ICD-9-CM Volume 3
Overview
Overview
ICD-9-CM Volume 3 is a system of procedural codes. It is a subset of ICD-9-CM (volumes 1 and 2 are used for diagnostic codes.)
The United States National Center for Health Statistics drafted ICD-10-PCS in 2000 as a potential replacement for ICD-9-CM Volume 3, but the World Health Organization (WHO) has neither set an implementation date for ICD-10-PCS nor set a phase-out date for ICD-9-CM. Hence, ICD-9-CM Volume 3 is still in effect.
Main sections
Main sections
(00) Procedures and interventions, not elsewhere classified
(00) Procedures and interventions, not elsewhere classified
- (Template:ICD9proc) Procedures and interventions, not elsewhere classified
- (Template:ICD9proc) Procedures on blood vessels
- (Template:ICD9proc) Percutaneous angioplasty or atherectomy of precerebral (extracranial) vessel(s)
- (Template:ICD9proc) Procedures on blood vessels
(01-05) Operations on the nervous system
(01-05) Operations on the nervous system
- (Template:ICD9proc) Incision and excision of skull, brain, and cerebral meninges
- (Template:ICD9proc) Craniotomy and craniectomy
- (Template:ICD9proc) Incision of brain and cerebral meninges
- (Template:ICD9proc) Other excision or destruction of brain and meninges
- (Template:ICD9proc) Other operations on skull, brain, and cerebral meninges
- (Template:ICD9proc) Operations on spinal cord and spinal canal structures
- (Template:ICD9proc) Exploration and decompression of spinal canal structures
- (Template:ICD9proc) Other exploration and decompression of spinal canal
- (Template:ICD9proc) Division of intraspinal nerve root
- (Template:ICD9proc) Chordotomy
- (Template:ICD9proc) Diagnostic procedures on spinal cord and spinal canal structures
- (Template:ICD9proc) Exploration and decompression of spinal canal structures
- (Template:ICD9proc) Operations on cranial and peripheral nerves
- (Template:ICD9proc) Incision, division, and excision of cranial and peripheral nerves
- (Template:ICD9proc) Gasserian ganglionectomy
- (Template:ICD9proc) Other cranial or peripheral ganglionectomy
- (Template:ICD9proc) Injection into peripheral nerve
- (Template:ICD9proc Injection of anesthetic into peripheral nerve for analgesia
- (Template:ICD9proc) Incision, division, and excision of cranial and peripheral nerves
- (Template:ICD9proc) Operations on sympathetic nerves or ganglia
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
The nervous system is a highly specialized network whose principal components are nerves called neurons. Neurons are interconnected to each other in complex arrangements, and have the property of conducting, using electrochemical signals, a great variety of stimuli both within the nervous tissue as well as from and towards most of the other tissues. Thus, neurons coordinate multiple functions in organisms. Nervous systems are found in many multicellular animals but differ greatly in complexity between species.

Nervous system in humans
The human nervous system can be observed both with gross anatomy, (which describes the parts that are large enough to be seen with the plain eye,) and microanatomy, (which describes the system at a cellular level.) At gross anatomy, the nervous system can be grouped in distinct organs, these being actually stations which the neural pathways cross through. Thus, with a didactical purpose, these organs, according to their ubication, can be divided in two parts: the central nervous system (CNS) and the peripheral nervous system (PNS).
Central nervous system
The central nervous system (CNS) represents the largest part of the nervous system, including the brain and the spinal cord. The CNS is contained within the dorsal cavity, with the brain within the cranial cavity, and the spinal cord in the spinal cavity. The CNS is covered by the meninges. The brain is also protected by the skull, and the spinal cord is also protected by the vertebrae. The nervous system can be connected into many systems that can function together. The two systems are central nervous system (CNS)and the peripheral nervous system (PNS).
Peripheral nervous system
The PNS consists of all the other nervous structures that do not lie within it. The large majority of what are commonly called nerves (which are actually axonal processes of nerve cells) are considered to be PNS.
Microanatomy
The nervous system is, on a small scale, primarily made up of neurons. However, glial cells also play a major role.
Neurons
They are the core components of both the central nervous system & peripheral nervous system. Neurons are sensors that send electric messages to the Central Nervous System which send the electric messages back to the neurons telling them how to react, where the messages are finally sent back directly to the brain. These messages travel at a usual pace of 100 meters per second.
Glial cells
Glial cells are non-neuronal cells that provide support and nutrition, maintain homeostasis, form myelin, and participate in signal transmission in the nervous system. In the human brain, glia are estimated to outnumber neurons by about 10 to 1.[1]
Glial cells provide support and protection for neurons. They are thus known as the “glue” of the nervous system. The four main functions of glial cells are to surround neurons and hold them in place, to supply nutrients and oxygen to neurons, to insulate one neuron from another, and to destroy pathogens and remove dead neurons.
Physiological division
A less anatomical but much more functional division of the human nervous system is that classifying it according to the role that the different neural pathways play, regardless whether these cross through the CNS or the PNS:
The somatic nervous system is responsible for coordinating the body’s movements, and also for receiving external stimuli. It is the system that regulates activities that are under conscious control.
The autonomic nervous system is then split into the sympathetic division, parasympathetic division, and enteric division. The sympathetic nervous system responds to impending danger or stress, and is responsible for the increase of one’s heartbeat and blood pressure, among other physiological changes, along with the sense of excitement one feels due to the increase of adrenaline in the system. The parasympathetic nervous system, on the other hand, is evident when a person is resting and feels relaxed, and is responsible for such things as the constriction of the pupil, the slowing of the heart, the dilation of the blood vessels, and the stimulation of the digestive and genitourinary systems. The role of the enteric nervous system is to manage every aspect of digestion, from the esophagus to the stomach, small intestine and colon.
In turn, these pathways can be divided according to the direction in which they conduct stimuli:
- Afferent system by sensory neurons, which carry impulses from a receptor to the CNS
- Efferent system by motor neurons, which carry impulses from the CNS to an effector
- Relay system by relay neurons (also called interneurons), which transmit impulses between the sensory and motor neurones.
A useful mnemonic to remember the nature of Afferent vs Efferent is SAME DAVE: Sensory Afferent, Motor Efferent; Dorsal Afferent, Ventral Efferent
However, there are relay neurons in the CNS as well.
The junction between two neurones is called a synapse. There is a very narrow gap (about 20nm in width) between the neurons – the synaptic cleft, where an action potential is transmitted from one neuron to a neighboring one. They do this by relaying the message with the use of neurotransmitters which the next neuron then receives the electrical signal, known as a nerve impulse. The nerve impulse is determined by the neurotransmitter to then carry the message to its appropriate destination. These nerve impulses are a change in ion balance in the nerve cell, which the central nervous system can then interpret. The fact that the nervous system uses a mixture of electrical and chemical signals makes it incredibly fast, which is necessary to acknowledge the presence of danger. For example, a hand touching a hot stove. If the nervous system was only comprised of chemical signals, the body would not tell the arm to move fast enough to escape dangerous burns. So the speed of the nervous system is a necessity for life.
| Physiological division | Somatic nervous system | Afferent system | ||
| Efferent system | ||||
| Autonomic nervous system | Sympathetic | Afferent system | ||
| Efferent system | ||||
| Parasympathetic | Afferent system | |||
| Efferent system | ||||
Development
Some landmarks of embryonic neural development include the birth and differentiation of neurons from stem cell precursors, the migration of immature neurons from their birthplaces in the embryo to their final positions, outgrowth of axons from neurons and guidance of the motile growth cone through the embryo towards postsynaptic partners, the generation of synapses between these axons and their postsynaptic partners, and finally the lifelong changes in synapses which are thought to underlie learning and memory.
Importance
Many people have lost basic motor skills and other skills because of spinal chord injuries. If this portion is damaged, the biggest nerve and the most important one gets damaged. This leads to paralysis or other permanent damages.
Abilities
The nervous system is able to make basic motor skills and other skills possible. The basic 5 senses of texture, taste, sight, smell,and hearing are powered by the nervous system. If disabled, basic motor skills may be lost.
Non-humans
Vertebrates
The nervous system of all vertebrate animals, is often divided into the central nervous system (CNS) and the peripheral nervous system (PNS). The CNS consists of the brain and spinal cord.
Worms
Planaria, a type of flatworm, have dual nerve cords running along the length of the body and merging at the tail and the mouth. These nerve cords are connected by transverse nerves like the rungs of a ladder. These transverse nerves help coordinate the two sides of the animal. Two large ganglia at the head end function similar to a simple brain. Photoreceptors on the animal’s eyespots provide sensory information on light and dark.
The nervous system of the roundworm Caenorhabditis elegans has been mapped out to the cellular level. Every neuron and its cellular lineage has been recorded and most, if not all, of the neural connections are known. In this species, the nervous system is sexually dimorphic; the nervous systems of the two sexes, males and hermaphrodites, have different numbers of neurons and groups of neurons that perform sex-specific functions. In C. elegans, males have exactly 383 neurons, while hermaphrodites have exactly 302 neurons [2]
Arthropoda
Arthropods, such as insects and crustaceans, have a nervous system made up of a series of ganglia, connected by a ventral nerve cord made up of two parallel connectives running along the length of the belly [3]. Typically, each body segment has one ganglion on each side, though some ganglia are fused to form the brain and other large ganglia [4].
The head segment contains the brain, also known as the supraesophageal ganglion. In the insect nervous system, the brain is anatomically divided into the protocerebrum, deutocerebrum, and tritocerebrum. Immediately behind the brain is the subesophageal ganglion, which is composed of three pairs of fused ganglia. It controls the mouthparts, the salivary glands and certain muscles.
Many arthropods have well-developed sensory organs, including compound eyes for vision and antennae for olfaction and pheromone sensation. The sensory information from these organs is processed by the brain.
Development
Neural development in most species have many similarities neural development in humans.
External links
- Neuroscience for Kids
- The Human Brain Project Homepage
- Kimball’s Biology Pages, CNS
- Kimball’s Biology Pages, PNS
Template:Organ systems Template:Nervous system Template:Somatosensory system
Template:Nervous system physiology Template:Diseases of the nervous system Template:Development of nervous system Template:Neurosurgical procedures
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(06-07) Operations on the endocrine system
(06-07) Operations on the endocrine system
- (Template:ICD9proc) Operations on thyroid and parathyroid glands
- (Template:ICD9proc) Incision of thyroid field
- (Template:ICD9proc) Diagnostic procedures on thyroid and parathyroid glands
- (Template:ICD9proc) Unilateral thyroid lobectomy
- (Template:ICD9proc) Other partial thyroidectomy
- (Template:ICD9proc) Complete thyroidectomy
- (Template:ICD9proc) Substernal thyroidectomy
- (Template:ICD9proc) Excision of lingual thyroid
- (Template:ICD9proc) Excision of thyroglossal duct or tract
- (Template:ICD9proc) Parathyroidectomy
- (Template:ICD9proc) Other operations on thyroid (region) and parathyroid
- (Template:ICD9proc) Operations on other endocrine glands
- (Template:ICD9proc) Exploration of adrenal field
- (Template:ICD9proc) Diagnostic procedures on adrenal glands, pituitary gland, pineal gland, and thymus
- (Template:ICD9proc) Partial adrenalectomy
- (Template:ICD9proc) Bilateral adrenalectomy
- (Template:ICD9proc) Other operations on adrenal glands, nerves, and vessels
- (Template:ICD9proc) Operations on pineal gland
- (Template:ICD9proc) Hypophysectomy
- (Template:ICD9proc) Other operations on hypophysis
- (Template:ICD9proc) Thymectomy
- (Template:ICD9proc) Other operations on thymus

Editors-In-Chief: C. Michael Gibson, M.S., M.D. [1] and Stephanie Fernandez, M.D. [2]
The endocrine system is an integrated system of small organs that involve the release of extracellular signaling molecules known as hormones. The endocrine system is instrumental in regulating metabolism, growth and development and puberty, tissue function, and plays a part also in mood.[1] The field of medicine that deals with disorders of endocrine glands is endocrinology, a branch of the wider field of internal medicine.
Function
The Endocrine system is an information signal system much like the nervous system. However, the nervous system uses nerves to conduct information, whereas the endocrine system mainly uses blood vessels as information channels. Glands located in many regions of the body release into the bloodstream specific chemical messengers called hormones. Hormones regulate the many and varied functions of an organism, e.g., mood, growth and development, tissue function, and metabolism, as well as sending messages and acting on them.
Types of signaling
The typical mode of cell signaling in the endocrine system is endocrine signaling. However, there are also other modes, i.e., paracrine, autocrine, and neuroendocrine signaling [2]. Purely neurocrine signaling between neurons, on the other hand, belongs completely to the nervous system.
Endocrine
A number of glands that signal each other in sequence is usually referred to as an axis, for example the Hypothalamic-pituitary-adrenal axis.
Typical endocrine glands are the pituitary, thyroid, and adrenal glands. Features of endocrine glands are, in general, their ductless nature, their vascularity, and usually the presence of intracellular vacuoles or granules storing their hormones. In contrast exocrine glands such as salivary glands, sweat glands, and glands within the gastrointestinal tract tend to be much less vascular and have ducts or a hollow lumen.
Autocrine
Other signaling can target the same cell.
Paracrine
Paracrine signaling is where the target cell is nearby.
Juxtacrine
Juxtacrine signals are transmitted along cell membranes via protein or lipid components integral to the membrane and are capable of affecting either the emitting cell or cells immediately adjacent.
Role in disease
Diseases of the endocrine system are common,[3] including diseases such as diabetes mellitus, thyroid disease, and obesity. Endocrine disease is characterised by dysregulated hormone release (a productive Pituitary adenoma), inappropriate response to signalling (Hypothyroidism), lack or destruction of a gland (Diabetes mellitus type 1, diminished erythropoiesis in Chronic renal failure), or structural enlargement in a critical site such as the neck (Toxic multinodular goitre). Hypofunction of endocrine glands can occur as result of loss of reserve, hyposecretion, agenesis, atrophy, or active destruction. Hyperfunction can occur as result of hypersecretion, loss of suppression, hyperplastic, or neoplastic change, or hyperstimulation.
Endocrinopathies are classified as primary, secondary, or tertiary. Primary endocrine disease inhibits the action of downstream glands. Tertiary endocrine disease is associated with dysfunction of the hypothalamus and its releasing hormones.
Cancer can occur in endocrine glands, such as the thyroid, and hormones have been implicated in signalling distant tissues to proliferate, for example the Estrogen receptor has been shown to be involved in certain breast cancers. Endocrine, Paracrine, and autocrine signalling have all been implicated in proliferation, one of the required steps of oncogenesis.[4]
Table of endocrine glands and secreted hormones
This is a table of the glands of the endocrine system, and their secreted hormones
| Secreted hormone | From cells | Effect |
|---|---|---|
| Melatonin (Primarily) | Pinealocytes | antioxidant and causes drowsiness |
Pituitary gland (hypophysis)
Anterior pituitary lobe (adenohypophysis)
| Secreted hormone | Abbreviation | From cells | Effect |
|---|---|---|---|
| Growth hormone | GH | Somatotropes | stimulates growth and cell reproduction
Release Insulin-like growth factor 1 from liver |
| Prolactin | PRL | Lactotropes | milk production in mammary glands sexual gratification after sexual acts |
| Adrenocorticotropic hormone or corticotropin | ACTH | Corticotropes | synthesis of corticosteroids (glucocorticoids and androgens) in adrenocortical cells |
| Lipotropin | Corticotropes | lipolysis and steroidogenesis, stimulates melanocytes to produce melanin | |
| Thyroid-stimulating hormone or thyrotropin | TSH | Thyrotropes | stimulates thyroid gland to secrete thyroxine (T4) and triiodothyronine (T3) |
| Follicle-stimulating hormone | FSH | Gonadotropes | In female: stimulates maturation of Graafian follicles in ovary.
In male: spermatogenesis, enhances production of androgen-binding protein by the Sertoli cells of the testes |
| Luteinizing hormone | LH | Gonadotropes | In female: ovulation
In male: stimulates Leydig cell production of testosterone |
Posterior pituitary lobe (neurohypophysis)
| Secreted hormone | Abbreviation | From cells | Effect |
|---|---|---|---|
| Oxytocin | Magnocellular neurosecretory cells | Contraction of cervix and vagina
Involved in orgasm, trust between people.[5] and circadian homeostasis (body temperature, activity level, wakefulness) [6]. release breast milk | |
| Vasopressin or antidiuretic hormone | AVP or ADH | Magnocellular neurosecretory cells | retention of water in kidneys
moderate vasoconstriction |
Intermediate pituitary lobe (pars intermedia)
| Secreted hormone | Abbreviation | From cells | Effect |
|---|---|---|---|
| Melanocyte-stimulating hormone | MSH | Melanotroph | melanogenesis by melanocytes in skin and hair. |
| Secreted hormone | Abbreviation | From cells | Effect |
|---|---|---|---|
| Triiodothyronine | T3 | Thyroid epithelial cell | potent form of thyroid hormone: increase the basal metabolic rate & sensitivity to catecholamines,
affect protein synthesis |
| Thyroxine or tetraiodothyronine | T4 | Thyroid epithelial cells | less active form of thyroid hormone: increase the basal metabolic rate & sensitivity to catecholamines,
affect protein synthesis |
| Calcitonin | Parafollicular cells | Construct bone
reduce blood Ca2+ |
| Secreted hormone | Abbreviation | From cells | Effect |
|---|---|---|---|
| Parathyroid hormone | PTH | Parathyroid chief cell | increase blood Ca2+: *indirectly stimulate osteoclasts
(Slightly) decrease blood phosphate: |
| Secreted hormone | Abbreviation | From cells | Effect |
|---|---|---|---|
| Atrial-natriuretic peptide | ANP | Cardiac myocytes | Reduce blood pressure by:
reducing systemic vascular resistance, reducing blood water, sodium and fats |
| Brain natriuretic peptide | BNP | Cardiac myocytes | (To a minor degree than ANP) reduce blood pressure by:
reducing systemic vascular resistance, reducing blood water, sodium and fats |
| Secreted hormone | From cells | Effect |
|---|---|---|
| Thrombopoietin | Myocytes | stimulates megakaryocytes to produce platelets[7] |
| Secreted hormone | From cells | Effect |
|---|---|---|
| Calcidiol (25-hydroxyvitamin D3) | Inactive form of Vitamin D3 |
| Secreted hormone | From cells | Effect |
|---|---|---|
| Leptin (Primarily) | Adipocytes | decrease of appetite and increase of metabolism. |
| Estrogens[8] (mainly Estrone) | Adipocytes |
| Secreted hormone | Abbreviation | From cells | Effect |
|---|---|---|---|
| Gastrin (Primarily) | G cells | Secretion of gastric acid by parietal cells | |
| Ghrelin | P/D1 cells | Stimulate appetite,
secretion of growth hormone from anterior pituitary gland | |
| Neuropeptide Y | NPY | increased food intake and decreased physical activity | |
| Secretin | S cells | Secretion of bicarbonate from liver, pancreas and duodenal Brunner’s glands
Enhances effects of cholecystokinin Stops production of gastric juice | |
| Somatostatin | D cells | Suppress release of gastrin, cholecystokinin (CCK), secretin, motilin, vasoactive intestinal peptide (VIP), gastric inhibitory polypeptide (GIP), enteroglucagon
Lowers rate of gastric emptying Reduces smooth muscle contractions and blood flow within the intestine [9] | |
| Histamine | ECL cells | stimulate gastric acid secretion | |
| Endothelin | X cells | Smooth muscle contraction of stomach [10] |
| Secreted hormone | From cells | Effect |
|---|---|---|
| Cholecystokinin | I cells | Release of digestive enzymes from pancreas
Release of bile from gallbladder hunger suppressant |
| Secreted hormone | Abbreviation | From cells | Effect |
|---|---|---|---|
| Insulin-like growth factor (or somatomedin) (Primarily) | IGF | Hepatocytes | insulin-like effects
regulate cell growth and development |
| Angiotensinogen and angiotensin | Hepatocytes | vasoconstriction
release of aldosterone from adrenal cortex dipsogen. | |
| Thrombopoietin | Hepatocytes | stimulates megakaryocytes to produce platelets[7] |
| Secreted hormone | From cells | Effect |
|---|---|---|
| Insulin (Primarily) | ß Islet cells | Intake of glucose, glycogenesis and glycolysis in liver and muscle from blood
intake of lipids and synthesis of triglycerides in adipocytes Other anabolic effects |
| Glucagon (Also Primarily) | a Islet cells | glycogenolysis and gluconeogenesis in liver
increases blood glucose level |
| Somatostatin | d Islet cells | Inhibit release of insulin [11]
Inhibit release of glucagon[11] Suppress the exocrine secretory action of pancreas. |
| Pancreatic polypeptide | PP cells | Unknown |
| Secreted hormone | From cells | Effect |
|---|---|---|
| Renin (Primarily) | Juxtaglomerular cells | Activates the renin-angiotensin system by producing angiotensin I of angiotensinogen |
| Erythropoietin (EPO) | Extraglomerular mesangial cells | Stimulate erythrocyte production |
| Calcitriol (1,25-dihydroxyvitamin D3) | Active form of vitamin D3
Increase absorption of calcium and phosphate from gastrointestinal tract and kidneys inhibit release of PTH | |
| Thrombopoietin | stimulates megakaryocytes to produce platelets[7] |
| Secreted hormone | From cells | Effect |
|---|---|---|
| Glucocorticoids (chiefly cortisol) | zona fasciculata and zona reticularis cells | Stimulation of gluconeogenesis
Inhibition of glucose uptake in muscle and adipose tissue Mobilization of amino acids from extrahepatic tissues Stimulation of fat breakdown in adipose tissue anti-inflammatory and immunosuppressive |
| Mineralocorticoids (chiefly aldosterone) | Zona glomerulosa cells | Increase blood volume by reabsorption of sodium in kidneys (primarily) |
| Androgens (including DHEA and testosterone) | Zona fasciculata and Zona reticularis cells | Virilization, anabolic |
| Secreted hormone | From cells | Effect |
|---|---|---|
| Adrenaline (epinephrine) (Primarily) | Chromaffin cells | Fight-or-flight response:
|
| Noradrenaline (norepinephrine) | Chromaffin cells | Fight-or-flight response:
|
| Dopamine | Chromaffin cells | Increase heart rate and blood pressure |
| Enkephalin | Chromaffin cells | Regulate pain |
| Secreted hormone | From cells | Effect |
|---|---|---|
| Androgens (chiefly testosterone) | Leydig cells | Anabolic: growth of muscle mass and strength, increased bone density, growth and strength,
Virilizing: maturation of sex organs, formation of scrotum, deepening of voice, growth of beard and axillary hair. |
| Estradiol | Sertoli cells | Prevent apoptosis of germ cells[12] |
| Inhibin | Sertoli cells | Inhibit production of FSH |
These originate either from the ovarian follicle or the corpus luteum.
| Secreted hormone | From cells | Effect |
|---|---|---|
| Progesterone | Granulosa cells, theca cells | Support pregnancy[13]:
Other:
|
| Androstenedione | Theca cells | Substrate for estrogen |
| Estrogens (mainly estradiol) | Granulosa cells | Structural:
Protein synthesis:
Fluid balance:
Gastrointestinal tract:
Melanin:
Cancer:
Lung function: |
| Inhibin | Granulosa cells | Inhibit production of FSH from anterior pituitary |
| Secreted hormone | Abbreviation | From cells | Effect |
|---|---|---|---|
| Progesterone (Primarily) | Support pregnancy[13]:
Other effects on mother similar to ovarian follicle-progesterone | ||
| Estrogens (mainly Estriol) (Also Primarily) | Effects on mother similar to ovarian follicle estrogen | ||
| Human chorionic gonadotropin | HCG | Syncytiotrophoblast | promote maintenance of corpus luteum during beginning of pregnancy
Inhibit immune response, towards the human embryo. |
| Human placental lactogen | HPL | Syncytiotrophoblast | increase production of insulin and IGF-1
increase insulin resistance and carbohydrate intolerance |
| Inhibin | Fetal Trophoblasts | suppress FSH |
| Secreted hormone | Abbreviation | From cells | Effect |
|---|---|---|---|
| Prolactin | PRL | Decidual cells | milk production in mammary glands |
| Relaxin | Decidual cells | Unclear in humans |
See also
- Releasing hormones
- Neuroendocrinology
- Nervous system
- Endocrine disruptor
- Major systems of the human body
Links
References
- ↑ Collier, Judith. et.al (2006). Oxford Handbook of Clinical Specialties 7th edn. Oxford. pp. 350–351. ISBN 0-19-853085-4.
- ↑ University of Virginia – HISTOLOGY OF THE ENDOCRINE GLANDS
- ↑ Kasper; et al. (2005). Harrison’s Principles of Internal Medicine. McGraw Hill. p. 2074. ISBN 0-07-139140-1.
- ↑ Bhowmick NA, Chytil A, Neilson EG, Moses HL (2004). “TGF-beta signaling in fibroblasts modulates the oncogenic potential of adjacent epithelia”. Science. Feb 6 303(5659): 848–51.
- ↑ Kosfeld M et al. (2005) Oxytocin increases trust in humans. Nature 435:673-676. PDF PMID 15931222
- ↑ Scientific American Mind, “Rhythm and Blues”; June/July 2007; Scientific American Mind; by Ulrich Kraft
- ↑ 7.0 7.1 7.2 Kaushansky K. Lineage-specific hematopoietic growth factors. N Engl J Med 2006;354:2034-45. PMID 16687716.
- ↑ The adipose tissue as a source of vasoactive factors. Frühbeck G. (Curr Med Chem Cardiovasc Hematol Agents. 2004 Jul;2(3):197-208.)
- ↑ http://www.vivo.colostate.edu/hbooks/pathphys/endocrine/otherendo/somatostatin.html Colorado State University – Biomedical Hypertextbooks – Somatostatin
- ↑ Diabetes-related changes in contractile responses of stomach fundus to endothelin-1 in streptozotocin-induced diabetic rats Journal of Smooth Muscle Research Vol. 41 (2005) , No. 1 35-47. Kazuki Endo1), Takayuki Matsumoto1), Tsuneo Kobayashi1), Yutaka Kasuya1) and Katsuo Kamata1)
- ↑ 11.0 11.1 Essentials of Human Physiology by Thomas M. Nosek. Section 5/5ch4/s5ch4_17.
- ↑ Pentikäinen V, Erkkilä K, Suomalainen L, Parvinen M, Dunkel L. Estradiol Acts as a Germ Cell Survival Factor in the Human Testis in vitro. The Journal of Clinical Endocrinology & Metabolism 2006;85:2057-67 PMID 10843196
- ↑ 13.0 13.1 13.2 13.3 http://www.vivo.colostate.edu/hbooks/pathphys/reprod/placenta/endocrine.html
- ↑ Essentials of Human Physiology by Thomas M. Nosek. Section 5/5ch9/s5ch9_13.
- ↑ Hould F, Fried G, Fazekas A, Tremblay S, Mersereau W (1988). “Progesterone receptors regulate gallbladder motility”. J Surg Res. 45 (6): 505–12. PMID 3184927.
- ↑ http://www.breastcancer.org/tre_sys_hrt_idx.html
- ↑ Massaro D, Massaro GD (2004). “Estrogen regulates pulmonary alveolar formation, loss, and regeneration in mice”. American Journal of Physiology. Lung Cellular and Molecular Physiology. 287 (6): L1154–9. PMID 15298854 url=http://ajplung.physiology.org/cgi/content/full/287/6/L1154.
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(08-16) Operations on the eye
(08-16) Operations on the eye
- (Template:ICD9proc) Operations on eyelids
- (Template:ICD9proc) Operations on lacrimal system
- (Template:ICD9proc) Operations on conjunctiva
- (Template:ICD9proc) Operations on cornea
- (Template:ICD9proc) Corneal transplant
- (Template:ICD9proc) Other reconstructive and refractive surgery on cornea
- (Template:ICD9proc) Operations on iris, ciliary body, sclera, and anterior chamber
- (Template:ICD9proc) Operations on lens
- Cataract surgery
- (Template:ICD9proc) Phacoemulsification and aspiration of cataract
- (Template:ICD9proc) Operations on retina, choroid, vitreous, and posterior chamber
- (Template:ICD9proc) Removal of foreign body from posterior segment of eye
- (Template:ICD9proc) Diagnostic procedures on retina, choroid, vitreous, and posterior chamber
- (Template:ICD9proc) Destruction of lesion of retina and choroid
- (Template:ICD9proc) Repair of retinal tear
- (Template:ICD9proc) Repair of retinal detachment with scleral buckling and implant
- (Template:ICD9proc) Other repair of retinal detachment
- (Template:ICD9proc) Removal of surgically implanted material from posterior segment of eye
- (Template:ICD9proc) Operations on vitreous
- (Template:ICD9proc) Other operations on retina, choroid, and posterior chamber
- (Template:ICD9proc) Operations on extraocular muscles
- (Template:ICD9proc) Operations on orbit and eyeball
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Eyes are organs that detect light. Different kinds of light-sensitive organs are found in a variety of animals. The simplest eyes do nothing but detect whether the surroundings are light or dark, which is sufficient for the entrainment of circadian rhythms but hardly can be called vision. More complex eyes can distinguish shapes and colors. The visual fields of some such complex eyes largely overlap, to allow better depth perception (binocular vision), as in humans; and others are placed so as to minimize the overlap, such as in rabbits and chameleons.
In the human eye, light enters the pupil and is focused on the retina by the lens. Light-sensitive nerve cells called rods (for brightness) and cones (for color) react to the light. They interact with each other and send messages to the brain that indicate brightness, color, and contour.
The first proto-eyes evolved among animals 540 million years ago. Almost all animals have eyes, or descend from animals that did.
In most vertebrates and some mollusks, the eye works by allowing light to enter it and project onto a light-sensitive panel of cells, known as the retina, at the rear of the eye. The cone cells (for colour) and the rod cells (for low-light contrasts) in the retina detect and convert light into neural signals. The visual signals are then transmitted to the brain via the optic nerve. Such eyes are typically roughly spherical, filled with a transparent gel-like substance called the vitreous humour, with a focusing lens and often an iris which regulates the intensity of the light that enters the eye. The eyes of cephalopods, fish, amphibians and snakes usually have fixed lens shapes, and focusing vision is achieved by telescoping the lens—similar to how a camera focuses.
Compound eyes are found among the arthropods and are composed of many simple facets which give a pixelated image (not multiple images, as is often believed). Each sensor has its own lens and photosensitive cell(s). Some eyes have up to 28,000 such sensors, which are arranged hexagonally, and which can give a full 360-degree field of vision. Compound eyes are very sensitive to motion. Some arthropods, including many Strepsiptera, have compound eyes of only a few facets, each with a retina capable of creating an image, creating multiple-image vision. With each eye viewing a different angle, a fused image from all the eyes is produced in the brain, providing very wide-angle, high-resolution images.
Possessing detailed hyperspectral color vision, the Mantis shrimp has been reported to have the world’s most complex color vision system.[1] Trilobites, which are now extinct, had unique compound eyes. They used clear calcite crystals to form the lenses of their eyes. In this, they differ from most other arthropods, which have soft eyes. The number of lenses in such an eye varied, however: some trilobites had only one, and some had thousands of lenses in one eye.
Some of the simplest eyes, called ocelli, can be found in animals like snails, who cannot actually “see” in the normal sense. They do have photosensitive cells, but no lens and no other means of projecting an image onto these cells. They can distinguish between light and dark, but no more. This enables snails to keep out of direct sunlight. Jumping spiders have simple eyes that are so large, supported by an array of other, smaller eyes, that they can get enough visual input to hunt and pounce on their prey. Some insect larvae, like caterpillars, have a different type of simple eye (stemmata) which gives a rough image.
Evolution of eyes
Biologists use the theory of evolution to explain the origin and development of eyes, as well as of organs in general.
The common origin (monophyly) of all animal eyes is established by shared anatomical and genetic features of all eyes; that is, all modern eyes, varied as they are, have their origins in a proto-eye evolved some 540 million years ago.[2][3][4] The majority of the advancements in early eyes are believed to have taken only a few million years to develop, as the first predator to gain true imaging would have touched off an “arms race”,[5] or rather, a phylogenetic radiation from the species with that first proto-eye, among the descendents of which, there may well have been an “arms race”. Prey animals and competing predators alike would be forced to rapidly match or exceed any such capabilities to survive. Hence multiple eye types and subtypes developed in parallel.
Vision in various animals shows adaptation to environmental requirements. For example, birds of prey have much greater visual acuity than humans, and some can see ultraviolet light. The different forms of eyes in, for example, vertebrates and mollusks are often cited as examples of parallel evolution, despite their distant common ancestry.
The earliest eyes, called “eyespots”, were simple patches of photoreceptor cells, or light-sensitive proteins in unicellular organisms, physically similar to the receptor patches for taste and smell. These eyespots could only sense ambient brightness: they could distinguish light and dark, but not the direction of the lightsource.[6] This gradually changed as the eyespot depressed into a shallow “cup” shape, granting the ability to slightly discriminate directional brightness by using the angle at which the light hit certain cells to identify the source. The pit deepened over time, the opening diminished in size, and the number of photoreceptor cells increased, forming an effective pinhole camera that was capable of slightly distinguishing dim shapes.[7]
The thin overgrowth of transparent cells over the eye’s aperture, originally formed to prevent damage to the eyespot, allowed the segregated contents of the eye chamber to specialize into a transparent humour that optimized color filtering, blocked harmful radiation, improved the eye’s refractive index, and allowed functionality outside of water. The transparent protective cells eventually split into two layers, with circulatory fluid in between that allowed wider viewing angles and greater imaging resolution, and the thickness of the transparent layer gradually increased, in most species with the transparent crystallin protein.[8]
Anatomy of the mammalian eye
Three layers
The structure of the mammalian eye can be divided into three main layers or tunics whose names reflect their basic functions: the fibrous tunic, the vascular tunic, and the nervous tunic.[9][10][11]
- The fibrous tunic, also known as the tunica fibrosa oculi, is the outer layer of the eyeball consisting of the cornea and sclera.[12] The sclera gives the eye most of its white color. It consists of dense connective tissue filled with the protein collagen to both protect the inner components of the eye and maintain its shape.[13]
- The vascular tunic, also known as the tunica vasculosa oculi, is the middle vascularized layer which includes the iris, ciliary body, and choroid.[12][14][15] The choroid contains blood vessels that supply the retinal cells with necessary oxygen and remove the waste products of respiration. The choroid gives the inner eye a dark color, which prevents disruptive reflections within the eye.
- The nervous tunic, also known as the tunica nervosa oculi, is the inner sensory which includes the retina.[12][15] The retina contains the photosensitive rod and cone cells and associated neurons. To maximise vision and light absorption, the retina is a relatively smooth (but curved) layer. It has two points at which it is different; the fovea and optic disc. The fovea is a dip in the retina directly opposite the lens, which is densely packed with cone cells. It is largely responsible for color vision in humans, and enables high acuity, such as is necessary in reading. The optic disc, sometimes referred to as the anatomical blind spot, is a point on the retina where the optic nerve pierces the retina to connect to the nerve cells on its inside. No photosensitive cells exist at this point, it is thus “blind”. In addition to the rods and cones, a small proportion (about 2% in humans) of the ganglion cells in the retina are photosensitive through the pigment melanopsin. They are generally most excitable by blue light, about 470 nm. Their information is sent to the SCN (suprachiasmatic nuclei), not to the visual center, through the retinohypothalamic tract, not via the optic nerve. It is these light signals which regulate circadian rhythms in mammals and several other animals. Many, but not all, totally blind individuals have their circadian rhythms adjusted daily in this way.
Anterior and posterior segments
The mammalian eye can also be divided into two main segments: the anterior segment and the posterior segment.[16]
Posterior segment

The posterior segment is the back two-thirds of the eye that includes the anterior hyaloid membrane and all structures behind it: the vitreous humor, retina, choroid, and optic nerve.[17] On the other side of the lens is the second humour, the vitreous humour, which is bounded on all sides: by the lens, ciliary body, suspensory ligaments and by the retina. It lets light through without refraction, helps maintain the shape of the eye and suspends the delicate lens. In some animals, the retina contains a reflective layer (the tapetum lucidum) which increases the amount of light each photosensitive cell perceives, allowing the animal to see better under low light conditions.
Extraocular anatomy
In many species, the eyes are inset in the portion of the skull known as the orbits or eyesockets. This placement of the eyes helps to protect them from injury.
In humans, the eyebrows redirect flowing substances (such as rainwater or sweat) away from the eye. Water in the eye can alter the refractive properties of the eye and blur vision. It can also wash away the tear fluid—along with it the protective lipid layer—and can alter corneal physiology, due to osmotic differences between tear fluid and freshwater. Osmotic effects are made apparent when swimming in freshwater pools, as the osmotic gradient draws “pool water” into the corneal tissue (the pool water is hypotonic), causing edema, and subsequently leaving the swimmer with “cloudy” or “misty” vision for a short period thereafter. The edema can be reversed by irrigating the eye with hypertonic saline which osmotically draws the excess water out of the eye.
In many animals, including humans, eyelids wipe the eye and prevent dehydration. They spread tears on the eyes, which contains substances which help fight bacterial infection as part of the immune system. Some aquatic animals have a second eyelid in each eye which refracts the light and helps them see clearly both above and below water. Most creatures will automatically react to a threat to its eyes (such as an object moving straight at the eye, or a bright light) by covering the eyes, and/or by turning the eyes away from the threat. Blinking the eyes is, of course, also a reflex.
In many animals, including humans, eyelashes prevent fine particles from entering the eye. Fine particles can be bacteria, but also simple dust which can cause irritation of the eye, and lead to tears and subsequent blurred vision.
Cytology
The structure of the mammalian eye owes itself completely to the task of focusing light onto the retina. This light causes chemical changes in the photosensitive cells of the retina, the products of which trigger nerve impulses which travel to the brain.
The retina contains two forms of photosensitive cells important to vision—rods and cones. Though structurally and metabolically similar, their function is quite different. Rod cells are highly sensitive to light, allowing them to respond in dim light and dark conditions; however, they cannot detect color differences. These are the cells that allow humans and other animals to see by moonlight, or with very little available light (as in a dark room). Cone cells, conversely, need high light intensities to respond and have high visual acuity. Different cone cells respond to different wavelengths of light, which allows an organism to see color. The shift from cone vision to rod vision is why the darker conditions become, the less color objects seem to have.
The differences between rods and cones are useful; apart from enabling sight in both dim and light conditions, they have further advantages. The fovea, directly behind the lens, consists of mostly densely-packed cone cells. The fovea gives humans a highly detailed central vision, allowing reading, bird watching, or any other task which primarily requires staring at things. Its requirement for high intensity light does cause problems for astronomers, as they cannot see dim stars, or other celestial objects, using central vision because the light from these is not enough to stimulate cone cells. Because cone cells are all that exist directly in the fovea, astronomers have to look at stars through the “corner of their eyes” (averted vision) where rods also exist, and where the light is sufficient to stimulate cells, allowing an individual to observe faint objects.
Rods and cones are both photosensitive, but respond differently to different frequencies of light. They contain different pigmented photoreceptor proteins. Rod cells contain the protein rhodopsin and cone cells contain different proteins for each color-range. The process through which these proteins go is quite similar — upon being subjected to electromagnetic radiation of a particular wavelength and intensity, the protein breaks down into two constituent products. Rhodopsin, of rods, breaks down into opsin and retinal; iodopsin of cones breaks down into photopsin and retinal. The opsin in each opens ion channels on the cell membrane, which leads to hyperpolarization; this hyperpolarization of the cell leads to a release of transmitter molecules at the synapse.
Differences between the rhodopsin and the iodopsins is the reason why cones and rods enable organisms to see in dark and light conditions — each of the photoreceptor proteins requires a different light intensity to break down into the constituent products. Further, synaptic convergence means that several rod cells are connected to a single bipolar cell, which then connects to a single ganglion cell by which information is relayed to the visual cortex. This convergence is in direct contrast to the situation with cones, where each cone cell is connected to a single bipolar cell. This divergence results in the high visual acuity, or the high ability to distinguish detail, of cone cells compared to rods. If a ray of light were to reach just one rod cell, the cell’s reponse may not be enough to hyperpolarize the connected bipolar cell. But because several “converge” onto a bipolar cell, enough transmitter molecules reach the synapses of the bipolar cell to hyperpolarize it.
Furthermore, color is distinguishable due to the different iodopsins of cone cells; there are three different kinds, in normal human vision, which is why we need three different primary colors to make a color space.
Acuity
Visual acuity is often measured in cycles per degree (CPD), which measures an angular resolution, or how much an eye can differentiate one object from another in terms of visual angles. Resolution in CPD can be measured by bar charts of different numbers of white–black stripe cycles. For example, if each pattern is 1.75 cm wide and is placed at 1 m distance from the eye, it will subtend an angle of 1 degree, so the number of white–black bar pairs on the pattern will be a measure of the cycles per degree of that pattern. The highest such number that the eye can resolve as stripes, or distinguish from a gray block, is then the measurement of visual acuity of the eye.
For a human eye with excellent acuity, the maximum theoretical resolution would be 50 CPD[18] (1.2 minute of arc per line pair, or a 0.35 mm line pair, at 1 m). However, the eye can only resolve a contrast of 5%. Taking this into account, the eye can resolve a maximum resolution of 37 CPD, or 1.6 minute of arc per line pair (0.47 mm line pair, at 1 m). [19] A rat can resolve only about 1 to 2 CPD.[20] A horse has higher acuity through most of the visual field of its eyes than a human has, but does not match the high acuity of the human eye’s central fovea region.
Equivalent resolution
A maximum resolution of the human eye in good light of 1.6 minute of arc per line pair will correspond to 1.25 lines per minute of arc. Assuming two pixels per line pair (one pixel per line) and a square field of 120 degrees, this would be equivalent to approximately 120×60×1.25 = 9000 pixels in each of the X and Y dimensions, or about 81 megapixels.
However, the human eye itself has only a small spot of sharp vision in the middle of the retina, the fovea centralis, the rest of the field of view being progressively lower resolution as it gets further from the fovea. The angle of the sharp vision being just a few degrees in the middle of the view, the sharp area thus barely achieves even a single megapixel resolution. The experience of wide sharp human vision is in fact based on turning the eyes towards the current point of interest in the field of view, the brain thus perceiving an observation of a wide sharp field of view.
The narrow beam of sharp vision is easy to test by putting a fingertip on a newspaper and trying to read the text while staring at the fingertip — it is very difficult to read text that’s just a few centimeters away from the fingertip.
Spectral response
Human eyes respond to light with wavelength in the range of approximately 400 to 700 nm. Other animals have other ranges, with many such as birds including a significant ultraviolet (shorter than 400 nm) response.
Dynamic range
The retina has a static contrast ratio of around 100:1 (about 6 1/2 stops). As soon as the eye moves (saccades) it re-adjusts its exposure both chemically and by adjusting the iris. Initial dark adaptation takes place in approximately four seconds of profound, uninterrupted darkness; full adaptation through adjustments in retinal chemistry (the Purkinje effect) are mostly complete in thirty minutes. Hence, a dynamic contrast ratio of about 1,000,000:1 (about 20 stops) is possible. The process is nonlinear and multifaceted, so an interruption by light nearly starts the adaptation process over again. Full adaptation is dependent on good blood flow; thus dark adaptation may be hampered by poor circulation, and vasoconstrictors like alcohol or tobacco.
Eye movement

The visual system in the brain is too slow to process that information if the images are slipping across the retina at more than a few degrees per second.[21] Thus, for humans to be able to see while moving, the brain must compensate for the motion of the head by turning the eyes. Another complication for vision in frontal-eyed animals is the development of a small area of the retina with a very high visual acuity. This area is called the fovea, and covers about 2 degrees of visual angle in people. To get a clear view of the world, the brain must turn the eyes so that the image of the object of regard falls on the fovea. Eye movements are thus very important for visual perception, and any failure to make them correctly can lead to serious visual disabilities.
Having two eyes is an added complication, because the brain must point both of them accurately enough that the object of regard falls on corresponding points of the two retinas; otherwise, double vision would occur. The movements of different body parts are controlled by striated muscles acting around joints. The movements of the eye are no exception, but they have special advantages not shared by skeletal muscles and joints, and so are considerably different.
Extraocular muscles
Each eye has six muscles that control its movements: the lateral rectus, the medial rectus, the inferior rectus, the superior rectus, the inferior oblique, and the superior oblique. When the muscles exert different tensions, a torque is exerted on the globe that causes it to turn, in almost pure rotation, with only about one millimeter of translation.[22] Thus, the eye can be considered as undergoing rotations about a single point in the center of the eye. Once the human eye sustains damage to the optic nerve, the impulses will not be taken to the brain. Eye transplants can happen but the person receiving the transplant will not be able to see. As for the optic nerve, once it is damaged it cannot be fixed.
Rapid eye movement
Rapid eye movement, or REM for short, typically refers to the stage during sleep during which the most vivid dreams occur. During this stage, the eyes move rapidly. It is not in itself a unique form of eye movement.
Saccades
Saccades are quick, simultaneous movements of both eyes in the same direction controlled by the frontal lobe of the brain.
Microsaccades
Even when looking intently at a single spot, the eyes drift around. This ensures that individual photosensitive cells are continually stimulated in different degrees. Without changing input, these cells would otherwise stop generating output. Microsaccades move the eye no more than a total of 0.2° in adult humans.
Vestibulo-ocular reflex
The vestibulo-ocular reflex is a reflex eye movement that stabilizes images on the retina during head movement by producing an eye movement in the direction opposite to head movement, thus preserving the image on the center of the visual field. For example, when the head moves to the right, the eyes move to the left, and vice versa.
Smooth pursuit movement
The eyes can also follow a moving object around. This tracking is less accurate than the vestibulo-ocular reflex, as it requires the brain to process incoming visual information and supply feedback. Following an object moving at constant speed is relatively easy, though the eyes will often make saccadic jerks to keep up. The smooth pursuit movement can move the eye at up to 100°/s in adult humans.
It is more difficult to visually estimate speed in low light conditions or while moving, unless there is another point of reference for determining speed.
Optokinetic reflex
The optokinetic reflex is a combination of a saccade and smooth pursuit movement. When, for example, looking out of the window in a moving train, the eyes can focus on a ‘moving’ tree for a short moment (through smooth pursuit), until the tree moves out of the field of vision. At this point, the optokinetic reflex kicks in, and moves the eye back to the point where it first saw the tree (through a saccade).
Vergence movement
File:Stereogram Tut Eye Convergence.png
When a creature with binocular vision looks at an object, the eyes must rotate around a vertical axis so that the projection of the image is in the centre of the retina in both eyes. To look at an object closer by, the eyes rotate ‘towards each other’ (convergence), while for an object farther away they rotate ‘away from each other’ (divergence). Exaggerated convergence is called cross eyed viewing (focusing on the nose for example) . When looking into the distance, or when ‘staring into nothingness’, the eyes neither converge nor diverge.
Vergence movements are closely connected to accommodation of the eye. Under normal conditions, changing the focus of the eyes to look at an object at a different distance will automatically cause vergence and accommodation.
Accommodation
To see clearly, the lens will be pulled flatter or allowed to regain its thicker form.
Diseases, disorders, and age-related changes

There are many diseases, disorders, and age-related changes that may affect the eyes and surrounding structures.
As the eye ages certain changes occur that can be attributed solely to the aging process. Most of these anatomic and physiologic processes follow a gradual decline. With aging, the quality of vision worsens due to reasons independent of aging eye diseases. While there are many changes of significance in the nondiseased eye, the most functionally important changes seem to be a reduction in pupil size and the loss of accommodation or focusing capability (presbyopia). The area of the pupil governs the amount of light that can reach the retina. The extent to which the pupil dilates also decreases with age. Because of the smaller pupil size, older eyes receive much less light at the retina. In comparison to younger people, it is as though older persons wear medium-density sunglasses in bright light and extremely dark glasses in dim light. Therefore, for any detailed visually guided tasks on which performance varies with illumination, older persons require extra lighting. Certain ocular diseases can come from sexually transmitted diseases such as herpes and genital warts. If contact between eye and area of infection occurs, the STD will be transmitted to the eye.[23]
With aging a prominent white ring develops in the periphery of the cornea- called arcus senilis. Aging causes laxity and downward shift of eyelid tissues and atrophy of the orbital fat. These changes contribute to the etiology of several eyelid disorders such as ectropion, entropion, dermatochalasis, and ptosis. The vitreous gel undergoes liquefaction (posterior vitreous detachment or PVD) and its opacities—visible as floaters—gradually increase in number.
Various eye care professionals, including ophthalmologists, optometrists, and opticians, are involved in the treatment and management of ocular and vision disorders. A Snellen chart is one type of eye chart used to measure visual acuity. At the conclusion of an eye examination, an eye doctor may provide the patient with an eyeglass prescription for corrective lenses
Eye injury/safety
Accidents involving common household products cause 125,000 eye injuries each year in the U.S.[24] More than 40,000 people a year suffer eye injuries while playing sports.[24] Sports-related eye injuries occur most frequently in baseball, basketball and racquet sports.[24]
Occupational eye injury
Each day about 2000 U.S. workers have a job-related eye injury that requires medical treatment.[25] About one third of the injuries are treated in hospital emergency departments and more than 100 of these injuries result in one or more days of lost work.[25] The majority of these injuries result from small particles or objects striking or abrading the eye. Examples include metal slivers, wood chips, dust, and cement chips that are ejected by tools, wind blown, or fall from above a worker. Some of these objects, such as nails, staples, or slivers of wood or metal penetrate the eyeball and result in a permanent loss of vision. Large objects may also strike the eye/face causing blunt force trauma to the eyeball or eye socket. Chemical burns to one or both eyes from splashes of industrial chemicals or cleaning products are common. Thermal burns to the eye occur as well. Among welders, their assistants, and nearby workers, UV radiation burns (welder’s flash) routinely damage workers’ eyes and surrounding tissue. In addition to common eye injuries, health care workers, laboratory staff, janitorial workers, animal handlers, and other workers may be at risk of acquiring infectious diseases via ocular exposure.[25]
See also
- Ophthalmology
- Eye exam
- Infant vision
- Annulus of Zinn
- Conjunctiva
- Macula
- Nictitating membrane
- Schlemm’s canal
- Trabecular meshwork
References
- ↑ http://www.nwf.org/nationalwildlife/article.cfm?issueID=77&articleID=1114
- ↑ Halder, G., Callaerts, P. and Gehring, W.J. (1995). “New perspectives on eye evolution.” Curr. Opin. Genet. Dev. 5 (pp. 602–609).
- ↑ Halder, G., Callaerts, P. and Gehring, W.J. (1995). “Induction of ectopic eyes by targeted expression of the eyeless gene in Drosophila“. Science 267 (pp. 1788–1792).
- ↑ Tomarev, S.I., Callaerts, P., Kos, L., Zinovieva, R., Halder, G., Gehring, W., and Piatigorsky, J. (1997). “Squid Pax-6 and eye development.” Proc. Natl. Acad. Sci. USA, 94 (pp. 2421–2426).
- ↑ Conway-Morris, S. (1998). The Crucible of Creation. Oxford: Oxford University Press.
- ↑ Land, M.F. and Fernald, Russell D. (1992). “The evolution of eyes.” Annu Rev Neurosci 15 (pp. 1–29).
- ↑ Eye-Evolution?
- ↑ Fernald, Russell D. (2001). The Evolution of Eyes: Where Do Lenses Come From? Karger Gazette 64: “The Eye in Focus”.
- ↑ “The Eye.” Accessed October 23, 2006.
- ↑ “General Anatomy of the Eye.” Accessed October 23, 2006.
- ↑ “Eye Anatomy and Function.” Accessed October 23, 2006.
- ↑ 12.0 12.1 12.2 Cline D; Hofstetter HW; Griffin JR. Dictionary of Visual Science. 4th ed. Butterworth-Heinemann, Boston 1997. ISBN 0-7506-9895-0
- ↑ http://www.bartleby.com/107/225.html
- ↑ Cassin, B. and Solomon, S. Dictionary of Eye Terminology. Gainsville, Florida: Triad Publishing Company, 1990.
- ↑ 15.0 15.1 “Medline Encyclopedia: Eye.” Accessed October 25, 2006.
- ↑ http://www.e-sunbear.com/anatomy_02.html
- ↑ Posterior segment anatomy
- ↑ John C. Russ (2006). The Image Processing Handbook. CRC Press. ISBN 0849372542.
- ↑ Optical System Design. McGraw-Hill Professional. 2000. ISBN 0071349162. Text ” Steve Chapman (editor) ” ignored (help)
- ↑ Curtis D. Klaassen (2001). Casarett and Doull’s Toxicology: The Basic Science of Poisons. McGraw-Hill Professional. ISBN 0071347216.
- ↑ Westheimer, Gerald & McKee, Suzanne P.; “Visual acuity in the presence of retinal-image motion”. Journal of the Optical Society of America 1975 65(7), 847-50.
- ↑ Roger H.S. Carpenter (1988); Movements of the Eyes (2nd ed.). Pion Ltd, London. ISBN 0-85086-109-8.
- ↑ AgingEye Times
- ↑ 24.0 24.1 24.2 “Eye Safety Prevent Eye Injuries at Home, at Work and at Play!”. Prevent Blindness America. Retrieved 2007-10-23.
- ↑ 25.0 25.1 25.2 “NIOSH Eye Safety”. United States National Institute for Occupational Safety and Health. Retrieved 2007-10-23.
- “Anatomy”. History of Ophthalmology. Unknown parameter
|accessdaymonth=ignored (help); Unknown parameter|accessyear=ignored (|access-date=suggested) (help) - Kandel ER, Schwartz JH, Jessell TM. Principles of Neural Science, 4th ed. McGraw-Hill, New York (2000). ISBN 0-8385-7701-6
External links
- DJO | Digital Journal of Ophthalmology
- Glossary of Eye Conditions
- Evolution of the Eye
- Diagram of the eye
- Webvision. The organisation of the retina and visual system.
- VisionSimulations.com | Images and vision simulators of various diseases and conditions of the eye
- Eyes and computers.
- Eyeatlas online (ophthalmological images) by Umberto Benelli, MD, PhD
- ClarkVision’s estimation of the resolution of the eye
- Video: Vision and How Our Eyes Work
- Summary of eye diseases and disorders
- Your Baby’s Eyes.
- National Institute for Occupational Safety and Health – Eye Safety
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(18-20) Operations on the ear
(18-20) Operations on the ear
- (Template:ICD9proc) Operations on external ear
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- (Template:ICD9proc) Diagnostic procedures on external ear
- (Template:ICD9proc) Excision or destruction of lesion of external ear
- (Template:ICD9proc) Other excision of external ear
- (Template:ICD9proc) Suture of laceration of external ear
- (Template:ICD9proc) Surgical correction of prominent ear
- (Template:ICD9proc) Reconstruction of external auditory canal
- (Template:ICD9proc) Other plastic repair of external ear
- (Template:ICD9proc) Other operations on external ear
- (Template:ICD9proc) Reconstructive operations on middle ear
- (Template:ICD9proc) Stapes mobilization
- (Template:ICD9proc) Stapedectomy
- (Template:ICD9proc) Revision of stapedectomy
- (Template:ICD9proc) Other operations on ossicular chain
- (Template:ICD9proc) Myringoplasty
- (Template:ICD9proc) Other tympanoplasty
- (Template:ICD9proc) Revision of tympanoplasty
- (Template:ICD9proc) Other repair of middle ear
- (Template:ICD9proc) Other operations on middle and inner ear
- (Template:ICD9proc) Myringotomy
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- (Template:ICD9proc) Incision of mastoid and middle ear
- (Template:ICD9proc) Diagnostic procedures on middle and inner ear
- (Template:ICD9proc) Mastoidectomy
- (Template:ICD9proc) Other excision of middle ear
- (Template:ICD9proc) Fenestration of inner ear
- (Template:ICD9proc) Incision, excision, and destruction of inner ear
- (Template:ICD9proc) Operations on Eustachian tube
- (Template:ICD9proc) Other operations on inner and middle ear
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

The ear is the sense organ that detects sounds. The vertebrate ear shows a common biology from fish to humans, with variations in structure according to order and species. It not only acts as a receiver for sound, but plays a major role in the sense of balance and body position. The ear is part of the auditory system.
The word “ear” may be used correctly to describe the entire organ or just the visible portion. In most animals, the visible ear is a flap of tissue that is also called the pinna. The pinna may be all that shows of the ear, but it serves only the first of many steps in hearing and plays no role in the sense of balance. In people, the pinna is often called the auricle. Vertebrates have a pair of ears, placed symmetrically on opposite sides of the head. This arrangement aids in the ability to localize sound sources.
Introduction to ears and hearing
Audition is the scientific name for the perception of sound. Sound is a form of energy that moves through air, water, and other matter, in waves of pressure. Sound is the means of auditory communication, including frog calls, bird songs and spoken language. Although the ear is the vertebrate sense organ that recognizes sound, it is the brain and central nervous system that “hears”. Sound waves are perceived by the brain through the firing of nerve cells in the auditory portion of the central nervous system. The ear changes sound pressure waves from the outside world into a signal of nerve impulses sent to the brain.

The outer part of the ear collects sound. That sound pressure is amplified through the middle portion of the ear and, in land animals, passed from the medium of air into a liquid medium. The change from air to liquid occurs because air surrounds the head and is contained in the ear canal and middle ear, but not in the inner ear. The inner ear is hollow, embedded in the temporal bone, the densest bone of the body. The hollow channels of the inner ear are filled with liquid, and contain a sensory epithelium that is studded with hair cells. The microscopic “hairs” of these cells are structural protein filaments that project out into the fluid. The hair cells are mechanoreceptors that release a chemical neurotransmitter when stimulated. Sound waves moving through fluid push the filaments; if the filaments bend over enough it causes the hair cells to fire. In this way sound waves are transformed into nerve impulses. In vision, the rods and cones of the retina play a similar role with light as the hair cells do with sound. The nerve impulses travel from the left and right ears through the eighth cranial nerve to both sides of the brain stem and up to the portion of the cerebral cortex dedicated to sound. This auditory part of the cerebral cortex is in the temporal lobe.
The part of the ear that is dedicated to sensing balance and position also sends impulses through the eighth cranial nerve, the VIIIth nerve’s Vestibular Portion. Those impulses are sent to the vestibular portion of the central nervous system. The human ear can generally hear sounds with frequencies between 20 Hz and 20 kHz (the audio range). Although the sensation of hearing requires an intact and functioning auditory portion of the central nervous system as well as a working ear, human deafness (extreme insensitivity to sound) most commonly occurs because of abnormalities of the inner ear, rather than the nerves or tracts of the central auditory system.[1]
Mammalian ear

The shape of outer ear of mammals varies widely across species. However the inner workings of mammalian ears (including humans’) are very similar.
Parts of the Ear
Outer ear (pinna, ear canal, surface of ear drum)
The outer ear is the most external portion of the ear. The outer ear includes the pinna (also called auricle), the ear canal, and the very most superficial layer of the ear drum (also called the tympanic membrane). In humans, and almost all vertebrates, the only visible portion of the ear is the outer ear. Although the word “ear” may properly refer to the pinna (the flesh covered cartilage appendage on either side of the head), this portion of the ear is not vital for hearing. The complicated design of the human outer ear does help capture sound (and imposes filtering that helps distinguish the direction of the sound source), but the most important functional aspect of the human outer ear is the ear canal itself. Unless the canal is open, hearing will be dampened. Ear wax (medical name – cerumen) is produced by glands in the skin of the outer portion of the ear canal. This outer ear canal skin is applied to cartilage; the thinner skin of the deep canal lies on the bone of the skull. Only the thicker cerumen-producing ear canal skin has hairs. The outer ear ends at the most superficial layer of the tympanic membrane. The tympanic membrane is commonly called the ear drum.
The pinna helps direct sound through the ear canal to the tympanic membrane (eardrum). The framework of the auricle consists of a single piece of yellow fibrocartilage with a complicated relief on the anterior, concave side and a fairly smooth configuration on the posterior, convex side. The Darwinian tubercle, which is present in some people, lies in the descending part of the helix and corresponds to the true ear tip of the long-eared mammals. The lobule merely contains subcutaneous tissue.[2] In some animals with mobile pinnae (like the horse), each pinna can be aimed independently to better receive the sound. For these animals, the pinnae help localize the direction of the sound source. Human beings localize sound within the central nervous system, by comparing arrival-time differences and loudness from each ear, in brain circuits that are connected to both ears.
Human outer ear and culture

The auricles also have an effect on facial appearance. In Western societies, protruding ears (present in about 5% of ethnic Europeans) have been considered unattractive, particularly if asymmetric. The first surgery to reduce the projection of prominent ears was published in the medical literature in 1881.
The ears have also been ornamented with jewellery for thousands of years, traditionally by piercing of the earlobe. In some cultures, ornaments are placed to stretch and enlarge the earlobes to make them very large. Tearing of the earlobe from the weight of heavy earrings, or from traumatic pull of an earring (for example by snagging on a sweater being removed), is fairly common.[3] The repair of such a tear is usually not difficult.
A cosmetic surgical procedure to reduce the size or change the shape of the ear is called an otoplasty. In the rare cases when no pinna is formed (atresia), or is extremely small (microtia) reconstruction the auricle is possible. Most often, a cartilage graft from another part of the body (generally, rib cartilage) is used to form the matrix of the ear, and skin grafts or rotation flaps are used to provide the covering skin. However, when babies are born without an auricle on one or both sides, or when the auricle is very tiny, the ear canal is ordinarily either small or absent, and the middle ear often has deformities. The initial medical intervention is aimed at assessing the baby’s hearing and the condition of the ear canal, as well as the middle and inner ear. Depending on the results of tests, reconstruction of the outer ear is done in stages, with planning for any possible repairs of the rest of the ear.[4][5][6]
Middle ear
The middle ear, an air-filled cavity behind the ear drum (tympanic membrane), includes the three ear bones or ossicles: the malleus (or hammer), incus (or anvil), and stapes (or stirrup). The opening of the Eustachian tube is also within the middle ear. The malleus has a long process (the manubrium, or handle) that is attached to the mobile portion of the eardrum. The incus is the bridge between the malleus and stapes. The stapes is the smallest named bone in the human body. The three bones are arranged so that movement of the tympanic membrane causes movement of the malleus, which causes movement of the incus, which causes movement of the stapes. When the stapes footplate pushes on the oval window, it causes movement of fluid within the cochlea (a portion of the inner ear).
In humans and other land animals the middle ear (like the ear canal) is normally filled with air. Unlike the open ear canal, however, the air of the middle ear is not in direct contact with the atmosphere outside the body. The Eustachian tube connects from the chamber of the middle ear to the back of the pharynx. The middle ear is very much like a specialized paranasal sinus, called the tympanic cavity; it, like the paranasal sinuses, is a hollow mucosa-lined cavity in the skull that is ventilated through the nose. The mastoid portion of the human temporal bone, which can be felt as a bump in the skull behind the pinna, also contains air, which is ventilated through the middle ear. Template:Middle ear map Normally, the Eustachian tube is collapsed, but it gapes open both with swallowing and with positive pressure. When taking off in an airplane, the surrounding air pressure goes from higher (on the ground) to lower (in the sky). The air in the middle ear expands as the plane gains altitude, and pushes its way into the back of the nose and mouth. On the way down, the volume of air in the middle ear shrinks, and a slight vacuum is produced. Active opening of the Eustachian tube is required to equalize the pressure between the middle ear and the surrounding atmosphere as the plane descends. The diver also experiences this change in pressure, but with greater rates of pressure change; active opening of the Eustachian tube is required more frequently as the diver goes deeper into higher pressure.
The arrangement of the tympanic membrane and ossicles works to efficiently couple the sound from the opening of the ear canal to the cochlea. There are several simple mechanisms that combine to increase the sound pressure. The first is the “hydraulic principle”. The surface area of the tympanic membrane is many times that of the stapes footplate. Sound energy strikes the tympanic membrane and is concentrated to the smaller footplate. A second mechanism is the “lever principle”. The dimensions of the articulating ear ossicles lead to an increase in the force applied to the stapes footplate compared with that applied to the malleus. A third mechanism channels the sound pressure to one end of the cochlea, and protects the other end from being struck by sound waves. In humans, this is called “round window protection”, and will be more fully discussed in the next section.
Abnormalities such as impacted ear wax (occlusion of the external ear canal), fixed or missing ossicles, or holes in the tympanic membrane generally produce conductive hearing loss. Conductive hearing loss may also result from middle ear inflammation causing fluid build-up in the normally air-filled space. Tympanoplasty is the general name of the operation to repair the middle ear’s tympanic membrane and ossicles. Grafts from muscle fascia are ordinarily used to rebuild an intact ear drum. Sometimes artificial ear bones are placed to substitute for damaged ones, or a disrupted ossicular chain is rebuilt in order to conduct sound effectively.
Inner ear: cochlea, vestibule, and semi-circular canals
Template:Inner ear map The inner ear includes both the organ of hearing (the cochlea) and a sense organ that is attuned to the effects of both gravity and motion (labyrinth or vestibular apparatus). The balance portion of the inner ear consists of three semi-circular canals and the vestibule. The inner ear is encased in the hardest bone of the body. Within this ivory hard bone, there are fluid-filled hollows. Within the cochlea are three fluid filled spaces: the tympanic canal, the vestibular canal, and the middle canal. The eighth cranial nerve comes from the brain stem to enter the inner ear. When sound strikes the ear drum, the movement is transferred to the footplate of the stapes, which presses into one of the fluid-filled ducts of the cochlea. The fluid inside this duct is moved, flowing against the receptor cells of the Organ of Corti, which fire. These stimulate the spiral ganglion, which sends information through the auditory portion of the eighth cranial nerve to the brain.
Hair cells are also the receptor cells involved in balance, although the hair cells of the auditory and vestibular systems of the ear are not identical. Vestibular hair cells are stimulated by movement of fluid in the semicircular canals and the utricle and saccule. Firing of vestibular hair cells stimulates the Vestibular portion of the eighth cranial nerve.[7]
Damage to the human ear
Outer ear trauma
Auricle

The auricle can be easily damaged. Because it is skin-covered cartilage, with only a thin padding of connective tissue, rough handling of the ear can cause enough swelling to jeopardize the blood-supply to its framework, the auricular cartilage. That entire cartilage framework is fed by a thin covering membrane called the perichondrium (meaning literally: around the cartilage). Any fluid from swelling or blood from injury that collects between the perichondrium and the underlying cartilage puts the cartilage in danger of being separated from its supply of nutrients. If portions of the cartilage starve and die, the ear never heals back into its normal shape. Instead, the cartilage becomes lumpy and distorted. Wrestler’s Ear is one term used to describe the result, because wrestling is one of the most common ways such an injury occurs. Cauliflower ear is another name for the same condition, because the thickened auricle can resemble that vegetable.
The lobule of the ear (ear lobe) is the one part of the human auricle that normally contains no cartilage. Instead, it is a wedge of adipose tissue (fat) covered by skin. There are many normal variations to the shape of the ear lobe, which may be small or large. Tears of the earlobe can be generally repaired with good results. Since there is no cartilage, there is not the risk of deformity from a blood clot or pressure injury to the ear lobe.
Other injuries to the external ear occur fairly frequently, and can leave a major deformity. Some of the more common ones include, laceration from glass, knives, and bite injuries, avulsion injuries, cancer, frostbite, and burns.
Ear canal
Ear canal injuries can come from firecrackers and other explosives, and mechanical trauma from placement of foreign bodies into the ear. The ear canal is most often self-traumatized from efforts at ear cleaning. The outer part of the ear canal rests on the flesh of the head; the inner part rests in the opening of the bony skull (called the external auditory meatus). The skin is very different on each part. The outer skin is thick, and contains glands as well as hair follicles. The glands make cerumen (also called ear wax). The skin of the outer part moves a bit if the pinna is pulled; it is only loosely applied to the underlying tissues. The skin of the bony canal, on the other hand, is not only among the most delicate skin in the human body, it is tightly applied to the underlying bone. A slender object used to blindly clean cerumen out of the ear often results instead with the wax being pushed in, and contact with the thin skin of the bony canal is likely to lead to laceration and bleeding.
Middle ear trauma

Like outer ear trauma, middle ear trauma most often comes from blast injuries and insertion of foreign objects into the ear. Skull fractures that go through the part of the skull containing the ear structures (the temporal bone) can also cause damage to the middle ear. Small perforations of the tympanic membrane usually heal on their own, but large perforations may require grafting. Displacement of the ossicles will cause a conductive hearing loss that can only be corrected with surgery. Forcible displacement of the stapes into the inner ear can cause a sensory neural hearing loss that cannot be corrected even if the ossicles are put back into proper position. Because human skin has a top waterproof layer of dead skin cells that are constantly shedding, displacement of portions of the tympanic membrane or ear canal into the middle ear or deeper areas by trauma can be particularly traumatic. If the displaced skin lives within a closed area, the shed surface builds up over months and years and forms a cholesteatoma. The -oma ending of that word indicates a tumour in medical terminology, and although cholesteatoma is not a neoplasm (but a skin cyst), it can expand and erode the ear structures. The treatment for cholesteatoma is surgical.
-
When the incus is eroded, broken or absent, the ossicular chain is reconstructed with an incus replacement prosthesis[10].
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When both the incus and malleus are eroded or absent, the ossicular chain is reconstructed with a partial ossicular replacement prosthesis (PORP)[11].
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When the incus and arch of the stapes are eroded, or when the malleus, incus and arch of the stapes are absent, the ossicular chain is reconstructed with a total ossicular replacement prosthesis (TORP)[12].
Inner ear trauma
There are two principal damage mechanisms to the inner ear in industrialized society, and both injure hair cells. The first is exposure to elevated sound levels (noise trauma), and the second is exposure to drugs and other substances (ototoxicity).
In 1972 the U.S. EPA told Congress that at least 34 million people were exposed to sound levels on a daily basis that are likely to lead to significant hearing loss.[13] The worldwide implication for industrialized countries would place this exposed population in the hundreds of millions.
Vestigial structures

It has long been known that humans, and indeed other primates such as the orangutan and chimpanzee have ear muscles that are minimally developed and non-functional, yet still large enough to be easily identifiable.[14] These undeveloped muscles are known as vestigial structures. A muscle that cannot move the ear, for whatever reason, can no longer be said to have any biological function. This serves as evidence of homology between related species. In humans there is variability in these muscles, such that some people are able to move their ears in various directions, and it has been said that it may be possible for others to gain such movement by repeated trials.[14]
Non-vertebrate hearing organs
Only vertebrate animals have ears, although many invertebrates are able to detect sound using other kinds of sense organs. In insects, tympanal organs are used to hear distant sounds. They are not confined to the head, but can occur in different locations depending on the group of insects.[15]
Simpler structures allow arthropods to detect near-at-hand sounds. Spiders and cockroaches, for example, have hairs on their legs which are used for detecting sound. Caterpillars may also have hairs on their body that perceive vibrations[16] and allow them to respond to the sound.
References
- ↑ Greinwald, John H. Jr MD; Hartnick, Christopher J. MD The Evaluation of Children With Hearing Loss. Archives of Otolaryngology — Head & Neck Surgery. 128(1):84-87, January 2002
- ↑ Stenström, J. Sten: Deformities of the ear; In: Grabb, W., C., Smith, J.S. (Edited): “Plastic Surgery”, Little, Brown and Company, Boston, 1979, ISBN 0-316-32269-5 (C), ISBN 0-316-32268-7 (P)
- ↑ Deborah S. Sarnoff, Robert H. Gotkin, and Joan Swirsky (2002). Instant Beauty: Getting Gorgeous on Your Lunch Break. St. Martin’s Press. ISBN 031228697X.
- ↑ Lam SM. Edward Talbot Ely: father of aesthetic otoplasty. [Biography. Historical Article. Journal Article] Archives of Facial Plastic Surgery. 6(1):64, 2004 Jan-Feb.
- ↑ Siegert R. Combined reconstruction of congenital auricular atresia and severe microtia. [Evaluation Studies. Journal Article] Laryngoscope. 113(11):2021-7; discussion 2028-9, 2003 Nov.
- ↑ Trigg DJ. Applebaum EL. Indications for the surgical repair of unilateral aural atresia in children. [Review] [33 refs] [Journal Article. Review] American Journal of Otology. 19(5):679-84; discussion 684-6, 1998 Sep.
- ↑ Anson and Donaldson, Surgical Anatomy of the Temporal Bone, 4th Edition, Raven Press, 1992
- ↑ http://www.ghorayeb.com
- ↑ http://www.ghorayeb.com
- ↑ http://www.ghorayeb.com
- ↑ http://www.ghorayeb.com
- ↑ http://www.ghorayeb.com
- ↑ Senate Public Works Committee, Noise Pollution and Abatement Act of 1972, S. Rep. No. 1160, 92nd Cong. 2nd session.
- ↑ 14.0 14.1 Darwin, Charles (1871). The Descent of Man, and Selection in Relation to Sex. John Murray: London.
- ↑ Yack, JE, and JH Fullard, 1993. What is an insect ear? Ann. Entomol. Soc. Am. 86(6): 677-682.
- ↑ Scoble, MJ. 1992. The Lepidoptera: Form, function, and diversity. Oxford Univ. Press.
See also
- WikiSaurus:ear — the WikiSaurus list of synonyms and slang words for ears in many languages
- Absolute threshold of hearing
- Acoustic reflex
- Cerumen
- Cholesteatoma
- Ear pick
- Ear piercing instrument
- Earring
- Georg von Békésy, winner of the 1961 Nobel Prize for his research on the cochlea
- Glossary of medical terms related to communications disorders
- Loudness
- Musical acoustics
- Noise health effects
- Otoplasty External Ear Surgery
- Pitch (music)
- Sound localization
- Timbre
- Tinnitus
- Vestibular system
- Auditory brainstem response (ABR) test
External links
| File:Wiktionary-logo-en-v2.svg | Look up ear in Wiktionary, the free dictionary. |
| Wikimedia Commons has media related to Ear. |
- Protein behind hearing
- 3D Ear page
- Details of various ear problems
- Ear wiggling mechanism unmasked
- Cotton swabs can pose serious health risk: coroner from ctv.ca
Template:Auditory system Template:Human anatomical features
af:Oor
ar:أذن
ay:Jinchu
az:Qulaq
bar:Ohrwaschl
bg:Ухо
bn:কর্ণ (অঙ্গ)
br:Skouarn
bs:Uho
ca:Orella
cdo:Ngê
cs:Ucho
cy:Clust
da:Øre
de:Ohr
diq:Goş
el:Αυτί
eo:Orelo
et:Kõrv
fi:Korva
fiu-vro:Kõrv
gd:Cluas
gl:Orella
he:אוזן
hi:कान
hr:Uho
hu:Fül
id:Telinga
ig:Nti
io:Orelo
is:Eyra
it:Orecchio
jbo:kerlo
ko:귀
la:Auris
lt:Ausis
ml:ചെവി
mr:कान
ms:Telinga
nah:Nacaztli
nl:Oor
nn:Øyre
no:Øre
nrm:Ouothelle
oc:Aurelha
ps:غوږ
qu:Rinri
scn:Aricchiu
simple:Ear
sk:Ucho
sl:Uho
sq:Veshi
sr:Уво
su:Ceuli
sv:Öra
te:చెవి
tg:Гӯш
th:หู
tl:Tainga
uk:Вухо
yi:אויער
yo:Etí
zh-min-nan:Hīⁿ
(21-29) Operations on the nose, mouth, and pharynx
- (Template:ICD9proc) Operations on nose
- (Template:ICD9proc) Control of epistaxis
- (Template:ICD9proc) Incision of nose
- (Template:ICD9proc) Diagnostic procedures on nose
- (Template:ICD9proc) Local excision or destruction of lesion of nose
- (Template:ICD9proc) Resection of nose
- (Template:ICD9proc) Submucous resection of nasal septum
- (Template:ICD9proc) Turbinectomy
- (Template:ICD9proc) Reduction of nasal fracture
- (Template:ICD9proc) Repair and plastic operations on the nose
- (Template:ICD9proc) Suture of laceration of nose
- (Template:ICD9proc) Closure of nasal fistula
- (Template:ICD9proc) Total nasal reconstruction
- (Template:ICD9proc) Revision rhinoplasty
- (Template:ICD9proc) Augmentation rhinoplasty
- (Template:ICD9proc) Limited rhinoplasty
- (Template:ICD9proc) Other rhinoplasty
- (Template:ICD9proc) Other septoplasty
- (Template:ICD9proc) Other repair and plastic operations on nose
- (Template:ICD9proc) Other operations on nose
- (Template:ICD9proc) Operations on nasal sinuses
- (Template:ICD9proc) Removal and restoration of teeth
- (Template:ICD9proc) Other operations on teeth, gums, and alveoli
- (Template:ICD9proc) Operations on tongue
- (Template:ICD9proc) Operations on salivary glands and ducts
- (Template:ICD9proc) Other operations on mouth and face
- (Template:ICD9proc) Operations on tonsils and adenoids
- (Template:ICD9proc) Tonsillectomy without adenoidectomy
- (Template:ICD9proc) Tonsillectomy with adenoidectomy
- (Template:ICD9proc) Adenoidectomy without tonsillectomy
- (Template:ICD9proc) Operations on pharynx
Overview




Anatomically, a nose is a protuberance in vertebrates that houses the nostrils, or nares, which admit and expel air for respiration in conjunction with the mouth.
In most humans, it also houses the nosehairs, which catch airborne particles and prevent them from reaching the lungs. Within and behind the nose is the olfactory mucosa and the sinuses. Behind the nasal cavity, air next passes through the pharynx, shared with the digestive system, and then into the rest of the respiratory system. In humans, the nose is located centrally on the face;on most other mammals, it is on the upper tip of the snout.
As an interface between the body and the external world, the nose and associated structures frequently perform additional functions concerned with conditioning entering air (for instance, by warming and/or humidifying it, also for flicking if moving and by mostly reclaiming moisture from the air before it is exhaled (as occurs most efficiently in camels).
In most mammals, the nose is the primary organ for smelling. As the animal sniffs, the air flows through the nose and over structures called turbinates in the nasal cavity. The turbulence caused by this disruption slows the air and directs it toward the olfactory epithelium. At the surface of the olfactory epithelium, odor molecules carried by the air contact olfactory receptor neurons which transduce the features of the molecule into non painful electrical impulses in the brain.
In cetaceans, the nose has been reduced to the nostrils, which have migrated to the top of the head, producing a more streamlined body shape and the ability to breathe while mostly submerged. Conversely, the elephant‘s nose has become elaborated into a long, muscular, manipulative organ called the trunk.
See also
ar:أنف
an:Naso
bs:Nos
br:Fri
bg:Нос (анатомия)
ca:Nas
cs:Nos
cy:Trwyn
da:Næse
de:Nase
dv:ނޭފަތް
et:Nina
el:Μύτη
eo:Nazo
eu:Sudur
fa:بینی
gd:Sròn
ko:코
hr:Nos
io:Nazo
id:Hidung
iu:ᕿᖓᖅ/qingaq
it:Naso (anatomia)
he:אף
ku:Poz
la:Nasus
lt:Nosis
jbo:nazbi
hu:Orr
mk:Нос
ml:മൂക്ക്
ms:Hidung
nl:Neus
no:Nese
oc:Nas
qu:Sinqa
sq:Hunda
scn:Nasu (anatumìa)
simple:Nose
sk:Nos
sl:Nos
fi:Nenä
sv:Näsa
tl:Ilong
tg:Бинӣ
uk:Ніс
fiu-vro:Nõna
yi:נאז
zh-yue:鼻
diq:Pırnıke
Template:Jb1
Template:WH
Template:WS
(30-34) Operations on the respiratory system
(30-34) Operations on the respiratory system
- (Template:ICD9proc) Excision of larynx
- (Template:ICD9proc) Excision or destruction of lesion or tissue of larynx
- (Template:ICD9proc) Hemilaryngectomy
- (Template:ICD9proc) Other partial laryngectomy
- (Template:ICD9proc) Complete laryngectomy
- (Template:ICD9proc) Radical laryngectomy
- (Template:ICD9proc) Other operations on larynx and trachea
- (Template:ICD9proc) Injection of larynx
- (Template:ICD9proc) Temporary tracheostomy
- (Template:ICD9proc) Permanent tracheostomy
- (Template:ICD9proc) Other incision of larynx or trachea
- (Template:ICD9proc) Diagnostic procedures on larynx and trachea
- (Template:ICD9proc) Local excision or destruction of lesion or tissue of trachea
- (Template:ICD9proc) Repair of larynx
- (Template:ICD9proc) Repair and plastic operations on trachea
- (Template:ICD9proc) Other operations on larynx and trachea
- (Template:ICD9proc) Excision of lung and bronchus
- (Template:ICD9proc) Local excision or destruction of lesion or tissue of bronchus
- (Template:ICD9proc) Other excision of bronchus
- (Template:ICD9proc) Local excision or destruction of lesion or tissue of lung
- (Template:ICD9proc) Segmental resection of lung
- (Template:ICD9proc) Lobectomy of lung
- (Template:ICD9proc) Complete pneumonectomy
- (Template:ICD9proc) Radical dissection of thoracic structures
- (Template:ICD9proc) Other excision of lung
- (Template:ICD9proc) Other operations on lung and bronchus
- (Template:ICD9proc) Incision of bronchus
- (Template:ICD9proc) Incision of lung
- (Template:ICD9proc) Diagnostic procedures on lung and bronchus
- (Template:ICD9proc) Surgical collapse of lung
- (Template:ICD9proc) Repair and plastic operation on lung and bronchus
- (Template:ICD9proc) Lung transplant
- (Template:ICD9proc) Combined heart-lung transplantation
- (Template:ICD9proc) Other operations on lung and bronchus
- (Template:ICD9proc) Operations on chest wall, pleura, mediastinum, and diaphragm
- (Template:ICD9proc) Incision of chest wall and pleura
- (Template:ICD9proc) Exploratory thoracotomy
- (Template:ICD9proc) Incision of mediastinum
- (Template:ICD9proc) Diagnostic procedures on chest wall, pleura, mediastinum, and diaphragm
- (Template:ICD9proc) Transpleural thoracoscopy
- (Template:ICD9proc) Mediastinoscopy
- (Template:ICD9proc) Biopsy of chest wall
- (Template:ICD9proc) Pleural biopsy
- (Template:ICD9proc) Closed (percutaneous) (needle) biopsy of mediastinum
- (Template:ICD9proc) Open mediastinal biopsy
- (Template:ICD9proc) Biopsy of diaphragm
- (Template:ICD9proc) Other diagnostic procedures on chest wall, pleura, and diaphragm
- (Template:ICD9proc) Other diagnostic procedures on mediastinum
- (Template:ICD9proc) Excision or destruction of lesion or tissue of mediastinum
- (Template:ICD9proc) Excision or destruction of lesion of chest wall
- (Template:ICD9proc) Pleurectomy
- (Template:ICD9proc) Scarification of pleura
- (Template:ICD9proc) Repair of chest wall
- (Template:ICD9proc) Operations on diaphragm
- (Template:ICD9proc) Other operations on thorax
- (Template:ICD9proc) Thoracentesis
- (Template:ICD9proc) Injection into thoracic cavity
- Chemical pleurodesis
- (Template:ICD9proc) Incision of chest wall and pleura

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Among quadrupeds, the respiratory system generally includes tubes, such as the bronchi, used to carry air to the lungs, where gas exchange takes place. A diaphragm pulls air in and pushes it out. Respiratory systems of various types are found in a wide variety of organisms.
In humans and other mammals, the respiratory system consists of the airways, the lungs, and the respiratory muscles that mediate the movement of air into and out of the body. Within the alveolar system of the lungs, molecules of oxygen and carbon dioxide are passively exchanged, by diffusion, between the gaseous environment and the blood. Thus, the respiratory system facilitates oxygenation of the blood with a concomitant removal of carbon dioxide and other gaseous metabolic wastes from the circulation. The system also helps to maintain the acid-base balance of the body through the efficient removal of carbon dioxide from the blood.
Anatomy
In humans and other animals, the respiratory system can be conveniently subdivided into an upper respiratory tract (or conducting zone) and lower respiratory tract (respiratory zone), trachea and lungs.
Air moves through the body in the following order:
- Nostrils
- Nasal cavity
- Pharynx (naso-, oro-, laryngo-)
- Larynx (voice box)
- Trachea (wind pipe)
- Thoracic cavity (chest)
- Bronchi (right and left)
- Alveoli (site of gas exchange)
Upper respiratory tract/conducting zone
The conducting zone begins with the nares (nostrils) of the nose, which open into the nasopharynx (nasal cavity). The primary functions of the nasal passages are to: 1) filter, 2) warm, 3) moisten, and 4) provide resonance in speech. The nasopharynx opens into the oropharynx (behind the oral cavity). The oropharynx leads to the laryngopharynx, and empties into the larynx (voicebox), which contains the vocal cords, passing through the glottis, connecting to the trachea (wind pipe).
Lower respiratory tract/respiratory zone
The trachea leads down to the thoracic cavity (chest) where it divides into the right and left “main stem” bronchi. The subdivision of the bronchus are: primary, secondary, and tertiary divisions (first, second and third levels). In all, they divide 16 more times into even smaller bronchioles.
The bronchioles lead to the respiratory zone of the lungs which consists of respiratory bronchioles, alveolar ducts and the alveoli, the multi-lobulated sacs in which most of the gas exchange occurs.
Ventilation
Ventilation of the lungs is carried out by the muscles of respiration.
Control
Ventilation occurs under the control of the autonomic nervous system from the part of the brain stem, the medulla oblongata and the pons. This area of the brain forms the respiration regulatory center, a series of interconnected neurons within the lower and middle brain stem which coordinate respiratory movements. The sections are the pneumotaxic center, the apneustic center, and the dorsal and ventral respiratory groups. This section is especially sensitive during infancy, and the neurons can be destroyed if the infant is dropped or shaken violently. The result can be death due to “shaken baby syndrome.”[1]
Inhalation
Inhalation is initiated by the diaphragm and supported by the external intercostal muscles. Normal resting respirations are 10 to 18 breaths per minute. Its time period is 2 seconds. During vigorous inhalation (at rates exceeding 35 breaths per minute), or in approaching respiratory failure, accessory muscles of respiration are recruited for support. These consist of sternocleidomastoid, platysma, and the strap muscles of the neck.
Inhalation is driven primarily by the diaphragm. When the diaphragm contracts, the ribcage expands and the contents of the abdomen are moved downward. This results in a larger thoracic volume, which in turn causes a decrease in intrathoracic pressure. As the pressure in the chest falls, air moves into the conducting zone. Here, the air is filtered, warmed, and humidified as it flows to the lungs.
During forced inhalation, as when taking a deep breath, the external intercostal muscles and accessory muscles further expand the thoracic cavity.
Exhalation
Exhalation is generally a passive process, however active or forced exhalation is achieved by the abdominal and the internal intercostal muscles. During this process air is forced or exhaled out.
The lungs have a natural elasticity; as they recoil from the stretch of inhalation, air flows back out until the pressures in the chest and the atmosphere reach equilibrium.[2]
During forced exhalation, as when blowing out a candle, expiratory muscles including the abdominal muscles and internal intercostal muscles, generate abdominal and thoracic pressure, which forces air out of the lungs.
Circulation
The right side of the heart pumps blood from the right ventricle through the pulmonary semilunar valve into the pulmonary trunk. The trunk branches into right and left pulmonary arteries to the pulmonary blood vessels. The vessels generally accompany the airways and also undergo numerous branchings. Once the gas exchange process is complete in the pulmonary capillaries, blood is returned to the left side of the heart through four pulmonary veins, two from each side. The pulmonary circulation has a very low resistance, due to the short distance within the lungs, compared to the systemic circulation, and for this reason, all the pressures within the pulmonary blood vessels are normally low as compared to the pressure of the systemic circulation loop.
Virtually all the body’s blood travels through the lungs every minute. The lungs add and remove many chemical messengers from the blood as it flows through pulmonary capillary bed . The fine capillaries also trap blood clots that have formed in systemic veins.
Gas exchange
The major function of the respiratory system is gas exchange. As gas exchange occurs, the acid-base balance of the body is maintained as part of homeostasis. If proper ventilation is not maintained two opposing conditions could occur: 1) respiratory acidosis, a life threatening condition, and 2) respiratory alkalosis.
Upon inhalation, gas exchange occurs at the alveoli, the tiny sacs which are the basic functional component of the lungs. The alveolar walls are extremely thin (approx. 0.2 micrometres), and are permeable to gases. The alveoli are lined with pulmonary capillaries, the walls of which are also thin enough to permit gas exchange. All gases diffuse from the alveolar air to the blood in the pulmonary capillaries, as carbon dioxide diffuses in the opposite direction, from capillary blood to alveolar air. At this point, the pulmonary blood is oxygen-rich, and the lungs are holding carbon dioxide. Exhalation follows, thereby ridding the body of the carbon dioxide and completing the cycle of respiration.
In an average resting adult, the lungs take up about 250ml of oxygen every minute while excreting about 200ml of carbon dioxide. During an average breath, an adult will exchange from 500 ml to 700 ml of air. This average breath capacity is called tidal volume.
Development
The respiratory system lies dormant in the human fetus during pregnancy. At birth, the respiratory system is drained of fluid and cleaned to assure proper functioning of the system. If an infant is born before forty weeks gestational age, the newborn may experience respiratory failure due to the under-developed lungs. This is due to the incomplete development of the alveoli type II cells in the lungs, necessary for the production of surfactant. The infant lungs do not function due to collapse of alveoli caused by surface tension of water remaining in the lungs, which in normal cases would be prohibited by the presence of surfactant. This condition may be avoided by giving the mother a series of steroid shots in the final week prior to delivery, which will enhance the development of type II alveolar cells.[3]
Role in communication
The movement of gas through the larynx, pharynx and mouth allows humans to speak, or phonate. Because of this, gas movement is extremely vital for communication purposes.
Conditions of the respiratory system
Disorders of the respiratory system can be classified into four general areas:
- Obstructive conditions (e.g., emphysema, bronchitis, asthma attacks)
- Restrictive conditions (e.g., fibrosis, sarcoidosis, alveolar damage, pleural effusion)
- Vascular diseases (e.g., pulmonary edema, pulmonary embolism, pulmonary hypertension)
- Infectious, environmental and other “diseases” (e.g., pneumonia, tuberculosis, asbestosis, particulate pollutants) coughing is of major importance, as it is the body’s main method to remove dust, mucus, saliva, and other debris from the lungs. Inability to cough can lead to infection. Deep breathing exercises may help keep finer structures of the lungs clear from particulate matter, etc.
The respiratory tract is constantly exposed to microbes due to the extensive surface area, which is why the respiratory system includes many mechanisms to defend itself and prevent pathogens from entering the body.
Disorders of the respiratory system are usually treated internally by a pulmonologist or Respiratory Physician.
Gas exchange in plants
Plants use carbon dioxide gas in the process of photosynthesis, and then exhale oxygen gas, a waste product of photosynthesis. However, plants also sometimes respire as humans do, using oxygen and producing carbon dioxide.
Plant respiration is limited by the process of diffusion. Plants take in carbon dioxide through holes on the undersides of their leaves known as stomata(sing:stoma). However, most plants require little air. Most plants have relatively few living cells outside of their surface because air (which is required for metabolic content) can penetrate only skin deep. However, most plants are not involved in highly aerobic activities, and thus have no need of these living cells.
See also
- Liquid breathing
- Aquatic respiration
- Involuntary control of respiration
- Gill
- Respiratory tract
- Major systems of the human body
- Muscles of respiration
References
- Perkins, M. 2003. Respiration Power Point Presentation. Biology 182 Course Handout. Orange Coast College, Costa Mesa, CA.
- Medical Dictionary
Notes
External links
- Science aid: Respiratory System A simple guide for high school students
- Introduction to Respiratory System
- A high school level description of the respiratory system
- The Respiratory System University level
Template:Organ systems Template:Respiratory system Template:Lung
Template:Respiratory pathology Template:Development of respiratory system
ar:جهاز التنفس zh-min-nan:Ho͘-khip hē-thóng ca:Sistema respiratori cs:Dýchací soustava cy:System respiradol el:Αναπνευστικό σύστημα eo:Spira sistemo eu:Arnas-aparatu hr:Dišni sustav io:Respirala sistemo it:Apparato respiratorio he:מערכת הנשימה mk:Систем за дишење ms:Sistem pernafasan no:Åndedrettssystemet sk:Dýchacia sústava sr:Систем органа за дисање tl:Sistemang respiratoryo
(35-39) Operations on the cardiovascular system
(35-39) Operations on the cardiovascular system
- (Template:ICD9proc) Operations on valves and septa of heart
- (Template:ICD9proc) Closed heart valvotomy
- (Template:ICD9proc) Open heart valvuloplasty without replacement
- (Template:ICD9proc) Replacement of heart valve
- (Template:ICD9proc) Operations on structures adjacent to heart valves
- (Template:ICD9proc) Production of septal defect in heart
- (Template:ICD9proc) Repair of atrial and ventricular septa with prosthesis
- (Template:ICD9proc) Repair of atrial and ventricular septa with tissue graft
- (Template:ICD9proc) Other and unspecified repair of atrial and ventricular septa
- (Template:ICD9proc) Total repair of certain congenital cardiac anomalies
- (Template:ICD9proc) Other operations on valves and septa of heart
- (Template:ICD9proc) Creation of conduit between atrium and pulmonary artery
- (Template:ICD9proc) Operations on vessels of heart
- (Template:ICD9proc) Removal of coronary artery obstruction and insertion of stent(s)
- (Template:ICD9proc) Bypass anastomosis for heart revascularization
- (Template:ICD9proc) Heart revascularization by arterial implant
- (Template:ICD9proc) Other heart revascularization
- (Template:ICD9proc) Other operations on vessels of heart
- (Template:ICD9proc) Other operations on heart and pericardium
- (Template:ICD9proc) Pericardiocentesis
- (Template:ICD9proc) Cardiotomy and pericardiotomy
- (Template:ICD9proc) Diagnostic procedures on heart and pericardium
- (Template:ICD9proc) Pericardiectomy and excision of lesion of heart
- (Template:ICD9proc) Pericardiectomy
- (Template:ICD9proc) Excision of aneurysm of heart
- (Template:ICD9proc) Excision or destruction of other lesion or tissue of heart, open approach
- (Template:ICD9proc) Excision or destruction of other lesion or tissue of heart, other approach
- (Template:ICD9proc) Partial ventriculectomy
- (Template:ICD9proc) Repair of heart and pericardium
- (Template:ICD9proc) Heart replacement procedures
- (Template:ICD9proc) Implantation of heart and circulatory assist system
- (Template:ICD9proc) Insertion, revision, replacement, and removal of pacemaker leads; insertion of temporary pacemaker system; or revision of cardiac device pocket
- (Template:ICD9proc) Insertion, replacement, removal, and revision of pacemaker device
- (Template:ICD9proc) Other operations on heart and pericardium
- (Template:ICD9proc) Incision, excision, and occlusion of vessels
- (Template:ICD9proc) Incision of vessel
- (Template:ICD9proc) Endarterectomy
- (Template:ICD9proc) Diagnostic procedures on blood vessels
- (Template:ICD9proc) Resection of vessel with anastomosis
- (Template:ICD9proc) Resection of vessel with replacement
- (Template:ICD9proc) Ligation and stripping of varicose veins
- (Template:ICD9proc) Other excision of vessel
- (Template:ICD9proc) Interruption of the vena cava
- (Template:ICD9proc) Other surgical occlusion of vessels
- (Template:ICD9proc) Puncture of vessel
- (Template:ICD9proc) Arterial catheterization
- (Template:ICD9proc) Umbilical vein catheterization
- (Template:ICD9proc) Venous catheterization, not elsewhere classified
- (Template:ICD9proc) Venous cutdown
- (Template:ICD9proc) Venous catheterization for renal dialysis
- (Template:ICD9proc) Other puncture of artery
- (Template:ICD9proc) Other puncture of vein
- (Template:ICD9proc) Other operations on vessels
- (Template:ICD9proc) Systemic to pulmonary artery shunt
- (Template:ICD9proc) Intra-abdominal venous shunt
- (Template:ICD9proc) Other shunt or vascular bypass
- (Template:ICD9proc) Suture of vessel
- (Template:ICD9proc) Revision of vascular procedure
- (Template:ICD9proc) Other repair of vessels
- (Template:ICD9proc) Extracorporeal circulation and procedures auxiliary to heart surgery
- (Template:ICD9proc) Extracorporeal circulation auxiliary to open heart surgery
- (Template:ICD9proc) Hypothermia (systemic) incidental to open heart surgery
- (Template:ICD9proc) Cardioplegia
- (Template:ICD9proc) Intraoperative cardiac pacemaker
- (Template:ICD9proc) Extracorporeal membrane oxygenation (ECMO)
- (Template:ICD9proc) Percutaneous cardiopulmonary bypass
- (Template:ICD9proc) Endovascular repair of vessel
- (Template:ICD9proc) Operations on carotid body and other vascular bodies
- (Template:ICD9proc) Other operations on vessels

Template:WikiDoc Cardiology News Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
The circulatory system (or cardiovascular system) is an organ system that moves nutrients, gases, and wastes to and from cells, and helps stabilize body temperature and pH to maintain homeostasis. While humans, as well as other vertebrates have a closed circulatory system, some invertebrate groups have open circulatory system. The most primitive animal phyla lack circulatory systems.
Human circulatory system
The main components of the human circulatory system are the heart, the blood, and the blood vessels.
Furthermore, these components can either belong to the systemic circulation and the pulmonary circulation. The systemic circulation is the main part of the circulatory system, while the pulmonary system oxygenates the blood.
Systemic circulation
Systemic circulation is the portion of the cardiovascular system which carries oxygenated blood away from the heart, to the body, and returns deoxygenated blood back to the heart.
In the systemic circulation, arteries bring oxygenated blood to the tissues. As blood circulates through the body, oxygen diffuses from the blood into cells surrounding the capillaries, and carbon dioxide diffuses into the blood from the capillary cells. Veins bring deoxygenated blood back to the heart.
The release of oxygen from red blood cells or erythrocytes is regulated in mammals. It increases with an increase of carbon dioxide in tissues, an increase in temperature, or a decrease in pH. Such characteristics are exhibited by tissues undergoing high metabolism, as they require increased levels of oxygen.
Pulmonary circulation
Pulmonary circulation is the portion of the cardiovascular system which carries oxygen-depleted blood away from the heart, to the lungs, and returns oxygenated blood back to the heart.
De-oxygenated blood enters the right atrium of the heart and flows into the right ventricle where it is pumped through the pulmonary arteries to the lungs. Pulmonary veins return the now oxygen-rich blood to the heart, where it enters the left atrium before flowing into the left ventricle. From the left ventricle the oxygen-rich blood is pumped out via the aorta, and on to the rest of the body.
Heart
In the heart there is one atrium and one ventricle for each circulation, and with both a systemic and a pulmonary circulation there are four chambers in total: left atrium, left ventricle, right atrium and right ventricle.
Closed circulatory system
The circulatory systems of humans is closed, meaning that the blood never leaves the system of blood vessels. In contrast, oxygen and nutrients diffuse across the blood vessel layers and enters interstitial fluid, which carries oxygen and nutrients to the target cells, and carbon dioxide and wastes in the opposite direction.
Other vertebrates
The circulatory systems of all vertebrates, as well as of annelids (for example, earthworms) and cephalopods (squid and octopus) are closed, just as in humans. Still, the systems of fish, amphibians, reptiles, and birds show various stages of the evolution of the circulatory system.
In fish, the system has only one circuit, with the blood being pumped through the capillaries of the gills and on to the capillaries of the body tissues. This is known as single circulation. The heart of fish is therefore only a single pump (consisting of two chambers). In amphibians and most reptiles, a double circulatory system is used, but the heart is not always completely separated into two pumps. Amphibians have a three-chambered heart.
Birds and mammals show complete separation of the heart into two pumps, for a total of four heart chambers; it is thought that the four-chambered heart of birds evolved independently from that of mammals.
Open circulatory system
The open circulatory system is an arrangement of internal transport present in animals such as molluscs and arthropods, in which fluid (called hemolymph) in a cavity called the hemocoel bathes the organs directly and there is no distinction between blood and interstitial fluid; this combined fluid is called hemolymph or haemolymph. Muscular movements by the animal during locomotion can facilitate hemolymph movement, but diverting flow from one area to another is limited. When the heart relaxes, blood is drawn back toward the heart through open-ended pores.
Hemolymph fills all of the interior hemocoel of the body and surrounds all cells. Hemolymph is composed of water, inorganic salts (mostly Na+, Cl–, K+, Mg2+, and Ca2+), and organic compounds (mostly carbohydrates, proteins, and lipids). The primary oxygen transporter molecule is hemocyanin.
There are free-floating cells, the hemocytes, within the hemolymph. They play a role in the arthropod immune system.
No circulatory system
Circulatory systems are absent in some animals, including flatworms (phylum Platyhelminthes). Their body cavity has no lining or enclosed fluid. Instead a muscular pharynx leads to an extensively branched digestive system that facilitates direct diffusion of nutrients to all cells. The flatworm’s dorso-ventrally flattened body shape also restricts the distance of any cell from the digestive system or the exterior of the organism. Oxygen can diffuse from the surrounding water into the cells, and carbon dioxide can diffuse out. Consequently every cell is able to obtain nutrients, water and oxygen without the need of a transport system.
Measurement techniques
Health and disease
History of discovery
The valves of the heart were discovered by a physician of the Hippocratean school around the 4th century BC. However their function was not properly understood then. Because blood pools in the veins after death, arteries look empty. Ancient anatomists assumed they were filled with air and that they were for transport of air.
Herophilus distinguished veins from arteries but thought that the pulse was a property of arteries themselves. Erasistratus observed that arteries that were cut during life bleed. He ascribed the fact to the phenomenon that air escaping from an artery is replaced with blood that entered by very small vessels between veins and arteries. Thus he apparently postulated capillaries but with reversed flow of blood.
The 2nd century AD Greek physician, Galen knew that blood vessels carried blood and identified venous (dark red) and arterial (brighter and thinner) blood, each with distinct and separate functions. Growth and energy were derived from venous blood created in the liver from chyle, while arterial blood gave vitality by containing pneuma (air) and originated in the heart. Blood flowed from both creating organs to all parts of the body where it was consumed and there was no return of blood to the heart or liver. The heart did not pump blood around, the heart’s motion sucked blood in during diastole and the blood moved by the pulsation of the arteries themselves.
Galen believed that the arterial blood was created by venous blood passing from the left ventricle to the right by passing through ‘pores’ in the interventricular septum, air passed from the lungs via the pulmonary artery to the left side of the heart. As the arterial blood was created ‘sooty’ vapors were created and passed to the lungs also via the pulmonary artery to be exhaled.
In 1242 the Arab physician Ibn al-Nafis became the first person to accurately describe the process of blood circulation in the human body, including pulmonary circulation. He stated:
“…the blood from the right chamber of the heart must arrive at the left chamber but there is no direct pathway between them. The thick septum of the heart is not perforated and does not have visible pores as some people thought or invisible pores as Galen thought. The blood from the right chamber must flow through the vena arteriosa (pulmonary artery) to the lungs, spread through its substances, be mingled there with air, pass through the arteria venosa (pulmonary vein) to reach the left chamber of the heart and there form the vital spirit…”
Contemporary drawings of this process have survived. In 1552, Michael Servetus described the same, and Realdo Colombo proved the concept, but it remained largely unknown in Europe.
Finally William Harvey, a pupil of Hieronymus Fabricius (who had earlier described the valves of the veins without recognizing their function), performed a sequence of experiments and announced in 1628 the discovery of the human circulatory system as his own and published an influential book about it. This work with its essentially correct exposition slowly convinced the medical world. Harvey was not able to identify the capillary system connecting arteries and veins; these were later described by Marcello Malpighi.
See also
- Cardiology
- Lymphatic system
- Noise health effects
- Blood vessels
- Innate heat
- Cardiac muscle
- Major systems of the human body
- Heart
- Amato Lusitano
- William Harvey
References
- Iskandar, Albert Z. “Comprehensive Book on the Art of Medicine by Ibn al-Nafis”. Retrieved May 2, 2005.
- Nie Jing-bao, ” Refutation of the Claim that the Ancient Chinese described the Circulation of Blood,” New Zealand Journal of Asian Studies 3, 2 (December, 2001): 119-135
External links
- The Circulatory System, a comprehensive overview
- The InVision Guide to a Healthy Heart An interactive website
- NCP Cardiovascular Medicine A Journal Covering Clinical Cardiovascular Medicine
Template:Development of circulatory system
ar:جهاز الدوران ast:Sistema cardiovascular bn:সংবহন তন্ত্র zh-min-nan:Sûn-khoân hē-thóng bs:Krvotok bg:Кръвообращение ca:Sistema cardiovascular cs:Oběhová soustava de:Blutkreislauf dv:ލޭދައުރުކުރާ ނިޒާމް eo:Kardiovaskula sistemo eu:Zirkulazio-aparatu gl:Aparello circulatorio hr:Krvožilni sustav id:Sistem kardiovaskular is:Blóðrásarkerfi it:Apparato circolatorio he:מחזור הדם pam:Circulatory system ku:Sîstema gera xwînê lv:Asinsrites orgānu sistēma lt:Kraujotakos sistema hu:Keringési rendszer mk:Циркулаторен систем nl:Hart- en vaatstelsel no:Sirkulasjonssystem nn:Kretsløpssystem qu:Sirk’a llika sq:Sistemi i qarkullimit të gjakut simple:Circulatory system sk:Obehová sústava sr:Крвни систем fi:Verenkierto sv:Kardiovaskulära systemet th:ระบบไหลเวียนโลหิต yi:בלוט צירקולאציע
(40-41) Operations on the hemic and lymphatic system
(40-41) Operations on the hemic and lymphatic system
- (Template:ICD9proc) Operations on lymphatic system
- (Template:ICD9proc) Incision of lymphatic structures
- (Template:ICD9proc) Diagnostic procedures on lymphatic structures
- (Template:ICD9proc) Simple excision of lymphatic structure
- (Template:ICD9proc) Excision of deep cervical lymph node
- (Template:ICD9proc) Excision of internal mammary lymph node
- (Template:ICD9proc) Excision of axillary lymph node
- (Template:ICD9proc) Excision of inguinal lymph node
- (Template:ICD9proc) Simple excision of other lymphatic structure
- Simple lymphadenectomy
- (Template:ICD9proc) Regional lymph node excision
- (Template:ICD9proc) Radical excision of cervical lymph nodes
- (Template:ICD9proc) Radical excision of other lymph nodes
- (Template:ICD9proc) Operations on thoracic duct
- (Template:ICD9proc) Other operations on lymphatic structures
- (Template:ICD9proc) Operations on bone marrow and spleen
- (Template:ICD9proc) Bone marrow or hematopoietic stem cell transplant
- (Template:ICD9proc) Puncture of spleen
- (Template:ICD9proc) Splenotomy
- (Template:ICD9proc) Diagnostic procedures on bone marrow and spleen
- (Template:ICD9proc) Excision or destruction of lesion or tissue of spleen
- (Template:ICD9proc) Marsupialization of splenic cyst
- (Template:ICD9proc) Excision of lesion or tissue of spleen
- (Template:ICD9proc) Partial splenectomy
- (Template:ICD9proc) Total splenectomy
- (Template:ICD9proc) Other operations on spleen and bone marrow
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

a – erythrocytes; b – neutrophil; c – eosinophil; d – lymphocyte.
Overview
Blood is a specialized biological fluid consisting of red blood cells (also called RBCs or erythrocytes), white blood cells (also called leukocytes) and platelets (also called thrombocytes) suspended in a complex fluid medium known as blood plasma.
By far the most abundant cells in blood are red blood cells. These contain hemoglobin which gives blood its red color. The iron-containing heme portion of Hemoglobin facilitates hemoglobin-bound transportation of oxygen and carbon dioxide by selectively binding to these respiratory gasses and greatly increasing their solubility in blood. White blood cells help to resist infections, and platelets are important in the clotting of blood.
Blood is circulated around the body through blood vessels by the pumping action of the heart. Blood is pumped from the strong left ventricle of the heart through arteries to peripheral tissues and returns to the right atrium of the heart through veins, blood then enters the right ventricle and is pumped through the pulmonary artery to the lungs and returns to the left atrium through the pulmonary veins, blood then enters the left ventricle to be circulated again. Arterial blood carries oxygen from inhaled air in the lungs to all of the cells of the body, and venous blood carries carbon dioxide, produced as a waste product of metabolism by cells, to the lungs to be exhaled.
Medical terms related to blood often begin with hemo- or hemato- (BE: haemo- and haemato-) from the Greek word “haima” for “blood.” Anatomically, blood is considered a connective tissue from both its origin in the bones and its function.
Functions
- Supply of oxygen to tissues (bound to hemoglobin which is carried in red cells)
- Supply of nutrients such as glucose, amino acids and fatty acids (dissolved in the blood or bound to plasma proteins)
- Removal of waste such as carbon dioxide, urea and lactic acid
- Immunological functions, including circulation of white cells, and detection of foreign material by antibodies
- Coagulation, which is one part of the body’s self-repair mechanism
- Messenger functions, including the transport of hormones and the signalling of tissue damage
- Regulation of body pH (the normal pH of blood is in the range of 7.35 – 7.45)
- Regulation of core body temperature
- Hydraulic functions
Problems with blood composition or circulation can lead to downstream tissue dysfunction. The term ischaemia refers to tissue which is inadequately perfused with blood.
The blood is circulated around the lungs and body by the pumping action of the heart. Additional return pressure may be generated by gravity and the actions of skeletal muscles. In mammals, blood is in equilibrium with lymph, which is continuously formed from blood (by capillary ultrafiltration) and returned to the blood (via the thoracic duct). The lymphatic circulation may be thought of as the “second circulation”.
Constituents of human blood
Blood accounts for 7% of the human body weight[1], with an average density of approximately 1060 kg/m³, very close to pure water’s density of 1000 kg/m3[2] The average adult has a blood volume of roughly 5 litres, composed of plasma (see below) and several kinds of cells (occasionally called corpuscles); these formed elements of the blood are erythrocytes (red blood cells), leukocytes (white blood cells), and thrombocytes (platelets). The red blood cells constitute about 45% of whole blood by volume.

Each litre of blood contains:[1]
- 5 × 1012 erythrocytes (45.0% of blood volume) : In mammals, mature red blood cells lack a nucleus and organelles. They contain the blood’s hemoglobin and distribute oxygen. The red blood cells (together with endothelial vessel cells and some other cells) are also marked by glycoproteins that define the different blood types. The proportion of blood occupied by red blood cells is referred to as the hematocrit. The combined surface area of all the red cells in the human body would be roughly 2,000 times as great as the body’s exterior surface.[3]
- 9 × 109 leukocytes (1.0% of blood volume) : White blood cells are part of the immune system; they destroy and remove old or aberrant cells and cellular debris, as well as attack infectious agents (pathogens) and foreign substances.
- 3 × 1011 thrombocytes (<1.0% of blood volume) : Platelets are responsible for blood clotting (coagulation). They change fibrinogen into fibrin. This fibrin creates a mesh onto which red blood cells collect and clot. This clot stops more blood from leaving the body and also helps to prevent bacteria from entering the body.
The other 55% (making up a total of 2.7-3.0 litres in an average human) is blood plasma, a fluid that is the blood’s liquid medium, appearing golden-yellow in color. Blood plasma is essentially an aqueous solution containing 92% water, 8% blood plasma proteins, and trace amounts of other materials. Some components are:
- Serum albumin
- Blood clotting factors (to facilitate coagulation)
- Immunoglobulins (antibodies)
- Hormones
- Carbon dioxide
- Various other proteins
- Various electrolytes (mainly sodium and chloride)
Together, plasma and cells form a non-Newtonian fluid whose flow properties are uniquely adapted to the architecture of the blood vessels. The term serum refers to plasma from which the clotting proteins have been removed. Most of the protein remaining is albumin and immunoglobulins.
The normal pH of human arterial blood is approximately 7.40 (normal range is 7.35-7.45), a weak alkaline solution. Blood that has a pH below 7.35 is considered overly acidic, while blood pH above 7.45 is too alkaline. Blood pH along with arterial carbon dioxide tension (PaCO2) and HCO3 readings are helpful in determining the acid-base balance of the body. The respiratory system and urinary system normally control the acid-base balance of blood as part of homeostasis.
Physiology
Production and degradation
Blood cells are produced in the bone marrow; this process is termed hematopoiesis. The proteinaceous component (including clotting proteins) is produced overwhelmingly in the liver, while hormones are produced by the endocrine glands and the watery fraction is regulated by the hypothalamus and maintained by the kidney and indirectly by the gut.
Blood cells are degraded by the spleen and the Kupffer cells in the liver. The liver also clears some proteins, lipids and amino acids. The kidney actively secretes waste products into the urine. Healthy erythrocytes have a plasma half-life of 120 days before they are systematically replaced by new erythrocytes created by the process of hematopoiesis.
Transport of oxygen
Blood oxygenation is measured in several ways, but the most important measure is the hemoglobin (Hb) saturation percentage. This is a non-linear (sigmoidal) function of the partial pressure of oxygen. About 98.5% of the oxygen in a sample of arterial blood in a healthy human breathing air at normal pressure is chemically combined with the Hb. Only 1.5% is physically dissolved in the other blood liquids and not connected to Hb. The hemoglobin molecule is the primary transporter of oxygen in mammals and many other species (for exceptions, see below).
With the exception of pulmonary and umbilical arteries and their corresponding veins, arteries carry oxygenated blood away from the heart and deliver it to the body via arterioles and capillaries, where the oxygen is consumed; afterwards, venules and veins carry deoxygenated blood back to the heart.
Differences in infrared absorption between oxygenated and deoxygenated blood form the basis for realtime oxygen saturation measurement in hospitals and ambulances.
Under normal conditions in humans at rest, hemoglobin in blood leaving the lungs is about 98-99% saturated with oxygen. In a healthy adult at rest, deoxygenated blood returning to the lungs is still approximately 75% saturated.[4][5] Increased oxygen consumption during sustained exercise reduces the oxygen saturation of venous blood, which can reach less than 15% in a trained athlete; although breathing rate and blood flow increase to compensate, oxygen saturation in arterial blood can drop to 95% or less under these conditions.[6] Oxygen saturation this low is considered dangerous in an individual at rest (for instance, during surgery under anesthesia): “As a general rule, any condition which leads to a sustained mixed venous saturation of less than 50% will be poorly tolerated and a mixed venous saturation of less than 30% should be viewed as a medical emergency.”[7]
A fetus, receiving oxygen via the placenta, is exposed to much lower oxygen pressures (about 21% of the level found in an adult’s lungs) and so fetuses produce another form of hemoglobin with a much higher affinity for oxygen (hemoglobin F) in order to function under these conditions.[8]
Substances other than oxygen can bind to the hemoglobin; in some cases this can cause irreversible damage to the body. Carbon monoxide for example is extremely dangerous when absorbed into the blood. When combined with the hemoglobin, it irreversibly makes carboxyhemoglobin which reduces the volume of oxygen that can be carried in the blood. This can very quickly cause suffocation, as oxygen is vital to many organisms (including humans). This damage can occur when smoking a cigarette (or similar item) or in event of a fire. Thus carbon monoxide is considered far more dangerous than the actual fire itself because it reduces the oxygen carrying content of the blood.
Invertebrates
In insects, the blood (more properly called hemolymph) is not involved in the transport of oxygen. (Openings called tracheae allow oxygen from the air to diffuse directly to the tissues). Insect blood moves nutrients to the tissues and removes waste products in an open system.
Other invertebrates use respiratory proteins to increase the oxygen carrying capacity. Hemoglobin is the most common respiratory protein found in nature. Hemocyanin (blue) contains copper and is found in crustaceans and mollusks. It is thought that tunicates (sea squirts) might use vanabins (proteins containing vanadium) for respiratory pigment (bright green, blue, or orange).
In many invertebrates, these oxygen-carrying proteins are freely soluble in the blood; in vertebrates they are contained in specialized red blood cells, allowing for a higher concentration of respiratory pigments without increasing viscosity or damaging blood filtering organs like the kidneys.
Giant tube worms have extraordinary hemoglobins that allow them to live in extraordinary environments. These hemoglobins also carry sulfides normally fatal in other animals.
Transport of carbon dioxide
When systemic arterial blood flows through capillaries, carbon dioxide diffuses from the tissues into the blood. Some carbon dioxide is dissolved in the blood. Some carbon dioxide reacts with hemoglobin and other proteins to form carbamino compounds. The remaining carbon dioxide is converted to bicarbonate and hydrogen ions through the action of RBC carbonic anhydrase. Most carbon dioxide is transported through the blood in the form of bicarbonate ions.
Transport of hydrogen ions
Some oxyhemoglobin loses oxygen and becomes deoxyhemoglobin. Deoxyhemoglobin has a much greater affinity for hydrogen ion (H+) than does oxyhemoglobin so it binds most of the hydrogen ions.
Thermoregulation
Blood circulation transports heat through the body, and adjustments to this flow are an important part of thermoregulation. Increasing blood flow to the surface (e.g. during warm weather or strenuous exercise) causes warmer skin, resulting in faster heat loss, while decreasing surface blood flow conserves heat.
Hydraulic functions
The restriction of blood flow can also be used in specialized tissues to cause engorgement resulting in an erection of that tissue. Examples of this would occur in a mammalian penis, clitoris or nipple.
Another example of a hydraulic function is the jumping spider, in which blood forced into the legs under pressure causes them to straighten for a powerful jump.
Color

In humans and other hemoglobin-using creatures, oxygenated blood is bright red. This is due to oxygenated iron-containing hemoglobin found in the red blood cells. Deoxygenated blood is a darker shade of red, which can be seen during blood donation and when venous blood samples are taken.
The blood of most molluscs, and some arthropods such as horseshoe crabs, is blue. This is a result of its high content of copper-based hemocyanin instead of the iron-based hemoglobin found, for example, in mammals. While mammalian blood is never blue, there is a rare condition (sulfhemoglobinemia) that results in green blood. Skinks in the genus Prasinohaema have green blood due to a buildup of the waste product biliverdin.
Health and disease
Ancient medicine
Hippocratic medicine considered blood one of the four humors (together with phlegm, yellow bile and black bile). As many diseases were thought to be due to an excess of blood, bloodletting and leeching were a common intervention until the 19th century (it is still used for some rare blood disorders).
In classical Greek medicine, blood was associated with air, springtime, and with a merry and gluttonous (sanguine) personality. It was also believed to be produced exclusively by the liver.
Diagnosis
Blood pressure and blood tests are amongst the most commonly performed diagnostic investigations that directly concern the blood.
Pathology
Problems with blood circulation and composition play a role in many diseases.
- Wounds can cause major blood loss (see bleeding). The thrombocytes cause the blood to coagulate, blocking relatively minor wounds, but larger ones must be repaired at speed to prevent exsanguination. Damage to the internal organs can cause severe internal bleeding, or hemorrhage.
- Circulation blockage can also create many medical conditions from ischemia in the short term to tissue necrosis and gangrene in the long term.
- Hemophilia is a genetic illness that causes dysfunction in one of the blood’s clotting mechanisms. This can allow otherwise inconsequential wounds to be life-threatening, but more commonly results in hemarthrosis, or bleeding into joint spaces, which can be crippling.
- Leukemia is a group of cancers of the blood-forming tissues.
- Major blood loss, whether traumatic or not (e.g. during surgery), as well as certain blood diseases like anemia and thalassemia, can require blood transfusion. Several countries have blood banks to fill the demand for transfusable blood. A person receiving a blood transfusion must have a blood type compatible with that of the donor.
- Overproduction of red blood cells is called polycythemia.
- Blood is an important vector of infection. HIV, the virus which causes AIDS, is transmitted through contact between blood, semen, or the bodily secretions of an infected person. Hepatitis B and C are transmitted primarily through blood contact. Owing to blood-borne infections, bloodstained objects are treated as a biohazard.
- Bacterial infection of the blood is bacteremia or sepsis. Viral Infection is viremia. Malaria and trypanosomiasis are blood-borne parasitic infections.
Treatment
Blood transfusion is the most direct therapeutic use of blood. It is obtained from human donors by blood donation. As there are different blood types, and transfusion of the incorrect blood may cause severe complications, crossmatching is done to ascertain the correct type is transfused.
Other blood products administered intravenously are platelets, blood plasma, cryoprecipitate and specific coagulation factor concentrates.
Many forms of medication (from antibiotics to chemotherapy) are administered intravenously, as they are not readily or adequately absorbed by the digestive tract.
As stated above, some diseases are still treated by removing blood from the circulation, eg. haemochromatosis.
It is the fluid part of the blood that saves lives where severe blood loss occurs, other preparations can be given such as ringers atopical plasma volume expander as a non-blood alternative, and these alternatives where used are rivalling blood use when used.
See also
- Blood substitutes often called Artificial blood
- List of human blood components
- blood phobia
- Medical technologist
References
- ↑ 1.0 1.1 Alberts, Bruce (2005). “Leukocyte functions and percentage breakdown”. Molecular Biology of the Cell. NCBI Bookshelf.
- ↑ “Density of Blood”. The Physics Factbook. 2004. External link in
|publisher=(help) - ↑ Martini, Frederic, et al (2006). Human Anatomy. 5th ed. Page 529. San Francisco, California: Pearson Education, Inc. ISBN 0-8053-7211-3
- ↑ Ventilation and Endurance Performance
- ↑ Transplant Support- Lung, Heart/Lung, Heart MSN groups
- ↑ J Physiol. 2005 July 1
- ↑ The ‘St George’ Guide To Pulmonary Artery Catheterisation
- ↑ Oxygen Carriage in Blood – High Altitude
ar:دم arc:ܕܡܐ zh-min-nan:Hoeh be-x-old:Кроў bar:Bluad bs:Krv bg:Кръв ca:Sang cs:Krev cy:Gwaed da:Blod de:Blut et:Veri el:Αίμα eo:Sango eu:Odol fa:خون gd:Fuil gl:Sangue ko:혈액 hr:Krv id:Darah ia:Sanguine is:Blóð it:Sangue he:דם pam:Daya ka:სისხლი kk:Қан ku:Xwîn la:Sanguis lv:Asinis lb:Blutt lt:Kraujas ln:Makilá hu:Vér mk:Крв mt:Demm ms:Darah cdo:Háik nl:Bloed no:Blod nn:Blod oc:Sang ps:وينه nds:Blood qu:Yawar sq:Gjaku simple:Blood sk:Krv sl:Kri sr:Крв sh:Krv su:Getih fi:Veri sv:Blod ta:குருதி te:రక్తం th:เลือด uk:Кров vls:Bloed yi:בלוט zh-yue:血 bat-smg:Kraus
(42-54) Operations on the digestive system
(42-54) Operations on the digestive system
- (Template:ICD9proc) Operations on esophagus
- (Template:ICD9proc) Excision of esophagus
- (Template:ICD9proc) Esophagectomy, not otherwise specified
- (Template:ICD9proc) Excision of esophagus
- (Template:ICD9proc) Incision and excision of stomach
- (Template:ICD9proc) Gastrotomy
- (Template:ICD9proc) Gastrostomy
- (Template:ICD9proc) Pyloromyotomy
- (Template:ICD9proc) Local excision or destruction of lesion or tissue of stomach
- (Template:ICD9proc) Partial gastrectomy with anastomosis to esophagus
- (Template:ICD9proc) Partial gastrectomy with anastomosis to duodenum
- (Template:ICD9proc) Partial gastrectomy with anastomosis to jejunum
- (Template:ICD9proc) Other partial gastrectomy
- (Template:ICD9proc) Total gastrectomy
- (Template:ICD9proc) Other operations on stomach
- (Template:ICD9proc) Vagotomy
- (Template:ICD9proc) Gastroenterostomy without gastrectomy
- (Template:ICD9proc) High gastric bypass
- (Template:ICD9proc) Percutaneous (endoscopic) gastrojejunostomy
- (Template:ICD9proc) Laparoscopic gastroenterostomy
- (Template:ICD9proc) Other gastroenterostomy
- (Template:ICD9proc) Incision, excision, and anastomosis of intestine
- (Template:ICD9proc) Diagnostic procedures on small intestine
- (Template:ICD9proc) Transabdominal endoscopy of small intestine
- (Template:ICD9proc) Endoscopy of small intestine through artificial stoma
- (Template:ICD9proc) Other endoscopy of small intestine
- (Template:ICD9proc) Closed (endoscopic) biopsy of small intestine
- (Template:ICD9proc) Open biopsy of small intestine
- (Template:ICD9proc) Esophagogastroduodenoscopy (EGD) with closed biopsy
- (Template:ICD9proc) Other diagnostic procedures on small intestine
- (Template:ICD9proc) Diagnostic procedures on large intestine
- (Template:ICD9proc) Partial excision of large intestine
- (Template:ICD9proc) Right hemicolectomy
- (Template:ICD9proc) Total intra-abdominal colectomy
- (Template:ICD9proc) Diagnostic procedures on small intestine
- (Template:ICD9proc) Other operations on intestine
- (Template:ICD9proc) Operations on appendix
- (Template:ICD9proc) Operations on rectum, rectosigmoid and perirectal tissue
- (Template:ICD9proc) Diagnostic procedures on rectum, rectosigmoid and perirectal tissue
- (Template:ICD9proc) Transabdominal proctosigmoidoscopy
- (Template:ICD9proc) Proctosigmoidoscopy through artificial stoma
- (Template:ICD9proc) Rigid proctosigmoidoscopy
- (Template:ICD9proc) Closed (endoscopic) biopsy of rectum
- (Template:ICD9proc) Open biopsy of rectum
- (Template:ICD9proc) Biopsy of perirectal tissue
- (Template:ICD9proc) Other diagnostic procedures on rectum, rectosigmoid and perirectal tissue
- (Template:ICD9proc) Diagnostic procedures on rectum, rectosigmoid and perirectal tissue
- (Template:ICD9proc) Operations on anus
- (Template:ICD9proc) Incision or excision of perianal tissue
- (Template:ICD9proc) Incision or excision of anal fistula
- (Template:ICD9proc) Diagnostic procedures on anus andperianal tissue
- (Template:ICD9proc) Local excision or destruction of other lesion or tissue of anus
- (Template:ICD9proc) Procedures on hemorrhoids
- (Template:ICD9proc) Excision of hemorrhoids
- Hemorrhoidectomy NOS
- (Template:ICD9proc) Excision of hemorrhoids
- (Template:ICD9proc) Division of anal sphincter
- (Template:ICD9proc) Excision of anus
- (Template:ICD9proc) Repair of anus
- (Template:ICD9proc) Other operations on anus
- (Template:ICD9proc) Operations on liver
- (Template:ICD9proc) Hepatotomy
- (Template:ICD9proc) Diagnostic procedures on liver
- (Template:ICD9proc) Local excision or destruction of liver tissue or lesion
- (Template:ICD9proc) Marsupialization of lesion of liver
- (Template:ICD9proc) Partial hepatectomy
- (Template:ICD9proc) Other destruction of lesion of liver
- (Template:ICD9proc) Lobectomy of liver
- (Template:ICD9proc) Total hepatectomy
- (Template:ICD9proc) Liver transplant
- (Template:ICD9proc) Repair of liver
- (Template:ICD9proc) Other operations on liver
- (Template:ICD9proc) Operations on gallbladder and biliary tract
- (Template:ICD9proc) Cholecystotomy and cholecystostomy
- (Template:ICD9proc) Diagnostic procedures on biliary tract
- (Template:ICD9proc) Cholecystectomy
- (Template:ICD9proc) Anastomosis of gallbladder or bile duct
- (Template:ICD9proc) Incision of bile duct for relief of obstruction
- (Template:ICD9proc) Other incision of bile duct
- (Template:ICD9proc) Local excision or destruction of lesion or tissue of biliary ducts and sphincter of Oddi
- (Template:ICD9proc) Repair of bile ducts
- (Template:ICD9proc) Other operations on biliary ducts and sphincter of Oddi
- (Template:ICD9proc) Other operations on biliary tract
- (Template:ICD9proc) Operations on pancreas
- (Template:ICD9proc) Pancreatotomy
- (Template:ICD9proc) Diagnostic procedures on pancreas
- (Template:ICD9proc) Local excision or destruction of pancreas and pancreatic duct
- (Template:ICD9proc) Marsupialization of pancreatic cyst
- (Template:ICD9proc) Internal drainage of pancreatic cyst
- (Template:ICD9proc) Partial pancreatectomy
- (Template:ICD9proc) Total pancreatectomy
- (Template:ICD9proc) Radical pancreaticoduodenectomy
- (Template:ICD9proc) Transplant of pancreas
- (Template:ICD9proc) Other operations on pancreas
- (Template:ICD9proc) Repair of hernia
- (Template:ICD9proc) Other operations on abdominal region
- (Template:ICD9proc) Laparotomy
- (Template:ICD9proc) Other operations of abdominal region
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
The digestive system is the organ system that breaks down and absorbs nutrients that are essential for growth and maintenance.
The digestive system includes the mouth, esophagus, stomach, pancreas, liver, gallbladder, duodenum, jejunum, ileum, (intestines), rectum, and anus.
This page contains links to all the parts of the digestive system.
External links
Template:Organ systems Template:Digestive tract Template:Digestive glands Template:Development of digestive system Template:Gastroenterology
af:Spysverteringstelsel ar:جهاز هضمي bn:পাচনতন্ত্র zh-min-nan:Siau-hoà hē-thóng mk:Систем за варење mt:Sistema diġestiva simple:Gastrointestinal system
(55-59) Operations on the urinary system
(55-59) Operations on the urinary system
- (Template:ICD9proc) Operations on kidney
- (Template:ICD9proc) Nephrotomy and nephrostomy
- (Template:ICD9proc) Pyelotomy and pyelostomy
- (Template:ICD9proc) Diagnostic procedures on kidney
- (Template:ICD9proc) Local excision or destruction of lesion or tissue of kidney
- (Template:ICD9proc) Partial nephrectomy
- (Template:ICD9proc) Complete nephrectomy
- (Template:ICD9proc) Transplant of kidney
- (Template:ICD9proc) Nephropexy
- (Template:ICD9proc) Other repair of kidney
- (Template:ICD9proc) Other operations on kidney
- (Template:ICD9proc) Operations on ureter
- (Template:ICD9proc) Transurethral removal of obstruction from ureter and renal pelvis
- (Template:ICD9proc) Ureteral meatotomy
- (Template:ICD9proc) Ureterotomy
- (Template:ICD9proc) Diagnostic procedures on ureter
- (Template:ICD9proc) Ureterectomy
- (Template:ICD9proc) Cutaneous uretero-ileostomy
- (Template:ICD9proc) Other external urinary diversion
- (Template:ICD9proc) Formation of other cutaneous ureterostomy
- Ureterostomy NOS
- (Template:ICD9proc) Formation of other cutaneous ureterostomy
- (Template:ICD9proc) Other anastomosis or bypass of ureter
- (Template:ICD9proc) Urinary diversion to intestine
- Internal urinary diversion NOS
- (Template:ICD9proc) Urinary diversion to intestine
- (Template:ICD9proc) Repair of ureter
- (Template:ICD9proc) Other operations on ureter
- (Template:ICD9proc) Operations on urinary bladder
- (Template:ICD9proc) Transurethral clearance of bladder
- (Template:ICD9proc) Cystotomy and cystostomy
- (Template:ICD9proc) Vesicostomy
- (Template:ICD9proc) Diagnostic procedures on bladder
- (Template:ICD9proc) Transurethral excision or destruction of bladder tissue
- (Template:ICD9proc) Other excision or destruction ofbladder tissue
- (Template:ICD9proc) Partial cystectomy
- (Template:ICD9proc) Total cystectomy
- (Template:ICD9proc) Other repair of urinary bladder
- (Template:ICD9proc) Other operations on bladder
- (Template:ICD9proc) Operations on urethra
- (Template:ICD9proc) Other operations on urinary tract
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Associate Editor-In-Chief: Cafer Zorkun, M.D., Ph.D. [2]
Overview
The urinary system is the organ system that produces, stores, and eliminates urine. In humans it includes two kidneys, two ureters, the bladder, and the urethra. The analogous organ in invertebrates is the nephridium (in animals).
Physiology

Typically, every human has two kidneys. The kidneys are bean-shaped organs about the size of a bar of soap. The kidneys lie in the abdomen, posterior or retroperitoneal to the organs of digestion, around or just below the ribcage and close to the lumbar spine. The kidneys are surrounded by what is called peri-nephric fat, and situated on the superior pole of each kidney is an adrenal gland. The kidneys receive their blood supply of 1.25 L/min (25% of the cardiac output) from the renal arteries which are fed by the Abdominal aorta. This is important because the kidneys’ main role is to filter water soluble waste products from the blood. The other attachment of the kidneys are at their functional endpoints the ureters, which lies more medial and runs down to the trigone of the bladder.
Functionally the kidney performs a number of tasks. In its role in the urinary system it concentrates urine, plays a crucial role in regulating electrolytes, and maintains acid-base homeostasis. The kidney excretes and re-absorbs electrolytes (e.g. sodium, potassium and calcium) under the influence of local and systemic hormones. pH balance is regulated by the excretion of bound acids and ammonium ions. In addition, they remove urea, a nitrogenous waste product from the metabolism of proteins from amino acids. The end point is a hyperosmolar solution carrying waste for storage in the bladder prior to urination.
Humans produce about 1.5 liters of urine over 24 hours, although this amount may vary according to circumstances. Because the rate of filtration at the kidney is proportional to the glomerular filtration rate, which is in turn related to the blood flow through the kidney, changes in body fluid status can affect kidney function. Hormones exogenous and endogenous to the kidney alter the amount of blood flowing through the glomerulus. Some medications interfere directly or indirectly with urine production. Diuretics achieve this by altering the amount of absorbed or excreted electrolytes or osmalites, which causes a diuresis.
Bladder
The urinary bladder is a hollow muscular organ shaped like a balloon. It is located in the anterior pelvis. The bladder stores urine; it swells into a round shape when it is full and gets smaller when empty. In the absence of bladder disease, it can hold up to 500 mL (17 fl. oz.) of urine comfortably for two to five hours. The epithelial tissue associated with the bladder is called transitional epithelium. It allows the bladder to stretch to accommodate urine without rupturing the tissue.
Normally the bladder is sterile.
Sphincters (circular muscles) regulate the flow of urine from the bladder. The bladder itself has a muscular layer (detrusor muscle) that, when contracted, increases pressure on the bladder and creates urinary flow.
Urination is a conscious process, generally initiated by stretch receptors in the bladder wall which signal to the brain that the bladder is full. This is felt as an urge to urinate. When urination is initiated, the sphincter relaxes and the detrusor muscle contracts, producing urinary flow.
Urethra
The endpoint of the urinary system is the urethra. Typically the urethra in humans is colonised by commensal bacteria below the external urethral sphincter. The urethra emerges from the end of the penis in males and between the clitoris and vagina in females.
Role in disease
Kidney diseases are normally investigated and treated by nephrologists, while the specialty of urology deals with problems in the other organs. Gynecologists may deal with problems of incontinence in women.
Diseases of other bodily systems also have a direct effect on urogenital function. For instance it has been shown that protein released by the kidneys in diabetes mellitus sensitises the kidney to the damaging effects of hypertension[1].
Diabetes also can have a direct effect in micturition due to peripheral neuropathies which occur in some individuals with poorly controlled diabetics.
Kidney disease
Renal failure is defined by functional impairment of the kidney. Renal failure can be acute or chronic, and can be further broken down into categories of pre-renal, intrinsic renal and post-renal.
Pre-renal failure refers to impairment of supply of blood to the functional nephrons including renal artery stenosis. Intrinsic renal diseases are the classic diseases of the kidney including drug toxicity and nephritis. Post-renal failure is outlet obstruction after the kidney, such as a renal stone or prostatic bladder outlet obstruction.
Renal failure may require medication, dietary and lifestyle modification and dialysis.
Primary renal cell carcinomas as well as metastatic cancers can affect the kidney.
Non-renal urinary tract disease
The causes of diseases of the body are common to the urinary tract. Structural and or traumatic change can lead to hemorrhage, functional blockage or inflammation. Colonisation by bacteria, protozoa or fungi can cause infection. Uncontrolled cell growth can cause neoplasia.
For example:
- Urinary tract infections (UTIs), interstitial cystitis
- incontinence (involuntary loss of urine), benign prostatic hyperplasia (where the prostate overgrows), prostatitis (inflammation of the prostate).
- Transitional cell carcinoma (bladder cancer), renal cell carcinoma (kidney cancer), and prostate cancer are examples of neoplasms affecting the urinary system.
The term “uropathy” refers to a disease of the urinary tract, while “nephropathy” refers to a disease of the kidney.
Testing
Biochemical blood tests determine the amount of typical markers of renal function in the blood serum, for instance serum urea and serum creatinine. Biochemistry can also be used to determine serum electrolytes. Special biochemical tests (arterial blood gas) can determine the amount of dissolved gases in the blood, indicating if pH imbalances are acute or chronic.
Urinalysis is a test that studies the content of urine for abnormal substances such as protein or signs of infection.
- A Full Ward Test, also known as dipstick urinalysis, involves the dipping of a biochemically active test strip into the urine specimen to determine levels of tell-tale chemicals in the urine.
- Urinalysis can also involve MC&S microscopy , culture and sensitivity
Urodynamic tests evaluate the storage of urine in the bladder and the flow of urine from the bladder through the urethra. It may be performed in cases of incontinence or neurological problems affecting the urinary tract.
Ultrasound is commonly performed to investigate problems of the kidney and/or urinary tract.
- KUB is plain radiography of the urinary system, e.g. to identify kidney stones.
- An intravenous pyelogram studies the shape of the urinary system.
- CAT scans and MRI can also be useful in localising urinary tract pathology.
Development
See also
References
- ↑ Baba T, Murabayashi S, Tomiyama T, Takebe K; Uncontrolled hypertension is associated with a rapid progression of nephropathy in type 2 diabetic patients with proteinuria and preserved renal function. Tohoku J Exp Med 1990 Aug;161(4):311-8 PMID 2256104
Template:Urinary system Template:Organ systems
ar:جهاز بولي de:Harnwege eo:Urina Sistemo eu:Gernu-aparatu fa:دستگاه ادراری lt:Šlapimo šalinimo sistema sr:Уринарни систем sv:Utsöndringen
(60-64) Operations on the male genital organs
(60-64) Operations on the male genital organs
- (Template:ICD9proc) Operations on prostate and seminal vesicles
- (Template:ICD9proc) Incision of prostate
- (Template:ICD9proc) Diagnostic procedures on prostate and seminal vesicles
- (Template:ICD9proc) Transurethral prostatectomy
- (Template:ICD9proc) Suprapubic prostatectomy
- (Template:ICD9proc) Retropubic prostatectomy
- (Template:ICD9proc) Radical prostatectomy
- (Template:ICD9proc) Other prostatectomy
- (Template:ICD9proc) Operations on seminal vesicles
- (Template:ICD9proc) Incision or excision of periprostatic tissue
- (Template:ICD9proc) Other operations on prostate
- (Template:ICD9proc) Operations on scrotum and tunica vaginalis
- (Template:ICD9proc) Operations on testes
- (Template:ICD9proc) Operations on spermatic cord, epididymis, and vas deferens
- (Template:ICD9proc) Vasectomy and ligation of vas deferens
- (Template:ICD9proc) Repair of vas deferens and epididymis
- (Template:ICD9proc) Reconstruction of surgically divided vas deferens
- (Template:ICD9proc) Operations on penis
- (Template:ICD9proc) Circumcision
- (Template:ICD9proc) Diagnostic procedures on the penis
- (Template:ICD9proc) Local excision or destruction of lesion of penis
- (Template:ICD9proc) Amputation of penis
- (Template:ICD9proc) Repair and plastic operation on penis
- (Template:ICD9proc) Operations for sex transformation, not elsewhere classified
- (Template:ICD9proc) Other operations on male genital organs
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
The human male reproductive system is a series of organs located outside of the body and around the pelvic region of a male that contribute towards the reproductive process.
The male contributes to reproduction by producing spermatozoa. The spermatozoa then fertilize the egg in the female body and the fertilized egg (zygote) gradually develops into a fetus, which is later born as a child.
Testes
The testes hang outside the abdominal cavity of the male within the scrotum. They begin their development in the abdominal cavity but descend into the scrotal sacs during the last 2 months of fetal development. This is required for the production of sperm because internal body temperatures are too high to produce viable sperm.
In the body of an average male, there are two testicles located in a sac called the scrotum. On top of these organs is the epididymis, the “housing area” for sperm that has been produced. The tightly coiled epididymis (6 meters or 20 feet when unraveled) store sperm cells for up to 4 weeks, while they are learning to swim.
Penis
The penis has a long shaft and enlarged tip called the glans penis. The penis is the copulatory organ of the males. When the male is sexually aroused, the penis becomes erect and ready for intercourse. Erection is achieved because blood sinuses within the erectile tissue of the penis become filled with blood. The arteries of the penis are dilated while the veins are passively compressed so that blood flows into the erectile cartilage under pressure. The male penis is made of two different tissues, soft spongey tissue and cartilage. is a pelvic bone in the front top of the penis.
Sperm & seminal fluid
A mature spermatoza, or spermatozoon, has 3 distinct parts: a head, a mid-piece, and a tail. The tail is made up of microtubules that form cilia and flagella, and the mid-piece contains energy-producing mitochondria. The head contains 23 chromosomes within a nucleus. The tip of the nucleus is covered by a cap called the acrosome, which is believed to contain enzymes needed to breach the egg for fertilization. A normal human male usually produces several hundred million sperm per day. Sperm are continually produced throughout a male’s reproductive life, though production decreases with age.
During ejaculation, sperm leaves the penis in a fluid called seminal fluid. This fluid is produced by 3 types of glands, the seminal vesicles, the prostate gland, and Cowper’s glands (bulbourethral glands). Each component of a seminal fluid has a particular function. Sperm are more viable in a basic solution, so seminal fluid has a slightly basic pH. Seminal fluid also acts as an energy source for the sperm, and contains chemicals that cause the uterus to contract.There is a tiny gland that holds sperm.
External links
Template:Male reproductive system
bs:Muški reproduktivni sistem da:Mandens kønsorganer fa:دستگاه تولید مثل در مردان ko:남성의 생식 기관 hr:Muški spolni sustav it:Apparato genitale maschile lt:Vyro lytiniai organai te:పురుష జననేంద్రియ వ్యవస్థ
(65-71) Operations on the female genital organs
(65-71) Operations on the female genital organs
- (Template:ICD9proc) Operations on ovary
- (Template:ICD9proc) Oophorotomy
- (Template:ICD9proc) Diagnostic procedures on ovaries
- (Template:ICD9proc) Local excision or destruction of ovarian lesion or tissue
- (Template:ICD9proc) Unilateral oophorectomy
- (Template:ICD9proc) Unilateral salpingo-oophorectomy
- (Template:ICD9proc) Bilateral oophorectomy
- (Template:ICD9proc) Bilateral salpingo-oophorectomy
- (Template:ICD9proc) Repair of ovary
- (Template:ICD9proc) Lysis of adhesions of ovary and fallopian tube
- (Template:ICD9proc) Other operations on ovary
- (Template:ICD9proc) Operations on fallopian tubes
- (Template:ICD9proc) Salpingotomy and salpingostomy
- (Template:ICD9proc) Diagnostic procedures on fallopian tubes
- (Template:ICD9proc) Bilateral endoscopic destruction or occlusion of fallopian tubes
- (Template:ICD9proc) Other bilateral destruction or occlusion of fallopian tubes
- (Template:ICD9proc) Total unilateral salpingectomy
- (Template:ICD9proc) Total bilateral salpingectomy
- (Template:ICD9proc) Other salpingectomy
- (Template:ICD9proc) Repair of fallopian tube
- (Template:ICD9proc) Insufflation of fallopian tube
- (Template:ICD9proc) Other operations on fallopian tubes
- (Template:ICD9proc) Operations on cervix
- (Template:ICD9proc) Other incision and excision of uterus
- (Template:ICD9proc) Hysterotomy
- (Template:ICD9proc) Diagnostic procedures on uterus and supporting structures
- (Template:ICD9proc) Vaginal hysterectomy
- (Template:ICD9proc) Other operations on uterus and supporting structures
- (Template:ICD9proc) Dilation and curettage of uterus
- (Template:ICD9proc) Excision or destruction of lesion or tissue of uterus and supporting structures
- (Template:ICD9proc) Repair of uterine supporting structures
- (Template:ICD9proc) Paracervical uterine denervation
- (Template:ICD9proc) Uterine repair
- (Template:ICD9proc) Aspiration curettage of uterus
- (Template:ICD9proc) Menstrual extraction or regulation
- (Template:ICD9proc) Insertion of intrauterine contraceptive device
- (Template:ICD9proc) Other operations on uterus, cervix, and supporting structures
- (Template:ICD9proc) Operations on vagina and cul-de-sac
- (Template:ICD9proc) Culdocentesis
- (Template:ICD9proc) Incision of vagina and cul-de-sac
- (Template:ICD9proc) Diagnostic procedures on vagina and cul-de-sac
- (Template:ICD9proc) Local excision or destruction of vagina and cul-de-sac
- (Template:ICD9proc) Obliteration and total excision of vagina
- (Template:ICD9proc) Repair of cystocele and rectocele
- (Template:ICD9proc) Vaginal construction and reconstruction
- (Template:ICD9proc) Other repair of vagina
- (Template:ICD9proc) Obliteration of vaginal vault
- (Template:ICD9proc) Other operations on vagina and cul-de-sac
- (Template:ICD9proc) Operations on vulva and perineum
- (Template:ICD9proc) Incision of vulva and perineum
- (Template:ICD9proc) Diagnostic procedures on vulva
- (Template:ICD9proc) Operations on Bartholin’s gland
- (Template:ICD9proc) Other local excision or destruction of vulva and perineum
- (Template:ICD9proc) Operations on clitoris
- (Template:ICD9proc) Radical vulvectomy
- (Template:ICD9proc) Other vulvectomy
- (Template:ICD9proc) Repair of vulva and perineum
- (Template:ICD9proc) Other operations on vulva
- (Template:ICD9proc) Other operations on female genital organs
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
The human female reproductive system contains two main parts: the vagina and uterus, which act as the receptacle for the male’s sperm, and the ovaries, which produce the female’s ova. All of these parts are always internal; the vagina meets the outside at the vulva, which also includes the labia, clitoris and urethra. The vagina is attached to the uterus through the cervix, while the uterus is attached to the ovaries via the Fallopian tubes. At certain intervals, the ovaries release an ovum, which passes through the fallopian tube into the uterus.
If, in this transit, it meets with sperm, the sperm penetrate and merge with the egg, fertilizing it. The fertilization usually occurs in the oviducts, but can happen in the uterus itself. The zygote then implants itself in the wall of the uterus, where it begins the processes of embryogenesis and morphogenesis. When developed enough to survive outside the womb, the cervix dilates and contractions of the uterus propel the fetus through the birth canal, which is the vagina.
The ova are larger than sperm and are generally all created by birth. Approximately every month, a process of oogenesis matures one ovum to be sent down the Fallopian tube attached to its ovary in anticipation of fertilization. If not fertilized, this egg is flushed out of the system through menstruation.
Vagina
The vagina is the tubular tract leading from the uterus to the exterior of the body in female mammals, or to the cloaca in female birds and some reptiles. Female insects and other invertebrates also have a vagina, which is the terminal part of the oviduct.
The vagina is the place where semen from the man is deposited into the woman’s body during sexual intercourse.
Cervix
The cervix is the lower, narrow portion of the uterus where it joins with the top end of the vagina. It is cylindrical or conical in shape and protrudes through the upper anterior vaginal wall. Approximately half its length is visible; the remainder lies above the vagina beyond view.
Uterus
The uterus or womb is the major female reproductive organ of humans. One end, the cervix, opens into the vagina; the other is connected on both sides to the fallopian tubes.
The uterus mostly consists of muscle, known as myometrium. Its major function is to accept a fertilized ovum which becomes implanted into the endometrium, and derives nourishment from blood vessels which develop exclusively for this purpose. The fertilized ovum becomes an embryo, develops into a fetus and gestates until childbirth.
Oviducts
The Fallopian tubes or oviducts are two very fine tubes leading from the ovaries of female mammals into the uterus.
On maturity of an ovum, the follicle and the ovary’s wall rupture, allowing the ovum to escape and enter the Fallopian tube. There it travels toward the uterus, pushed along by movements of cilia on the inner lining of the tubes. This trip takes hours or days. If the ovum is fertilized while in the Fallopian tube, then it normally implants in the endometrium when it reaches the uterus, which signals the beginning of pregnancy.
Ovaries
The ovaries are the place inside the female body where ova or eggs are produced. The process by which the ovum is released is called ovulation. The speed of ovulation is periodic and impacts directly to the length of a menstrual cycle.
After ovulation, the ovum is captured by the oviduct, where it travelled down the oviduct to the uterus, occasionally being fertilised on its way by an incoming sperm, leading to pregnancy.
The Fallopian tubes are often called the oviducts and they have small hairs (cilia) to help the egg cell travel.
External Links
- OBGYN.net – Obstetrics, Gynaecology, Infertility, Pregnancy, Birth, & Women’s Health top online resource
Template:Female reproductive system
bg:Женски полови органи da:Kvindens kønsorganer ko:여성의 생식 기관 it:Apparato genitale femminile lt:Moters lytiniai organai
(72-75) Obstetrical procedures
(72-75) Obstetrical procedures
- (Template:ICD9proc) Other procedures inducing or assisting delivery
- (Template:ICD9proc) Artificial rupture of membranes
- (Template:ICD9proc) Other surgical induction of labor
- (Template:ICD9proc) Internal and combined version and extraction
- (Template:ICD9proc) Failed forceps
- (Template:ICD9proc) Medical induction of labor
- (Template:ICD9proc) Manually assisted delivery
- (Template:ICD9proc) Episiotomy
- (Template:ICD9proc) Operations on fetus to facilitate delivery
- (Template:ICD9proc) Other operations assisting delivery
- (Template:ICD9proc) Cesarean section and removal of fetus
- (Template:ICD9proc) Other obstetric operations
- (Template:ICD9proc) Diagnostic amniocentesis
- (Template:ICD9proc) Other intrauterine operations on fetus and amnion
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Obstetrics (from the Latin obstare, “to stand by”) is the surgical specialty dealing with the care of a woman and her offspring during pregnancy, childbirth and the puerperium (the period shortly after birth). Midwifery is the equivalent non-surgical specialty. Most obstetricians are also gynaecologists. See Obstetrics and gynaecology.
The average gestational period for humans is 40 weeks by gestational age and 38 weeks by fertilization age. This is divided into three trimesters.
Antenatal care
In obstetric practice, an obstetrician or midwife sees a pregnant woman on a regular basis to check the progress of the pregnancy, to verify the absence of ex-novo disease, to monitor the state of preexisting disease and its possible effect on the ongoing pregnancy. A woman’s schedule of antenatal appointment varies according to the presence of risk factors, such as diabetes, and local resources.
Some of the clinically and statistically more important risk factors that must be systematically excluded, especially in advancing pregnancy, are pre-eclampsia, abnormal placentation, abnormal fetal presentation and Intrauterine Growth Retardation.
For example, to identify pre-eclampsia, blood-pressure and albuminuria (level of urine protein) are checked at every opportunity.
Placenta praevia must be excluded (PP = low lying placenta that, at least partially, obstructs the birth canal and therefore warrants elective caesarean delivery); this can only be achieved with the use of an ultrasound scan.
In late pregnancy fetal presentation must be established: cepfalic presentation (head first) is the norm but the fetus may present feet-first or buttocks-first (breech), side-on (transverse), or at an angle (oblique presentation).
Intrauterine Growth Retardation is a general designation, where the fetus is smaller than expected when compared to its gestational age (in this case fetal growth parameters show a tendency to drop off from the 50th percentile eventually falling below the 10th percentile, when plotted on a fetal growth chart). Causes can be intrinsic (to the fetus) or extrinsic (maternal or placental problems).
Signs

Trimesters
First trimester: elevated β-hCG (human chorionic gonadotrophin) of up to 100,000 mIU/mL by 10 weeks GA is thought to contribute to morning sickness, fatigue, mood swings and food cravings. The symptoms can last through 12 to 16 weeks of gestation.
Second trimester: The abdomen shows an obvious swelling arising from the pelvis, starting the “obvious phase” of pregnancy. Hyperpigmentation, including linea nigra, may appear.
Third trimester: The mother may experience backaches due to increased strain. Typically, the curvature of the spine is changed as pregnancy evolves in order to counteract the change in weight distribution. The mother may also suffer mild urinary incontinence due to pressure on the bladder by the pregnant uterus, as well as heartburn(due to compression of the stomach).
Overall
- Bluish discoloration of vagina and cervix (Chadwick’s sign)
- Softening and cyanosis of cervix after 4 weeks (Goodell’s sign)
- Softening of uterus after 6 weeks (Hegar’s or Ladin’s sign)
- Breast swelling and tenderness
- Linea nigra from umbilicus to pubis
- Telangiectasias
- Palmar erythema
- Amenorrhea
- Nausea and vomiting
- Breast pain
- Fetal movement
- Sciatica (Pain caused by compression of the sciatic nerve)
Maternal physiology
During pregnancy, the woman undergoes many physiological changes, which are entirely normal, including cardiovascular, hematologic, metabolic, renal and respiratory changes that become very important in the event of complications.
Cardiovascular
The woman is the sole provider of nourishment for the embryo and later, the fetus, and so her plasma and blood volume slowly increase by 40-50% over the course of the pregnancy to accommodate the changes. This results in overall vasodilation, an increase in heart rate (15 beats/min more than usual), stroke volume, and cardiac output. Cardiac output increases by about 50%, mostly during the first trimester. The systemic vascular resistance also drops due to the smooth muscle relaxation caused by elevated progesterone, leading to a fall in blood pressure. Diastolic blood pressure consequently decreases between 12-26 weeks, and increases again to prepregnancy levels by 36 weeks. If the blood pressure remains abnormal beyond 36 weeks, the woman should be investigated for pre-eclampsia, a condition that precedes eclampsia.
Hematology
- The plasma volume increases by 50% and the red blood cell volume increases only by 20-30%.
- Consequently, the hematocrit decreases.
- White blood cell count increases and may peak at over 20 mil/mL in stressful conditions.
- Decrease in platelet concentration to a minimal normal values of 100-150 mil/mL
- The pregnant woman also becomes hypercoagulable due to increased liver production of coagulation factors, mainly fibrinogen and factor VIII.
Metabolism
During pregnancy, both protein metabolism and carbohydrate metabolism are affected. One kilogram of extra protein is deposited, with half going to the fetus and placenta, and another half going to uterine contractile proteins, breast glandular tissue, plasma protein, and hemoglobin.
Nutrition
- Increased caloric requirement by 300 kcal/day
- Gain of 20 to 30 lb (10 to 15 kg)
- Increased protein requirement to 70 or 75 g/day
- Increased folate requirement from 0.4 to 0.8 mg/day (important in preventing neural tube defects)
All patients are advised to take prenatal vitamins to compensate for the increased nutritional requirements. The use of Omega 3 fatty acids supports mental and visual development of infants.[1] Choline supplementation of research mammals supports mental development that lasts throughout life.[2]
Gastrointestinal
- nausea and vomiting (“morning sickness“) may be due to elevated Beta-hCG, which should resolve by 14 to 16 weeks
- prolonged gastric empty time
- decreased gastroesophageal sphincter tone, which can lead to acid reflux
- decreased colonic motility, which leads to increased water absorption and constipation
Renal
- Increase in kidney and ureter size
- Increased glomerular filtration rate (GFR) by 50%, which subsides around 20 weeks postpartum
- Decreased BUN (blood urea nitrogen) and creatinine, and glucosuria (due to saturated tubular reabsorption)
- Persistent glucosuria can suggest gestational diabetes
- Decreased BUN (blood urea nitrogen) and creatinine, and glucosuria (due to saturated tubular reabsorption)
- Increased renin-angiotensin system, causing increased aldosterone levels
- Plasma sodium does not change because this is offset by the increase in GFR
Pulmonary
- Increased tidal volume (30-40%)
- Decreased total lung capacity (TLC) by 5% due to elevation of diaphragm from uteral compression
- Decreased expiratory reserve volume
- Increased minute ventilation (30-40%) which causes a decrease in PaCO2 and a compensated respiratory alkalosis
All of these changes can contribute to the dyspnea (shortness of breath) that a pregnant woman may experience.
Endocrine
- Increased estrogen, which is mainly produced in the placenta
- Fetal well being is associated with maternal estrogen levels
- Causes an increase in thyroxine-binding globulin (TBG)
- Increased human chorionic gonadotropin (β-hCG), which is produced by the placenta. This maintains progesterone production by the corpus luteum
- Human placental lactogen (hPL) is produced by the placenta and ensures nutrient supply to the fetus. It also causes lipolysis and is an insulin antagonist, which is a diabetogenic effect.
- Increased progesterone production, first by corpus luteum and later by the placenta. Its main course of action is to relax smooth muscle.
- Increased prolactin
- Increased alkaline phosphatase
Musculoskeleton and dermatology
- Lower back pain due to a shift in gravity
- Increased estrogen can cause spider angiomata and palmar erythema
- Increase melanocyte stimulating hormone (MSH) can cause hyperpigmentation of nipples, umbilicus, abdominal midline (linea nigra), perineum, and face (melasma or chloasma)
Others
- Edema, or swelling, of the feet is common during pregnancy, partly because the enlarging uterus compresses veins and lymphatic drainage from the legs.
Prenatal care
Prenatal care is important in screening for various complications of pregnancy. This includes routine office visits with physical exams and routine lab tests:
First trimester
- complete blood count (CBC)
- blood type (blood transfusion may be needed in an emergency)
- general antibody screen (indirect Coombs test) for HDN
- Rh D negative antenatal patients should receive RhoGam at 28 weeks to prevent Rh disease.
- Rapid plasma reagent (RPR) which screens for syphilis
- Rubella antibody screen
- Hepatitis B surface antigen
- Gonorrhea and Chlamydia culture
- PPD for tuberculosis
- Pap smear
- Urinalysis and culture
- HIV screen
- Group B Streptococcus screen — will receive IV penicillin if positive (if mother is allergic, alternative therapies include IV clindamycin or IV vancomycin)
Second trimester
- MSAFP/triple screen (maternal serum alpha-fetoprotein) – elevation correlated with neural tube defects and decrease correlated with Down’s syndrome
- ultrasound
- amniocentesis in older patients
Third trimester
- hematocrit (if low, mother will receive iron supplementation)
- Glucose loading test (OGTT, GLT, GTT) – screens for gestational diabetes; if > 140 mg/dL, a glucose tolerance test (GTT) is administered; a fasting glucose > 105 mg/dL suggests gestational diabetes.
Complications
See Complications of pregnancy
Fetal assessments
- Common
- ultrasound is used for many functions:
- Dating the gestational age of a pregnancy, most accurate in first trimester
- Detecting fetal anomalies in the second trimester
- biophysical profiles (BPP)
- Blood flow velocity in umbilical cord — decrease/absence/reversal or diastolic blood flow in the umbilical artery is worrisome.
- Congenital anomalies can be diagnosed with second trimester ultrasound
- Fetal karyotype for the screening of genetic diseases can be obtained via amniocentesis or chorionic villus sampling (CVS)
- Uncommon
- Fetal hematocrit for the assessment of fetal anemia, Rh isoimmunization, or hydrops can be determined by percutaneous umbilical blood sampling (PUBS) which is done by placing a needle through the abdomen into the uterus and taking a portion of the umbilical cord.
- Fetal lung maturity is associated with how much surfactant the fetus is producing. Reduced production of surfactant indicates decreased lung maturity and is a high risk factor for neonatal respiratory distress syndrome (NRDS). Typically a lecithin:sphingomyelin ratio greater than 1.5 is associated with increased lung maturity.
- Nonstress test (NST) for fetal heart rate
- Oxytocin challenge test
Induction
Reasons to induce include:
- pre-eclampsia
- IUGR
- diabetes
- other general medical condition, such as renal disease
- “postdates” – the pregnancy has lasted longer than 41 weeks after the last menstrual period
Induction may occur any time after 34 weeks of gestation if the risk to the fetus or mother is greater than the risk of delivering a premature fetus regardless of lung maturity.
If a woman does not eventually labour by 41-42 weeks, induction may be performed, as the placenta may become unstable after this date.
Induction may be achieved via several methods:
- pessary of Prostin cream, prostaglandin E2
- iv. or oral administration of misoprostol
- cervical insertion of a 30-mL Foley catheter
- rupturing the amniotic membranes
- intravenous infusion of synthetic oxytocin (Pitocin or Syntocinon)
Labor
During labor itself, the obstetrician may be called on to do a number of things:
- monitor the progress of labor, by reviewing the nursing chart, performing vaginal examination, and assessing the trace produced by a fetal monitoring device (the cardiotocograph)
- accelerate the progress of labor by infusion of the hormone oxytocin
- provide pain relief, either by nitrous oxide (nowadays uncommon, at least in the U.S.), opiates, or by epidural anesthesia done by anaethestists, an anesthesiologist, or a nurse anesthetist.
- surgically assisting labor, by forceps or the Ventouse (a suction cap applied to the fetus’ head)
- Caesarean section, if vaginal delivery is decided against or appears too difficult. Caesarean section can either be elective, that is, arranged before labor, or decided during labor as an alternative to hours of waiting. True “emergency” Cesarean sections (where minutes count) are a rarity.
Antenatal
During the time immediately after birth both baby as well as mother are hormonally cued to bond, the mother through the release of oxytocin a hormone also released with breastfeeding.
Emergencies in obstetrics
Two main emergencies are ectopic pregnancy and (pre)eclampsia.
- Ectopic pregnancy is when an embryo implants in the Fallopian tube or (rarely) on the ovary or inside the peritoneal cavity. This may cause massive internal bleeding.
- Pre-eclampsia is a disease which is defined by a combination of signs and symptoms that are related to maternal hypertension. The cause is unknown, and markers are being sought to predict its development from the earlist stages of pregnancy.
Some unknown factors cause vascular damage in the [endothelium], causing hypertension and proteinuria. If severe, it progresses to fulminant pre-eclampsia, with headaches and visual disturbances. This is a prelude to eclampsia, where a convulsion occurs, which can be fatal.
Imaging, monitoring and care
In present society, medical science has developed a number of procedures to monitor pregnancy.
Antenatal record
On the first visit to her obstetrician or midwife, the pregnant woman is asked to carry out the antenatal record, which constitutes a medical history and physical examination.
On subsequent visits, the gestational age (GA) is rechecked with each visit.
Symphysis-fundal height (SFH; in cm) should equal gestational age after 20 weeks of gestation, and the fetal growth should be plotted on a curve during the antenatal visits.
The fetus is palpated by the midwife or obstetrician using Leopold maneuver to determine the position of the baby. Blood pressure should also be monitored, and may be up to 140/90 in normal pregnancies. High blood pressure indicates hypertension and possibly pre-eclampsia, if severe swelling (edema) and spilled protein in the urine are also present.
Fetal screening is also used to help assess the viability of the fetus, as well as congenital problems. Genetic counseling is often offered for families who may be at an increased risk to have a child with a genetic condition.
Amniocentesis at around the 20th week is sometimes done for women 35 or older to check for Down’s Syndrome and other chromosome abnormalities in the fetus.
Even earlier than amniocentesis is performed, the mother may undergo the triple test, nuchal screening, nasal bone, alpha-fetoprotein screening and Chorionic villus sampling, also to check for disorders such as Down Syndrome. Amniocentesis is a prenatal genetic screening of the fetus, which involves inserting a needle through the mother’s abdominal wall and uterine wall, to extract fetal DNA from the amniotic fluid. There is a risk of miscarriage and fetal injury with amniocentesis because it involves penetrating the uterus with the baby still in utero.
Imaging

Imaging is another important way to monitor a pregnancy. The mother and fetus are also usually imaged in the first trimester of pregnancy. This is done to predict problems with the mother; confirm that a pregnancy is present inside the uterus; guess the gestational age; determine the number of fetuses and placentae; evaluate for an ectopic pregnancy and first trimester bleeding; and assess for early signs of anomalies.
X-rays and computerized tomography (CT) are not used, especially in the first trimester, due to the ionizing radiation, which has teratogenic effects on the fetus. Instead, ultrasound is the imaging method of choice in the first trimester and throughout the pregnancy, because it emits no radiation, is portable, and allows for realtime imaging. Ultrasound imaging may be done at any time throughout the pregnancy, but usually happens at the 12th week (dating scan) and the 20th week (detailed scan).
A normal gestation would reveal a gestational sac, yolk sac, and fetal pole. The gestational age can be assessed by evaluating the mean gestation sac diameter (MGD) before week 6, and the crown-rump length after week 6. Multiple gestation is evaluated by the number of placentae and amniotic sacs present.
Pregnancy has different cultural aspects related to the perception of the body, the relationship with partner and to the meaning of the event.
Terms and definitions
- embryo – conceptus between time of fertilization to 10 weeks of gestation
- fetus – from 10 weeks of gestation to time of birth
- infant – time of birth to 1 year of age
- gestational age – time from last menstrual period (LMP) up to present
- first trimester – up to 14 weeks of gestation
- second trimester – 14 to 28 weeks of gestation
- third trimester – 28 weeks to delivery
- viability – minimum age for fetus survival, ca. third trimester
- previable infant – delivered prior to 24 weeks
- preterm infant – delivered between 24-37 weeks
- term infant – delivered between 37-42 weeks
- gravidity (G) – number of times a woman has been pregnant
- parity (P) – number of pregnancies with a birth beyond 20 weeks GA or an infant weighing more than 500 g
- Ga Pw-x-y-z – a = number of pregnancies, w = number of term births, x = number of preterm births, y = number of abortions (spontaneous or therapeutic), z = number of living children; for example, G4P1-2-1-3 means the woman had a total of 4 pregnancies, of which 1 is of term, 2 are preterm, 1 miscarriage or therapeutic abortion, and 3 total living children (1 term + 2 preterm).
See also
- List of obstetric topics
- Gynecology
- Home birth
- Maternal health
- Midwifery
- Obstetric ultrasonography
- Puerperium
References
- ↑ “Omega-3 least known of pregnancy “Big 3““. Retrieved 2008-01-01.
- ↑ Tees RC, Mohammadi E (1999). <226::AID-DEV7>3.0.CO;2-H “The effects of neonatal choline dietary supplementation on adult spatial and configural learning and memory in rats”. Dev Psychobiol. 35 (3): 226–40. PMID 10531535.
Further reading
- J Lane (July 1987). “A provincial surgeon and his obstetric practice: Thomas W. Jones of Henley-in-Arden, 1764–1846”. Medical History. 31 (3): 333&ndash, 348.
Template:Obstetrical procedures Template:Urogenital surgical and other procedures
bn:ধাত্রীবিদ্যা bg:Акушерство da:Obstetrik de:Geburtshilfe el:Μαιευτική ga:Cnáimhseachas id:Obstetrik ia:Obstetricia it:Ostetricia ne:प्रसवशास्त्र nl:Verloskunde qu:Wachachiq sv:Obstetrik uk:Акушерство
(76-84) Operations on the musculoskeletal system
(76-84) Operations on the musculoskeletal system
- (Template:ICD9proc) Operations on facial bones and joints
- (Template:ICD9proc) Incision of facial bone without division
- (Template:ICD9proc) Diagnostic procedures on facial bones and joints
- (Template:ICD9proc) Local excision or destruction of lesion of facial bone
- (Template:ICD9proc) Partial ostectomy of facial bone
- (Template:ICD9proc) Excision and reconstruction of facial bones
- (Template:ICD9proc) Temporomandibular arthroplasty
- (Template:ICD9proc) Other facial bone repair and orthognathic surgery
- (Template:ICD9proc) Augmentation genioplasty
- Mentoplasty NOS
- (Template:ICD9proc) Augmentation genioplasty
- (Template:ICD9proc) Reduction of facial fracture
- (Template:ICD9proc) Other operations on facial bones and joints
- (Template:ICD9proc) Incision, excision, and division of other bones
- (Template:ICD9proc) Sequestrectomy
- (Template:ICD9proc) Other incision of bone without division
- (Template:ICD9proc) Wedge osteotomy
- (Template:ICD9proc) Other division of bone
- (Template:ICD9proc) Biopsy of bone
- (Template:ICD9proc) Excision and repair of bunion and other toe deformities
- (Template:ICD9proc) Local excision of lesion or tissue of bone
- (Template:ICD9proc) Excision of bone for graft
- (Template:ICD9proc) Other partial ostectomy
- (Template:ICD9proc) Total ostectomy
- (Template:ICD9proc) Other operations on bones, except facial bones
- (Template:ICD9proc) Bone graft
- (Template:ICD9proc) Application of external fixator device
- (Template:ICD9proc) Limb shortening procedures]
- (Template:ICD9proc) Limb lengthening procedures
- (Template:ICD9proc) Other repair or plastic operations on bone
- (Template:ICD9proc) Internal fixation of bone without fracture reduction
- (Template:ICD9proc) Removal of implanted devices from bone
- (Template:ICD9proc) Osteoclasis
- (Template:ICD9proc) Diagnostic procedures on bone, not elsewhere classified
- (Template:ICD9proc) Insertion of bone growth stimulator
- (Template:ICD9proc) Reduction of fracture and dislocation
- (Template:ICD9proc) Closed reduction of fracture without internal fixation
- (Template:ICD9proc) Closed reduction of fracture with internal fixation
- (Template:ICD9proc) Open reduction of fracture without internal fixation
- (Template:ICD9proc) Open reduction of fracture with internal fixation
- (Template:ICD9proc) Closed reduction of separated epiphysis
- (Template:ICD9proc) Open reduction of separated epiphysis
- (Template:ICD9proc) Debridement of open fracture site
- (Template:ICD9proc) Closed reduction of dislocation
- (Template:ICD9proc) Open reduction of dislocation
- (Template:ICD9proc) Unspecified operation on bone injury
- (Template:ICD9proc) Incision and excision of joint structures
- (Template:ICD9proc) Arthroscopy
- (Template:ICD9proc) Excision or destruction of intervertebral disc
- (Template:ICD9proc) Excision of intervertebral disc
- (Template:ICD9proc) Repair and plastic operations on joint structures
- (Template:ICD9proc) Spinal fusion
- (Template:ICD9proc) Arthrodesis and arthroereisis of foot and ankle
- (Template:ICD9proc) Arthrodesis of other joint
- (Template:ICD9proc) Refusion of spine
- (Template:ICD9proc) Other repair of joint of lower extremity
- (Template:ICD9proc) Joint replacement of lower extremity
- (Template:ICD9proc) Total hip replacement
- (Template:ICD9proc) Partial hip replacement
- (Template:ICD9proc) Revision of hip replacement, not otherwise specified
- (Template:ICD9proc) Total knee replacement
- (Template:ICD9proc) Revision of knee replacement, not otherwise specified
- (Template:ICD9proc) Total ankle replacement
- (Template:ICD9proc) Replacement of joint of foot and toe
- (Template:ICD9proc) Revision of joint replacement of lower extremity, not elsewhere classified
- (Template:ICD9proc) Other procedures on spine
- (Template:ICD9proc) Arthroplasty and repair of hand, fingers and wrist
- (Template:ICD9proc) Arthroplasty and repair of shoulder and elbow
- (Template:ICD9proc) Other operations on joint structures
- (Template:ICD9proc) Operations on muscle, tendon, and fascia of hand
- (Template:ICD9proc) Incision of muscle, tendon, fascia, and bursa of hand
- (Template:ICD9proc) Division of muscle, tendon, and fascia of hand
- (Template:ICD9proc) Excision of lesion of muscle, tendon, and fascia of hand
- (Template:ICD9proc) Other excision of soft tissue of hand
- (Template:ICD9proc) Suture of muscle, tendon, and fascia of hand
- (Template:ICD9proc) Transplantation of muscle and tendon of hand
- (Template:ICD9proc) Reconstruction of thumb
- (Template:ICD9proc) Plastic operation on hand with graft or implant
- (Template:ICD9proc) Other plastic operations on hand
- (Template:ICD9proc) Other operations on muscle, tendon, and fascia of hand
- (Template:ICD9proc) Operations on muscle, tendon, fascia, and bursa, except hand
- (Template:ICD9proc) Incision of muscle, tendon, fascia, and bursa
- (Template:ICD9proc) Division of muscle, tendon, and fascia
- (Template:ICD9proc) Diagnostic procedures on muscle, tendon, fascia, and bursa, including that of hand
- (Template:ICD9proc) Excision of lesion of muscle, tendon, fascia, and bursa
- (Template:ICD9proc) Other excision of muscle, tendon, and fascia
- (Template:ICD9proc) Bursectomy
- (Template:ICD9proc) Suture of muscle, tendon, and fascia
- (Template:ICD9proc) Reconstruction of muscle and tendon
- (Template:ICD9proc) Other plastic operations on muscle, tendon, and fascia
- (Template:ICD9proc) Other operations on muscle, tendon, fascia, and bursa
- (Template:ICD9proc) Other procedures on musculoskeletal system
- (Template:ICD9proc) Amputation of upper limb
- (Template:ICD9proc) Amputation of lower limb
- (Template:ICD9proc) Reattachment of extremity
- (Template:ICD9proc) Revision of amputation stump
- (Template:ICD9proc) Implantation or fitting of prosthetic limb device
- (Template:ICD9proc) Implantation of other musculoskeletal devices and substances
- (Template:ICD9proc) Replacement of spinal disc
- (Template:ICD9proc) Adjunct codes for external fixator devices
- (Template:ICD9proc) Other operations on musculoskeletal system
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
The musculoskeletal system (also known as the locomotor system) is an organ system that gives animals the ability to physically move using the muscles and skeletal system.
The human musculoskeletal system consists of the human skeleton, made by bones attached to other bones with joints, and skeletal muscle attached to the skeleton by tendons.
Hydrostatic musculoskeletal system
Among others, cnidarians and annelids, have a hydrostatic skeleton similar to a water-filled balloon, these animals can move by contracting the muscles surrounding the fluid-filled pouch, creating pressure within the pouch that causes movement. Animals such as earthworms use their hydrostatic skeletons to change their body shape as they move forward, from long and skinny to short and stumpy. Arthropoda have their muscles attached to an exoskeleton.
Muscle contraction initiation
In mammals, when a muscle contracts, a series of reactions occur. Muscle contraction is stimulated by the motor neuron sending a message to the muscles from the somatic nervous system. Depolarization of the motor neuron results in neurotransmitters being released from the nerve terminal. The space between the nerve teminal and the muscle cell is called the neuromuscular junction. These neurotransmitters diffuse across the synapse and bind to specific receptor sites on the sarcolemma (cell membrane of the muscle fiber). When enough receptors are stimulated, an action potential is generated and the permeability of the sarcolemma is altered. This process is known as initiation.
(85-86) Operations on the integumentary system
(85-86) Operations on the integumentary system
- (Template:ICD9proc) Operations on the breast
- (Template:ICD9proc) Mastotomy
- (Template:ICD9proc) Diagnostic procedures on breast
- (Template:ICD9proc) Excision or destruction of breast tissue
- (Template:ICD9proc) Local excision of lesion of breast
- (Template:ICD9proc) Reduction mammoplasty and subcutaneous mammectomy
- (Template:ICD9proc) Mastectomy
- (Template:ICD9proc) Augmentation mammoplasty
- (Template:ICD9proc) Mastopexy
- (Template:ICD9proc) Total reconstruction of breast
- (Template:ICD9proc) Other repair and plastic operations on breast
- (Template:ICD9proc) Other operations on the breast
- (Template:ICD9proc) Operations on skin and subcutaneous tissue
- (Template:ICD9proc) Incision of skin and subcutaneous tissue
- (Template:ICD9proc) Diagnostic procedures on skin and subcutaneous tissue
- (Template:ICD9proc) Excision or destruction of lesion or tissue of skin and subcutaneous tissue
- (Template:ICD9proc) Other local excision or destruction of lesion or tissue of skin and subcutaneous tissue
- (Template:ICD9proc) Radical excision of skin lesion
- (Template:ICD9proc) Suture or other closure of skin and subcutaneous tissue
- (Template:ICD9proc) Free skin graft
- (Template:ICD9proc) Pedicle grafts or flaps
- (Template:ICD9proc) Other repair and reconstruction of skin and subcutaneous tissue
- (Template:ICD9proc) Other operations on skin and subcutaneous tissue
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
In zootomy, the integumentary system is the external covering of the body, comprising the skin, hair, scales, nails, sweat glands and their products (sweat and mucus). The integumentary system has a variety of functions; in animals, it may serve to waterproof, cushion and protect the deeper tissues, excrete wastes, regulate temperature and is the location of sensory receptors for pain, pressure and temperature. The name derives from the Latin integumentum, which means ‘a covering’.
As an organ system
The integumentary system is often the largest organ system. It distinguishes, separates, protects and informs the animal with regard to its surroundings. Small-bodied invertebrates of aquatic or continually moist habitats respire using the outer layer (integument). This gas exchange system, where gases simply diffuse into and out of the interstitial fluid, is called integumentary exchange.
Anatomy
The cutaneous membrane (skin) and its accessory structures (hair, scales, feathers, nails, exocrine glands) make up the integumentary system.
There are three layers of skin:
Below the dermis, the subcutis acts to protect underlying muscles, tissues, and other organs. Hair on the surface of the skin helps maintain body temperature and filter out harmful particles.
Cutaneous glands include:
- Sweat glands (also known as sudoriferous glands) – excrete sweat to regulate temperature
- Sebaceous glands – oil-producing glands that keep skin and hair moist and soft
- Ceruminous glands – glands of the ear canal that produce earwax
- Mammary glands – milk-producing glands located in the breasts.
Layers
Epidermis
The epidermis is the thin outer layer of skin that contains melanin which gives skin its color and allows for the skin to tan. Carotene, and oxygen-rich hemoglobin also contributes to the color of skin. The epidermis also encompasses the protein keratin which stiffens epidermal tissue to form finger nails. The outermost layer consists of 25-30 layers of dead cells. Further levels include:
- Scaly Cells form the surface of the skin
- Melanocytes give the skin color
- Langerhans cells are formed in the bone marrow and work to fight infection
It is divided into the following sub-layers:
Sublayers
Epidermis is divided into the following 5 sublayers or strata:
- Stratum corneum
- Stratum lucidum…..
- Stratum granulosum
- Stratum spinosum
- Stratum germinativum (also called “stratum basale”)
Dermis
The dermis is the bottom-most, thick inner layer of skin, which comprises blood vessels, connective tissue, nerves, lymph vessels, sweat glands and hair shafts. It has two main layers:
- Upper Papillary: Contains touch receptors which communicate with the central nervous system and is responsible for the folds of the fingerprints
- Lower Reticular: Made of dense elastic fibers that house the hair follicles, nerves, gland, and that gives the skin most of its stretchiness and strength.
The dermis papillary or the upper part of the skin produces the fngerprints and its receptors communicate with central nervous system that includes, touch, pressure, hot, cold, and pain by; me
Subcutaneous tissue
The subcutaneous tissue or subcutis is the layer of tissue directly underlying the cutis. It is mainly composed of adipose tissue. Its physiological function includes insulation and storage of nutrients. It also cushions the body for extra protection.
Functions
The integumentary system has multiple roles in homeostasis. All body systems work in an interconnected manner to maintain the internal conditions essential to the function of the body. The skin has an important job of protecting the body and acts somewhat as the body’s first line of defense against infection, temperature change or other challenges to homeostasis. Functions include:
- Protects the body’s internal living tissues and organs
- Protects against invasion by infectious organisms
- Protects the body from dehydration
- Protects the body against abrupt changes in temperature
- Helps excrete waste materials through perspiration
- Acts as a receptor for touch, pressure, pain, heat, and cold (see Somatosensory system)
- Protects the body against sunburns
- Generates vitamin D through exposure to ultraviolet light
- Stores water, fat, and vitamin D
Diseases and injuries
Possible diseases and injuries to the human integumentary system include:
Australian Institute of Health and Welfare National Perinatal Statistics Unit, UNSW published congenital malformation rate 1981-92 / 10,000, shows that only a 0.5% of birth defects are in the integumentary system.
See also
- Exoskeleton and shell
- Major systems of the human body
References
- Kardong, Kenneth V. (1998). Vertebrates: Comparative Anatomy, Function, Evolution (second edition ed.). USA: McGraw-Hill. pp. 747 pp. ISBN 0-07-115356-X/0-697-28654-1 Check
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External links
- Aquatic Path Details of the integumentary system of the fathead minnow
- biology4kids
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(87-99) Miscellaneous diagnostic and therapeutic procedures
(87-99) Miscellaneous diagnostic and therapeutic procedures
- (Template:ICD9proc) Diagnostic radiology
- (Template:ICD9proc) Other diagnostic radiology and related techniques
- (Template:ICD9proc) Interview, evaluation, consultation, and examination
- (Template:ICD9proc) Anatomic and physiologic measurements and manual examinations — nervous system and sense organs
- (Template:ICD9proc) Cardiac stress tests, pacemaker and defibrillator checks
- (Template:ICD9proc) Microscopic examination-II
- (Template:ICD9proc) Physical therapy, respiratory therapy, rehabilitation, and related procedures
- (Template:ICD9proc) Skeletal traction and other traction
- (Template:ICD9proc) Procedures related to the psyche
- (Template:ICD9proc) Ophthalmologic and otologic diagnosis and treatment
- (Template:ICD9proc) General and subjective eye examination
- (Template:ICD9proc) Nonoperative intubation and irrigation
- (Template:ICD9proc) Replacement and removal of therapeutic appliances
- (Template:ICD9proc) Nonoperative removal of foreign body or calculus
- (Template:ICD9proc) Removal of intraluminal foreign body from digestive system without incision
- (Template:ICD9proc) Removal of intraluminal foreign body from other sites without incision
- (Template:ICD9proc) Removal of other foreign body without incision
- (Template:ICD9proc) Extracorporeal shockwave lithotripsy (ESWL)
- (Template:ICD9proc) Other nonoperative procedures
- (Template:ICD9proc) Transfusion of blood and blood components
- (Template:ICD9proc) Injection or infusion of therapeutic or prophylactic substance
- (Template:ICD9proc) Injection or infusion of other therapeutic or prophylactic substance
- (Template:ICD9proc) Prophylactic vaccination and inoculation against certain bacterial diseases
- (Template:ICD9proc) Prophylactic vaccination and inoculation against certain viral diseases
- (Template:ICD9proc) Other vaccination and inoculation
- (Template:ICD9proc) Conversion of cardiac rhythm
- (Template:ICD9proc) Cardiopulmonary resuscitation, not otherwise specified
- (Template:ICD9proc) Atrial cardioversion
- (Template:ICD9proc) Other electric countershock of heart
- (Template:ICD9proc) Closed chest cardiac massage
- (Template:ICD9proc) Carotid sinus stimulation
- (Template:ICD9proc) Other conversion of cardiac rhythm
- (Template:ICD9proc) Therapeutic apheresis or other injection, administration, or infusion of other therapeutic or prophylactic substance
- (Template:ICD9proc) Miscellaneous physical procedures
- (Template:ICD9proc) Other miscellaneous procedures
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Sumanth Khadke, MD[2]
Overview
In general, diagnosis (plural diagnoses) has two distinct dictionary definitions. The first definition is “the recognition of a disease or condition by its outward signs and symptoms”, while the second definition is “the analysis of the underlying physiological/biochemical cause(s) of a disease or condition”.
Diagnosis covers a broad spectrum, or spectra, of testing in some form of analysis; collective reasoning using such tests is called the method of diagnostics, leading then to the results of those tests by ideal (ethics) would then be considered a diagnosis, but not necessarily the correct one.
In medicine, diagnosis or diagnostics is the process of identifying a medical condition or disease by its signs, symptoms, and from the results of various diagnostic procedures. The conclusion reached through this process is called a diagnosis. The term “diagnostic criteria” designates the combination of symptoms which allows the doctor to ascertain the diagnosis of the respective disease.
Typically, someone with abnormal symptoms will consult a physician, who will then obtain a history of the patient‘s illness and examine him for signs of disease. The physician will formulate a hypothesis of likely diagnoses and in many cases will obtain further testing to confirm or clarify the diagnosis before providing treatment.
Medical tests commonly performed are measuring blood pressure, checking the pulse rate, listening to the heart with a stethoscope, urine tests, fecal tests, saliva tests, blood tests, medical imaging, electrocardiogram, hydrogen breath test and occasionally biopsy.
The word diagnosis is derived from the Greek words dia which means “by”, and gnosis which means “knowledge”. The verb is diagnose and a person diagnosing could be considered a diagnostician.
Relationship of diagnosis to medical practice
A physician‘s job is to know the human body and its functions in terms of normality (homeostasis). The four cornerstones of diagnostic medicine, each essential for understanding homeostasis, are: anatomy (the structure of the human body), physiology (how the body works), pathology (what can go wrong with the anatomy and physiology) and psychology (thought and behavior). Once the doctor knows what is normal and can measure the patient’s current condition against those norms, she or he can then determine the patient’s particular departure from homeostasis and the degree of departure. This is called the diagnosis. Once a diagnosis has been reached, the doctor is able to propose a management plan, which will include treatment as well as plans for follow-up. From this point on, in addition to treating the patient’s condition, the doctor educates the patient about the causes, progression, outcomes, and possible treatments of his ailments, as well as providing advice for maintaining health.
It should be noted however, that medical diagnosis in psychology or psychiatry is problematic. Apart from the fact that there are differing theoretical views toward mental conditions and that there are few “lab” tests available for various major disorders (e.g., clinical depression), a causal analysis with respect to symptomatology and disorder/disease is not always possible. As a result, most if not all mental conditions, function as both symptoms as well as disorders. There are often functional descriptions provided for psychological disorders and these are vulnerable to circular reasoning due to the etiological fuzziness inherent of these diagnostic categories. (BDG, 2006)
Diagnostic procedure
Diagnosis is a fluid process in which the physician responds to information garnered from the patient and others, from a physical examination of the patient, and from medical tests performed upon the patient.
The doctor should consider the patient in his ‘well’ context rather than simply as a walking medical condition. This entails assessing the socio-political context of the patient (family, work, stress, beliefs), in addition to the patient’s physical body, as this often offers vital clues to the patient’s condition and its management.
The process of diagnosis begins when the patient consults the doctor and presents a set of complaints (the symptoms). If the patient is unconscious, this condition is the de facto complaint. The doctor then obtains further information from the patient himself (and from those who know him, if present) about the patient’s symptoms, his previous state of health, living conditions, and so forth.
Rather than consider the myriad diseases that could afflict the patient, the physician narrows down the possibilities to the illnesses likely to account for the apparent symptoms, making a list of only those conditions that could account for what is wrong with the patient. These are generally ranked in order of probability.
The doctor then conducts a physical examination of the patient, studies the patient’s medical record, and asks further questions as he goes, in an effort to rule out as many of the potential conditions as possible. When the list is narrowed down to a single condition, this is called the differential diagnosis, and provides the basis for a hypothesis of what is ailing the patient.
Unless the physician is certain of the condition present, further medical tests are performed or scheduled (such as medical imaging), in part to confirm or disprove the diagnosis but also to document the patient’s status to keep the patient’s medical history up to date. Consultations with other physicians and specialists in the field may be sought. If unexpected findings are made during this process, the initial hypothesis may be ruled out and the physician must then consider other hypotheses.
Despite all of these complexities, most patient consultations are relatively brief, because many diseases are obvious, or the physician’s experience may enable him to recognize the condition quickly. Another factor is that the decision trees used for most diagnostic hypothesis testing are relatively short.
Once the physician has completed the diagnosis, he explains the prognosis to the patient and proposes a treatment plan which includes therapy and follow-up (further consultations and tests to monitor the condition and the progress of the treatment, if needed), usually according to the guideline provided by the medical field on the treatment of the particular illness.
Treatment itself may indicate a need for review of the diagnosis if there is a failure to respond to treatments that would normally work.
History of medical diagnostics
The history of medical diagnosis began in earnest from the enlightened days of Hippocrates in ancient Greece but is far from perfect despite the enormous bounty of information made available by medical research including the sequencing of the human genome. The practice of diagnosis continues to be dominated by theories set down in the early 1900s.
Ancient Greece
Over two thousand years ago, Hippocrates recorded the association between disease and heredity. In similar fashion, Pythagoras noted the association between metabolism and heredity (allergy to Fava beans). The medical community, however, has only recently acknowledged the importance of genetics and its relevance to mainstream medicine.
The Oslerian ideal
The ideals of William Osler who transformed the practice of medicine in the early 1900s were based on the principles of the diagnosis and treatment of disease. According to Osler, the functions of a physician were to be able to identify disease and its manifestations, understand its mechanisms, how it may be prevented and how it may be cured. For his medical students he believed that the best textbook was the patient himself – analysis of morbid anatomy and pathology were the keys. The Oslerian ideal continues today, as the basis of the Doctor’s strategy is, “What disease does this patient have and what is the best way for treatment?” The emphasis is on the classification of the disease in order to use the remedies available for its effects to be reversed or ameliorated. The human being in question is representative of a class of people with this type of disease whereas the biological individuality of this person is not given any great weight.
Garrod’s view
The successor to William Osler as Regius Professor at Oxford was Archibald Garrod. Garrod echoed the observations of his Greek counterparts of two millennia ago, …our chemical individualities are due to our chemical merits as well as our chemical shortcomings; and it is more nearly true to say that the factors which confer upon us our predispositions to and immunities from various mishaps which are spoken of as diseases, are inherent in our very chemical structure; and even in the molecular groupings which confer upon us our individualities, and which went into the making of the chromosomes from which we sprang. Considering that the time that he formulated these ideas were the early 1900’s, and the knowledge of DNA encoding genes that in turn encoded proteins responsible for bodily structure and functions not being discovered until some fifty years later it took some time before medicine could fully appreciate the fundamental importance of his concept of diagnosis.
Present-day Oslerian practice
Whereas Osler laid the founding principles by which medicine should be practiced, Garrod placed these principles in a greater context of a chemical individuality that is inherited and is subject to the mechanisms of evolutionary selection. The Oslerian ideal of medical practice continues to dominate medical philosophy today. The patient is a collective of symptoms to be characterized and analyzed algorithmically in order to draw a diagnosis and subsequently produce a strategy of treatment. Medicine is about problems based solutions. In keeping with this philosophy, today’s pathology reports provide a momentary snapshot of the patient’s biochemical profile, highlighting the end result of the disease process.
Influence of DNA technology
Garrod’s conception of biological individuality was confirmed with the advent of the sequencing of the human genome. Finally the subtle relationship between inheritance, individuality and environment became apparent via the variations detected in DNA. In each patient’s DNA lies a script for how their bodies will change and become ill as well as how they will handle the assaults of the environment from the beginning of their life to its end. It is hoped that by knowing a patient’s genes that the biological strengths and weaknesses in respect to these assaults will be revealed and disease processes can be predicted before they have the opportunity to manifest. Although knowledge in this area is far from complete, there are already medical interventions based on this. More importantly, the physician, forewarned with this knowledge can guide the patient towards appropriate lifestyle changes to anticipate and mitigate disease processes.
See also
Lists
External links
- GPnotebook web site GPnotebook is a British medical database for GPs that provides an immediate reference resource for clinicians worldwide. The database consists of over 30,000 pages of information.
- Free 24/7 DRG & ICD-9-CM lookup powered by Flash Code at icd9coding.com
- Differential Diagnosis
- Merck Manual of Diagnosis and Therapy
als:Diagnostik bg:Диагноза de:Diagnose eu:Diagnostiko it:Diagnosi he:אבחנה ms:Diagnosis nl:Diagnose no:Diagnose nn:Diagnose simple:Diagnosis sk:Diagnóza sr:Дијагностика sh:Dijagnoza fi:Lääketieteellinen diagnoosi sv:Diagnostik ta:அறுதியிடல்
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![When the incus is eroded, broken or absent, the ossicular chain is reconstructed with an incus replacement prosthesis[10].](https://www.wikidoc.org/images/7/72/Incus_replacement_gif320.gif)
![When both the incus and malleus are eroded or absent, the ossicular chain is reconstructed with a partial ossicular replacement prosthesis (PORP)[11].](https://www.wikidoc.org/images/d/d1/Porp_labeled.gif)
![When the incus and arch of the stapes are eroded, or when the malleus, incus and arch of the stapes are absent, the ossicular chain is reconstructed with a total ossicular replacement prosthesis (TORP)[12].](https://www.wikidoc.org/images/4/4b/Torplabeled.gif)