Nausea and vomiting
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Tayebah Chaudhry[2]; Associate Editor-In-Chief: M.Umer Tariq [3]
Synonyms and Keywords: Emesis
Overview
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Vishnu Vardhan Serla M.B.B.S. [2]
Overview
Nausea (Latin: Nausea, Greek: Template:Polytonic, “sea-sickness“) is an ‘unpleasant painless subjective feeling that one will imminently vomit’. Nausea is often indicative of an underlying condition elsewhere in the body. Travel sickness, which is due to confusion between perceived movement and actual movement, is an example. The sense of equilibrium lies in the ear and works together with eyesight. When these two don’t “agree” to what extent the body is actually moving the symptom is presented as nausea even though the stomach itself has nothing to do with the situation. Nausea is also an adverse effect of many drugs. Nausea may also be an effect of a large intake of sugary foods. In medicine, nausea can be a problem during some chemotherapy regimens and following general anesthesia. Nausea is also a common symptom of pregnancy. Mild nausea experienced during pregnancy can be normal, and should not be considered an immediate cause for alarm. Vomiting (also throwing up or emesis) is the forceful expulsion of the contents of one’s stomach through the mouth and sometimes the nose resulting from contractions of gut and thoracoabdominal wall musculature. Vomiting may result from many causes, ranging from gastritis or poisoning to brain tumors, or elevated intracranial pressure (ICP). The feeling that one is about to vomit is called nausea. It usually precedes but does not always lead to vomiting. Antiemetics are sometimes necessary to suppress nausea and vomiting, and in severe cases where dehydration develops, intravenous fluid may need to be administered to replace fluid volume. The medical branch investigating vomiting, emetics, and antiemetics is called emetology.
Historical Perspective
The medical term ‘nausea’ is derived from the classical Greek terms ναυτια and ναυσια, which designated the signs and symptoms of seasickness. The descriptions of the development of seasickness in monographs from the latter half of the 19th and early 20th centuries provide a context for understanding the evolution of the demarcation of symptom clusters associated with the original term ‘nausea”. The term ‘nausea’ has been used to denote both a disorder (diagnosis of seasickness) and a symptom (or symptom cluster) associated with other disorders. This pattern also appeared for terms for vertigo, such as ‘vertigine’, dinos, scotomatikos and skotodininos. Hence, one must ask whether the term nausea denoted seasickness explicitly or whether it denoted the appearance of a ‘cluster of signs and symptoms of seasickness’ as a component of other primary disorders.
Classification
Nausea and vomiting can be classified into acute or chronic
Acute nausea and vomiting
Acute vomiting which typically lasts from a few hours to few days is the most common presentation in the emergency department. Acute vomiting needs an extensive workup to exclude life-threatening conditions like bowel obstruction, mesenteric ischemia, acute pancreatitis, and possibly myocardial infarction.
Chronic nausea and vomiting
Chronic vomiting which lasts from weeks to months is initially evaluated in an outpatient setting.
Pathophysiology
It is understood that nausea and vomiting are complex and encompass psychological states, the central nervous system, the autonomic nervous system, gastric dysrhythmias, and the endocrine system. Each individual has a threshold for nausea that changes minute by minute. At any given moment, the threshold depends on the interaction of certain inherent factors of the individual with the more changeable psychological states of anxiety, anticipation, expectation, and adaptation. Stimuli giving rise to nausea and vomiting originate from visceral, vestibular, and chemoreceptor trigger zone inputs which are mediated by serotonin/dopamine, histamine/acetylcholine, and serotonin/dopamine, respectively.
Causes
Life threatening causes of nausea and vomiting include acute coronary syndrome, anaphylaxis, and heart failure. Other common causes of nausea and vomiting are food allergies, food poisoning, gastroenteritis, and gastroesophageal reflux.
Differentiating Nausea and vomiting from Other Diseases
Epidemiology and Demographics
Risk Factors
Screening
Natural History, Complications, and Prognosis
Diagnosis
Diagnostic Study of Choice
History and Symptoms
Physical Examination
Laboratory Findings
Electrocardiogram
X-ray
Echocardiography and Ultrasound
ECG is done to rule out an inferior MI or arrhythmia.
CT scan
MRI
Other Imaging Findings
Other Diagnostic Studies
Treatment
Medical Therapy
Interventions
Surgery
Primary Prevention
Secondary Prevention
References
Historical Perspective
Overview
The medical term ‘nausea’ is derived from the classical Greek terms ναυτια and ναυσια, which designated the signs and symptoms of seasickness. The descriptions of the development of seasickness in monographs from the latter half of the 19th and early 20th centuries provide a context for understanding the evolution of the demarcation of symptom clusters associated with the original term ‘nausea”. The term ‘nausea’ has been used to denote both a disorder (diagnosis of seasickness) and a symptom (or symptom cluster) associated with other disorders. This pattern also appeared for terms for vertigo, such as ‘vertigine’, dinos, scotomatikos and skotodininos. Hence, one must ask whether the term nausea denoted seasickness explicitly or whether it denoted the appearance of a ‘cluster of signs and symptoms of seasickness’ as a component of other primary disorders.
Historical perspective
Discovery
- In 1830, Marshall Hall was the first to discover the reflex theory and the association between nervous mechanisms and the development of nausea and vomiting
- In 1865, Gianuzzi speculated on the possible existence of a regulating center of the emetic reflex in the brain .
- In 1881, Thumas, pointed to an area on the floor of the fourth ventricle in animals which, if damaged, made apomorphine’s emetic action impossible
- In 1889, Clarke described a case of an 8-year-old boy with uncontrollable hiccups and vomiting. The outcome of the case was the death of the patient, and a tumorin the middle of the fourth ventricle was found at the postmortem examination, leaving the author curious about the absence of manifestations other thanvomiting.
- Retzius produced the most important work on the macroscopic anatomy of the encephalon and he described a structure on thefloor of the fourth ventricle, adjacent to the nucleus of the solitary tract, named it as the area postrema (AP), in Latin meaning, the hindmost area. [1]
- In 1906, Wilson in a descriptive work on the human bulb, mentioned the AP as being richly vascularized, as well as detailing histological aspects and pointing out the high density of neurons in area postrema.
- In 1924, Wislocki and Putnam speculated about the postrema region as an area of diffusion between blood andcerebrospinal fluid, after observing dye granules deposited in the perivascular space, especially amongependymal cells.
- In 1942, Dow and Berglund, in an article on the vascular patterns ofmultiple sclerosis lesions, also described the case of a 38-year-old woman with some of the symptoms involving incessantvomiting, and showing postmortem plaques on the pons andmedulla oblongata.
- In 1951, Borison and Brizzee while studying the medulla oblongata of cats, identified the AP as a chemoreceptor zone sensitive to the vomiting reflex, integrating the hypothesis of the researchers of late 19 th century, and in 1974, Borison published a review article condensing the advances made by countless other researchers since the early 1950s, concluding that the AP acted primarily as a chemoreceptor trigger zone to the emetic response.
- In 1979, McFarling and Susac13, reported on patients with multiple sclerosis with intractablehiccups, a symptom not reported within their clinical manifestations, relating to probable disinhibition of the hiccup reflex by the multiple sclerosisplaques.
- In 1986, Leslie published a meticulous comparative study between several animal species and humans, detailing the microscopic ultrastructure of the AP, and demonstrating that it was an area of permeability of the blood-brain barrier serving as a zone of fine control of autonomic and neurochemical information.
- In the 2000s, a profusion of papers correlated area postrema syndrome cases to neuromyelitis optica spectrum disorders, with AP in a central role as the target of anti-aquaporin 4 antibodies.[2]
References
- ↑ DE SOUZA, Thiago Ferreira Simões (2020). “A concise historical perspective of the area postrema structure and function”. Arquivos de Neuro-Psiquiatria. 78 (2): 121–123. doi:10.1590/0004-282×20190118. ISSN 1678-4227.
- ↑ Sarikcioglu, Levent; Yildirim, Fatos Belgin (2008). “Area Postrema: One of the Terms Described by Magnus Gustaf Retzius”. Journal of the History of the Neurosciences. 17 (1): 109–110. doi:10.1080/09647040701236578. ISSN 0964-704X.
Classification
Overview
Nausea and vomiting can be classified into acute or chronic
Acute vomiting which typically lasts from a few hours to few days is the most common presentation in the emergency department. Acute vomiting needs an extensive workup to exclude life-threatening conditions like bowel obstruction, mesenteric ischemia, acute pancreatitis, and possibly myocardial infarction.
Chronic vomiting which lasts from weeks to months is initially evaluated in an outpatient setting. Cyclical vomiting syndrome is the most common cause of chronic nausea and vomiting.
Classification
Based on the duration of symptoms it can be classified as
Acute:
Acute nausea and vomiting can be caused by food allergies, viral gastroenteritis etc
It typically lasts from few hours to few days
Chronic:
Chronic nausea, vomiting can last from weeks to months. [1]
Chemotherapy is one of the most common cause of nausea and vomiting, and
Chemotherapy induced nausea and vomiting can be classified as
Acute:
Acute Chemotherapy induced nausea and vomiting (CINV) occur with in 24 hours of chemotherapy administration
Delayed:
Delayed CINV can occur at least 24 hours after chemotherapy and peaks between 48-72 hours [2]
Anticipatory:
Nausea and vomiting that is triggered by stimuli associated withchemotherapy and can be due to prior poor control of nausea and vomiting during chemotherapy [3] [4]
Refractory:
CINV that occurs despite maximum antiemetics
Breakthrough:
CINV that occurs within 5 days of chemotherapy despite of antiemetics. May require rescue therapy
References
- ↑ Lacy BE, Parkman HP, Camilleri M (May 2018). “Chronic nausea and vomiting: evaluation and treatment”. Am J Gastroenterol. 113 (5): 647–659. doi:10.1038/s41395-018-0039-2. PMID 29545633.
- ↑ Navari RM (2003). “Pathogenesis-based treatment of chemotherapy-induced nausea and vomiting–two new agents”. J Support Oncol. 1 (2): 89–103. PMID 15352652.
- ↑ . doi:10.1002/j.1875-9114.1990.tb02560.x. Missing or empty
|title=(help) - ↑ Jordan K, Kasper C, Schmoll HJ (January 2005). “Chemotherapy-induced nausea and vomiting: current and new standards in the antiemetic prophylaxis and treatment”. Eur J Cancer. 41 (2): 199–205. doi:10.1016/j.ejca.2004.09.026. PMID 15661543.
Pathophysiology
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Vishnu Vardhan Serla M.B.B.S. [2]
Overview
The physiology of nausea and vomiting encompass psychological states, the central nervous system, the autonomic nervous system, gastric dysrhythmias, and the endocrine system. Each individual has a threshold for nausea that changes minute by minute. Stimuli giving rise to nausea and vomiting originate from visceral, vestibular, and chemoreceptor trigger zone inputs which are mediated by serotonin/dopamine, histamine/acetylcholine, and serotonin/dopamine, respectively.
Pathophysiology
The physiology of nausea and vomiting encompass psychological states, the central nervous system, the autonomic nervous system, gastric dysrhythmias, and the endocrine system. Each individual has a threshold for nausea that changes minute by minute. At any given moment, the threshold depends on the interaction of certain inherent factors of the individual with the more changeable psychological states of anxiety, anticipation, expectation, and adaptation. Stimuli giving rise to nausea and vomiting originate from visceral, vestibular, and chemoreceptor trigger zone inputs which are mediated by serotonin/dopamine, histamine/acetylcholine, and serotonin/dopamine, respectively. These relationships between these areas are the basis of the pharmacotherapy.[1]
Vomiting Center
The vomiting center lies in the medulla oblongata and comprises the reticular formation and the nucleus of the tractus solitarius.
When there is stimulus, it activates motor pathways descend from this center and trigger vomiting.
These efferent pathways travel within the 5th, 7th, 9th, 10th, and 12th cranial nerves to the upper gastrointestinal tract, within vagal and sympathetic nerves to the lower tract, and within spinal nerves to the diaphragm and abdominal muscles.
The vomiting center can be activated directly by irritants or indirectly following input from gastrointestinal tract, cerebral cortex and thalamus, vestibular region, and chemoreceptor trigger zone (CRTZ). [2]
The CRTZ is closest in proximity, lying between the medulla and the floor of the fourth ventricle, and it is not protected by the blood-brain barrier.
The chemoreceptor trigger zone at the base of the fourth ventricle has numerous dopamine D2 receptors, serotonin 5-HT3 receptors, opioid receptors, acetylcholine receptors, and receptors for substance P. Stimulation of different receptors are involved in different pathways leading to emesis, in the final common pathway substance P appears to be involved.[3]
The vestibular system which sends information to the brain via cranial nerve VIII (vestibulocochlear nerve). It plays a major role in motion sickness and is rich in muscarinic receptors and histamine H1 receptors.
Cranial nerve X (vagus nerve), which is activated when the pharynx is irritated, leading to a gag reflex.
Vagal and enteric nervous system inputs that transmit information regarding the state of the gastrointestinal system. Irritation of the GI mucosa by chemotherapy, radiation, distention or acute infectious gastroenteritis activates the 5-HT3 receptors of these inputs.
The CNS mediates vomiting arising from psychiatric disorders and stress.
Vomiting:
The act of vomiting consists of 3 steps:[4]
- ”’Nausea”’ is an unpleasant and difficult to describe psychic experience. Physiologically,nausea is typically associated with decreased gastric motility and increased tone in the small intestine. Also, there is often reverse peristalsis in the proximal small intestine.
- ”’Retching”’ (“dry heaves”) refers to spasmodic respiratory movements conducted with a closedglottis. While this is occurring, the antrum of the stomach contracts and the fundus and cardia relax.
- ”’Emesis”’ is when gastric and often small intestinal contents are propelled up to and out of the mouth.
and is caused by three types of outputs initiated by themedulla:Motor, parasympathetic nervous system (PNS) and sympathetic nervous system (SNS).
- Increased salivation to protect the enamel of teeth from stomach acids (excessive vomiting leads to caries). This is part of the PNS output.
- Reverse peristalsis, starting from the middle of the small intestine, sweeping up the contents of the digestive tract into the stomach, through the relaxed pyloric sphincter.
- A lowering of intrathoracic pressure (by inspiration against a closed glottis), coupled with an increase in abdominal pressure as the abdominal muscles contract, propels stomach contents into the esophagus without involvement of the reverse peristalsis. The lower esophageal sphincter relaxes.
- Vomiting also initiates a SNS response causing both sweating and increased heart rate.
The neurotransmitters that regulate vomiting are poorly understood, but inhibitors of dopamine, histamine and serotonin are all used to suppress vomiting, suggesting that these play a role in the initiation or maintenance of a vomiting cycle. Vasopressin and neurokinin may also be involved.
Content
As the stomach secretes acid, vomit contains a high concentration of hydronium ions and is thus strongly acidic. Recent food intake will be reflected in the gastric vomit.
The content of the vomitus (vomit) may be of medical interest.
Fresh blood in the vomit is called hematemesis (“blood vomiting”).
Old blood bears resemblance to coffee grounds (as the iron in the blood is oxidized), and is termed “coffee ground vomiting”.
Bile can enter the vomit during subsequent heaves due to duodenal contraction if the vomiting is severe.
Fecal vomiting is often a consequence of intestinal obstruction, and is treated as a warning sign of this potentially serious problem (“signum mali ominis”); such vomiting is sometimes called “miserere”. If food has recently been consumed, then partly digested food may show up in the vomit.
References
- ↑ Singh P, Yoon SS, Kuo B (January 2016). “Nausea: a review of pathophysiology and therapeutics”. Therap Adv Gastroenterol. 9 (1): 98–112. doi:10.1177/1756283X15618131. PMC 4699282. PMID 26770271.
- ↑ Hornby PJ. Central neurocircuitry associated with emesis. Am J Med 2001;111:106S-12S. PMID 11749934.
- ↑ Rhodes VA (December 1990). “Nausea, vomiting, and retching”. Nurs Clin North Am. 25 (4): 885–900. PMID 2235641.
Causes
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Vishnu Vardhan Serla M.B.B.S. [2] Kiran Singh, M.D. [3]
Overview
Life threatening causes of nausea and vomiting include acute coronary syndrome, anaphylaxis, and heart failure. Other common causes of nausea and vomiting are food allergies, food poisoning, gastroenteritis, and gastroesophageal reflux.
Causes
Life Threatening Causes
Common Causes
Causes by Organ System
References
- ↑ Ahmed SS, Gupta RC, Brancato RR (May 1978). “Significance of nausea and vomiting during acute myocardial infarction”. Am Heart J. 95 (5): 671–2. doi:10.1016/0002-8703(78)90311-3. PMID 637006.
- ↑ . doi:10.1002/j.1875-9114.1990.tb02560.x. Missing or empty
|title=(help) - ↑ Scorza K, Williams A, Phillips JD, Shaw J (July 2007). “Evaluation of nausea and vomiting”. Am Fam Physician. 76 (1): 76–84. PMID 17668843.
- ↑ Hasler WL, Chey WD (December 2003). “Nausea and vomiting”. Gastroenterology. 125 (6): 1860–7. doi:10.1053/j.gastro.2003.09.040. PMID 14724837.
- ↑ Swanson DW, Swenson WM, Huizenga KA, Melson SJ (May 1976). “Persistent Nausea without organic cause”. Mayo Clin Proc. 51 (5): 257–62. PMID 1263596.
Differentiating Nausea and Vomiting from other Conditions
Overview
Differential diagnosis of vomiting may be a result of a range of causes, including GI (obstructive and inflammatory) etiologies, CNS disease, pulmonary problems, renal disease, endocrine/metabolic disorders, drugs (either as side effects or in over dosages), psychiatric disorders, strep throat, pregnancy or stress.[1]
Differential diagnosis
The causes of nausea and vomiting can be differentiated as GI and Non GI causes:
GI causes
Esophageal malignancies
Gastric outlet obstruction , may be due tomalignancy
Strangulated hernias
Small bowel obstruction due toadhesion,intussusception orvolvulus
Functional:
Gastroparesis due to autonomic dysfunction
Non GI causes can be
CNS causes:
Space occupying lesions
Metabolic:
Acidosis- DKA, Lactic acidosis
Others:
Opiate therapy
References
- ↑ Scorza K, Williams A, Phillips JD, Shaw J (July 2007). “Evaluation of nausea and vomiting”. Am Fam Physician. 76 (1): 76–84. PMID 17668843.
- ↑ Hasler WL, Chey WD (December 2003). “Nausea and vomiting”. Gastroenterology. 125 (6): 1860–7. doi:10.1053/j.gastro.2003.09.040. PMID 14724837.
- ↑ . doi:10.1002/j.1875-9114.1990.tb02560.x. Missing or empty
|title=(help)
Epidemiology and Demographics
Overview
Epidemiology and demographics
- In population studies, at least one episode of nausea was reported in more than 50% of adults, and one episode of vomiting in more than 30% of adults within the preceding 12 months, with nausea seen more in women than men. [1] [2]
- A significant psychological and economic impact of nausea and vomiting is seen with an estimated economic burden of $4-16 billion on US economy. [2]
- Only 25% of people with acute symptoms of nausea and vomiting seek medical help. [3]
Incidence
- Incidence of nausea and vomiting varies with the underlying cause.
- Nausea and vomiting of pregnancy effects 70% to 80% of all pregnant women. [4]
- Approximately 40% of patients experience nausea and 15%-25% patients experience vomiting with opioid use. [5]
- Incidence of postoperative nausea and vomiting varies from 8%-92%. [5]
Prevalence
- In population studies, at least one episode of nausea was reported in more than 50% of adults, and one episode of vomiting in more than 30% of adults within the preceding 12 months, with nausea seen more in women than men. [1]
- Only 25% of people with acute symptoms of nausea and vomiting seek medical help. [3]
- The exact prevalence of idiopathic nausea and vomiting is not known. [2]
Age
- In a study of patients with nausea and vomiting in Australia, between April 2000 and March 2006. vomiting was more often presented in children aged <15 years and decreased steadily with age. [6]
- Nausea was more often presented in age 15-25 years and less frequently in all other age groups.
Race
Gender
- Prevalence of nausea is more in females than males. [9]
- Nausea and vomiting associated with gastroenteritis is significantly more in males than in females. [6]
- Undiagnosed cases of nausea and vomiting are more commonly seen in females than males. [6]
Developed Countries
- In a study, nausea and vomiting was reported more commonly by less educated pregnant females (hence less common in developed countries due to high literacy rate) [10]
Developing Countries
- Developing countries may have more cases of nausea and vomiting due to low literacy and low socioeconomic status according to a study that involved cases of nausea and vomiting in pregnant females. [10]
References
- ↑ 1.0 1.1 “Mechanisms and Control of Emesis: A Satellite Symposium of the European … – Google Books”.
- ↑ 2.0 2.1 2.2 Singh P, Yoon SS, Kuo B (January 2016). “Nausea: a review of pathophysiology and therapeutics”. Therap Adv Gastroenterol. 9 (1): 98–112. doi:10.1177/1756283X15618131. PMC 4699282. PMID 26770271.
- ↑ 3.0 3.1 Metz A, Hebbard G (September 2007). “Nausea and vomiting in adults–a diagnostic approach”. Aust Fam Physician. 36 (9): 688–92. PMID 17885699.
- ↑ Lee NM, Saha S (June 2011). “Nausea and vomiting of pregnancy”. Gastroenterol Clin North Am. 40 (2): 309–34, vii. doi:10.1016/j.gtc.2011.03.009. PMC 3676933. PMID 21601782.
- ↑ 5.0 5.1 Mallick-Searle T, Fillman M (November 2017). “The pathophysiology, incidence, impact, and treatment of opioid-induced nausea and vomiting”. J Am Assoc Nurse Pract. 29 (11): 704–710. doi:10.1002/2327-6924.12532. PMID 29131554.
- ↑ 6.0 6.1 6.2 Britt H, Fahridin S (September 2007). “Presentations of nausea and vomiting”. Aust Fam Physician. 36 (9): 682–3. PMID 17885697.
- ↑ Stern RM, Hu S, LeBlanc R, Koch KL (September 1993). “Chinese hyper-susceptibility to vection-induced motion sickness”. Aviat Space Environ Med. 64 (9 Pt 1): 827–30. PMID 8216144.
- ↑ Stern RM, Hu S, Uijtdehaage SH, Muth ER, Xu LH, Koch KL (1996). “Asian hypersusceptibility to motion sickness”. Hum Hered. 46 (1): 7–14. doi:10.1159/000154318. PMID 8825456.
- ↑ Haug TT, Mykletun A, Dahl AA (2002). “The prevalence of nausea in the community: psychological, social and somatic factors”. Gen Hosp Psychiatry. 24 (2): 81–6. doi:10.1016/s0163-8343(01)00184-0. PMID 11869741.
- ↑ 10.0 10.1 Louik C, Hernandez-Diaz S, Werler MM, Mitchell AA (July 2006). “Nausea and vomiting in pregnancy: maternal characteristics and risk factors”. Paediatr Perinat Epidemiol. 20 (4): 270–8. doi:10.1111/j.1365-3016.2006.00723.x. PMID 16879499.
Risk Factors
Overview
Risk factors
- Well established risk factors for postoperative nausea and vomiting include: [1]
- female gender post puberty
- nonsmoking status
- history of postoperative nausea and vomiting
- history of motion sickness
- childhood after infancy and younger adulthood
- increasing duration of surgery
- use of volatile anesthetics, nitrous oxide, large-dose neostigmine, or intraoperative or postoperative opioids
- Possible risk factors for postoperative nausea and vomiting include: [1]
- history of migraine
- history of postoperative nausea and vomiting or motion sickness in a child’s parent or sibling
- intense preoperative anxiety
- certain ethnicities or surgery types
- decreased perioperative fluids
- crystalloid versus colloid administration
- increasing duration of anesthesia
- general versus regional anesthesia or sedation
- balanced versus total IV anesthesia
- use of longer-acting versus shorter-acting opioids
- Risk factors for nausea and vomiting in pregnancy include: [2]
- increased number of prior miscarriages
- increased gravidity
- risk decreased with increasing age
- twin births
- Increased risk of nausea and vomiting after first trimester is seen in women who are less well educated, have lower incomes, and more likely in black women.
- Risk factors for chemotherapy induced nausea and vomiting: [3] [4]
- age less than 50 years
- female gender
- history of nausea and vomiting or motion sickness
- type of antineoplastic agent and how it is used
References
- ↑ 1.0 1.1 Gan TJ (June 2006). “Risk factors for postoperative nausea and vomiting”. Anesth Analg. 102 (6): 1884–98. doi:10.1213/01.ANE.0000219597.16143.4D. PMID 16717343.
- ↑ Louik C, Hernandez-Diaz S, Werler MM, Mitchell AA (July 2006). “Nausea and vomiting in pregnancy: maternal characteristics and risk factors”. Paediatr Perinat Epidemiol. 20 (4): 270–8. doi:10.1111/j.1365-3016.2006.00723.x. PMID 16879499.
- ↑ Sekine I, Segawa Y, Kubota K, Saeki T (June 2013). “Risk factors of chemotherapy-induced nausea and vomiting: index for personalized antiemetic prophylaxis”. Cancer Sci. 104 (6): 711–7. doi:10.1111/cas.12146. PMC 7657206 Check
|pmc=value (help). PMID 23480814. - ↑ Hesketh, Paul J.; Aapro, Matti; Street, James C.; Carides, Alexandra D. (2009). “Evaluation of risk factors predictive of nausea and vomiting with current standard-of-care antiemetic treatment: analysis of two phase III trials of aprepitant in patients receiving cisplatin-based chemotherapy”. Supportive Care in Cancer. 18 (9): 1171–1177. doi:10.1007/s00520-009-0737-9. ISSN 0941-4355.
Natural History, Complications and Prognosis
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Vishnu Vardhan Serla M.B.B.S. [2]
Overview
Natural history, complications and prognosis
Natural history
- Nausea starts as an urge of vomiting. There is a diffuse sensation of unease and discomfort (often described as feeling sick or queasy feeling). Discomfort in chest, upper abdomen or back of throat might be present. It is often accompanied by excessive salivation. If vomiting follows, there is involuntary expulsion of stomach contents through mouth and sometimes nose. If nausea and vomiting are left untreated, the general feeing of distress can progress to life threatening complications.
Complications
- aspiration of gastric content [1]
- dehydration [2]
- electrolyte imbalance leading to metabolic alkalosis (increased blood pH), showing hypokalemia and hypochloremia [2] [1]
- cachexia due to loss of intake of food [2]
- antepartum hemorrhage of indeterminate origin in early pregnancy [3]
- callus formation and abrasions on skin of hands in case of self induced vomiting [1]
- pressure on ear, nose and eyes sometimes leading to subconjunctival hemorrhage and nose bleeds due to prolonged retching [1]
- dental erosion, discoloration and sensitivity of teeth, gum disease due to acidic gastric content [1]
- mucositis of hard palate and throat [1]
- salivary gland enlargement and parotid gland hypertrophy in bulimics [1] [4]
- Cardiovascular symptoms including hypotention, sinus tachycardia, arrythmias and orthostasis in bulimic patients [1]
Prognosis
Prognosis for nausea and vomiting depends on the underlying cause.
References
- ↑ 1.00 1.01 1.02 1.03 1.04 1.05 1.06 1.07 1.08 1.09 1.10 1.11 1.12 1.13 Brown, Carrie A.; Mehler, Philip S. (2013). “Medical Complications of Self-Induced Vomiting”. Eating Disorders. 21 (4): 287–294. doi:10.1080/10640266.2013.797317. ISSN 1064-0266.
- ↑ 2.0 2.1 2.2 Kim GH, Jung KW (December 2017). “[Vomiting]”. Korean J Gastroenterol (in Korean). 70 (6): 283–287. doi:10.4166/kjg.2017.70.6.283. PMID 29277090.
- ↑ Chin RK (December 1989). “Antenatal complications and perinatal outcome in patients with nausea and vomiting-complicated pregnancy”. Eur J Obstet Gynecol Reprod Biol. 33 (3): 215–9. doi:10.1016/0028-2243(89)90132-9. PMID 2599251.
- ↑ 4.0 4.1 Metzger ED, Levine JM, McArdle CR, Wolfe BE, Jimerson DC (June 1999). “Salivary gland enlargement and elevated serum amylase in bulimia nervosa”. Biol Psychiatry. 45 (11): 1520–2. doi:10.1016/s0006-3223(98)00221-2. PMID 10356637.
Diagnosis
Diagnosis
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