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Melena

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief:

Synonyms and keywords: Black and tarry stools, Clinical manifestation of upper GI bleed

Overview

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Melena or melaena refers to the black, “tarry” feces that are associated with gastrointestinal hemorrhage. The black color is caused by oxidation of the iron in hemoglobin during its passage through the ileum and colon.

Historical Perspective

Classification

Pathophysiology

Melena, is stool with blood, that has been altered by the gut flora, and appears black/”tarry“.

Causes

The most common cause of melena is peptic ulcer disease. Any other cause of bleeding from the upper gastro-intestinal tract, or even the ascending colon, can also cause melena. Melena may also be a sign of drug overdose if a patient is taking anti-coagulants, such as warfarin. A less serious, self-limiting case of melena can occur in newborns two to three days after delivery, due to swallowed maternal blood.

Differentiating Melena overview from Other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications, and Prognosis

Natural History

Complications

Prognosis

Diagnosis

Diagnostic Criteria

History and Symptoms

Physical Examination

Laboratory Findings

Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Surgery

Prevention

References

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Historical Perspective

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief:

Overview

Historical Perspective

  • Melena is a manifestation of upper gastrointestinal bleeding (UGIB). The term melena is defined as black or tarry stools as a result of blood loss originating proximal to the ligament of Treitz, in the esophagus, stomach, or duodenum.[1]
  • Melena, or black stool, may develop with as little as 50 ml of blood loss from the GI tract per day.[2]

Reference

  1. Kamboj AK, Hoversten P, Leggett CL (2019). “Upper Gastrointestinal Bleeding: Etiologies and Management”. Mayo Clin Proc. 94 (4): 697–703. doi:10.1016/j.mayocp.2019.01.022. PMID 30947833.
  2. “Melena – an overview | ScienceDirect Topics”.

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Classification

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief:

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Overview

Classification

References

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Pathophysiology

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Pathophysiology

Melena, is stool with blood, that has been altered by the gut flora, and appears black/”tarry“.

Melena vs. Hematochezia

Bleeding originating from the lower GI tract (such as the sigmoid colon and rectum) is generally associated with the passage of bright red blood, or hematochezia, particularly when brisk. Blood acts as a cathartic agent in the intestine, promoting its prompt passage. Only blood that originates from a high source (such as the small intestine), or bleeding from a lower source that occurs slowly enough to allow for oxidation, is associated with melena. For this reason, melena is often associated with hemorrhage in the stomach or duodenum (upper gastrointestinal tract), for example by a peptic ulcer. A rough estimate is that it takes about 14 hours for blood to be broken down within the intestinal lumen; therefore if transit time is less than 14 hours the patient will have hematochezia and if greater than 14 hours the patient will exhibit melena. One often-stated rule of thumb is that melena only occurs if the source of bleeding is above the ligament of Treitz.

Reference

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Causes

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ogheneochuko Ajari, MB.BS, MS [2]

Overview

The most common cause of melena is peptic ulcer disease. Any other cause of bleeding from the upper gastro-intestinal tract, or even the ascending colon, can also cause melena. Melena may also be a sign of drug overdose if a patient is taking anti-coagulants, such as warfarin. A less serious, self-limiting case of melena can occur in newborns two to three days after delivery, due to swallowed maternal blood.

Causes

Life Threatening Causes

Life-threatening causes include conditions which may result in death or permanent disability within 24 hours if left untreated.

Common Causes

Causes by Organ System

Cardiovascular Cholesterol embolism, mesenteric vascular occlusion, vasculitis
Chemical/Poisoning Arsenic trioxide, arsenicals, caustic ingestion, ethylene glycol, mercury
Dental No underlying causes
Dermatologic Craniomandibular dermatodysostosis, Degos disease, dermatomyositis, hereditary haemorrhagic telangiectasia, Osler-Weber-Rendu syndrome, vasculitis
Drug Side Effect Alendronate, alosetron, anticoagulants, aspirin, bevacizumab, Bicalutamide, Ceftibuten, clopidogrel, Cidofovir, colchicine, dicoumarol, indomethacin, iron compounds, melarsoprol, Meropenem, miltefosine, Nilutamide, NSAIDS, Oxaprozin, Pergolide, phenprocoumon, phenylbutazone, potassium chloride, quinidine, sertraline, tetracycline, Tiagabine, warfarin, zinc, ziv-aflibercept, Zonisamide
Ear Nose Throat Hereditary haemorrhagic telangiectasia, Osler-Weber-Rendu syndrome
Endocrine Carcinoid
Environmental No underlying causes
Gastroenterologic Alcoholic cirrhosis, alcoholic fatty liver, anal fissure, angiodysplasia, aortoenteric fistula, Banti’s syndrome, biliary atresia, bowel ischemia, bowel obstruction, bowel strangulation, Budd-Chiari syndrome, chronic portal vein thrombosis, coats plus syndrome, colitis cystica profunda, colitis, colonic diverticulosis, colonic tubular adenomata, colonic villous adenomata, colonoscopy, colorectal cancer, Crohn’s disease, Degos disease, Dieulafoy’s ulcer, duodenal polypectomy, duodenal ulcer, duodenal webs, duplication cysts, esophageal cancer, esophageal cyst, esophageal varices, familial adenomatous polyposis, Gardner syndrome, gastric antral vascular ectasia, Gastric cancer, gastric polyps, gastric ulcer, gastric volvulus, gastric webs, gastritis, gastroduodenal ulcers, gastrointestinal duplications, hemorrhoids, hemobilia, hepatic arterioportal fistula, intussusception, liver cirrhosis, Mallory-Weiss syndrome, Mallory-Weiss tear, Meckel’s diverticulum, Ménétrier’s disease, mesenteric vascular occlusion, peptic ulcer, Peutz-Jeghers syndrome, pneumatosis cystoides intestinalis, portal hypertension, portal hypertensive gastropathy, proctitis, ruptured esophageal varices, solitary rectal ulcer syndrome, stomach cancer, stress gastritis, stress ulcer, superior mesenteric artery occlusion, ulcerative colitis, watermelon stomach, Zollinger-Ellison syndrome
Genetic Banti’s syndrome, carbamoylphosphate synthetase deficiency, coats plus syndrome, Crohn’s disease, Ehlers-Danlos syndrome, familial adenomatous polyposis, Gardner syndrome, hepatorenal tyrosinemia, Kasabach-Merritt syndrome, neurofibromatosis type I, Peutz-Jeghers syndrome, pseudoxanthoma elasticum, Wiskott-Aldrich syndrome
Hematologic Blood clotting disorders, carcinoid, coagulopathy, essential thrombocytosis, hemophilia, haemorrhagic disease of the newborn, hemorrhagic thrombocythemia, Henoch-Schoenlein purpura, iron deficiency anemia, Kasabach-Merritt syndrome, systemic mastocytosis, thrombocytopenia, Wiskott-Aldrich syndrome
Iatrogenic Parenteral nutrition-induced liver disease, post-surgical anastomosis, radiation-induced telangiectasia
Infectious Disease Acanthocephaliasis, ancylostoma duodenale, angiostrongyliasis, anthrax, bacillary dysentery, balantidiasis, candida albicans, cytomegalovirus, ebola virus, entamoeba histolytica, giardiasis, helicobacter pylori, herpes simplex virus, Katayama fever , necator americanus (hookworm), parasites, schistosoma mansoni, strongyloidiasis, trichuriasis, typhoid fever, yellow fever
Musculoskeletal/Orthopedic Craniomandibular dermatodysostosis, Ehlers-Danlos syndrome, pelvic fracture
Neurologic Degos disease, hereditary haemorrhagic telangiectasia, Labrune syndrome, neurofibromatosis type I, Osler-Weber-Rendu syndrome
Nutritional/Metabolic Carbamoylphosphate synthetase deficiency, hepatorenal tyrosinemia, milk protein intolerance
Obstetric/Gynecologic Choriocarcinoma, endometriosis, leiomyoma
Oncologic Adenocarcinoma, anal cancer, blue rubber bleb nevus syndrome, carcinoid, cecal carcinoma, choriocarcinoma, colorectal cancer, esophageal cancer, familial adenomatous polyposis, Gardner syndrome, gastric cancer, hemangiomas, kaposi sarcoma, lipoma, lymphoma, malignancy, melanoma, mesenchymal neoplasm, metastatic tumor, Peutz-Jeghers syndrome, small bowel cancer, small bowel lymphoma, small bowel tumors, stomach cancer, systemic mastocytosis, tumors
Ophthalmologic Coats plus syndrome
Overdose/Toxicity Drug overdose
Psychiatric No underlying causes
Pulmonary No underlying causes
Renal/Electrolyte Cholesterol embolism, chronic renal failure, craniomandibular dermatodysostosis, Henoch-Schoenlein purpura
Rheumatology/Immunology/Allergy Crohn’s disease, dermatomyositis, food allergy, food protein-induced enterocolitis syndrome (FPIES), Henoch-Schoenlein purpura, microscopic polyangiitis, polyarteritis nodosa, systemic mastocytosis, vasculitis, Wiskott-Aldrich syndrome
Sexual No underlying causes
Trauma Trauma
Urologic No underlying causes
Miscellaneous Foreign body, swallowed maternal blood

Causes in Alphabetical Order

References

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Differentiating Melena from Other Diseases

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Reference

Epidemiology and Demographics

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Tayyaba Ali, M.D.[2]

Overview

Epidemiology and Demographics

Incidence

  • The annual incidence of hospitalization for acute upper gastrointestinal bleeding (UGIB) in the United States is approximately 65 per 100,000 individuals.[1]

Prevalence

  • The prevalence of melena is almost the same as incidence, as it is a manifestation of an acute condition and is not a chronic disease.

Case-fatality rate/Mortality rate

  • Overall mortality decreased from 17.1 to 8.2 per 100,000/y which corresponded to a 60.8% decrease after adjustment for age (95% CI, 46.5%-75.1%). The age-standardized mortality rate for ulcer bleeding decreased by 56.5% (95% CI, 41.9%-71.1%).[2]

Age

  • The incidence of upper gastrointestinal bleed increases with age and decreases in people younger than 70 years of age.[2]

Race

  • According to one study done in 2196 patients with upper gastrointestinal bleeding. 620 (28%) were black, 625 (29%) white, 881 (40%) Hispanic, and 70 (3%) were members of other ethnicities.
  • In all ethnicities, gastrointestinal ulcer disease is the most common cause of bleeding or melena in patients younger than 35 or older than 65 years. Certain differences in terms of etiology of melena were observed among patients aged 35 to 64 years.
  • Blacks aged 50 to 64 years frequently experienced gastroduodenal ulcers, whereas Hispanics aged 35 to 49 years typically had esophageal varices. Rebleeding rates were significantly lower in whites (5.8%) than in Hispanics (9.9%) or blacks (8.7%) (P=0.02).[3]

Gender

  • The incidence of UGIB is higher in males than in females (128 versus 65 per 100,000 in one study).[4]

Reference

  1. Wuerth BA, Rockey DC (2018). “Changing Epidemiology of Upper Gastrointestinal Hemorrhage in the Last Decade: A Nationwide Analysis”. Dig Dis Sci. 63 (5): 1286–1293. doi:10.1007/s10620-017-4882-6. PMID 29282637.
  2. 2.0 2.1 Loperfido S, Baldo V, Piovesana E, Bellina L, Rossi K, Groppo M; et al. (2009). “Changing trends in acute upper-GI bleeding: a population-based study”. Gastrointest Endosc. 70 (2): 212–24. doi:10.1016/j.gie.2008.10.051. PMID 19409558.
  3. Wollenman CS, Chason R, Reisch JS, Rockey DC (2014). “Impact of ethnicity in upper gastrointestinal hemorrhage”. J Clin Gastroenterol. 48 (4): 343–50. doi:10.1097/MCG.0000000000000025. PMC 4157370. PMID 24275716.
  4. Enestvedt BK, Gralnek IM, Mattek N, Lieberman DA, Eisen G (2008). “An evaluation of endoscopic indications and findings related to nonvariceal upper-GI hemorrhage in a large multicenter consortium”. Gastrointest Endosc. 67 (3): 422–9. doi:10.1016/j.gie.2007.09.024. PMID 18206878.

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Risk Factors

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief:

Overview

Risk Factors

Reference

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Screening

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief:

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Overview

Screening

References

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Natural History, Complications and Prognosis

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief:

Overview

Natural History

Complications

Prognosis

Reference

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Diagnosis

Diagnosis

History and Symptoms | Physical Examination | Laboratory Findings | X Ray | CT | MRI | Other Imaging Findings | Other Diagnostic Studies

Treatment

Treatment

Medical Therapy | Surgery | Primary Prevention | Secondary Prevention | Cost-Effectiveness of Therapy | Future or Investigational Therapies

Case Studies

Case Studies

Case #1

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