Fecal occult blood

From Wikipedia, the free encyclopedia
(Redirected from Stool occult blood)
Fecal occult blood
Cards and bottle used for the Hemoccult test, a type of stool guaiac test
SpecialtyGastroenterology, general surgery

Fecal occult blood (FOB) refers to blood in the feces that is not visibly apparent (unlike other types of blood in stool such as melena or hematochezia). A fecal occult blood test (FOBT) checks for hidden (occult) blood in the stool (feces).[1]

The American College of Gastroenterology has recommended the abandoning of gFOBT testing as a colorectal cancer screening tool, in favor of the fecal immunochemical test (FIT).[2] The newer and recommended tests look for globin, DNA, or other blood factors including transferrin, while conventional stool guaiac tests look for heme.

Medical uses[edit]

Fecal occult blood testing (FOBT), as its name implies, aims to detect subtle blood loss in the gastrointestinal tract, anywhere from the mouth to the colon. Positive tests ("positive stool") may result from either upper gastrointestinal bleeding or lower gastrointestinal bleeding and warrant further investigation for peptic ulcers or a malignancy (such as colorectal cancer or gastric cancer). The test does not directly detect colon cancer but is often used in clinical screening for that disease. It can also be used to look for active occult blood loss in anemia[3] or when there are gastrointestinal symptoms.[4]

Colorectal cancer screening[edit]

An estimated 1–5% of large tested populations have a positive fecal occult blood test.[citation needed] Of those, about 2–10% have cancer, while 20–30% have adenomas. Screening methods for colon cancer depend on detecting either precancerous changes such as certain kinds of polyps or on finding early and thus more treatable cancer. The extent to which screening procedures reduce the risk of gastrointestinal cancer or deaths depends on the rate of precancerous and cancerous disease in that population. gFOBT (guaiac fecal occult blood test) and flexible sigmoidoscopy screening have each shown benefit. Other colon cancer screening tools such as iFOBT (immunochemical fecal occult blood test) or colonoscopy are also included in guidelines.[5]

In 2009 the American College of Gastroenterology (ACG) suggested that colon cancer screening modalities that are also directly preventive by removing precursor lesions should be given precedence, and prefer a colonoscopy every ten years in average-risk individuals, beginning at age 50.[6] The ACG suggests that cancer detection tests such as any type of FOB are an alternative that is less preferred, and if a colonoscopy is declined, the FIT (fecal immunochemical test, or iFOBT) should be offered instead. The 2017 US Multi-Society Task Force (MSTF)'s recommended first-tier tests are a colonoscopy every 10 years or annual FIT test.[7] If FIT is utilized, proper steps must be taken to ensure appropriate use and follow-up of abnormal FIT results.[8] FIT tests however are not that useful in picking up adenomas, even when advanced.[9]

The United States Preventive Services Task Force (USPSTF)'s 2016 recommendation, instead of emphasizing specific screening approaches, has instead chosen to highlight that there is convincing evidence that colorectal cancer screening substantially reduces deaths from the disease among adults aged 50 to 75 years and that not enough adults are using this effective preventive intervention.[10] The ACG and MSTF also included CT colonography every five years, and fecal DNA testing as considerations. All three recommendation panels recommended replacing any older low-sensitivity, guaiac-based fecal occult blood testing (gFOBT) with either newer high-sensitivity guaiac-based fecal occult blood testing (hs gFOBT) or fecal immunochemical testing (FIT). MSTF looked at six studies that compared high-sensitivity gFOBT (Hemoccult SENSA) to FIT, and concluded that there was no clear difference in overall performance between these methods.

The English National Health Service (NHS) introduced a Bowel Cancer Screening Program in 2006.[11] It is now offered to patients aged 60–74 years. In 2019 FIT was introduced as the primary screening test in England and Wales, replacing gFOBt. [12][13] However, research carried out in the UK has suggested that the FIT threshold for further investigation is set at a point that may miss more than half of bowel cancer cases and only identifies one in four high-risk polyps.[14][15]

The American College of Gastroenterology has recommended the abandoning of gFOBT testing as a colorectal cancer screening tool, in favor of the fecal immunochemical test.[6] Though the FIT test is preferred, even the guaiac FOB testing of average risk populations may have been sufficient to reduce the mortality associated with colon cancer by about 25%.[16] With this lower efficacy, it was not always cost-effective to screen a large population with gFOBT.[17][18][19][20]

A LabCorp fecal occult blood immunoassay testing kit.

If colon cancer is suspected in an individual (such as in someone with an unexplained anemia), fecal occult blood tests may not be clinically helpful. If a doctor suspects colon cancer, more rigorous investigation is necessary, whether or not the test is positive.[citation needed]

In 2006, the Australian Government introduced the National Bowel Cancer Program which has been updated several times since; targeted screening will be done of all Australians aged from 50 to 74 by 2020. Cancer Council Australia recommended that FOBT should be done every two years. People over 50 not yet eligible for the national program can arrange with their doctor for an FOBT.[21] The Canadian Cancer Society recommends that men and women aged 50 and over have an FOBT at least every two years.[22] In colon cancer screening, using only one sample of feces collected by a doctor performing a digital rectal examination is discouraged.[23]

The use of the M2-PK Test is encouraged over gFOBT for routine screening, as it may pick up tumors whether or not they are bleeding.[24] It is able to detect 80 percent of colorectal cancers and 44 percent for adenoma > 1 centimeter, while gFOBT picks up 13 to 50 percent of colorectal cancers.[24]

Other sources of bleeding[edit]

Gastrointestinal bleeding has many potential sources, and positive results usually result in further testing for the bleeding site, usually looking for lower gastrointestinal bleeding before upper gastrointestinal bleeding causes unless there are other clues.[25] Colonoscopy is usually preferred to computerized tomographic colonography.[26]

A positive test can result from upper gastrointestinal bleeding or lower gastrointestinal bleeding. The common causes are:

In the event of a positive fecal occult blood test, the next step in the workup is a form of visualization of the gastrointestinal tract by one of several means:

  1. Sigmoidoscopy, an examination of the rectum and lower colon with a lighted instrument to look for abnormalities, such as polyps.
  2. Colonoscopy, a more thorough examination of the rectum and entire colon.
  3. Virtual colonoscopy
  4. Upper gastrointestinal endoscopy. It is sometimes performed with chromoendoscopy, a method that assists the endoscopist by enhancing the visual difference between cancerous and normal tissue, by either marking the abnormally increased DNA content (toluidine blue) or failing to stain the tumor, possibly due to decreased surface glycogen on tumor cells(Lugol).[28][29] Infrared fluorescent endoscopy[citation needed] and ultrasonic endoscopy[citation needed] can interrogate vascular abnormalities such as esophageal varices.
  5. Double-contrast barium enema: a series of x-rays of the colon and rectum.

Testing secretions for blood[edit]

The use of an FOBT for bleeding from the mouth, nose, esophagus, lungs, stomach and the initial portion of the small intestine, while the same as fecal testing, is discouraged, due to technical considerations including poorly characterized test performance characteristics such as sensitivity, specificity, and analytical interference.[30] However, chemical confirmation that coloration is due to blood rather than coffee, beets, medications, or food additives can be of significant clinical assistance.

Marathon runners[edit]

Gastrointestinal (GI) complaints and low-intensity GI bleeding frequently occur in marathon runners.[31] Strenuous exercise, particularly in elite athlete runners and less frequently in other exercise activities, can cause acute incapacitating gastrointestinal symptoms including heartburn, nausea, vomiting, abdominal pain, diarrhea and gastrointestinal bleeding.[32] Approximately one third of endurance runners experience transient but exercise-limiting symptoms, and repetitive gastrointestinal bleeding occasionally causes iron deficiency and anaemia.[33][34] Runners can sometimes experience significant symptoms including hematemesis.[35] Exercise is associated with extensive changes in gastrointestinal (GI) tract physiology, including diversion of blood flow from the GI tract to muscles and lungs, decreased GI absorption and small intestinal motility, increased colonic transit, neuroimmunoendocrine changes in hormones and peptides such as vasoactive intestinal peptide, secretin and peptide-histidine-methionine.[36] Substantial changes occur in stress hormones including cortisol, in circulating concentrations and metabolic behavior of various leucocytes, and in immunoglobulin levels and major histocompatibility complex expression.[37] Symptoms can be exacerbated by dehydration or by pre-exercise ingestion of certain foods and hypertonic liquids, and lessened by adequate training.[36]

Ingestion of 800 mg of cimetidine two hours before running a marathon did not significantly affect the frequency of gastrointestinal symptoms or occult gastrointestinal bleeding.[38] Conversely, 800 mg of cimetidine 1 hr before the start and again at 50 miles of a 100-mile running race substantially decreased GI symptoms and post-race guaiac test positivity but did not affect race performance.[39]


There are four methods in clinical use to test for occult blood in feces. These look at different properties, such as antibodies, heme, globin, or porphyrins in blood, or at DNA from cellular material such as from lesions of the intestinal mucosa.

  • Fecal immunochemical testing (FIT), and immunochemical fecal occult blood test (iFOBT). FIT products utilize specific antibodies to detect globin. FIT screening is more effective in terms of health outcomes and cost compared with guaiac FOBT.[40] According to the guidelines of the American College of Gastroenterology, "Annual fecal immunochemical testing is the preferred colorectal cancer detection test."[6][41] A FIT test detects globin levels in feces at or above 50 nanograms per mL, the established cutoff by the World Health Organization for Colorectal Cancer Screening.[citation needed] FIT testing has replaced most gFOBT tests as the colon cancer screening test of choice.[42][43] This methodology can be adapted for automated test reading and to report quantitative results, which are potential factors in design of a widescale screening strategy.[44] The number of fecal samples submitted for FIT may affect the clinical sensitivity and specificity of the methodology.[8] High-sensitivity gFOBT tests such as Hemoccult SENSA remain an accepted option[8] and may retain a role in monitoring gastrointestinal conditions such as ulcerative colitis;[45] however, the FIT test is preferred in recent guidelines.[6] FIT is widely used outside of the US, and generally cost less than US$20 per test in 2020, compared to US$1,000 or more for a colonoscopy.[46]
A positive traditional guaiac fecal occult blood test
  • Stool guaiac test for fecal occult blood (gFOBT): – The stool guaiac test involves smearing some feces onto some absorbent paper that has been treated with a chemical. Hydrogen peroxide is then dropped onto the paper; if trace amounts of blood are present, the paper will change color in one or two seconds. This method works as the heme component in hemoglobin has a peroxidase-like effect, rapidly breaking down hydrogen peroxide. In some settings such as gastric or proximal upper intestinal bleeding, the guaiac method may be more sensitive than tests detecting globin because globin is broken down in the upper intestine to a greater extent than is heme.[47] There are various commercially available gFOBT tests which have been categorized as being of low or high sensitivity, and only high-sensitivity tests remain an acceptable alternative to FIT testing, which is now the best-practices recommendation in colon cancer screening. Optimal clinical performance of the stool guaiac test depends on preparatory dietary adjustment.[48] The stool guaiac test for hidden (occult) blood in the stool should be used at home following the test kit's directions with spontaneously passed stool[23] or on samples submitted to a clinical laboratory. Testing kits are available at pharmacies in some countries without a prescription, or a health professional may order a testing kit for use at home. If a home fecal occult blood test detects blood in the stool it is recommended to see a health professional to arrange further testing.[49]
  • Stool DNA screening tests look for DNA alterations that have been associated with cancer.

Additional methods of looking for occult blood are being explored, including transferrin dipstick[50] and stool cytology.[51]

Test performance[edit]

Reference standards[edit]

The estimates for test performance characteristics are based on comparison with a variety of reference methods including 51-chromium studies,[citation needed] analytical recovery studies in spiked stool samples, analytical recovery after ingestion of autologous blood, rarer studies of carefully quantified blood instilled at bowel surgery[citation needed], as well as other research approaches.[citation needed] Additionally, clinical studies look at a variety of additional factors.

Gastrointestinal blood loss[edit]

In healthy people about 0.5 to 1.5 ml of blood escapes blood vessels into the stool each day.[52][53][54] Significant amounts of blood can be lost without producing visible blood in the stool, estimated as 200 ml in the stomach,[55] 100 ml in the duodenum, and lesser amounts in the lower intestine. Tests for occult blood identify lesser blood loss.

Clinical sensitivity and specificity[edit]

Fecal immunochemical testing (FIT) can identify as little as 0.3 ml of daily blood in the stool; yet this test threshold doesn't cause undue false positives from normal upper intestinal blood leakage because it does not detect occult blood from the stomach and upper small intestine. Thus, the FIT test is much more specific for bleeding from the colon or lower gastrointestinal tract than alternatives.[56] The detection rate of the test decreases if the time from sample collection to laboratory processing is delayed; processing the sample in under five days from collection is recommended.[57] It does not appear to be affected by aspirin, anticoagulants, or nonsteroidal anti-inflammatory drugs.[58]

Stool guaiac test for fecal occult blood (gFOBT) sensitivity varies depending on the site of bleeding. Moderately sensitive gFOBT can pick up a daily blood loss of about 10 ml (about two teaspoonfuls), and higher sensitivity gFOBT can pick up lesser amounts, requires at least 2 ml to become positive. The sensitivity of a single-stool guaiac test to pick up bleeding has been quoted at 10 to 30%, but if a standard three tests are done as recommended the sensitivity rises to 92%.[59] Reduced patient compliance with the collection of three samples hampers the usefulness of this test. Further discussion of sensitivity and specificity issues that relate particularly to the guaiac method is found in the stool guaiac test article.

Fecal porphyrin quantification by HemoQuant can yield a false positive result due to exogenous blood and various porphyrins. HemoQuant is the most sensitive test for upper gastrointestinal bleeding and therefore may be most appropriate fecal occult blood test to use in the evaluation of iron deficiency.[60] It is advisable to stop ingesting red meat and aspirin for three days prior to specimen collection.[61] False positives can occur with myoglobin, catalase, or protohemes[62] and in certain types of porphyria.[citation needed]

Fecal DNA tests as of 2008 had not been studied enough to support widespread use.[63]


Safety regulations from US accreditor the Joint Commission may have unintentionally decreased digital rectal examination and FOBT in hospital settings such as Emergency Departments.[64][65]


  1. ^ Beg M, Singh M, Saraswat MK, Rewari BB (2002). "Occult Gastrointestinal Bleeding: Detection, Interpretation, and Evaluation" (PDF). JIACM. 3 (2): 153–58. Archived (PDF) from the original on 2010-11-22.
  2. ^ Rex DK, Johnson DA, Anderson JC, Schoenfeld PS, Burke CA, Inadomi JM (March 2009). "American College of Gastroenterology guidelines for colorectal cancer screening 2009 [corrected]". The American Journal of Gastroenterology. 104 (3): 739–750. doi:10.1038/ajg.2009.104. PMID 19240699. S2CID 295873.
  3. ^ Harewood GC, Ahlquist DA (2000). "Fecal occult blood testing for iron deficiency: a reappraisal". Digestive Diseases. 18 (2): 75–82. doi:10.1159/000016968. PMID 11060470. S2CID 29966595.
  4. ^ Bardhan PK, Beltinger J, Beltinger RW, Hossain A, Mahalanabis D, Gyr K (January 2000). "Screening of patients with acute infectious diarrhoea: evaluation of clinical features, faecal microscopy, and faecal occult blood testing". Scandinavian Journal of Gastroenterology. 35 (1): 54–60. doi:10.1080/003655200750024533. PMID 10672835. S2CID 218910557.
  5. ^ Robertson DJ, Lee JK, Boland CR, Dominitz JA, Giardiello FM, Johnson DA, et al. (April 2017). "Recommendations on Fecal Immunochemical Testing to Screen for Colorectal Neoplasia: A Consensus Statement by the US Multi-Society Task Force on Colorectal Cancer". Gastroenterology. 152 (5): 1217–1237.e3. doi:10.1053/j.gastro.2016.08.053. PMID 27769517.
  6. ^ a b c d Rex DK, Johnson DA, Anderson JC, Schoenfeld PS, Burke CA, Inadomi JM (March 2009). "American College of Gastroenterology guidelines for colorectal cancer screening 2009 [corrected]". The American Journal of Gastroenterology. 104 (3): 739–750. doi:10.1038/ajg.2009.104. PMID 19240699. S2CID 295873.
  7. ^ Rex DK, Boland CR, Dominitz JA, Giardiello FM, Johnson DA, Kaltenbach T, et al. (July 2017). "Colorectal Cancer Screening: Recommendations for Physicians and Patients From the U.S. Multi-Society Task Force on Colorectal Cancer". Gastroenterology. Elsevier BV. 153 (1): 307–323. doi:10.1053/j.gastro.2017.05.013. PMID 28600072.
  8. ^ Cusumano VT, May FP (June 2020). "Making FIT Count: Maximizing Appropriate Use of the Fecal Immunochemical Test for Colorectal Cancer Screening Programs". Journal of General Internal Medicine. JGIM. 35 (6): 1870–1874. doi:10.1007/s11606-020-05728-y. PMC 7280423. PMID 32128688.
  9. ^ Imperiale TF, Gruber RN, Stump TE, Emmett TW, Monahan PO (March 2019). "Performance Characteristics of Fecal Immunochemical Tests for Colorectal Cancer and Advanced Adenomatous Polyps: A Systematic Review and Meta-analysis". Annals of Internal Medicine. 170 (5): 319–329. doi:10.7326/M18-2390. hdl:1805/21570. PMID 30802902. S2CID 67876943.
  10. ^ "Final Recommendation Statement: Colorectal Cancer: Screening". U.S. Preventive Services Task Force. June 2016. Retrieved 7 April 2019.
  11. ^ Koo S, Neilson LJ, Von Wagner C, Rees CJ (2017-12-04). "The NHS Bowel Cancer Screening Program: current perspectives on strategies for improvement". Risk Management and Healthcare Policy. 10: 177–187. doi:10.2147/RMHP.S109116. PMC 5720037. PMID 29270036.
  12. ^ "CKS is only available in the UK". NICE. Retrieved 2022-08-05.
  13. ^ "Bowel cancer screening". nhs.uk. 2017-10-20. Retrieved 2022-08-05.
  14. ^ "New pathways could improve bowel cancer screening". NIHR Evidence. 2021-09-13. doi:10.3310/alert_47581. S2CID 239113610. Retrieved 2022-08-05.
  15. ^ Li SJ, Sharples LD, Benton SC, Blyuss O, Mathews C, Sasieni P, Duffy SW (September 2021). "Faecal immunochemical testing in bowel cancer screening: Estimating outcomes for different diagnostic policies". Journal of Medical Screening. 28 (3): 277–285. doi:10.1177/0969141320980501. PMC 8366184. PMID 33342370.
  16. ^ Bretthauer M (August 2010). "Evidence for colorectal cancer screening". Best Practice & Research. Clinical Gastroenterology. 24 (4): 417–425. doi:10.1016/j.bpg.2010.06.005. PMID 20833346.
  17. ^ Mandel JS, Bond JH, Church TR, Snover DC, Bradley GM, Schuman LM, Ederer F (May 1993). "Reducing mortality from colorectal cancer by screening for fecal occult blood. Minnesota Colon Cancer Control Study". The New England Journal of Medicine. 328 (19): 1365–1371. doi:10.1056/NEJM199305133281901. PMID 8474513. S2CID 6756273.
  18. ^ Hardcastle JD, Chamberlain JO, Robinson MH, Moss SM, Amar SS, Balfour TW, et al. (November 1996). "Randomised controlled trial of faecal-occult-blood screening for colorectal cancer". Lancet. 348 (9040): 1472–1477. doi:10.1016/S0140-6736(96)03386-7. PMID 8942775. S2CID 11395104.
  19. ^ Kronborg O, Fenger C, Olsen J, Jørgensen OD, Søndergaard O (November 1996). "Randomised study of screening for colorectal cancer with faecal-occult-blood test". Lancet. 348 (9040): 1467–1471. doi:10.1016/S0140-6736(96)03430-7. PMID 8942774. S2CID 37515050.
  20. ^ Kewenter J, Brevinge H, Engarås B, Haglind E, Ahrén C (May 1994). "Results of screening, rescreening, and follow-up in a prospective randomized study for detection of colorectal cancer by fecal occult blood testing. Results for 68,308 subjects". Scandinavian Journal of Gastroenterology. 29 (5): 468–473. doi:10.3109/00365529409096840. PMID 8036464.
  21. ^ "Bowel cancer screening program". Cancer Council Australia. 19 June 2018. Retrieved 11 December 2018.
  22. ^ "Screening for colorectal cancer". Canadian Cancer Society. 2018. Retrieved 11 December 2018.
  23. ^ a b Collins JF, Lieberman DA, Durbin TE, Weiss DG (January 2005). "Accuracy of screening for fecal occult blood on a single stool sample obtained by digital rectal examination: a comparison with recommended sampling practice". Annals of Internal Medicine. 142 (2): 81–85. CiteSeerX doi:10.7326/0003-4819-142-2-200501180-00006. PMID 15657155. S2CID 29833684.
  24. ^ a b Tonus C, Sellinger M, Koss K, Neupert G (August 2012). "Faecal pyruvate kinase isoenzyme type M2 for colorectal cancer screening: a meta-analysis". World Journal of Gastroenterology. 18 (30): 4004–4011. doi:10.3748/wjg.v18.i30.4004. PMC 3419997. PMID 22912551.
  25. ^ Rockey DC (December 2005). "Occult gastrointestinal bleeding". Gastroenterology Clinics of North America. 34 (4): 699–718. doi:10.1016/j.gtc.2005.08.010. PMID 16303578.
  26. ^ Walleser S, Griffiths A, Lord SJ, Howard K, Solomon MJ, Gebski V (December 2007). "What is the value of computered tomography colonography in patients screening positive for fecal occult blood? A systematic review and economic evaluation". Clinical Gastroenterology and Hepatology. 5 (12): 1439–46, quiz 1368. doi:10.1016/j.cgh.2007.09.003. PMID 18054752.
  27. ^ a b c Bevan R, Lee TJ, Nickerson C, Rubin G, Rees CJ (June 2014). "Non-neoplastic findings at colonoscopy after positive faecal occult blood testing: data from the English Bowel Cancer Screening Programme". Journal of Medical Screening. 21 (2): 89–94. doi:10.1177/0969141314528889. PMID 24644029. S2CID 40548811.
  28. ^ Endo M, Sakakibara N, Suzuki H (1972). "Observation of esophageal lesions with the use of endoscopic dyes". Progress of Digestive Endoscopy. 1: 34.
  29. ^ Endo M, Takeshita K, Yoshida M (September 1986). "How can we diagnose the early stage of esophageal cancer? Endoscopic diagnosis". Endoscopy. 18 (Suppl 3): 11–18. doi:10.1055/s-2007-1018435. PMID 2428607. S2CID 34757654.
  30. ^ Mathews B, Ratcliffe T, Sehgal R, Abraham J, Monash B (July 2017). "Fecal Occult Blood Testing in Hospitalized Patients with Upper Gastrointestinal Bleeding". Journal of Hospital Medicine. 12 (7): 567–569. doi:10.12788/jhm.2773. PMID 28699947.
  31. ^ Halvorsen FA, Lyng J, Ritland S (May 1986). "Gastrointestinal bleeding in marathon runners". Scandinavian Journal of Gastroenterology. 21 (4): 493–497. doi:10.3109/00365528609015168. PMID 3487825.
  32. ^ de Oliveira EP, Burini RC (September 2009). "The impact of physical exercise on the gastrointestinal tract". Current Opinion in Clinical Nutrition and Metabolic Care. 12 (5): 533–538. doi:10.1097/MCO.0b013e32832e6776. PMID 19535976. S2CID 21085826.
  33. ^ Peters HP, De Vries WR, Vanberge-Henegouwen GP, Akkermans LM (March 2001). "Potential benefits and hazards of physical activity and exercise on the gastrointestinal tract". Gut. 48 (3): 435–439. doi:10.1136/gut.48.3.435. PMC 1760153. PMID 11171839.
  34. ^ Toy KA, Conran RM (2022-01-01). "Educational Case: Diverticulosis". Academic Pathology. 9 (1): 100014. doi:10.1016/j.acpath.2022.100014. PMC 9115725. PMID 35600744.
  35. ^ Weaver LT (1984). "Do some marathon runners bleed into the gut? (letter response to a previous article)". BMJ. 288 (6410): 65. doi:10.1136/bmj.288.6410.65-b. PMC 1444190.
  36. ^ a b Brouns F, Beckers E (April 1993). "Is the gut an athletic organ? Digestion, absorption and exercise". Sports Medicine. 15 (4): 242–257. doi:10.2165/00007256-199315040-00003. PMID 8460288. S2CID 26732943.
  37. ^ Venkatraman JT, Pendergast DR (2002). "Effect of dietary intake on immune function in athletes". Sports Medicine. 32 (5): 323–337. CiteSeerX doi:10.2165/00007256-200232050-00004. PMID 11929359. S2CID 25330480.
  38. ^ Moses FM, Baska RS, Peura DA, Deuster PA (October 1991). "Effect of cimetidine on marathon-associated gastrointestinal symptoms and bleeding". Digestive Diseases and Sciences. 36 (10): 1390–1394. doi:10.1007/BF01296804. PMID 1914760. S2CID 8264981.
  39. ^ Baska RS, Moses FM, Deuster PA (August 1990). "Cimetidine reduces running-associated gastrointestinal bleeding. A prospective observation". Digestive Diseases and Sciences. 35 (8): 956–960. doi:10.1007/BF01537243. PMID 2384041. S2CID 1978110.
  40. ^ Quintero E (October 2009). "[Chemical or immunological tests for the detection of fecal occult blood in colorectal cancer screening?]". Gastroenterologia y Hepatologia (in Spanish). 32 (8): 565–576. doi:10.1016/j.gastrohep.2009.01.179. PMID 19577340.
  41. ^ Colorectal Cancer http://patients.gi.org/topics/colorectal-cancer
  42. ^ Young GP, Cole SR (March 2009). "Which fecal occult blood test is best to screen for colorectal cancer?". Nature Clinical Practice. Gastroenterology & Hepatology. 6 (3): 140–141. doi:10.1038/ncpgasthep1358. PMID 19174764. S2CID 26481612.
  43. ^ Quintero E (October 2009). "[Chemical or immunological tests for the detection of fecal occult blood in colorectal cancer screening?]". Gastroenterologia y Hepatologia (in Spanish). 32 (8): 565–576. doi:10.1016/j.gastrohep.2009.01.179. PMID 19577340.
  44. ^ Berchi C, Bouvier V, Réaud JM, Launoy G (March 2004). "Cost-effectiveness analysis of two strategies for mass screening for colorectal cancer in France". Health Economics. 13 (3): 227–238. doi:10.1002/hec.819. PMID 14981648.
  45. ^ Kuriyama M, Kato J, Takemoto K, Hiraoka S, Okada H, Yamamoto K (March 2010). "Prediction of flare-ups of ulcerative colitis using quantitative immunochemical fecal occult blood test". World Journal of Gastroenterology. 16 (9): 1110–1114. doi:10.3748/wjg.v16.i9.1110. PMC 2835788. PMID 20205282.
  46. ^ Span P (2021-01-11). "A Colonoscopy Alternative Comes Home". The New York Times. ISSN 0362-4331. Retrieved 2021-01-12.
  47. ^ Rockey DC (July 1999). "Occult gastrointestinal bleeding". The New England Journal of Medicine. 341 (1): 38–46. doi:10.1056/NEJM199907013410107. PMID 10387941.
  48. ^ "Diagnostic Tests — Fecal Occult Blood Test". Archived from the original on 2007-07-07. Retrieved 2007-07-18.
  49. ^ "Fecal Occult Blood Test (FOBT)". WebMD. Retrieved 2007-07-18.
  50. ^ Sheng JQ, Li SR, Wu ZT, Xia CH, Wu X, Chen J, Rao J (August 2009). "Transferrin dipstick as a potential novel test for colon cancer screening: a comparative study with immuno fecal occult blood test". Cancer Epidemiology, Biomarkers & Prevention. 18 (8): 2182–2185. doi:10.1158/1055-9965.EPI-09-0309. PMID 19661074.
  51. ^ Sheng JQ, Li SR, Su H, Li JS, Sun ZQ, Wu ZT, et al. (June 2010). "Fecal cytology in conjunction with immunofecal occult blood test for colorectal cancer screening". Analytical and Quantitative Cytology and Histology. 32 (3): 131–135. PMID 20701065.
  52. ^ Ahlquist DA, McGill DB, Schwartz S, Taylor WF, Owen RA (May 1985). "Fecal blood levels in health and disease. A study using HemoQuant". The New England Journal of Medicine. 312 (22): 1422–1428. doi:10.1056/NEJM198505303122204. PMID 3873009.
  53. ^ Dybdahl JH, Daae LN, Larsen S (1981). "Occult faecal blood loss determined by chemical tests and a 51 Cr method". Scandinavian Journal of Gastroenterology. 16 (2): 245–252. doi:10.3109/00365528109181963. PMID 7313535.
  54. ^ St John DJ, Young GP (April 1978). "Evaluation of radiochromium blood loss studies in unexplained iron-deficiency anaemia". Australian and New Zealand Journal of Medicine. 8 (2): 121–126. doi:10.1111/j.1445-5994.1978.tb04496.x. PMID 307949.
  55. ^ Schiff L, Stevens RJ, Shapiro N, et al. Observations on the oral administration of citrate blood in man. Am J Med Sci 1942; 203: 409.
  56. ^ "What Does a Positive Fecal Occult Blood Test Mean? – B01". Retrieved 2007-07-18.
  57. ^ van Rossum LG, van Rijn AF, van Oijen MG, Fockens P, Laheij RJ, Verbeek AL, et al. (August 2009). "False negative fecal occult blood tests due to delayed sample return in colorectal cancer screening". International Journal of Cancer. 125 (4): 746–750. doi:10.1002/ijc.24458. PMID 19408302.
  58. ^ Nieuwenburg SA, Vuik FE, Kruip MJ, Kuipers EJ, Spaander MC (May 2019). "Effect of anticoagulants and NSAIDs on accuracy of faecal immunochemical tests (FITs) in colorectal cancer screening: a systematic review and meta-analysis". Gut. 68 (5): 866–872. doi:10.1136/gutjnl-2018-316344. PMID 29871970. S2CID 46949140.
  59. ^ "Screening average risk patients for colorectal cancer – B01". Retrieved 2007-10-25.
  60. ^ Harewood GC, McConnell JP, Harrington JJ, Mahoney DW, Ahlquist DA (January 2002). "Detection of occult upper gastrointestinal tract bleeding: performance differences in fecal occult blood tests". Mayo Clinic Proceedings. 77 (1): 23–28. doi:10.4065/77.1.23. PMID 11794453.
  61. ^ "Test ID: HQ HemoQuant, Feces". Mayo Clinic: Mayo Clinical Laboratories.
  62. ^ Schwartz S, Dahl J, Ellefson M, Ahlquist D (December 1983). "The "HemoQuant" test: a specific and quantitative determination of heme (hemoglobin) in feces and other materials". Clinical Chemistry. 29 (12): 2061–2067. doi:10.1093/clinchem/29.12.2061. PMID 6640900.
  63. ^ Whitlock EP, Lin J, Liles E, Beil T, Fu R, O'Connor E, Thompson RN, Cardenas T (2008). "Screening for Colorectal Cancer: An Updated Systematic Review". Agency for Healthcare Research and Quality. PMID 20722162. Report No.: 08-05-05124-EF-1.
  64. ^ Adams BD, McHugh KJ, Bryson SA, Dabulewicz J (February 2008). "The law of unintended consequences: The Joint Commission regulations and the digital rectal examination". Annals of Emergency Medicine. 51 (2): 197–201, 201.e1. doi:10.1016/j.annemergmed.2007.07.022. PMID 17961818.
  65. ^ Cleveland NJ, Yaron M, Ginde AA (August 2010). "The effect of removal of point-of-care fecal occult blood testing on performance of digital rectal examinations in the emergency department". Annals of Emergency Medicine. 56 (2): 135–141. doi:10.1016/j.annemergmed.2009.12.021. PMID 20060198.

External links[edit]