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GIT Bleeding
Prepared by:
Zana Hossam
Learning objectives
• To realize the importance of GI bleeding in clinical practice
• To define the different manifestations of GIB
• To identify the causes of GIB
• To be able to risk stratify cases of GIB
• To be able to manage cases of GIB
GIT bleeding
• GI bleeding is the most common gastrointestinal emergency
• Sites:
– 50% of admissions for GI bleeding are for upper GIB (UGIB; from
esophagus, stomach, duodenum).
– 40% are for lower GI (LGIB; from the colon and anorectum).
– 10% are for obscure bleeding.
Classified into:
– Upper GI bleeding (proximal ligament of Treitz)
– Lower GI bleeding (distal to ligament of Treitz)
• Upper GI bleeding 4x more common than lower GI
bleeding and is a major cause of morbidity and mortality.
GI Bleeding
Upper GIT Bleeding
Upper GIT Bleeding
• Upper gastrointestinal bleeding is defined as bleeding derived
from a source proximal to the ligament of Treitz.
• Upper GI bleed remains a major medical problem.
• About 75% of patient presenting to the emergency room with
GI bleeding have an upper source.
• Bleeding is self-limited in 80% of patients with UGI
hemorrhage, even without specific therapy.
• In-hospital mortality of 5-10% can be expected.
Causes of Upper GIT Bleeding
Clinical presentation
• Haematemesis
• Melaena
• Hematochezia
• Haematemesis without melaena
• Melaena without haematomesis
• Epigastric pain or diffuse abdominal pain
• Weakness ,Dizziness , Syncope or Presyncope .
• Dyspepsia
• Dysphagia
• Jaundice
• Weight loss
Clinical presentation
History
Important information to obtain includes potential comorbid
conditions, medication history, and potential toxic exposures, as well
as the severity, timing, duration, and volume of the bleeding.
Physical Examination
The goal of the patient's physical examination is to evaluate for
shock and blood loss & assessing the patient for hemodynamic
instability and clinical signs of poor perfusion
Severe GIT Bleeding
Is defined as GIT bleeding accompanied by shock or
orthostatic hypotension & a decrease in the hematocrit
value by at least 6% or a decrease in Hb of at least 2 g/dL
or transfusion of at least two units of packed RBC.
Risk Stratification
• Risk scoring systems have been developed to stratify risk
of mortality, rebleeding or need for endoscopic therapy .
• In general, all these scoring systems are better at
determining mortality than rebleeding.
• Blatchford Score
• Rockall Scoring System
13
Variable Score 0 Score 1 Score 2 Score 3 Score
Calculate on admission
Age < 60 60-79 > 80
Shock No shock Pulse > 100 , SBP >100 SBP < 100
Comorbidity Nil major CHF, IHD, major comorbidity Renal/liver
failure
Metastatic cancer
Calculate after endoscopy
Diagnosis Mallory-Weiss tear or
normal
All other diagnoses GI malignancy1
Evidence of
bleeding
None Blood in stomach Adherent clot
Visible or
spurting vessel
Rockall score Final score (range 0-11)
Management
1. start by protecting the airway and giving high-flow O2
2. Intravenous access
Insert at least one large-bore cannula (14- or 16-gauge). Two if ongoing bleeding
3. Initial clinical assessment by history & physical examination.
Management cont…
3. Basic investigations
– Full blood count.
– Urea & Electrolyte
– Liver function tests
– Prothrombin time & INR
– Cross-matching
4. Prepare blood (2-8 units of packed RBC according to the
severity of bleeding).
Management cont…
5. Resuscitation
– Give 1-2 liters of normal saline as fast as possible to keep SBP > 100
mmHg and PR <100 BPM.
– Give packed RBC if the patient remains unstable after 2 L of crystalloids.
Also give packed RBC to keep Hb 7-9 g/dl (> 9 g/dl if acute coronary
syndrome or Child Pugh class-C cirrhosis or symptoms attributable to
anemia).
– Transfuse platelets & fresh frozen plasma to keep platelet > 50,000/mm3
& PT < 15 Sec, respectively
– Comorbidities should be managed as appropriate.
– Consult surgeon in cases of massive bleeding that cannot be medically
resuscitated.
6. Monitoring
• Patients should be closely observed, with hourly
measurements of pulse, blood pressure
• Insert a urinary catheter and monitor hourly urine output
• CVP monitoring is useful in sever bleeding particularly in
patient with cardiac disease and to guide fluid
replacement & identification of rebleeding
Management cont…
7. Endoscopy
– It should be done after adequate resuscitation, ideally within 24
hours, and will yield a diagnosis in 80% of cases.
– Patients with major endoscopic stigmata of haemorrhage can
be treated endoscopically using a thermal or mechanical
modality, combined with adrenaline injection (Dual therapy).
– This may stop active bleeding and combined with intravenous
proton pump inhibitor (PPI) therapy (infusion for 72 hours),
prevent rebleeding, thus avoiding the need for surgery
(mortality is not reduced significantly).
8. Surgery
– Surgery is indicated when endoscopic hemostasis fails to stop
active bleeding and if rebleeding occurs on one occasion in an
elderly or frail patient, or twice in a younger, fitter patient.
– If available, angiographic embolization is an effective
alternative to surgery in frail patients.
Management cont…
9. Prevention of recurrent ulcer bleeding:
– All patients should be tested for H. pylori and treated with H. pylori
eradication therapy if they test positive,
– Successful eradication should be confirmed by urea breath or faecal
antigen testing
– They should avoid NSAIDs.
– Repeated OGD in gastric ulcer after 6-10 weeks of PPI to confirm
healing & exclude malignancy
Post-care
1. In patients who underwent endoscopic therapy: absolute
bed rest for 24 hours, start oral intake after 6 hours.
2. Monitor for features of rebleeding
3. Consult endoscopist for rebleeding.
4. Test for H. pylori and eradicate if positive testing. Confirm
eradication.
5. Revise NSAID use.
6. Give long term maintenance acid suppression for 2-5
years in high risk patients.
Use of IV PPI
• Intravenous PPI given to patients subjected to endoscopic
therapy for major peptic ulcer hemorrhage reduce rebleeding
and need for surgery, but not mortality.
• When PPI are given prior to endoscopy, they reduce the need
for endoscopic therapy and hospital stay, but not the need for
surgery or mortality.
Lower GITBleeding
• Lower GI bleed refers to bleeding arising distal to the
ligament of Treitz
• Although this includes jejunum and ileum but bleeding
from these sites is rare (<5%)
• Vast majority of lower GI bleeding arises from
colon/rectum/anus
Lower GI bleeding
Causes of lower gastrointestinal bleeding
Severe acute
• Diverticular disease
• Angiodysplasia
• Ischaemia
• Meckel's diverticulum
• Inflammatory bowel disease
Moderate, chronic/subacute
• Anal disease e.g. fissure,
haemorrhoids
• Inflammatory bowel disease
• Carcinoma
• Large polyps
• Angiodysplasia
• Radiation enteritis
• Solitary rectal ulcer
Signs and symptoms
• The clinical presentation of Lower GIT Bleeding varies with
the anatomical source of the bleeding, as follows:
• Maroon stools, with LGIB from the right side of the colon
• Bright red blood per rectum with LGIB from the left side of the
colon
• Melena with cecal bleeding
• In practice, however, patients with upper GI bleeding and
right-sided colonic bleeding may also present with bright red
blood per rectum if the bleeding is brisk and massive.
Obscure GIT Bleeding
• Obscure is commonly defined as GIB of uncertain cause after a non-
diagnostic upper endoscopy, colonoscopy, and small bowel barium
follow through.
• Overt obscure GIB: patient has visible GIB (e.g., melena, maroon stool,
hematochezia)
• Occult obscure GIB patients has positive fecal occult blood test (FOBT)
or unexplained iron deficiency anemia (IDA).
Major GIB of unknown cause
• In some patients with major GIB, upper endoscopy and colonoscopy
fail to reveal a diagnosis.
1.When severe life-threatening bleeding continues, urgent CT mesenteric
angiography is indicated.
2.If angiography is negative or bleeding is less severe, push or double
balloon enteroscopy can visualize the small intestine and treat the
bleeding source.
3. Wireless capsule endoscopy is often used to define a source of
bleeding prior to enteroscopy.
4.When all else fails, laparotomy with on-table endoscopy is indicated.
Chronic occult GIT Bleeding
• Occult means that blood or its breakdown products are present in the
stool but cannot be seen by the naked eye.
• Occult bleeding may reach 200 mL per day and cause iron deficiency
anemia.
• Any cause of GIB may be responsible but the most important is
colorectal cancer, particularly carcinoma of the caecum, which may
produce no gastrointestinal symptoms.
• Many colorectal cancer patients are FOBT-negative at presentation,
and the only value of FOB testing is as a means of screening for
colonic disease in asymptomatic populations
Differentiation of UGIB from LGIB
1. Hematemesis indicates UGIB.
2. Melena indicates presence of blood in GIT for at least 14 h. It generally
indicates UGIB but Small Intestine or proximal colonic GIB.
3. Hematochezia indicates LGIB or brisk UGIB (hemodynamic instability).
4. Small bowel bleeding present with melena or hematochezia
5. Other clues to UGIB are hyperactive bowel sounds and an elevated blood
urea nitrogen
6. Non-bloody nasogastric aspirate occur in 18% of UGIB.
7. Even a bile-stained aspirate does not exclude a bleeding post-pyloric lesion
because reports of bile in the aspirate are incorrect in -50% of cases.
8. Testing of aspirates that are not grossly bloody for occult blood is not useful
References
• Davidson's Principles and Practice of Medicine 21st Ed
• GIT Bleeding PDF prepared By Dr. Ali A. Ramadhan
• www.medscape.com
Git bleeding 2

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Git bleeding 2

  • 2. Learning objectives • To realize the importance of GI bleeding in clinical practice • To define the different manifestations of GIB • To identify the causes of GIB • To be able to risk stratify cases of GIB • To be able to manage cases of GIB
  • 3. GIT bleeding • GI bleeding is the most common gastrointestinal emergency • Sites: – 50% of admissions for GI bleeding are for upper GIB (UGIB; from esophagus, stomach, duodenum). – 40% are for lower GI (LGIB; from the colon and anorectum). – 10% are for obscure bleeding.
  • 4. Classified into: – Upper GI bleeding (proximal ligament of Treitz) – Lower GI bleeding (distal to ligament of Treitz) • Upper GI bleeding 4x more common than lower GI bleeding and is a major cause of morbidity and mortality. GI Bleeding
  • 5.
  • 7. Upper GIT Bleeding • Upper gastrointestinal bleeding is defined as bleeding derived from a source proximal to the ligament of Treitz. • Upper GI bleed remains a major medical problem. • About 75% of patient presenting to the emergency room with GI bleeding have an upper source. • Bleeding is self-limited in 80% of patients with UGI hemorrhage, even without specific therapy. • In-hospital mortality of 5-10% can be expected.
  • 8. Causes of Upper GIT Bleeding
  • 9. Clinical presentation • Haematemesis • Melaena • Hematochezia • Haematemesis without melaena • Melaena without haematomesis • Epigastric pain or diffuse abdominal pain • Weakness ,Dizziness , Syncope or Presyncope . • Dyspepsia • Dysphagia • Jaundice • Weight loss
  • 10. Clinical presentation History Important information to obtain includes potential comorbid conditions, medication history, and potential toxic exposures, as well as the severity, timing, duration, and volume of the bleeding. Physical Examination The goal of the patient's physical examination is to evaluate for shock and blood loss & assessing the patient for hemodynamic instability and clinical signs of poor perfusion
  • 11. Severe GIT Bleeding Is defined as GIT bleeding accompanied by shock or orthostatic hypotension & a decrease in the hematocrit value by at least 6% or a decrease in Hb of at least 2 g/dL or transfusion of at least two units of packed RBC.
  • 12. Risk Stratification • Risk scoring systems have been developed to stratify risk of mortality, rebleeding or need for endoscopic therapy . • In general, all these scoring systems are better at determining mortality than rebleeding. • Blatchford Score • Rockall Scoring System
  • 13. 13
  • 14. Variable Score 0 Score 1 Score 2 Score 3 Score Calculate on admission Age < 60 60-79 > 80 Shock No shock Pulse > 100 , SBP >100 SBP < 100 Comorbidity Nil major CHF, IHD, major comorbidity Renal/liver failure Metastatic cancer Calculate after endoscopy Diagnosis Mallory-Weiss tear or normal All other diagnoses GI malignancy1 Evidence of bleeding None Blood in stomach Adherent clot Visible or spurting vessel Rockall score Final score (range 0-11)
  • 15. Management 1. start by protecting the airway and giving high-flow O2 2. Intravenous access Insert at least one large-bore cannula (14- or 16-gauge). Two if ongoing bleeding 3. Initial clinical assessment by history & physical examination.
  • 16. Management cont… 3. Basic investigations – Full blood count. – Urea & Electrolyte – Liver function tests – Prothrombin time & INR – Cross-matching 4. Prepare blood (2-8 units of packed RBC according to the severity of bleeding).
  • 17. Management cont… 5. Resuscitation – Give 1-2 liters of normal saline as fast as possible to keep SBP > 100 mmHg and PR <100 BPM. – Give packed RBC if the patient remains unstable after 2 L of crystalloids. Also give packed RBC to keep Hb 7-9 g/dl (> 9 g/dl if acute coronary syndrome or Child Pugh class-C cirrhosis or symptoms attributable to anemia). – Transfuse platelets & fresh frozen plasma to keep platelet > 50,000/mm3 & PT < 15 Sec, respectively – Comorbidities should be managed as appropriate. – Consult surgeon in cases of massive bleeding that cannot be medically resuscitated.
  • 18. 6. Monitoring • Patients should be closely observed, with hourly measurements of pulse, blood pressure • Insert a urinary catheter and monitor hourly urine output • CVP monitoring is useful in sever bleeding particularly in patient with cardiac disease and to guide fluid replacement & identification of rebleeding
  • 19. Management cont… 7. Endoscopy – It should be done after adequate resuscitation, ideally within 24 hours, and will yield a diagnosis in 80% of cases. – Patients with major endoscopic stigmata of haemorrhage can be treated endoscopically using a thermal or mechanical modality, combined with adrenaline injection (Dual therapy). – This may stop active bleeding and combined with intravenous proton pump inhibitor (PPI) therapy (infusion for 72 hours), prevent rebleeding, thus avoiding the need for surgery (mortality is not reduced significantly).
  • 20. 8. Surgery – Surgery is indicated when endoscopic hemostasis fails to stop active bleeding and if rebleeding occurs on one occasion in an elderly or frail patient, or twice in a younger, fitter patient. – If available, angiographic embolization is an effective alternative to surgery in frail patients.
  • 21. Management cont… 9. Prevention of recurrent ulcer bleeding: – All patients should be tested for H. pylori and treated with H. pylori eradication therapy if they test positive, – Successful eradication should be confirmed by urea breath or faecal antigen testing – They should avoid NSAIDs. – Repeated OGD in gastric ulcer after 6-10 weeks of PPI to confirm healing & exclude malignancy
  • 22.
  • 23.
  • 24. Post-care 1. In patients who underwent endoscopic therapy: absolute bed rest for 24 hours, start oral intake after 6 hours. 2. Monitor for features of rebleeding 3. Consult endoscopist for rebleeding. 4. Test for H. pylori and eradicate if positive testing. Confirm eradication. 5. Revise NSAID use. 6. Give long term maintenance acid suppression for 2-5 years in high risk patients.
  • 25. Use of IV PPI • Intravenous PPI given to patients subjected to endoscopic therapy for major peptic ulcer hemorrhage reduce rebleeding and need for surgery, but not mortality. • When PPI are given prior to endoscopy, they reduce the need for endoscopic therapy and hospital stay, but not the need for surgery or mortality.
  • 27. • Lower GI bleed refers to bleeding arising distal to the ligament of Treitz • Although this includes jejunum and ileum but bleeding from these sites is rare (<5%) • Vast majority of lower GI bleeding arises from colon/rectum/anus Lower GI bleeding
  • 28. Causes of lower gastrointestinal bleeding Severe acute • Diverticular disease • Angiodysplasia • Ischaemia • Meckel's diverticulum • Inflammatory bowel disease Moderate, chronic/subacute • Anal disease e.g. fissure, haemorrhoids • Inflammatory bowel disease • Carcinoma • Large polyps • Angiodysplasia • Radiation enteritis • Solitary rectal ulcer
  • 29. Signs and symptoms • The clinical presentation of Lower GIT Bleeding varies with the anatomical source of the bleeding, as follows: • Maroon stools, with LGIB from the right side of the colon • Bright red blood per rectum with LGIB from the left side of the colon • Melena with cecal bleeding • In practice, however, patients with upper GI bleeding and right-sided colonic bleeding may also present with bright red blood per rectum if the bleeding is brisk and massive.
  • 30. Obscure GIT Bleeding • Obscure is commonly defined as GIB of uncertain cause after a non- diagnostic upper endoscopy, colonoscopy, and small bowel barium follow through. • Overt obscure GIB: patient has visible GIB (e.g., melena, maroon stool, hematochezia) • Occult obscure GIB patients has positive fecal occult blood test (FOBT) or unexplained iron deficiency anemia (IDA).
  • 31. Major GIB of unknown cause • In some patients with major GIB, upper endoscopy and colonoscopy fail to reveal a diagnosis. 1.When severe life-threatening bleeding continues, urgent CT mesenteric angiography is indicated. 2.If angiography is negative or bleeding is less severe, push or double balloon enteroscopy can visualize the small intestine and treat the bleeding source. 3. Wireless capsule endoscopy is often used to define a source of bleeding prior to enteroscopy. 4.When all else fails, laparotomy with on-table endoscopy is indicated.
  • 32. Chronic occult GIT Bleeding • Occult means that blood or its breakdown products are present in the stool but cannot be seen by the naked eye. • Occult bleeding may reach 200 mL per day and cause iron deficiency anemia. • Any cause of GIB may be responsible but the most important is colorectal cancer, particularly carcinoma of the caecum, which may produce no gastrointestinal symptoms. • Many colorectal cancer patients are FOBT-negative at presentation, and the only value of FOB testing is as a means of screening for colonic disease in asymptomatic populations
  • 33.
  • 34. Differentiation of UGIB from LGIB 1. Hematemesis indicates UGIB. 2. Melena indicates presence of blood in GIT for at least 14 h. It generally indicates UGIB but Small Intestine or proximal colonic GIB. 3. Hematochezia indicates LGIB or brisk UGIB (hemodynamic instability). 4. Small bowel bleeding present with melena or hematochezia 5. Other clues to UGIB are hyperactive bowel sounds and an elevated blood urea nitrogen 6. Non-bloody nasogastric aspirate occur in 18% of UGIB. 7. Even a bile-stained aspirate does not exclude a bleeding post-pyloric lesion because reports of bile in the aspirate are incorrect in -50% of cases. 8. Testing of aspirates that are not grossly bloody for occult blood is not useful
  • 35. References • Davidson's Principles and Practice of Medicine 21st Ed • GIT Bleeding PDF prepared By Dr. Ali A. Ramadhan • www.medscape.com

Editor's Notes

  1. a band of smooth muscle extending from the junction of the duodenum and jejunum to the rt crus of the diaphragm and functioning as a suspensory ligament
  2. Oesophagus -Oesophageal varices -Oesophageal CA -Reflux oesophagitis -Mallory-Weiss syndrome Stomach -Gastric ulcer Erosive gastritis -Gastric CA -gastric lymphoma -gastric leiomyoma -Dielafoy’s syndrome Duodenum -Duodenal ulcer -Duodenitis -Periampullary tumour -Aorto-duodenal fistula General Haemophilia -Leukemia -Thrombocytopenia -Anti-coagulant therapy
  3. Hematemesis: vomiting of blood, which is indicative of upper GI bleeding. It includes vomiting of bright red blood or dark material (coffee-ground emesis). Melena: black tarry foul-smelling stool and results from degradation of blood to hematin or other hemochromes by intestinal bacteria and digestive enzymes giving the stool characteristic color and smell. It generally occurs when 50 to 100 mL or more of blood is delivered into the GIT. Hematochezia: bright red blood per rectum, and suggests distal colonic or anorectal bleeding or active UGI or small bowel bleeding.
  4. http://emedicine.medscape.com/article/187857-clinical#b1
  5. The advantage of the Blatchford score is that it may be used before endoscopy to predict the need for intervention to treat bleeding.
  6. Low scores (2 or less) are associated with a very low risk of adverse outcome. These patients may be discharged early Score 6 or more need intervention . Such blood transfusion or endoscopic intervension
  7. Score less than 3 have good prognosis , more than 8 have high mortality rate
  8. Define circulatory status. Severe bleeding causes tachycardia, hypotension and oliguria. The patient is cold, sweating & may be agitated. There may be syncope. Symptoms of anemia suggest chronic bleeding. Orthostatic hypotension: drop in SBP ≥20 mmHg or DBP ≥10 mm Hg on assuming standing position B. Seek evidence of liver disease Jaundice, cutaneous stigmata, hepatosplenomegaly and ascites may be present in decompensated cirrhosis C. Identify comorbidity: The presence of cardiorespiratory, cerebrovascular or renal disease is important (worsened by acute bleeding and they increase the hazards of endoscopy & surgery) These factors can be combined using the Rockall scoring system to predict severity A score < 3 is associated with a good prognosis while a total score > 8 carries a high risk of mortality.
  9. Chronic or subacute bleeding leads to anaemia Haemoglobin concentration may be normal after sudden, major bleeding until haemodilution occurs. Thrombocytopenia may indicate hypersplenism in cirrhosis It may show renal failure. Blood urea rises as the absorbed products of luminal blood are metabolized by the liver. Elevated blood urea with normal creatinine concentration implies severe bleeding. : may show evidence of CLD. Check with clinical suggestion of liver disease or in anticoagulated patients.
  10. Patients with suspected chronic liver disease should receive broad-spectrum antibiotics. IV Ciprofloxacin 400 bid IV levofloxacin 500mg /day for 7 day
  11. Management Treatment includes the following: Secure the airway Insert bilateral, 16-gauge (minimum), upper extremity, peripheral intravenous lines Replace each milliliter of blood loss with 3 mL of crystalloid fluid In patients with severe coexisting medical illnesses, pulmonary artery catheter insertion for monitoring hemodynamic cardiac performance Foley catheter placement for continuous evaluation of urinary output as a guide to renal perfusion Endoscopic hemostatic therapy for bleeding ulcers and varices Surgical repair of perforated viscus For high-risk peptic ulcer patients, high-dose intravenous proton pump inhibitors Indications for surgery in patients with bleeding peptic ulcers include the following: Severe, life-threatening hemorrhage not responsive to resuscitative efforts Failure of medical therapy and endoscopic hemostasis with persistent recurrent bleeding A coexisting reason for surgery (eg, perforation, obstruction, malignancy) Prolonged bleeding, with loss of 50% or more of the patient's blood volume A second hospitalization for peptic ulcer hemorrhage
  12. This may stop active bleeding and, combined with intravenous proton pump inhibitor (PPI) therapy (infusion for 72 hours), prevent rebleeding, thus avoiding the need for surgery (mortality is not reduced significantly). Patients found to have varices should be treated by band ligation
  13. Prokinetic (benzamide, metoclopramid, erythromycin) octreotide ( sandostatin)
  14. Non bleeeding visible vessels
  15. Features of re-bleeding: • Hematemesis or bloody NG aspirate > 6 hours after endoscopy • Melena or hematochezia after normalization of stool color • PR ≥110 BPM or SBP ≤90mmHg after at least one hour of hemodynamic stability in the absence of an alternative explanation • Hemoglobin drop of ≥2 g/dL over 24 hours • Tachycardia or hypotension that does not resolve within 8 hours after index endoscopy despite resuscitation (in the absence of an alternative explanation).
  16. An older patient with diverticular bleeding or angiodysplasia may present with painless bleeding and minimal symptoms. Ischemic colitis, abdominal pain, and varying degrees of bleeding are usually observed in patients with multiple comorbidities such as congestive heart failure (CHF), atrial fibrillation, or chronic renal failure (CRF). LGIB can be mild and intermittent, as often is the case of angiodysplasia and colon carcinoma, or moderate or severe, as may be the situation in diverticula-related bleeding. Colon carcinoma rarely causes significant LGIB.
  17. Investigations for obscure GIB: Repeat upper endoscopy or colonoscopy according to suspicion and clinical presentation. Video capsule endoscopy Enteroscopy Angiography Laparotomy & Intraoperative endoscopy
  18. 1-This will usually identify the site if the bleeding rate exceeds 1 mL/min and then formal angiographic embolisation can often stop the bleeding.
  19. should not influence whether or not GIT is imaged because bleeding from tumors is often intermittent and a negative FOBT does not exclude malignancy In clinical practice Any pt with unexplained IDA U&L GIT should be investigated