Gastrointestinal Tract Bleeding: DR Stefanus Nangoi, M.Biomed, SPB
Gastrointestinal Tract Bleeding: DR Stefanus Nangoi, M.Biomed, SPB
Gastrointestinal Tract Bleeding: DR Stefanus Nangoi, M.Biomed, SPB
BLEEDING
dr Stefanus Nangoi, M.Biomed, SpB.
Epidemiology
•Upper GI bleeding:
• Perdarahan di proximal lig Treitz
• Lebih sering dibanding Lower GI bleeding
• incidence 149-172/100,000. per tahun
• Terutama pada pria dan usia lanjut
• 50% of upper GI bleeds are due to erosive or
ulcerative disease of the stomach or duodenum.
• The mortality 5% to 11%.
• Faktor yg mempengaruhi mortality rate in upper GI bleeding :
• Age > 60.
• Co morbid diseases especially pulmonary and hepatic diseases.
• Physical findings consistent with cardiorespiratory or
hemodynamic compromise.
• Blood transfusion requirement greater than 5 units.
• Requirement for surgery (patients requiring emergency surgery
had increased mortality compared with those undergoing more
elective surgery).
• Recurrent bleeding after hospitalization.
• Those who develop GI bleeding after hospitalization for other
reasons.
Epidemiology
• lower GI bleeding:
• Is defined as bleeding distal to the ligament of Treitz. It can
range in severity from trivial to massive.
• LGIB accounts for approximately 20% of all major GI bleeds.
• More commonly bleeding is from a colonic rather than a
small bowel source.
• Annual incidence 21 cases per 100,000.
• Increased in males and in older patients (mean age at
presentation of 63 to 77 years).
• 80-90% of cases will stop bleeding spontaneously.
• As many as 25% will re-bleed either during or after their
hospital admission.
• While most patients have a self-limited illness, the
reported mortality ranges from 2-4%.
• Among all patients presenting with lower GI bleeding,
diverticular disease is the most common cause, followed
by, vascular anomaliesor ischemic colitis.
Etiology- Upper GI bleeding
• Mallory-Weiss tear:
• A mucosal laceration of the gastric cardia or gastroesophageal junction.
• Account for approximately 5% to 15% of all cases of upper GI bleeding and
are relatively common in alcoholics.
• The classic presentation is that of repeated retching, vomiting or coughing
followed by hematemesis .
• Up to 50% of patients do not give a history of antecedent retching or
vomiting.
• Esophageal/gastric varices.
• The incidence of bleeding is approximately 10% to 15% per year, and in patients
with large varices is 20% to 30%.
• Bleeding due to varices is typically brisk and associated with hemodynamic
compromise.
• The mortality associated with the first variceal bleed ranges from 30% to 50%.
• Treatment :
• Endoscopic sclerotherapy and band ligation of varices are the mainstay of emergent therapy.
• medical therapy for variceal hemorrhage has been extensively studied, the benefit of such
vasopressin , More recently
therapy remains uncertain (
somatostatin and the somatostatin analogue,
octreotide)
• The Senkstaken-Blakemore tube remains an important therapeutic tool in patients with brisk
esophageal or gastric variceal hemorrhage that cannot be controlled on initial endoscopy.
• Patients who continue to bleed or who have more than one rebleeding episode despite
endoscopic and medical therapy should be considered for portal decompression.
Etiology- Upper GI bleeding
• Neoplasm
• Gastric cancer
• Esophageal cancer
• Stromal tumor
Etiology- Upper GI bleeding
• Vascular anomalies
• An unusual cause of upper GI bleeding, accounting for only 5% of cases..
• Angiodysplasia, whether sporadic or secondary, is the most common vascular anomaly seen
in the GI tract.
• Angiodysplasia/ectasia
• Dieulafoy lesion
• Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu)
• Arteriovenous malformation
Etiology- Upper GI bleeding
• Anorectal causes :
• Include hemorrhoids -anal fissure and rectal ulcer.
• Bleeding from hemorrhoids and fissure is uncommonly associated with
hemodynamic instability or large volume of blood loss.
• While rectal ulcer can cause severe hemorrhage and hemodynamic instability
• Diverticular disease:
• Contributes 20-60% of the cases of LGIB.
• In 75% of patients bleeding will stop spontaneously.
• Rebleeding rate after first episode 25% and increase to 50% after two
episodes.
• 5% will have severe hemorrhage .
• diverticular bleeding is distributed equally between the right and left sides
of the colon.
• Observation alone is generally recommended following the first episode of
diverticular hemorrhage. However, following a second episode, the risk of
subsequent episodes appears to approximate 50%, and thus elective
resection has been recommended .
Etiology- lower GI bleeding
• Angiodysplasia:
• Only about 15% of patients with vascular ectasia will develop gastrointestinal
hemorrhage.
• The incidence in most recent studies is only 3% compared to 15-27%
previously as cause of LGIB.
• Colorectal neoplasm
• Although colorectal cancer is most commonly associated with occult blood
loss rather than overt bleeding, patients with rectosigmoid lesions may
present with hematochezia .
• CR-cancers are source of LGIB in 9-13% of patients.
Etiology- lower GI bleeding
• Ischemic colitis
• Patients tend to be elderly, often with significant atherosclerosis or cardiac
disease.
• Other colonic etiologies:
• Inflammatory bowel disease:
• Acute hemorrhage occurs 0.9-6% in CD and 1.4-4% in UC.
• Bleeding occurred in both young and old patients and not related to
disease duration.
• Malignant lesion must be considered in patient with long standing history
of IBD and LGIB.
• Infectious colitis or enteritis :
• Radiation colitis/proctitis.
• Trauma, hematologic disorders and NSAIDs.
• Post polypectomy (occurs in 0.3% to 6.1% of polypectomies).
• Bleeding from CR-anastomosis (o.5-1.8%).
Etiology- lower GI bleeding
• Meckel’s diverticula,
• neoplasia,
• Crohn’s disease,
• aorto-enteric fistulas .
Obscure Gastrointestinal Bleeding
• During the initial stabilization and evaluation, a complete history and physical should be performed .
• History :
• Physical examination
• Orthostatic blood pressure and pulse even if the patient appears stable.
• cutaneous stigmata of liver disease
• splenomegaly or ascites, abdominal tenderness, an abdominal mass or lymphadenopathy
• cutaneous or mucocutaneous manifestations of systemic disorders associated with GI
bleeding
• ENT EXAMINATION,RECTAL EXAMINATION.
MANAGEMENT OF GI BLEEDING
• Diagnostic studies:
• Upper GI endoscopy:
• the preferred diagnostic modality in patients with upper GI bleeding
• advantages of endoscopy include:
• the ability to obtain biopsies for an accurate histologic diagnosis,
• Determine the risk of rebleeding .
• Provide endoscopic therapy.
• Patients with severe upper GI bleeding should have an upper endoscopy, or
esophagogastroduodenoscopy (EGD), performed as soon as they are stable.
• Patients in whom endoscopy cannot be performed due to torrential bleeding should be
considered for laparotomy, with or without prior mesenteric angiography
MANAGEMENT OF GI BLEEDING
• Angiography:
• bleeding rate of 0.5 mL/min is necessary in order for angiography to be positive
• helpful in the patient with massive GI bleeding from either an upper or lower source
• reveals a bleeding site in up to 75% of patients with massive upper GI bleeding
• success rate in LGIB 60-90% rebleeding rate 0-33% and significant ischemia 7%
MANAGEMENT OF GI BLEEDING
• Radionuclide scanning :
• Red blood cells obtained by venipuncture are labeled with technetium 99m (99mTc) and
reinjected into the patient.
• red blood cell scans detect lower rates of bleeding (0.1cc/min)
• Since prolonged or repeated scanning is possible, bleeding can be detected even if it is
intermittent or too slow to be detected on angiography.
• If the red blood cell scan is negative, the angiogram is very unlikely to demonstrate active
bleeding
• Helpful in some patients with recurrent lower GI bleeding in whom all other diagnostic
studies are negative.
• is particularly helpful in the setting of bleeding from a Meckel’s diverticulum
• Multidetector row CT:
• Blood flow can be detected at the rate of 0.3 ml\min
• Considered positive when vascular contrast material is extravasated into bowel lumen.