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Fast Facts
A brief refresher with useful tables, figures, and research summaries
Gastrointestinal Bleeding
Gastrointestinal (GI) bleeding can present in several ways, with the presentation often providing clues about the location and etiology of the bleed. Common presentations and definitions are listed below.
Definition | Indication of upper or lower bleed? | Other details | |
---|---|---|---|
Hematemesis | Bloody emesis | Upper | Bright-red emesis indicates active bleeding. Coffee-ground emesis (due to the effect of gastric acid on blood) indicates a slower rate or resolved bleeding. |
Melena | Dark, tarry stools | Upper or lower | Due to oxidation of hemoglobin by intestinal bacteria. This requires time, so usually represents either an upper GI bleed or a bleed from the proximal colon. |
Hematochezia | Bright-red blood per rectum | Usually lower but also can indicate a brisk upper GI bleed | This presentation of upper GI bleed is more common in children due to shorter intestinal transit time. |
Causes of GI Bleeding
Although the etiologies of GI bleeding overlap among different age groups, some causes are more common in younger individuals, particularly neonates. The causes of GI bleeding are stratified by age group in the following tables.
Etiologies | Examples (a few of many) |
---|---|
Hemorrhagic disease of the newborn | Vitamin K deficiency |
Stress gastritis or gastric ulcers | Critical illness; can also occur spontaneously |
Congenital anomalies | Intestinal duplications, vascular anomalies |
Coagulopathy | Liver failure, congenital factor deficiencies, sepsis |
Swallowed maternal blood | During breastfeeding (from cracked nipples) |
Note: One of the most common causes of apparent hematemesis is swallowed maternal blood. Maternal blood can be distinguished from fetal blood by the Apt test performed on vomitus or stool. The test relies on the fact that fetal hemoglobin resists alkali denaturation. To perform the test, 1% sodium hydroxide is added to the supernatant of centrifuged sample of blood mixed with water. A positive test (sample turns yellow-brown) indicates the presence of maternal blood. In contrast, fetal hemoglobin resists the alkali denaturation and remains pinkish or red.
Etiologies | Details |
---|---|
Esophagitis | Examples include reflux, eosinophilic esophagitis, pill esophagitis, and caustic ingestion. |
Mallory-Weiss syndrome | An acute mucosal laceration (usually in the gastric cardia or GE junction) following forceful retching, vomiting, or coughing. |
Gastritis or ulcers | Possible etiologies include critical illness, NSAID use, Helicobacter pylori, CMV, and alcohol use. |
Variceal bleeding | Potential causes include cirrhosis, portal vein thrombosis, and Budd-Chiari syndrome. |
Foreign body | Foreign bodies rarely can cause ulceration, perforation, or may serve as a lead point for intussusception. |
Dieulafoy lesion | A submucosal artery that aberrantly protrudes through a defect in the mucosa. Most commonly found along the lesser curvature of the stomach, near the GE junction. |
Causes of Lower GI Bleeding in Neonates |
---|
Anal fissures |
Cow’s milk protein sensitivity |
Volvulus |
Necrotizing enterocolitis (NEC) |
Hirschsprung-associated enterocolitis |
Etiologies | Examples |
---|---|
Enteric infections | Salmonella, Shigella, Campylobacter, Escherichia coli O157:H7, Clostridium difficile, CMV (in immunocompromised state or IBD) |
Anal fissure | |
Juvenile polyps | |
Meckel diverticulum | |
Intussusception | |
Vasculitis | Henoch-Schönlein purpura (HSP) |
Rectal prolapse | |
Inflammatory bowel disease | Crohn disease, ulcerative colitis |
Vascular anomolies | Hereditary hemorrhagic telangiectasia, blue rubber bleb nevus syndrome |
Evaluation of GI Bleeding
Initial evaluation should focus on the identification of ill-appearing patients and subsequent stabilization, with fluid and blood product resuscitation taking precedence over the below diagnostic workup.
Guaiac test of stool or emesis can be performed to confirm the presence of blood. Mimickers of blood include food coloring, gelatin, sports drinks, red candy, beets, tomatoes, antibiotic syrups, iron, and licorice.
Physical exam: A targeted physical exam should be completed to identify clues about the etiology of the bleeding such as:
Head, eyes, ears, nose, and throat: scleral icterus, mucosal/lip pallor, trauma
cardiovascular: murmur, perfusion
abdominal: focal tenderness, ascites, hepatosplenomegaly
rectal: anal fissures, hemorrhoids, fistulae
skin: pallor, jaundice, vascular malformations
Basic laboratory workup should include complete blood count (CBC), blood urea nitrogen (BUN), creatinine, coagulation profile, liver transaminases, and type and cross. Other laboratory studies should be considered based on patient presentation (e.g., infectious stool studies if concern for infection, inflammatory markers if concern for inflammatory bowel disease).
Nasogastric (NG) lavage can be considered in situations of diagnostic uncertainty. The presence of blood in the lavage indicates an upper GI bleed (which could originate from the stomach or duodenum). Clearing of blood with lavage suggests that the bleeding has stopped.
Imaging: The following imaging modalities may be considered, depending on the patient’s presentation and symptoms.
abdominal x-ray: consider for suspicion of intestinal obstruction, pneumatosis intestinalis, or foreign body
ultrasound: for suspicion of intussusception or portal hypertension
Meckel scan: for suspicion of Meckel diverticulum
radioisotope-tagged red blood cell (RBC) scan: requires active bleeding; may be used for partial localization of an obscure bleed
angiography: requires active bleeding; may be used for brisk bleeds after other diagnostic modalities (e.g., endoscopy) have failed to identify a source; interventional angiography can offer therapy for patients who are poor surgical candidates or who have obscure GI bleeding
CT angiography: an emerging modality for bleed localization; does not allow option for therapeutic intervention (unlike regular angiography)
capsule endoscopy: may be used to identify bleeding in the small intestine not reachable by endoscopy
Endoscopy: Typically involves both esophagogastroduodenoscopy (EGD) and colonoscopy; allows for diagnosis of many etiologies of GI bleeding and also treatment of pathology in some cases:
Emergent endoscopy is reserved for life-threatening bleeding.
In stable patients with GI bleeding of unclear etiology, endoscopy typically is performed within 1 to 2 days of presentation (see endoscopic treatment of GI bleeding below).
Management of GI Bleeding
In all patients with GI bleeding, management starts with stabilization of the patient’s hemodynamic status (intravenous [IV] resuscitation with crystalloid or blood products) and correction of coagulation or platelet abnormalities. Signs of significant bleeding in children include tachycardia, hypotension, orthostasis, and prolonged capillary refill.
Pharmacologic Management
Active Bleeding |
---|
Intravenous inhibitors of gastric acid secretion:
|
Intravenous vasoactive agents:
|
Prevention of Rebleeding |
Oral inhibitors of gastric acid secretion:
|
Oral adhesive protection of ulcerated mucosa:
|
Oral prevention of variceal rebleeding:
|
Acid suppression with either proton pump inhibitors (PPIs) or H2-receptor antagonists is commonly utilized when upper GI bleeding is suspected. In the case of severe bleeds, acid suppression classically is given as an IV bolus followed by a continuous infusion. This regimen is based on research in adults, with few studies in children investigating pharmacologic treatment of GI bleeding. In one study in adults, intermittent dosing of PPIs was noninferior to continuous dosing, suggesting that continuous PPI therapy may be unnecessary.
Octreotide is commonly used for variceal bleeding with an initial IV bolus followed by a continuous infusion. This therapy also is not widely studied in pediatrics; however, it is used in clinical practice. Read a review on the usage of octreotide in children here.
Endoscopic Treatment
-
Definitive treatment for many causes of GI bleeding can be achieved through endoscopic hemostasis. For mucosal lesions (e.g., ulcers), options include:
injection therapy with (epinephrine) usually only has temporary effect but allows for other more definitive therapies
contact thermal coagulation (e.g., argon plasma coagulation or bipolar cautery)
clip placement
topical hemostatic agents
-
For acute variceal bleeding, options include:
injection sclerotherapy
variceal band ligation therapy
For colonic lesion (e.g., polyps), treatment involves endoscopic polypectomy.
The Sheffield Scoring System can be used to predict the need for endoscopic therapy.
Read a review of endoscopic approaches to GI bleeding in children here.
Research
Landmark clinical trials and other important studies
Attard TM et al. J Pediatr 2017.
This study found that hospital readmission after gastrointestinal bleeding is common in children, with the highest rates of readmission seen in patients with esophageal varices and chronic comorbidities. Lower rates of readmission were seen in patients who underwent endoscopy or Meckel scan on the first admission.
![[Image]](content_item_thumbnails/r360.i053994_res1.jpg)
Sachar H et al. JAMA Intern Med 2014.
This meta-analysis of adult patients with peptic ulcers found that intermittent PPI therapy was noninferior to continuous therapy.
![[Image]](content_item_thumbnails/r360.i053994_res2.jpg)
Freedman SB et al. J Pediatr Gastroenterol Nutr 2012.
This study found low rates of clinically significant bleeding in children presenting to the emergency room with hematemesis. Traits associated with significant bleeding included unwell appearance, older age, and presentation with melena or hematochezia.
![[Image]](content_item_thumbnails/r360.i053994_res3.jpg)
Lau JYW et al. N Engl J Med 2000.
This study on adults with peptic ulcers found a lower rate of recurrent bleeding after endoscopic treatment when patients also were given intravenous PPI therapy versus endoscopic treatment alone.
![[Image]](content_item_thumbnails/r360.i053994_res4.jpg)
Reviews
The best overviews of the literature on this topic
Boyle JT. Pediatr Rev 2008.
A review of the differential diagnosis, evaluation, and management of gastrointestinal bleeding in children
![[Image]](content_item_thumbnails/r360.i053994_rev1.jpg)
Kay MH and Wyllie R. J Pediatr Gastroenterol Nutr 2007.
A review of endoscopic treatment of gastrointestinal bleeding in children
![[Image]](content_item_thumbnails/r360.i053994_rev2.jpg)
Heikenen JB et al. J Pediatr Gastroenterol Nutr 2002.
A review of the uses of octreotide in children
![[Image]](content_item_thumbnails/r360.i053994_rev3.jpg)
Guidelines
The current guidelines from the major specialty associations in the field
Laine L et al. Am J Gastroenterol 2021.
![[Image]](content_item_thumbnails/r360.i053994_guide1.jpg)
Friedlander JA et al. J Pediatr Gastroenterol Nutr 2017.
This guideline reviews use of capsule endoscopy in children, including in cases of gastrointestinal bleeding.
![[Image]](content_item_thumbnails/r360.i053994_guide2.jpg)
Jones NL et al. J Pediatr Gastroenterol Nutr 2017.
![[Image]](content_item_thumbnails/r360.i053994_guide3.jpg)