AssessmentsPediatric gastrointestinal bleeding: Clinical practice
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An 8-month-old boy comes to the clinic with his parents because of new skin lesions. The parents state that the child has recently developed multiple blue-black lesions on his chest and upper extremities. The boy is otherwise in good health and there is no family history skin cancer. Physical examination shows compressible, rubber-like lesions that are wrinkled in appearance as shown in the image. The child does not cry when the the lesions are palpated. The rest of the exam is normal. Which of the following is a complication of the most likely diagnosis?
Content Reviewers:Rishi Desai, MD, MPH
Pediatric gastrointestinal bleeding can be divided into upper and lower GI bleeding.
Common causes of lower GI bleeding include anal fissures, allergic, necrotizing or infectious enterocolitis, malrotation with volvulus, intussusception, Meckel’s diverticulum, juvenile polyps and inflammatory bowel disease.
Now, both upper and lower GI bleedings can be either visible or occult- meaning that there’s no visible evidence of bleeding. This is usually detected by a fecal occult blood test or if there are signs of iron deficiency anemia.
Okay, first things first. Visible upper GI bleeds may cause blood in the vomit, which might be fresh and bright red, known as hematemesis- and suggests moderate to severe ongoing bleeding, or it might look like coffee- grounds, which suggests that the blood has been oxidized by acid in the stomach so that the iron in the blood has turned black. This is a sign that bleeding was a small quantity or has stopped.
Blood in the stool or diaper may present as black and tarry stools, known as melena, which suggest small quantity bleeding, about 50 milliliters of blood, and that most often results from upper GI bleeding.
If there is fresh, bright red blood passing through the anus which may or may not be mixed with stool, it’s usually lower GI bleeding, known as hematochezia.
In rare cases, if there’s a large upper GI bleed, that can cause hematochezia as well.
In any child with active GI bleed, the first thing to do is evaluate the general appearance, meaning the activity, muscle tone, level of consciousness and skin color, along with hemodynamic stability.
In mild hypovolemia, 3 to 5% of volume was lost, and it causes a slightly dry mouth, increased thirst, and slightly decreased urine output, like one wet diaper or void in six hours.
In moderate hypovolemia, 6% to 9% of the blood volume is lost, and it causes a markedly reduced urine output, with less than one wet diaper or void in six hours, tachycardia, orthostatic hypotension- which is a decrease of over 20 mm Hg in the systolic blood pressure, decreased skin turgor, dry mucous membranes, irritability, delayed capillary refill between two and three seconds, and deep respirations with or without an increase in respiratory rate. In infants, we might also see lack of tears when crying and a sunken open fontanelle.
In severe hypovolemia, over 10% of the blood volume is lost, and it causes anuria, or absence of any urine output, hypotension, a capillary refill of greater than three seconds, cool and mottled extremities, lethargy, and deep respirations with an increase in rate.
Active GI bleeding also requires a prompt workup. Lab work includes a CBC which usually shows a normal hemoglobin level, because the individual is losing whole blood.
Over the next 24 hours, there’s a physiologic compensation of holding onto more water, and intravenous fluids are usually given - and that decreases the hemoglobin level.
Coagulation studies including fibrinogen, a PT, PTT, and INR are done to rule out bleeding disorders.
Importantly, cross-matching for blood transfusions are also done.
Well-appearing children, are those that are physically active, with a normal muscle tone, posture and level of consciousness, and are hemodynamically stable.
In these children, if upper GI bleeding is suspected, then an upper endoscopy is done within 24 hours, and when lower GI bleeding is suspected, a colonoscopy is done within 24 hours to identify the source of bleeding.
Otherwise, in hemodynamically stable children, blood transfusions are done in infants younger than 4 months for a hemoglobin below 12 grams per deciliter and after 4 months of age, when hemoglobin drops below 7 grams per deciliter.
Ill-appearing children, are those that have little or no energy, decreased muscle tone, decreased level of consciousness, or are hemodynamically unstable with signs of hypovolemia.
In these children, two large caliber peripheral IV catheters are placed, and fluid resuscitation begins immediately with 20 milliliters per kilogram of weight of normal saline or lactated Ringer’s solution given over 5 to 10 minutes. This can be repeated, as needed, up to three times in children without improvement, provided there are no signs of fluid overload, such as decreased oxygenation, crackles, gallop rhythm or hepatomegaly.
Blood transfusions may be done if the child remains hemodynamically unstable.
If there’s a suspected upper GI bleed, it’s important to have surgical and interventional radiology teams nearby, because an upper endoscopy can precipitate complications like perforation.
Alternatively, if there’s a suspected lower GI bleed, then nasogastric lavage or upper endoscopy are done, followed by a colonoscopy.
Now specific causes of bleeding, vary by age.
In a neonate below one month of age, maternal blood ingestion is the most common cause of GI bleeding.
To differentiate between maternal and fetal blood, we can use the Apt-Downey test. That’s where a sample of the newborn's stool or vomit is placed in a test tube and hemolyzed to yield free hemoglobin and then mixed with sodium hydroxide.
If the solution turns yellow-brown, the hemoglobin is maternal or adult hemoglobin. If it remains the same color, it’s fetal hemoglobin; so, the newborn is the source of the bleeding. But, if the stool or vomit has been exposed to air longer than 30 minutes, the Apt-Downey test isn’t reliable.
In this case, we can quantify the fetal and maternal hemoglobin in the stool or vomit with a spectrophotometric assay. If maternal hemoglobin level is higher than 50% of the total hemoglobin detected in the sample, then this points to a maternal blood ingestion. No treatment is needed for maternal blood ingestion.
Another source of bleeding is an anal fissure which usually causes pain and bleeding with bowel movements. It can come from anal trauma, for example from rectal thermometers, birth injury, or even sexual abuse.
Most of the time, these are located in the posterior midline of the anal canal, and less often they can be in the anterior midline.
Sometimes, there are fissures in both the anterior and posterior midline, and these are called "kissing fissures".
Primary fissures require no routine workup. But if there’s suspicion of a secondary cause, additional tests may be required like PCR for HIV, dark field microscopy and VDRL or RPR for syphilis and culture or PPD skin testing for tuberculosis.
Most neonatal anal fissures heal on their own. Frequent diaper changes and thorough cleaning of the also help the healing process.
Now, another cause is food protein-induced allergic proctocolitis. This is triggered by cow’s milk proteins, or occasionally soy proteins, which are found in most infant formulas and can even be transmitted through a mother’s breast milk, if the mother has been drinking cow’s or soy milk herself.
To diagnose this in a breastfed infant, cow and soy milk is removed from the mother’s diet. In a formula-fed infant, cow or soy milk containing formula is stopped and an elemental formula, which doesn’t contain any cow milk or soy protein is used instead. After a few weeks, the cow or soy milk is reintroduced for seven days, either by having the mother consume lots of that milk, or by switching back to the old formula. If no symptoms reappear, there’s no milk-protein allergy, but if there are symptoms, then a diagnosis of milk-protein allergy is confirmed and the elimination diet should restart.
Alright, now, let’s switch gears to an ill-appearing neonate, with signs of hemodynamic instability.
One cause is necrotizing enterocolitis, which is where a portion of the intestine, typically the distal small bowel and large bowel, becomes ischemic and dies - typically due to inflammation from infectious pathogens. It’s most common in premature babies weighing less than 1500 grams, but can also occur in term and near-term babies.
A risk factor for necrotizing enterocolitis is formula-feeding, possibly due to loss of protective immunity and bacteria of breastmilk, causing alterations in the flora of the bowel. It typically occurs after the first week of life and symptoms include poor feeding, bloating, bilious vomiting, and bloody stools.
On physical examination, there can be abdominal distention from a right lower quadrant mass, abdominal wall erythema, tenderness, visible intestinal loops, and decreased bowel sounds. At late stages, the baby might go in shock, with bradycardia, apnea, and hypotension.
Diagnosis is made with an abdominal radiograph, which shows multiple loops of dilated bowel, along with the pathognomonic pneumatosis intestinalis. That’s air in the bowel wall produced by gas-forming bacteria. Sometimes, the air extends into portal vein.
Labs can show hyponatremia due to "third spacing" of fluid, metabolic acidosis due to build-up of lactic acid from ischemic bowel injury, thrombocytopenia due to disseminated intravascular coagulation, and neutrophilia or neutropenia due to sepsis. Blood cultures should be obtained to look for the causative pathogen.
Necrotizing enterocolitis is staged using Bell’s criteria.
In Stage I, necrotizing enterocolitis is only suspected.
It’s divided into stage IA, which includes mild symptoms like an unstable temperature, mild abdominal distension, occult blood in the stool, and normal or non-specific radiographic findings of bowel dilatation.
In stage IB, there’s also gross blood in the stool.
In Stage IIA, the diagnosis is now definite. The baby has absent bowel sounds or abdominal tenderness and radiographic findings like pneumatosis intestinalis.
In stage IIB, there are also lab changes such as metabolic acidosis and thrombocytopenia, and findings like abdominal cellulitis and right quadrant mass, and sometimes radiographic findings of gas in the portal vein.
Management includes discontinuing enteral feeds and switching to parenteral nutrition, which may require a central venous catheter, along with gastric decompression with a nasogastric tube to provide bowel rest. Empiric broad-spectrum antibiotics, such as ampicillin, gentamicin and metronidazole, are also initiated.
Empiric antibiotics should be continued for 3 days in stages IA and IB, 7 to 10 days in stage IIA, and 14 days in stage IIB, IIIA, and IIIB.
In stage IIIA, fluid replacement and inotropes are often needed, along with supplemental oxygen and mechanical ventilation.
In stage IIIB or if there’s progressive deterioration, such as worsening metabolic acidosis, severe and persistent thrombocytopenia, rising leukocytosis or declining leukopenia, surgical resection of the affected sections of bowel is also indicated.
Next, there’s intestinal malrotation with volvulus, which is where there’s twisting of the mesentery around the superior mesenteric artery leading to intestinal obstruction, infarction, and necrosis. This causes acute, bilious vomiting, abdominal distention and bloody diarrhea.
Diagnosis is usually made with ultrasound or with an abdominal X-ray in an upright position, which will show distended loops of bowel with air-fluid levels. That’s followed by an upper GI contrast series, which shows a corkscrew-like or spiral shaped duodenum in the right lower quadrant instead of the left upper quadrant.
Management starts with discontinuing feedings, fluid resuscitation with normal saline, nasogastric tube decompression, and broad spectrum IV antibiotics, like vancomycin or 4th generation cephalosporins, to treat sepsis.
Emergency surgery, known as a Ladd procedure, should be performed, which is where necrotic bowel is resected and reoriented within the abdominal cavity.
Moving on to infants over 1 month and young children up to 5 years old, GI bleeding is most commonly due to infectious colitis, Meckel’s diverticulum, or intussusception, and more rarely, due to peptic ulcer disease, juvenile polyposis, or arteriovenous malformations.
Infectious colitis is typically caused by bacteria, like Shigella, Salmonella, Yersinia, Campylobacter, Enterohemorrhagic E Coli 0157:H7 - SSYCE, and Clostridium difficile, but can also be caused by viruses, like CMV, and parasites, like Entamoeba histolytica.
There’s usually acute, bloody diarrhea, lasting up to a week, along with fever, abdominal pain, and cramps. E Coli 0157:H7 can also lead to hemolytic uremic syndrome, which is a life- threatening disease characterised by microangiopathic hemolytic anemia, thrombocytopenia, and renal failure.