Approach to diarrhea (pediatrics): Clinical sciences

Last updated: January 30, 2025

Approach to diarrhea (pediatrics): Clinical sciences

STAGE DE PÉDIATRIE

STAGE DE PÉDIATRIE

Henoch-Schonlein purpura: Clinical sciences
Approach to inborn errors of metabolism (progressive or chronic): Clinical sciences
Meningitis (pediatrics): Clinical sciences
Approach to anemia in the newborn and infant (destruction and blood loss): Clinical sciences
Approach to anemia in the newborn and infant (underproduction): Clinical sciences
Approach to anemia (destruction and sequestration): Clinical sciences
Approach to anemia (underproduction): Clinical sciences
Sickle cell disease: Clinical sciences
Sepsis (pediatrics): Clinical sciences
Approach to constipation (pediatrics): Clinical sciences
Approach to a cough (pediatrics): Clinical sciences
Bronchiolitis: Clinical sciences
Pneumonia (pediatrics): Clinical sciences
Upper respiratory tract infections: Clinical sciences
Influenza: Clinical sciences
Croup and epiglottitis: Clinical sciences
Congestive heart failure: Clinical sciences
Asthma: Clinical sciences
Approach to diarrhea (pediatrics): Clinical sciences
Infectious gastroenteritis (acute) (pediatrics): Clinical sciences
Infectious gastroenteritis (subacute) (pediatrics): Clinical sciences
Approach to a fever (over 2 months): Clinical sciences
Osteomyelitis (pediatrics): Clinical sciences
Pharyngitis, peritonsillar abscess, and retropharyngeal abscess (pediatrics): Clinical sciences
Otitis media and externa (pediatrics): Clinical sciences
Septic arthritis and transient synovitis (pediatrics): Clinical sciences
Stevens-Johnson syndrome and toxic epidermal necrolysis: Clinical sciences
Urinary tract infection (pediatrics): Clinical sciences
Approach to viral exanthems (pediatrics): Clinical sciences
Approach to bacterial causes of fever and rash (pediatrics): Clinical sciences
Juvenile idiopathic arthritis: Clinical sciences
Kawasaki disease: Clinical sciences
Acute group A streptococcal infections and sequelae (pediatrics): Clinical sciences
Approach to congenital infections: Clinical sciences
Staphylococcal scalded skin syndrome and impetigo: Clinical sciences
Approach to head and neck masses (pediatrics): Clinical sciences
Periorbital and orbital cellulitis (pediatrics): Clinical sciences
Approach to a murmur (pediatrics): Clinical sciences
Approach to congenital heart diseases (cyanotic): Clinical sciences
Approach to hematuria (pediatrics): Clinical sciences
Nephritic syndromes (pediatrics): Clinical sciences
Approach to leukocoria (pediatrics): Clinical sciences
Hepatitis B: Clinical sciences
Approach to a limp (pediatrics): Clinical sciences
Approach to common musculoskeletal injuries (pediatrics): Clinical sciences
Developmental dysplasia of the hip: Clinical sciences
Legg-Calve-Perthes disease and slipped capital femoral epiphysis: Clinical sciences
Human immunodeficiency virus (HIV) infection: Clinical sciences
Approach to proteinuria (pediatrics): Clinical sciences
Approach to a red eye: Clinical sciences
Conjunctival disorders: Clinical sciences
Eyelid disorders: Clinical sciences
Approach to vomiting (newborn and infant): Clinical sciences
Approach to vomiting (pediatrics): Clinical sciences
Gastroesophageal reflux disease (pediatrics): Clinical sciences
Approach to increased intracranial pressure: Clinical sciences
Peptic ulcers, gastritis, and duodenitis (pediatrics): Clinical sciences
Large bowel obstruction: Clinical sciences
Small bowel obstruction: Clinical sciences
Approach to acid-base disorders: Clinical sciences
Approach to metabolic acidosis: Clinical sciences
Approach to metabolic alkalosis: Clinical sciences
Approach to respiratory acidosis: Clinical sciences
Approach to respiratory alkalosis: Clinical sciences
Approach to hypocalcemia (pediatrics): Clinical sciences
Approach to hypoglycemia (pediatrics): Clinical sciences
Approach to hypernatremia (pediatrics): Clinical sciences
Approach to hyponatremia (pediatrics): Clinical sciences
Adrenal insufficiency: Clinical sciences
Syndrome of inappropriate antidiuretic hormone secretion: Clinical sciences
Approach to a fever (0-60 days): Clinical sciences
Approach to hypotonia (newborn and infant): Clinical sciences
Approach to jaundice (newborn and infant): Clinical sciences
Approach to poor feeding (newborn and infant): Clinical sciences
Approach to complications of prematurity (early): Clinical sciences
Approach to complications of prematurity (late): Clinical sciences
Necrotizing enterocolitis: Clinical sciences
Neonatal respiratory distress syndrome: Clinical sciences
Approach to prenatal teratogen exposure: Clinical sciences
Respiratory failure (pediatrics): Clinical sciences
Foreign body aspiration and ingestion (pediatrics): Clinical sciences
Approach to upper airway obstruction (pediatrics): Clinical sciences
Anaphylaxis: Clinical sciences
Approach to epilepsy: Clinical sciences
Approach to a first unprovoked seizure (pediatrics): Clinical sciences
Febrile seizure (pediatrics): Clinical sciences
Diabetes mellitus (pediatrics): Clinical sciences
Dehydration (pediatrics): Clinical sciences
Brief, resolved, unexplained event (BRUE): Clinical sciences
Approach to bradycardia: Clinical sciences
Approach to tachycardia: Clinical sciences
Approach to melena and hematemesis (pediatrics): Clinical sciences
Burns: Clinical sciences
Approach to trauma (pediatrics): Clinical sciences
Approach to a child with Down syndrome (trisomy 21): Clinical sciences
Cystic fibrosis and primary ciliary dyskinesia: Clinical sciences
Approach to delay or regression in developmental milestones: Clinical sciences
Approach to growth faltering: Clinical sciences
Approach to neurodevelopmental disorders: Clinical sciences
Approach to short stature: Clinical sciences
Approach to feeding and eating disorders: Clinical sciences
Allergic rhinitis: Clinical sciences
Essential hypertension: Clinical sciences
Approach to a rash in the well newborn and infant: Clinical sciences
Immunizations (pediatrics): Clinical sciences
Well-child visit (newborn and infant): Clinical sciences
Well-child visit (toddler and child): Clinical sciences
Well-child visit (adolescent): Clinical sciences
Bacterial and viral skin infections: Pathology review
Nasal, oral and pharyngeal diseases: Pathology review
Pediatric musculoskeletal disorders: Pathology review
Viral exanthems of childhood: Pathology review
Seizures: Pathology review
Congenital TORCH infections: Pathology review
Central nervous system infections: Pathology review
Developmental and learning disorders: Pathology review
Breastfeeding
Anatomy clinical correlates: Eye

Decision-Making Tree

Transcript

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Diarrhea refers to stools that are unusually loose or frequent when compared to a patient’s normal stooling pattern. In pediatric patients, acute diarrhea is commonly caused by infection, whereas chronic diarrhea often represents a pathologic condition or a functional gastrointestinal disorder. The underlying cause of diarrhea can be determined after assessing its chronicity and associated symptoms.

Now, if a pediatric patient presents with diarrhea, first perform an ABCDE assessment to determine if they are unstable or stable. If unstable, stabilize their airway, breathing, and circulation. Next, obtain IV access, administer IV fluids, and place your patient on continuous vital sign monitoring, including respiratory rate, pulse oximetry, and cardiac monitoring. Finally, if needed, don’t forget to provide supplemental oxygen.

Alright, now let’s go back to the ABCDE assessment and look at stable patients. First, obtain a focused history and physical examination. Patients or caregivers typically describe loose or frequent stools, while the physical exam might demonstrate abdominal tenderness, hyperactive bowel sounds, or dry mucous membranes. At this point, diagnose diarrhea and assess the duration of your patient’s symptoms.

First, let’s focus on acute diarrhea, or diarrhea that lasts for less than two weeks. In this case, your next step is to assess for red flag signs and symptoms, including high fever, blood or mucus in the stool, severe abdominal pain, and signs of dehydration.

If your patient reports no red flag signs or symptoms, consider mild viral gastroenteritis, which is the most common cause of acute diarrhea in children. These patients often report a known sick contact, and symptoms including vomiting and watery stool, possibly in combination with a low-grade fever. Additionally, the exam may reveal mild abdominal tenderness and increased bowel sounds. These findings are highly suggestive of mild viral gastroenteritis, which is a clinical diagnosis that doesn’t require laboratory evaluation.

This self-limited infection is commonly caused by rotavirus in unimmunized patients or by norovirus during outbreaks in closed environments like daycare centers and schools. However, if your patient has one or more red flag signs or symptoms, consider severe viral gastroenteritis or bacterial gastroenteritis. Then, order a CBC, CMP, and stool studies, including culture, viral antigen testing, and ova and parasites, or O&P.

First, let’s focus on severe viral gastroenteritis. In addition to vomiting and watery stools, these patients also report symptoms of dehydration, like decreased urine output and weight loss. Physical exam typically reveals dry mucous membranes and delayed capillary refill; and some patients may have significant abdominal tenderness.

Labs might reveal a normal anion gap hyperchloremic metabolic acidosis from bicarbonate loss in the stool. Stool studies will reveal no ova, parasites, or bacterial pathogens; and the viral antigen test will often be positive, which confirms your diagnosis of severe viral gastroenteritis.

On the flip side, individuals with bacterial gastroenteritis often have bloody stools, severe abdominal pain, and high fever. The exam may demonstrate abdominal tenderness and hyperactive bowel sounds;

while labs might show an elevated white blood cell count and normal anion gap hyperchloremic metabolic acidosis. The stool culture will identify a pathogen such as Salmonella, Shigella, Campylobacter, or E. coli; while the O&P and viral antigen tests will be negative. These findings indicate bacterial gastroenteritis.

In this case, historical clues can occasionally suggest the causative pathogen; for example, if a patient became sick after eating poultry, eggs, or dairy, think of Salmonella; while high fever and seizures suggest Shigella. Finally, recent travel suggests enterotoxigenic E. coli, and animal exposure suggests Campylobacter jejuni.

Now, switching gears and moving on to individuals with chronic diarrhea, which persists for 2 or more weeks. Again, the first step is to assess for red flag signs and symptoms, including blood in the stool, weight loss, or fever.

If any of these are present, order labs including CBC, CMP, and an ESR or CRP; and obtain stool studies, including a culture and O&P. Then, assess for bloody stools. If your patient reports bloody stools, order a fecal calprotectin, which is a sensitive marker of gastrointestinal inflammation.

An elevated fecal calprotectin should make you consider an inflammatory bowel disease like Crohn disease or ulcerative colitis. To differentiate these conditions, order an upper or lower gastrointestinal endoscopy with biopsies.

First, let’s look at findings you’ll see in Crohn disease. In this case, labs typically demonstrate a low hemoglobin; elevated platelets; elevated ESR or CRP; and negative stool studies. Endoscopic findings include cobblestoning and ulcerations with a discontinuous pattern of disease, or skip lesions; along with creeping fat anywhere along the GI tract. With these findings, diagnose Crohn disease.

Next let’s focus on findings you’ll see in ulcerative colitis. Labs will also demonstrate a low hemoglobin; elevated platelets; elevated ESR or CRP; and negative stool studies. Endoscopic findings will reveal a continuous pattern of ulcerations in the large intestine and loss of haustra, which are the pouches in the large intestine giving it a segmented appearance. With these findings, diagnose ulcerative colitis.

Here’s a clinical pearl! In addition to bloody diarrhea, fever, abdominal pain, and weight loss; patients with inflammatory bowel disease may experience extraintestinal manifestations, like polyarthralgia, uveitis, or erythema nodosum. On the other hand, if the fecal calprotectin level is normal, consider a gastrointestinal food allergy such as eosinophilic gastroenteropathy.

In this condition, patients often have a family or personal history of atopy, and many report sensitivity to cow’s milk, soy, or egg whites. Patients also demonstrate poor weight gain and may have recurrent vomiting. In severe cases, the physical exam might reveal generalized edema as a result of protein malabsorption. As far as labs go, hemoglobin is often low; eosinophils are usually elevated; and stool studies are negative.

To evaluate further, you could order a food skin-prick test or upper and lower gastrointestinal endoscopy with biopsies. The skin-prick test might identify the offending food protein. The endoscopy will show erythema, edema, erosions, or ulcerations of the intestinal mucosa; and the biopsy typically reveals eosinophilic infiltration of the gastrointestinal mucosa, which confirms eosinophilic gastroenteropathy.

Sources

  1. "Childhood Functional Gastrointestinal Disorders: Neonate/Toddler. " Gastroenterology. (Published online February 15, 2016. )
  2. "Childhood Functional Gastrointestinal Disorders: Child/Adolescent. " Gastroenterology. (2016;150(6):1456-1468.e2. )
  3. "Update on Diarrhea. " Pediatr Rev. (2016;37(8):313-322. )
  4. "Chronic diarrhea in children. " Pediatr Rev. (2012;33(5):207-218. )
  5. "Nelson Essentials of Pediatrics. 8th ed. " Elsevier (2023)
  6. "American Academy of Pediatrics Textbook of Pediatric Care. 2nd ed. " American Academy of Pediatrics; (2017)