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Pediatrics: General Medicine > Infectious Disease
Gastroenteritis
Article Last Updated: Apr 25, 2008
AUTHOR AND EDITOR INFORMATION
Section 1 of 10
Author: Randy P Prescilla, MD, Instructor in Anesthesia, Harvard Medical School; Assistant in Perioperative Anesthesia, Children's Hospital Boston
Editors: Ashir Kumar, MBBS, MD, FAAP, Professor, Department of Pediatrics and Human Development, College of Human Medicine, Michigan State University; Consulting Staff, Department of Pediatrics, EW Sparrow Hospital; Mary L Windle, PharmD, Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy, Pharmacy Editor, eMedicine.com, Inc; Joseph Domachowske, MD, Associate Professor, Department of Pediatrics, Division of Infectious Diseases, State University of New York-Upstate Medical University; Robert W Tolan Jr, MD, Chief, Division of Allergy, Immunology and Infectious Diseases, The Children's Hospital at Saint Peter's University Hospital; Clinical Associate Professor of Pediatrics, Drexel University College of Medicine; Russell W Steele, MD, Head, Division of Pediatric Infectious Diseases, Ochsner Children's Health Center; Clinical Professor, Department of Pediatrics, Tulane University School of Medicine
Author and Editor Disclosure
Synonyms and related keywords:
gastroenteritis, enterogastritis
Background
Gastroenteritis is a very common pediatric condition and is second only to respiratory infections as the most common reason for unscheduled visits to pediatricians.
Pathophysiology
Gastroenteritis is a clinical syndrome caused by a variety of viral, bacterial, and parasitic enteropathogens. The mechanisms potentially responsible for viral diarrhea include lysis of enterocytes, interference with the brush border function that leads to malabsorption of electrolytes, stimulation of cyclic adenosine monophosphate (cAMP), and carbohydrate malabsorption. The proposed pathophysiology of bacterial gastroenteritis involves the elaboration of toxin by enterotoxigenic pathogens and the invasion and inflammation of mucosa by invasive pathogens. Parasitic organisms invade epithelial cells and cause villus atrophy and eventual malabsorption.
Frequency
United States
Incidence rates for diarrhea are 1-2.5 episodes per child per year, which annually leads to approximately 38 million cases, 2-3.7 million physician visits, 320,000 hospitalizations, and 325-425 deaths.
International
More than 1 billion cases and at least 4 million deaths per year are attributed to diarrhea worldwide.
Mortality/Morbidity
Mortality and morbidity from diarrhea relate to the degree of dehydration. Most deaths in the United States correlate to lower maternal socioeconomic factors and prematurity.
Age
Dehydration risk in children relates to age, and infants are most susceptible.
History
- Pertinent information includes the following:
- Presence or absence of vomiting
- Frequency, duration, and character of diarrhea
- Travel history
- Contacts with sick individuals
- Antibiotic use
- Seafood ingestion
- Possible ingestion of toxic substances
- Chronic illness
- Determine the amount and type of fluids ingested for the past 24 hours and the child's urine output.
- Seizures in a patient with diarrhea should raise the possibility of gastroenteritis caused by Shigella species, enterohemorrhagic Escherichia coli, or an electrolyte imbalance. Hyponatremia is more common than hypernatremia.
- Consider hyponatremic dehydration in children who have been fed bland and dilute fluids (eg, tea, rice water, dilute formula).
- Consider hypernatremic dehydration in patients who have been drinking mainly salt solutions and other hypertonic solutions, who have been losing hypotonic fluids (eg, profuse watery diarrhea), and who present with a depressed sensorium beyond what would be expected from the apparently mild signs of dehydration.
Physical
- The criterion standard and most accurate clinical indicator of the extent of dehydration is the percentage loss of body weight during the illness, which represents the child's fluid deficit.
- Other vital clinical findings
- Thirst
- Listlessness
- Dry mucous membranes
- Sunken fontanelles
- Sunken eyes
- Absence of tears
- Decreased skin turgor
- Decreased capillary filling time
- Tachycardia
- Weak pulse
- Reduced blood pressure
- Examine the stools to check for mucus, blood streaks, or gross blood
- Tenting or loss of skin turgor (eg, when pinched skin does not return to the original flat shape) usually occurs in moderate-to-severe cases of dehydration yet is not always present in dehydration. Tenting or skin turgor loss seldom occurs with hypernatremic dehydration, a condition in which doughy skin is more common.
Causes
- Bacterial infections cause most gastroenteritis cases in less affluent nations.
- The most important causal agent in these countries is diarrhea-causing E coli (eg, enteropathogenic [EPEC], enterotoxigenic [ETEC], enteroaggregative [EAEC], enteroinvasive [EIEC], enterohemorrhagic [EHEC]).
- Other bacteria that cause gastroenteritis less often are Campylobacter, Aeromonas, Shigella, and Salmonella species.
- Vibrios species, especially Vibrios cholerae, play major roles in epidemics. In seafood poisoning, Vibrio parahaemolyticus is associated with gastroenteritis.
- Viral infections cause 30-40% of gastroenteritis cases in affluent countries.
- The most common bacterial agents in the United States are Salmonella, Shigella, Campylobacter, and Yersinia species and E coli. Enteroaggregative E coli has recently been shown to be an unrecognized cause of community-acquired diarrhea in infants in the United States. Campylobacter jejuni affects approximately 2 million people in the United States annually. Clostridium difficile is the most common cause of pseudomembranous colitis, a condition often observed in patients who develop severe diarrhea during or following a course of antibiotics. Clindamycin is the most common antibiotic identified, although almost all antibiotics have been implicated.
- In patients with sickle cell disease, Salmonella species are the most frequent cause of gastroenteritis.
- Giardia lamblia is the only parasite frequently isolated from patients with diarrhea. Other parasites include Cryptosporidium parvum and Cyclospora cayetanensis.
- Nonpathogenic isolates are Entamoeba coli, Endolimax nana, Iodamoeba butschlii, and Blastocystis hominis.
- In patients with HIV/AIDS, Mycobacterium avium is another causative agent, in addition to the other bacteria mentioned above. Protozoal agents include Cryptosporidium species, Isospora belli, G lamblia, Entamoeba histolytica, Cyclospora species, and microsporidia. Viral causes include cytomegalovirus and rotavirus.
- Persistent infectious diarrhea may be caused by Shigella, Giardia, and Cryptosporidium species, EPEC, EAEC, and Entamoeba histolytica.
- Additional information on bacterial foodborne and diarrheal diseases is available from the CDC.
Crohn Disease
Cystic Fibrosis
Hemolytic-Uremic Syndrome
Lactose Intolerance
Other Problems to be Considered
Chronic nonspecific diarrhea of childhood (toddler diarrhea)
Lab Studies
- Most cases of children with mild-to-moderate dehydration require no laboratory tests. Electrolyte, BUN, serum creatinine, and glucose levels may be obtained for severely dehydrated children or those with atypical or inconsistent histories and physical examination results. Other laboratory tests may be ordered to assess hydration status, including hematocrit and urine specific gravity tests.
- Fecal leukocytes usually are observed in infections caused by invasive E coli and Shigella and Campylobacter species. This test's predictive value varies, as does that of occult blood testing.
- Gram stain of the stools may help differentiate infectious from noninfectious diarrhea. Gram-negative seagull-shaped bacteria visible with Gram stain strongly suggest campylobacteriosis. An ova and parasite examination and specialized staining procedures are necessary to diagnose a parasitic etiology.
- Stool cultures usually are reserved for cases of children with bloody diarrhea and those who are severely dehydrated, chronically ill or immunocompromised, or who have the appearance of toxemia.
- Metabolic acidosis with a normal anion gap occurs with loss of bicarbonate, including the following conditions:
- Ureterostomy
- Small bowel fistula
- Extra chloride
- Diarrhea
- Carbonic anhydrase inhibitors
- Early chronic renal failure
- Addison disease
- Renal tubular acidosis
- Pancreatic fistula
- Parenteral nutrition
Imaging Studies
- Although imaging studies are not routine for gastroenteritis, anatomical abnormalities (eg, obstruction) should be excluded in cases involving vomiting without diarrhea. Consider the possibility of intussusception in very young patients. Exclude an appendicitis diagnosis for patients in whom abdominal pain is a greater presenting symptom than diarrhea.
Histologic Findings
Stool examination for patients whose gastroenteritis is caused by invasive enteropathogens usually reveals small amounts of mucoid stools containing leukocytes, red blood cells, and/or gross blood. Both tests, however, have low specificity and are better used for their negative predictive value (ie, up to 95%). The probability of an invasive bacterial pathogen is very low when both test results are negative.
Medical Care
The American Academy of Pediatrics (AAP) states, "oral rehydration therapy is the preferred treatment of fluid and electrolytes lost by diarrhea in children with mild-to-moderate dehydration." In addition, both the AAP and the European Society for Paediatric Gastroenterology, Hepatology, and Nutrition (ESPGHAN) recommend rapid rehydration over 3-4 hours. A useful method is to administer 100 mL/kg/d for the first 10 kg of body weight (BW), 50 mL/kg for the next 10 kg BW, and 20 mL/kg for each additional kg BW.
The latest CDC recommendations for managing acute gastroenteritis in children can be viewed online at Managing Acute Gastroenteritis Among Children (King CK, 2003).
- Oral rehydration therapy in the home environment
- Several oral rehydration solutions (ORSs) and pediatric maintenance solutions are available commercially (eg, Pedialyte, Rehydralyte, Kaolectrolyte, CeraLyte, Infalyte, Equalyte).
- A general guideline is to provide 4-8 oz for every episode of loose or watery stools until the diarrhea resolves.
- These fluids are not recommended for rehydration: tea, juices, pop, Kool-Aid, Gatorade (or similar sport drinks), boiled rice water, or boiled skim milk.
- Rehydration therapy in healthcare settings
- Oral rehydration is possible in a doctor's office with available space for at least 4 hours monitoring, adequately trained staff, and adequate mechanisms for billing this service. Intravenous rehydration also is feasible in these settings for mildly dehydrated patients who do not tolerate oral rehydration.
- Provide rapid intravenous rehydration for patients with the following conditions:
- Severe dehydration with cardiovascular involvement (ie, hypotension or shock)
- Failure of oral rehydration because of persistent vomiting
- High stool output (ie, usually >10 mL/kg BW/h)
- Monosaccharide malabsorption, evidenced by the presence of glucose or reducing substances in the stool and a significant increase in the stool volume following administration of the ORS
- Cerebral edema is the most serious potential consequence of rapidly infusing hypotonic fluids in a patient with hypernatremic dehydration.
- Medications
- Loperamide, opiates, opiate-and-atropine combination drugs, anticholinergic drugs, and absorbents are not recommended to treat diarrhea in children. No evidence exists that these are effective, and use may lead to possible adverse events.
- Similarly, routine use of bismuth subsalicylate and lactobacillus-containing compounds is not recommended.
- Most authorities do not recommend routine antiemetic use for children. Clinical evidence is currently insufficient to justify the use of ondansetron or metoclopramide in children with acute viral gastroenteritis.
- While antibiotic treatment clearly shortens the clinical illness and duration of pathogen excretion in dysentery caused by Shigella species, routine antibiotic use provides no clear advantage to treat gastroenteritis caused by Campylobacter jejuni, Yersinia enterocolitica, E coli, and Salmonella species.
- Antibiotic administration may be considered for very young patients with Salmonella-caused gastroenteritis, for patients who are immunocompromised, and for patients who are systemically ill.
- Recent evidence suggests that antibiotic treatment of enterohemorrhagic E coli infection may increase the risk for developing hemolytic uremic syndrome.
- Rifaximin has excellent antibacterial activity and was approved in 2004 for the treatment for traveler's diarrhea caused by noninvasive strains of E coli.
Diet
- Rapidly reintroducing normal feeding is the optimal rehydration method for children who are mildly to moderately dehydrated.
- For infants, the AAP, ESPGHAN, and other groups currently recommend full-strength formula. The recommended rehydration method for breastfed infants is to continue to receive mother's milk.
- For older children, the usual advice is to eat bananas, rice cereals, applesauce, and toast (ie, BRAT diet). Also on the recommended list are complex carbohydrates (eg, rice, wheat, bread, cereals), lean meats, yogurt, fruits, and vegetables.
Drug Category: Antibiotics
In cases of Shigella enteritis, antibiotic treatment provides more rapid resolution of symptoms and faster fecal shedding of the organism. Trimethoprim-sulfamethoxazole (TMP-SMZ) is the drug of choice. In uncomplicated enteritis caused by nontyphoidal Salmonella species, antibiotics have no beneficial effect and may prolong the carrier state. The role of antimicrobials to treat enteritis caused by Campylobacter species, Y enterocolitica, and E coli remains controversial. Metronidazole is the recommended medication for G lamblia.
| Drug Name | Sulfamethoxazole and Trimethoprim (Bactrim, Cotrim, Septra) |
| Description | An antibacterial combination that may be used to treat enteritis caused by susceptible strains of Shigella flexneri and Shigella sonnei when antibacterial therapy is indicated. |
| Adult Dose | 160 mg (based on trimethoprim component)/800 mg (based on sulfamethoxazole component) PO bid for 5 d (ie, 1 double-strength tab bid) |
| Pediatric Dose | 8 mg/kg/d (based on trimethoprim component) PO divided bid for 5 d |
| Contraindications | Documented hypersensitivity; documented megaloblastic anemia from folate deficiency; pregnant and nursing mothers; infants <2 mo; marked hepatic damage and renal insufficiency |
| Interactions | May increase PT when used with warfarin (perform coagulation tests and adjust dose accordingly); coadministration with dapsone may increase blood levels of both drugs; coadministration of diuretics increases incidence of thrombocytopenia purpura in elderly; phenytoin levels may increase with coadministration; may potentiate effects of methotrexate in bone marrow depression; hypoglycemic response to sulfonylureas may increase with coadministration; may increase levels of zidovudine |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
|
| Precautions | Do not use in pregnancy near term (risk of kernicterus in newborn); discontinue at first appearance of rash or sign of adverse reaction; obtain CBC counts regularly when used for more than 5 d; discontinue therapy if significant hematologic changes occur; goiter, diuresis, and hypoglycemia may occur with sulfonamides; caution in folate deficiency (eg, patients with chronic alcoholism, older patients, patients receiving anticonvulsant therapy, patients with malabsorption syndrome); hemolysis may occur in patients with G-6-PD deficiency; patients with AIDS may not tolerate or respond to TMP-SMZ; caution in patients with renal or hepatic impairment (perform urinalyses and renal function tests during therapy); administer fluids to prevent crystalluria and stone formation |
| Drug Name | Metronidazole (Flagyl) |
| Description | Appears to be absorbed into cells where intermediate-metabolized compounds are formed that bind DNA and inhibit protein synthesis. |
| Adult Dose | 250 mg PO tid for 5 d |
| Pediatric Dose | 5 mg/kg PO tid for 5 d |
| Contraindications | Documented hypersensitivity; first trimester of pregnancy |
| Interactions | Cimetidine may increase toxicity; may increase effects of anticoagulants; may increase toxicity of lithium and phenytoin; disulfiramlike reaction may occur with orally ingested ethanol |
| Pregnancy | B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
|
| Precautions | Contraindicated in pregnancy during first trimester; adjust dose in patients with hepatic disease; monitor for seizures and development of peripheral neuropathy |
| Drug Name | Rifaximin (Xifaxan, RedActiv, Flonorm) |
| Description | Nonabsorbed ( <0.4%), broad-spectrum antibiotic specific for enteric pathogens of the gastrointestinal tract (ie, Gram-positive, Gram-negative, aerobic and anaerobic). Rifampin structural analog. Binds to beta-subunit of bacterial DNA-dependent RNA polymerase, thereby inhibiting RNA synthesis. Indicated for E coli (enterotoxigenic and enteroaggregative strains) associated with travelers' diarrhea. |
| Adult Dose | 200 mg PO tid |
| Pediatric Dose | <12 years: Not established >12 years: Administer as in adults |
| Contraindications | Documented hypersensitivity to rifaximin or rifamycin antimicrobial agents (eg, rifampin) |
| Interactions | Induces CYP450 3A4 in vitro; limited data exist; no significant interactions shown in single dose studies with midazolam and oral contraceptives |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
|
| Precautions | May promote intestinal bacterial overgrowth and cause superinfection; discontinue if diarrhea persists more than 24-48 h or worsens; seek immediate medical care if fever and/or bloody stools emerge (tablets not effective); not effective for travelers' diarrhea due to suspected pathogens other than E coli; postmarketing reports include allergic dermatitis, rash, angioneurotic edema, urticaria, and pruritus |
Drug Category: Vaccines
These agents elicit active immunization to increase resistance to infection. Vaccines consist of microorganisms or cellular components, which act as antigens. Administration of the vaccine stimulates the production of antibodies with specific protective properties.
| Drug Name | Rotavirus vaccine (RotaTeq, Rotarix) |
| Description | Currently, 2 orally administered live-virus vaccine. Indicated to prevent rotavirus gastroenteritis, a major cause of severe diarrhea in infants. RotaTeq is a pentavalent vaccine that contains 5 live reassortant rotaviruses and is administered as a 3-dose regimen against G1, G2, G3, and G4 serotypes, the 4 most common rotavirus group A serotypes. It also contains attachment protein P1A (genotype P[8]). Rotarix protects against rotavirus gastroenteritis caused by G1, G3, G4, and G9 strains and is administered as a 2-dose series in infants aged 6-24 wk. Clinical trials found that the vaccines prevented 74-78% of all rotavirus gastroenteritis cases, nearly all severe rotavirus gastroenteritis cases, and nearly all hospitalizations due to rotavirus. |
| Adult Dose | Not indicated |
| Pediatric Dose | <6 weeks: Not established 6-12 weeks: 2 mL PO as a single dose, followed by 2 additional doses at 4- to 10-wk intervals; do not administer after age 32 wk >32 weeks: Not established |
| Contraindications | Documented hypersensitivity |
| Interactions | Immunosuppressive therapies (eg, irradiation, antimetabolites, alkylating agents, cytotoxic drugs, high-dose corticosteroids) may decrease immune response |
| Pregnancy | C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
|
| Precautions | Common adverse effects include diarrhea, vomiting, otitis media, inflamed nasal passages, and bronchospasm; refrigerate and protect from light; handle and discard empty tube according to biological waste procedures; previously marketed rotavirus vaccine (RotaShield) was associated with intussusception, but RotaTeq did not show an increased risk compared with placebo in clinical trials (monitor for signs of intestinal blockage); do not mix with other vaccines or solutions |
Transfer
- Transfer by emergency medical service unit any patient with moderate-to-severe dehydration to the nearest emergency department for intravenous rehydration.
Prognosis
- Prognosis is excellent because gastroenteritis usually is self-limited. Children usually improve after an intravenous bolus. Patients who receive ORS improve gradually.
Patient Education
Medical/Legal Pitfalls
- Failure to assess the extent of dehydration (sometimes due to insufficient information provided by parents who have telephoned the physician for advice)
- Failure by parents/patients to understand instructions
- Failure to schedule a follow-up visit
- Failure to diagnose ingestion(s)
- Failure to diagnose renal or acid-base abnormalities
- Failure to exclude anatomical abnormalities (eg, obstruction, abdominal infections)
Special Concerns
- Manage dehydration aggressively in patients who have sickle cell disease to prevent sequelae (eg, infarction, stroke, splenic sequestration). Administration of 1.5 times the normal rate of maintenance fluid infusion is a routine practice.
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Gastroenteritis excerpt Article Last Updated: Apr 25, 2008
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