Gastroenteritis in Emergency Medicine Medication

  • Author: Arthur Diskin, MD; Chief Editor: Steven C Dronen, MD, FAAEM   more...
 
Updated: Mar 19, 2012
 

Medication Summary

The goals of pharmacotherapy are to reduce morbidity, to prevent complications, and to possibly decrease the duration of illness.

In February 2006, the United States Food and Drug Administration (FDA) approved an oral vaccine for rotavirus (RotaTeq). RotaTeq is administered in a 3-dose series starting between age 6-12 weeks and completed before age 32 weeks. It protects against types G1, G2, G3 and G4.

In April 2008, the FDA approved Rotarix, another oral vaccine, for prevention of rotavirus gastroenteritis. The current recommendation is to administer 2 separate doses of Rotarix to patients aged 6-24 weeks. Rotarix was efficacious in a large study, which reported that Rotarix protected patients with severe rotavirus gastroenteritis and decreased the rate of severe diarrhea or gastroenteritis of any cause.[8] In March 2010, Rotarix was temporarily taken off the market due to concerns with contamination with porcine circovirus type 1 (PCV1), but in May 2010 the FDA cleared use of the product again. Rotarix should not be given to children with latex allergy. It protects against type G1, G3, G4, and G 9. Rotashield, an earlier vaccine, was withdrawn from the market due to concerns with intussusception.

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Antibiotics

Class Summary

Therapy must cover all likely pathogens in the context of the clinical setting.

Ciprofloxacin (Cipro)

 

Fluoroquinolones are the agents of choice for the empiric treatment of invasive and traveler's diarrhea syndromes in adult patients. They are also the agents of choice when treatment is indicated and the organism involved is known to be Campylobacter, E coli (non-O157:H7), nontyphoid Salmonella (although antibiotic treatment may prolong bacterial shedding), Shigella, or Yersinia.

Trimethoprim-sulfamethoxazole (Bactrim)

 

Excellent second choice for empiric therapy, although it is not effective against Campylobacter organisms. Increasing resistance. First drug of choice for patients younger than 18 years. Specifically recommended for 5 d for shigellosis.

Rifaximin (Xifaxan, RedActiv, Flonorm)

 

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.

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Antiemetics

Class Summary

All these drugs are indicated in the control of nausea and vomiting. All have been associated with extrapyramidal adverse effects, especially in patients who are acutely ill, dehydrated, or children. They should be used with caution and only in the lowest effective dose. A weak association with Reye syndrome exists, and all may mask the vomiting associated with underlying CNS lesions.

Prochlorperazine (Compazine)

 

Antidopaminergic drug that blocks the postsynaptic mesolimbic dopamine receptors. Has an anticholinergic effect and can depress the reticular activating system, possibly responsible for relieving nausea and vomiting.

Promethazine (Phenergan)

 

Antidopaminergic agent effective in the treatment of emesis. Blocks postsynaptic mesolimbic dopaminergic receptors in the brain and reduces stimuli to the brainstem reticular system.

Trimethobenzamide (Tigan)

 

Has central effects in which it inhibits the medullary receptor trigger zone.

Ondansetron (Zofran)

 

Selective 5-HT3 receptor antagonist that blocks serotonin both peripherally and centrally. Indicated for nausea and vomiting due to radiation and/or chemotherapy and for postoperative nausea and vomiting. Cost considerations.

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Antidiarrheal agents

Class Summary

These agents are used to decrease the frequency of diarrheal stools and possibly the duration. They should be used with caution in children and in patients with dysentery, as some reports of prolonged illness and development of toxic megacolon exist.

Loperamide (Imodium)

 

Antimotility DOC. Generally safe and indicated in the early treatment of travelers' diarrhea.

Diphenoxylate HCl 2.5 mg/atropine sulfate 0.025 mg (Lomotil)

 

Antidiarrheal agent chemically related to narcotic analgesic meperidine. A subtherapeutic dose of anticholinergic atropine sulfate is added to discourage overdosage, in which case diphenoxylate may clinically mimic the effects of codeine.

Each tab of Lomotil or 5 cc of elixir contains 2.5 mg diphenoxylate hydrochloride and 0.025 mg atropine sulfate.

Almost always the preferred antimotility agent.

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Vaccines

Class Summary

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.

Rotavirus vaccine (RotaTeq, Rotarix)

 

Currently, 2 orally administered live-virus vaccines are marketed in the United States. Each is 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.

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Contributor Information and Disclosures
Author

Arthur Diskin, MD  Vice-President, Global Chief Medical Officer, Royal Caribbean Cruise Lines; Voluntary Associate Professor, University of Miami, Leonard M Miller School of Medicine

Arthur Diskin, MD is a member of the following medical societies: American College of Emergency Physicians

Disclosure: Royal Caribbean Cruise Lines Salary Employment

Specialty Editor Board

Michelle Ervin, MD  Chair, Department of Emergency Medicine, Howard University Hospital

Michelle Ervin, MD is a member of the following medical societies: American Academy of Emergency Medicine, American College of Emergency Physicians, American Medical Association, National Medical Association, and Society for Academic Emergency Medicine

Disclosure: Nothing to disclose.

Francisco Talavera, PharmD, PhD  Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference

Disclosure: Medscape Salary Employment

Eugene Hardin, MD, FAAEM, FACEP  Former Chair and Associate Professor, Department of Emergency Medicine, Charles Drew University of Medicine and Science; Former Chair, Department of Emergency Medicine, Martin Luther King Jr/Drew Medical Center

Disclosure: Nothing to disclose.

John D Halamka, MD, MS  Associate Professor of Medicine, Harvard Medical School, Beth Israel Deaconess Medical Center; Chief Information Officer, CareGroup Healthcare System and Harvard Medical School; Attending Physician, Division of Emergency Medicine, Beth Israel Deaconess Medical Center

John D Halamka, MD, MS is a member of the following medical societies: American College of Emergency Physicians, American Medical Informatics Association, Phi Beta Kappa, and Society for Academic Emergency Medicine

Disclosure: Nothing to disclose.

Chief Editor

Steven C Dronen, MD, FAAEM  Chair, Department of Emergency Medicine, LeConte Medical Center

Steven C Dronen, MD, FAAEM is a member of the following medical societies: American Academy of Emergency Medicine and Society for Academic Emergency Medicine

Disclosure: Nothing to disclose.

References
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  2. Centers for Disease Control and Prevention. Vessel Sanitation Program: Cruise Ship Inspection. Available at http://wwwn.cdc.gov/InspectionQueryTool/Forms/InspectionSearch.aspx.

  3. Centers for Disease Control and Prevention. Investigation Update: Outbreak of Salmonella Typhimurium Infections, 2008-2009. Available at http://www.cdc.gov/salmonella/typhimurium/update.html.

  4. Rasko DA, Webster DR, Sahl JW, et al. Origins of the E. coli strain causing an outbreak of hemolytic-uremic syndrome in Germany. N Engl J Med. Aug 25 2011;365(8):709-17. [Medline]. [Full Text].

  5. Farthing M, Lindberg G, Dite P, et al. World Gastroenterology Organisation practice guideline: Acute diarrhea. World Gastroenterology Organisation. Available at http://www.worldgastroenterology.org/acute-diarrhea-in-adults.html. Accessed September 2011.

  6. CDC research shows outbreaks linked to imported foods increasing. Available at http://www.cdc.gov/media/releases/2012/p0314_foodborne.html. Accessed March 14, 2012.

  7. Belliot G, Lavaux A, Souihel D, Agnello D, Pothier P. Use of murine norovirus as a surrogate to evaluate resistance of human norovirus to disinfectants. Appl Environ Microbiol. May 2008;74(10):3315-8. [Medline]. [Full Text].

  8. [Best Evidence] Ruiz-Palacios GM, Perez-Schael I, Velazquez FR, et al. Safety and efficacy of an attenuated vaccine against severe rotavirus gastroenteritis. N Engl J Med. Jan 5 2006;354(1):11-22. [Medline].

  9. DuPont HL, Jiang ZD, Okhuysen PC, Ericsson CD, de la Cabada FJ, Ke S, et al. A randomized, double-blind, placebo-controlled trial of rifaximin to prevent travelers' diarrhea. Ann Intern Med. May 17 2005;142(10):805-12. [Medline].

  10. Caeiro JP, DuPont HL. Management of travellers' diarrhoea. Drugs. Jul 1998;56(1):73-81. [Medline].

  11. Centers for Disease Control and Prevention. Outbreaks of gastroenteritis associated with noroviruses on cruise ships--United States, 2002. MMWR Morb Mortal Wkly Rep. Dec 13 2002;51(49):1112-5. [Medline]. [Full Text].

  12. Heymann DL. Control of communicable diseases manual. 19th ed. Washington, DC: American Public Health Association; 2008:258-260, 534-539.

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  14. DuPont HL. Clinical practice. Bacterial diarrhea. N Engl J Med. Oct 15 2009;361(16):1560-9. [Medline].

  15. [Guideline] DuPont HL. Guidelines on acute infectious diarrhea in adults. The Practice Parameters Committee of the American College of Gastroenterology. Am J Gastroenterol. Nov 1997;92(11):1962-75. [Medline].

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  18. [Guideline] Guerrant RL, Van Gilder T, Steiner TS, Thielman NM, Slutsker L, Tauxe RV, et al. Practice guidelines for the management of infectious diarrhea. Clin Infect Dis. Feb 1 2001;32(3):331-51. [Medline].

  19. Health Protection Agency Centre for Infections. Guidance for the Management of Norovirus Infection in Cruise Ships - Norovirus Working Group. Available at http://www.hpa.org.uk/publications/2007/cruiseliners/cruiseliners.pdf.

  20. Hom J. Do probiotics reduce the duration and symptoms of acute infectious diarrhea?. Ann Emerg Med. November 2011;58:445-446.

  21. Musher DM, Musher BL. Contagious acute gastrointestinal infections. N Engl J Med. Dec 2 2004;351(23):2417-27. [Medline].

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Hektoen enteric agar with Escherichia coli colonies. Different growth media are necessary for identifying different enteric pathogens, suppressing the growth of nonpathogens, and allowing for chemical reactions to assist in identification. The appearance results from the organism's ability to ferment lactose placed in the medium. This results in the production of acid, which lowers the pH and causes a change in the pH indicator placed in the medium. Salmonella and Shigella organisms do not ferment lactose.
Example of Salmonella on Hektoen enteric agar. The medium also contains ferric ammonium citrate, which indicates the production of hydrogen sulfide by the appearance of a black precipitate.
The MacConkey medium is commonly used and differentiates lactose fermenters, which produce acid, decrease the pH, and cause the neutral red indicator to give the colonies a pink-to-red color.
The Christensen method is used to determine if an organism produces the enzyme urease (Yersinia) or not (Salmonella, Shigella, Vibrio). Hydrolysis of urea produces ammonia and carbon dioxide, alkalinizing the medium and turning the phenol red from light orange to magenta (pink).
Often, a combination of methods may be used for identification. The tube on the left is triple sugar iron (TSI) agar. The alkaline slant and acid butt (K/A) indicates an organism that ferments glucose only (not lactose or sucrose). The middle tube is indole positive, as indicated by the pink ring, and indicates the organism's ability to split tryptophan to form indole. The tube on the right is urease negative. Taken together, these tests indicate the organism is likely Shigella.
Gram stain may be helpful in identifying an etiologic agent. This stain shows gram-negative bacilli, which could be Salmonella or Shigella with 2 polymorphonucleocyte cells (PMNs).
 
 
 
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