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Meta-Analysis
. 2011 Sep 7;2011(9):CD005506.
doi: 10.1002/14651858.CD005506.pub5.

Antiemetics for reducing vomiting related to acute gastroenteritis in children and adolescents

Affiliations
Meta-Analysis

Antiemetics for reducing vomiting related to acute gastroenteritis in children and adolescents

Zbys Fedorowicz et al. Cochrane Database Syst Rev. .

Abstract

Background: Vomiting is a common manifestation of acute gastroenteritis in children and adolescents. When untreated it can be a hindrance to oral rehydration therapy, which is the cornerstone in the management of acute gastroenteritis. Evidence is needed concerning the safety and efficacy of antiemetic use for vomiting in acute gastroenteritis in children.

Objectives: To assess the safety and effectiveness of antiemetics on gastroenteritis induced vomiting in children and adolescents.

Search strategy: We searched the Cochrane Upper Gastrointestinal and Pancreatic Diseases Group Trials Register comprising references identified from comprehensive electronic database searches and hand searches of relevant journals and abstract books of conferences.The search was re-run and is up to date as on 20 July 2010.

Selection criteria: Randomized controlled trials comparing antiemetics with placebo or no treatment, in children and adolescents under the age of 18, for vomiting due to gastroenteritis.

Data collection and analysis: Two review authors independently assessed trial quality and extracted data.

Main results: We included seven trials involving 1,020 participants. Mean time to cessation of vomiting in one study was 0.34 days less with dimenhydrinate suppository compared to placebo (P value = 0.036). Pooled data from three studies comparing oral ondansetron with placebo showed: a reduction in the immediate hospital admission rate (RR 0.40, NNT 17, 95% CI 10 to 100) but no difference between the hospitalization rates at 72 hours after discharge from the Emergency Department (ED); a reduction in IV rehydration rates both during the ED stay (RR 0.41, NNT 5, 95% CI 4 to 8), and in follow-up to 72 hours after discharge from the ED stay (worst-best scenario for ondansetron RR 0.57, NNT 6, 95% CI 4 to 13) and an increase in the proportion of patients with cessation of vomiting (RR 1.34, NNT 5, 95% CI 3 to 7)). No significant difference was noted in the revisit rates or adverse events, although diarrhea was reported as a side effect in four of the five ondansetron studies. In one study the proportion of patients with cessation of vomiting in 24 hours was (58%) with IV ondansetron, (17%) placebo and (33%) in the metoclopramide group (P value = 0.039).

Authors' conclusions: Oral ondansetron increased the proportion of patients who had ceased vomiting and reduced the number needing intravenous rehydration and immediate hospital admission. Intravenous ondansetron and metoclopramide reduced the number of episodes of vomiting and hospital admission, and dimenhydrinate as a suppository reduced the duration of vomiting.

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Conflict of interest statement

There are no financial conflicts of interest and the reviewers declare that they do not have any associations with any parties who may have vested interests in the results of this review. Dr Cathy Bennett is the proprietor of Systematic Research Ltd. and received payment for her contribution to the process of updating an earlier version of the review.

Figures

1
1
Study flow diagram (PRISMA).
2
2
Risk of bias graph: review authors' judgements about each risk of bias item presented as percentages across all included studies.
3
3
Risk of bias summary: review authors' judgements about each risk of bias item for each included study.
4
4
Forest plot of comparison: 1 Oral ondansetron (weight dependent dose) vs placebo, outcome: 1.1 Rate of admission to hospital (during ED stay).
5
5
Forest plot of comparison: 1 Oral ondansetron (weight dependent dose) vs placebo, outcome: 1.6 Rate of intravenous rehydration (up to 72 hrs following discharge from the ED stay), worst‐best case scenario.
6
6
Forest plot of comparison: 1 Oral ondansetron (weight dependent dose) vs placebo, outcome: 1.7 Proportion of participants with cessation of vomiting.
1.1
1.1. Analysis
Comparison 1 Oral ondansetron (weight dependent dose) vs placebo, Outcome 1 Rate of admission to hospital (during ED stay).
1.2
1.2. Analysis
Comparison 1 Oral ondansetron (weight dependent dose) vs placebo, Outcome 2 Rate of admission to hospital (up to 72 hrs following discharge from ED stay) best‐worst case scenario.
1.3
1.3. Analysis
Comparison 1 Oral ondansetron (weight dependent dose) vs placebo, Outcome 3 Rate of admission to hospital (up to 72 hrs following discharge from ED stay) worst‐best case scenario.
1.4
1.4. Analysis
Comparison 1 Oral ondansetron (weight dependent dose) vs placebo, Outcome 4 Rate of intravenous rehydration (during ED stay).
1.5
1.5. Analysis
Comparison 1 Oral ondansetron (weight dependent dose) vs placebo, Outcome 5 Rate of intravenous rehydration (up to 72 hrs following discharge from the ED stay), best‐worst case scenario.
1.6
1.6. Analysis
Comparison 1 Oral ondansetron (weight dependent dose) vs placebo, Outcome 6 Rate of intravenous rehydration (up to 72 hrs following discharge from the ED stay), worst‐best case scenario.
1.7
1.7. Analysis
Comparison 1 Oral ondansetron (weight dependent dose) vs placebo, Outcome 7 Proportion of participants with cessation of vomiting.
1.8
1.8. Analysis
Comparison 1 Oral ondansetron (weight dependent dose) vs placebo, Outcome 8 Revisit rate.

Update of

Comment in

References

References to studies included in this review

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Ginsburg 1980 {published data only}
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NCT01257672 {published data only}
    1. NCT0125762. Symptomatic treatment of acute gastroenteritis. http://clinicaltrials.gov/ct2/show/NCT0125762 (accessed 14 June 2011).

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