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Antiemetics for reducing vomiting related to acute ... - Update Software

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Why it is important <strong>to</strong> do this review<br />

Physicians who provide care <strong>to</strong> paediatric patients in the emergency<br />

department (ED) usually prescribe intravenous fluid therapy<br />

(IVT) <strong>for</strong> mild or moderate dehydration when <strong>vomiting</strong> is<br />

the major symp<strong>to</strong>m. Additional symp<strong>to</strong>matic treatment of <strong>vomiting</strong><br />

with antiemetics could lead <strong>to</strong> an important reduction in<br />

the use of intravenous rehydration as well as hospitalization, and<br />

a resumption of oral rehydration therapy (ORT). Concerns have<br />

also been expressed about the side effects of some antiemetics.<br />

A number of randomized control trials have investigated the effectiveness<br />

of different antiemetics, some of which have been assessed<br />

in several recent non-Cochrane systematic reviews.<br />

O B J E C T I V E S<br />

The objective of this review was <strong>to</strong> provide reliable evidence regarding<br />

the clinical effectiveness and safety of antiemetics prescribed<br />

<strong>for</strong> <strong>vomiting</strong> due <strong>to</strong> gastroenteritis by comparing clinical<br />

outcomes expressed as cessation of <strong>vomiting</strong>, reduction in the need<br />

<strong>for</strong> intravenous rehydration or hospitalization and the eventual<br />

resumption of oral rehydration therapy.<br />

M E T H O D S<br />

Criteria <strong>for</strong> considering studies <strong>for</strong> this review<br />

Types of studies<br />

We considered only randomized controlled clinical trials in this<br />

review.<br />

Types of participants<br />

Studies which had recruited children and adolescents who were<br />

under the age of 18 and who presented with <strong>vomiting</strong> and a confirmed<br />

clinical diagnosis of gastroenteritis.<br />

We excluded any studies in which patients were <strong>vomiting</strong> as a result<br />

of general anaesthesia or due <strong>to</strong> chemotherapy. In addition,<br />

we excluded studies in which patients were suffering from surgical<br />

conditions (<strong>for</strong> example, <strong>acute</strong> appendicitis/pelvic abscess, inflamma<strong>to</strong>ry<br />

bowel disease), or systemic infections (such as urinary<br />

tract infections, pneumonia, meningitis), or metabolic conditions<br />

(diabetes mellitus or any other previously diagnosed disorders, including<br />

immunodeficiency).<br />

Types of interventions<br />

Active interventions<br />

We considered any antiemetics administered orally, intravenously<br />

or as supposi<strong>to</strong>ries at any dosage, prescribed <strong>to</strong> terminate or reduce<br />

<strong>vomiting</strong>.<br />

Control<br />

Administration of placebo, vehicle or nothing prescribed <strong>to</strong> terminate<br />

<strong>vomiting</strong>. We included studies which compared different<br />

antiemetics.<br />

Types of outcome measures<br />

Primary outcomes<br />

Time taken from the first administration of the treatment until<br />

cessation of <strong>vomiting</strong>.<br />

Secondary outcomes<br />

We also considered the following secondary outcomes <strong>for</strong> this<br />

review.<br />

• Parental satisfaction as assessed by questionnaire or<br />

interview<br />

• Number of participants who required hospitalization:<br />

during the ED stay; and up <strong>to</strong> 72 hours following discharge from<br />

the ED stay<br />

• Number of participants who required intravenous<br />

rehydration during the ED stay; and up <strong>to</strong> 72 hours following<br />

discharge from the ED stay<br />

• Mean number of episodes of <strong>vomiting</strong><br />

• Proportion of participants with cessation of <strong>vomiting</strong><br />

• Number of participants who revisited<br />

• Number of participants who resumed oral rehydration<br />

Adverse events<br />

• Any clinically documented or patient reported adverse<br />

events.<br />

Search methods <strong>for</strong> identification of studies<br />

Electronic searches<br />

<strong>Antiemetics</strong> <strong>for</strong> <strong>reducing</strong> <strong>vomiting</strong> <strong>related</strong> <strong>to</strong> <strong>acute</strong> gastroenteritis in children and adolescents (Review)<br />

Copyright © 2011 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.<br />

We conducted searches on 28th July 2005, and have updated these<br />

subsequently (July 2006, June 2008, and July 2010), <strong>to</strong> identify<br />

all published and unpublished randomized controlled trials. There<br />

were no language or date restrictions in the electronic searches.<br />

7

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