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Evidence-based clinical update: does premedication with oral midazolam lead to improved behavioural outcomes in
Robin G Cox1, Ulyana Nemish, Alastair Ewen
1Division of Pediatric Anesthesia, Alberta Children's Hospital, Calgary, Alberta T3B 6A8, Canada. robin.cox@calgaryhealthregion.ca
Insights
Oral midazolam effectively reduces pre-anesthesia anxiety in children but doesn't consistently improve home behavior. This evidence-based review confirms its benefits for separation and induction anxiety.
Area of Science:
- Pediatric Anesthesiology
- Evidence-Based Medicine
- Clinical Pharmacology
Background:
- Preoperative anxiety in children is a common challenge.
- Oral midazolam is frequently used for pediatric premedication.
- Assessing its impact on behavioral outcomes is crucial for clinical practice.
Purpose of the Study:
- To evaluate the evidence for improved behavioral outcomes in children receiving oral midazolam before anesthesia.
- To synthesize findings from randomized controlled trials (RCTs) on oral midazolam's efficacy.
Main Methods:
- Conducted a systematic literature search on PubMed and OVID for RCTs (1990-2006) involving oral midazolam in children (0-18 years).
- Included studies with placebo or control arms, focusing on premedication for general anesthesia.
- Assigned levels of evidence and grades of recommendation using the Centre for Evidence-Based Medicine criteria.
Main Results:
- Oral midazolam significantly reduces anxiety related to parental separation and anesthesia induction.
- No significant delays in recovery times were observed.
- Evidence for reducing emergence agitation and improving postoperative behavior at home is inconsistent.
Conclusions:
- A Grade A recommendation supports oral midazolam (0.5 mg/kg) 20-30 minutes preoperatively for reducing separation and induction anxiety in children.
- Minimal impact on recovery times is noted.
- Consistent improvement in postoperative behavioral outcomes, either in the postanesthesia care unit or at home, cannot be reliably predicted.
Purpose:
The purpose of this evidence-based clinical update was to identify the best evidence to determine if behavioural outcomes are improved in children after oral midazolam premedication.
Methods:
A literature search was conducted using both PubMed and OVID programs, utilizing the terms "midazolam", and either "premedication" or "preoperative treatment". Search limits that were employed included randomized controlled trials (RCTs), English language, human studies, children aged 0-18 yr, and publication dates 1990 - present (January 2006). A review of the 171 abstracts obtained was undertaken and, of these, 30 papers were identified that concerned oral midazolam in children prior to general anesthesia, and that involved a RCT with a placebo or control arm. These studies were assigned levels of evidence, and grades of recommendation were made according to Centre for Evidence-Based Medicine criteria.
Results:
Oral midazolam premedication in children was found to reduce the anxiety associated with separation from parents/guardians, and with induction of anesthesia. Recovery times are not significantly delayed. There is no consistent evidence to suggest a reduction in the phenomenon of emergence agitation. Evidence suggesting an improvement in behavioural outcomes at home is also inconsistent.
Conclusion:
Premedication with midazolam 0.5 mg x kg(-1) po administered 20-30 min preoperatively, is effective in reducing both separation and induction anxiety in children (grade A recommendation), with minimal effect on recovery times. However improved postoperative behavioural outcomes in the postanesthesia care unit, or at home cannot be predicted on a consistent basis.
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