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Published on: January 17, 2011
Oral midazolam premedication and postoperative behaviour in children
1Oregon Health Sciences University, Portland 97201, USA.
Insights
Oral midazolam premedication in children reduced crying during anesthesia induction. However, it was associated with a higher incidence of adverse postoperative behavioral changes, such as nightmares and anxiety, one week later.
Area of Science:
- Pediatric Anesthesiology
- Behavioral Pediatrics
Background:
- Preoperative anxiety and behavioral distress are common in children undergoing anesthesia.
- Sedative premedication aims to alleviate these issues, but its long-term effects require careful evaluation.
Purpose of the Study:
- To investigate the impact of oral midazolam premedication on children's behavior during anesthesia induction and in the postoperative period.
- To assess the incidence of adverse behavioral changes following midazolam administration.
Main Methods:
- A prospective, randomized, blinded study involving 70 children (ASA Physical Status 1 and 2; aged 1-10 years).
- Participants received either oral midazolam (0.5 mg/kg, max 10 mg) or placebo.
- Behavioral assessments were conducted before medication, during induction, and 15 minutes post-recovery.
Main Results:
- Children receiving midazolam exhibited significantly less crying during anesthesia induction (P < 0.02).
- One week post-procedure, 19 of 35 children in the midazolam group reported adverse behavioral changes (e.g., nightmares, anxiety), compared to 8 of 35 in the placebo group (P < 0.02).
- Most behavioral changes resolved by four weeks post-procedure.
Conclusions:
- Oral midazolam effectively reduces crying and distress during anesthesia induction in pediatric patients.
- Preoperative midazolam is associated with an increased incidence of adverse postoperative behavioral changes, necessitating careful consideration of risks and benefits.
Abstract:
We examined the effect of oral midazolam premedication on postoperative behaviour. Seventy children (ASA Physical Status 1 and 2; aged 1-10 yrs) were assigned randomly in a prospective, blinded fashion to receive either midazolam 0.5 mg.kg-1 (maximum 10 mg) or placebo. Behaviour assessments were made prior to medication, during induction of anaesthesia and 15 min following arrival to recovery room. The baseline behavioural evaluation scores were not significantly different. The children receiving midazolam cried significantly less during induction (P < or = 0.02). At one week follow-up, eight of 35 subjects receiving placebo had experienced adverse behaviour changes (nightmares, night terrors, food rejection, anxiety, negativism); 19 of 35 of the midazolam group experienced these changes (P < or = 0.02). At four week follow-up, most behaviour changes had resolved. Children given preoperative oral midazolam were less likely to cry and fight while being anaesthetized, and preoperative sedation was associated with increased incidence of adverse postoperative behaviour changes.
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