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. 1983;16(Suppl 1):97S–102S. doi: 10.1111/j.1365-2125.1983.tb02278.x

Efficacy and safety of midazolam in the treatment of night terrors in children

L Popoviciu, O Corfariu
PMCID: PMC1428090  PMID: 6138089

Abstract

1 Midazolam, in an oral dose of 15 mg, and placebo were administered to 15 children aged 6-15 years in treatment of night terrors.

2 After an initial adaptation night, the patients received placebo for 2 nights, followed by 15 mg midazolam for 2 nights and placebo again on the final 2 nights. Eight-hour nocturnal polygraphic recordings were made after the administration of both placebo and midazolam. The patients were continuously monitored by means of closed circuit infra-red television.

3 Ten of the patients manifested simple episodes while five had attacks associated with motor automatisms and EEG anomalies.

4 The total sleep time was lengthened by midazolam in most of the children; sleep architecture was favourably modified, mainly in terms of the amount and proportion of REM sleep (accompanied by dreams) and stage 2 sleep. Night terrors were eliminated by midazolam in all except one patient. REM sleep latency also decreased as did the number of nocturnal arousals (clinical and/or EEG). In the five cases with a background of organic cerebral disorders, the EEG anomalies and these attacks were suppressed by midazolam especially during the first sleep cycles.

5 Patients' subjective assessment of the quality of sleep was favourable. Midazolam was well tolerated with no side-effects.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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