Incidence of serious adverse events during nocturnal polysomnography
- PMID: 15586791
- PMCID: PMC2734412
- DOI: 10.1093/sleep/27.7.1379
Incidence of serious adverse events during nocturnal polysomnography
Abstract
Objectives: The purpose of the study was to verify whether minimal concern is warranted in regard to serious adverse effects in the sleep laboratory.
Design: A prospective multicenter study
Participants: Three scoring teams for 17 sleep laboratories.
Methods: Reports of adverse events occurring during polysomnography or identified upon scoring a study were collected over an 18-month time period. Incidence of mortality and adverse events were evaluated using a binomial distribution based on the Bernoulli process.
Results: Of 16,084 studies, the mortality rate during or 2 weeks after an adverse event, as noted, was 0.006%, and the overall rate of adverse events was 0.35%.
Conclusions: Adverse event rates are low; however, procedures for handling medical emergencies or adverse events during or after polysomnography are prudent, and those studies performed for research should include preparedness for the possibility of adverse events.
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Comment in
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Polysomnography entails no more than minimal risk.Sleep. 2005 Feb;28(2):276; author reply 277. doi: 10.1093/sleep/28.2.276. Sleep. 2005. PMID: 16171253 No abstract available.
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