Literature DB >> 15586791

Incidence of serious adverse events during nocturnal polysomnography.

Reena Mehra1, Kingman P Strohl.   

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.

Entities:  

Mesh:

Year:  2004        PMID: 15586791      PMCID: PMC2734412          DOI: 10.1093/sleep/27.7.1379

Source DB:  PubMed          Journal:  Sleep        ISSN: 0161-8105            Impact factor:   5.849


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