Description and validation of the apnea risk evaluation system: a novel method to diagnose sleep apnea-hypopnea in the home.

Abstract:

STUDY OBJECTIVES:To evaluate the accuracy and practicality of the Apnea Risk Evaluation System (ARES; Advanced Brain Monitoring; Carlsbad, CA), a limited-channel system for diagnosing sleep apnea/hypopnea in the home. DESIGN:Prospective randomized study with blinded analysis. SETTINGS:Two independent, community-based, sleep-disorders centers and the participants' homes. PARTICIPANTS:Two hundred ninety-nine subjects were recruited, including 210 consecutive willing patients referred by community physicians to the centers because of suspected sleep apnea; 36 "general medical" patients recruited from community physicians' offices; and 53 "presumably healthy" subjects recruited from community centers. MEASUREMENTS AND RESULTS:Manual scoring of attended in-laboratory full-night or split-night polysomnography by trained technologists supervised by physicians board certified in sleep medicine, and automated scoring of the limited-channel system used attended in the laboratory and unattended at home. The definition of the polysomnography apnea-hypopnea index (AHI) and the ARES respiratory disturbance index was the total number of events divided by the study duration in hours. Two hundred eighty-four valid comparisons of in-laboratory simultaneous polysomnography and ARES and 187 valid comparisons of in-laboratory polysomnography with a separate 2 nights of unattended self-applied ARES Unicorder (Advanced Brain Monitoring) were obtained. A diagnostic AHI cutoff of > 10 was used to establish the accuracy and validity of the ARES. The concurrent in-laboratory comparison yielded a sensitivity of 97.4, a specificity of 85.6, a positive predictive value of 93.6, and a negative predictive value of 93.9; in-home comparison sensitivity, specificity, positive predictive value, and negative predictive value were 91.5, 85.7, 91.5, and 85.7, respectively. CONCLUSIONS:The ARES demonstrated consistently high sensitivity and specificity for both in-laboratory and in-home recordings. In patients at risk for sleep apnea who do not a priori need an attended study, the ARES could provide a low-cost alternative to traditional polysomnography.

journal_name

Chest

journal_title

Chest

authors

Westbrook PR,Levendowski DJ,Cvetinovic M,Zavora T,Velimirovic V,Henninger D,Nicholson D

doi

10.1378/chest.128.4.2166

subject

Has Abstract

pub_date

2005-10-01 00:00:00

pages

2166-75

issue

4

eissn

0012-3692

issn

1931-3543

pii

S0012-3692(15)52618-4

journal_volume

128

pub_type

临床试验,杂志文章,随机对照试验

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