Li Qing Yun, Berry Richard B, Goetting Mark G, Staley Bethany, Soto-Calderon Haideliza, Tsai Sheila C, Jasko Jeffrey G, Pack Allan I, Kuna Samuel T
Department of Respiratory Medicine, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Department of Medicine, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA.
Sleep. 2015 Apr 1;38(4):597-605. doi: 10.5665/sleep.4578.
To compare a positive airway pressure (PAP) device's detection of respiratory events and airway status during device-detected apneas with events scored on simultaneous polysomnography (PSG).
Prospective PSGs of patients with sleep apnea using a new-generation PAP device.
Four clinical and academic sleep centers.
Forty-five patients with obstructive sleep apnea (OSA) and complex sleep apnea (Comp SA) performed a PSG on PAP levels adjusted to induce respiratory events.
None.
PAP device data identifying the type of respiratory event and whether the airway during a device-detected apnea was open or obstructed were compared to time-synced, manually scored respiratory events on simultaneous PSG recording. Intraclass correlation coefficients between device-detected and PSG scored events were 0.854 for apnea-hypopnea index (AHI), 0.783 for apnea index, 0.252 for hypopnea index, and 0.098 for respiratory event-related arousals index. At a device AHI (AHIFlow) of 10 events/h, area under the receiver operating characteristic curve was 0.98, with sensitivity 0.92 and specificity 0.84. AHIFlow tended to overestimate AHI on PSG at values less than 10 events/h. The device detected that the airway was obstructed in 87.4% of manually scored obstructive apneas. Of the device-detected apneas with clear airway, a minority (15.8%) were manually scored as obstructive apneas.
A device-detected apnea-hypopnea index (AHIFlow) < 10 events/h on a positive airway pressure device is strong evidence of good treatment efficacy. Device-detected airway status agrees closely with the presumed airway status during polysomnography scored events, but should not be equated with a specific type of respiratory event.
比较在设备检测到的呼吸暂停期间,正压通气(PAP)设备对呼吸事件和气道状态的检测结果与同步多导睡眠图(PSG)评分的事件。
使用新一代PAP设备对睡眠呼吸暂停患者进行前瞻性PSG检查。
四个临床和学术睡眠中心。
45例阻塞性睡眠呼吸暂停(OSA)和复杂性睡眠呼吸暂停(Comp SA)患者在调整PAP水平以诱发呼吸事件的情况下进行了PSG检查。
无。
将识别呼吸事件类型以及设备检测到的呼吸暂停期间气道是否通畅的PAP设备数据与同步PSG记录上时间同步、人工评分的呼吸事件进行比较。设备检测到的事件与PSG评分事件之间的组内相关系数,呼吸暂停低通气指数(AHI)为0.854,呼吸暂停指数为0.783,低通气指数为0.252,呼吸事件相关觉醒指数为0.098。在设备AHI(AHIFlow)为每小时10次事件时,受试者操作特征曲线下面积为0.98,灵敏度为0.92,特异性为0.84。当PSG上的AHI值小于每小时10次事件时,AHIFlow往往会高估AHI。该设备在87.4%的人工评分阻塞性呼吸暂停中检测到气道阻塞。在设备检测到气道通畅的呼吸暂停中,少数(15.8%)被人工评分为阻塞性呼吸暂停。
正压通气设备上设备检测到的呼吸暂停低通气指数(AHIFlow)<每小时10次事件是治疗效果良好的有力证据。设备检测到的气道状态与多导睡眠图评分事件期间假定的气道状态密切一致,但不应等同于特定类型的呼吸事件。