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临床参数和血氧饱和度在疑似阻塞性睡眠呼吸暂停患者中启动 CPAP 的准确性。

Accuracy of the clinical parameters and oximetry to initiate CPAP in patients with suspected obstructive sleep apnea.

机构信息

Sleep Laboratory, Pneumonology Unit, Hospital Alemán, Buenos Aires, Argentina.

出版信息

Sleep Breath. 2012 Dec;16(4):1073-9. doi: 10.1007/s11325-011-0603-0. Epub 2011 Oct 14.

Abstract

OBJECTIVE

The aim of this study was to assess the accuracy of oximetry and the clinical parameters for the prescription of continuous positive airway pressure (CPAP) in patients with suspected obstructive sleep apnea syndrome (OSAS).

METHODS

All participants (135) performed oximetry (WristOx 3100™) and polysomnography (PSG) simultaneously in the sleep laboratory. The patients completed the Epworth sleepiness scale, the Berlin questionnaire, and a clinical history. Two blind independent observers decided to prescribe CPAP according to the results of the PSG (gold standard, observer A), oximetry (alternative method, observer B), and the clinical parameters. The accuracy of observer B on the indication of CPAP, using different cutoff points of the adjusted desaturation index (ADI3 and ADI4), was evaluated by the area under the receiver operating characteristics curve (AUC-ROC). The interobserver agreement for the indication of CPAP was assessed using kappa statistics.

RESULTS

One hundred nineteen subjects were included (92 men; mean age, 53; median respiratory disturbance index, 22.6; median BMI, 27.5 kg/m(2)). Depending on the criteria used in oximetry, the sensitivity and specificity of observer B to initiate a CPAP trial ranged from 79.8% to 92.5% and of 92% to 96%, respectively. The best performance for the indication of CPAP was noted with the adjusted O(2) desaturation index ≥ 3% (AUC-ROC, 0.923). The inter-rater agreement for the prescription of CPAP was good (kappa, 0.60 to 0.79).

CONCLUSION

This simulated study has shown that the use of oximetry plus clinical data has made it possible to indicate CPAP reliably in nearly 90% of the population with OSAS.

摘要

目的

本研究旨在评估血氧仪和临床参数在疑似阻塞性睡眠呼吸暂停综合征(OSAS)患者持续气道正压通气(CPAP)处方中的准确性。

方法

所有参与者(135 人)均在睡眠实验室同时进行血氧仪(WristOx 3100™)和多导睡眠图(PSG)检查。患者完成了 Epworth 嗜睡量表、柏林问卷和临床病史。两名独立的盲法观察员根据 PSG 结果(金标准,观察员 A)、血氧仪(替代方法,观察员 B)和临床参数决定是否开具 CPAP。使用调整后的脱氧指数(ADI3 和 ADI4)不同截断值,通过受试者工作特征曲线下面积(AUC-ROC)评估观察者 B 对 CPAP 适应证的准确性。使用 Kappa 统计评估 CPAP 适应证的观察者间一致性。

结果

共纳入 119 例患者(92 例男性;平均年龄 53 岁;中位呼吸暂停低通气指数 22.6;中位 BMI 27.5 kg/m²)。根据血氧仪标准,观察者 B 启动 CPAP 试验的敏感性和特异性范围分别为 79.8%至 92.5%和 92%至 96%。用于 CPAP 适应证的最佳指标是调整后的 O(2)脱氧指数≥3%(AUC-ROC,0.923)。CPAP 处方的观察者间一致性良好(kappa 值为 0.60 至 0.79)。

结论

本模拟研究表明,使用血氧仪加临床数据可以在近 90%的 OSAS 患者中可靠地提示 CPAP。

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