Melbourne School of Population and Global Health, University of Melbourne, Melbourne, VIC.
University of Sri Jayewardenepura, Nugegoda, Sri Lanka.
Med J Aust. 2019 Jul;211(2):65-70. doi: 10.5694/mja2.50145. Epub 2019 May 3.
To examine the utility of apnoea screening questionnaires, alone and in combination with the Epworth sleepiness scale (ESS), for detecting obstructive sleep apnoea (OSA) in primary care.
DESIGN, SETTING: Prospective validation study in an Australian general population cohort.
424 of 772 randomly invited Tasmanian Longitudinal Health Study, 6th decade follow-up participants with OSA symptoms (mean age, 52.9 years; SD, 0.9 year) who completed OSA screening questionnaires and underwent type 4 sleep studies.
Clinically relevant OSA, defined as moderate to severe OSA (15 or more oxygen desaturation events/hour), or mild OSA (5-14 events/hour) and excessive daytime sleepiness (ESS ≥ 8); diagnostic test properties of the Berlin (BQ), STOP-Bang and OSA-50 questionnaires, alone or combined with an ESS ≥ 8.
STOP-Bang and OSA-50 correctly identified most participants with clinically relevant OSA (sensitivity, 81% and 86% respectively), but with poor specificity (36% and 21% respectively); the specificity (59%) and sensitivity of the BQ (65%) were both low. When combined with the criterion ESS ≥ 8, the specificity of each questionnaire was high (94-96%), but sensitivity was low (36-51%). Sensitivity and specificity could be adjusted according to specific needs by varying the STOP-Bang cut-off score when combined with the ESS ≥ 8 criterion.
For people likely to trigger OSA assessment in primary care, the STOP-Bang, BQ, and OSA-50 questionnaires, combined with the ESS, can be used to rule in, but not to rule out clinically relevant OSA. Combined use of the STOP-Bang with different cut-off scores and the ESS facilitates a flexible balance between sensitivity and specificity.
探讨单独使用和联合使用嗜睡量表(Epworth sleepiness scale,ESS)的睡眠呼吸暂停筛查问卷对初级保健中阻塞性睡眠呼吸暂停(obstructive sleep apnea,OSA)的检测效果。
设计、设置:澳大利亚普通人群队列的前瞻性验证研究。
424 名随机邀请的塔斯马尼亚纵向健康研究(Tasmanian Longitudinal Health Study)第 6 个十年随访参与者,具有 OSA 症状(平均年龄 52.9 岁,标准差 0.9 岁),他们完成了 OSA 筛查问卷并接受了 4 型睡眠研究。
临床相关 OSA,定义为中重度 OSA(每小时 15 次或更多的血氧饱和度下降事件)或轻度 OSA(每小时 5-14 次事件)和日间过度嗜睡(ESS≥8);柏林问卷(Berlin Questionnaire,BQ)、STOP-Bang 问卷和 OSA-50 问卷的诊断测试特性,单独使用或与 ESS≥8 联合使用。
STOP-Bang 和 OSA-50 正确识别了大多数具有临床相关 OSA 的参与者(敏感性分别为 81%和 86%),但特异性较低(分别为 36%和 21%);BQ(65%)和 OSA-50 问卷(65%)的特异性均较低。当与 ESS≥8 标准相结合时,每个问卷的特异性均较高(94%-96%),但敏感性较低(36%-51%)。通过改变 STOP-Bang 与 ESS≥8 标准相结合时的切点值,可以根据特定需求调整敏感性和特异性。
对于可能在初级保健中触发 OSA 评估的人群,STOP-Bang、BQ 和 OSA-50 问卷联合 ESS 可用于确定但不能排除临床相关 OSA。STOP-Bang 与不同切点值和 ESS 联合使用有助于在敏感性和特异性之间灵活平衡。