Validity of sheet-type portable monitoring device for screening obstructive sleep apnea syndrome

被引:18
作者
Kobayashi, Mina [1 ,2 ,3 ]
Namba, Kazuyoshi [1 ,2 ]
Tsuiki, Satoru [1 ,2 ,3 ]
Nakamura, Masaki [1 ,2 ,3 ]
Hayashi, Masamichi [4 ]
Mieno, Yuuki [4 ]
Imizu, Hiromi [4 ]
Fujita, Shiho [5 ]
Yoshikawa, Atsushi [5 ]
Sakakibara, Hiroki [4 ]
Inoue, Yuichi [1 ,2 ,3 ]
机构
[1] Japan Somnol Ctr, Neuropsychiat Res Inst, Shibuya Ku, Tokyo 1510053, Japan
[2] Yoyogi Sleep Disorder Ctr, Shibuya Ku, Tokyo 1510053, Japan
[3] Tokyo Med Univ, Dept Somnol, Shinjyuku Ku, Tokyo 1600023, Japan
[4] Fujita Hlth Univ, Sch Med, Div Resp Med & Clin Allergy, Dept Internal Med, Toyoake, Aichi 4701192, Japan
[5] Fujita Hlth Univ Hosp, Dept Lab Med, Toyoake, Aichi 4701192, Japan
关键词
Obstructive sleep apnea syndrome; Oximetry; Sheet-like monitoring device; Polysomnography; Validation; CARDIOVASCULAR-DISEASE; DIAGNOSIS; ASSOCIATION; SYSTEM; VALIDATION;
D O I
10.1007/s11325-012-0725-z
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The SD-101 is a non-restrictive sheet-like medical device that measures sleep-disordered breathing using pressure sensors that can detect the gravitational alterations in the body that accompany respiratory movement. One report has described that the screening specificity of the SD-101 for mild to moderate obstructive sleep apnea syndrome (OSAS) is relatively low. The present study examines whether the accuracy of the SD-101 for OSAS screening is improved by simultaneously measuring percutaneous oxygen saturation (SpO(2)). Sixty consecutive individuals with suspected OSAS consented to undergo overnight polysomnography (PSG) together with simultaneous measurements of SD-101 and SpO(2) at our laboratory. The apnea-hypopnea index (AHI) determined from PSG and the respiratory disturbance index determined from SD-101 measurements significantly correlated (SD-101 alone: r = 0.871, p < 0.0001; SD-101 with SpO(2): r = 0.965, p < 0.0001). Bland-Altman plots showed a smaller dispersion for the SD-101 with SpO(2) than for the SD-101 alone. The SD-101 with SpO(2) detected an AHI of > 15 on PSG with a sensitivity and specificity of 96.9 and 90.5 % compared with 87.5 and of 85.7 %, respectively, of the SD-101 alone. Simultaneously measuring SpO(2) improved the accuracy of the SD-101 for OSAS screening. Furthermore, this modality appears to offer high sensitivity and specificity for detecting even moderately severe OSAS.
引用
收藏
页码:589 / 595
页数:7
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