A Multisite Randomized Trial of Portable Sleep Studies and Positive Airway Pressure Autotitration Versus Laboratory-Based Polysomnography for the Diagnosis and Treatment of Obstructive Sleep Apnea: The HomePAP Study

被引:248
作者
Rosen, Carol L. [1 ]
Auckley, Dennis [2 ]
Benca, Ruth [3 ]
Foldvary-Schaefer, Nancy [4 ]
Iber, Conrad [5 ]
Kapur, Vishesh [6 ]
Rueschman, Michael [7 ]
Zee, Phyllis [8 ]
Redline, Susan [7 ,9 ]
机构
[1] Case Western Reserve Univ, Sch Med, Univ Hosp, Case Med Ctr, Cleveland, OH USA
[2] Case Western Reserve Univ, Sch Med, MetroHlth Med Ctr, Cleveland, OH USA
[3] Univ Wisconsin, Madison, WI USA
[4] Case Western Reserve Univ, Cleveland Clin, Cleveland, OH 44106 USA
[5] Univ Minnesota, Hennepin Cty Med Ctr, Minneapolis, MN 55415 USA
[6] Univ Washington, Harborview Med Ctr, Seattle, WA 98104 USA
[7] Brigham & Womens Hosp, Boston, MA 02115 USA
[8] Northwestern Univ, Feinberg Sch Med, Chicago, IL 60611 USA
[9] Harvard Univ, Beth Israel Deaconess Med Ctr, Sch Med, Boston, MA 02215 USA
关键词
OSA; portable monitoring; diagnosis; randomized clinical trial; autotitration; PRACTICE PARAMETERS; SHORT-FORM; MANAGEMENT; DISORDERS; OUTCOMES; INDEX; CPAP;
D O I
10.5665/sleep.1870
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Study Objectives: To test the utility of an integrated clinical pathway for obstructive sleep apnea (OSA) diagnosis and continuous positive airway pressure (CPAP) treatment using portable monitoring devices. Design: Randomized, open-label, parallel group, unblinded, multicenter clinical trial comparing home-based, unattended portable monitoring for diagnosis and autotitrating CPAP (autoPAP) compared with in-laboratory polysomnography (PSG) and CPAP titration. Setting: Seven American Academy of Sleep Medicine (AASM) accredited sleep centers. Participants: Consecutive new referrals, age 18 yr or older with high probability of moderate to severe OSA (apnea-hypopnea index [AHI] >= 15) identified by clinical algorithm and Epworth Sleepiness Scale (ESS) score >= 12. Interventions: Home-based level 3 testing followed by 1 wk of autoPAP with a fixed pressure CPAP prescription based on the 90% pressure from autotitration of PAP therapy (autoPAP) device (HOME) compared with attended, in-laboratory studies (LAB). Measurements: CPAP acceptance, time to treatment, adherence at 1 and 3 mo; changes in ESS, and functional outcomes. Results: Of 373 participants, approximately one-half in each study arm remained eligible (AHI >= 15) to continue in the study. At 3 mo, PAP usage (nightly time at pressure) was 1 hr greater: 4.7 +/- 2.1 hr (HOME) compared with 3.7 +/- 2.4 hr (LAB). Adherence (percentage of night used >= 4 hr) was 12.6% higher: 62.8 +/- 29.2% compared with 49.4 +/- 36.1% in the HOME versus LAB. Acceptance of PAP therapy, titration pressures, effective titrations, time to treatment, and ESS score change did not differ between arms. Conclusions: A home-based strategy for diagnosis and treatment compared with in-laboratory PSG was not inferior in terms of acceptance, adherence, time to treatment, and functional improvements.
引用
收藏
页码:757 / 767
页数:11
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