Guzman Michelle A, Sgambati Francis P, Pho Huy, Arias Rafael S, Hawks Erin M, Wolfe Erica M, Ötvös Tamás, Rosenberg Russell, Dakheel Riad, Schneider Hartmut, Kirkness Jason P, Smith Philip L, Schwartz Alan R
Johns Hopkins Sleep Disorders Center, Center for Interdisciplinary Sleep Research and Education, Baltimore, Maryland.
NeuroTrials Research, Inc., Atlanta, Georgia.
J Clin Sleep Med. 2017 May 15;13(5):703-711. doi: 10.5664/jcsm.6588.
To assess effects of low-level continuous positive airway pressure (CPAP) on snoring in habitual snorers without obstructive sleep apnea (OSA).
A multicenter prospective in-laboratory reversal crossover intervention trial was conducted between September 2013 and August 2014. Habitual snorers were included if they snored (inspiratory sound pressure level ≥ 40 dBA) for ≥ 30% all sleep breaths on a baseline sleep study (Night 1), and if significant OSA and daytime somnolence were absent. Included participants then underwent a CPAP titration study at 2, 4, or 6 cm HO (Night 2) to examine snoring responses to step-increases in nasal pressure, a treatment night at optimal pressure (Night 3), followed by baseline night (Night 4). At each pressure, snoring intensity was measured on each breath. Snoring frequency was quantified as a percentage of sleep breaths at thresholds of 40, 45, 50, and 55 dBA. Sleep architecture and OSA severity were characterized using standard measurements.
On baseline sleep studies, participants demonstrated snoring at ≥ 40 dBA on 53 ± 3% and ≥ 45 dBA on 35 ± 4% of breaths. Snoring frequency decreased progressively as nasal pressure increased from 0 to 4 cm HO at each threshold, and plateaued thereafter. CPAP decreased snoring frequency by 67% and 85% at 40 and 45 dBA, respectively. Intervention did not alter sleep architecture and sleep apnea decreased minimally.
Low-level CPAP below the range required to treat OSA diminished nocturnal snoring, and produced uniform reduction in nightly noise production below the World Health Organization's limit of 45 dBA.
ClinicalTrials.gov, identifier: NCT01949584.
评估低水平持续气道正压通气(CPAP)对无阻塞性睡眠呼吸暂停(OSA)的习惯性打鼾者打鼾情况的影响。
2013年9月至2014年8月进行了一项多中心前瞻性实验室反向交叉干预试验。纳入的习惯性打鼾者需满足在基线睡眠研究(第1晚)中,打鼾(吸气声压水平≥40分贝)占所有睡眠呼吸的≥30%,且无明显的OSA和日间嗜睡。纳入的参与者随后在第2晚进行CPAP滴定研究,压力分别为2、4或6厘米水柱,以检查打鼾对鼻压力逐步增加的反应,在最佳压力下进行治疗晚(第3晚),随后是基线晚(第4晚)。在每个压力水平下,测量每次呼吸时的打鼾强度。打鼾频率被量化为在40、45、50和55分贝阈值下睡眠呼吸的百分比。使用标准测量方法对睡眠结构和OSA严重程度进行表征。
在基线睡眠研究中,参与者在53±3%的呼吸中打鼾声压≥40分贝,在35±4%的呼吸中打鼾声压≥45分贝。在每个阈值下,随着鼻压力从0增加到4厘米水柱,打鼾频率逐渐降低,此后趋于平稳。CPAP在40和45分贝时分别使打鼾频率降低了67%和85%。干预未改变睡眠结构,睡眠呼吸暂停略有减少。
低于治疗OSA所需范围的低水平CPAP可减少夜间打鼾,并使夜间噪音产生均匀降低至低于世界卫生组织45分贝的限值。
ClinicalTrials.gov,标识符:NCT01949584