Wang Yeying, Ai Li, Luo Jiahong, Li Ran, Chai Yanlin, He Xiaojie, Cao Yu, Li Yongxia
Department of Respiratory Medicine, The Second Affiliated Hospital of Kunming Medical University.
Department of Epidemiology and Biostatistics, School of Public Health, Kunming Medical University, Chenggong New City, Kunming, Yunnan Province, People's Republic of China.
Patient Prefer Adherence. 2017 Apr 12;11:769-779. doi: 10.2147/PPA.S128217. eCollection 2017.
The aims of this study were to describe changes in day- and nighttime symptoms and the adherence to nasal continuous positive airway pressure (nCPAP) during the first 3-month nCPAP therapy among newly diagnosed patients with obstructive sleep apnea/hypopnea syndrome (OSAS) and to identify the effect of adherence on the changes in day- and nighttime symptoms during the first 3 months.
Newly diagnosed OSAS patients were consecutively recruited from March to August 2013. Baseline clinical information and measures of the Epworth Sleepiness Scale (ESS), Fatigue Severity Scale (FSS), Zung's Self-Rating Depression Scale (SDS) and the Pittsburgh Sleep Quality Index (PSQI) at baseline and the end of 3rd, 6th, 9th and 12th week of therapy were collected. Twelve weeks' adherence was calculated as the average of each 3-week period. Mixed model was used to explore the effect of adherence to nCPAP therapy on ESS, FSS, SDS and PSQI in each 3-week phase.
Seventy-six patients completed the 12-week follow-up. The mixed-effects models showed that under the control of therapy phase adherence in the range of <4 hours per night, using nCPAP could independently improve daytime sleepiness, in terms of ESS (coefficient, [95% confidence interval] unit; -4.49 [-5.62, -3.36]). Adherence at 4-6 hours per night could independently improve all variables of day- and nighttime symptoms included in this study, namely ESS -6.69 (-7.40, -5.99), FSS -6.02 (-7.14, -4.91), SDS -2.40 (-2.95, -1.85) and PSQI -0.20 (-0.52, -0.12). Further improvement in symptoms could be achieved at ≥6 hours per night using nCPAP, which was ESS -8.35 (-9.26, -7.44), FSS -10.30 (-11.78, -8.83), SDS -4.42 (-5.15, -3.68) and PSQI -0.40 (-0.82, -0.02). The interaction between adherence level and therapy phase was not significant in day- and nighttime symptoms.
The effect of adherence on the above-mentioned symptoms is stable through the first 3 months. Under the control of therapy phase, the nCPAP therapy effectively improves day- and nighttime symptoms with ≥4 hours adherence, and the patients can achieve a further improvement with ≥6 hours adherence.
本研究旨在描述新诊断的阻塞性睡眠呼吸暂停低通气综合征(OSAS)患者在接受鼻持续气道正压通气(nCPAP)治疗的前3个月中白天和夜间症状的变化以及对nCPAP的依从性,并确定依从性对前3个月白天和夜间症状变化的影响。
2013年3月至8月连续招募新诊断的OSAS患者。收集基线临床信息以及治疗第3、6、9和12周结束时的Epworth嗜睡量表(ESS)、疲劳严重程度量表(FSS)、zung自评抑郁量表(SDS)和匹兹堡睡眠质量指数(PSQI)的测量值。将12周的依从性计算为每个3周时间段的平均值。使用混合模型探讨每个3周阶段nCPAP治疗依从性对ESS、FSS、SDS和PSQI的影响。
76例患者完成了12周的随访。混合效应模型显示,在每晚<4小时的治疗阶段依从性控制下,使用nCPAP可独立改善白天嗜睡,就ESS而言(系数,[95%置信区间]单位;-4.49[-5.62,-3.36])。每晚4-6小时的依从性可独立改善本研究中包括的白天和夜间症状的所有变量,即ESS -6.69(-7.40,-5.99)、FSS -6.02(-7.14,-4.91)、SDS -2.40(-2.95,-1.85)和PSQI -0.20(-0.52,-0.12)。每晚使用nCPAP≥6小时可进一步改善症状,即ESS -8.35(-9.26,-7.44)、FSS -10.30(-11.78,-8.83)、SDS -4.42(-5.15,-3.68)和PSQI -0.40(-0.82,-0.02)。依从水平与治疗阶段之间的相互作用在白天和夜间症状方面不显著。
依从性对上述症状的影响在最初3个月内是稳定的。在治疗阶段的控制下,nCPAP治疗在依从性≥4小时时有效改善白天和夜间症状,依从性≥6小时时患者可进一步改善。