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Effect of adherence on daytime sleepiness, fatigue, depression and sleep quality in the obstructive sleep apnea/hypopnea syndrome patients undertaking nasal continuous positive airway pressure therapy

OBJECTIVES: 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 identif...

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Detalles Bibliográficos
Autores principales: Wang, Yeying, Ai, Li, Luo, Jiahong, Li, Ran, Chai, Yanlin, He, Xiaojie, Cao, Yu, Li, Yongxia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5396979/
https://www.ncbi.nlm.nih.gov/pubmed/28442894
http://dx.doi.org/10.2147/PPA.S128217
Descripción
Sumario:OBJECTIVES: 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. METHODS: 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. RESULTS: 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. CONCLUSION: 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.