Respiratory measurements, respiratory symptoms, and quality of life in ALS: results from the REVEALS study.

IF 2.8
Deirdre Murray, James Rooney, Dara Meldrum, Ammar Al-Chalabi, Tommy M Bunte, Theresa Chiwera, Mutahhara Choudhury, Adriano Chio, Lauren Fenton, Jennifer Fortune, Lindsay Maidment, Umberto Manera, Christopher J McDermott, Myrte Meyjes, Rachel Tattersall, Maria Claudia Torrieri, Philip Van Damme, Elien Vanderlinden, Claire Wood, Leonard H Van Den Berg, Orla Hardiman
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Abstract

Objective: Progressing respiratory weakness throughout the course of amyotrophic lateral sclerosis (ALS) is clinically associated with distressing symptoms, including dyspnea, orthopnea, and difficulty clearing secretions. Fatigue, poor sleep, and reduced quality of life are also considered to be associated with declining respiratory function. Respiratory measurements guide prescription of interventions, which aim to alleviate symptoms. The relationships between respiratory measurements and patient reported symptoms are currently unclear. Method: The REVEALS study was a longitudinal, observational, multisite study of decline in respiratory function in people with ALS attending six European centers. Respiratory measures (forced and slow vital capacity (F/SVC), sniff nasal inspiratory pressure (SNIP), and peak cough flow) were collected, as were the presence of respiratory symptoms and simple quality of life, fatigue and sleep measures. We used Bayesian's multivariate models to explore the associations of the respiratory measures with outcome variables. Results: Two hundred and eighty participants completed in-person assessments over a median of 8 (IQR 2.3, 14.1) months, with 974 data collection timepoints. The probability of reporting symptoms including dyspnea, orthopnea, and difficulty clearing secretions increased with decreasing respiratory measurement scores. The probability of reporting moderately low quality of life and moderate fatigue also increased with decreasing test scores, but reported sleep quality was not associated with respiratory scores. Conclusion: Respiratory weakness in people with ALS was associated with symptoms including dyspnea, orthopnea, and difficulty clearing secretions. The probability of reporting symptoms increased incrementally as respiratory weakness increased, supporting the use of both respiratory measurements and the presence of symptoms in making decisions about clinical interventions.

ALS患者的呼吸测量、呼吸症状和生活质量:来自reveal研究的结果
目的:在肌萎缩性侧索硬化症(ALS)的整个病程中,进行性呼吸无力在临床上与令人痛苦的症状相关,包括呼吸困难、直立呼吸和分泌物清除困难。疲劳、睡眠不足和生活质量下降也被认为与呼吸功能下降有关。呼吸测量指导干预措施的处方,其目的是减轻症状。呼吸测量与患者报告的症状之间的关系目前尚不清楚。方法:reveal研究是一项纵向、观察性、多地点研究,研究在六个欧洲中心就诊的ALS患者呼吸功能下降。收集呼吸测量(用力肺活量和慢速肺活量(F/SVC)、嗅鼻吸气压(SNIP)和峰值咳嗽流量),以及呼吸症状的存在和简单的生活质量、疲劳和睡眠测量。我们使用贝叶斯多变量模型来探讨呼吸测量与结果变量的关系。结果:280名参与者在中位8个月(IQR 2.3, 14.1)个月的时间内完成了亲自评估,共有974个数据收集时间点。随着呼吸测量评分的降低,报告呼吸困难、直立呼吸和分泌物清除困难等症状的可能性增加。随着测试分数的降低,报告中度低生活质量和中度疲劳的可能性也会增加,但报告的睡眠质量与呼吸评分无关。结论:肌萎缩侧索硬化症患者的呼吸无力与呼吸困难、直立呼吸和分泌物清除困难等症状相关。随着呼吸无力的加重,报告症状的可能性逐渐增加,这支持在决定临床干预措施时同时使用呼吸测量和症状的存在。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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