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

被引:0
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作者
Murray, Deirdre [1 ,2 ]
Rooney, James [1 ,3 ]
Meldrum, Dara [1 ]
Al-Chalabi, Ammar [4 ,5 ]
Bunte, Tommy M. [6 ]
Chiwera, Theresa [4 ,5 ]
Choudhury, Mutahhara [4 ,5 ]
Chio, Adriano [7 ,8 ]
Fenton, Lauren [1 ]
Fortune, Jennifer [1 ]
Maidment, Lindsay [9 ]
Manera, Umberto [7 ,8 ]
Mcdermott, Christopher J. [9 ,10 ]
Meyjes, Myrte [6 ]
Tattersall, Rachel [1 ,2 ]
Torrieri, Maria Claudia [7 ]
Van Damme, Philip [11 ,12 ]
Vanderlinden, Elien [11 ]
Wood, Claire [4 ,5 ]
van den Berg, Leonard H. [6 ]
Hardiman, Orla [1 ,2 ]
机构
[1] Trinity Coll Dublin, Acad Unit Neurol, Dublin, Ireland
[2] Beaumont Hosp, Dublin, Ireland
[3] Ludwig Maximilians Univ Munchen, Univ Hosp, Inst & Clin Occupat Social & Environm Med, Munich, Germany
[4] Kings Coll London, Maurice Wohl Clin Neurosci Inst, Dept Basic & Clin Neurosci, London, England
[5] Kings Coll Hosp London, Dept Neurol, London, England
[6] UMC Utrecht, Utrecht, Netherlands
[7] Univ Turin, Als Ctr, Rita Levi Montalcini Dept Neurosci, Turin, Italy
[8] Azienda Osped Univ Citta Salute & Sci, Neurol 1, Turin, Italy
[9] Sheffield Teaching Hosp NHS Fdn Trust, Sheffield, England
[10] Univ Sheffield, Sheffield Inst Translat Neurosci, Div Neurosci, Sheffield, England
[11] Univ Hosp Leuven, Neurol Dept, Leuven, Belgium
[12] Univ Leuven KU Leuven, Leuven Brain Inst, Dept Neurosci, Leuven, Belgium
基金
英国医学研究理事会; 英国经济与社会研究理事会;
关键词
Respiratory measurement; respiratory symptoms; amyotrophic lateral sclerosis; AMYOTROPHIC-LATERAL-SCLEROSIS; FATIGUE; MANAGEMENT;
D O I
10.1080/21678421.2025.2471421
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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.
引用
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页数:11
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