Remote pulmonary function testing allows for early identification of need for non-invasive ventilation in a subset of persons with ALS.

Amyotrophic lateral sclerosis Pulmonary function testing Remote monitoring

Journal

Journal of the neurological sciences
ISSN: 1878-5883
Titre abrégé: J Neurol Sci
Pays: Netherlands
ID NLM: 0375403

Informations de publication

Date de publication:
19 Mar 2024
Historique:
received: 12 01 2024
revised: 24 02 2024
accepted: 17 03 2024
medline: 25 3 2024
pubmed: 25 3 2024
entrez: 24 3 2024
Statut: aheadofprint

Résumé

The traditional ALS multidisciplinary clinical practice of quarterly respiratory assessment may leave some individuals in danger of developing untreated respiratory insufficiency between visits or beginning non-invasive ventilation (NIV) later than would be optimal. Remote, or home-based, pulmonary function testing (rPFT) allows patients with ALS to perform regular respiratory testing at more frequent intervals in the home. The aim of this study was to determine the clinical benefit of weekly rPFT compared to standard, quarterly in-clinic respiratory assessments: the number of individuals with earlier identification of NIV need, the magnitude of this advance notice, and the individual factors predicting benefit. Participants with ALS (n = 39) completed rPFT training via telemedicine and then completed one year of weekly self-guided assessments in the home. Over this period, 17 individuals exhibited remotely-measured FVC dropping below 50% of predicted, the value often used for recommendation of NIV initiation. In 13 individuals with clinical detection of this event, the median and range of advance notice of need for NIV was 53 (-61-294) days. Prescription of NIV occurred for 21 individuals on the study, six of whom began NIV as a result of remote testing, prior to indication of need as determined by in-person assessments. Weekly home assessments appeared to be of greatest clinical value in a subset of patients with low baseline respiratory test values and rapid respiratory decline. This has potential implications for clinical management of ALS as well as the conduct of clinical trials that rely on respiratory endpoints.

Identifiants

pubmed: 38522245
pii: S0022-510X(24)00106-0
doi: 10.1016/j.jns.2024.122971
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

122971

Informations de copyright

Copyright © 2024. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of competing interest Dr. Simmons has received consulting fees from Amylyx, Clene, Biogen, and Corcept Therapeutics, and research funding to his institution from Sanofi, Mitsubishi Tanabe, Cytokinetics, and the ALS Association. All other authors report no financial and personal relationships with other people or organizations that could inappropriately influence this work.

Auteurs

Andrew Geronimo (A)

Departments of Neurology and Neurosurgery, Penn State College of Medicine, Hershey, PA 17033, United States of America. Electronic address: ageronimo@pennstatehealth.psu.edu.

Zachary Simmons (Z)

Department of Neurology, Penn State College of Medicine, Hershey, PA 17033, United States of America.

Classifications MeSH