Scientific Reports (Mar 2025)

Provision, cough efficacy and treatment satisfaction of mechanical insufflation-exsufflation in a large multicenter cohort of patients with amyotrophic lateral sclerosis

  • André Maier,
  • Dagmar Kettemann,
  • Ute Weyen,
  • Torsten Grehl,
  • Peter Caspar Schulte,
  • Robert Steinbach,
  • Annekathrin Rödiger,
  • Patrick Weydt,
  • Susanne Petri,
  • Joachim Wolf,
  • Julian Grosskreutz,
  • Jan Christoph Koch,
  • Jochen H. Weishaupt,
  • Simone Rosseau,
  • Jenny Norden,
  • Peter Körtvélyessy,
  • Birgit Koch,
  • Teresa Holm,
  • Barbara Hildebrandt,
  • Peggy Schumann,
  • Bertram Walter,
  • Alessio Riitano,
  • Christoph Münch,
  • Thomas Meyer,
  • Susanne Spittel

DOI
https://doi.org/10.1038/s41598-025-91692-8
Journal volume & issue
Vol. 15, no. 1
pp. 1 – 14

Abstract

Read online

Abstract In patients with amyotrophic lateral sclerosis (ALS), mechanical insufflation-exsufflation (MI-E) addresses cough deficiency to achieve major therapeutic goals: improving costal muscle and joint function, reducing atelectasis through insufflation, and clearing bronchial secretions via exsufflation. Despite its perceived benefits, there is limited systematic research on MI-E provision, symptom alleviation, or patient satisfaction. The research platform Ambulanzpartner coordinated this longitudinal observational study conducted in 12 German ALS centers from July 2018 to September 2023. Patients were enrolled based on ALS-related cough deficiency requiring MI-E therapy. The study recorded provision, reasons for withholding MI-E, clinical parameters, therapy frequency, subjective cough deficiency, and symptomatic relief. Satisfaction with MI-E therapy was determined by the likelihood of recommendation. Out of 694 ALS patients indicated for MI-E, 527 (75.9%) received the therapy. The primary reason for non-provision was that the patient had died before provision (n = 66 of 167; 39.5%). These patients were significantly more affected as represented by higher progression rates and lower cough peak flows (CPF) at the time of MI-E indication (p < 0.05). Most patients who received MI-E used it daily (n = 290 of 370; 78.4%). Self-assessed cough deficiency correlated with clinical measurements, especially for patients with higher deficits. At follow-up visits, patients reported reduced cough deficiency (p < 0.001). Frequent MI-E use was linked to greater symptom relief and higher likelihood of recommending the therapy. This study highlights the symptomatic and palliative potential of MI-E therapy for ALS patients.