Using patient-reported symptoms of dyspnea for screening reduced respiratory function in patients with motor neuron diseases

Jochem Helleman, Esther T Kruitwagen-van Reenen, J Bakers, Willeke J Kruithof, Annerieke C van Groenestijn, Rineke J H Jaspers Focks, Arthur de Grund, Leonard H van den Berg, Johanna M A Visser-Meily, Anita Beelen

Research output: Contribution to journalArticleAcademicpeer-review

14 Downloads (Pure)

Abstract

BACKGROUND: Poor monitoring of respiratory function may lead to late initiation of non-invasive ventilation (NIV) in patients with motor neuron diseases (MND). Monitoring could be improved by remotely assessing hypoventilation symptoms between clinic visits. We aimed to determine which patient-reported hypoventilation symptoms are best for screening reduced respiratory function in patients with MND, and compared them to the respiratory domain of the amyotrophic lateral sclerosis functional rating scale (ALSFRS-R).

METHODS: This prospective multi-center study included 100 patients with MND, who were able to perform a supine vital capacity test. Reduced respiratory function was defined as a predicted supine vital capacity ≤ 80%. We developed a 14-item hypoventilation symptom questionnaire (HYSQ) based on guidelines, expert opinion and think-aloud interviews with patients. Symptoms of the HYSQ were related to dyspnea, sleep quality, sleepiness/fatigue and pneumonia. The diagnostic performances of these symptoms and the ALSFRS-R respiratory domain were determined from the receiver operating characteristic (ROC) curves, area under the curve (AUC), sensitivity, specificity, predictive values and accuracy.

RESULTS: Dyspnea-related symptoms (dyspnea while eating/talking, while lying flat and during light activity) were combined into the MND Dyspnea Scale (MND-DS). ROC curves showed that the MND-DS had the best diagnostic performance, with the highest AUC = 0.72, sensitivity = 75% and accuracy = 71%. Sleep-quality symptoms, sleepiness/fatigue-related symptoms and the ALSFRS-R respiratory domain showed weak diagnostic performance.

CONCLUSION: The diagnostic performance of the MND-DS was better than the respiratory domain of the ALSFRS-R for screening reduced respiratory function in patients with MND, and is, therefore, the preferred method for (remotely) monitoring respiratory function.

Original languageEnglish
Pages (from-to)3310-3318
Number of pages9
JournalJournal of Neurology
Volume267
Issue number11
Early online date23 Jun 2020
DOIs
Publication statusPublished - Nov 2020

Keywords

  • Amyotrophic lateral sclerosis
  • Dyspnea
  • Motor neuron disease
  • Patient-reported outcome measure
  • Respiratory function
  • Vital capacity

Fingerprint

Dive into the research topics of 'Using patient-reported symptoms of dyspnea for screening reduced respiratory function in patients with motor neuron diseases'. Together they form a unique fingerprint.

Cite this