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

Publication date

2020-11

Authors

Helleman, Jochem
Kruitwagen-van Reenen, Esther T
Bakers, Jaap N EORCID 0000-0001-9881-7710
Kruithof, WJ
van Groenestijn, Annerieke C
Jaspers Focks, Rineke J H
de Grund, Arthur
van den Berg, LeonardISNI 0000000388137302
Visser-Meily, Johanna MaISNI 0000000387554577
Beelen, AnitaORCID 0000-0002-1269-0710

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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.

Keywords

Amyotrophic lateral sclerosis, Dyspnea, Motor neuron disease, Patient-reported outcome measure, Respiratory function, Vital capacity, Clinical Neurology, Neurology, Journal Article

Citation

Helleman, J, Kruitwagen-van Reenen, E T, Bakers, J, Kruithof, W J, van Groenestijn, A C, Jaspers Focks, R J H, de Grund, A, van den Berg, L H, Visser-Meily, J M A & Beelen, A 2020, 'Using patient-reported symptoms of dyspnea for screening reduced respiratory function in patients with motor neuron diseases', Journal of Neurology, vol. 267, no. 11, pp. 3310-3318. https://doi.org/10.1007/s00415-020-10003-5