Bettine Ah Vosse, Leandre André la Fontaine, Nicolle Cobben, Danielle Kock-Cordeiro, Anda Hazenberg, Michael Gaytant, P J Wijkstra, Catharina Faber
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引用次数: 0
Abstract
Myotonic dystrophy type 1 (DM1) frequently leads to chronic respiratory failure, yet the effectiveness of noninvasive home mechanical ventilation (HMV) remains understudied. Our objective was to assess the effects of HMV on gas exchange, health-related quality of life (HRQL), and daily functioning, and to explore baseline predictors of treatment response. A prospective multicenter study was conducted in which clinical data, pulmonary function tests, blood gas analysis, polysomnography and overnight pulse oximetry with transcutaneous CO2 monitoring, and validated questionnaires were collected at baseline and after six months of treatment. Paired t-tests and correlation analyses assessed treatment outcomes and predictive factors. Forty participants (mean age 46.6 years, 63% male) were enrolled, and follow-up data of 38 participants were available for analysis. After six months of treatment, significant improvements in gas exchange were observed with a reduction in daytime pCO2 of 0.48 ± 0.81 kPa (p = 0.001) and nocturnal mean pCO2 of 0.92 ± 0.81 kPa (p < 0.001). HRQL, assessed with the Severe Respiratory Insufficiency (SRI) questionnaire, improved significantly, with a mean increase of 9.9 ± 8.9 points (p < 0.001).No significant changes were seen in daily functioning measured with the DM1-ActivC questionnaire. Improvements in nocturnal pCO2 correlated with HRQL gains (r = 0.427, p < 0.021), while baseline characteristics were not predictive of response. This prospective multicenter study demonstrates that nocturnal HMV is associated with significant improvements in gas exchange and HRQL in patients with DM1 over six months.
期刊介绍:
The Journal of Neuromuscular Diseases aims to facilitate progress in understanding the molecular genetics/correlates, pathogenesis, pharmacology, diagnosis and treatment of acquired and genetic neuromuscular diseases (including muscular dystrophy, myasthenia gravis, spinal muscular atrophy, neuropathies, myopathies, myotonias and myositis). The journal publishes research reports, reviews, short communications, letters-to-the-editor, and will consider research that has negative findings. The journal is dedicated to providing an open forum for original research in basic science, translational and clinical research that will improve our fundamental understanding and lead to effective treatments of neuromuscular diseases.