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Published on: February 14, 2022
Lung Volume Recruitment Slows Pulmonary Functional Decline and Prolongs Survival in ALS
Taiyo Kawaguchi1, Keisuke Yorimoto, Michiyuki Kawakami
1Department of Rehabilitation Medicine, Keio University School of Medicine, 35 Shinanomachi, Shinjuku-ku, Tokyo 160-8582, Japan (T.K., M.K., Y.M., D.N., T.T.); Department of Rehabilitation Medicine, National Center of Neurology and Psychiatry, Tokyo, Japan (T.K., K.Y., T.H., Y.M., D.N.); Department of Rehabilitation Medicine, The Jikei University School of Medicine, Tokyo, Japan (T.H.); Department of Nursing, National Center of Neurology and Psychiatry, Tokyo, Japan (A.H.); Department of Medical Cooperation and Welfare, National Center of Neurology and Psychiatry, Tokyo, Japan (A.H.); and Department of Neurology, National Center of Neurology and Psychiatry, Tokyo, Japan (Y. T.).
Lung volume recruitment (LVR) may slow respiratory decline and improve survival in amyotrophic lateral sclerosis (ALS) patients. Continued LVR use of six months or more showed a significant association with longer survival.
Area of Science:
- Neurology
- Pulmonology
- Respiratory Medicine
Background:
- Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease impacting respiratory function.
- Long-term effects of lung volume recruitment (LVR) in ALS patients remain under-examined.
- Understanding interventions that may impact ALS progression is crucial.
Purpose of the Study:
- To evaluate the long-term impact of LVR on respiratory function in ALS patients.
- To determine if LVR influences survival rates in individuals with ALS.
Main Methods:
- Retrospective cohort study of hospitalized ALS patients undergoing LVR between 2015-2020.
- Longitudinal assessment of forced vital capacity (%FVC) changes at 3-month intervals pre- and post-LVR.
- Survival analysis incorporating patient data including LVR duration.
Main Results:
- Forced vital capacity (%FVC) decline slowed from ~2% per month to <1% per month after LVR initiation.
- No significant %FVC decrease was observed at 3, 6, 9, or 12 months post-LVR.
- Patients using LVR for ≥6 months demonstrated longer survival, with LVR duration identified as a prognostic factor (HR=0.42).
Conclusions:
- Continued LVR use is associated with a slower rate of respiratory decline in ALS.
- Prolonged LVR (≥6 months) may be linked to improved survival outcomes in ALS patients.
- Further prospective research is recommended to validate these findings.
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