Abstract
Background Coronavirus disease 2019 (COVID-19) can result in a large variety of chronic health issues such as impaired lung function, reduced exercise performance and diminished quality of life. Our study aimed to investigate the efficacy, feasibility and safety of pulmonary rehabilitation in COVID-19 patients and to compare outcomes between patients with a mild/moderate and a severe/critical course of the disease.
Methods Patients in the post-acute phase of a mild to critical course of COVID-19 admitted to a comprehensive 3-week inpatient pulmonary rehabilitation programme were included in this prospective, observational cohort study. Several measures of exercise performance (6-min walk distance (6MWD)), lung function (forced vital capacity (FVC)) and quality of life (36-question short-form health survey (SF-36)) were assessed before and after pulmonary rehabilitation.
Results 50 patients were included in the study (24 with mild/moderate and 26 with severe/critical COVID-19). On admission, patients had a reduced 6MWD (mild: median 509 m, interquartile range (IQR) 426–539 m; severe: 344 m, 244–392 m), an impaired FVC (mild: 80%, 59–91%; severe: 75%, 60–91%) and a low SF-36 mental health score (mild: 49 points, 37–54 points; severe: 39 points, 30–53 points). Patients attended a median (IQR) 100% (94–100%) of all provided pulmonary rehabilitation sessions. At discharge, patients in both subgroups improved in 6MWD (mild/moderate: +48 m, 35–113 m; severe/critical: +124 m, 75–145 m; both p<0.001), FVC (mild/moderate: +7.7%, 1.0–17.8%, p=0.002; severe/critical: +11.3%, 1.0–16.9%, p<0.001) and SF-36 mental component (mild/moderate: +5.6 points, 1.4–9.2 points, p=0.071; severe/critical: +14.4 points, −0.6–24.5, p<0.001). No adverse event was observed.
Conclusion Our study shows that pulmonary rehabilitation is a feasible, safe and effective therapeutic option in COVID-19 patients independent of disease severity.
Abstract
Pulmonary rehabilitation is effective, feasible and safe to improve exercise performance, lung function and quality of life in patients with persistent impairments due to a mild to critical course of #COVID19 https://bit.ly/3kQFIbs
Footnotes
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This study is registered at www.clinicaltrials.gov with identifier number NCT04649918.
Data availability: A pseudonymised dataset will be made available upon reasonable request to the corresponding author. The request must include a statistical analysis plan.
Author contributions: R. Gloeckl, D. Leitl, T. Schneeberger, I. Jarosch, K. Kenn and A.R. Koczulla designed the study. R. Gloeckl, D. Leitl, T. Schneeberger, I. Jarosch and A.R. Koczulla were involved in recruiting patients and collecting the data. D. Leitl and R. Gloeckl verified the underlying data. R. Gloeckl and C. Nell performed statistical analyses. R. Gloeckl and D. Leitl drafted the manuscript. R. Gloeckl, D. Leitl, T. Schneeberger, I. Jarosch, C. Nell, N. Stenzel, C.F. Vogelmeier, K. Kenn and A.R. Koczulla provided scientific discussion and revised the initial draft. All authors had full access to all the data in the study and accept responsibility to submit for publication. All authors approved the final version of the manuscript.
Conflict of interest: R. Gloeckl has nothing to disclose.
Conflict of interest: D. Leitl has nothing to disclose.
Conflict of interest: I. Jarosch has nothing to disclose.
Conflict of interest: T. Schneeberger has nothing to disclose.
Conflict of interest: C. Nell has nothing to disclose.
Conflict of interest: N. Stenzel has nothing to disclose.
Conflict of interest: C.F. Vogelmeier has nothing to disclose.
Conflict of interest: K. Kenn has nothing to disclose.
Conflict of interest: A.R. Koczulla has nothing to disclose.
Support statement: This study was funded by own resources of the study centre (Schoen Klinik Berchtesgadener Land, Schoenau am Koenigssee, Germany) and did not receive any external funding.
- Received February 12, 2021.
- Accepted February 23, 2021.
- Copyright ©The authors 2021
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