In-Patient Pulmonary Rehabilitation to Improve Asthma Control A Randomized Controlled Study (EPRA, Effectiveness of Pulmonary Rehabilitation for Patients with Asthma)

被引:29
作者
Schultz, Konrad [1 ]
Wittmann, Michael [1 ]
Wagner, Rupert [1 ]
Lehbert, Nicola [1 ]
Schwarzkopf, Larissa [2 ,6 ]
Szentes, Boglarka [2 ]
Nowak, Dennis [3 ]
Faller, Hermann [5 ]
Schuler, Michael [4 ]
机构
[1] Deutsch Rentenversicherung Bayern Sud, Clin Bad Reichenhall, Ctr Rehabil Pneumol & Orthoped, Bad Reichenhall, Germany
[2] Deutsch Forschungszentrum Gesundheit & Umwelt Gmb, Helmholtz Zentrum Munchen, Inst Hlth Econ & Hlth Care Management, Comprehens Pneumol Ctr Munich CPC M,German Ctr Lu, Munich, Germany
[3] Klinikum Univ Munchen, Inst & Poliklin Arbeits Sozial & Umweltmed, German Ctr Lung Res DZL, Comprehens Pneumol Ctr Munich CPC M, Munich, Germany
[4] Univ Wurzburg, Inst Clin Epidemiol & Biometry, Wurzburg, Germany
[5] Univ Wurzburg, Chair Rehabil Sci, Wurzburg, Germany
[6] IFT Inst Therapieforsch GmbH, Munich, Germany
来源
DEUTSCHES ARZTEBLATT INTERNATIONAL | 2021年 / 118卷 / 03期
关键词
ADULTS; QUESTIONNAIRE; PEOPLE; TRIAL;
D O I
10.3238/arztebl.m2021.0003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Despite the availability of effective pharmaceutical treatment options, many patients with asthma do not manage to control their illness. This randomized trial with a waiting-list control group examined whether a 3-week course of inpatient pulmonary rehabilitation (PR) improves asthma control (primary endpoint) and other secondary endpoints (e.g., quality of life, cardinal symptoms, mental stress). The subsequent observational segment of the study investigated the long-term outcome after PR. Methods: After approval of the rehabilitation' by the insurance providers (T0), 412 adults with uncontrolled asthma (Asthma Control Test [ACT] score < 20 points) undergoing rehabilitation were assigned to either the intervention group (IG) or the waiting-list control group (CG). PR commenced 1 month (T1) after randomization in the IG and 5 months after randomization (T3) in the CG. Asthma control and the secondary endpoints were assessed 3 months after PR in the IG (T3) as an intention-to-treat analysis by means of analyses of covariance. Moreover, both groups were observed for a period of 12 months after the end of PR. Results: At T3 the mean ACT score was 15.76 points in the CG, 20.38 points in the IG. The adjusted mean difference of 4.71 points was clinically relevant (95% confidence interval [3.99; 5.43]; effect size, Cohen's d = 1.27). The secondary endpoints also showed clinically relevant effects in favor of the IG. A year after the end of rehabilitation the mean ACT score was 19.00 points, still clinically relevant at 3.54 points higher than when rehabilitation began. Secondary endpoints such as quality of life and cardinal symptoms (dyspnea, cough, expectoration, pain) and self-management showed moderate to large effects. Conclusion: The trial showed that a 3-week course of PR leads to clinically relevant improvement in asthma control and secondary endpoints. Patients who do not achieve control of their asthma despite outpatient treatment therefore benefit from rehabilitation.
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页码:23 / +
页数:18
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