The role of pulmonary rehabilitation in idiopathic pulmonary fibrosis: An overview of systematic reviews

被引:2
作者
Song, Shangyue [1 ,2 ]
Feng, Zhenzhen [1 ,2 ,3 ]
Liu, Wenrui [1 ,2 ]
Li, Jiansheng [1 ,2 ,3 ]
机构
[1] Henan Univ Chinese Med, Clin Med Coll 1, Zhengzhou, Henan, Peoples R China
[2] Henan Univ Chinese Med, Coconstruct Collaborat Innovat Ctr Chinese Med & R, Henan & Educ Minist PR China, Zhengzhou, Henan, Peoples R China
[3] Henan Univ Chinese Med, Affiliated Hosp 1, Dept Resp Dis, Zhengzhou, Henan, Peoples R China
来源
PLOS ONE | 2023年 / 18卷 / 12期
关键词
MANAGEMENT;
D O I
10.1371/journal.pone.0295367
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background The role of pulmonary rehabilitation (PR) in idiopathic pulmonary fibrosis (IPF) has been studied in several systematic reviews (SRs), but no definitive conclusions have been drawn due to the wide variation in the quality and outcomes of the studies. And there are no studies to assess the quality of relevant published SRs. This overview aims to determine the effectiveness of PR in patients with IPF and to summarize and critically evaluate the risk of bias, methodological, and evidence quality of SRs on this related topic.Methods With no language restrictions, eight databases were searched from inception to March 10, 2023. The literature search, screening, and data extraction were carried out separately by two reviewers. We assessed the risk of bias using the ROBIS tool, the reporting quality using PRISMA statements, the methodological quality using AMSTAR-2, and the evidence quality using Grades of Recommendations, Assessment, Development, and Evaluation (GRADE).Results Seven SRs from 2018-2023 (including 1836 participants) on PR for the treatment of IPF were selected, all of which included patients with a definitive diagnosis of IPF. After strict evaluation by the ROBIS tool and AMSTAR-2 tool, 42.86% of the SRs had a high risk of bias and 85.71% of the SRs had critically low methodological quality in this overview. PR might be effective for patients with IPF on exercise capacity, quality of life, and pulmonary function-related outcomes, but we did not find high quality evidence to confirm the effectiveness.Conclusion PR may appear to be an effective and safe treatment for patients with IPF, but the results of this overview should be interpreted dialectically and with caution. Further high-quality, rigorous studies are urgently needed to draw definitive conclusions and provide scientific evidence.
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