Article Text
Abstract
Objectives We aimed to assess the available evidence for corticosteroids in fibrotic interstitial lung disease (fILD) to inform the randomised embedded multifactorial adaptive platform ILD.
Design Systematic review and meta-analysis.
Data sources We searched Embase, Medline, Cochrane CENTRAL and Web of Science databases from inception to April 17 2023.
Eligibility criteria We included studies that compared corticosteroids with standard care, placebo or no treatment in adult patients with fILD.
Data extraction and synthesis We report on the change in forced vital capacity (FVC) and mortality. We used random-effects meta-analysis to estimate relative risk (RR) for dichotomous outcomes, and mean difference (MD) and standardised MDs for continuous outcomes, with 95% CIs.
Results Of the 13 229 unique citations identified, we included 10 observational studies comprising 1639 patients. Corticosteroids had an uncertain effect on mortality compared with no treatment (RR 1.03 (95% CI 0.85 to 1.25); very low certainty evidence). The effect of corticosteroids on the rate of decline in FVC (% predicted) was uncertain when compared with no treatment (MD 4.29% (95% CI −8.26% to 16.83%); very low certainty evidence). However, corticosteroids might reduce the rate of decline in FVC in patients with non-idiopathic pulmonary fibrosis (IPF) fILD (MD 10.89% (95% CI 5.25% to 16.53%); low certainty evidence), while an uncertain effect was observed in patients with IPF (MD −3.80% (95% CI −8.94% to 1.34%); very low certainty evidence).
Conclusions The current evidence on the efficacy and safety of corticosteroids in fILD is limited and of low certainty. Randomised trials are needed to address this significant research gap.
- Interstitial Fibrosis
- Systemic disease and lungs
- Clinical Epidemiology
Data availability statement
Data are available on reasonable request.
This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
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Data availability statement
Data are available on reasonable request.
Supplementary materials
Supplementary Data
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Footnotes
Twitter @IPFdoc
Collaborators On behalf of the REMAP-ILD consortium collaborators listed in online supplemental file 1.
Contributors TP, LK-D, GJ and DZ came up with the study design, methods and data collection methods. TP, GVK, DL, GL and CZ screened titles and abstracts, full text and collected data. TP analysed and performed risk of bias and GRADE assessments in duplicate with DZ. TP wrote the first draft. WA, MF-C, MK, IS, CJR, LK-D and GJ provided content expertise, critical appraisal of the manuscript and helped write the final draft. DZ supervised the study. TP is the data guarantor.
Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.
Competing interests None declared.
Patient and public involvement Patients and/or the public were not involved in the design, or conduct, or reporting, or dissemination plans of this research.
Provenance and peer review Not commissioned; externally peer reviewed.
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