Survival of adults with rheumatoid arthritis associated interstitial lung disease - A systematic review and meta-analysis.

Interstitial lung disease Meta-analysis Rheumatoid arthritis Survival Systematic review

Journal

Seminars in arthritis and rheumatism
ISSN: 1532-866X
Titre abrégé: Semin Arthritis Rheum
Pays: United States
ID NLM: 1306053

Informations de publication

Date de publication:
06 2023
Historique:
received: 18 09 2022
revised: 16 01 2023
accepted: 02 03 2023
medline: 1 5 2023
pubmed: 19 3 2023
entrez: 18 3 2023
Statut: ppublish

Résumé

Rheumatoid arthritis associated interstitial lung disease (RA-ILD) is associated with high levels of morbidity and mortality. The primary aim of this systematic review was to determine the duration of survival, from time of diagnosis of RA-ILD. Medline (Ovid), Embase (OVID), CINAHL (EBSCO), PubMed, and the Cochrane Library were searched for studies that reported duration of survival from time of diagnosis of RA-ILD. Risk of bias of included studies was assessed based upon 4 domains of the Quality In Prognosis Studies tool. Results for median survival were presented by tabulation and discussed qualitatively. Meta-analysis of cumulative mortality at 1 year, >1y to ≤3 years, >3 years to ≤5 years, and >5 years to≤ 10 years was undertaken, for total RA-ILD population, and according to ILD pattern. 78 studies were included. Median survival for the total RA-ILD population ranged from 2 to 14 years. Pooled estimates for cumulative percentage mortality up to 1 year were 9.0% (95% CI 6.1, 12.5, I This review summarises the high mortality of RA-ILD, however the strength of conclusions that can be made is limited by the heterogeneity of the available studies, due to methodological and clinical factors. Further studies are needed to better understand the natural history of this condition.

Sections du résumé

BACKGROUND
Rheumatoid arthritis associated interstitial lung disease (RA-ILD) is associated with high levels of morbidity and mortality. The primary aim of this systematic review was to determine the duration of survival, from time of diagnosis of RA-ILD.
METHODS
Medline (Ovid), Embase (OVID), CINAHL (EBSCO), PubMed, and the Cochrane Library were searched for studies that reported duration of survival from time of diagnosis of RA-ILD. Risk of bias of included studies was assessed based upon 4 domains of the Quality In Prognosis Studies tool. Results for median survival were presented by tabulation and discussed qualitatively. Meta-analysis of cumulative mortality at 1 year, >1y to ≤3 years, >3 years to ≤5 years, and >5 years to≤ 10 years was undertaken, for total RA-ILD population, and according to ILD pattern.
RESULTS
78 studies were included. Median survival for the total RA-ILD population ranged from 2 to 14 years. Pooled estimates for cumulative percentage mortality up to 1 year were 9.0% (95% CI 6.1, 12.5, I
CONCLUSION
This review summarises the high mortality of RA-ILD, however the strength of conclusions that can be made is limited by the heterogeneity of the available studies, due to methodological and clinical factors. Further studies are needed to better understand the natural history of this condition.

Identifiants

pubmed: 36933302
pii: S0049-0172(23)00027-6
doi: 10.1016/j.semarthrit.2023.152187
pii:
doi:

Types de publication

Meta-Analysis Systematic Review Journal Article Review Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

152187

Informations de copyright

Copyright © 2023 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest LKS has received grants or contracts to from Health Research Council of New Zealand paid to their institution, royalties or licenses from UpToDate, and consulting fees from Pharmac paid to them and their institution. ELM has received royalties or licenses from UpToDate, consulting fees from Beohringer-Ingelheim and Alvotech Inc, Payment or honoraria for lectures, presentations, speakers bureaus, manuscript writing or educational events from Practice Point Communications/Simply Speaking, Beohringer-Ingelheim, Novartis, Participation on a Data Safety Monitoring Board or Advisory Board for Horizon Therapeutics and National Institute of Health USA, Leadership or fiduciary role in other board, society, committee or advocacy group, paid or unpaid The American College of Rheumatology.

Auteurs

H J Farquhar (HJ)

Department of Medicine, University of Otago, Christchurch, Christchurch, New Zealand. Electronic address: hamish.farquhar@cdhb.health.nz.

N Beckert (N)

Department of Medicine, University of Otago, Christchurch, Christchurch, New Zealand.

L Beckert (L)

Department of Medicine, University of Otago, Christchurch, Christchurch, New Zealand.

A L Edwards (AL)

Respiratory Department, Christchurch Hospital, Christchurch, New Zealand.

E L Matteson (EL)

Division of Rheumatology and Department of Health Sciences Research, Mayo Clinic College of Medicine, Rochester, Minnesota.

C Frampton (C)

Department of Medicine, University of Otago, Christchurch, Christchurch, New Zealand.

L K Stamp (LK)

Department of Medicine, University of Otago, Christchurch, Christchurch, New Zealand.

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Classifications MeSH