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类风湿关节炎相关间质性肺疾病成年患者的生存率——一项系统评价和荟萃分析。

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

作者信息

Farquhar H J, Beckert N, Beckert L, Edwards A L, Matteson E L, Frampton C, Stamp L K

机构信息

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

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

出版信息

Semin Arthritis Rheum. 2023 Jun;60:152187. doi: 10.1016/j.semarthrit.2023.152187. Epub 2023 Mar 9.

Abstract

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 88.9%), >1 to ≤3 years 21.4% (17.3, 25.9, I 85.7%), >3 to ≤ 5 years 30.2% (24.8, 35.9, I 87.7%), and > 5 to ≤ 10 years 49.1% (40.6, 57.7 I 85.0%). Heterogeneity was high. Only 15 studies were rated as low risk of bias in all 4 domains assessed.

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.

摘要

背景

类风湿关节炎相关间质性肺疾病(RA - ILD)与高发病率和死亡率相关。本系统评价的主要目的是确定自RA - ILD诊断之时起的生存时长。

方法

检索了Medline(Ovid)、Embase(OVID)、CINAHL(EBSCO)、PubMed和Cochrane图书馆,查找报告自RA - ILD诊断之时起生存时长的研究。根据“预后研究质量”工具的4个领域评估纳入研究的偏倚风险。以表格形式呈现中位生存结果并进行定性讨论。对整个RA - ILD人群以及根据ILD模式,在1年、>1年至≤3年、>3年至≤5年和>5年至≤10年时的累积死亡率进行荟萃分析。

结果

纳入78项研究。整个RA - ILD人群的中位生存时长为2至14年。1年时累积死亡率的合并估计值为9.0%(95%置信区间6.1, 12.5,I² 88.9%),>1年至≤3年为21.4%(17.3, 25.9,I² 85.7%),>3年至≤5年为30.2%(24.8, 35.9,I² 87.7%),>5年至≤10年为49.1%(40.6, 57.7,I² 85.0%)。异质性较高。在评估的所有4个领域中,只有15项研究被评为低偏倚风险。

结论

本综述总结了RA - ILD的高死亡率,然而,由于方法学和临床因素,现有研究的异质性限制了可得出结论的力度。需要进一步研究以更好地了解这种疾病的自然史。

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