4.4 Article

Intravenous cyclophosphamide in acute exacerbation of rheumatoid arthritis-related interstitial lung disease: A propensity-matched analysis using a nationwide inpatient database

期刊

SEMINARS IN ARTHRITIS AND RHEUMATISM
卷 51, 期 5, 页码 977-982

出版社

W B SAUNDERS CO-ELSEVIER INC
DOI: 10.1016/j.semarthrit.2021.07.008

关键词

Rheumatoid arthritis; Interstitial lung disease; Cyclophosphamide; Mortality; Administrative data; Propensity score matching

资金

  1. Ministry of Health, Labour and Welfare, Japan [19AA2007, 20AA2005]
  2. Minis-try of Education, Culture, Sports, Science and Technology, Japan [20H03907]

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The study aimed to investigate the effect of intravenous cyclophosphamide (CYC) as initial therapy in patients with acute exacerbation of rheumatoid arthritis-related interstitial lung disease. The results showed that CYC did not demonstrate a survival benefit in this patient population but was associated with a higher proportion of platelet transfusion.
Objectives: We aimed to investigate the effect of intravenous cyclophosphamide (CYC) as the initial therapy in patients with acute exacerbation of rheumatoid arthritis-related interstitial lung disease. Methods: This was a retrospective observational study. Using the Japanese Diagnosis Procedure Combination inpatient database from July 2010 to March 2018, we identified patients with acute exacerbation of rheumatoid arthritis-related interstitial lung disease (RA-ILD) who received high-dose methylprednisolone within 3 days after admission. RA-ILD was defined as having either the diagnosis of RA-ILD or the diagnoses of both RA and ILD, based on the ICD-10 codes recorded by attending physicians. Patients were divided into two groups: those receiving intravenous CYC within 3 days after admission (CYC group) and those who did not (control group). One-to-four propensity-score matching analyses were performed. Results: A total of 6130 eligible patients were included. After propensity score matching, 129 patients in the CYC group and 516 patients in the control group were further analyzed. 90-day in-hospital mortality, defined as all-cause mortality during hospitalization within 90 days after admission, was not significantly different between the CYC and control groups (50.4% versus 42.2%, hazard ratio 1.20, 95% confidence interval 0.91-1.58). A larger proportion of patients in the CYC group received platelet transfusion than that in the control group (7.0% versus 2.3%, odds ratio 3.05, 95% confidence interval 1.20-7.73). Conclusion: In this retrospective database study, the initial therapy with CYC did not show a survival benefit in patients with acute exacerbation of RA-ILD. CYC was associated with a larger proportion of platelet transfusion. (c) 2021 Elsevier Inc. All rights reserved.

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