TY - JOUR
T1 - Clinical course of patients with rheumatoid arthritis who continue or discontinue biologic therapy after hospitalization for infection
T2 - a retrospective observational study
AU - Kashiwado, Yusuke
AU - Kiyohara, Chikako
AU - Kimoto, Yasutaka
AU - Nagano, Shuji
AU - Sawabe, Takuya
AU - Oryoji, Kensuke
AU - Mizuki, Shinichi
AU - Nishizaka, Hiroaki
AU - Yoshizawa, Seiji
AU - Yoshizawa, Shigeru
AU - Tsuru, Tomomi
AU - Inoue, Yasushi
AU - Ueda, Naoyasu
AU - Ota, Shun ichiro
AU - Suenaga, Yasuo
AU - Miyamura, Tomoya
AU - Tada, Yoshifumi
AU - Niiro, Hiroaki
AU - Akashi, Koichi
AU - Horiuchi, Takahiko
N1 - Funding Information:
TH has received research grant support from Mitsubishi-Tanabe Pharma, Chugai Pharma, Astellas Pharma, Bristol-Myers Squibb, Takeda Industrial Pharma, Eli Lilly and Company, CSL Behring KK, Asahi-Kasei Pharma, Santen Pharma, Teijin Pharma, and Daiichi-Sankyo. TM has received research grant support from Mitsubishi-Tanabe Pharma, Chugai Pharma, Pfizer, and AbbVie Pharma. YT received research grants and speaker’s fees from Chugai Pharmaceutical. HN has received research grant support from Astellas Pharma, Chugai Pharmaceutical, Daiichi-Sankyo, and Asahi-kasei Pharma. The other authors have no conflict of interest to disclose.
Publisher Copyright:
© 2022, The Author(s).
PY - 2022/12
Y1 - 2022/12
N2 - Background: To analyse the subsequent clinical course of patients with rheumatoid arthritis (RA) who either continued or discontinued biologic agents after hospitalization for infections. Methods: We retrospectively reviewed the clinical records of 230 RA patients with 307 hospitalizations for infections under biologic therapy between September 2008 and May 2014 in 15 institutions for up to 18 months after discharge. The risks of RA flares and subsequent hospitalizations for infections from 61 days to 18 months after discharge were evaluated. Results: Survival analyses indicated that patients who continued biologic therapy had a significantly lower risk of RA flares (31.4% vs. 60.6%, P < 0.01) and a slightly lower risk of subsequent infections (28.7% vs. 34.5%, P = 0.37). Multivariate analysis showed that discontinuation of biologic therapy, diabetes, and a history of hospitalization for infection under biologic therapy were associated with RA flares. Oral steroid therapy equivalent to prednisolone 5 mg/day or more and chronic renal dysfunction were independent risk factors for subsequent hospitalizations for infections. Conclusions: Discontinuation of biologic therapy after hospitalization for infections may result in RA flares. Continuation of biologic therapy is preferable, particularly in patients without immunodeficiency.
AB - Background: To analyse the subsequent clinical course of patients with rheumatoid arthritis (RA) who either continued or discontinued biologic agents after hospitalization for infections. Methods: We retrospectively reviewed the clinical records of 230 RA patients with 307 hospitalizations for infections under biologic therapy between September 2008 and May 2014 in 15 institutions for up to 18 months after discharge. The risks of RA flares and subsequent hospitalizations for infections from 61 days to 18 months after discharge were evaluated. Results: Survival analyses indicated that patients who continued biologic therapy had a significantly lower risk of RA flares (31.4% vs. 60.6%, P < 0.01) and a slightly lower risk of subsequent infections (28.7% vs. 34.5%, P = 0.37). Multivariate analysis showed that discontinuation of biologic therapy, diabetes, and a history of hospitalization for infection under biologic therapy were associated with RA flares. Oral steroid therapy equivalent to prednisolone 5 mg/day or more and chronic renal dysfunction were independent risk factors for subsequent hospitalizations for infections. Conclusions: Discontinuation of biologic therapy after hospitalization for infections may result in RA flares. Continuation of biologic therapy is preferable, particularly in patients without immunodeficiency.
UR - http://www.scopus.com/inward/record.url?scp=85131157924&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85131157924&partnerID=8YFLogxK
U2 - 10.1186/s13075-022-02820-y
DO - 10.1186/s13075-022-02820-y
M3 - Article
C2 - 35650638
AN - SCOPUS:85131157924
SN - 1478-6354
VL - 24
JO - Arthritis Research and Therapy
JF - Arthritis Research and Therapy
IS - 1
M1 - 131
ER -