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Ann Rheum Dis. 2018;77(5):644-649.

Prophylactic effect of trimethoprim-sulfamethoxazole for pneumocystis pneumonia in patients with rheumatic diseases exposed to prolonged high-dose glucocorticoids.

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제1저자 박준원 · 교신저자 이은봉

소속 (4)
  1. Division of Rheumatology, Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea.
  2. Division of Clinical Immunology and Rheumatology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
  3. Division of Nephrology, Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea.
  4. Seoul Kidney Clinic, Seoul, Republic of Korea.

Abstract

OBJECTIVES To investigate the efficacy and safety of trimethoprim/sulfamethoxazole (TMP-SMX) as primary prophylaxis for pneumocystis pneumonia (PCP) in patients with rheumatic diseases receiving high-dose steroids.

METHODS The study included 1522 treatment episodes with prolonged (≥4 weeks) high-dose (≥30 mg/day prednisone) steroids in 1092 patients over a 12-year period. Of these, 262 treatment episodes involved TMP-SMX (prophylaxis group) while other episodes involved no prophylaxis (control group). Differences in 1-year PCP incidence and its mortality between the two groups were estimated using Cox regression. To minimise baseline imbalance, propensity score matching was performed and efficacy outcome was mainly assessed in the postmatched population (n=235 in both groups).

RESULTS During a total of 1474.4 person-years, 30 PCP cases occurred with a mortality rate of 36.7%. One non-fatal case occurred in the prophylaxis group. TMP-SMX significantly reduced the 1-year PCP incidence (adjusted HR=0.07(95% CI 0.01 to 0.53)) and related mortality (adjusted HR=0.08 (95% CI 0.0006 to 0.71)) in the postmatched population. The result of the same analysis performed in the whole population was consistent with that of the primary analysis. Incidence rate of adverse drug reactions (ADR) related to TMP-SMX was 21.2 (14.8-29.3)/100 person-years. Only two serious ADRs (including one Stevens-Johnson syndrome case) occurred. The number needed to treat for preventing one PCP (52 (33-124)) was lower than the number needed to harm for serious ADR (131 (55-∞)).

CONCLUSION TMP-SMX prophylaxis significantly reduces the PCP incidence with a favourable safety profile in patients with rheumatic disease receiving prolonged, high-dose steroids.

© Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted.

Keywords

autoimmune diseasescorticosteroidsepidemiologyinfectionsoutcomes research

Figures

Figure 1
Figure 1 Kaplan-Meier curve showing pneumocystis pneumonia (PCP)-free survival according to the initial dose of steroids (30–45 mg/day prednisone, 45–60 mg/day and ≥60 mg/day) in the whole population. PD, prednisone.

그림 출처: PubMed Central 공개 논문 (PMC5909751)

Comment · 정정

Conflict of interest statement

Competing interests: EBL has acted as a consultant to Pfizer, and received research grants from Green Cross Corp and Hanmi Pharm Company. The other authors declare no conflicts of interest.

그 밖의 정보
출판 형태
Evaluation Study, Journal Article, Research Support, Non-U.S. Gov't
저널
Annals of the rheumatic diseases · eISSN 1468-2060
전자 출판
2017-11-01
MeSH
Adult · Antifungal Agents / therapeutic use · Female · Glucocorticoids / administration & dosage / adverse effects · Humans · Incidence · Male · Middle Aged · Pneumonia, Pneumocystis / chemically induced / epidemiology / prevention & control · Propensity Score · Retrospective Studies · Rheumatic Diseases / drug therapy · Time Factors · Trimethoprim, Sulfamethoxazole Drug Combination / therapeutic use
Substances
Antifungal Agents · Glucocorticoids · Trimethoprim, Sulfamethoxazole Drug Combination
참고문헌
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