Division of Rheumatology, Department of Internal Medicine, Seoul National University College of Medicine, Seoul, Republic of Korea.
Division of Clinical Immunology and Rheumatology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Ann Rheum Dis. 2018 May;77(5):644-649. doi: 10.1136/annrheumdis-2017-211796. Epub 2017 Nov 1.
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.
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).
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-∞)).
TMP-SMX prophylaxis significantly reduces the PCP incidence with a favourable safety profile in patients with rheumatic disease receiving prolonged, high-dose steroids.
研究复方磺胺甲噁唑(TMP-SMX)作为风湿性疾病患者接受大剂量类固醇治疗时预防卡氏肺孢子虫肺炎(PCP)的疗效和安全性。
本研究纳入了 1092 例患者 1522 个疗程的长期(≥4 周)大剂量(≥30mg/天泼尼松)类固醇治疗,其中 262 个疗程使用 TMP-SMX(预防组),而其他疗程未使用预防措施(对照组)。使用 Cox 回归估计两组患者 1 年 PCP 发生率及其死亡率的差异。为了最小化基线不平衡,进行了倾向评分匹配,主要在匹配后的人群(每组 235 人)中评估疗效结果。
在总共 1474.4 人年中,发生了 30 例 PCP 病例,死亡率为 36.7%。预防组发生了 1 例非致命病例。TMP-SMX 显著降低了匹配后人群(调整后的 HR=0.07(95%CI 0.01 至 0.53))和相关死亡率(调整后的 HR=0.08(95%CI 0.0006 至 0.71))的 1 年 PCP 发生率。在全人群中进行的相同分析结果与主要分析结果一致。与 TMP-SMX 相关的药物不良反应(ADR)发生率为 21.2(14.8-29.3)/100 人年。仅发生了 2 例严重 ADR(包括 1 例 Stevens-Johnson 综合征病例)。预防 1 例 PCP 所需的治疗人数(52(33-124))低于严重 ADR 所需的治疗人数(131(55-∞))。
在接受长期大剂量类固醇治疗的风湿性疾病患者中,TMP-SMX 预防可显著降低 PCP 发生率,且安全性良好。