Jinno Sadao, Akashi Kengo, Onishi Akira, Nose Yoko, Yamashita Mai, Saegusa Jun
Department of Rheumatology and Clinical Immunology, University Graduate School of Medicine, 7-5-2 Kusunoki-chou, Kobe, Hyogo, 650-0017, Japan.
Department of Advanced Medicine for Rheumatic Diseases, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Rheumatol Int. 2022 Aug;42(8):1403-1409. doi: 10.1007/s00296-021-04945-w. Epub 2021 Jul 14.
We compared the prophylactic effect of trimethoprim-sulfamethoxazole (TMP-SMX) with atovaquone for pneumocystis pneumonia (PCP) in patients with connective tissue diseases (CTDs) receiving high-dose glucocorticoids. Patients with CTDs aged ≥ 18 years who were treated with a prolonged course (≥ 4 weeks) of glucocorticoids (≥ 20 mg/day prednisone) in a Japanese tertiary center between 2013 and 2017 were included. The patients were categorized into two groups: TMP-SMX and atovaquone group. Adjusted cumulative incidence of PCP was compared between the two groups after propensity score weighting for differences in confounding factors. A total of 480 patients with a prolonged high-dose glucocorticoid treatment were identified. Out of 383 patients with TMP-SMX prophylaxis, 102 (26.8%) patients experienced adverse events leading to discontinuation within 4 weeks of initiation, while no patient in the atovaquone discontinued the therapy. Two hundred eighty-one patients received TMP-SMX, while 107 received atovaquone for PCP prophylaxis. During a total of 397.0 person-years, 7 PCP cases (2 in the TMP-SMX, 5 in the atovaquone) occurred with a mortality rate of 54.5%. After adjusting for differences in baseline characteristics, the adjusted cumulative incidence of PCP was similar between the two group (HR 0.97, 95% CI 0.19-5.09, p = 0.97). Prophylactic effects for PCP in CTDs patients receiving prolonged high-dose glucocorticoids were similar between TMP-SMX and atovaquone. Atovaquone was well-tolerated with no side effects.
我们比较了甲氧苄啶-磺胺甲恶唑(TMP-SMX)与阿托伐醌对接受大剂量糖皮质激素治疗的结缔组织病(CTD)患者预防肺孢子菌肺炎(PCP)的效果。纳入了2013年至2017年期间在日本一家三级中心接受延长疗程(≥4周)糖皮质激素(≥20mg/天泼尼松)治疗的年龄≥18岁的CTD患者。患者被分为两组:TMP-SMX组和阿托伐醌组。在对混杂因素差异进行倾向评分加权后,比较两组PCP的调整累积发病率。共确定了480例接受延长疗程大剂量糖皮质激素治疗的患者。在383例接受TMP-SMX预防的患者中,102例(26.8%)患者在开始治疗后4周内出现不良事件导致停药,而阿托伐醌组没有患者停药。281例患者接受TMP-SMX预防,107例接受阿托伐醌预防PCP。在总共397.0人年的时间里,发生了7例PCP病例(TMP-SMX组2例,阿托伐醌组5例),死亡率为54.5%。在调整基线特征差异后,两组PCP的调整累积发病率相似(HR 0.97,95%CI 0.19 - 5.09,p = 0.97)。TMP-SMX和阿托伐醌对接受延长疗程大剂量糖皮质激素治疗的CTD患者预防PCP的效果相似。阿托伐醌耐受性良好,无副作用。