Abe Yoshiyuki, Fujibayashi Kazutoshi, Nishizaki Yuji, Yanagisawa Naotake, Nojiri Shuko, Nakano Soichiro, Tada Kurisu, Yamaji Ken, Tamura Naoto
Department of Internal Medicine and Rheumatology, Juntendo University School of Medicine, Bunkyo-ku, Tokyo 113-8421, Japan.
Acta Med Okayama. 2019 Feb;73(1):85-89. doi: 10.18926/AMO/56464.
Pneumocystis pneumonia (PCP) due to Pneumocystis jirovecii infection is the leading cause of fatal opportunistic infections in immunocompromised patients. We will determine whether a daily sulfamethoxazole-trimethoprim (SMX/TMP) dose of 200/40 mg was non-inferior to 400/80 mg for PCP prevention in patients with systemic rheumatic disease under immunosuppressive therapy. This is a randomized, open-label, multicenter controlled trial. The primary outcome is the rate of PCP prevention at 52 weeks. The secondary outcome is the discontinuation rate of SMX/TMP. The trial will evaluate the optimal dose of SMX/TMP for PCP prevention in patients with systemic rheumatic disease under immunosuppressive therapy.
由耶氏肺孢子菌感染引起的肺孢子菌肺炎(PCP)是免疫功能低下患者致命性机会性感染的主要原因。我们将确定对于接受免疫抑制治疗的系统性风湿性疾病患者,每日200/40毫克的磺胺甲恶唑-甲氧苄啶(SMX/TMP)剂量在预防PCP方面是否不劣于400/80毫克。这是一项随机、开放标签、多中心对照试验。主要结局是52周时PCP的预防率。次要结局是SMX/TMP的停药率。该试验将评估接受免疫抑制治疗的系统性风湿性疾病患者预防PCP的SMX/TMP最佳剂量。