Sue Soichiro, Sasaki Tomohiko, Kaneko Hiroaki, Irie Kuniyasu, Kondo Masaaki, Maeda Shin
Department of Gastroenterology Yokohama City University Graduate School of Medicine Yokohama Japan.
JGH Open. 2021 Jan 23;5(2):307-311. doi: 10.1002/jgh3.12492. eCollection 2021 Feb.
To assess the efficacy and safety of 7-day rescue treatment consisting of a vonoprazan (VPZ), metronidazole (MNZ), and sitafloxacin (STFX) regimen (VPZ-MNZ-STFX therapy) in patients with penicillin allergy.
This was a registered prospective intervention study. Patients with penicillin allergy who were diagnosed with infection and had a history of eradication were eligible for inclusion. Seventeen patients were prospectively treated with VPZ 20 mg bid, MNZ 250 mg bid, and STFX 100 mg bid for 7 days. Safety was evaluated using a questionnaire on adverse effects.
The eradication rate of 7-day VPZ-MNZ-SFTX therapy was 88.2% (95% confidence interval: 63.6-98.5%; = 17) in both intention-to-treat and per-protocol analyses. On the questionnaire, 25% of patients reported experiencing diarrhea, with a score of 2 or 3. All patients undergoing VPZ-MNZ-STFX therapy completed 100% of their medication course.
Rescue eradication with VPZ-MNZ-STFX therapy is effective and well tolerated in patients with penicillin allergy (UMIN000016335, jRCTs031180133).
评估由沃克拉唑(VPZ)、甲硝唑(MNZ)和西他沙星(STFX)组成的7天挽救治疗方案(VPZ-MNZ-STFX疗法)在青霉素过敏患者中的疗效和安全性。
这是一项注册前瞻性干预研究。被诊断为感染且有根除治疗史的青霉素过敏患者符合纳入标准。17例患者前瞻性地接受VPZ 20mg每日两次、MNZ 250mg每日两次和STFX 100mg每日两次治疗7天。使用不良反应问卷评估安全性。
在意向性分析和符合方案分析中,7天VPZ-MNZ-SFTX疗法的根除率均为88.2%(95%置信区间:63.6-98.5%;n=17)。在问卷中,25%的患者报告有腹泻,评分为2或3分。所有接受VPZ-MNZ-STFX治疗的患者均完成了100%的疗程。
VPZ-MNZ-STFX疗法的挽救性根除治疗对青霉素过敏患者有效且耐受性良好(UMIN000016335,jRCTs031180133)。