Mile Bosilkovski, Valerija Kirova, Krsto Grozdanovski, Ivan Vidinic, Ilir Demiri, Nikola Labacevski
University Clinic for Infectious Diseases and Febrile Conditions, Skopje, Republic of Macedonia.
Trop Doct. 2012 Jan;42(1):13-7. doi: 10.1258/td.2011.110284.
This prospective, non-randomized trial, compared the efficacy and tolerance of a doxycycline-rifampin regimen, administered for 45 days, versus doxycycline-rifampin given for 45 days plus gentamicin for the first 7-10 days, in the treatment of human brucellosis. Of 238 patients that were initially included in the study, 181 were finally evaluated. Ninety-four were treated with the doxycycline-rifampin and 87 with the doxycycline-rifampin-gentamicin regimens. In the doxycycline-rifampin group: relapses were noted in 13 (13.8%) patients; therapeutic failures in five (5.3%); and mild adverse effects in 28 (29.8%). In the doxycycline-rifampin-gentamicin group: four (4.6%) relapsed; and five (5.7%) therapeutic failures were registered. Mild adverse effects were registered in 29 (33.3%) patients. The doxycycline-rifampin-gentamicin regimen demonstrated a significantly lower relapse rate compared to the doxycycline-rifampin combination (P = 0.034). We conclude that adding gentamicin for the first 7-10 days to the standard oral doxycycline-rifampin regimen can decrease the rate of relapses.
这项前瞻性、非随机试验比较了为期45天的强力霉素-利福平治疗方案与为期45天的强力霉素-利福平联合头7至10天加用庆大霉素的方案在治疗人类布鲁氏菌病方面的疗效和耐受性。在最初纳入研究的238例患者中,最终对181例进行了评估。94例接受强力霉素-利福平治疗,87例接受强力霉素-利福平-庆大霉素治疗方案。在强力霉素-利福平组:13例(13.8%)患者出现复发;5例(5.3%)治疗失败;28例(29.8%)出现轻度不良反应。在强力霉素-利福平-庆大霉素组:4例(4.6%)复发;5例(5.7%)治疗失败。29例(33.3%)患者出现轻度不良反应。与强力霉素-利福平联合方案相比,强力霉素-利福平-庆大霉素方案的复发率显著降低(P = 0.034)。我们得出结论,在标准口服强力霉素-利福平方案的头7至10天加用庆大霉素可降低复发率。