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多西环素-利福平与多西环素-利福平-庆大霉素治疗人类布鲁氏菌病的比较

Doxycycline-rifampin versus doxycycline-rifampin-gentamicin in treatment of human brucellosis.

作者信息

Mile Bosilkovski, Valerija Kirova, Krsto Grozdanovski, Ivan Vidinic, Ilir Demiri, Nikola Labacevski

机构信息

University Clinic for Infectious Diseases and Febrile Conditions, Skopje, Republic of Macedonia.

出版信息

Trop Doct. 2012 Jan;42(1):13-7. doi: 10.1258/td.2011.110284.

Abstract

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.

摘要

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。

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