首页> 美国卫生研究院文献>Antimicrobial Agents and Chemotherapy >Doxycycline-rifampin versus doxycycline-streptomycin in treatment of human brucellosis due to Brucella melitensis. The GECMEI Group. Grupo de Estudio de Castilla-la Mancha de Enfermedades Infecciosas.
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Doxycycline-rifampin versus doxycycline-streptomycin in treatment of human brucellosis due to Brucella melitensis. The GECMEI Group. Grupo de Estudio de Castilla-la Mancha de Enfermedades Infecciosas.

机译:强力霉素-利福平与强力霉素-链霉素在治疗布鲁氏菌引起的人类布鲁氏菌病中的应用。 GECMEI集团。卡斯蒂利亚-拉曼恰传染病研究组。

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摘要

Brucellosis is a common zoonosis in many parts of the world; the best regimen for the treatment of brucellosis has not been clearly determined. We have carried out a multicenter, open, controlled trial in five general hospitals in Spain to compare the efficacy and safety of doxycycline and rifampin (DR) versus doxycycline and streptomycin (DS) for the treatment of human brucellosis. The study included 194 ambulatory or hospitalized patients with acute brucellosis, without endocarditis or neurobrucellosis. The diagnostic criterion was isolation of Brucella species from blood or other tissues (n = 120) or a standard tube agglutination titer of 1/160 or more for anti-Brucella antibodies with compatible clinical findings (n = 74). Patients were randomly assigned to receive either 100 mg of doxycycline twice daily plus rifampin, 900 mg/day, in a single morning dose for 45 days (DR group) or the same dose of doxycycline for 45 days plus streptomycin, 1 g/day, intramuscularly for 14 days (DS group). A lack of therapeutic efficacy developed in 8 of the 100 patients in the DR group (8%) and in 2 of the 94 patients in the DS group (2%)(P = 0.10). Relapses occurred in 16 of the 100 patients in the DR group (16%) but in only 5 of the 94 patients in the DS group (5.3%) (P = 0.02). When relapse was considered in combination with initial lack of efficacy, 26 patients in the DR group (24%) and 7 patients in the DS group (7.45%) failed to respond to therapy (P = 0.0016). In general, therapy was well tolerated and only four patients (4%) in the DR group and two (2%) in the DS group had episodes of adverse effects necessitating discontinuation of treatment (P> 0.2). We conclude that a doxycycline-and-rifampin regimen is less effective than the doxycycline-and-streptomycin regimen in patients with acute brucellosis.
机译:布鲁氏菌病是世界许多地方的常见人畜共患病。尚没有确定治疗布鲁氏菌病的最佳方案。我们在西班牙的五家综合医院进行了一项多中心,开放,对照试验,比较了强力霉素和利福平(DR)与强力霉素和链霉素(DS)在治疗人类布鲁氏菌病中的疗效和安全性。该研究纳入了194例急性布鲁氏菌病,无心内膜炎或神经布鲁氏菌病的非卧床或住院患者。诊断标准是从血液或其他组织中分离出布鲁氏菌种(n = 120),或者对具有临床意义的抗布鲁氏菌抗体,标准管凝集滴度为1/160或更高(n = 74)。患者被随机分配为每天两次,每天一次,每天一次,每次100 mg强力霉素加利福平,900 mg /天,连续45天(DR组),或者连续45天,相同剂量的强力霉素加链霉素,每天1 g,肌肉注射14天(DS组)。 DR组的100名患者中有8名(8%)和DS组的94名患者中有2名(2%)缺乏治疗功效(P = 0.10)。 DR组100例患者中有16例(16%)复发,而DS组94例中仅5例(5.3%)复发(P = 0.02)。当考虑到复发与最初缺乏疗效相结合时,DR组的26例患者(24%)和DS组的7例患者(7.45%)对治疗无效(P = 0.0016)。通常,治疗耐受性良好,DR组只有4例患者(4%),DS组只有2例(2%)出现不良反应发作,因此必须停止治疗(P> 0.2)。我们得出的结论是,在急性布鲁氏菌病患者中,强力霉素和利福平治疗方案比强力霉素和链霉素治疗效果差。

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