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首页> 外文期刊>Brazilian Journal of Infectious Diseases >A randomized, comparative study of dual therapy (doxycyclinea??rifampin) versus triple therapy (doxycyclinea??rifampina??levofloxacin) for treating acute/subacute brucellosis
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A randomized, comparative study of dual therapy (doxycyclinea??rifampin) versus triple therapy (doxycyclinea??rifampina??levofloxacin) for treating acute/subacute brucellosis

机译:双重疗法(强力霉素?利福平)与三重疗法(强力霉素?利福平?左氧氟沙星)治疗急性/亚急性布鲁氏菌病的随机对照研究

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Aim The aim of this study was to compare both the efficacy and safety profile of the WHO-recommended, dual therapy (doxycyclinea??rifampin) to a quinolone-based, triple therapy (doxycyclinea??rifampina??levofloxacin) for treating acute/subacute brucellosis. Patients and methods We studied 107 consecutive, na?ˉve patients with acute/subacute brucellosis admitted to Assiut University Hospital. Patients were randomly allocated to receive the dual therapy of doxycyclinea??rifampin (group-A) or to receive the triple therapy of doxycyclinea??rifampina??levofloxacin (group-B). Acute/subacute brucellosis was diagnosed based on the presence of: (1) contact with animals or fresh animal products, (2) suggestive clinical manifestations of less than one-year duration, and (3) positive antibody titer (1:160) by standard tube agglutination test. Results There was no significant difference between the two groups regarding their demographic data. Fever was the most frequent manifestation (96.3%). Epigastric pain was the most frequent adverse effect of treatment (12.1%). Group-A patients had a significantly higher relapse rate compared to group-B patients (22.6% versus 9.3%, p -value = 0.01). The rate of treatment adverse effects was higher among group-B patients, although not reaching statistical significance (20.4% versus 11.3%, p -value = 0.059). Conclusions Adding levofloxacin to the dual therapy for acute/subacute brucellosis (doxycyclinea??rifampin) may increase its efficacy in terms of lowering the relapse rate of the disease. Further, larger scale studies are needed before considering modifying the standard, dual therapy for brucellosis.
机译:目的本研究的目的是比较WHO推荐的双重疗法(强力霉素?利福平)与基于喹诺酮的三联疗法(强力霉素?利福平?左氧氟沙星)的疗效和安全性。亚急性布鲁氏菌病。患者和方法我们研究了107例连续不断的急性或亚急性布鲁氏菌病患者,这些患者均入Assiut大学医院接受治疗。患者被随机分配接受强力霉素-利福平的双重治疗(A组)或接受强力霉素-利福平-左氧氟沙星的三联治疗(B组)。急性/亚急性布鲁氏菌病的诊断依据是:(1)与动物或新鲜动物产品接触;(2)持续时间少于一年的暗示性临床表现;(3)抗体滴度呈阳性(1:160)标准管凝集试验。结果两组在人口统计学数据上无显着差异。发烧是最常见的表现(96.3%)。上腹痛是最常见的治疗不良反应(12.1%)。与B组患者相比,A组患者的复发率显着更高(22.6%比9.3%,p值= 0.01)。 B组患者的治疗不良反应率较高,尽管未​​达到统计学显着性(20.4%对11.3%,p值= 0.059)。结论将左氧氟沙星用于急性/亚急性布鲁氏菌病(强力霉素,利福平)双重疗法可降低其复发率,从而提高其疗效。此外,在考虑修改布鲁氏菌病的标准双重疗法之前,需要进行大规模研究。

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