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Meropenem monotherapy for the treatment of hospital-acquired pneumonia: results of a multicenter trial.

机译:美罗培南单药治疗医院获得性肺炎:一项多中心试验的结果。

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摘要

The efficacy and tolerability of meropenem as empirical treatment in patients with hospital-acquired pneumonia was determined in a prospective, open-label, non-randomized trial. Patients from 28 centers in the USA received meropenem 1 g every 8 h intravenously. Of 255 patients enrolled, 111 were evaluable for efficacy, including 60 patients with ventilator-associated pneumonia. At end of treatment 74% of patients had a satisfactory clinical response and 64% had this response at follow-up, which could last up to 28 days after treatment. In patients with ventilator-associated pneumonia, a satisfactory clinical response was observed in 68% at the end of treatment and 63% at follow-up. The overall satisfactory response rate for individual pretreatment pathogens ranged from 65% to 100%. This study demonstrates that meropenem monotherapy is effective and well tolerated for patients with hospital-acquired pneumonia, including a subgroup of patients with ventilator-associated pneumonia.
机译:在一项前瞻性,开放标签,非随机试验中确定了美罗培南作为经验性治疗在医院获得性肺炎患者中的疗效和耐受性。来自美国28个中心的患者每8小时静脉注射1 g美罗培南。在255名患者中,有111名可评估疗效,包括60名呼吸机相关性肺炎患者。在治疗结束时,有74%的患者有满意的临床反应,而64%的患者在随访时有此反应,治疗后可持续长达28天。在呼吸机相关性肺炎患者中,在治疗结束时观察到令人满意的临床反应,在治疗结束时为68%,在随访时为63%。单个预处理病原体的总体满意响应率范围为65%至100%。这项研究表明,美洛培南单药疗法对于医院获得性肺炎患者(包括呼吸机相关性肺炎亚组患者)有效且耐受性良好。

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