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Influence of Colistin Dose on Global Cure in Patients with Bacteremia Due to Carbapenem-Resistant Gram-Negative Bacilli

机译:Colistin剂量对耐碳青霉烯类革兰阴性杆菌的细菌血症患者整体治愈的影响

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摘要

The increasing prevalence of multidrug-resistant (MDR) nosocomial infections accounts for increased morbidity and mortality of such infections. Infections with MDR Gram-negative isolates are frequently treated with colistin. Based on recent pharmacokinetic studies, current colistin dosing regimens may result in a prolonged time to therapeutic concentrations, leading to suboptimal and delayed effective treatment. In addition, studies have demonstrated an association between an increased colistin dose and improved clinical outcomes. However, the specific dose at which these outcomes are observed is unknown and warrants further investigation. This retrospective study utilized classification and regression tree (CART) analysis to determine the dose of colistin most predictive of global cure at day 7 of therapy. Patients were assigned to high- and low-dose cohorts based on the CART-established breakpoint. The secondary outcomes included microbiologic outcomes, clinical cure, global cure, lengths of intensive care unit (ICU) and hospital stays, and 7- and 28-day mortalities. Additionally, safety outcomes focused on the incidence of nephrotoxicity associated with high-dose colistin therapy. The CART-established breakpoint for high-dose colistin was determined to be >4.4 mg/kg of body weight/day, based on ideal body weight. This study evaluated 127 patients; 45 (35%) received high-dose colistin, and 82 (65%) received low-dose colistin. High-dose colistin was associated with day 7 global cure (40% versus 19.5%; P = 0.013) in bivariate and multivariate analyses (odds ratio [OR] = 3.40; 95% confidence interval [CI], 1.37 to 8.45; P = 0.008). High-dose colistin therapy was also associated with day 7 clinical cure, microbiologic success, and mortality but not with the development of acute kidney injury. We concluded that high-dose colistin (>4.4 mg/kg/day) is independently associated with day 7 global cure.
机译:多药耐药性(MDR)医院感染的流行率增加,导致此类感染的发病率和死亡率增加。 MDR革兰氏阴性菌的感染经常用粘菌素治疗。根据最近的药代动力学研究,目前的大肠菌素给药方案可能导致治疗浓度延长时间,导致次优治疗和延迟治疗。此外,研究表明,粘菌素剂量增加与临床结果改善之间存在关联。但是,观察到这些结果的具体剂量尚不清楚,需要进一步研究。这项回顾性研究利用分类和回归树(CART)分析来确定最能预测治疗第7天整体治愈的大肠菌素的剂量。根据CART确定的断点将患者分为高剂量组和低剂量组。次要结果包括微生物学结果,临床治愈,整体治愈,重症监护病房(ICU)的长度和住院时间以及7天和28天死亡率。此外,安全性结果集中在与大剂量粘菌素治疗相关的肾毒性发生率。根据理想体重,CART确定的大剂量粘菌素断点为> 4.4 mg / kg体重/天。这项研究评估了127例患者。 45(35%)人接受大剂量粘菌素,82(65%)人接受低剂量粘菌素。在双变量和多变量分析中,大剂量粘菌素与第7天的总体治愈率相关(40%比19.5%; P = 0.013)(优势比[OR] = 3.40; 95%置信区间[CI]为1.37至8.45; P = 0.008)。大剂量粘菌素治疗还与第7天临床治愈,微生物学成功率和死亡率相关,但与急性肾损伤的发生无关。我们得出的结论是,大剂量粘菌素(> 4.4 mg / kg /天)与第7天的总体治愈独立相关。

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