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Antimicrobial de-escalation in the critically ill patient and assessment of clinical cure: the DIANA study

机译:患者患者的抗菌脱升升级和临床治疗评估:戴安娜研究

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Purpose The DIANA study aimed to evaluate how often antimicrobial de-escalation (ADE) of empirical treatment is performed in the intensive care unit (ICU) and to estimate the effect of ADE on clinical cure on day 7 following treatment initiation. Methods Adult ICU patients receiving empirical antimicrobial therapy for bacterial infection were studied in a prospective observational study from October 2016 until May 2018. ADE was defined as (1) discontinuation of an antimicrobial in case of empirical combination therapy or (2) replacement of an antimicrobial with the intention to narrow the antimicrobial spectrum, within the first 3 days of therapy. Inverse probability (IP) weighting was used to account for time-varying confounding when estimating the effect of ADE on clinical cure. Results Overall, 1495 patients from 152 ICUs in 28 countries were studied. Combination therapy was prescribed in 50%, and carbapenems were prescribed in 26% of patients. Empirical therapy underwent ADE, no change and change other than ADE within the first 3 days in 16%, 63% and 22%, respectively. Unadjusted mortality at day 28 was 15.8% in the ADE cohort and 19.4% in patients with no change [p = 0.27; RR 0.83 (95% CI 0.60-1.14)]. The IP-weighted relative risk estimate for clinical cure comparing ADE with no-ADE patients (no change or change other than ADE) was 1.37 (95% CI 1.14-1.64). Conclusion ADE was infrequently applied in critically ill-infected patients. The observational effect estimate on clinical cure suggested no deleterious impact of ADE compared to no-ADE. However, residual confounding is likely.
机译:目的,戴安娜的研究旨在评估经验治疗的抗微生物脱升(ADE)在重症监护室(ICU)中进行频率,并在治疗开始后第7天估计脂肪对临床治疗的影响。方法研究来自2016年10月至2018年5月至2018年5月的前瞻性观察研究中接受了对细菌感染的经验抗微生物治疗的成年ICU患者。在经验联合治疗或(2)替代抗菌药物的情况下,Ade被定义为(1)抗菌药物中止抗菌药物随着缩小抗菌谱的意图,在治疗的前3天内。逆概率(IP)加权用于考虑在估计脂肪对临床治疗的影响时的时变混淆。结果总体而言,在28个国家的152名ICU患者中,1495名患者进行了研究。组合疗法在50%方案中规定,肉豆蔻蛋白在26%的患者中规定。经验疗法在前3天内,分别在前3天内进行了近期的ade,没有变化和变化,分别为16%,63%和22%。在第28天的未经调整的死亡率为15.8%,在乙型队队中的15.8%,没有变化的患者19.4%[P = 0.27; RR 0.83(95%CI 0.60-14)]。临床固化的IP加权相对风险估算与无脂患者的ade(没有变化或除ade以外的变化)为1.37(95%CI 1.14-1.64)。结论Ade不经常应用于危重感染患者。与禁止饮料相比,临床治疗的观察效应估计表明,与缺水相比,Ade没有任何有害影响。然而,可能的剩余混杂可能。

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