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A multinational, preregistered cohort study of beta-lactam/beta-lactamase inhibitor combinations for treatment of bloodstream infections due to extended-spectrum-beta-lactamase-producing Enterobacteriaceae

机译:一项针对β-内酰胺/β-内酰胺酶抑制剂组合的跨国预注册队列研究,用于治疗因产生广谱β-内酰胺酶的肠杆菌科引起的血流感染

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摘要

The spread of extended-spectrum-β-lactamase (ESBL)-producing Enterobacteriaceae (ESBL-E) is leading to increased carbapenem consumption. Alternatives to carbapenems need to be investigated. We investigated whether β-lactam/β-lactamase inhibitor (BLBLI) combinations are as effective as carbapenems in the treatment of bloodstream infections (BSI) due to ESBL-E. A multinational, retrospective cohort study was performed. Patients with monomicrobial BSI due to ESBL-E were studied; specific criteria were applied for inclusion of patients in the empirical-therapy (ET) cohort (ETC; 365 patients), targeted-therapy (TT) cohort (TTC; 601 patients), and global cohort (GC; 627 patients). The main outcome variables were cure/improvement rate at day 14 and all-cause 30-day mortality. Multivariate analysis, propensity scores (PS), and sensitivity analyses were used to control for confounding. The cure/improvement rates with BLBLIs and carbapenems were 80.0% and 78.9% in the ETC and 90.2% and 85.5% in the TTC, respectively. The 30-day mortality rates were 17.6% and 20% in the ETC and 9.8% and 13.9% in the TTC, respectively. The adjusted odds ratio (OR) (95% confidence interval [CI]) values for cure/improvement rate with ET with BLBLIs were 1.37 (0.69 to 2.76); for TT, they were 1.61 (0.58 to 4.86). Regarding 30-day mortality, the adjusted OR (95% CI) values were 0.55 (0.25 to 1.18) for ET and 0.59 (0.19 to 1.71) for TT. The results were consistent in all subgroups studied, in a stratified analysis according to quartiles of PS, in PS-matched cases, and in the GC. BLBLIs, if active in vitro, appear to be as effective as carbapenems for ET and TT of BSI due to ESLB-E regardless of the source and specific species. These data may help to avoid the overuse of carbapenems. (This study has been registered at ClinicalTrials.gov under registration no. NCT01764490.).
机译:产生广谱β-内酰胺酶(ESBL)的肠杆菌科细菌(ESBL-E)的扩散导致碳青霉烯的消耗量增加。碳青霉烯的替代品需要研究。我们研究了β-内酰胺/β-内酰胺酶抑制剂(BLBLI)组合在治疗因ESBL-E引起的血流感染(BSI)中是否与碳青霉烯类药物一样有效。进行了一项跨国回顾性队列研究。研究了由ESBL-E引起的单微生物BSI患者;应用特定标准将患者纳入经验治疗(ET)队列(ETC; 365例患者),靶向治疗(TT)队列(TTC; 601例患者)和整体队列(GC; 627例)。主要结局变量是第14天的治愈/改善率和全天30天的死亡率。多变量分析,倾向评分(PS)和敏感性分析用于控制混淆。 ETC中BLBLI和碳青霉烯类药物的治愈/改善率分别为80.0%和78.9%,TTC中分别为90.2%和85.5%。 30天死亡率在ETC中分别为17.6%和20%,在TTC中分别为9.8%和13.9%。使用BLBLI的ET的治愈/改善率的校正比值比(OR)(95%置信区间[CI])值为1.37(0.69至2.76); TT则为1.61(0.58至4.86)。关于30天死亡率,ET的校正OR值(95%CI)为0.55(0.25至1.18),TT的校正值为OR9(0.59(0.19至1.71))。在根据PS四分位数,PS匹配病例和GC进行的分层分析中,所有研究亚组的结果均一致。如果在体外具有活性,则BLBLI似乎与碳青霉烯类药物对BSI的ET和TT一样有效,这归因于ESLB-E,无论来源和具体物种如何。这些数据可能有助于避免碳青霉烯类药物的过度使用。 (该研究已在ClinicalTrials.gov上注册,注册号为NCT01764490。)。

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