首页> 外文期刊>Hepatology international >Clinical outcomes of spontaneous bacterial peritonitis due to extended-spectrum beta-lactamase-producing Escherichia coli or Klebsiella pneumoniae: a retrospective cohort study
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Clinical outcomes of spontaneous bacterial peritonitis due to extended-spectrum beta-lactamase-producing Escherichia coli or Klebsiella pneumoniae: a retrospective cohort study

机译:产生广谱β-内酰胺酶的大肠杆菌或肺炎克雷伯菌引起的自发性细菌性腹膜炎的临床结局:一项回顾性队列研究

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PurposeThe aim of this study was to (1) evaluate the clinical outcomes of spontaneous bacterial peritonitis (SBP) due to extended-spectrum beta-lactamase (ESBL)-producing Escherichia coli or Klebsiella pneumoniae (EK) and (2) investigate the relationship between the adequacy of initial antibiotic treatments and patient outcomes.MethodsWe conducted a retrospective cohort study of cirrhotic patients with SBP caused by EK. We evaluated the 30-day mortality rate and used Cox proportional hazard models to identify risk factors for mortality.ResultsBetween January 2006 and December 2012, a total of 231 episodes of SBP due to EK were recorded. Among them, 52 were caused by ESBL-producing EK (ESBL-EK). The 30-day mortality rate was significantly higher in patients with SBP due to ESBL-EK than in those with non-ESBL-producing EK (non-ESBL-EK) (34.6 vs. 18.4?%, respectively; p?=?0.013). Multivariate analysis revealed that ESBL production [adjusted HR (aHR) 1.82, 95?% confidence interval (CI) 1.00–3.31], nosocomial infection (aHR 2.24, 95?% CI 1.26–3.95), septic shock (aHR 4.84, 95?% CI 2.70–8.65), higher Child-Pugh score (aHR 1.57, 95?% CI 1.28–1.92), and higher Charlson comorbidity index (aHR 1.37, 95?% CI 1.15–1.64) were independent risk factors for 30-day mortality in the total cohort. When we analyzed patients with SBP due to ESBL-EK separately, septic shock (aHR 3.64, 95?% CI 1.40–9.77), accompanying bacteremia (aHR 3.71, 95?% CI 1.37–10.08), and hepatocellular carcinoma (aHR 3.21, 95?% CI 1.20–8.56) were independent risk factors.ConclusionsBoth 7- and 30-day mortalities for SBP due to ESBL-EK were significantly higher than for SBP due to non-ESBL-EK. Initial antibiotic choice was not associated with poor clinical outcomes in patients with SBP due to ESBL-EK.
机译:目的本研究的目的是(1)评估由于产生大范围β-内酰胺酶(ESBL)的大肠杆菌或肺炎克雷伯菌(EK)引起的自发性细菌性腹膜炎(SBP)的临床结果,以及(2)研究两者之间的关系方法我们对由EK引起的肝硬化SBP患者进行了一项回顾性队列研究。我们评估了30天的死亡率,并使用Cox比例风险模型确定了死亡率的危险因素。结果在2006年1月至2012年12月之间,共记录了231次因EK引起的SBP发作。其中,52个是由产生ESBL的EK(ESBL-EK)引起的。由ESBL-EK引起的SBP患者的30天死亡率显着高于非ESBL产生EK(non-ESBL-EK)的患者(分别为34.6%和18.4%); p?=?0.013 )。多因素分析显示,ESBL的产生[调整后的HR(aHR)为1.82,95%置信区间(CI)为1.00–3.31],医院感染(aHR 2.24、95%CI为1.26–3.95),败血性休克(aHR 4.84、95? %CI 2.70–8.65),较高的Child-Pugh评分(aHR 1.57,95%CI 1.28–1.92)和较高的Charlson合并症指数(aHR 1.37,95%CI 1.15-1.64)是30天的独立危险因素总队列死亡率。当我们分别分析由ESBL-EK引起的SBP患者,败血性休克(aHR 3.64,95%CI 1.40–9.77),伴有菌血症(aHR 3.71、95%CI 1.37-10.08)和肝细胞癌(aHR 3.21, 95%CI(1.20–8.56)是独立的危险因素。结论ESBL-EK致SBP的7天和30天死亡率均高于非ESBL-EK致SBP的死亡率。由于ESBL-EK,最初的抗生素选择与SBP患者不良的临床预后无关。

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