重症监护病房中产kpc肺炎克雷伯菌血流感染患者的感染危险因素和死亡率预测因素

Matthaios Papadimitriou-Olivgeris, Markos Marangos, Myrto Christofidou, Fotini Fligou, Christina Bartzavali, Eleftheria S Panteli, Sophia Vamvakopoulou, Kriton S Filos, Evangelos D Anastassiou
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引用次数: 52

摘要

背景:产碳青霉烯酶(KPC)的肺炎克雷伯菌(KPC- kp)感染在重症监护病房(icu)与死亡率增加相关。我们的目的是确定感染的危险因素和KPC-Kp血流感染(BSI) ICU患者30天死亡率的预测因素。方法:将273例在希腊帕特雷大学医院ICU住院6天以上的患者分为2组,分别为KPC-Kp BSI组和未发生KPC-Kp BSI组。采用Vitek 2技术鉴定肺炎克雷伯菌。采用琼脂纸片扩散法进行药敏试验。最低抑菌浓度用Etest测定。PCR证实了blaKPC基因的存在。采用脉冲场凝胶电泳对xbai限制性基因组DNA进行分子分型。流行病学资料通过患者图表收集。结果:5例患者入院时出现菌血症,48例患者(17.6%)在入院后6天出现BSI。后一组KPC-Kp BSI的危险因素为氨基糖苷类药物的使用、第3天后插入导管的次数和气管切开术。30天死亡率为43.4%(23/53)。多因素分析显示,年龄、BSI发病时SAPS II评分、对粘菌素、庆大霉素或替加环素的耐药性以及感染性休克与死亡率独立相关。用至少2种适当的抗生素治疗被确定为预后良好的预测因子。结论:ICU患者KPC-Kp BSI与多种危险因素有关。ICU中KPC-KP BSI患者的高死亡率要求实施适当的感染控制措施。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Risk factors for infection and predictors of mortality among patients with KPC-producing Klebsiella pneumoniae bloodstream infections in the intensive care unit.

Background: Klebsiella pneumoniae carbapenemase (KPC)-producing Klebsiella pneumoniae (KPC-Kp) infections in intensive care units (ICUs) are associated with increased mortality. We aimed to determine risk factors for infection and predictors of 30-day mortality in ICU patients with KPC-Kp bloodstream infections (BSI).

Methods: During a 26-month period, patients (n = 273) who stayed more than 6 days in the ICU of the University Hospital of Patras, Greece, were divided into 2 groups, those who developed KPC-Kp BSI and those who did not. K. pneumoniae was identified by Vitek 2 technology. Antibiotic susceptibility testing was performed by agar disk diffusion method. Minimum inhibitory concentrations were determined by Etest. The presence of the blaKPC gene was confirmed by PCR. Molecular typing was performed by pulsed-field gel electrophoresis of XbaI-restricted genomic DNA. Epidemiological data were collected by patient chart review.

Results: Five patients had bacteraemia upon admission, while in 48 (17.6%) the BSI developed after 6 days of hospitalization. Risk factors for KPC-Kp BSI in the latter group were the administration of aminoglycosides, number of invasive catheters inserted after the third day, and tracheostomy. The 30-day mortality was 43.4% (23/53 patients). Multivariate analysis revealed that age, SAPS II score at onset of BSI, resistance to colistin, gentamicin, or tigecycline, and septic shock were independently associated with mortality. Treatment with at least 2 appropriate antibiotics was identified as a predictor of a good prognosis.

Conclusions: Many risk factors are involved in KPC-Kp BSI among ICU patients. The high mortality in patients with KPC-KP BSI in the ICU requires the implementation of appropriate infection control measures.

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