耐碳青霉烯肺炎克雷伯菌血流感染患者死亡的危险因素

E. Eren, A. Ulu-Kilic, Zeynep Türe, F. Cevahir, H. Kılıç, Emine Alp-Meşe
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引用次数: 1

摘要

目的:碳青霉烯耐药肺炎克雷伯菌(CRKp)是全球医院获得性感染的主要原因之一,并导致严重和危及生命的感染。血流感染(bsi)的治疗选择非常有限,由于多药耐药性的增加,预后很差。本研究的目的是评估CRKp-BSI导致死亡的危险因素。方法:2013年9月至2017年10月在某大学医院进行回顾性研究。CRKp-BSI患者(年龄0 ~ 16岁)纳入本研究。从电子病历和微生物数据库中收集数据,包括人口统计数据、Charlson合并症指数(CCI)、住院日期的急性生理和慢性健康评估II (APACHE II)评分、CRKp的最低抑制浓度(MIC)、抗生素治疗和结局(30天死亡率)数据。结果:共分析了82例crkp - bsi患者。年龄中位数为54.5岁,男性48例(58.5%)。住院时APACHEⅱ评分中位数为14 (IQR 6-28), CCI为4.0 (IQR 0-12)。46例(56.1%)患者为icu获得性菌血症,36例(43.9%)为中央静脉相关菌血症,25例(30.5%)为原发性菌血症。50例(61.0%)患者采用联合治疗,粘菌素/替加环素(28%)是使用最多的抗生素联合治疗。所有患者的死亡率为56.1% (46/82),ICU患者死亡率为65.2%(30/46)。在单因素分析中,CRKp-BSI死亡率的危险因素为高CCI、治疗第5天无临床反应、住院和感染日期高APACHE II评分和多器官功能障碍综合征。在多因素分析中,最显著的死亡危险因素是感染当日APACHE II评分(OR: 1.190;95% ci: 1.088-1.301)。治疗方案和联合治疗与单一治疗未发现与生存率显著相关。此外,CRKp的MIC值与死亡率无关。结论:CRKp-BSI患者死亡率高(56.1%)。感染日APACHEⅱ评分与死亡率显著相关。接受联合治疗(54.3%)或单一治疗(45.7%)的患者的结果相似。
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 of Mortality in Patients with Bloodstream Infections Due to Carbapenem Resistant Klebsiella pneumoniae
Objective: Carbapenem-resistant Klebsiella pneumoniae (CRKp) is among the leading causes of hospital-acquired infections worldwide and causes serious and life-threatening infections. Treatment options are very limited for blood stream infections (BSIs) and prognosis is poor due to increasing multi-drug resistance. The aim of this study was to assess risk factors for the mortality due to CRKp-BSI. Methods: A retrospective study was conducted in a university hospital from September 2013 to October 2017. Patients (aged >16 years) with CRKp-BSI were included in this study. Data, including demographics, Charlson comorbidity index (CCI), acute physiology and chronic health evaluation II (APACHE II) score on hospitalisation date, minimum inhibitory concentration (MIC) of CRKp, antibiotic treatment and outcome (30-day mortality) data were collected from the electronic medical records and microbiology databases. Results: A total of 82 patients with CRKP-BSIs were analysed. The median age was 54.5 years, and 48 (58.5%) of them were male. The median APACHE II score on hospitalisation was 14 (IQR 6-28) and CCI was 4.0 (IQR 0-12). Forty-six (56.1%) patients had ICU-acquired bacteremia and 36 (43.9%) had central-line associated bacteremia and 25 (30.5%) had primary bacteremia. Fifty (61.0%) patients had combination therapy, colistin/tigecycline (28%) was the most used antibiotic combination. The mortality of all patients was 56.1% (46/82) and 65.2% (30/46) in ICU patients. In univariate analysis, risk factors for the mortality of CRKp-BSI were high CCI, not having clinical response on the fifth day of treatment, high APACHE II score on hospitalisation and infection date and multiple organ dysfunction syndrome. In multivariate analysis, the most significant risk factor for mortality was APACHE II score on infection day (OR: 1.190; 95% CI: 1.088-1.301). Treatment regimens and combination therapy vs. monotherapy were not found to be significantly associated with survival. In addition, MIC values of CRKp were not associated with mortality. Conclusions: Patients with CRKp-BSI had high mortality (56.1%). APACHE II score on infection day was significantly associated with mortality. The outcome was similar between patients receiving combination (54.3%) or monotherapy (45.7%).
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