Division of Clinical Pharmacy, Department of Pharmacy, Faculty of Pharmacy, Mahidol University, Bangkok, Thailand.
Department of Pharmacy Practice, College of Pharmacy, Rangsit University, Pathum Thani, Thailand.
Clin Transl Sci. 2024 Jun;17(6):e13855. doi: 10.1111/cts.13855.
Bloodstream infections (BSI) caused by carbapenem-resistant Enterobacterales (CRE) are associated with a high mortality rate. This study aimed to investigate factors associated with 14-day mortality and identify a potential treatment option. A retrospective cohort study was conducted on patients with CRE-BSI in Thailand from 2015 to 2020. The multivariate Cox proportional-hazards model was employed to identify factors influencing 14-day mortality. Out of 134 diagnosed cases of CRE-BSI, the all-cause 14-day mortality rate was 35.1%. The most prevalent organism isolated was Klebsiella pneumoniae (85.8%), followed by Escherichia coli (11.9%). Among the 60 isolates tested for carbapenemase genes, the majority exhibited co-occurring bla and bla (51.7%), followed by bla (31.7%) and bla (15.0%). In the multivariate analysis, neutropenia (adjusted hazard ratio [aHR] 2.55; 95% confidence interval [95%CI] 1.28-5.06; p = 0.008), sepsis/septic shock (aHR 3.02; 95%CI 1.33-6.86; p = 0.008), and previous metronidazole exposures (aHR 3.58; 95%CI 1.89-6.71; p < 0.001) were identified as independent factors for 14-day mortality. The fosfomycin-based regimen was found to be protective (aHR 0.37; 95%CI 0.15-0.92; p = 0.032). In patients with CRE-BSI, particularly in regions with a high occurrence of co-occurring bla and bla, neutropenia, sepsis/septic shock, and previous metronidazole exposures emerged as independent risk factors for mortality. Moreover, the fosfomycin-based regimen showed an improvement in the survival rate.
血流感染(BSI)由碳青霉烯类耐药肠杆菌科(CRE)引起,死亡率高。本研究旨在探讨与 14 天死亡率相关的因素,并确定潜在的治疗选择。对 2015 年至 2020 年泰国 CRE-BSI 患者进行了回顾性队列研究。采用多变量 Cox 比例风险模型确定影响 14 天死亡率的因素。在确诊的 134 例 CRE-BSI 患者中,全因 14 天死亡率为 35.1%。最常见的分离菌为肺炎克雷伯菌(85.8%),其次是大肠埃希菌(11.9%)。在对 60 株碳青霉烯酶基因进行检测的菌株中,大多数同时存在 bla 和 bla(51.7%),其次是 bla(31.7%)和 bla(15.0%)。多变量分析显示,中性粒细胞减少症(调整后的危险比[aHR] 2.55;95%置信区间[95%CI] 1.28-5.06;p=0.008)、败血症/感染性休克(aHR 3.02;95%CI 1.33-6.86;p=0.008)和先前甲硝唑暴露(aHR 3.58;95%CI 1.89-6.71;p<0.001)是 14 天死亡率的独立因素。磷霉素方案被发现具有保护作用(aHR 0.37;95%CI 0.15-0.92;p=0.032)。在 CRE-BSI 患者中,特别是在同时存在 bla 和 bla 的高发地区,中性粒细胞减少症、败血症/感染性休克和先前甲硝唑暴露是死亡率的独立危险因素。此外,基于磷霉素的方案显示出生存率的提高。
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