Department of Internal Medicine and Center for Infection Control, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Department of Internal Medicine and Center for Infection Control, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan; Department of Medicine, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
J Microbiol Immunol Infect. 2024 Aug;57(4):594-600. doi: 10.1016/j.jmii.2024.05.010. Epub 2024 May 30.
As limited antibiotic options are available for the treatment of carbapenem-resistant Klebsiella pneumoniae (CRKP) bloodstream infections (BSIs), the optimal treatment duration for CRKP BSIs is unclear. Our objective was to investigate whether short courses (6-10 days) are as effective as prolonged courses (≥11 days) of active antibiotic therapy for CRKP BSIs.
A retrospective cohort study comprising adults with monomicrobial CRKP BSI receiving a short or prolonged course of in vitro active therapy at a medical center was conducted between 2010 and 2021. Comparisons of two therapeutic strategies were assessed by the logistic regression model and propensity score analysis. The primary endpoint was 30-day crude mortality. Secondary outcomes included recurrent BSIs, the emergence of multidrug-resistant organisms and candidemia during hospitalization after completing antibiotic therapy for CRKP BSIs.
Of 263 eligible adults, 160 (60.8%) were male, and the median (interquartile range) age was 69.0 (53.0-76.0) years. Common comorbidities included diabetes (143 patients, 54.4%), malignancy (75, 28.5%), cerebrovascular accident (58, 22.1%), and hemodialysis (49, 18.6%). The 30-day mortality rate was 8.4% (22 patients). Of 84 propensity score well-balanced matched pairs, the 30-day mortality was similar in the short-course and prolonged-course group (6.0% and 7.1%, respectively; P = 1.00). However, there were less episodes candidemia in the short-course group (1.2% versus 13.1%; odds ratio, 0.08; 95% confidence interval, 0.01-0.63; P = 0.005).
Short courses of active therapy for CRKP BSIs demonstrate comparable clinical outcomes to prolonged courses and are associated with a lower risk of subsequent candidemia.
由于可供治疗耐碳青霉烯类肺炎克雷伯菌(CRKP)血流感染(BSI)的抗生素选择有限,CRKP BSI 的最佳治疗持续时间尚不清楚。我们的目的是研究短疗程(6-10 天)是否与延长疗程(≥11 天)的活性抗生素治疗对 CRKP BSI 同样有效。
一项回顾性队列研究纳入了 2010 年至 2021 年期间在一家医疗中心接受短疗程或长疗程体外活性治疗的成人单一致病菌 CRKP BSI 患者。通过逻辑回归模型和倾向评分分析评估两种治疗策略的比较。主要终点为 30 天粗死亡率。次要结局包括复发性 BSI、在完成 CRKP BSI 抗生素治疗后住院期间出现多重耐药菌和念珠菌血症。
在 263 名符合条件的成年人中,160 名(60.8%)为男性,中位(四分位距)年龄为 69.0(53.0-76.0)岁。常见合并症包括糖尿病(143 例,54.4%)、恶性肿瘤(75 例,28.5%)、脑血管意外(58 例,22.1%)和血液透析(49 例,18.6%)。30 天死亡率为 8.4%(22 例)。在 84 对匹配良好的倾向评分中,短疗程和长疗程组的 30 天死亡率相似(分别为 6.0%和 7.1%;P=1.00)。然而,短疗程组念珠菌血症的发作次数较少(1.2%比 13.1%;比值比,0.08;95%置信区间,0.01-0.63;P=0.005)。
CRKP BSI 的短疗程活性治疗与长疗程治疗具有相当的临床结局,并且与随后发生念珠菌血症的风险较低相关。