Infections due to multidrug‐resistant organisms following heart transplantation: Epidemiology, microbiology, and outcomes

医学 肺炎克雷伯菌 铜绿假单胞菌 多重耐药 移植 流行病学 内科学 抗药性 碳青霉烯 抗生素 重症监护医学 微生物学 大肠杆菌 生物 细菌 生物化学 遗传学 基因
作者
Pinki J. Bhatt,Mohsin Ali,Meenakshi Rana,Gopi Patel,Timothy Sullivan,Joseph Murphy,Sean Pinney,Anelechi Anyanwu,Shirish Huprikar,Sarah Taimur
出处
期刊:Transplant Infectious Disease [Wiley]
卷期号:22 (1) 被引量:33
标识
DOI:10.1111/tid.13215
摘要

Abstract Background Infections secondary to multidrug‐resistant organisms (MDRO) have emerged as a growing problem in solid organ transplantation (SOT). Most of the published data on MDRO infections in SOT pertains to abdominal organ transplantation and data specific to heart transplantation (HT) are limited. Methods This is a retrospective review of HT recipients at our institution from 2011 to 2016; with the aim to investigate the epidemiology, microbiologic spectrum, and outcomes in patients with post‐HT MDRO infections, classified as multidrug‐resistant (MDR), extensively drug‐resistant (XDR), and pandrug‐resistant (PDR) using standardized definitions. Results Of the 149 HT recipients, 82 episodes of bacterial infection were seen in 46 patients (31%) in the year following HT. Thirty (37%) were due to MDR pathogens and 13 (16%) were XDR. The most common gram‐negative MDR pathogens were extended‐spectrum beta‐lactamase (ESBL) Escherichia coli and Klebsiella pneumoniae ; while XDR pathogens were most commonly Pseudomonas aeruginosa followed by carbapenem‐resistant Klebsiella pneumoniae . Majority of infection episodes were bloodstream (54, 66%) followed by pulmonary infection (20, 24%). Within a year after transplant, HT recipients with any bacterial infection had significantly higher mortality versus those without infection; and XDR infections were associated with a 26‐fold greater hazard of death on average compared to those without infection (adjusted HR, 26.1; 95% CI, 6.4‐107.0; P < .001). There were no PDR infections. Conclusion Bacterial infections were a significant predictor of 1‐year post‐HT mortality, which was highest among those with XDR infections. This study highlights the burden of MDRO infections in HT recipients and identifies an area of future research.
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