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评估念珠菌血症中的抗菌药物管理策略:一种比较血培养与T2念珠菌诊断方法的新型结局排名合意性(DOOR)分析

Evaluating antimicrobial stewardship strategies in candidemia: a novel desirability of outcome ranking (DOOR) analysis comparing blood culture versus T2Candida diagnostic approaches.

作者信息

Caniff Kaylee E, Al Musawa Mohammed, Judd Chloe, Shupp Macy, Veve Michael P, Alangaden George, Claeys Kimberly C, Scipione Marco R, Walsh Thomas J, Rybak Michael J

机构信息

Wayne State University Eugene Applebaum College of Pharmacy and Health Sciences, Detroit, Michigan, USA.

Henry Ford Health System, Detroit, Michigan, USA.

出版信息

J Clin Microbiol. 2025 May 14;63(5):e0004325. doi: 10.1128/jcm.00043-25. Epub 2025 Apr 11.

Abstract

The T2Candida Panel (T2 Biosystems, Lexington, MA) is a rapid diagnostic test that detects from whole blood within 3-5 hours. We developed and applied a desirability of outcome ranking (DOOR) analysis to investigate if an antimicrobial stewardship program (ASP) strategy centered on T2Candida diagnosis is associated with improved outcomes compared to an ASP strategy that relies on conventional blood culture diagnosis in critically ill patients with candidemia. This is a retrospective, observational cohort of patients with candidemia identified ≤72 h of intensive care unit admission at two medical centers in Detroit, MI (one T2Candida site and one blood culture site) from 2016 to 2023. Management strategies for candidemia were compared using an original DOOR analysis with inverse probability of treatment weighting (IPTW) to account for confounding. Two hundred patients were included, 100 from each site. Baseline illness severity, race, and species varied between groups; however, source control procedures, echocardiogram, and ophthalmologic exam occurred at similar frequencies. T2Candida/ASP was associated with faster median (interquartile range [IQR]) detection of candidemia (7.0 [5.0-10.75] h vs 45.5 h [34.25-68.75], < 0.001) and timelier median (IQR) initiation of directed antifungal therapy (6.0 [0-11.0] h vs 49.0 [34.0-77.0] h, < 0.001). T2Candida/ASP patients had a 58.0% probability of achieving an overall better outcome compared to those managed with blood culture/ASP (95% confidence interval: 50.4-65.2%) in IPTW-adjusted DOOR analysis. An ASP strategy incorporating T2Candida was associated with an overall better patient outcome compared to patients managed via conventional blood culture diagnosis.IMPORTANCE species are a significant cause of bloodstream infections in critically ill patients. Conventional diagnostic methods, such as blood cultures, have poor sensitivity and delayed results. The T2Candida Panel is a diagnostic tool that rapidly detects directly from the blood in 3-5 h, enabling faster initiation of antifungal therapy. Antimicrobial stewardship programs (ASPs) optimize the management of bloodstream infections and may benefit from incorporating T2Candida to improve patient outcomes. This study examined whether an ASP intervention based on T2Candida diagnosis, compared to one relying on traditional blood culture methods, could improve outcomes in candidemia using a desirability of outcome ranking (DOOR) analysis. The DOOR method provides a comprehensive evaluation by integrating multiple outcomes into a single end point, which is ideal given the complexity of patients with candidemia. The T2Candida/ASP intervention resulted in an overall better patient outcome, considering infectious complications, treatment failure, and all-cause mortality.

摘要

T2念珠菌检测试剂盒(T2 Biosystems公司,马萨诸塞州列克星敦)是一种快速诊断测试,可在3 - 5小时内从全血中检测出念珠菌。我们开发并应用了结果期望排名(DOOR)分析,以研究与依赖传统血培养诊断的抗菌药物管理计划(ASP)策略相比,以T2念珠菌诊断为中心的ASP策略在念珠菌血症重症患者中是否与更好的结果相关。这是一项回顾性观察队列研究,研究对象为2016年至2023年在密歇根州底特律的两个医疗中心(一个T2念珠菌检测点和一个血培养检测点)入住重症监护病房≤72小时内确诊为念珠菌血症的患者。使用原始的DOOR分析和逆概率治疗加权(IPTW)来比较念珠菌血症的管理策略,以考虑混杂因素。共纳入200例患者,每个检测点100例。两组之间的基线疾病严重程度、种族和念珠菌种类各不相同;然而,感染源控制程序、超声心动图和眼科检查的发生频率相似。T2念珠菌检测/ASP与念珠菌血症的中位(四分位间距[IQR])检测速度更快相关(7.0 [5.0 - 10.75]小时对45.5小时[34.25 - 68.75],P < 0.001),且中位(IQR)启动针对性抗真菌治疗的时间也更早(6.0 [0 - 11.0]小时对49.0 [34.0 - 77.0]小时,P < 0.001)。在IPTW调整后的DOOR分析中,与采用血培养/ASP管理的患者相比,T2念珠菌检测/ASP患者实现总体更好结果的概率为58.0%(95%置信区间:50.4 - 65.2%)。与通过传统血培养诊断管理的患者相比,纳入T2念珠菌检测的ASP策略与总体更好的患者结局相关。重要性念珠菌是重症患者血流感染的重要原因。传统诊断方法,如血培养,敏感性差且结果延迟。T2念珠菌检测试剂盒是一种诊断工具,可在3 - 5小时内直接从血液中快速检测出念珠菌,从而能够更快地启动抗真菌治疗。抗菌药物管理计划(ASP)优化血流感染的管理,并可能受益于纳入T2念珠菌检测以改善患者结局。本研究使用结果期望排名(DOOR)分析,研究了与依赖传统血培养方法的ASP干预相比,基于T2念珠菌诊断的ASP干预是否能改善念珠菌血症的结局。DOOR方法通过将多个结局整合到一个单一终点来提供全面评估,鉴于念珠菌血症患者的复杂性,这是理想的方法。考虑到感染并发症、治疗失败和全因死亡率,T2念珠菌检测/ASP干预导致总体更好的患者结局。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d6dc/12077142/7089f53c7fff/jcm.00043-25.f001.jpg

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