Department of Infectious Diseases, St. Jude Children's Research Hospital, Memphis, Tennessee.
Department of Oncology, Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Boston, Massachusetts.
Pediatr Blood Cancer. 2020 Aug;67(8):e28234. doi: 10.1002/pbc.28234. Epub 2020 May 9.
Single-center reports of central line-associated bloodstream infection (CLABSI) and the subcategory of mucosal barrier injury laboratory-confirmed bloodstream infection (MBI-LCBI) in pediatric hematology oncology transplant (PHO) patients have focused on the inpatient setting. Characterization of MBI-LCBI across PHO centers and management settings (inpatient and ambulatory) is urgently needed to inform surveillance and prevention strategies.
Prospectively collected data from August 1, 2013, to December 31, 2015, on CLABSI (including MBI-LCBI) from a US PHO multicenter quality improvement network database was analyzed. CDC National Healthcare Safety Network definitions were applied for inpatient events and adapted for ambulatory events.
Thirty-five PHO centers reported 401 ambulatory and 416 inpatient MBI-LCBI events. Ambulatory and inpatient MBI-LCBI rates were 0.085 and 1.01 per 1000 line days, respectively. Fifty-three percent of inpatient CLABSIs were MBI-LCBIs versus 32% in the ambulatory setting (P < 0.01). Neutropenia was the most common criterion defining MBI-LCBI in both settings, being present in ≥90% of events. The most common organisms isolated in MBI-LCBI events were Escherichia coli (in 28% of events), Klebsiella spp. (23%), and viridans streptococci (12%) in the ambulatory setting and viridans streptococci (in 29% of events), E. coli (14%), and Klebsiella spp. (14%) in the inpatient setting.
In this largest study of PHO MBI-LCBI inpatient events and the first such study in the ambulatory setting, the burden of MBI-LCBI across the continuum of care of PHO patients was substantial. These data should raise awareness of MBI-LCBI among healthcare providers for PHO patients, help benchmarking across centers, and help inform prevention and treatment strategies.
有关小儿血液肿瘤移植(PHO)患者中心静脉相关血流感染(CLABSI)和黏膜屏障损伤实验室确诊血流感染(MBI-LCBI)的单中心报告侧重于住院环境。迫切需要描述 PHO 中心之间以及管理环境(住院和门诊)的 MBI-LCBI,以告知监测和预防策略。
从 2013 年 8 月 1 日至 2015 年 12 月 31 日,使用美国 PHO 多中心质量改进网络数据库前瞻性收集了 CLABSI(包括 MBI-LCBI)的数据。应用 CDC 国家医疗保健安全网络定义用于住院事件,并针对门诊事件进行了调整。
35 个 PHO 中心报告了 401 例门诊和 416 例住院 MBI-LCBI 事件。门诊和住院 MBI-LCBI 发生率分别为每 1000 个线路日 0.085 和 1.01。53%的住院 CLABSI 为 MBI-LCBI,而门诊为 32%(P<0.01)。中性粒细胞减少症是两种环境中定义 MBI-LCBI 的最常见标准,存在于≥90%的事件中。MBI-LCBI 事件中最常见的分离物为大肠埃希菌(28%的事件)、克雷伯氏菌属(23%)和草绿色链球菌(12%)在门诊环境中,草绿色链球菌(29%的事件)、大肠埃希菌(14%)和克雷伯氏菌属(14%)在住院环境中。
在这项针对 PHO MBI-LCBI 住院患者的最大研究和第一项针对门诊患者的此类研究中,PHO 患者整个护理过程中 MBI-LCBI 的负担相当大。这些数据应提高医护人员对 PHO 患者 MBI-LCBI 的认识,帮助各中心之间进行基准测试,并为预防和治疗策略提供信息。