Heston Sarah M, Young Rebecca R, Hong Hwanhee, Akinboyo Ibukunoluwa C, Tanaka John S, Martin Paul L, Vinesett Richard, Jenkins Kirsten, McGill Lauren E, Hazen Kevin C, Seed Patrick C, Kelly Matthew S
Division of Pediatric Infectious Diseases, Duke University Medical Center, Durham, North Carolina, USA.
Department of Biostatistics and Bioinformatics, Duke University School of Medicine, Durham, North Carolina, USA.
Open Forum Infect Dis. 2020 Sep 30;7(11):ofaa465. doi: 10.1093/ofid/ofaa465. eCollection 2020 Nov.
Bloodstream infections (BSIs) occur frequently after hematopoietic stem cell transplantation (HSCT). We examined the microbiology of BSI in pediatric HSCT recipients over a 2-decade period at our institution to inform empirical antimicrobial prescribing and infection prevention strategies.
We conducted a retrospective cohort study of children (<18 years) who underwent HSCT at Duke University between 1997 and 2015. We used recurrent-event gap-time Cox proportional hazards models to determine the hazards of all-cause and cause-specific BSI according to HSCT year. We compared the median time to BSI by causative organism type and evaluated for temporal trends in the prevalence of antibiotic resistance among causative organisms.
A total of 865 BSI occurred in 1311 children, including 412 (48%) Gram-positive bacterial, 196 (23%) Gram-negative bacterial, 56 (6%) fungal, 23 (3%) mycobacterial, and 178 (21%) polymicrobial BSI. The hazard of all BSIs did not change substantially over time during the study period, but the hazard of fungal BSIs declined over time during the study period ( = .04). Most fungal BSIs (82%) occurred in the first 100 days after HSCT, whereas mycobacterial BSIs occurred later after HSCT than BSIs caused by other organisms ( < .0001). The prevalence of vancomycin resistance among BSIs caused by increased during the study period ( = .0007). The risk of 2-year mortality in children was increased with BSI ( = .02), Gram-negative bacterial BSI ( = .02), and fungal BSI ( < .0001).
Despite expanded practices for BSI prevention over the past several decades, the incidence of BSI remains high in pediatric HSCT recipients at our institution. Additional strategies are urgently needed to effectively prevent BSIs in this high-risk population.
造血干细胞移植(HSCT)后血流感染(BSI)频繁发生。我们在本机构对20年间儿科HSCT受者的BSI微生物学进行了研究,以指导经验性抗菌药物处方和感染预防策略。
我们对1997年至2015年在杜克大学接受HSCT的儿童(<18岁)进行了一项回顾性队列研究。我们使用复发事件间隔时间Cox比例风险模型来确定根据HSCT年份的全因和特定原因BSI的风险。我们比较了不同病原体类型导致BSI的中位时间,并评估了病原体中抗生素耐药性流行率的时间趋势。
1311名儿童共发生865例BSI,包括412例(48%)革兰氏阳性菌、196例(23%)革兰氏阴性菌、56例(6%)真菌、23例(3%)分枝杆菌和178例(21%)多微生物BSI。在研究期间,所有BSI的风险随时间变化不大,但真菌性BSI的风险在研究期间随时间下降(P = 0.04)。大多数真菌性BSI(82%)发生在HSCT后的前100天,而分枝杆菌性BSI在HSCT后出现的时间比其他病原体导致的BSI更晚(P < 0.0001)。在研究期间,由肠球菌引起的BSI中万古霉素耐药性的流行率增加(P = 0.0007)。儿童发生BSI(P = 0.02)、革兰氏阴性菌BSI(P = 0.02)和真菌性BSI(P < 0.0001)时2年死亡率风险增加。
尽管在过去几十年中BSI预防措施有所扩展,但在我们机构儿科HSCT受者中BSI的发生率仍然很高。迫切需要额外的策略来有效预防这一高危人群中的BSI。