儿童短肠综合征中央线相关血流感染的危险因素。

IF 4.1
JPEN. Journal of parenteral and enteral nutrition Pub Date : 2020-03-01 Epub Date: 2019-06-09 DOI:10.1002/jpen.1667
Talal B Seddik, Lu Tian, Colleen Nespor, John Kerner, Yvonne Maldonado, Hayley Gans
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引用次数: 10

摘要

背景:接受家庭肠外营养(HPN)的短肠综合征(SBS)儿童易发生动态中央线相关血流感染(A-CLABSI)。描述儿童中这种感染的危险因素的数据有限。方法:对2012年1月至2016年12月接受HPN治疗的≤18岁SBS患儿进行回顾性队列、单中心、病例交叉研究。单因素和多因素混合效应泊松回归确定了A-CLABSI的相对危险度(RR)与提出的危险因素。结果:确诊35例;中位随访时间为30个月。A-CLABSI发生率为4.2 / 1000中央线(CL)天。单因素分析发现年龄更年轻(RR: 0.92 / 12个月)[95%可信区间{CI}: 0.85-0.99;P = 0.036]),小肠长度较短(RR: 0.96 / 10厘米增加[95% CI: 0.92-0.99;P = 0.008]),瓜氨酸水平降低(RR: 0.86 / 5-nmol/mL) [95% CI: 0.75-0.99;P = 0.036]),近期CL断裂(RR: 1.55 [95% CI: 1.06-2.28;P = 0.024])为A-CLABSI的危险因素。多因素分析显示,临床诊断为小肠细菌过度生长(SIBO)时,A-CLABSI升高(RR: 1.87 [95% CI: 1.1-3.17;P = 0.021])和CL断裂(RR: 1.49 [95% CI: 1-2.22;P = 0.024])。结论:影响肠道完整性的因素增加了A-CLABSI的发生率,支持易位作为预防的重要机制和靶点。SIBO的临床诊断增加了A-CLABSI的发生率,但究竟是生态失调还是腹泻的原因是未来的研究领域。CL的维护是至关重要的,预防断裂可能会降低A-CLABSI的发生率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Risk Factors of Ambulatory Central Line-Associated Bloodstream Infection in Pediatric Short Bowel Syndrome.

Background: Children with short bowel syndrome (SBS) receiving home parenteral nutrition (HPN) are predisposed to ambulatory central line-associated bloodstream infection (A-CLABSI). Data describing risk factors of this infection in children are limited.

Methods: Retrospective cohort, single-center, case-crossover study of children ≤18 years old with SBS receiving HPN from January 2012 to December 2016. Univariate and multivariate mixed effect Poisson regression identified the relative risk (RR) of A-CLABSI with proposed risk factors.

Results: Thirty-five children were identified; median follow-up was 30 months. A-CLABSI rate was 4.2 per 1000 central line (CL) days. Univariate analysis identified younger age (RR: 0.92 per 12-month increase [95% confidence interval {CI}: 0.85-0.99; P = 0.036]), shorter small intestine length (RR: 0.96 per 10-cm increase [95% CI: 0.92-0.99; P = 0.008]), lower citrulline level (RR: 0.86 per 5-nmol/mL increase [95% CI: 0.75-0.99; P = 0.036]), and recent CL break (RR: 1.55 [95% CI: 1.06-2.28; P = 0.024]) as risk factors for A-CLABSI. Multivariate analysis showed increased A-CLABSI with clinical diagnosis of small intestine bacterial overgrowth (SIBO) (RR: 1.87 [95% CI: 1.1-3.17; P = 0.021]) and CL breaks (RR: 1.49 [95% CI: 1-2.22; P = 0.024]).

Conclusions: Factors influencing gut integrity increase A-CLABSI rate, supporting translocation as an important mechanism and target for prevention. Clinical diagnosis of SIBO increases A-CLABSI rate, but whether dysbiosis or diarrhea is responsible is an area for future research. CL maintenance is crucial, and prevention of breaks would likely decrease A-CLABSI rate.

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