高危白血病儿童和青少年实施左氧氟沙星预防后中央线相关血流感染率的变化

IF 1 4区 医学 Q3 NURSING
Lauri A Linder, Cheryl Gerdy, Yeonjung Jo, Crystal Stark, Andrew Wilson
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引用次数: 0

摘要

背景:尽管采取了减少中心线相关血流感染(CLABSI)的措施,患有恶性血液病的儿童和青少年,以及那些疾病复发的儿童和青少年,仍然是感染的最大风险。这个单机构项目评估了高危血液恶性肿瘤患者在实施左氧氟沙星抗菌预防后CLABSI率的变化。方法:纳入2006年1月1日至2019年12月31日期间符合国家卫生安全网监测标准的CLABSIs阳性血培养事件。根据clabsi减少干预措施的实施情况,将数据分为四个时间段进行比较。使用条件泊松回归模型评估时间(干预期)对CLABSI率的影响,并在四个时间段之间进行事后Tukey两两比较。结果:从2006年到2019年,227名患者经历了310次clabsi。实施儿童医院协会(CHA)捆绑治疗(每1000行日3.29例)后,CLABSI发生率较基线(每1000行日4.84例)显著降低;然而,这种差异并不显著(p = 0.16)。随着正式支持性护理的增加,CLABSI率从基线下降(每1000个线日2.66;发病率比[IRR] = 0.60;pp p = .011)和CHA包加正式支持性护理(IRR = 0.58;p = .046)。讨论:结果表明,使用基于实践的证据方法来指导clabsi减少干预措施取得了持续成功。后续研究,应用机器学习算法,可能会发现额外的风险因素,并为未来的干预措施提供信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Changes in Central Line-Associated Bloodstream Infection (CLABSI) Rates Following Implementation of Levofloxacin Prophylaxis for Children and Adolescents With High-Risk Leukemia.

Background: Despite initiatives to reduce central line-associated bloodstream infection (CLABSI), children and adolescents with hematologic malignancies, as well as those with relapsed disease, remain at the greatest risk for infection. This single-institution project evaluated changes in CLABSI rates following implementation of antibacterial prophylaxis with levofloxacin for patients with high-risk hematologic malignancies. Methods: Positive blood culture events meeting National Health Safety Network surveillance criteria to be classified as CLABSIs from January 1, 2006, to December 31, 2019, were included. Data were organized into four time periods for comparison based on implementation of CLABSI-reduction interventions. Conditional Poisson regression models were used to evaluate the effect of time (intervention period) on CLABSI rates with post hoc Tukey pairwise comparisons between each of the four time periods. Results: From 2006 and 2019, 227 patients experienced 310 CLABSIs. Clinically important decreases in CLABSI rates from baseline (4.84 per 1,000 line days) occurred with implementation of Children's Hospital Association (CHA) bundles (3.29 per 1,000 line days); however, this difference was not significant (p  =  .16). CLABSI rates decreased from baseline with the addition of formalized supportive cares (2.66 per 1,000 line days; incidence rate ratio [IRR]  =  0.60; p < .01), and with the use of antibacterial prophylaxis (1.66 per 1,000 line days; IRR  =  0.35; p < .01). Post hoc comparisons indicated decreased CLABSI rates with the use of antibacterial prophylaxis compared with CHA bundles alone (IRR  =  0.49; p  =  .011) and CHA bundles plus formalized supportive cares (IRR  =  0.58; p  =  .046). Discussion: Results demonstrate sustained success using a practice-based evidence approach to guide CLABSI-reduction interventions. Follow-up research, applying machine learning algorithms, may identify additional risk factors and inform future interventions.

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