评估使用混合油脂注射乳剂与接受肠外营养的儿科患者30天死亡率或真菌导管相关血流感染持续感染之间的关系:一项回顾性队列研究。

IF 2.9 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Pharmacotherapy Pub Date : 2025-07-01 DOI:10.1002/phar.70037
Gustavo R Alvira-Arill, April Yarbrough, Jessica Tansmore, Caroline M Sierra, Ferras Bashqoy, Oscar R Herrera, Brian M Peters, Jeremy S Stultz
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引用次数: 0

摘要

背景:与大豆油和鱼油制剂相比,在接受肠外营养的儿科患者中,使用混合油脂注射乳剂可降低导管相关血流感染率。本研究的目的是比较接受混合油(smof脂)脂类注射乳剂或其他配方(大豆油[Intralipid]或鱼油[Omegaven])肠外营养的儿科患者真菌导管相关血流感染的临床结果。方法:回顾性队列研究美国5家儿科医院5年期间给予肠外营养和注射脂质乳剂后发生真菌导管相关血流感染的儿童患者。根据感染前接受的脂质注射乳剂的类型,通过二项分布的广义线性混合模型评估了首次血培养阳性和/或感染持续30天死亡率的综合结果的差异。结果:104例患者在感染前接受了混合油脂注射乳剂(n = 43)或其他制剂(n = 69),共评估了112例真菌导管相关血流感染。39例感染符合复合结局(32例持续感染,3例30天死亡,4例两者均有)。在多变量分析中,接受混合油脂注射乳剂显示复合结局无统计学意义的增加(优势比[OR][95%可信区间{CI}]: 1.80 [0.75-4.34];p = 0.19)。与综合结果独立相关的因素包括接受全身抗真菌预防治疗(OR [95% CI]: 5.72 [1.33-24.7];p = 0.019)和延迟中心静脉导管拔除(OR [95% CI]: 1.09 [1.01-1.19];p = 0.03)。与复合结果无关的显著因素包括持续接受脂质注射乳剂,经验性抗真菌选择,抗真菌给药时间以及感染前90天内的胃肠道手术。结论:与其他配方(大豆油或鱼油)相比,使用混合油脂注射乳剂在接受肠外营养的儿科患者的30天死亡率和/或真菌导管相关血流感染的持续感染方面具有非统计学显著性增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assessment of the association between mixed-oil lipid injectable emulsion use and 30-day mortality or infection persistence from fungal catheter-related bloodstream infections in pediatric patients following receipt of parenteral nutrition: A retrospective cohort study.

Background: Compared to soybean-oil and fish-oil formulations, the use of mixed-oil lipid injectable emulsion is associated with reduced catheter-related bloodstream infection rates in pediatric patients receiving parenteral nutrition. The objective of this study was to compare clinical outcomes of fungal catheter-related bloodstream infections in pediatric patients following receipt of parenteral nutrition with mixed-oil (SMOFlipid) lipid injectable emulsion or other formulations (soybean-oil [Intralipid] or fish-oil [Omegaven]).

Methods: A retrospective cohort study of pediatric patients with fungal catheter-related bloodstream infections following administration of parenteral nutrition and injectable lipid emulsion from five pediatric hospitals in the United States during a 5-year period was conducted. Differences in a composite outcome of 30-day mortality from first positive blood culture and/or infection persistence based on type of lipid injectable emulsion received prior to infection were assessed through generalized linear mixed models with binomial distribution.

Results: One-hundred twelve fungal catheter-related bloodstream infections were assessed from 104 patients who received mixed-oil lipid injectable emulsion (n = 43) or other formulations (n = 69) prior to infection. Thirty-nine infections met the composite outcome (32 with persistent infection, three with 30-day mortality, and four with both). On multivariable analysis, receipt of mixed-oil lipid injectable emulsion demonstrated a non-statistically significant increase in the composite outcome (odds ratio [OR] [95% confidence interval {CI}]: 1.80 [0.75-4.34]; p = 0.19). Factors independently associated with the composite outcome include receipt of systemic antifungal prophylaxis (OR [95% CI]: 5.72 [1.33-24.7]; p = 0.019) and delay in central venous catheter removal (OR [95% CI]: 1.09 [1.01-1.19]; p = 0.03). Notable factors not associated with the composite outcome included continued receipt of lipid injectable emulsion, empiric antifungal choice, time to antifungal administration, and gastrointestinal surgery within 90 days prior to infection.

Conclusion: Use of mixed-oil lipid injectable emulsion compared to other formulations (soybean-oil or fish-oil) demonstrated a non-statistically significant increase in 30-day mortality and/or infection persistence from fungal catheter-related bloodstream infections in pediatric patients receiving parenteral nutrition.

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来源期刊
Pharmacotherapy
Pharmacotherapy 医学-药学
CiteScore
7.80
自引率
2.40%
发文量
93
审稿时长
4-8 weeks
期刊介绍: Pharmacotherapy is devoted to publication of original research articles on all aspects of human pharmacology and review articles on drugs and drug therapy. The Editors and Editorial Board invite original research reports on pharmacokinetic, bioavailability, and drug interaction studies, clinical trials, investigations of specific pharmacological properties of drugs, and related topics.
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