重新评估风险:股骨、颈内和锁骨下中心静脉导管CLABSI风险的回顾性分析。

IF 1.8 Q3 CRITICAL CARE MEDICINE
Critical Care Research and Practice Pub Date : 2025-04-29 eCollection Date: 2025-01-01 DOI:10.1155/ccrp/8193419
Alexandra Vaughan-Masamitsu, Wesley Paulson, Robert Hodes, Cain Dudek
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引用次数: 0

摘要

背景:中心线相关性血流感染(CLABSIs)由于其与发病率、死亡率增加和经济负担相关,是一个重大的医疗保健挑战。目前的指南不鼓励使用股静脉(FV)放置中心静脉导管(CVC),因为与颈内静脉(IJV)或锁骨下(SCV)位置相比,股静脉(FV)的感染风险更高。然而,最近的证据对这一假设提出了质疑,并表明股动脉粥样硬化可能与其他部位具有相似的风险,强调需要更新分析。目的:本研究的目的是消除一种误解,即与其他中心线部位相比,股骨cvc发生CLABSI的相关风险更高。本研究评估了FV、IJV和SCV部位CLABSI的风险。方法:使用TriNetX研究网络进行回顾性队列分析,初步查询确定了2014年至2025年间遇到的99,216例CVC安置患者。倾向评分匹配后,保留65,265例患者进行统计分析。根据解剖CVC放置位置将患者分为IJV、SCV和FV组。在cvc植入后1天至1个月内,使用ICD-10-CM编码测定CLABSI发生率。对2014-2025年、2014-2019年和2019-2025年进行敏感性分析,以评估总体风险,并评估解剖部位CLABSI风险随时间的变化。采用风险百分比、风险比和95%置信区间的优势比对结果进行比较,比较不同部位CLABSI的风险差异。结果:总体而言,2014-2025年期间,与IJV或FV cvc相比,股骨cvc与CLABSI的风险增加没有统计学意义。2014-2025年间,只有合资企业和SCV的风险差异有统计学意义。与SCV cvc相比,IJV cvc与CLABSI风险较高相关,风险差异为0.089% (95% CI: 0.006%, 0.171%, Z = 2.11, p=0.0348),风险比为1.708 (95% CI:1.033, 2.826),优势比为1.71 (95% CI:1.033, 2.831)。2014-2019年期间,IJV组和FV组之间的风险差异无统计学意义(风险差异0.09%,95% CI: -0.035%, 0.215%, Z = 1.415, p=0.1569)。比较2014-2019年期间IJV与SCV的CLABSI率,风险差异为0.112% (95% CI: -0.009%, 0.234%, Z = 1.81, p=0.07)。2019-2025年期间,IJV组和FV组的风险差异为-0.077% (FV组风险更高),差异无统计学意义(95% CI: -0.193%, 0.04%, Z = -1.289, p=0.1974)。比较2019-2025年期间IJV与SCV的CLABSI率,风险差异为0.117% (95% CI: = -0.006%, 0.24%, Z = 1.861, p=0.0627),差异无统计学意义。结论:本研究挑战了普遍的假设,即与IJV和SCV部位相比,股骨cvc发生CLABSI的风险更高,风险没有显着差异。这些发现表明,出于对感染的担忧而避免FV放置CVC可能会不必要地限制临床选择,而不会改善患者的预后。强调部位特异性风险,如技术并发症和解剖学考虑,而不是感染问题,可以简化CVC放置的决策并增强个性化护理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reassessing the Risk: A Retrospective Analysis of CLABSI Risk in Femoral, Internal Jugular, and Subclavian Central Venous Catheters.

Background: Central line-associated bloodstream infections (CLABSIs) represent a significant healthcare challenge due to their association with increased morbidity, mortality, and financial burden. Current guidelines discourage the use of the femoral vein (FV) for central venous catheter (CVC) placement due to a perceived higher infection risk compared to the internal jugular vein (IJV) or subclavian (SCV) sites. However, recent evidence questions this assumption and suggests that femoral CVCs may carry similar risks to other sites, emphasizing the need for updated analyses. Objective: The goal of this study was to address the misconception that femoral CVCs have a higher associated risk for developing CLABSI compared to other central line sites. This study evaluates risk for CLABSI across FV, IJV, and SCV sites. Methods: Using the TriNetX Research Network to conduct a retrospective cohort analysis, initial queries identified 99,216 patients who were encountered between 2014 and 2025 for CVC placement. Following propensity score matching, 65,265 of these patients were retained for statistical analysis. Patients were categorized based on anatomic CVC placement sites into IJV, SCV, and FV cohorts. CLABSI incidence was determined using ICD-10-CM codes within 1 day to 1 month post-CVC insertion. Sensitivity analyses were conducted for the 2014-2025 period, as well as for the 2014-2019 and 2019-2025 periods to assess overall risk and evaluate for changes in CLABSI risk by anatomic site over time. Outcomes were compared using risk percentages, risk ratios, and odds ratios with 95% confidence intervals to compare differences in risk for CLABSI across different sites. Results: Overall, femoral CVCs were not associated with a statistically significant higher risk of CLABSI compared to IJV or FV CVCs from the overall period of 2014-2025. Only the risk difference between IJV and SCV CVCs over 2014-2025 showed a statistically significant difference. IJV CVCs were associated with a higher risk of CLABSI compared with SCV CVCs, with a risk difference of 0.089% (95% CI: 0.006%, 0.171%, Z = 2.11, p=0.0348), a risk ratio of 1.708 (95% CI: 1.033, 2.826), and an odds ratio of 1.71 (95% CI:1.033, 2.831). Over the 2014-2019 period, there was no statistically significant risk difference between the IJV and FV cohorts (risk difference 0.09%, 95% CI: -0.035%, 0.215%, Z = 1.415, p=0.1569). Comparing the IJV to SCV CLABSI rates for the 2014-2019 period, the risk difference was 0.112% (95% CI: -0.009%, 0.234%, Z = 1.81, p=0.07). For the 2019-2025 period between the IJV and FV cohorts, the risk difference was -0.077% (higher risk in the FV cohort), which was not a statistically significant difference (95% CI: -0.193%, 0.04%, Z = -1.289, p=0.1974). Comparing the IJV to SCV CLABSI rates for the 2019-2025 period, the risk difference was 0.117% (95% CI: = -0.006%, 0.24%, Z = 1.861, p=0.0627), which was not a statistically significant difference. Conclusions: This study challenges the prevailing assumption that femoral CVCs carry a higher risk of CLABSI compared to IJV and SCV sites, showing no significant difference in risk. These findings suggest that avoidance of the FV for CVC placement out of concern for infection may unnecessarily limit clinical options without improving patient outcomes. Emphasizing site-specific risks like technical complications and anatomical considerations over infection concerns could simplify decision-making and enhance personalized care in CVC placement.

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来源期刊
Critical Care Research and Practice
Critical Care Research and Practice CRITICAL CARE MEDICINE-
CiteScore
3.60
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34
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14 weeks
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