Risk of thrombophlebitis associated with continuous peripheral infusion of vancomycin: The effect of dilution.

Q3 Medicine JAVA - Journal of the Association for Vascular Access Pub Date : 2024-01-01 Epub Date: 2022-05-24 DOI:10.1177/11297298221095778
Marianna Scarano, Sonia D'Arrigo, Sestilio De Letteriis, Salvatore Grasso, Mauro Pittiruti, Giancarlo Scoppettuolo
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Abstract

Introduction: Although several guidelines recommend that prolonged administration of vancomycin should be preferably carried out by a central venous access, vancomycin is often given peripherally. Whether such risk may be affected by different modalities of administration in terms of dilution and time of infusion, it is a matter of controversy.

Methods: This single-center prospective study enrolled all consecutive patients requiring prolonged intravenous infusion of vancomycin (1 g/day) using long peripheral cannula "mini-midline." Patients were randomized in study group (4 mg/ml) and control group (20 mg/ml). All patients were systematically evaluated every 24 h by the Visual Exit-Site Score and a daily ultrasound scan of the veins of the arm.

Results: The daily ultrasound evaluation showed venous thrombosis at the distal tip of the cannula in all patients, in both groups. After this finding in the first 14 patients, the study was interrupted. All thromboses were completely asymptomatic and occurred in absence of any sign of catheter malfunction. The onset of thrombosis was significantly earlier in the control group (ranging from 24 to 48 h) than in the study group (ranging from 48 to 96 h), with an average of 30 ± 11 versus 68 ± 16 h (p < 0.001).

Conclusion: Continuous intravenous infusion of vancomycin should be preferably delivered by a central venous access, as largely recommended by current guidelines, since peripheral infusion is inevitably associated with venous thrombosis, independently from the type of peripheral venous access device adopted (short peripheral cannula vs long peripheral cannula) and from the extent of dilution.

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持续外周输注万古霉素的血栓性静脉炎风险:稀释的影响。
简介尽管一些指南建议,万古霉素的长期给药最好通过中心静脉通路进行,但万古霉素通常通过外周给药。这种风险是否会受到不同给药方式在稀释和输注时间方面的影响,目前还存在争议:这项单中心前瞻性研究招募了所有需要使用外周长插管 "迷你中线 "长期静脉输注万古霉素(1 克/天)的连续患者。患者被随机分为研究组(4 毫克/毫升)和对照组(20 毫克/毫升)。所有患者每 24 小时接受一次视觉出口部位评分和每日手臂静脉超声波扫描的系统评估:结果:每日超声波评估显示,两组所有患者的插管远端都出现了静脉血栓。在前 14 名患者发现这一情况后,研究中断。所有血栓均完全无症状,且发生时导管无任何故障迹象。对照组血栓形成的时间(24 至 48 小时不等)明显早于研究组(48 至 96 小时不等),平均为 30 ± 11 小时对 68 ± 16 小时(P < 0.001):万古霉素的连续静脉输注最好通过中心静脉通路进行,这也是当前指南的主要建议,因为外周输注不可避免地与静脉血栓形成有关,这与采用的外周静脉通路装置类型(短外周插管与长外周插管)和稀释程度无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
JAVA - Journal of the Association for Vascular Access
JAVA - Journal of the Association for Vascular Access Medicine-Medicine (miscellaneous)
CiteScore
1.10
自引率
0.00%
发文量
22
期刊介绍: The Association for Vascular Access (AVA) is an association of healthcare professionals founded in 1985 to promote the emerging vascular access specialty. Today, its multidisciplinary membership advances research, professional and public education to shape practice and enhance patient outcomes, and partners with the device manufacturing community to bring about evidence-based innovations in vascular access.
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