A GAVeCeLT bundle for central venous catheterization in neonates and children: A prospective clinical study on 729 cases.

Q2 Biochemistry, Genetics and Molecular Biology
Genes and Cancer Pub Date : 2023-11-01 Epub Date: 2022-05-09 DOI:10.1177/11297298221074472
Mauro Pittiruti, Davide Celentano, Giovanni Barone, Vito D'Andrea, Maria Giuseppina Annetta, Giorgio Conti
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引用次数: 10

Abstract

Background: In the pediatric patient, central venous catheterization may be associated with relevant complications. Though, most of them may be prevented by a wise choice of materials, methods, and techniques. Evidence-based insertion bundles for central venous catheterization have been developed in the adult patient, but not in neonates and children.

Methods: The Italian Group for Long Term Venous Access Devices (GAVeCeLT) has developed an insertion bundle for central venous catheterization in neonates, infants, and children, which includes seven evidence-based strategies: (1) preprocedural ultrasound evaluation, (2) appropriate aseptic technique, (3) ultrasound guided venipuncture, (4) intraprocedural tip location by non-radiological methods, (5) proper choice of the exit site by tunneling, (6) sutureless securement, and (7) protection of the exit site using glue and transparent membranes. The effectiveness and safety of this bundle has been tested in a prospective study.

Results: All neonates, infants and children requiring a non-emergency central line (except for umbilical venous catheters and epicutaneo-cava catheters) were included in the study. Out of 729 central line insertions, there were no immediate complications (no pneumothorax, no arterial puncture, no malposition); the incidence of early and late complications (local ecchymosis, dislodgment, local pain, exit site infection) was 3.7%; in the first 2 weeks after insertion, no catheter-related bacterial infection or catheter-related thrombosis was recorded.

Conclusion: The results of this prospective study strongly validate the hypothesis that an insertion bundle is highly effective in optimizing the safety of the maneuver, reducing immediate, early, and late complications.

用于新生儿和儿童中心静脉导管插入术的 GAVeCeLT 管束:729 例前瞻性临床研究。
背景:在儿科患者中,中心静脉导管插入术可能会引起相关并发症。不过,通过明智地选择材料、方法和技术,大多数并发症是可以避免的。以证据为基础的中心静脉导管插入捆绑术已在成人患者中应用,但尚未在新生儿和儿童中应用:方法:意大利长期静脉通路设备小组(GAVeCeLT)已制定了新生儿、婴儿和儿童中心静脉导管插入捆绑包,其中包括七项循证策略:(1) 术前超声评估;(2) 适当的无菌技术;(3) 超声引导下的静脉穿刺;(4) 用非放射学方法进行术中尖端定位;(5) 用隧道法正确选择出口部位;(6) 无缝线固定;(7) 用胶水和透明膜保护出口部位。一项前瞻性研究对这种捆绑方法的有效性和安全性进行了测试:所有需要非急诊中心静脉置管(脐静脉导管和腔外导管除外)的新生儿、婴儿和儿童都被纳入研究范围。在 729 例中心静脉置管手术中,没有出现直接并发症(无气胸、无动脉穿刺、无错位);早期和晚期并发症(局部瘀斑、脱落、局部疼痛、出口感染)的发生率为 3.7%;在置管后的头两周内,没有发生导管相关细菌感染或导管相关血栓形成:这项前瞻性研究的结果有力地验证了插入捆绑包能有效优化操作安全性、减少即时、早期和晚期并发症的假设。
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
Genes and Cancer
Genes and Cancer Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
3.90
自引率
0.00%
发文量
6
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