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多药静脉注射治疗期间总体微粒污染暴露的体外分析:输液器的影响

In vitro analysis of overall particulate contamination exposure during multidrug IV therapy: impact of infusion sets.

作者信息

Perez Maxime, Décaudin Bertrand, Abou Chahla Wadih, Nelken Brigitte, Barthélémy Christine, Lebuffe Gilles, Odou Pascal

机构信息

EA GRITA, University Lille Nord de France, Lille, France; Institute of Pharmacy, Lille University Hospital, Lille, France.

出版信息

Pediatr Blood Cancer. 2015 Jun;62(6):1042-7. doi: 10.1002/pbc.25442. Epub 2015 Mar 8.

Abstract

BACKGROUND

Drug incompatibilities, recognizable through precipitate, may have clinical consequences for patients, especially during multidrug IV therapies, where vancomycin and piperacillin are present. Drug concentration and infusion set influence the overall particulate contamination of pediatric infusion protocols. The use of multi-lumen infusion sets could prevent such incompatibilities. Our goal was to define and assess a new way to infuse these drugs during leukemia treatment in children.

PROCEDURES

This in vitro study focused on a pediatric multidrug protocol for patients diagnosed with lymphoblastic leukemia and receiving allogeneic transplantation. Different vancomycin concentrations were tested to infuse incompatible drugs simultaneously without any particle formation (optimized multidrug protocol). A dynamic particle count test was used over 24 hr to evaluate the overall particulate contamination of our standard and optimized multidrug protocols, using both a standard and a multi-lumen infusion set.

RESULTS

No visible particles were detected on a decreased vancomycin concentration compared to the standard dose. For the optimized multidrug protocol, the use of a multi-lumen infusion set reduced overall particulate contamination by 68%, compared to the standard infusion set (P = 0.002). Large-sized particles were significantly reduced when using the multi-lumen infusion set approximately 60% (P = 0.027) and 90% (P = 0.009) for particle sizes ≥10 μm and 25 μm, respectively.

CONCLUSIONS

This study demonstrates that a large number of particles can be administered during parenteral multidrug infusion. The choice of drug concentration and/or the type of infusion set may reduce this. Further studies are required to evaluate adverse clinical effects.

摘要

背景

药物不相容性可通过沉淀识别,这可能对患者产生临床后果,尤其是在同时使用万古霉素和哌拉西林的多药静脉治疗期间。药物浓度和输液器会影响儿科输液方案中的总体微粒污染。使用多腔输液器可预防此类不相容性。我们的目标是确定并评估一种在儿童白血病治疗期间输注这些药物的新方法。

程序

这项体外研究聚焦于针对被诊断为淋巴细胞白血病并接受同种异体移植的患者的儿科多药方案。测试了不同的万古霉素浓度,以便在不形成任何微粒的情况下同时输注不相容药物(优化的多药方案)。使用动态微粒计数测试在24小时内评估我们的标准和优化多药方案的总体微粒污染情况,同时使用标准输液器和多腔输液器。

结果

与标准剂量相比,在降低万古霉素浓度时未检测到可见微粒。对于优化的多药方案,与标准输液器相比,使用多腔输液器可使总体微粒污染减少68%(P = 0.002)。使用多腔输液器时,对于粒径≥10μm和25μm的微粒,大尺寸微粒分别显著减少约60%(P = 0.027)和90%(P = 0.009)。

结论

本研究表明,在胃肠外多药输注期间可输注大量微粒。药物浓度的选择和/或输液器类型可能会减少这种情况。需要进一步研究以评估不良临床影响。

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