重症监护病房常用静脉注射药物的y位点相容性:涉及9种主要药物的75种混合物的实验室试验

Gillian Ayari, E. D’huart, J. Vigneron, B. Demoré
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引用次数: 1

摘要

摘要目的重症监护病房住院患者经常需要多种药物输注。由于静脉输注途径有限,常常需要在同一输注线上同时给药。文献中有关于y位点给药的相容性研究,但缺乏几种组合的数据。d 'Huart等人在之前的工作中对三个成人icu的注射药物给药进行了观察,并确定了一个没有相容性数据的y位点给药列表。本研究的目的是测试该清单中主要药物在重症监护病房y点输注中成对使用的物理相容性,为文献提供新的相容性数据,并为静脉给药提供保障。方法对重症监护病房常用的9种药物与其他药物的y位物理相容性进行检测。75种混合物在制备后、储存1和4小时后进行检测。该评估包括视觉检查,包括寻找沉淀形成、颜色变化、气体形成,以及亚视觉评估:在350、410和550 nm处通过紫外可见分光光度法测量吸光度,以及光遮挡颗粒计数测试。每次分析时进行pH值评估。结果实验室测试表明,本研究获得的所有混合物的总体相容性为68.0%。耐福泮与其他药物的配伍性较好(95.0%)。盐酸胺碘酮(84.6%)、乙酰水杨酸(80.0%)、盐酸可乐定(75.0%)和胰岛素(71.4%)也与其他药物配伍。阿替洛尔(42.9%)、呋塞米(25.0%)、肝素钠(25.0%)相容性较差。泮托拉唑钠(0.0%)与所分析的其他药物完全不相容。通过这些实验室测试的结果,缺失的相容性数据现在是可用的,为文献提供了额外的信息。
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Y-site compatibility of intravenous medications commonly used in intensive care units: laboratory tests on 75 mixtures involving nine main drugs
Abstract Objectives Patients hospitalized in intensive care units often require multiple drug infusions. Due to limited intravenous accesses, concomitant administration of drugs in the same infusion line is often necessary. Compatibility studies of Y-site administration are available in the literature, but data of several combinations are lacking. Previous work from d’Huart et al. have performed an observation of the administration of injectable drugs in three adults ICUs and identified a list of Y-site administration without compatibility data. The objective of this study was to test the physical compatibility of the main drugs of this list used in pairs in Y-site infusions in critical care units, in order to provide new compatibility data to the literature, and to secure the administration of intravenous drugs. Methods The physical compatibility in Y-site of nine drugs with other drugs commonly used in intensive care units has been tested. Examinations were performed on 75 mixtures after their preparation, after 1 and 4-h storage. This evaluation included a visual examination with a search for precipitation formation, color change, gas formation, and a subvisual evaluation: absorbance measurements by UV-visible spectrophotometry at 350, 410 and 550 nm, and Light Obscuration Particle Count Test. The pH evaluation was performed at each time of analysis. Results Laboratory tests led to an overall compatibility of 68.0% for all mixtures obtained in this study. Nefopam was found to be quite compatible with other drugs (95.0%). Amiodarone hydrochloride (84.6%), acetylsalicylic acid (80.0%), clonidine hydrochloride (75.0%) and insulin (71.4%) were compatible with other drugs too. Atenolol (42.9%), furosemide (25.0%), heparin sodium (25.0%) showed less compatible results. Pantoprazole sodium (0.0%) was not at all compatible with the other drugs analyzed. Conclusions By the results of these laboratory tests, missing compatibility data are now available, providing additional information to the literature.
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