Y-site simulation compatibility study of 10% calcium salts with various injectable solutions during toxicological resuscitation.

IF 1.6 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Arianne Hamelin, Félix Thompson-Desormeaux, Audrée Elliott, Mihaela Friciu, Jean-Marc Forest, Gregoire Leclair
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引用次数: 0

Abstract

Purpose: To determine the physical compatibility of 10% calcium chloride and 10% calcium gluconate in combination with injectable solutions, administered in the paediatric and adult intensive care unit setting during toxicological resuscitation involving calcium channel blockers and beta-blockers.

Methods: Forty-eight combinations were prepared at room temperature, including the following products: calcium chloride, calcium gluconate, insulin, epinephrine, norepinephrine, highly concentrated dextrose solution, sodium chloride, Plasma-Lyte A and Ringer's lactate. A visual evaluation at times 0, 1, 4, 24, 48 and 72 hours and a particle count test with the LS-20 particle counter at times 0, 4, 24 and 72 hours were performed. The admixtures were considered incompatible if there was a precipitate, a colour change, turbidity, viscosity or a gas formation. The stability of calcium salts was also tested in empty IV bags and syringes by the particle count test.

Results: All drug mixtures were found to be compatible by visual evaluation and using the particle counter based on United States Pharmacopoeia chapter 788 (USP<788>) specifications. Calcium salts were compatible with insulin and vasopressors in the tested combinations. The stability of 10% calcium salts in empty IV bags and polypropylene syringes was demonstrated for up to 48 hours at room temperature.

Conclusion: All the combinations tested were physically compatible for up to 72 hours at room temperature. Clinical use of calcium salt infusions, at an undiluted concentration, in combination with these injectable solutions in a toxicological resuscitation context is considered clinically acceptable.

中毒复苏期间 10%钙盐与各种注射液的 Y-site 模拟兼容性研究。
目的:确定 10%氯化钙和 10%葡萄糖酸钙与注射溶液的物理相容性:在室温下配制了 48 种混合溶液,包括以下产品:氯化钙、葡萄糖酸钙、胰岛素、肾上腺素、去甲肾上腺素、高浓度葡萄糖溶液、氯化钠、Plasma-Lyte A 和林格乳酸盐。在 0、1、4、24、48 和 72 小时时进行目测评估,在 0、4、24 和 72 小时时使用 LS-20 粒子计数器进行粒子计数测试。如果出现沉淀、颜色变化、浑浊、粘度或气体形成,则认为外加剂不相容。此外,还通过粒子计数测试法检测了钙盐在空静脉注射袋和注射器中的稳定性:根据美国药典第 788 章(USP)的规定,通过目测评估和使用粒子计数器,发现所有药物混合物都是相容的。在测试的组合中,钙盐与胰岛素和血管加压剂相容。在室温下,10% 的钙盐在空静脉注射袋和聚丙烯注射器中的稳定性可长达 48 小时:结论:所有测试组合在室温下的物理相容性可达 72 小时。在临床上,将未稀释浓度的钙盐输液与这些注射溶液结合起来用于毒物复苏是可以接受的。
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来源期刊
CiteScore
3.40
自引率
5.90%
发文量
104
审稿时长
6-12 weeks
期刊介绍: European Journal of Hospital Pharmacy (EJHP) offers a high quality, peer-reviewed platform for the publication of practical and innovative research which aims to strengthen the profile and professional status of hospital pharmacists. EJHP is committed to being the leading journal on all aspects of hospital pharmacy, thereby advancing the science, practice and profession of hospital pharmacy. The journal aims to become a major source for education and inspiration to improve practice and the standard of patient care in hospitals and related institutions worldwide. EJHP is the only official journal of the European Association of Hospital Pharmacists.
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