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毒理学复苏期间不同注射溶液与 10% 钙剂的 Y 型部位模拟兼容性研究。

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

机构信息

Université de Montréal, Montreal, Québec, Canada.

CIUSSS du Centre-Ouest-de-l'Ile-de-Montreal, Montreal, Québec, Canada.

出版信息

Eur J Hosp Pharm. 2024 Oct 25;31(6):583-587. doi: 10.1136/ejhpharm-2023-003689.

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.

摘要

目的

确定 10%氯化钙和 10%葡萄糖酸钙与注射溶液在儿科和成人重症监护病房中的组合的物理相容性,这些溶液用于涉及钙通道阻滞剂和β-受体阻滞剂的毒理学复苏。

方法

在室温下制备了 48 种组合,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 和林格氏乳酸盐。在 0、1、4、24、48 和 72 小时进行了目视评估,并在 0、4、24 和 72 小时使用 LS-20 粒子计数器进行了粒子计数测试。如果出现沉淀、颜色变化、混浊、粘度或气体形成,则认为混合物不相容。还通过粒子计数测试在空 IV 袋和注射器中测试了钙盐的稳定性。

结果

通过目视评估和基于美国药典第 788 章(USP<788>)规格的粒子计数器,发现所有药物混合物均相容。钙盐与胰岛素和血管加压素在测试组合中相容。在室温下,10%钙盐在空 IV 袋和聚丙烯注射器中的稳定性可长达 48 小时。

结论

在室温下,所有测试的组合在 72 小时内均具有物理相容性。在毒理学复苏背景下,以未稀释浓度将钙盐输注与这些注射溶液联合使用被认为在临床上是可接受的。

相似文献

本文引用的文献

1
Treatment for beta-blocker poisoning: a systematic review.β受体阻滞剂中毒的治疗:一项系统评价。
Clin Toxicol (Phila). 2020 Oct;58(10):943-983. doi: 10.1080/15563650.2020.1752918. Epub 2020 Apr 20.
2
Treatment for calcium channel blocker poisoning: a systematic review.钙通道阻滞剂中毒的治疗:系统评价。
Clin Toxicol (Phila). 2014 Nov;52(9):926-44. doi: 10.3109/15563650.2014.965827. Epub 2014 Oct 6.

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