Chemical Compatibility of N-Acetylcysteine After the Simultaneous Intravenous Administration of Ondansetron.

Q2 Medicine
Stacy Brown, Benjamin Kennard, Jim Thigpen
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引用次数: 0

Abstract

Objective: This study evaluated the chemical compatibility of N-acetylcysteine (NAC) and ondansetron to simplify the treatment of acute nausea and vomiting during intravenous (IV) NAC administration. NAC is commonly used to treat acetaminophen overdose, but its 21-hour IV infusion is often interrupted for ondansetron administration, which can pose risks.

Methods: High-performance liquid chromatography with ultraviolet detection was used to quantify NAC. To simulate IV administration, a closed-circuit pump with multiple independent lines, was plumbed with Y-sites to circulate NAC at concentrations matching 30- and 100-kg loading doses and 4-mg ondansetron was pushed into the flow paths. Control lines without ondansetron were also maintained. Samples were collected at 10, 20, and 30 minutes postondansetron introduction. NAC concentrations in single-drug and combination lines were compared using an unpaired t-test with Welch's correction (p = 0.05).

Results: The mean concentrations for the 100-kg dose were 55.23 and 55.28 mg/mL for control and with ondansetron, respectively. The 30-kg cohort included 36.38 mg/mL for control and 36.49 mg/mL with ondansetron. The results of the unpaired t-test for either weight illustrated that no statistical significance was achieved. Furthermore, the t-values of 0.2013 for 100 kg and 0.8556 for 30 kg support a less likely chance of significant difference.

Conclusion: Based on this experiment, ondansetron can be introduced into an NAC infusion via IV push in vitro without affecting the NAC concentration in the solution. The likelihood of IV compatibility for NAC and ondansetron could permit no infusion interruptions, reducing unnecessary risk of acetaminophen toxicity.

同时静脉给药昂丹司琼后n -乙酰半胱氨酸的化学相容性。
目的:评价n -乙酰半胱氨酸(NAC)与昂丹司琼的化学相容性,以简化静脉注射NAC时急性恶心呕吐的治疗。NAC通常用于治疗对乙酰氨基酚过量,但其21小时静脉输注经常因使用昂丹司琼而中断,这可能会造成风险。方法:采用高效液相色谱-紫外检测法定量测定NAC。为了模拟静脉给药,一个带有多条独立管线的闭环泵,与y位点相连,以30和100公斤负荷剂量的浓度循环NAC,并将4毫克昂丹司琼推入流动路径。没有昂丹司琼的控制线也被维持。在使用丹西酮后10分钟、20分钟和30分钟采集样本。单药系和联合用药系NAC浓度比较采用Welch校正的非配对t检验(p = 0.05)。结果:对照组和昂丹司琼组的平均浓度分别为55.23和55.28 mg/mL。30公斤的队列包括36.38 mg/mL的对照组和36.49 mg/mL的昂丹司琼组。对任意一个权重进行非配对t检验的结果表明,没有达到统计学意义。此外,100公斤的t值为0.2013,30公斤的t值为0.8556,支持显著差异的可能性较小。结论:在本实验基础上,体外静脉推注昂丹司琼可在不影响NAC浓度的情况下,将昂丹司琼引入NAC输注中。NAC和昂丹司琼的静脉相容性可能不允许输注中断,减少不必要的对乙酰氨基酚毒性风险。
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
Journal of Pediatric Pharmacology and Therapeutics
Journal of Pediatric Pharmacology and Therapeutics Medicine-Pediatrics, Perinatology and Child Health
CiteScore
2.40
自引率
0.00%
发文量
90
期刊介绍: The Journal of Pediatric Pharmacology and Therapeutics is the official journal of the Pediatric Pharmacy Advocacy Group. JPPT is a peer-reviewed multi disciplinary journal that is devoted to promoting the safe and effective use of medications in infants and children. To this end, the journal publishes practical information for all practitioners who provide care to pediatric patients. Each issue includes review articles, original clinical investigations, case reports, editorials, and other information relevant to pediatric medication therapy. The Journal focuses all work on issues related to the practice of pediatric pharmacology and therapeutics. The scope of content includes pharmacotherapy, extemporaneous compounding, dosing, methods of medication administration, medication error prevention, and legislative issues. The Journal will contain original research, review articles, short subjects, case reports, clinical investigations, editorials, and news from such organizations as the Pediatric Pharmacy Advocacy Group, the FDA, the American Academy of Pediatrics, the American Society of Health-System Pharmacists, and so on.
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