静脉注射治疗的用药安全性:依托泊苷与模拟y部位给药期间肿瘤重症监护常用药物的相容性。

IF 4.7 2区 医学 Q1 CHEMISTRY, MEDICINAL
Drug Design, Development and Therapy Pub Date : 2025-02-18 eCollection Date: 2025-01-01 DOI:10.2147/DDDT.S489534
Haiwen Ding, Tong Tong, Sheng Liu, Liqin Tang, Zhaolin Chen
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引用次数: 0

摘要

目的:依托泊苷是一种广泛用于治疗儿童和成人肿瘤的抗肿瘤药物。危重病人在入院时预计会接受几种静脉注射药物。当相容性数据可用时,静脉注射药物可同时通过y位点给药。本研究旨在确定依托泊苷在模拟y位点给药过程中与45种持续输注药物的相容性,这些药物通常在肿瘤重症监护病房中使用。方法:将依托泊苷在0.9%氯化钠(NS)中稀释至0.25 mg/mL,其他静脉试验药物按照厂家推荐的最终临床所需浓度进行复配。在无菌条件下,将5ml依托泊苷与其他稀释的静脉注射药物按1:1的比例混合,模拟体外y部位给药。混合后,以一定的时间间隔(0,1,2,4小时)取出相容溶液,并使用廷德尔光束,pH,浊度,不溶性颗粒和紫外线吸收作为相容性的测量,进行目测测试。结果:45种药物中有38种(84%)在4小时内与依托泊苷相容。谷胱甘肽和人粒细胞集落刺激因子立即显示与依托泊苷不相容。1 h内4种药物(头孢呋辛钠、伊拉唑钠、霉酚酸酯、血必净)出现不相容。在4 h内,观察还发现有一种药物(头孢他啶)与依托泊苷不相容。结论:45种肿瘤危重监护常用药物中,有7种在4 h内出现不配伍,如需同时给药且经端口导管输注,应在输注依托泊苷前后用较大体积的生理盐水(NS)或5%水葡萄糖(D5W)冲洗端口导管,以清洁端口导管管腔。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Medication Safety in Intravenous Therapy: Compatibility of Etoposide with Frequently Drugs Used in Tumour Critical Care During Simulated Y-Site Administration.

Objective: Etoposide is an antineoplastic agent widely used to treat pediatric and adult cancers. Critically ill patients are expected to receive several intravenous pharmaceutical drugs while admitted to hospitals. When compatibility data are available, intravenous drugs may be administered simultaneously through the Y-site. This study aimed to determine the compatibility of etoposide during simulated Y-site administration with 45 continuous-infusion drugs that are commonly administered in tumor critical care units.

Methods: Etoposide was diluted to a concentration of 0.25 mg/mL in 0.9% sodium chloride (NS) and other intravenously tested drugs were reconstituted according to the manufacturer's recommendations to the final clinical desired concentrations. Y-site administration was simulated in vitro by mixing 5 mL etoposide with other diluted intravenous medications under aseptic conditions in a 1:1 ratio. Compatible solutions were withdrawn at certain time intervals (0, 1, 2, 4 hours) after mixing and tested visually, using a Tyndall beam, pH, turbidity, insoluble particles, and UV absorption as measures of compatibility.

Results: Etoposide was compatible with 38 (84%) of the 45 drugs tested within four hours. Glutathione and human granulocyte colony-stimulating factor immediately showed incompatibility with etoposide. Within 1 h, four medications (cefuroxime sodium, ilaprazole sodium, mycophenolate, and xuebijing) were incompatible. Within 4 h, one medications (ceftazidime) were also found to be incompatible with etoposide under observation.

Conclusion: Seven of the 45 common medications in tumor critical care tested with etoposide were incompatible within 4 h. If co administration is inevitable and the drug is infused through a port catheter, a larger volume of saline (NS) or dextrose 5% in water (D5W) should be used to flush the port catheter before and after the etoposide infusion to clean the lumen of the port catheter.

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来源期刊
Drug Design, Development and Therapy
Drug Design, Development and Therapy CHEMISTRY, MEDICINAL-PHARMACOLOGY & PHARMACY
CiteScore
9.00
自引率
0.00%
发文量
382
审稿时长
>12 weeks
期刊介绍: Drug Design, Development and Therapy is an international, peer-reviewed, open access journal that spans the spectrum of drug design, discovery and development through to clinical applications. The journal is characterized by the rapid reporting of high-quality original research, reviews, expert opinions, commentary and clinical studies in all therapeutic areas. Specific topics covered by the journal include: Drug target identification and validation Phenotypic screening and target deconvolution Biochemical analyses of drug targets and their pathways New methods or relevant applications in molecular/drug design and computer-aided drug discovery* Design, synthesis, and biological evaluation of novel biologically active compounds (including diagnostics or chemical probes) Structural or molecular biological studies elucidating molecular recognition processes Fragment-based drug discovery Pharmaceutical/red biotechnology Isolation, structural characterization, (bio)synthesis, bioengineering and pharmacological evaluation of natural products** Distribution, pharmacokinetics and metabolic transformations of drugs or biologically active compounds in drug development Drug delivery and formulation (design and characterization of dosage forms, release mechanisms and in vivo testing) Preclinical development studies Translational animal models Mechanisms of action and signalling pathways Toxicology Gene therapy, cell therapy and immunotherapy Personalized medicine and pharmacogenomics Clinical drug evaluation Patient safety and sustained use of medicines.
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