Physical compatibility of ceftriaxone and cefepime in 0.45% sodium chloride, Ringer's lactate solution, and Plasma-Lyte A.

IF 1.6 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Megan Kelley, Chloe Spooneybarger, Mitchell Howard, Justin Reinert, Mariann D Churchwell, Gabriella Baki
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Abstract

Objectives: The compatibility of intravenous fluids with medications is of paramount concern to pharmacists and is an imperative component of ensuring patient safety. Data regarding the physical compatibility of medications with intravenous fluids has not been examined, or published with conflicting results or the concentrations studied were not consistent with current practice. Our objective was to determine the physical compatibility of ceftriaxone and cefepime in 0.45% sodium chloride, Ringer's lactate solution, and Plasma-Lyte A.

Methods: An in vitro analysis of the physical compatibility of ceftriaxone and cefepime at 10 mg/mL, 20 mg/mL, and 40 mg/mL concentrations was conducted in 0.45% sodium chloride, Ringer's lactate solution, and Plasma-Lyte A. Admixtures were evaluated in triplicate at hours 0, 1, 5, 8, and 24. Physical compatibility was assessed by visual inspection, spectrophotometry, and pH analysis.

Results: Ceftriaxone 40 mg/mL was found to be physically incompatible in 0.45% sodium chloride and Ringer's lactate solution beyond 5 hours and in Plasma-Lyte A beyond 8 hours. Cefepime was found to be physically incompatible with all fluids and in all concentrations beyond 1 hour.

Conclusions: This work contributes to the body of literature dedicated to the evaluation of intravenous drug and fluid physical compatibility by identifying demonstrable changes in admixtures containing 0.45% sodium chloride, Plasma-Lyte A, and Ringer's lactate solution. Ceftriaxone should not be administered with 0.45% sodium chloride, Ringer's lactated solution, or Plasma-Lyte A at selected concentrations and time points and cefepime is not considered to be physically compatible at 10 mg/mL, 20 mg/mL, or 40 mg/mL in any of the studied fluids beyond 1 hour.

头孢曲松和头孢吡肟在 0.45%氯化钠、林格乳酸盐溶液和 Plasma-Lyte A 中的物理相容性。
目的:静脉注射液与药物的相容性是药剂师最为关心的问题,也是确保患者安全的必要组成部分。有关药物与静脉注射液物理相容性的数据尚未经过研究,或公布的结果相互矛盾,或研究的浓度与当前的实践不一致。我们的目的是确定头孢曲松和头孢吡肟在 0.45% 氯化钠、林格乳酸盐溶液和 Plasma-Lyte A 中的物理相容性:在 0.45% 氯化钠、林格氏乳酸盐溶液和 Plasma-Lyte A 中对头孢曲松和头孢吡肟在 10 mg/mL、20 mg/mL 和 40 mg/mL 浓度下的物理相容性进行了体外分析。物理相容性通过目测、分光光度法和 pH 值分析进行评估:结果:发现头孢曲松 40 毫克/毫升在 0.45%氯化钠和林格乳酸盐溶液中超过 5 小时,在 Plasma-Lyte A 溶液中超过 8 小时,物理不相容。头孢吡肟与所有液体和所有浓度的头孢吡肟的物理不相容时间超过 1 小时:这项研究通过确定含有 0.45% 氯化钠、Plasma-Lyte A 和林格乳酸盐溶液的混合液中的明显变化,为专门评估静脉注射药物和液体物理兼容性的文献做出了贡献。在选定的浓度和时间点,头孢曲松不应与 0.45% 氯化钠、林格氏乳酸盐溶液或 Plasma-Lyte A 混合给药,而头孢吡肟在 10 毫克/毫升、20 毫克/毫升或 40 毫克/毫升的任何研究液体中超过 1 小时后也不被认为具有物理兼容性。
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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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