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多利培南在模拟Y型静脉给药过程中与其他药物的配伍性。

Compatibility of doripenem with other drugs during simulated Y-site administration.

作者信息

Brammer Matthew K, Chan Pak, Heatherly Kathy, Trusley Craig, Kupiec Thomas C, Trissel Lawrence A, Psathas Petros A, Gilmor Timothy, Schaufelberger Daniel

机构信息

Analytical Research Laboratories, Oklahoma City, OK, USA.

出版信息

Am J Health Syst Pharm. 2008 Jul 1;65(13):1261-5. doi: 10.2146/ajhp070574.

Abstract

PURPOSE

The compatibility of doripenem diluted for infusion with 82 other drugs during simulated Y-site administration was studied.

METHODS

Five-milliliter samples of doripenem 5 mg/mL in 5% dextrose injection and separately in 0.9% sodium chloride injection were combined with 5 mL of 82 other drugs, undiluted or diluted in 5% dextrose injection or 0.9% sodium chloride injection. Visual examinations were performed with the unaided eye in fluorescent light and using a Tyndall beam to enhance visualization of small particles and low-level turbidity. The turbidity of each sample was measured, and particulate content was evaluated. Samples were inspected initially and one and four hours after preparation.

RESULTS

Of the drugs tested, doripenem 5 mg/mL in 5% dextrose injection and in 0.9% sodium chloride injection was incompatible with diazepam, potassium phosphates, and undiluted propofol. Doripenem 5 mg/mL in 0.9% sodium chloride injection but not in 5% dextrose injection was incompatible with amphotericin B-containing drugs due to the diluent. Doripenem was found to be compatible when combined with the other 75 drugs for at least four hours.

CONCLUSION

Doripenem 5 mg/mL in 5% dextrose injection or in 0.9% sodium chloride injection was physically compatible for four hours at room temperature with 75 drugs during simulated Y-site administration. Three drugs combined with doripenem in 5% dextrose injection or 0.9% sodium chloride injection and 7 drugs combined with doripenem in 0.9% sodium chloride injection resulted in unacceptable precipitation or an increase in measured haze and should not be simultaneously administered with doripenem admixtures.

摘要

目的

研究在模拟Y型给药过程中,多利培南稀释用于输注时与其他82种药物的配伍性。

方法

将5mg/mL的多利培南5mL样品分别加入5%葡萄糖注射液和0.9%氯化钠注射液中,再与5mL其他82种未稀释或已在5%葡萄糖注射液或0.9%氯化钠注射液中稀释的药物混合。在荧光灯下肉眼观察,并使用丁达尔光束增强对小颗粒和低水平浑浊度的可视化。测量每个样品的浑浊度,并评估颗粒含量。在制备后立即、1小时和4小时对样品进行检查。

结果

在所测试的药物中,5%葡萄糖注射液和0.9%氯化钠注射液中的5mg/mL多利培南与地西泮、磷酸钾和未稀释的丙泊酚不相容。由于稀释剂的原因,0.9%氯化钠注射液中而非5%葡萄糖注射液中的5mg/mL多利培南与含两性霉素B的药物不相容。发现多利培南与其他75种药物混合至少4小时是相容的。

结论

在模拟Y型给药过程中,5%葡萄糖注射液或0.9%氯化钠注射液中的5mg/mL多利培南在室温下与75种药物在4小时内物理相容。5%葡萄糖注射液或0.9%氯化钠注射液中的多利培南与3种药物混合,以及0.9%氯化钠注射液中的多利培南与7种药物混合会导致不可接受的沉淀或测量的浑浊度增加,不应与多利培南混合液同时给药。

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