Brammer Matthew K, Chan Pak, Heatherly Kathy, Trusley Craig, Kupiec Thomas C, Trissel Lawrence A, Psathas Petros A, Gilmor Timothy, Schaufelberger Daniel
Analytical Research Laboratories, Oklahoma City, OK, USA.
Am J Health Syst Pharm. 2008 Jul 1;65(13):1261-5. doi: 10.2146/ajhp070574.
The compatibility of doripenem diluted for infusion with 82 other drugs during simulated Y-site administration was studied.
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.
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.
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.
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。
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。
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。
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。