Lessard Jean-Justin, Caron Elaine, Schérer Hugo, Forest Jean-Marc, Leclair Grégoire
Chisasibi Hospital, QC, Canada.
CHU Sainte-Justine, Montreal, QC, Canada.
Hosp Pharm. 2020 Oct;55(5):332-337. doi: 10.1177/0018578719844168. Epub 2019 May 3.
The objective of the study was to establish the compatibility of injectable meropenem with 101 other drugs during Y-site administration. Meropenem (50 mg/mL, 10 mL) was combined with 101 undiluted injectable drugs (10 mL each) at room temperature. Each preparation was performed twice. The first sample underwent a visual evaluation and a particle count test by light obstruction immediately after mixing. These tests were repeated 4 hours after mixing using the second preparation. Incompatibility was defined as precipitation or other visual change (turbidity, crystal formation, gas formation, color change) or failure to meet United States Pharmacopeia (USP) <788> 1.B specifications at any time point. A total of 83 of the 101 injectable drugs tested with meropenem were found to be compatible both visually and using the USP <788> particle counter. The gross incompatibility of the other 17 drugs was determined by visual observation. One mixture complied with the specifications, but showed an increase of temperature upon mixing and was removed from the study. Of the 101 drugs tested, 83 were found to be compatible while the remaining 17 were incompatible. One drug was removed from the study as its compatibility was unclear.
该研究的目的是确定注射用美罗培南在Y型接口给药时与其他101种药物的配伍性。将美罗培南(50 mg/mL,10 mL)与101种未稀释的注射用药物(各10 mL)在室温下混合。每种制剂制备两次。第一个样品在混合后立即进行外观评估和光阻法颗粒计数测试。使用第二个制剂在混合4小时后重复这些测试。配伍禁忌定义为在任何时间点出现沉淀或其他外观变化(浑浊、晶体形成、气体形成、颜色变化)或不符合美国药典(USP)<788> 1.B规格。在用美罗培南测试的101种注射用药物中,共有83种在外观和使用USP <788>颗粒计数器检测时被发现是可配伍的。另外17种药物的明显配伍禁忌通过外观观察确定。有一种混合物符合规格,但在混合时温度升高,因此被排除在研究之外。在测试的101种药物中,83种被发现是可配伍的,而其余17种是不可配伍的。有一种药物因配伍性不明确而被排除在研究之外。