Center for Anti-Infective Research and Development, Hartford Hospital, Hartford, Connecticut.
Center for Anti-Infective Research and Development, Hartford Hospital, Hartford, Connecticut.
Clin Ther. 2018 Feb;40(2):261-269. doi: 10.1016/j.clinthera.2017.12.007. Epub 2017 Dec 28.
Meropenem/vaborbactam is a novel intravenous antibiotic combining the carbapenem, meropenem, with a novel β-lactamase inhibitor, vaborbactam. Meropenem/vaborbactam is administered as a 3-hour infusion given every 8 hours, thereby potentially restricting an intravenous line for 9 h/d. Intravenous medications may be given concurrently via Y-site when compatibility data are available. Herein, physical compatibility was determined for the identification which medications can be coadministered with meropenem/vaborbactam via Y-site.
Y-site administration was simulated in vitro by admixing 5 mL of meropenem 8 mg/mL and vaborbactam 8 mg/mL with an equal volume of 88 other diluted intravenous medications, including 34 antimicrobials. All other medications were diluted with 0.9% sodium chloride to the upper range of concentrations considered standard for intravenous infusion. Visual inspection, turbidity measurement, and pH measurement were performed prior to admixture, directly after admixture, and at time points up to 3 hours after admixture.
Of the 88 medications tested, meropenem/vaborbactam was compatible with 73 (83%), including many antibiotics such as aminoglycosides (amikacin, gentamicin, and tobramycin), colistin, fosfomycin, linezolid, tedizolid, tigecycline, and vancomycin. Physical incompatibility was observed with albumin, amiodarone, anidulafungin, calcium chloride, caspofungin, ceftaroline, ciprofloxacin, daptomycin, diphenhydramine, dobutamine, isavuconazole, midazolam, nicardipine, ondansetron, and phenytoin.
The majority of intravenous medications tested were found to be physically compatible with meropenem/vaborbactam. These data will help pharmacists and nurses to improve line access in patients receiving meropenem/vaborbactam.
美罗培南/沃博巴坦是一种新型的静脉注射抗生素,由碳青霉烯类美罗培南与新型β-内酰胺酶抑制剂沃博巴坦组成。美罗培南/沃博巴坦每 8 小时静脉输注 3 小时,因此每天最多可限制静脉通路 9 小时。当有相容性数据时,可通过 Y 型部位同时给予静脉药物。在此,通过体内实验确定物理相容性,以确定哪些药物可以通过 Y 型部位与美罗培南/沃博巴坦同时给药。
通过将 5 mL 8 mg/mL 的美罗培南和 8 mg/mL 的沃博巴坦与 88 种其他稀释的静脉药物(包括 34 种抗菌药物)等体积混合,模拟 Y 型部位给药。所有其他药物均用 0.9%氯化钠稀释至认为标准的静脉输注最高浓度范围。在混合前、混合后直接和混合后 3 小时内进行目测、浊度测量和 pH 值测量。
在所测试的 88 种药物中,美罗培南/沃博巴坦与 73 种(83%)药物相容,包括许多抗生素,如氨基糖苷类(阿米卡星、庆大霉素和妥布霉素)、黏菌素、磷霉素、利奈唑胺、替加环素、万古霉素。物理不相容性观察到与白蛋白、胺碘酮、阿尼达fungin、氯化钙、卡泊芬净、头孢洛林、环丙沙星、达托霉素、苯海拉明、多巴酚丁胺、伊曲康唑、咪达唑仑、尼卡地平、昂丹司琼和苯妥英。
大多数测试的静脉药物与美罗培南/沃博巴坦在物理上是相容的。这些数据将帮助药剂师和护士改善接受美罗培南/沃博巴坦治疗的患者的线路通道。