Dasta J F, Hale K N, Stauffer G L, Tschampel M M
College of Pharmacy, Department of Anesthesiology, Ohio State University, Columbus.
Am J Hosp Pharm. 1988 Nov;45(11):2361-6.
Visual and turbidimetric methods for determining the short-term compatibility of critical-care i.v. drugs were compared. In phase 1, serial dilutions of calcium chloride and magnesium sulfate were examined visually and turbidimetrically to test the sensitivity of the spectrophotometric method used. In phase 2, i.v. solutions of dobutamine, dopamine, lidocaine, nitroglycerin, and nitroprusside were prepared and studied in all possible combinations of two, three, four and five drugs, for a total of 26 different combinations. In phase 3, 45 two-drug combinations previously reported as physically incompatible were studied. Visual inspection was conducted against a dark and a light background; changes were graded as slight, moderate, or gross. Absorbance was determined at 650 nm; an absorbance value of greater than 0.010 was considered to be evidence of turbidity. Visual, turbidimetric, and pH measurements were done at zero, one, and three hours after mixing. Samples of the calcium chloride-magnesium sulfate mixture that were graded visually as having a slight precipitate had absorbance readings less than 0.010. No physical evidence of incompatibility was observed by either method for dobutamine, dopamine, lidocaine, nitroglycerin, and nitroprusside in any combination. In phase 3, 19 drug combinations were shown to be incompatible; however, only 6 of these (31%) had absorbance readings greater than 0.010 when the visual incompatibility was first observed. There was no physical evidence of incompatibility for several drug combinations that have been listed as incompatible in commonly used references. Turbidimetry does not appear to be as reliable a method for determining the compatibility of drugs as is visual inspection against a dark and a light background.
对用于确定重症监护静脉注射药物短期相容性的目视法和比浊法进行了比较。在第1阶段,对氯化钙和硫酸镁的系列稀释液进行了目视检查和比浊检查,以测试所使用的分光光度法的灵敏度。在第2阶段,制备了多巴酚丁胺、多巴胺、利多卡因、硝酸甘油和硝普钠的静脉注射液,并对两种、三种、四种和五种药物的所有可能组合进行了研究,总共26种不同组合。在第3阶段,对先前报道在物理上不相容的45种两药组合进行了研究。在深色和浅色背景下进行目视检查;变化分为轻微、中度或明显。在650nm处测定吸光度;吸光度值大于0.010被认为是浑浊的证据。在混合后0小时、1小时和3小时进行目视、比浊和pH测量。氯化钙 - 硫酸镁混合物的样品,目视分级为有轻微沉淀,其吸光度读数小于0.010。对于任何组合的多巴酚丁胺、多巴胺、利多卡因、硝酸甘油和硝普钠,两种方法均未观察到不相容的物理证据。在第3阶段,有19种药物组合显示不相容;然而,在首次观察到目视不相容时,其中只有6种(31%)的吸光度读数大于0.010。对于常用参考文献中列为不相容的几种药物组合,没有不相容的物理证据。与在深色和浅色背景下进行目视检查相比,比浊法似乎不是一种确定药物相容性的可靠方法。