Gottschling H D, Reuter W, Ronquist G, Steinmetz A, Hattemer A
Diabetesinstitut Karlsburg, Germany.
Eur J Clin Chem Clin Biochem. 1995 Jun;33(6):373-81.
Accutrend Cholesterol, a non-wipe test for the determination of total cholesterol in capillary blood, was evaluated at four clinical centres. Cholesterol determinations with the Accutrend system using capillary blood were compared with results obtained with the cholesterol oxidase/p-aminophenazone (CHOD-PAP) method using the respective capillary sera. Triacylglycerols, uric acid and haematocrit were determined to evaluate potential interference. Imprecision measurements were performed with venous blood. To examine the reproducibility of results from lot to lot, three different lots of test strips were included in these investigations. Results with Accutrend Cholesterol agree with those of the comparison method within systematic differences of +2.5% to -3.2%, depending on the lot. There was no interference by triacylglycerols up to 10.28 mmol/l (900 mg/dl), by uric acid 60 to 400 mumol/l (1 mg/dl to 7 mg/dl), or by haematocrits between 0.35 and 0.54. Impression data show coefficients of variation of generally less than 5%. Thus Accutrend Cholesterol proved to be a reliable system for the determination of total cholesterol.
Accutrend胆固醇检测法是一种用于测定毛细血管血中总胆固醇的免擦拭检测方法,在四个临床中心进行了评估。将使用Accutrend系统通过毛细血管血进行的胆固醇测定结果与使用相应毛细血管血清的胆固醇氧化酶/对氨基苯乙酮(CHOD-PAP)法获得的结果进行比较。测定了甘油三酯、尿酸和血细胞比容以评估潜在干扰。使用静脉血进行不精密度测量。为了检验不同批次结果的可重复性,这些研究中纳入了三个不同批次的测试条。Accutrend胆固醇检测法的结果与比较方法的结果相符,系统差异在+2.5%至-3.2%之间,具体取决于批次。甘油三酯浓度高达10.28 mmol/l(900 mg/dl)、尿酸浓度在60至400 μmol/l(1 mg/dl至7 mg/dl)之间或血细胞比容在0.35至0.54之间时均无干扰。精密度数据显示变异系数一般小于5%。因此,Accutrend胆固醇检测法被证明是一种可靠的总胆固醇测定系统。