Bergdahl B, Dahlström G, Molin L, Bertler A
Acta Pharmacol Toxicol (Copenh). 1979 Jul;45(1):66-72. doi: 10.1111/j.1600-0773.1979.tb02362.x.
Samples from two pools were sent 10 times to 27 laboratories for assay of digoxin. One pool contained digoxin 2.60 nmol/l in normal plasma (SP); the other was pooled plasma from patients treated with digoxin (PP). Ten radioimmunoassay (RIA) methods were used. The mean of SP assays was 2.59 nmol/l, not significantly different from 2.60 nmol/l. The mean of PP determinations was 2.46 nmol/l. Within each of the 10 assay rounds, the concentrations showed an almost twofold variation and S.D. averaged 0.33 nmol/l and 0.31 nmol/l for SP and PP respectively. Significant differences (P less than 0.001) were found between mean concentrations obtained for the pools at various laboratories (SP range 2.15-2.85 nmol/l; PP range 2.12-2.72 nmol/l). The laboratory means obtained for SP and PP correlated significantly (P less than 0.001). Nevertheless, significant (P less than 0.01) variations between laboratories were found also concerning the mean difference between SP and PP concentrations. The interassay SD of the assays differed significantly between laboratories (range 0.05-0.61 nmol/l. Between and within groups of laboratories using the same RIA method and between various types of laboratories, differences were also found concerning both accuracy and precision of the assays. It is concluded that a better control of digoxin assay is needed.
来自两个样本池的样本被10次送往27个实验室进行地高辛检测。一个样本池含有正常血浆(SP)中浓度为2.60纳摩尔/升的地高辛;另一个是用地高辛治疗的患者的混合血浆(PP)。使用了10种放射免疫测定(RIA)方法。SP检测的平均值为2.59纳摩尔/升,与2.60纳摩尔/升无显著差异。PP测定的平均值为2.46纳摩尔/升。在10次检测轮次中的每一轮内,浓度显示出近两倍的变化,SP和PP的标准差分别平均为0.33纳摩尔/升和0.31纳摩尔/升。在各个实验室获得的两个样本池的平均浓度之间发现了显著差异(P小于0.001)(SP范围为2.15 - 2.85纳摩尔/升;PP范围为2.12 - 2.72纳摩尔/升)。获得的SP和PP的实验室平均值显著相关(P小于0.001)。然而,在SP和PP浓度的平均差异方面,实验室之间也发现了显著(P小于0.01)差异。各实验室检测的批间标准差差异显著(范围为0.05 - 0.61纳摩尔/升)。在使用相同RIA方法的实验室组之间以及不同类型的实验室之间,在检测的准确性和精密度方面也发现了差异。结论是需要更好地控制地高辛检测。