Bandi Z L, Schoen I, DeLara M
Clin Chem. 1987 May;33(5):677-81.
We screened six highly sensitive kits, designed for serum pregnancy tests, for false-positive results. The two best were then evaluated more extensively. The "BETA-hCG MAIA-clone" (I) and the "TANDEM ICON" (II) kits gave only negative results for 100 sera from men at 5, 10, and 25 int. units/L (1st IRP). Of 100 serum specimens from post-menopausal women three and 10 were hCG positive by the II and the I reagents, respectively, but only at the 5 int. units (1st IRP) of hCG per liter level of sensitivity. At 10 and 25 int. units/L, all specimens were negative by both tests. The manufacturers of these kits recommend pregnancy testing only at the 25 int. units/L level of analytical sensitivity. By quantitative methods, hCG concentrations in the II positive samples ranged from 6 to 20 int. units/L (1st IRP) and lutropin concentrations were between 130 to greater than 150 int. units/L. The medical records of the corresponding patients did not support the presence of trophoblast or any other hCG-secreting tissues. During 15 months of routine use of the II reagents at an analytical sensitivity of 25 int. units/L (1st IRP) hCG for pregnancy testing (greater than 4000 serum specimens from pre-menopausal women), the staff has not reported to us any suspected false-positive findings.
我们筛选了六种用于血清妊娠检测的高灵敏度试剂盒,以检测其假阳性结果。然后对其中性能最佳的两种试剂盒进行了更广泛的评估。“BETA-hCG MAIA克隆”(I)试剂盒和“串联ICON”(II)试剂盒对100份男性血清样本在5、10和25国际单位/升(第一国际参考品)时仅给出阴性结果。在100份绝经后女性血清样本中,分别有3份和10份通过II试剂和I试剂检测hCG呈阳性,但仅在每升5国际单位(第一国际参考品)的hCG灵敏度水平时呈阳性。在10和25国际单位/升时,两种检测方法对所有样本均呈阴性。这些试剂盒的制造商建议仅在25国际单位/升的分析灵敏度水平进行妊娠检测。通过定量方法,II阳性样本中的hCG浓度范围为6至20国际单位/升(第一国际参考品),促黄体生成素浓度在130至大于150国际单位/升之间。相应患者的病历不支持存在滋养层或任何其他分泌hCG的组织。在以25国际单位/升(第一国际参考品)的分析灵敏度常规使用II试剂进行妊娠检测的15个月期间(超过4000份绝经前女性血清样本),工作人员未向我们报告任何疑似假阳性结果。