Gochis P, Hasenyager C, Aiman J
Department of Obstetrics and Gynecology, Medical College of Wisconsin, Milwaukee.
Obstet Gynecol. 1988 Apr;71(4):652-6.
Human chorionic gonadotropin (hCG) was measured in 117 serum samples with known quantities of hCG after a dilutional modification of a reliable, simple, and inexpensive qualitative assay for hCG. The modification yielded a semiquantitative assay for hCG with a sensitivity of 5000 mIU/mL. At hCG concentrations below 4000 mIU/mL, the assay had no false-negative or false-positive results; above 6500 mIU/mL, there were also no false-negative or false-positive results. In the range of 4000-6500 mIU/mL, the clinical false-positive rate was 28%. Using the described dilutional modification of this qualitative hCG assay, the test is semiquantitative, and is useful in selecting the appropriate time to perform ultrasound and laparoscopy in women suspected of having an ectopic pregnancy.
在对一种可靠、简单且廉价的人绒毛膜促性腺激素(hCG)定性检测方法进行稀释改良后,对117份已知hCG含量的血清样本进行了hCG检测。改良后的方法产生了一种hCG半定量检测方法,其灵敏度为5000 mIU/mL。在hCG浓度低于4000 mIU/mL时,该检测方法无假阴性或假阳性结果;高于6500 mIU/mL时,也无假阴性或假阳性结果。在4000 - 6500 mIU/mL范围内,临床假阳性率为28%。使用所描述的这种hCG定性检测方法的稀释改良法,该检测为半定量检测,有助于为疑似异位妊娠的女性选择进行超声检查和腹腔镜检查的合适时间。