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酶联免疫吸附尿液妊娠试验。临床特异性研究。

Enzyme-linked immunosorbent urine pregnancy tests. Clinical specificity studies.

作者信息

Bandi Z L, Schoen I, DeLara M

出版信息

Am J Clin Pathol. 1987 Feb;87(2):236-42. doi: 10.1093/ajcp/87.2.236.

DOI:10.1093/ajcp/87.2.236
PMID:3812355
Abstract

The performance of six recently introduced highly sensitive enzyme-linked immunosorbent (ELISA) urine pregnancy test reagent kits was evaluated for false positive results using 100 male and 100 postmenopausal female urine specimens and the findings were compared with those of a qualitative radioimmunoassay (RIA) procedure. Based on the findings, the most suitable pregnancy test reagent kit was then selected for doing routine pregnancy testing of urine samples of premenopausal patients. The less sensitive PregnaSTICK ELISA method and Concept RIA procedure did not give any positive results. Positive results for postmenopausal female and male urine samples were obtained as follows: Testpack, 2 and 0 (greater than 50 mIU/mL [IU/L]); Icon, 2 and 0 (greater than 50 mIU/mL [IU/L]); Quest, 4 and 2 (greater than 50 mIU/mL [IU/L]); Nimbus, 17 and 4 (greater than 25 mIU/mL [IU/L]); and Sensi-Chrome, 33 and 19 (greater than 50 mIU/mL [IU/L]), respectively. The medical records of the patients whose urine samples gave positive results were examined for information that would have explained the positive results, but no clear-cut reasons were found. Comparison of the routine urinalysis findings showed that there was a correlation between the mucus content of female (but not of male) urine samples and the incidence of false positive human chorionic gonadotropin results. During 12 months of routine use of the Icon reagents for pregnancy testing of premenopausal urine samples, the University of Texas Medical Branch staff has not reported any suspected false positive findings to the authors.

摘要

使用100份男性尿液标本和100份绝经后女性尿液标本,对最近推出的6种高灵敏度酶联免疫吸附(ELISA)尿液妊娠试验试剂盒进行假阳性结果评估,并将结果与定性放射免疫分析(RIA)方法的结果进行比较。基于这些结果,随后选择最合适的妊娠试验试剂盒用于绝经前患者尿液样本的常规妊娠检测。灵敏度较低的PregnaSTICK ELISA方法和Concept RIA方法未得出任何阳性结果。绝经后女性和男性尿液样本的阳性结果如下:Testpack分别为2例和0例(大于50 mIU/mL [IU/L]);Icon分别为2例和0例(大于50 mIU/mL [IU/L]);Quest分别为4例和2例(大于50 mIU/mL [IU/L]);Nimbus分别为17例和4例(大于25 mIU/mL [IU/L]);Sensi - Chrome分别为33例和19例(大于50 mIU/mL [IU/L])。对尿液样本呈阳性结果的患者病历进行检查,以寻找可能解释阳性结果的信息,但未发现明确原因。常规尿液分析结果的比较表明,女性(而非男性)尿液样本中的黏液含量与假阳性人绒毛膜促性腺激素结果的发生率之间存在相关性。在使用Icon试剂对绝经前尿液样本进行12个月的常规妊娠检测期间,德克萨斯大学医学分校的工作人员未向作者报告任何疑似假阳性结果。

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1
Enzyme-linked immunosorbent urine pregnancy tests. Clinical specificity studies.酶联免疫吸附尿液妊娠试验。临床特异性研究。
Am J Clin Pathol. 1987 Feb;87(2):236-42. doi: 10.1093/ajcp/87.2.236.
2
Performance of a new enzyme-linked immunoassay urine pregnancy test for the detection of ectopic gestation.
Ann Emerg Med. 1986 Oct;15(10):1198-9. doi: 10.1016/s0196-0644(86)80865-4.
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The development and evaluation of Sevatest ELISA hCG Micro I. kit as a test for pregnancy.Sevatest ELISA hCG Micro I.试剂盒作为妊娠检测方法的开发与评估。
J Hyg Epidemiol Microbiol Immunol. 1988;32(4):467-76.
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Evaluation of methods for the prospective identification of early fetal losses in environmental epidemiology studies.环境流行病学研究中早期胎儿丢失前瞻性识别方法的评估
Am J Epidemiol. 1988 Apr;127(4):843-50. doi: 10.1093/oxfordjournals.aje.a114867.
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Three highly sensitive "bedside" serum and urine tests for pregnancy compared.三种高灵敏度的“床边”妊娠血清和尿液检测方法的比较。
Clin Chem. 1990 Sep;36(9):1686-8.
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Am J Obstet Gynecol. 1988 Mar;158(3 Pt 1):613-6. doi: 10.1016/0002-9378(88)90040-3.
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Emergency urinary HCG testing with the Tandem ICON.使用串联式 ICON 进行紧急尿液人绒毛膜促性腺激素检测。
Clin Chem. 1985 Aug;31(8):1405.
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Highly sensitive qualitative methods for serum choriogonadotropin (hCG): clinical specificity studies.血清绒毛膜促性腺激素(hCG)的高灵敏度定性检测方法:临床特异性研究
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A commercial pregnancy test modified for field studies of fetal loss.一种为胎儿丢失的现场研究而改良的商用妊娠试验。
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