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用于大规模筛查的胎粪药物检测的适应性调整。

Adaptation of the meconium drug test for mass screening.

作者信息

Ostrea E M, Romero A, Yee H

机构信息

Department of Pediatrics, Wayne State University, Detroit, Michigan.

出版信息

J Pediatr. 1993 Jan;122(1):152-4. doi: 10.1016/s0022-3476(05)83509-7.

Abstract

For purposes of mass drug screening, the procedure for analysis of meconium for drugs was modified into a one-step extraction and analysis by enzyme immunoassay. The accuracy of this modified method was tested by comparing the results of simultaneous analysis of 61 meconium samples for cocaine opiate and cannabinoid metabolites by both the original and the modified methods. In 61 samples analyzed, opiate was detected in 8 (13%) samples by the original method and in 9 (15%) by the modified method; cocaine was detected in 39 (64%) samples by the original method and in 39 (64%) by the modified method. The concordance between the negative and positive results of the modified versus the original methods was 98% and 100%, respectively, for opiate and 95% and 98%, respectively, for cocaine. Only one sample was positive for cannabinoid. Thus a comparison of positive results for cannabinoid was not done; however, all the negative results obtained by the modified method were confirmed by the original method. The clinical experience of mass meconium drug testing using the modified method in 1991 is also reported. In four centers tested (total tests = 4409), the prevalence of presence of drug was consistent with the high- or low-risk status of the population. This simplified, rapid procedure can be performed in most clinical laboratories. This adaptation has made the meconium drug test feasible for large-scale clinical and research use.

摘要

为了进行大规模药物筛查,将胎粪药物分析程序修改为通过酶免疫测定进行一步提取和分析。通过比较用原始方法和修改后方法同时分析61份胎粪样本中的可卡因、阿片类药物和大麻素代谢物的结果,对这种修改后方法的准确性进行了测试。在分析的61份样本中,原始方法检测出8份(13%)样本含有阿片类药物,修改后方法检测出9份(15%);原始方法检测出39份(64%)样本含有可卡因,修改后方法检测出39份(64%)。修改后方法与原始方法的阴性和阳性结果之间的一致性,阿片类药物分别为98%和100%,可卡因为95%和98%。只有1份样本大麻素呈阳性。因此,未对大麻素的阳性结果进行比较;然而,修改后方法获得的所有阴性结果均得到原始方法的证实。还报告了1991年使用修改后方法进行大规模胎粪药物检测的临床经验。在四个检测中心(总检测数 = 4409),药物存在的患病率与人群的高风险或低风险状况一致。这种简化、快速的程序可在大多数临床实验室进行。这种调整使胎粪药物检测适用于大规模临床和研究用途。

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