Mei J V, Hannon W H, Dobbs T L, Bell C J, Spruill C, Gwinn M
Newborn Screening Quality Assurance Program, Centers for Disease Control and Prevention, Atlanta, GA 30341-3724, USA. (SMTP)jvm0@.cdc.gov
Clin Chem. 1998 Feb;44(2):281-6.
We modified and evaluated a RIA for serum and used the modified RIA to measure zidovudine in dried blood spot specimens (DBSs) routinely collected for newborn screening and tested anonymously for maternally acquired HIV antibodies in the national HIV Seroprevalence Survey Among Childbearing Women. DBS calibration and quality-control materials were used to adapt the serum assay to the DBS matrix. The assay had a limit of detection of 24 micrograms/L serum and was used to measure zidovudine from both whole DBSs and the eluate remaining after HIV antibody screening. We initiated a pilot study to investigate the assay's performance and assess its potential to determine the implementation of the US Public Health Service recommendations that HIV-infected pregnant women and newborns receive zidovudine treatment to reduce the risk of perinatal HIV transmission.
我们对一种血清放射免疫分析方法进行了改进和评估,并使用改进后的放射免疫分析方法来检测干血斑样本(DBS)中的齐多夫定。这些干血斑样本是在全国育龄妇女艾滋病毒血清流行率调查中为新生儿筛查常规采集的,且对母体获得性艾滋病毒抗体进行了匿名检测。使用DBS校准和质量控制材料使血清检测方法适用于DBS基质。该检测方法的血清检测限为24微克/升,用于检测全血干血斑样本以及艾滋病毒抗体筛查后剩余洗脱液中的齐多夫定。我们启动了一项试点研究,以调查该检测方法的性能,并评估其确定美国公共卫生服务建议实施情况的潜力,该建议要求感染艾滋病毒的孕妇和新生儿接受齐多夫定治疗,以降低围产期艾滋病毒传播的风险。