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首页> 外文期刊>Human Reproduction >Prostate-specific antigen in vaginal fluid after exposure to known amounts of semen and after condom use: comparison of self-collected and nurse-collected samples.
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Prostate-specific antigen in vaginal fluid after exposure to known amounts of semen and after condom use: comparison of self-collected and nurse-collected samples.

机译:暴露于已知量的精液后和使用安全套后,阴道液中的前列腺特异性抗原:比较自我收集和护士收集的样本。

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摘要

BACKGROUND: Prostate-specific antigen (PSA) in vaginal fluid indicates exposure to semen, and was used to assess condom effectiveness, although validity and reliability have not been fully evaluated. Our objective was to compare PSA in self-collected samples with samples collected by a nurse. METHODS: We conducted two studies, each with 100 women aged 18-48 years. In the first, a nurse exposed each participant to her partner's semen (10, 100 and 1000 microl), and nurse and participant collected samples. In the second, each participant sampled before and after using two male condoms (MC) and two female condoms (FC); a nurse collected another sample afterwards. RESULTS: PSA concentration increased with semen exposure, but was lower in nurse-collected samples. Both procedures were sensitive, almost 100% after exposure to 100-1000 microl of semen. PSA detection rates with MC and FC were 13% and 28% in self-collected samples, 8% and 9% in nurse-collected samples. Concordance between sample types was 93% with the MC (95% CI: 89%; 96%), 78% with the FC (95% CI: 72%; 84%). PSA decay between sampling times may explain higher values in self-collected samples. CONCLUSIONS: PSA is a highly sensitive surrogate endpoint for condom effectiveness studies. Self-collected and nurse-collected samples are equivalent, but sample collection timing is critical.
机译:背景:阴道液中的前列腺特异性抗原(PSA)表明已接触精液,并被用于评估避孕套的有效性,尽管其有效性和可靠性尚未得到充分评估。我们的目标是将自我收集的样本中的PSA与护士收集的样本进行比较。方法:我们进行了两项研究,每个研究对象为100名18-48岁的女性。首先,护士将每个参与者暴露于伴侣伴侣的精液中(10、100和1000微升),然后护士和参与者采集样本。在第二个样本中,每个参与者在使用两个男用避孕套(MC)和两个女用避孕套(FC)之前和之后进行了抽样;一位护士随后收集了另一份样本。结果:PSA浓度随精液暴露而增加,但在护士采集的样品中降低。两种方法都是敏感的,暴露于100-1000微升精液后几乎100%。自收集样品中MC和FC的PSA检测率分别为13%和28%,护士收集样品中分别为8%和9%。 MC(95%CI:89%; 96%)为93%,FC(95%CI:72%; 84%)为78%。采样时间之间的PSA衰减可能解释了自收集样本中的较高值。结论:PSA是安全套有效性研究的高度敏感的替代终点。自我收集和护士收集的样本是等效的,但是样本收集的时间至关重要。

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