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一种新的输精管结扎术后精液分析方法消除了评估新鲜标本的需要。

A new approach to postvasectomy semen analyses eliminates the need to evaluate a fresh specimen.

机构信息

Bedford Research Foundation Clinical Laboratory, Bedford, Massachusetts, USA.

Harvard Medical School, Boston, Massachusetts, USA.

出版信息

Andrology. 2023 Mar;11(3):464-470. doi: 10.1111/andr.13331. Epub 2022 Nov 23.

Abstract

BACKGROUND

According to current guidelines, confirmation that vasectomy results in sterility depends on microscopic examination of postvasectomy semen for the presence of spermatozoa. Guidelines established in 2012 require examination of a fresh specimen within 2 h of collection, which necessitates the patient making an appointment with either the surgeon's office or a licensed clinical laboratory. Twenty-five to 42% of patients fail to comply with postvasectomy semen analysis (PVSA).

OBJECTIVES

To determine if an at-home semen collection kit can substitute for the evaluation of a fresh specimen and improve patient compliance with postvasectomy spermatozoa assessment.

MATERIALS AND METHODS

The kit contains a patented aldehyde-fixative that maintains spermatozoa and semen cells in suspension for quantitation. Patients order a PVSA kit to be delivered to their home and can collect a semen specimen and return it to the laboratory through regular US mail.

RESULTS

From January 2011 through December 2018, 6096 men undergoing vasectomy by 184 urologists in 33 states in the US ordered PVSA kits, of which 5408 (89%) returned at least one for analysis. Of those, 398 men (7.4%) returned the first kit with greater than 10,000 spermatozoa/ml within a year of vasectomy, of which only 4.4% contained greater than 100,000 spermatozoa/ml 12 weeks postsurgery. This suggests that fewer than 5% of postvasectomy patients might need follow-up fresh semen analyses, greatly easing the logistical burden of PVSA. Ninety percent of surgeons returning a patient satisfaction questionnaire said their patients "never" complained about using PVSA kits.

DISCUSSION AND CONCLUSION

These data support the adoption of a new standard for PVSA that does not involve an initial evaluation of a fresh semen specimen.

摘要

背景

根据当前的指南,确认输精管结扎术导致不育需要通过显微镜检查输精管结扎术后精液中是否存在精子。2012 年制定的指南要求在采集后 2 小时内检查新鲜标本,这就需要患者预约外科医生办公室或获得许可的临床实验室。有 25%至 42%的患者未能遵守输精管结扎术后精液分析(PVSA)的规定。

目的

确定家庭用精液采集套件是否可以替代新鲜标本的评估,并提高患者对输精管结扎术后精子评估的依从性。

材料和方法

该套件包含一种专利的醛固定剂,可使精子和精液细胞悬浮在其中进行定量。患者订购 PVSA 套件并将其寄送到家中,然后可以通过普通美国邮件将精液标本寄回实验室。

结果

从 2011 年 1 月至 2018 年 12 月,美国 33 个州的 184 名泌尿科医生为 6096 名男性进行了输精管结扎术,其中 5408 名(89%)至少返回了一个用于分析。在这些人中,有 398 名男性(7.4%)在输精管结扎术后一年内首次返回的试剂盒中含有大于 10,000 个精子/ml,但其中只有 4.4%在术后 12 周时含有大于 100,000 个精子/ml。这表明少于 5%的输精管结扎术后患者可能需要进行后续的新鲜精液分析,从而大大减轻了 PVSA 的后勤负担。90%返回患者满意度问卷的外科医生表示,他们的患者“从不”抱怨使用 PVSA 套件。

讨论和结论

这些数据支持采用一种新的 PVSA 标准,该标准不涉及初始新鲜精液标本的评估。

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