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新型基于智能手机的精液分析仪与实验室精子质量分析仪的准确性比较研究。

Accuracy comparison study of new smartphone-based semen analyzer versus laboratory sperm quality analyzer.

机构信息

The Korea Institute for Public Sperm Bank, Busan, Korea.

Department of Urology, Pusan National University School of Medicine, Busan, Korea.

出版信息

Investig Clin Urol. 2021 Nov;62(6):672-680. doi: 10.4111/icu.20210266.

Abstract

PURPOSE

This study aimed to test the clinical efficacy of a portable smartphone-based App assisted semen analysis (SA) system, O'VIEW-M PRO® to clinically accurate in comparison with results of laboratory-based conventional semen analyses including manual microscopic and computer-assisted semen analysis (CASA) for self-evaluation of seminal parameters.

MATERIALS AND METHODS

From January to May 2021, a total of 39 semen samples were analyzed for the sperm concentration and motility with new smartphone-based App assisted semen analyzer, O'VIEW-M PRO®, and results compared with those from laboratory-based manual microscopic SA with Makler Counting Chamber and CASA.

RESULTS

The coefficient factors among the results of the measurement with Makler chamber and laboratory-based CASA comparing to O'VIEW-M PRO® were 0.666 and 0.655 for sperm density, 0.662 and 0.658 for sperm motility, respectively. There were no particular problems with clinical use of the O'VIEW-M PRO®. Device performance in classifying samples is positive (<15×10 sperm/mL) and negative (>15×10 sperm/mL) for sperm concentration criteria, and positive (<40%) and negative (>40%) for sperm motility criteria. The smartphone-based App assisted SA O'VIEW-M PRO® showed a sensitivity of 92.6%, a specificity of 66.7%, and overall accuracy rate of 84.6%.

CONCLUSIONS

This study shows a novel smartphone-based App assisted SA system. O'VIEW-M PRO® can easily obtain semen parameter information through self-diagnosis at home and induce infertile men's treatment and help patients after receiving infertile men's treatment before receiving treatment.

摘要

目的

本研究旨在测试基于智能手机的 O'VIEW-M PRO® 便携式应用程序辅助精液分析 (SA) 系统的临床疗效,与实验室基础的常规精液分析(包括手动显微镜检查和计算机辅助精液分析 [CASA])相比,该系统在自我评估精液参数方面的结果是否准确。

材料和方法

2021 年 1 月至 5 月,使用基于新智能手机的 O'VIEW-M PRO® 辅助精液分析仪对 39 份精液样本的精子浓度和活力进行分析,并将结果与使用 Makler 计数室的实验室手动显微镜 SA 和 CASA 进行比较。

结果

与 Makler 室和实验室基础 CASA 的结果相比,O'VIEW-M PRO® 的测量结果的系数因子分别为精子密度为 0.666 和 0.655,精子活力为 0.662 和 0.658。临床使用 O'VIEW-M PRO® 没有出现特别的问题。该设备在对精子浓度标准进行分类时表现为阳性(<15×10 精子/mL)和阴性(>15×10 精子/mL),在对精子活力标准进行分类时表现为阳性(<40%)和阴性(>40%)。基于智能手机的应用程序辅助 SA O'VIEW-M PRO® 显示出 92.6%的敏感性、66.7%的特异性和 84.6%的总准确率。

结论

本研究展示了一种新型的基于智能手机的应用程序辅助 SA 系统。O'VIEW-M PRO® 可以通过在家中进行自我诊断轻松获得精液参数信息,并在接受治疗前帮助不孕男性进行治疗并帮助接受治疗后的患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3fd8/8566791/8c88512792c3/icu-62-672-g001.jpg

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