质量保证
精液
精液分析
中国
国家(计算机科学)
统计
基础(证据)
误差分析
质量(理念)
活力
数学
精液质量
可靠性(半导体)
医学
统计分析
工程类
精子活力
精子质量
运营管理
作者
Yan Zheng,Lin Yu,Ying-Bi Wu,Y P Jia,shasha liu,Jiao Qin,Jintao Yuan,Y. Liu,fuping li
标识
DOI:10.1515/cclm-2025-1222
摘要
Abstract Objectives To establish evidence-based analytical performance specifications (APS), specifically allowable total error (TE a ), for five fundamental semen analysis parameters (sperm concentration, progressive motility, total motility, morphology, and vitality) in China utilizing the state-of-the-art model, and to compare these specifications with existing international benchmarks. Methods We examined national external quality assessment (EQA) data from 2019 to 2025, encompassing 315 laboratories across 30 provinces in China. TE a was calculated using the state-of-the-art model as half the 10th–90th percentile range of result deviations from assigned values. Given that the participant count was below 100 from 2019 to 2022, this study eventually utilized data from 2023 to 2025 for the calculation of TE a . The pass rate of participating laboratories was evaluated against the established TE a criteria. Results The established TE a values as follows: sperm concentration, 34.3 %; progressive motility, 26.9 % (for assigned value ≤40 %) and 13.5 % (>40 %); total motility, 26.3 % (≤50 %) and 10.5 % (>50 %); morphology, 67.7 %; vitality, 24.6 % (≤60 %) and 7.9 % (>60 %). The pass rates for all parameters in recent EQA cycles were approximately 80 %, supporting the practical achievability of the proposed specifications. Comparisons showed that the derived TE a values are generally consistent with or more refined than previous state-of-the-art and biological variation-based standards. Conclusions This study provides the first large-scale, evidence-based TE a for semen analysis in China. The stratified TE a for motility and vitality based on clinical thresholds, improves diagnostic accuracy. The proposed specifications are practical, achievable, and clinically relevant, providing a consistent foundation for quality assurance in reproductive medicine laboratories.
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