台湾实施全民小池核酸检测后供体感染概况趋势及输血传播人类免疫缺陷病毒、丙型肝炎病毒和乙型肝炎病毒残留风险

IF 1.6 4区 医学 Q3 HEMATOLOGY
Vox Sanguinis Pub Date : 2025-08-06 DOI:10.1111/vox.70083
Wen-Jie Liu, Ching-Mei Yu, Yun-Yuan Chen, Jen-Wei Chen, Sheng-Tang Wei, Sheng-Mou Hou
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引用次数: 0

摘要

本研究旨在评估NAT实施后献血者感染概况和这些病毒输血传播感染(tti)残留风险的变化。材料和方法:2013年1月15日至2023年12月的捐赠均纳入本研究。与窗口期(WP)和隐匿性HBV感染(OBI)相关的剩余风险均进行了估计。结果:献血19,756,973例中,HIV、HCV和HBV分别阳性465例、5592例和23,534例。在hbv阳性的献血者中,有很大比例是nat产献血者(19.5%),特别是在重复献血者中(61.3%)。无论是首次或重复供体,这些病毒的供体流行率都有所下降。估计2022-2023年每百万次捐献的WP的剩余风险,HIV-TTI为0.08(95%置信区间[CI]: 0.02-0.17), HCV-TTI为0.31 (95% CI: 0.24-0.55), HBV-TTI为26.38 (95% CI: 12.81-50.06),自普遍实施NAT以来,HIV-TTI和HBV-TTI呈显著下降趋势。OBI的剩余风险相对较高,但正在下降,占2022-2023年HBV-TTI总剩余风险的一半以上。结论:台湾实施NAT后,HIV、HCV和HBV的TTI患病率和残留风险均有所下降。尽管HBV-TTI的残留风险仍然相对较高,但与其他流行地区相当,并且自NAT实施以来未报告这些病毒的TTI病例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Trends in donor infection profiles and residual risks of transfusion-transmitted human immunodeficiency virus, hepatitis C virus and hepatitis B virus after the implementation of universal mini-pool nucleic acid testing in Taiwan.

Background and objectives: Universal mini-pool nucleic acid testing (NAT) for human immunodeficiency virus (HIV), hepatitis C virus (HCV) and hepatitis B virus (HBV) in blood donations has been introduced in Taiwan since 2013. This study aimed to evaluate changes in donors' infection profiles and residual risks of transfusion-transmitted infections (TTIs) for these viruses after NAT implementation.

Materials and methods: Donations from 15 January 2013 to December 2023 were included in this study. Residual risks associated with the window period (WP) and occult HBV infection (OBI) were both estimated.

Results: Among 19,756,973 donations, 465, 5592 and 23,534 were confirmed positive for HIV, HCV and HBV, respectively. A high proportion of HBV-positive donations was NAT-yield donations (19.5%), particularly among repeat donors (61.3%). Donor prevalences for these viruses declined regardless of first-time or repeat donors. The residual risks of WP per million donations in 2022-2023 were estimated at 0.08 (95% confidence interval [CI]: 0.02-0.17) for HIV-TTI, 0.31 (95% CI: 0.24-0.55) for HCV-TTI and 26.38 (95% CI: 12.81-50.06) for HBV-TTI, with significant declining trends for HIV-TTI and HBV-TTI since universal NAT implementation. The residual risk of OBI was relatively high yet decreasing, accounting for more than half of the total residual risk for HBV-TTI in 2022-2023.

Conclusion: After NAT implementation in Taiwan, prevalences and residual risks of TTI for HIV, HCV and HBV have declined. Although the residual risk of HBV-TTI remains relatively high, it is comparable to that in other endemic areas, and no cases of TTI from these viruses have been reported since NAT implementation.

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来源期刊
Vox Sanguinis
Vox Sanguinis 医学-血液学
CiteScore
4.40
自引率
11.10%
发文量
156
审稿时长
6-12 weeks
期刊介绍: Vox Sanguinis reports on important, novel developments in transfusion medicine. Original papers, reviews and international fora are published on all aspects of blood transfusion and tissue transplantation, comprising five main sections: 1) Transfusion - Transmitted Disease and its Prevention: Identification and epidemiology of infectious agents transmissible by blood; Bacterial contamination of blood components; Donor recruitment and selection methods; Pathogen inactivation. 2) Blood Component Collection and Production: Blood collection methods and devices (including apheresis); Plasma fractionation techniques and plasma derivatives; Preparation of labile blood components; Inventory management; Hematopoietic progenitor cell collection and storage; Collection and storage of tissues; Quality management and good manufacturing practice; Automation and information technology. 3) Transfusion Medicine and New Therapies: Transfusion thresholds and audits; Haemovigilance; Clinical trials regarding appropriate haemotherapy; Non-infectious adverse affects of transfusion; Therapeutic apheresis; Support of transplant patients; Gene therapy and immunotherapy. 4) Immunohaematology and Immunogenetics: Autoimmunity in haematology; Alloimmunity of blood; Pre-transfusion testing; Immunodiagnostics; Immunobiology; Complement in immunohaematology; Blood typing reagents; Genetic markers of blood cells and serum proteins: polymorphisms and function; Genetic markers and disease; Parentage testing and forensic immunohaematology. 5) Cellular Therapy: Cell-based therapies; Stem cell sources; Stem cell processing and storage; Stem cell products; Stem cell plasticity; Regenerative medicine with cells; Cellular immunotherapy; Molecular therapy; Gene therapy.
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