管理澳大利亚献血中输血传播疟疾的风险:推荐新的筛查策略。

IF 1.8 4区 医学 Q3 HEMATOLOGY Vox Sanguinis Pub Date : 2024-09-01 Epub Date: 2024-07-24 DOI:10.1111/vox.13706
Katia Schenberg, Veronica C Hoad, Robert Harley, Peter Bentley
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引用次数: 0

摘要

背景和目标:为了降低可输血成分导致输血传播疟疾(TTM)的风险,澳大利亚对从疟疾流行地区返回的旅行者和曾经居住在该地区的居民进行疟疾抗体检测。检测在最后一次可能接触后至少 120 天进行。TTM 是一种极为罕见的事件,管理这种风险增加了相当大的复杂性。本研究的目的是分析各种检测和推迟策略,同时考虑风险、捐赠数量和操作复杂性:建立了一个残余风险模型,以计算五种检测/推迟策略中发生 TTM 的风险。该模型使用了 2020 年和 2021 年的澳大利亚献血者数据,并纳入了寄生虫病发病率、疟原虫种类和疟疾酶免疫测定试验的失败率。对捐献者和捐献者的损失或收益进行了操作评估:当前模型估计的 TTM 风险为每 6790 万个输血单位中有 1 例。对居民进行 120 天血浆限制检测,对未进行检测的来访者进行检测,发现估计风险相同,预计每年增加 342 例捐赠,显著节约成本,并将需要评估的捐赠者人数减少 62%:结论:只对疟疾地区的居民进行检测并对其实施 120 天血浆旅行限制的策略不会显著增加发生 TTM 的风险,而且操作更简单、成本更低,并能少量增加捐赠。
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Managing the risk of transfusion-transmitted malaria from Australian blood donations: Recommendation of a new screening strategy.

Background and objectives: To reduce the risk of transfusion-transmitted malaria (TTM) from transfusible components, Australia tests for malaria antibodies in both travellers returning from and former residents of malaria-endemic areas. The testing is performed a minimum of 120 days after last potential exposure. TTM is an extremely rare event and managing the risk adds considerable complexity. The objectives of this study were to analyse various testing and deferral strategies, considering the risk, donation numbers and operational complexities.

Materials and methods: A residual risk model was developed to calculate the risk of TTM in five testing/deferral strategies. Australian blood donor data from 2020 and 2021 were used and incorporated the incidence of parasitaemia, Plasmodium species and the malaria enzyme immunoassay test's failure rate. Donor and donation loss or gain and an operational assessment were performed.

Results: The current model's estimated risk of TTM is 1 in 67.9 million transfused units. Testing residents with a 120-day plasma restriction for visitors without testing was found to have the same estimated risk, with an expected increase of 342 donations per year, significant cost savings and a 62% reduction in the number of donors requiring assessment.

Conclusion: A strategy that involves testing residents of malaria areas only and a 120-day plasma travel restriction would not significantly increase the risk of TTM, is operationally simpler, costs less and results in a small increase in donations.

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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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