澳大利亚献血者疟疾筛查的最佳策略:成本效益分析。

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.13705
Qinglu Cheng, Veronica C Hoad, Peter Bentley, Robert Harley, Katia Schenberg, Virginia Wiseman
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引用次数: 0

摘要

背景和目的:在澳大利亚,输血传播疟疾(TTM)感染的风险极低,而目前筛查策略的成本效益尚未得到评估。本研究旨在对不同献血者疟疾筛查策略进行成本效益分析,作为基于风险的决策框架的一部分:开发了一个决策树模型,从医疗保健部门的角度评估五种备选疟疾筛查策略的成本效益。该模型考虑了完全或部分取消疟疾检测以及不同推迟期的筛查策略。重症和无并发症 TTM 的发病概率是根据 2000 年以来非流行地区病例的文献回顾得出的。健康结果采用残疾调整生命年进行量化。此外,还包括因推迟捐献而导致的未返回捐献者的成本。进行了确定性和概率敏感性分析,以考虑数据的不确定性:所有策略的剩余风险都很低,因此与 TTM 相关的成本、死亡率和发病率几乎可以忽略不计。总成本主要受不返回献血者成本的影响。因此,在所有考虑过的方案中,取消疟疾检测和对高危献血者实行 28 天延期是成本最低、最具成本效益的方案:结论:澳大利亚现行的献血者疟疾筛查策略并未有效利用医疗资源。部分或全部取消疟疾检测将大大节约成本,同时又不会严重影响血液安全。
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Optimal malarial screening strategy in Australian blood donors: A cost-effectiveness analysis.

Background and objectives: The risk of transfusion-transmitted malaria (TTM) infections is extremely low in Australia, and the cost-effectiveness of the current screening strategy has not been assessed. This study aims to conduct a cost-effectiveness analysis of different malaria screening strategies in blood donors as part of the risk-based decision-making framework.

Materials and methods: A decision tree model was developed to assess the cost-effectiveness of five alternative malaria screening strategies from a healthcare sector perspective. Screening strategies combining total or partial removal of malaria testing with different deferral periods were considered. The probabilities of developing severe and uncomplicated TTM were based on a literature review of cases in non-endemic areas since 2000. The health outcomes were quantified using disability-adjusted life years. The costs of non-returning donors due to deferral were also included. Deterministic and probabilistic sensitivity analyses were conducted to account for data uncertainty.

Results: The residual risks for all strategies were so low that the costs, mortality and morbidity associated with TTM are almost negligible. The overall costs were predominantly influenced by the costs of non-returning blood donors. As a result, removal of malaria testing and applying a 28-day deferral for at-risk donors were the least costly and most cost-effective of all the options considered.

Conclusion: The current screening strategy for malaria in blood donors in Australia is not an efficient use of healthcare resources. Partial or total removal of malaria testing would bring significant cost savings without significantly compromising blood safety.

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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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