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优化血液匹配策略的概念框架:平衡患者并发症与总费用

A Conceptual Framework for Optimizing Blood Matching Strategies: Balancing Patient Complications Against Total Costs Incurred.

作者信息

van Sambeeck Joost H J, de Wit Puck D, Luken Jessie, Veldhuisen Barbera, van den Hurk Katja, van Dongen Anne, Koopman Maria M W, van Kraaij Marian G J, van der Schoot C Ellen, Schonewille Henk, de Kort Wim L A M, Janssen Mart P

机构信息

Department of Transfusion Technology Assessment, Sanquin Research, Amsterdam, Netherlands.

Center for Healthcare Operations Improvement and Research, University of Twente, Enschede, Netherlands.

出版信息

Front Med (Lausanne). 2018 Jul 25;5:199. doi: 10.3389/fmed.2018.00199. eCollection 2018.

DOI:10.3389/fmed.2018.00199
PMID:30090809
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6069448/
Abstract

Alloimmunization is currently the most frequent adverse blood transfusion event. Whilst completely matched donor blood would nullify the alloimmunization risk, this is practically infeasible. Current matching strategies therefore aim at matching a limited number of blood groups only, and have evolved over time by systematically including matching strategies for those blood groups for which (serious) alloimmunization complications most frequently occurred. An optimal matching strategy for controlling the risk of alloimmunization however, would balance alloimmunization complications and costs within the entire blood supply chain, whilst fulfilling all practical requirements and limitations. In this article the outline of an integrated blood management model is described and various potential challenges and prospects foreseen with the development of such a model are discussed.

摘要

目前,同种免疫是最常见的输血不良事件。虽然完全匹配的供体血液可消除同种免疫风险,但这在实际中并不可行。因此,当前的匹配策略仅旨在匹配有限数量的血型,并且随着时间的推移,通过系统地纳入针对(严重)同种免疫并发症最常发生的血型的匹配策略而不断发展。然而,一种用于控制同种免疫风险的最佳匹配策略应在整个血液供应链中平衡同种免疫并发症和成本,同时满足所有实际要求和限制。本文描述了一种综合血液管理模型的概要,并讨论了随着这种模型的发展所预见的各种潜在挑战和前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db06/6069448/0feafa7208f5/fmed-05-00199-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db06/6069448/31721e0f6883/fmed-05-00199-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db06/6069448/0feafa7208f5/fmed-05-00199-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db06/6069448/31721e0f6883/fmed-05-00199-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db06/6069448/0feafa7208f5/fmed-05-00199-g0002.jpg

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本文引用的文献

1
Direct costs of transfusion reactions - an expert judgement approach.输血反应的直接成本——一种专家判断方法。
Vox Sang. 2018 Feb;113(2):143-151. doi: 10.1111/vox.12614. Epub 2017 Nov 9.
2
Nonclassical haplotype is associated with protection from red blood cell alloimmunization in sickle cell disease.非经典单倍型与镰状细胞病中红细胞同种免疫的保护有关。
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Medical and economic implications of strategies to prevent alloimmunization in sickle cell disease.
荷兰非裔人群的献血行为:阻碍因素和促进因素如何与献血意愿相关联?
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Impact of red blood cell alloimmunization on sickle cell disease mortality: a case series.红细胞同种免疫对镰状细胞病死亡率的影响:病例系列研究
Transfusion. 2016 Jan;56(1):107-14. doi: 10.1111/trf.13379. Epub 2015 Oct 28.
6
Protective effect of HLA-DQB1 alleles against alloimmunization in patients with sickle cell disease.HLA - DQB1等位基因对镰状细胞病患者同种免疫的保护作用。
Hum Immunol. 2016 Jan;77(1):35-40. doi: 10.1016/j.humimm.2015.10.010. Epub 2015 Oct 22.
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Incidence of alloantibody formation after ABO-D or extended matched red blood cell transfusions: a randomized trial (MATCH study).ABO-D 或扩展匹配红细胞输血后同种抗体形成的发生率:一项随机试验(MATCH 研究)。
Transfusion. 2016 Feb;56(2):311-20. doi: 10.1111/trf.13347. Epub 2015 Oct 7.
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Mechanisms of sickle cell alloimmunization.镰状细胞同种免疫的机制。
Transfus Clin Biol. 2015 Aug;22(3):178-81. doi: 10.1016/j.tracli.2015.05.005. Epub 2015 Jun 6.
9
Female sex of older patients is an independent risk factor for red blood cell alloimmunization after transfusion.老年患者的女性性别是输血后红细胞同种免疫的独立危险因素。
Transfusion. 2015 Jun;55(6 Pt 2):1478-85. doi: 10.1111/trf.13111. Epub 2015 Apr 6.
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Hyperhemolysis syndrome in patients with sickle cell anemia: report of three cases.镰状细胞贫血患者的高溶血综合征:三例报告。
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