The prototypical UK blood donor, homophily and blood donation: Blood donors are like you, not me.

IF 1.8 4区 医学 Q3 HEMATOLOGY
Vox Sanguinis Pub Date : 2024-09-02 DOI:10.1111/vox.13731
Eamonn Ferguson, Sarah Bowen, Richard Mills, Claire Reynolds, Katy Davison, Claire Lawrence, Roanna Maharaj, Chris Starmer, Abigail Barr, Tracy Williams, Mark Croucher, Susan R Brailsford
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Abstract

Background and objectives: Homophily represents the extent to which people feel others are like them and encourages the uptake of activities they feel people like them do. Currently, there are no data on blood donor homophily with respect to (i) people's representation of the average prototypical UK blood donor and (ii) the degree of homophily with this prototype for current donors, non-donors, groups blood services wish to encourage (ethnic minorities), those who are now eligible following policy changes (e.g., men-who-have-sex-with-men: MSM) and recipients. We aim to fill these gaps in knowledge.

Materials and methods: We surveyed the UK general population MSM, long-term blood recipients, current donors, non-donors and ethnic minorities (n = 785) to assess perceptions of the prototypical donor in terms of ethnicity, age, gender, social class, educational level and political ideology. Homophily was indexed with respect to age, gender and ethnicity.

Results: The prototypical UK blood donor is perceived as White, middle-aged, middle-class, college-level educated and left-wing. Current donors and MSM are more homophilous with this prototype, whereas recipients and ethnic minorities have the lowest homophily. Higher levels of homophily are associated with an increased likelihood of committing to donate.

Conclusion: The prototype of the UK donor defined this as a White activity. This, in part, may explain why ethnic minorities are less likely to be donors. As well as traditional recruitment strategies, blood services need to consider broader structural changes such as the ethnic diversity of staff and co-designing donor spaces with local communities.

英国献血者原型、同质性和献血:献血者就像你,而不是我。
背景和目的:同质性是指人们认为他人与自己相似的程度,它鼓励人们参加他们认为与自己相似的人所从事的活动。目前,还没有关于献血者同质性的数据:(i)人们对英国献血者平均原型的代表性;(ii)当前献血者、非献血者、血液服务机构希望鼓励的群体(少数民族)、政策变化后符合献血条件的人(如男性同性性行为者:MSM)和受血者与该原型的同质性程度。我们旨在填补这些知识空白:我们对英国普通人群中的 MSM、长期受血者、当前献血者、非献血者和少数民族(n = 785)进行了调查,从种族、年龄、性别、社会阶层、教育水平和政治意识形态等方面评估了人们对献血者原型的看法。对年龄、性别和种族进行了同质性分析:结果:英国献血者的原型被认为是白人、中年、中产阶级、受过高等教育和左翼。目前的献血者和男男性行为者与这一原型的亲缘性更高,而受血者和少数民族的亲缘性最低。同质性越高,承诺捐赠的可能性就越大:英国捐赠者的原型将其定义为白人活动。这在一定程度上解释了为什么少数民族不太可能成为献血者。除了传统的招募策略外,血液服务机构还需要考虑更广泛的结构性变化,如工作人员的种族多样性以及与当地社区共同设计捐献者空间。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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