The UK Infected Blood Inquiry: A Personal Reflection.

IF 3 2区 医学 Q2 HEMATOLOGY
Haemophilia Pub Date : 2025-04-02 DOI:10.1111/hae.70043
Christine A Lee
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引用次数: 0

Abstract

The UK Infected Blood Inquiry (IBI) considered the transfusion transmitted infections hepatitis B and C, HIV, and vCJD. The inquiry lasted 6 years during 2018 to 2024 and reported to the UK parliament on 20 May, 2024. It concluded that at least 3000 people died because of the recklessness and obstinacy of officialdom and it has been reported that victims may be compensated an estimated £12 bn-£14 bn ($16 bn-$18 bn). This personal reflection considers people with the bleeding disorder haemophilia, who were infected with blood products. The longevity of both the understanding of the infections, as well as the long natural history of the infections themselves, is set in the context of the medicine practiced by physicians with whom the author was taught and practiced over a period of 40 years. These physicians used blood products to advance the care and life expectancy of patients whilst the ill understood and unforeseen side effects of treatment were slowly elucidated: their contributions were severely criticised but their evidence could not be presented through ill health or death. It is recommended that 'no-fault compensation' schemes should be provided, especially in the era of new and sometimes irreversible therapies, and evidence-based medicine is protected.

英国受感染血液调查:个人反思。
英国感染血液调查(IBI)考虑了输血传播感染乙型肝炎和丙型肝炎,艾滋病毒和vCJD。调查从2018年到2024年持续了6年,并于2024年5月20日向英国议会报告。报告得出的结论是,至少有3000人死于官员的鲁莽和固执,据报道,受害者可能获得约120亿至140亿英镑(160亿至180亿美元)的赔偿。这种个人反思考虑的是患有血友病出血性疾病的人,他们感染了血液制品。对感染的长期理解,以及感染本身漫长的自然历史,都是在作者与医生一起学习和实践了40多年的医学背景下建立起来的。这些医生使用血液制品来提高病人的护理和预期寿命,而治疗的不了解和不可预见的副作用却慢慢被阐明:他们的贡献受到严厉批评,但他们的证据不能通过疾病或死亡来提出。建议应该提供“无过错补偿”方案,特别是在新的、有时是不可逆的疗法出现的时代,并保护循证医学。
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来源期刊
Haemophilia
Haemophilia 医学-血液学
CiteScore
6.50
自引率
28.20%
发文量
226
审稿时长
3-6 weeks
期刊介绍: Haemophilia is an international journal dedicated to the exchange of information regarding the comprehensive care of haemophilia. The Journal contains review articles, original scientific papers and case reports related to haemophilia care, with frequent supplements. Subjects covered include: clotting factor deficiencies, both inherited and acquired: haemophilia A, B, von Willebrand''s disease, deficiencies of factor V, VII, X and XI replacement therapy for clotting factor deficiencies component therapy in the developing world transfusion transmitted disease haemophilia care and paediatrics, orthopaedics, gynaecology and obstetrics nursing laboratory diagnosis carrier detection psycho-social concerns economic issues audit inherited platelet disorders.
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