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Decision to reject screening for familial hypercholesterolaemia is flawed.

作者信息

Wald David S, Martin Andrew C

机构信息

Wolfson Institute of Preventive Medicine, Queen Mary University of London, London, UK

Dept of Paediatric and Adolescent Medicine, Princess Margaret Hospital for Children, Perth, Western Australia, Australia.

出版信息

Arch Dis Child. 2021 Jun;106(6):525-526. doi: 10.1136/archdischild-2020-319168. Epub 2020 Jun 29.

DOI:10.1136/archdischild-2020-319168
PMID:32601084
Abstract
摘要

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1
Decision to reject screening for familial hypercholesterolaemia is flawed.拒绝进行家族性高胆固醇血症筛查的决定存在缺陷。
Arch Dis Child. 2021 Jun;106(6):525-526. doi: 10.1136/archdischild-2020-319168. Epub 2020 Jun 29.
2
Further response to 'Decision to reject screening for familial hypercholesterolaemia is flawed' by Wald and Martin.对瓦尔德和马丁所著《拒绝筛查家族性高胆固醇血症的决定存在缺陷》的进一步回应
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How To Identify Familial Premature Myocardial Infarction: Comparing Approaches To Identify Familial Hypercholesterolemia.如何识别家族性早发性心肌梗死:比较识别家族性高胆固醇血症的方法。
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People at risk of familial hypercholesterolaemia should have DNA test, says NICE.英国国家卫生与临床优化研究所表示,有家族性高胆固醇血症风险的人应该进行DNA检测。
BMJ. 2017 Nov 2;359:j5112. doi: 10.1136/bmj.j5112.
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Universal screening at age 1-2 years as an adjunct to cascade testing for familial hypercholesterolaemia in the UK: A cost-utility analysis.1-2 岁时进行普遍筛查以作为英国家族性高胆固醇血症级联检测的辅助手段:成本效用分析。
Atherosclerosis. 2018 Aug;275:434-443. doi: 10.1016/j.atherosclerosis.2018.05.047. Epub 2018 Jun 4.
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Responses to 'Decision to reject screening for familial hypercholesterolaemia is flawed' by Wald and Martin.对沃尔德和马丁所著《拒绝进行家族性高胆固醇血症筛查的决定存在缺陷》的回应。
Arch Dis Child. 2022 Jan;107(1):102. doi: 10.1136/archdischild-2021-322642. Epub 2021 Jul 21.
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Mutation screening in patients for familial hypercholesterolaemia (ADH).对家族性高胆固醇血症(ADH)患者进行突变筛查。
Clin Genet. 2010 Jan;77(1):97-9. doi: 10.1111/j.1399-0004.2009.01279.x. Epub 2009 Oct 14.
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The UK National Screening Committee's position on child-parent screening for familial hypercholesterolaemia.英国国家筛查委员会关于家族性高胆固醇血症的儿童-父母筛查的立场。
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Screening for hypercholesterolaemia versus case finding for familial hypercholesterolaemia: a systematic review and cost-effectiveness analysis.高胆固醇血症筛查与家族性高胆固醇血症病例发现:系统评价与成本效益分析
Health Technol Assess. 2000;4(29):1-123.
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Screening for familial hypercholesterolaemia in primary care: Time for general practice to play its part.在初级保健中筛查家族性高胆固醇血症:是时候让全科医生发挥作用了。
Atherosclerosis. 2018 Oct;277:399-406. doi: 10.1016/j.atherosclerosis.2018.08.019.

引用本文的文献

1
Modelling a two-stage adult population screen for autosomal dominant familial hypercholesterolaemia: cross-sectional analysis within the UK Biobank.对常染色体显性家族性高胆固醇血症进行两阶段成年人群筛查的模型构建:英国生物银行内的横断面分析
BMJ Public Health. 2023 Oct 29;1(1):e000021. doi: 10.1136/bmjph-2023-000021. eCollection 2023 Nov.
2
Population-based screening in children for early diagnosis and treatment of familial hypercholesterolemia: design of the VRONI study.基于人群的儿童家族性高胆固醇血症早期诊断和治疗筛查:VRONI 研究的设计。
Eur J Public Health. 2022 Jun 1;32(3):422-428. doi: 10.1093/eurpub/ckac007.
3
The UK National Screening Committee's position on child-parent screening for familial hypercholesterolaemia.
英国国家筛查委员会关于家族性高胆固醇血症的儿童-父母筛查的立场。
J Med Screen. 2021 Sep;28(3):217-220. doi: 10.1177/09691413211025426. Epub 2021 Jul 22.