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2020 APHRS/HRS expert consensus statement on the investigation of decedents with sudden unexplained death and patients with sudden cardiac arrest, and of their families.2020年亚太心律学会/美国心律学会关于不明原因猝死死者及心脏骤停患者及其家属调查的专家共识声明
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2020 APHRS/HRS expert consensus statement on the investigation of decedents with sudden unexplained death and patients with sudden cardiac arrest, and of their families.2020 年 APHRS/HRS 关于猝死和心搏骤停患者及其家属尸检调查的专家共识声明
Heart Rhythm. 2021 Jan;18(1):e1-e50. doi: 10.1016/j.hrthm.2020.10.010. Epub 2020 Oct 19.
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The composition and capacity of the clinical genetics workforce in high-income countries: a scoping review.高收入国家临床遗传学劳动力的构成和能力:范围综述。
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本文引用的文献

1
Genetic Testing in the Evaluation of Unexplained Cardiac Arrest: From the CASPER (Cardiac Arrest Survivors With Preserved Ejection Fraction Registry).不明原因心脏骤停评估中的基因检测:来自CASPER(射血分数保留的心脏骤停幸存者注册研究)
Circ Cardiovasc Genet. 2017 Jun;10(3). doi: 10.1161/CIRCGENETICS.116.001686.
2
Cost Analysis of Patients Referred for Inherited Heart Rhythm Disorder Evaluation.遗传性心律失常评估转诊患者的成本分析
Can J Cardiol. 2017 Jun;33(6):814-821. doi: 10.1016/j.cjca.2016.12.009. Epub 2016 Dec 20.
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Molecular Autopsy for Sudden Unexpected Death.猝死的分子尸检
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4
Cardiac Abnormalities in First-Degree Relatives of Unexplained Cardiac Arrest Victims: A Report From the Cardiac Arrest Survivors With Preserved Ejection Fraction Registry.不明原因心脏骤停受害者一级亲属的心脏异常:来自左心室射血分数保留的心脏骤停幸存者注册研究的报告
Circ Arrhythm Electrophysiol. 2016 Sep;9(9). doi: 10.1161/CIRCEP.115.004274.
5
A Prospective Study of Sudden Cardiac Death among Children and Young Adults.前瞻性研究儿童和青年人群中心脏性猝死。
N Engl J Med. 2016 Jun 23;374(25):2441-52. doi: 10.1056/NEJMoa1510687.
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Interdisciplinary psychosocial care for families with inherited cardiovascular diseases.遗传性心血管疾病患者家庭的跨学科心理社会照护。
Trends Cardiovasc Med. 2016 Oct;26(7):647-53. doi: 10.1016/j.tcm.2016.04.010. Epub 2016 Apr 28.
7
Posttraumatic Stress and Prolonged Grief After the Sudden Cardiac Death of a Young Relative.年轻亲属心源性猝死后的创伤后应激和持续性悲伤
JAMA Intern Med. 2016 Mar;176(3):402-5. doi: 10.1001/jamainternmed.2015.7808.
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Outcome of Apparently Unexplained Cardiac Arrest: Results From Investigation and Follow-Up of the Prospective Cardiac Arrest Survivors With Preserved Ejection Fraction Registry.不明原因心搏骤停的转归:前瞻性射血分数保留的心脏骤停幸存者调查和随访登记研究结果。
Circ Arrhythm Electrophysiol. 2016 Jan;9(1):e003619. doi: 10.1161/CIRCEP.115.003619.
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Patient Outcomes From a Specialized Inherited Arrhythmia Clinic.从专门的遗传性心律失常诊所获得的患者结果。
Circ Arrhythm Electrophysiol. 2016 Jan;9(1):e003440. doi: 10.1161/CIRCEP.115.003440.
10
Genetic purgatory and the cardiac channelopathies: Exposing the variants of uncertain/unknown significance issue.遗传困境与心脏通道病学:揭示不确定/未知意义变异体问题。
Heart Rhythm. 2015 Nov;12(11):2325-31. doi: 10.1016/j.hrthm.2015.07.002. Epub 2015 Jul 2.

The accessibility and utilization of genetic testing for inherited heart rhythm disorders: a Canadian cross-sectional survey study.

作者信息

Roston Thomas M, Dewar Laura, Franciosi Sonia, Hathaway Julie, Bartels Kirsten, Cunningham Taylor, Gibbs Karen A, Sheps Sam, Laksman Zachary W M, Sanatani Shubhayan, Krahn Andrew D

机构信息

BC Inherited Arrhythmia Program, Vancouver, BC, Canada.

Heart Rhythm Vancouver, Division of Cardiology, University of British Columbia, Vancouver, BC, Canada.

出版信息

J Community Genet. 2018 Jul;9(3):257-262. doi: 10.1007/s12687-017-0348-y. Epub 2017 Nov 23.

DOI:10.1007/s12687-017-0348-y
PMID:29170972
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6002300/
Abstract

The genetic basis of many sudden death-related conditions has been elucidated. These include inherited arrhythmias and arrhythmogenic cardiomyopathies, termed inherited heart rhythm disorders (IHRD). Advising on and interpreting genetic testing is challenging for the general cardiologist. This has led to the development of interdisciplinary clinics for IHRD in varying stages of establishment in Canada. We sought the viewpoints and patterns of practice of Canadian IHRD experts, and assessed their ability to access genetic testing for IHRD using a national cross-sectional survey. Of 56 participants, most were physicians (68%) or genetic counselors (19%). Despite working collaboratively, most genetic counselors (59%) were either not satisfied or only somewhat satisfied with their relationships with physicians. Ninety percent of participants were involved in offering genetic evaluation, including 80% who felt that testing was usually/always accessible. Most offered genetic testing to confirm clinical diagnosis and/or direct family screening. Post-mortem genetic analysis was sought by 69% of respondents; however, a lack of retained tissue and/or poor tissue preparation hindered this process. Family screening was usually recommended in the setting of a pathogenic/likely pathogenic variant. The most commonly perceived barrier to genetic testing was cost to the healthcare system. More than a quarter of patients waited ≥ 6 months for funding. An ability to engage at-risk relatives was rated as limited/poor by 34% of participants. Despite the establishment of several interdisciplinary clinics, timely access to affordable testing, supported by strong team communication, continues to be a barrier to genetic testing in Canada.

摘要