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Genetic risk assessments in individuals at high risk for inherited breast cancer in the breast oncology care setting.在肿瘤护理环境中,对遗传性乳腺癌高危个体进行遗传风险评估。
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2
Communicating BRCA1/2 genetic test results within the family: a qualitative analysis.家族内沟通 BRCA1/2 基因检测结果:定性分析。
Psychol Health. 2011 Aug;26(8):1018-35. doi: 10.1080/08870446.2010.525640. Epub 2011 Jul 28.
3
Family communication matters: the impact of telling relatives about unclassified variants and uninformative DNA-test results.家庭沟通很重要:告知亲属未分类变异体和无信息 DNA 检测结果的影响。
Genet Med. 2011 Apr;13(4):333-41. doi: 10.1097/GIM.0b013e318204cfed.
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Effects of communicating DNA-based disease risk estimates on risk-reducing behaviours.传达基于DNA的疾病风险评估对降低风险行为的影响。
Cochrane Database Syst Rev. 2010 Oct 6(10):CD007275. doi: 10.1002/14651858.CD007275.pub2.
5
A whisper-game perspective on the family communication of DNA-test results: a retrospective study on the communication process of BRCA1/2-test results between proband and relatives.从耳语游戏的角度探讨 DNA 检测结果的家庭沟通:BRCA1/2 检测结果在患者与亲属之间沟通过程的回顾性研究。
Fam Cancer. 2011 Mar;10(1):87-96. doi: 10.1007/s10689-010-9385-y.
6
The development of a methodology for examining the process of family communication of genetic test results.一种用于检验基因检测结果家庭沟通流程的方法的开发。
J Genet Couns. 2011 Feb;20(1):23-34. doi: 10.1007/s10897-010-9317-x. Epub 2010 Sep 11.
7
Comparing family members' motivations and attitudes towards genetic testing for hereditary breast and ovarian cancer: a qualitative analysis.比较家族成员对遗传性乳腺癌和卵巢癌基因检测的动机和态度:定性分析。
Eur J Hum Genet. 2010 Dec;18(12):1289-95. doi: 10.1038/ejhg.2010.114. Epub 2010 Jul 21.
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Disclosing cancer genetic information within families: perspectives of counselees and their at-risk relatives.在家庭中披露癌症遗传信息:咨询对象及其高危亲属的观点。
Fam Cancer. 2010 Dec;9(4):669-79. doi: 10.1007/s10689-010-9364-3.
9
Genetic health professionals and the communication of genetic information in families: Practice during and after a genetic consultation.遗传健康专业人员及其在家庭中的遗传信息沟通:遗传咨询期间和之后的实践。
Am J Med Genet A. 2010 Jun;152A(6):1458-66. doi: 10.1002/ajmg.a.33385.
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What facilitates or impedes family communication following genetic testing for cancer risk? A systematic review and meta-synthesis of primary qualitative research.癌症风险基因检测后,哪些因素促进或阻碍了家庭沟通?一项关于原发性定性研究的系统评价和元综合分析。
J Genet Couns. 2010 Aug;19(4):330-42. doi: 10.1007/s10897-010-9296-y. Epub 2010 Apr 9.

患者及其亲属对癌症易感BRCA1/2基因突变信息的回忆准确性。

Accuracy of recall of information about a cancer-predisposing BRCA1/2 gene mutation among patients and relatives.

作者信息

Jacobs Chris, Dancyger Caroline, Smith Jonathan A, Michie Susan

机构信息

Department of Clinical Genetics, Guy's and St Thomas' NHS Foundation Trust, London, UK.

Cancer Psychological Services, Bart's Health NHS Trust, London, UK.

出版信息

Eur J Hum Genet. 2015 Feb;23(2):147-51. doi: 10.1038/ejhg.2014.84. Epub 2014 May 21.

DOI:10.1038/ejhg.2014.84
PMID:24848747
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4297912/
Abstract

This observational study aimed to (i) compare the accuracy of information recalled by patients and relatives following genetic counselling about a newly identified BRCA1/2 mutation, (ii) identify differences in accuracy of information about genetics and hereditary cancer and (iii) investigate whether accuracy among relatives improved when information was provided directly by genetics health professionals. Semistructured interviews following results from consultations with 10 breast/ovarian cancer patients and 22 relatives were audio-recorded and transcribed. Information provided by the genetics health professional was tracked through the families and coded for accuracy. Accuracy was analysed using the Wilcoxon Signed-Ranks test. Sources of information were tested using Spearman's rank-order correlation coefficient. Fifty-three percent of the information recalled by patients was accurate. Accuracy of recall among relatives was significantly lower than that among patients (P=0.017). Both groups recalled a lower proportion of information about hereditary cancer than about genetics (P=0.005). Relatives who learnt the information from the patient alone recalled significantly less accurate information than those informed directly by genetics health professionals (P=0.001). Following genetic counselling about a BRCA1/2 mutation, accuracy of recall was low among patients and relatives, particularly about hereditary cancer. Multiple sources of information, including direct contact with genetics health professionals, may improve the accuracy of information among relatives.

摘要

这项观察性研究旨在

(i)比较在接受关于新发现的BRCA1/2突变的遗传咨询后患者及其亲属回忆信息的准确性;(ii)确定关于遗传学和遗传性癌症的信息准确性方面的差异;(iii)调查当遗传学健康专业人员直接提供信息时亲属的信息准确性是否会提高。对10名乳腺癌/卵巢癌患者和22名亲属咨询结果后的半结构化访谈进行了录音和转录。追踪遗传学健康专业人员提供的信息在家庭中的传播情况并对其准确性进行编码。使用Wilcoxon符号秩检验分析准确性。使用Spearman等级相关系数检验信息来源。患者回忆的信息中有53%是准确的。亲属回忆信息的准确性显著低于患者(P=0.017)。两组回忆的关于遗传性癌症的信息比例均低于关于遗传学的信息比例(P=0.005)。仅从患者那里获取信息的亲属回忆的准确信息明显少于直接从遗传学健康专业人员那里得知信息的亲属(P=0.001)。在接受关于BRCA1/2突变的遗传咨询后,患者和亲属回忆信息的准确性较低,尤其是关于遗传性癌症的信息。包括与遗传学健康专业人员直接接触在内的多种信息来源可能会提高亲属信息的准确性。