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本文引用的文献

1
How is genetic testing evaluated? A systematic review of the literature.遗传检测如何评估?文献系统评价。
Eur J Hum Genet. 2018 May;26(5):605-615. doi: 10.1038/s41431-018-0095-5. Epub 2018 Feb 8.
2
Personal utility in genomic testing: a systematic literature review.基因检测中的个人效用:一项系统的文献综述
Eur J Hum Genet. 2017 Jun;25(6):662-668. doi: 10.1038/ejhg.2017.10. Epub 2017 Mar 15.
3
Utility of thrombophilia testing in patients with venous thrombo-embolism.血栓形成倾向检测在静脉血栓栓塞症患者中的应用价值。
J Thorac Dis. 2016 Dec;8(12):3697-3703. doi: 10.21037/jtd.2016.12.40.
4
Which BRCA genetic testing programs are ready for implementation in health care? A systematic review of economic evaluations.哪些BRCA基因检测项目已准备好在医疗保健中实施?一项经济评估的系统综述。
Genet Med. 2016 Dec;18(12):1171-1180. doi: 10.1038/gim.2016.29. Epub 2016 Apr 14.
5
A qualitative study of patients' perceptions of the value of molecular diagnosis for familial hypercholesterolemia (FH).一项关于患者对家族性高胆固醇血症(FH)分子诊断价值认知的定性研究。
J Community Genet. 2017 Jan;8(1):45-52. doi: 10.1007/s12687-016-0286-0. Epub 2016 Nov 19.
6
Current state of genomic policies in healthcare among EU member states: results of a survey of chief medical officers.欧盟成员国医疗保健中基因组政策的现状:首席医疗官调查结果。
Eur J Public Health. 2017 Oct 1;27(5):931-937. doi: 10.1093/eurpub/ckw155.
7
Guidance for the evaluation and treatment of hereditary and acquired thrombophilia.遗传性和获得性血栓形成倾向的评估与治疗指南。
J Thromb Thrombolysis. 2016 Jan;41(1):154-64. doi: 10.1007/s11239-015-1316-1.
8
Delivering value by focusing on patient experience.通过关注患者体验来传递价值。
Am J Manag Care. 2015 Oct;21(10):735-7.
9
Genetic testing and economic evaluations: a systematic review of the literature.基因检测与经济评估:文献系统综述
Epidemiol Prev. 2015 Jul-Aug;39(4 Suppl 1):45-50.
10
Experiences of Women Who Underwent Predictive BRCA 1/2 Mutation Testing Before the Age of 30.30岁之前接受BRCA 1/2基因预测性突变检测的女性的经历
J Genet Couns. 2016 Feb;25(1):90-100. doi: 10.1007/s10897-015-9845-5. Epub 2015 May 19.

患者对遗传信息的体验和利用:一项针对癌症易感性和血栓形成倾向检测患者的横断面研究。

Patient experience and utility of genetic information: a cross-sectional study among patients tested for cancer susceptibility and thrombophilia.

机构信息

Department of Public Health and Infectious Diseases, Sapienza University of Rome, Rome, Italy.

Brigham and Women's Hospital, Harvard Medical School, Boston, USA.

出版信息

Eur J Hum Genet. 2018 Apr;26(4):518-526. doi: 10.1038/s41431-017-0083-1. Epub 2018 Jan 26.

DOI:10.1038/s41431-017-0083-1
PMID:29374276
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5891505/
Abstract

We evaluated whether genetic tests with evidence of clinical and personal utility (i.e. APC and BRCA1/2 tests) are associated with higher satisfaction and a more positive perception of care experience than those with undefined utility (i.e. tests for thrombophilia). A cross-sectional survey was performed through telephone interviews to patients tested for deleterious variants in APC or BRCA1/2 genes, or for inherited thrombophilia (FV Leiden and/or FIIG20210A) during a 5-year period (2008-2012). Three aspects of patient experience were assessed: effective communication through pre- and post-test genetic counselling; collaboration between caregivers on the management of patient care; and impact of genetic testing on quality of life. Overall 237 patients had telephone interviews. Multivariate logistic regression analyses showed that patients tested for APC or BRCA1/2 variants were more likely to be satisfied with both pre- and post-test counselling than those tested for inherited thrombophilia (APC vs. thrombophilia, p = 0.039 and 0.005; BRCA1/2 vs. thrombophilia, p = 0.030 and <0.001). Patients tested for APC were more likely to report an improvement in quality of life than those for thrombophilia (OR = 2.97, 95%CI 1.14, 7.72; p = 0.025). A positive association was observed between patients who underwent BRCA1/2 testing, and self-perceived improvement in quality of life (OR = 1.41, 95%CI 0.74, 2.69; p = 0.294). Tests of undefined clinical and personal utility are associated with a lower degree of patient satisfaction with genetic counselling and no clear opinions on changes in quality of life compared with those with well-defined utility.

摘要

我们评估了具有临床和个人效用证据的基因检测(即 APC 和 BRCA1/2 检测)是否与更高的满意度和更积极的护理体验认知相关,而与效用未定义的检测(即血栓形成倾向检测)相比。通过电话访谈对在 5 年内(2008-2012 年)接受 APC 或 BRCA1/2 基因有害变异或遗传性血栓形成倾向(FV Leiden 和/或 FII G20210A)检测的患者进行了横断面调查。评估了患者体验的三个方面:通过检测前和检测后遗传咨询进行有效的沟通;护理人员在患者护理管理方面的协作;以及基因检测对生活质量的影响。共有 237 名患者接受了电话访谈。多变量逻辑回归分析显示,与接受遗传性血栓形成倾向检测的患者相比,接受 APC 或 BRCA1/2 变异检测的患者对检测前和检测后咨询均更满意(APC 与血栓形成倾向相比,p=0.039 和 0.005;BRCA1/2 与血栓形成倾向相比,p=0.030 和 <0.001)。与接受血栓形成倾向检测的患者相比,接受 APC 检测的患者更有可能报告生活质量改善(OR=2.97,95%CI 1.14,7.72;p=0.025)。观察到接受 BRCA1/2 检测的患者与自我感知生活质量改善之间存在正相关(OR=1.41,95%CI 0.74,2.69;p=0.294)。与具有明确临床和个人效用的检测相比,具有未定义临床和个人效用的检测与患者对遗传咨询的满意度较低以及对生活质量变化的看法不明确相关。