Shared decision making: Implications for return of results from whole-exome and whole-genome sequencing

被引:4
|
作者
Vadaparampil, Susan T. [1 ,2 ]
Cragun, Deborah [1 ,3 ]
机构
[1] H Lee Moffitt Canc Ctr & Res Inst, Div Populat Sci, Hlth Outcomes & Behav Program, Tampa, FL 33612 USA
[2] Univ S Florida, Morsani Coll Med, Dept Oncol Sci, Tampa, FL 33612 USA
[3] Univ S Florida, Coll Publ Hlth, Dept Global Hlth, Tampa, FL 33612 USA
关键词
Shared decision making; While exome sequencing; Whole genome sequencing; Return of results; POPULATION-BASED SAMPLE; INFORMATION NONDISCRIMINATION ACT; BREAST-CANCER; INCIDENTAL FINDINGS; SECONDARY FINDINGS; CLINICAL EXOME; AWARENESS; HEALTH; RECOMMENDATIONS; DISCRIMINATION;
D O I
10.1093/tbm/ibx048
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
In this issue, Kaphingst and colleagues report on young breast cancer patient's preferences for learning about various results from genomic sequencing. In our commentary, we discuss the results in light of the burgeoning clinical use of whole-exome and whole-genome sequencing (WES/WGS). In particular, we consider findings in the context of a Shared Decision Making approach to return of results. We also identify additional important factors to consider that may influence patient preferences that were largely absent from the paper by Kaphingst and colleagues, including cultural context, costs of testing, and provider factors.
引用
收藏
页码:80 / 84
页数:5
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