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决策诊断性遗传检测中的框架效应:一项随机试验的结果。

Framing Effects on Decision-Making for Diagnostic Genetic Testing: Results from a Randomized Trial.

机构信息

William F. Connell School of Nursing, Boston College, Chestnut Hill, MA 02467, USA.

Massachusetts General Hospital-Harvard Center for Reproductive Medicine, Massachusetts General Hospital, Boston, MA 02114, USA.

出版信息

Genes (Basel). 2021 Jun 20;12(6):941. doi: 10.3390/genes12060941.

Abstract

Genetic testing is increasingly part of routine clinical care. However, testing decisions may be characterized by regret as findings also implicate blood relatives. It is not known if genetic testing decisions are affected by the way information is presented (i.e., framing effects). We employed a randomized factorial design to examine framing effects on hypothetical genetic testing scenarios (common, life-threatening disease and rare, life-altering disease). Participants ( = 1012) received one of six decision frames: choice, default ( = 2; opt-in, opt-out), or enhanced choice ( = 3, based on the Theory of Planned Behavior). We compared testing decision, satisfaction, regret, and decision cognitions across decision frames and between scenarios. Participants randomized to 'choice' were least likely to opt for genetic testing compared with default and enhanced choice frames (78% vs. 83-91%, < 0.05). Neither satisfaction nor regret differed across frames. Perceived autonomy (behavioral control) predicted satisfaction (B = 0.085, < 0.001) while lack of control predicted regret (B = 0.346, < 0.001). Opting for genetic testing did not differ between disease scenarios ( = 0.23). Results suggest framing can nudge individuals towards opting for genetic testing. These findings have important implications for individual self-determination in the genomic era. Similarities between scenarios with disparate disease trajectories point to possible modular approaches for web-based decisional support.

摘要

基因检测越来越成为常规临床护理的一部分。然而,由于检测结果也暗示了血缘亲属的情况,检测决策可能会让人感到遗憾。目前尚不清楚基因检测决策是否会受到信息呈现方式(即框架效应)的影响。我们采用随机因子设计来研究假设的基因检测场景(常见的危及生命的疾病和罕见的改变生活的疾病)中的框架效应。参与者(n=1012)接受了六种决策框架中的一种:选择、默认(=2;选择加入、选择退出)或增强选择(=3,基于计划行为理论)。我们比较了不同决策框架和不同场景下的检测决策、满意度、遗憾和决策认知。与默认和增强选择框架相比,随机分配到“选择”框架的参与者选择进行基因检测的可能性最低(78%对 83-91%,<0.05)。框架之间的满意度和遗憾均无差异。感知自主性(行为控制)预测满意度(B=0.085,<0.001),而缺乏控制则预测遗憾(B=0.346,<0.001)。不同疾病场景之间的基因检测选择(=0.23)并无差异。结果表明,框架可以促使个人倾向于选择基因检测。这些发现对基因组时代的个体自主决策具有重要意义。不同疾病轨迹场景之间的相似性表明,可能需要采用模块化方法来为基于网络的决策支持提供服务。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9bd/8234313/f6dd52b8d069/genes-12-00941-g001.jpg

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