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ORCA,一种基于价值的决策辅助工具,用于选择成年人基因组测序中的附加发现:一项随机试验的疗效结果。

ORCA, a values-based decision aid for selecting additional findings from genomic sequencing in adults: Efficacy results from a randomized trial.

机构信息

Kaiser Permanente Center for Health Research, Portland, OR.

Kaiser Permanente Center for Health Research, Portland, OR.

出版信息

Genet Med. 2022 Aug;24(8):1664-1674. doi: 10.1016/j.gim.2022.04.008. Epub 2022 May 6.

DOI:10.1016/j.gim.2022.04.008
PMID:35522237
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9586129/
Abstract

PURPOSE

Individuals having genomic sequencing can choose to be notified about pathogenic variants in genes unrelated to the testing indication. A decision aid can facilitate weighing one's values before making a choice about these additional results.

METHODS

We conducted a randomized trial (N = 231) comparing informed values-choice congruence among adults at risk for a hereditary cancer syndrome who viewed either the Optional Results Choice Aid (ORCA) or web-based additional findings information alone. ORCA is values-focused with a low-literacy design.

RESULTS

Individuals in both arms had informed values-choice congruence (75% and 73% in the decision aid and web-based groups, respectively; odds ratio [OR] = 1.10, 95% CI = 0.58-2.08). Most participants had adequate knowledge (79% and 76% in the decision aid and web-based groups, respectively; OR = 1.20, 95% CI = 0.61-2.34), with no significant difference between groups. Most had information-seeking values (97% and 98% in the decision aid and web-based groups, respectively; OR = 0.59, 95% CI = 0.10-3.61) and chose to receive additional findings.

CONCLUSION

The ORCA decision aid did not significantly improve informed values-choice congruence over web-based information in this cohort of adults deciding about genomic results. Both web-based approaches may be effective for adults to decide about receiving medically actionable additional results.

摘要

目的

进行基因组测序的个体可以选择获知与检测指征无关的基因中的致病性变异。决策辅助工具可以在做出有关这些额外结果的选择之前,帮助权衡个人的价值观。

方法

我们进行了一项随机试验(N=231),比较了有遗传性癌症综合征风险的成年人在查看可选结果选择辅助工具(ORCA)或仅查看基于网络的附加发现信息时,其知情价值观选择一致性。ORCA 是一个以价值观为重点且具有低识字设计的工具。

结果

两个组的个体都具有知情价值观选择一致性(决策辅助组和基于网络组分别为 75%和 73%;优势比[OR]=1.10,95%置信区间[CI]为 0.58-2.08)。大多数参与者具有足够的知识(决策辅助组和基于网络组分别为 79%和 76%;OR=1.20,95%CI 为 0.61-2.34),两组之间没有显著差异。大多数参与者有信息寻求价值观(决策辅助组和基于网络组分别为 97%和 98%;OR=0.59,95%CI 为 0.10-3.61),并选择接收附加发现。

结论

在决定基因组结果的这组成年人中,ORCA 决策辅助工具并没有比基于网络的信息显著提高知情价值观选择一致性。基于网络的这两种方法都可能对成年人决定是否接受具有医学可操作性的附加结果有效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/439f/9586129/22b42e3431b6/nihms-1810472-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/439f/9586129/6d8f7f2d28d3/nihms-1810472-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/439f/9586129/9a9f52f60c52/nihms-1810472-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/439f/9586129/22b42e3431b6/nihms-1810472-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/439f/9586129/6d8f7f2d28d3/nihms-1810472-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/439f/9586129/9a9f52f60c52/nihms-1810472-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/439f/9586129/22b42e3431b6/nihms-1810472-f0003.jpg

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