Haga Susanne B, Tindall Genevieve, O'Daniel Julianne M
Institute for Genome Sciences and Policy, Duke University, Durham, North Carolina 27708, USA.
Genet Test Mol Biomarkers. 2012 Mar;16(3):193-7. doi: 10.1089/gtmb.2011.0118. Epub 2011 Nov 2.
Pharmacogenetic (PGx) tests are intended to improve therapeutic outcomes through predicting a patient's likelihood to respond to or experience an adverse effect from a specific treatment. In addition, PGx testing may also generate ancillary, or incidental, disease information unrelated to the purpose for which the test was ordered. To assess public attitudes toward PGx testing, ancillary disease risk information and related clinical issues, we conducted a series of focus groups.
Forty-five individuals recruited from Durham, NC, participated in four focus groups. Overall, participants were enthusiastic about PGx testing, though expressed concerns about privacy, confidentiality, and psychological harms associated with ancillary information. Focus group participants believed that physicians had a responsibility to disclose ancillary risk information, but were concerned about managing and coping with unexpected disease risk information.
We find that participants welcomed the integration of PGx testing into therapeutic decision-making. Public concerns about PGx testing and ancillary information specifically centered on personal implications of learning such additional information, suggesting that patient-provider discussion of the benefits and risks of testing will be necessary until public familiarity with these tests increases.
药物遗传学(PGx)检测旨在通过预测患者对特定治疗产生反应或出现不良反应的可能性来改善治疗效果。此外,PGx检测还可能产生与检测目的无关的辅助性或偶然性疾病信息。为了评估公众对PGx检测、辅助性疾病风险信息及相关临床问题的态度,我们开展了一系列焦点小组讨论。
从北卡罗来纳州达勒姆招募的45人参加了4个焦点小组讨论。总体而言,参与者对PGx检测充满热情,但对与辅助性信息相关的隐私、保密和心理伤害表示担忧。焦点小组参与者认为医生有责任披露辅助性风险信息,但担心如何管理和应对意外的疾病风险信息。
我们发现参与者欢迎将PGx检测纳入治疗决策。公众对PGx检测和辅助性信息的担忧具体集中在了解此类额外信息对个人的影响上,这表明在公众对这些检测的熟悉程度提高之前,患者与医疗服务提供者讨论检测的益处和风险是必要的。