患者在BRCA1/2基因咨询中对风险信息的抵触情绪。
Patients' resistance to risk information in genetic counseling for BRCA1/2.
作者信息
Gurmankin Andrea D, Domchek Susan, Stopfer Jill, Fels Christina, Armstrong Katrina
机构信息
Department of Society, Human Development, and Health, Harvard School of Public Health, Dana-Farber Cancer Institute, 44 Binney Street, Boston, MA 02115, USA.
出版信息
Arch Intern Med. 2005 Mar 14;165(5):523-9. doi: 10.1001/archinte.165.5.523.
BACKGROUND
Risk information from health care providers is relevant to and used in nearly all medical decisions. Patients often misunderstand their risks, yet little is known about the risk perception that patients derive from risk communications with health care providers. This study examines patients' risk perceptions following communication with health care providers during genetic counseling about the risks of breast cancer and BRCA1/2 mutations.
METHODS
A prospective, longitudinal study was conducted from October 2002 to February 2004 of women who received genetic counseling. The women completed a survey before their counseling and a telephone interview in the week after the counseling. Main outcome measures included change from precounseling in risk perception and accuracy of postcounseling risk perception (relative to actual risk information communicated).
RESULTS
A total of 108 women agreed to participate in the study. The women's postcounseling risk perceptions were significantly lower than their precounseling risk perceptions (breast cancer: 17%, P<.001; mutation: 13%, P<.001) but were significantly higher than the actual risk information communicated (breast cancer: 19%, P<.001; mutation: 24%, P<.001). Accuracy of breast cancer risk perception but not mutation risk perception was associated with precounseling worry (P = .04), even after adjusting for trait anxiety (P = .01).
CONCLUSIONS
This research demonstrates patients' resistance to risk information. Inappropriately high risk perception derived from a risk communication with a health care provider can lead patients to make different, and potentially worse, medical decisions than they would with an accurate risk perception and to be unnecessarily distressed about their risk.
背景
医疗保健提供者提供的风险信息与几乎所有医疗决策都相关且被应用于其中。患者常常误解自身风险,但对于患者从与医疗保健提供者的风险沟通中所获得的风险认知却知之甚少。本研究调查了在关于乳腺癌风险和BRCA1/2基因突变的遗传咨询过程中,患者与医疗保健提供者沟通后对风险的认知情况。
方法
2002年10月至2004年2月,对接受遗传咨询的女性进行了一项前瞻性纵向研究。这些女性在咨询前完成一份调查问卷,并在咨询后一周接受电话访谈。主要结局指标包括咨询前后风险认知的变化以及咨询后风险认知的准确性(相对于所传达的实际风险信息)。
结果
共有108名女性同意参与该研究。这些女性咨询后的风险认知显著低于咨询前的风险认知(乳腺癌:降低17%,P<0.001;基因突变:降低13%,P<0.001),但显著高于所传达的实际风险信息(乳腺癌:高19%,P<0.001;基因突变:高24%,P<0.001)。即使在调整特质焦虑因素后(P = 0.01),乳腺癌风险认知的准确性而非基因突变风险认知的准确性仍与咨询前的担忧相关(P = 0.04)。
结论
本研究表明患者对风险信息存在抵触情绪。与医疗保健提供者的风险沟通产生的过高风险认知可能会导致患者做出与准确风险认知时不同且可能更糟糕的医疗决策,并使其对自身风险产生不必要的担忧。