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遗传咨询对有乳腺癌家族史女性的风险认知和心理健康的影响。

The impact of genetic counselling on risk perception and mental health in women with a family history of breast cancer.

作者信息

Watson M, Lloyd S, Davidson J, Meyer L, Eeles R, Ebbs S, Murday V

机构信息

Royal Marsden NHS Trust and Institute of Cancer Research, Sutton, Surrey, UK.

出版信息

Br J Cancer. 1999 Feb;79(5-6):868-74. doi: 10.1038/sj.bjc.6690139.

Abstract

The present study investigated: (1) perception of genetic risk and, (2) the psychological effects of genetic counselling in women with a family history of breast cancer. Using a prospective design, with assessment pre- and post-genetic counselling at clinics and by postal follow-up at 1, 6 and 12 months, attenders at four South London genetic clinics were assessed. Participants included 282 women with a family history of breast cancer. Outcome was measured in terms of mental health, cancer-specific distress and risk perception. High levels of cancer-specific distress were found pre-genetic counselling, with 28% of participants reporting that they worried about breast cancer 'frequently or constantly' and 18% that worry about breast cancer was 'a severe or definite problem'. Following genetic counselling, levels of cancer-specific distress were unchanged. General mental health remained unchanged over time (33% psychiatric cases detected pre-genetic counselling, 27% at 12 months after genetic counselling). Prior to their genetics consultation, participants showed poor knowledge of their lifetime risk of breast cancer since there was no association between their perceived lifetime risk (when they were asked to express this as a 1 in x odds ratio) and their actual risk, when the latter was calculated by the geneticist at the clinic using the CASH model. In contrast, women were more accurate about their risk of breast cancer pre-genetic counselling when this was assessed in broad categorical terms (i.e. very much lower/very much higher than the average woman) with a significant association between this rating and the subsequently calculated CASH risk figure (P = 0.001). Genetic counselling produced a modest shift in the accuracy of perceived lifetime risk, expressed as an odds ratio, which was maintained at 12 months' follow-up. A significant minority failed to benefit from genetic counselling; 77 women continued to over-estimate their risk and maintain high levels of cancer-related worry. Most clinic attenders were inaccurate in their estimates of the population risk of breast cancer with only 24% able to give the correct figure prior to genetic counselling and 36% over-estimating this risk. There was some improvement following genetic counselling with 62% able to give the correct figure, but this information was poorly retained and this figure had dropped to 34% by the 1-year follow-up. The study showed that women attending for genetic counselling are worried about breast cancer, with 34% indicating that they had initiated the referral to the genetic clinic themselves. This anxiety is not alleviated by genetic counselling, although women reported that it was less of a problem at follow-up. Women who continue to over-estimate their risk and worry about breast cancer are likely to go on seeking unnecessary screening if they are not reassured.

摘要

本研究调查了

(1)乳腺癌家族史女性对遗传风险的认知,以及(2)遗传咨询的心理影响。采用前瞻性设计,在诊所进行遗传咨询前后进行评估,并在1个月、6个月和12个月时通过邮寄方式进行随访,对伦敦南部四家遗传诊所的就诊者进行了评估。参与者包括282名有乳腺癌家族史的女性。结果通过心理健康、癌症特异性困扰和风险认知来衡量。在遗传咨询前发现癌症特异性困扰水平较高,28%的参与者报告称他们“经常或持续”担心乳腺癌,18%的参与者称担心乳腺癌是“一个严重或明确的问题”。遗传咨询后,癌症特异性困扰水平没有变化。总体心理健康随着时间推移保持不变(遗传咨询前检测出33%有精神疾病病例,遗传咨询后12个月为27%)。在进行基因咨询之前,参与者对自己患乳腺癌的终生风险了解甚少,因为他们感知到的终生风险(当被要求以x分之一的比值比来表达时)与实际风险之间没有关联,而实际风险是由诊所的遗传学家使用CASH模型计算得出的。相比之下,当以宽泛的分类术语(即远低于/远高于普通女性)评估时,女性在遗传咨询前对自己患乳腺癌的风险判断更准确,这种评级与随后计算出的CASH风险数字之间存在显著关联(P = 0.001)。遗传咨询使感知终生风险的准确性有适度转变,以比值比表示,这种转变在12个月的随访中得以维持。相当一部分人未能从遗传咨询中受益;77名女性继续高估自己的风险并维持高水平的癌症相关担忧。大多数诊所就诊者对乳腺癌人群风险的估计不准确,遗传咨询前只有24%的人能给出正确数字,36%的人高估了这一风险。遗传咨询后有一定改善,62%的人能给出正确数字,但这一信息保留情况不佳,到1年随访时这一数字已降至34%。该研究表明,前来进行遗传咨询的女性担心乳腺癌,34%的人表示是自己主动转诊到遗传诊所的。遗传咨询并未减轻这种焦虑,尽管女性报告称随访时这一问题有所减轻。如果得不到安心,那些继续高估自身风险并担心乳腺癌的女性可能会继续寻求不必要的筛查。

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