Rose P W, Watson E, Yudkin P, Emery J, Murphy M, Fuller A, Lucassen A
Department of Primary Health Care, University of Oxford, Oxford, UK.
Fam Pract. 2001 Oct;18(5):487-90. doi: 10.1093/fampra/18.5.487.
Primary care is expected to play a significant role in the management of patients with genetic problems. Currently, this particularly involves patients with a family history of cancer. If GPs are to exercise their gatekeeper role efficiently in this area, they must be able to evaluate genetic risk and make appropriate referral decisions.
The aim of this study was to examine GPs' ability to assess risk and to make appropriate referral decisions for women with a family history of breast/ovarian cancer, and to determine their expectations of a referral to secondary care.
A questionnaire survey was carried out of the 282 GP principals working within Bedfordshire Health Authority. GPs were asked to make decisions for six simulated cases of women presenting with a family history of breast or ovarian cancer.
A total of 164 (58%) GPs returned completed questionnaires. Across the six family histories, the percentage of GPs making an appropriate risk assessment ranged from 21% [95% confidence interval (CI) 14-27%] to 63% (95% CI 56-71%), and an appropriate referral decision ranged from 40% (95% CI 32-48%) to 80% (95% CI 73-86%). Regardless of their accuracy of risk assessment, most GPs were consistent in deciding not to refer low risk women and to refer moderate and high risk women (range 71-85% of GPs for the six family histories). Only 43 (26%, 95% CI 20-33%) of GPs knew the three most important criteria for risk assessment.
GPs require more help and education to enable them to perform their gatekeeper role satisfactorily when assessing patients with a family history of breast/ovarian cancer.
初级保健有望在遗传问题患者的管理中发挥重要作用。目前,这尤其涉及有癌症家族史的患者。如果全科医生要在这一领域有效地发挥把关人的作用,他们必须能够评估遗传风险并做出适当的转诊决定。
本研究的目的是检验全科医生评估风险的能力,以及为有乳腺癌/卵巢癌家族史的女性做出适当转诊决定的能力,并确定他们对转诊至二级保健机构的期望。
对在贝德福德郡卫生局工作的282名全科医生负责人进行了问卷调查。要求全科医生对6例有乳腺癌或卵巢癌家族史的女性模拟病例做出决定。
共有164名(58%)全科医生返回了完整的问卷。在这6种家族病史中,做出适当风险评估的全科医生比例从21%[95%置信区间(CI)14 - 27%]到63%(95%CI 56 - 71%)不等,做出适当转诊决定的比例从40%(95%CI 32 - 48%)到80%(95%CI 73 - 86%)不等。无论风险评估的准确性如何,大多数全科医生在决定不转诊低风险女性以及转诊中度和高风险女性方面是一致的(6种家族病史中全科医生的比例范围为71 - 85%)。只有43名(26%,95%CI 20 - 33%)全科医生知道风险评估的三个最重要标准。
全科医生需要更多的帮助和教育,以便在评估有乳腺癌/卵巢癌家族史的患者时能够令人满意地发挥其把关人的作用。