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Patient satisfaction with two different models of cancer genetic services in south-east Scotland

机译:患者对苏格兰东南部两种不同的癌症遗传服务模式的满意度

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There is a need to integrate primary- and secondary-care cancer genetic services, but the most appropriate model of service delivery remains unclear. This study reports patients’ expectations of breast cancer genetic services and a comparison of their satisfaction with two service models. In the first model, risk assessment was carried out using mailed family history data. Women estimated as being at high/moderate risk were offered an appointment at the familial breast cancer clinic, and those at low risk were sent a letter of reassurance. In the second model, all women were seen by a genetic nurse specialist, who assessed risk, referred high/moderate-risk women to the above clinic and discharged those at low risk. Over 60% of all women in the study regarded access to breast screening by mammogram and regular check-ups as very important. This underlines the demand for a multidisciplinary service providing both clinical genetic and surgical services. Satisfaction was high with both models of service, although significantly lower among women not at increased cancer risk and thus not offered a clinical check-up and mammography. Increased cancer worry was associated with a greater expressed need for information and for reassurance through follow-up clinical checks and mammography. Better targeting of counselling to the expressed concerns and needs of these women is required to improve the service offered. GPs and patients expressed no clear preference for any specific service location or staffing configuration. The novel community service was less expensive in terms of both staff and patient costs. The potential to decrease health staff/patient contact time and to employ nurse practitioners with both clinical genetic and oncology training should be explored further. The rapidly rising demand for these services suggests that the evaluation of further new models needs to continue to be given priority to guide the development of cancer genetic services.
机译:有必要整合初级保健和二级保健的癌症遗传服务,但最合适的服务提供模式仍不清楚。这项研究报告了患者对乳腺癌基因服务的期望以及他们对两种服务模型的满意度的比较。在第一个模型中,使用邮寄的家族史数据进行了风险评估。估计处于高/中度风险中的妇女在家族性乳腺癌诊所接受了任命,向处于低风险中的妇女发送了保证书。在第二种模型中,所有妇女均由遗传护士专家看望,该专家评估了风险,将高/中度风险的妇女转诊到上述诊所,并把低风险的妇女出院。该研究中超过60%的女性认为通过乳房X线照片进行乳房筛查和定期检查非常重要。这突出了对提供临床遗传和外科服务的多学科服务的需求。两种服务模式的满意度都很高,尽管在未患癌症风险增加的女性中满意度明显较低,因此没有提供临床检查和乳房X线照相。通过后续的临床检查和乳房X线照相术,对癌症的担忧增加与对信息的更多需求以及对安全性的更大需求有关。需要更好地将咨询针对这些妇女所表达的关切和需求,以改善所提供的服务。全科医生和患者对任何特定的服务地点或人员配置都没有明确表示偏爱。就员工和患者的费用而言,新颖的社区服务的价格较低。应进一步探索减少医务人员/患者接触时间并聘请护士从业人员进行临床遗传和肿瘤学培训的潜力。对这些服务的需求迅速增长表明,需要继续优先考虑对其他新模型的评估,以指导癌症遗传服务的发展。

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