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Patient preferences and National Health Service costs: a cost-consequences analysis of cancer genetic services.

机译:患者偏好和国家卫生服务费用:癌症遗传服务的费用后果分析。

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摘要

The study has three aims; firstly to establish if, having been informed of their risk status and that gene testing is inappropriate for them, low and moderate risk patients have misunderstood or failed to grasp this and want a test that is inappropriate for them. Secondly, to elicit patients' willingness to pay for cancer genetic services. Thirdly, to ascertain the aspects of cancer genetics services that are important to high risk patients and present service configurations prioritised in terms of preferences accompanied by their costs (cost-consequences analysis). Patient preferences were gathered from 120 patients returning a self-administered discrete choice questionnaire issued post genetic risk assessment. Patients at low and moderate risk of developing breast cancer desired inappropriate testing. Patients at high, moderate and low risk of developing genetic cancer were willing to pay up to 3,000 pounds for genetic serviced, which exceeds the current estimated cost of providing testing and counselling. Counselling by a genetics associate accompanied by favourable levels of other attributes provided high utility and substantial cost savings.
机译:该研究有三个目的;首先,要确定中低风险患者在被告知其风险状况并且基因检测不适合他们之后,是否被误解或未能理解并希望进行不适合他们的检测。其次,激发患者愿意为癌症基因服务付费。第三,确定对于高风险患者而言重要的癌症遗传学服务方面,并根据偏好及其费用(费用后果分析)对服务结构进行优先排序。从120名患者中收集了患者的偏好,这些患者返回了在遗传风险评估后发布的自我管理的离散选择调查表。中低患乳腺癌风险的患者需要进行不适当的检查。高,中,低患遗传性癌症风险的患者愿意为遗传服务支付高达3,000英镑的费用,这超出了目前提供检测和咨询服务的估计费用。遗传学助理提供的咨询服务以及其他属性的有利水平提供了很高的实用性并节省了大量成本。

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