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首页> 外文期刊>Frontiers in Medicine >Social Preferences for Orphan Drugs: A Discrete Choice Experiment Among the French General Population
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Social Preferences for Orphan Drugs: A Discrete Choice Experiment Among the French General Population

机译:孤儿药物的社会偏好:法国普通人群中的离散选择实验

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Objectives: While several authors have suggested using a multi-criteria approach for orphan drug assessment and proposed lists of determinants of orphan drug value, studies on social preferences regarding these determinants remain limited. The current study aimed to identify preferences of the French general population regarding attributes characterizing the value of orphan drugs in a discrete choice experiment. Methods: The list of attributes was formed based on a literature search and was refined through expert interviews, a focus group, and a pilot study. The final list included nine attributes: disease-associated disability, disease-associated mortality, number of patients, availability of alternative treatments, treatment impact on disease disability, treatment impact on mortality, treatment safety, uncertainty around therapeutic effect, and annual treatment cost per patient. Members of the General Public were presented with 12 choice sets containing two drug profiles described according to the attributes and an option to fund neither of these treatments. The questionnaire was disseminated online. A conditional logit model with random effects was used to estimate the weight of each attribute. Results: A total of 958 persons participated in the study (48.7% male, mean age: 47.5 years). All attributes except for disease-associated disability had a statistically significant influence on the choices made by participants. The attribute with the highest weight was treatment impact on mortality ( p 0.0001), followed by uncertainty around therapeutic effect ( p 0.0001). The direction of results was generally consistent with intuition: patients preferred a drug with a larger impact on mortality, a larger impact on disability, with mild or no adverse events, with less uncertainty. Although patients appeared to prefer drugs with a lower budget impact, the relationship between patient preferences and costs was more complex. Conclusions: Preferences of the general public between orphan drugs are mostly driven by the impact on mortality and the degree of certainty regarding the available evidence.
机译:目的:虽然有几位作者用孤儿药物评估的多标准方法建议,并提出了孤儿药物价值的决定因素列表,关于这些决定因素的社会偏好的研究仍然有限。目前的研究旨在识别法国一般人群关于特征在离散选择实验中孤儿药物价值的属性的偏好。方法:通过文献搜索,通过专家访谈,焦点小组和试点研究来提炼属性列表。最终清单包括九个属性:疾病相关的残疾,疾病相关死亡率,患者数量,替代治疗的可用性,治疗对疾病残疾的影响,治疗对死亡率的影响,治疗安全,治疗效果周围的不确定性,以及每年的年度治疗费用病人。普通公众的成员介绍了12套,其中包含了根据属性描述的两种药物档案,也是既不用于这些治疗的选项。调查问卷在线传播。随机效果的条件Logit模型用于估计每个属性的权重。结果:共有958人参加该研究(男性48.7%,意思年龄:47.5岁)。除疾病相关的残疾外的所有属性对参与者制作的选择具有统计上显着的影响。具有最高重量的属性是对死亡率的影响(P <0.0001),然后在治疗效果周围的不确定性(P <0.0001)。结果的方向通常与直觉一致:患者优雅的一种药物对死亡率影响较大,对残疾的影响较大,具有轻微或没有不良事件,不确定。虽然患者似乎更喜欢具有较低预算效果的药物,但患者偏好与成本之间的关系更复杂。结论:孤儿药物之间的公众偏好主要受到对死亡率的影响以及关于可用证据的确定性程度。

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