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Attributes Development for Pharmaceutical Subsidization: A Qualitative Study

机译:药物补贴的归属发展:定性研究

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摘要

Discrete choice experiments (DCES) as a stated preference method have used increasingly to determine preferences attached to some attributes associated to health. Although, the validity of this type of studies comprehensively depends on the appropriate determination of attributes and attribute-levels for DCES, there is little rigorous evidence regarding which factors or attributes and attribute- levels should be counted for eliciting public preferences in health resource allocation. This paper responds to such question by carefully doing a qualitative study. A qualitative study used semi-structured interviews, which were audio recorded, transcribed and subject to thematic analysis. Sixteen participants had been key informants and decision makers of pharmaceutical and health system. Initially, by conducting a meticulous literature review, an inclusive list of attributes associated with intended policy was identified. Qualitative data for the development of attributes and their levels were collected using 16 key informant interviews and were analyzed by software MAXQDA followed by a focus group discussion (FGD) with 7 people, well-familiar with the notion pharmaceutical policy and Pharmacoeconomics. The 311 codes in four main dimensions were initially identified by conducting interviews. However, for being manageable within a DCE, they were classified and limited to four attributes, including severity of disease without treatment, health gain after treatment, frequency of patients, and cost of treatment per patient. This qualitative study provides enough evidence for designing and doing a precise discrete choice experiment answering the question about public preferences in pharmaceutical subsidization and contributes empirical evidence to the limited methodological literature on attributes development for DCE, specifically within low and middle-income countries.
机译:作为所说的偏好方法的离散选择实验(DCE)越来越多地用于确定附加到与健康相关的某些属性的偏好。虽然,这种类型研究的有效性全面地取决于对某种形式的属性和属性水平的适当确定,关于应计入哪些因素或属性和属性的严格证据,以赋予卫生资源分配的公共偏好。本文通过仔细执行定性研究来回答这些问题。定性研究使用了半结构化访谈,这些访谈是录制的,转录并受专题分析。十六名参与者一直是药品和卫生系统的主要信息人和决策者。最初,通过进行细致的文献综述,确定了与预期策略相关的包含属性列表。使用16个关键信息面试,通过Software MaxQDA进行分析,随后通过7人,熟悉药物政策和药物经济学和药物经济学和药物经济学和药物经济学和药物经济学和药物经济学和药物经济学和药物经济学熟悉的焦点小组讨论(FGD)进行分析。最初通过进行访谈来识别四个主要尺寸的311个代码。然而,为了在DCE中可管理,它们被分类和限于四个属性,包括疾病的严重程度,无需治疗,治疗后的健康增益,患者的频率和每位患者治疗的成本。这种定性研究提供了足够的依据来设计和做出精确的离散选择实验,回答了关于药物补贴的公共偏好的问题,并为中低收入和中等收入国家的归属发展有限的方法学文学作出了有限的方法。

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