Attributes Development for Pharmaceutical Subsidization: A Qualitative Study.

Gita Afsharmanesh, Gholamhossein Mehralian, Farzad Peiravian
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引用次数: 4

Abstract

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.

药品补贴属性发展:定性研究。
离散选择实验(DCES)作为一种明确的偏好方法,越来越多地用于确定与健康相关的某些属性的偏好。虽然这类研究的有效性完全取决于对DCES属性和属性水平的适当确定,但很少有严格的证据表明,哪些因素或属性和属性水平应该被计算在内,以引起公众在卫生资源分配中的偏好。本文通过细致的定性研究来回答这一问题。一项定性研究采用半结构化访谈,对访谈进行录音、转录并进行专题分析。16名与会者是医药和卫生系统的关键信息提供者和决策者。最初,通过进行细致的文献回顾,确定了与预期政策相关的属性的包含列表。通过16个关键信息者访谈,收集了属性发展及其水平的定性数据,并通过MAXQDA软件进行分析,随后由熟悉药物政策和药物经济学概念的7人进行焦点小组讨论(FGD)。311准则的四个主要维度最初是通过访谈确定的。然而,为了在DCE内进行管理,它们被分类并限制为四个属性,包括未经治疗的疾病严重程度、治疗后的健康状况改善、患者频率和每位患者的治疗成本。这项定性研究为设计和做一个精确的离散选择实验提供了足够的证据,以回答公众对药品补贴的偏好问题,并为有限的关于DCE属性发展的方法学文献提供了经验证据,特别是在低收入和中等收入国家。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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