从定性研究到定量偏好激发:以侵袭性脑膜炎球菌病为例。

IF 3.4 3区 医学 Q1 HEALTH CARE SCIENCES & SERVICES
Joshua Coulter, Chiara Whichello, Sebastian Heidenreich, Brett Hauber, Christine Michaels-Igbokwe, Joseph C Cappelleri, Paula Peyrani, Jessica Vespa Presa, Malavika Venkatraman, Katharina Schley
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引用次数: 0

摘要

背景:定性研究是设计离散选择实验 (DCE) 的基础,但在偏好研究文献中往往未得到充分报道。我们开发了一种 DCE,以了解美国青少年(AYP)及父母和法定监护人(PLG)对侵入性脑膜炎球菌病(IMD)疫苗接种的偏好。本文报告了为 DCE 设计提供依据的目标文献综述和定性访谈,并展示了如何在偏好研究中应用最新的定性发展工作报告指南:本研究包括两部分:有针对性的文献综述和定性访谈。在 Medline 和 Embase 数据库中搜索了有关 IMD 和免疫接种的定量和定性研究。有针对性的文献综述结果为定性访谈指南提供了参考。通过对 AYP 和 PLG 进行 60 分钟的在线半结构化访谈,确定了与接种 IMD 疫苗意愿相关的主题。参与者是通过第三方招募者数据库和商业在线面板招募的。访谈包括有关 IMD 和疫苗接种的小故事,以及三个阈值练习,分别考察发病率、致残率和死亡率对疫苗接种偏好的影响。对参与者与主题相关的回答进行了统计:有针对性的文献综述确定了 31 个概念,并将其归纳为定性访谈的六个主题。对 20 名年龄在 16-23 岁之间的青少年和 20 名年龄在 11-17 岁之间的青少年群体进行了访谈。出现了四个与接种意愿有关的主题:对接种疫苗的态度、知识和信息、对 IMD 的看法以及疫苗属性。大多数参与者关注综合症(青少年占 60%;儿童占 85%),并对疫苗接种持积极态度(青少年占 80%;儿童占 60%)。90%的AYP和75%的PLG总是选择接种疫苗而不是不接种,这与IMD发病率、致残率或死亡率无关:结论:接种 IMD 疫苗的意愿受疫苗属性的影响,但对 IMD 发病率和严重程度基本不敏感。本文举例说明了如何在偏好研究中应用最新的定性发展工作报告指南,并考虑了指南中 22 个项目中的 21 个。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

From Qualitative Research to Quantitative Preference Elicitation: An Example in Invasive Meningococcal Disease.

From Qualitative Research to Quantitative Preference Elicitation: An Example in Invasive Meningococcal Disease.

Background: Qualitative research is fundamental for designing discrete choice experiments (DCEs) but is often underreported in the preference literature. We developed a DCE to elicit preferences for vaccination against invasive meningococcal disease (IMD) among adolescents and young people (AYP) and parents and legal guardians (PLG) in the United States. This article reports the targeted literature review and qualitative interviews that informed the DCE design and demonstrates how to apply the recent reporting guidelines for qualitative developmental work in preference studies.

Methods: This study included two parts: a targeted literature review and qualitative interviews. The Medline and Embase databases were searched for quantitative and qualitative studies on IMD and immunization. The results of the targeted literature review informed a qualitative interview guide. Sixty-minute, online, semi-structured interviews with AYP and PLG were used to identify themes related to willingness to be vaccinated against IMD. Participants were recruited through a third-party recruiter's database and commercial online panels. Interviews included vignettes about IMD and vaccinations and three thresholding exercises examining the effect of incidence rate, disability rate, and fatality rate on vaccination preferences. Participant responses related to the themes were counted.

Results: The targeted literature review identified 31 concepts that were synthesized into six topics for the qualitative interviews. Twenty AYP aged 16-23 years and 20 PLG of adolescents aged 11-17 years were interviewed. Four themes related to willingness to be vaccinated emerged: attitudes towards vaccination, knowledge and information, perception of IMD, and vaccine attributes. Most participants were concerned about IMD (AYP 60%; PLG 85%) and had positive views of vaccination (AYP 80%; PLG 60%). Ninety percent of AYP and 75% of PLG always chose vaccination over no vaccination, independent of IMD incidence rate, disability rate, or fatality rate.

Conclusion: Willingness to be vaccinated against IMD was affected by vaccine attributes but largely insensitive to IMD incidence and severity. This article provides an example of how to apply the recent reporting guidelines for qualitative developmental work in preference studies, with 21 out of 22 items in the guidelines being considered.

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来源期刊
Patient-Patient Centered Outcomes Research
Patient-Patient Centered Outcomes Research HEALTH CARE SCIENCES & SERVICES-
CiteScore
6.60
自引率
8.30%
发文量
44
审稿时长
>12 weeks
期刊介绍: The Patient provides a venue for scientifically rigorous, timely, and relevant research to promote the development, evaluation and implementation of therapies, technologies, and innovations that will enhance the patient experience. It is an international forum for research that advances and/or applies qualitative or quantitative methods to promote the generation, synthesis, or interpretation of evidence. The journal has specific interest in receiving original research, reviews and commentaries related to qualitative and mixed methods research, stated-preference methods, patient reported outcomes, and shared decision making. Advances in regulatory science, patient-focused drug development, patient-centered benefit-risk and health technology assessment will also be considered. Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in The Patient may be accompanied by plain language summaries to assist readers who have some knowledge of, but not in-depth expertise in, the area to understand important medical advances. All manuscripts are subject to peer review by international experts.
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