Concept elicitation

概念启发
  • 文章类型: Journal Article
    背景:为了比较在三种不同的定性数据来源中获得的有关老花眼(与年龄相关的近视力受损)个体经历的见解:结构化的针对性文献综述,社交媒体收听(SML)评论,以及对老花眼患者和医疗保健专业人员(HCP)的定性概念启发(CE)访谈。确定的概念数量,数据深度,成本和时间影响,探索并比较了每种方法产生的患者见解的价值。
    方法:在书目数据库中进行的关键词搜索和对摘要的回顾确定了120种相关出版物;对定性研究的深入有针对性的文献回顾确定了关键症状/功能概念。SML是使用可公开访问的社交媒体来源进行的,重点是眼科疾病,使用预定义的搜索字符串。分析了老花眼患者(n=270)的相关帖子,并确定了关键概念。对老花眼患者进行了半结构化CE访谈(美国n=30,德国n=10,法国n=10),和有治疗老花眼经验的HCP(美国=3,法国n=2,德国n=1,日本n=1)。使用主题分析对逐字记录进行编码。在三个来源中确定的158个概念中,定性CE访谈产生的概念数量最多(n=151/158,96%),SML产生了三分之一的概念(n=51/158,32%),文献综述产生的概念最少(n=33/158,21%)。定性CE访谈提供了比SML和文献综述更深入的数据。与定性CE访谈相比,SML和文献综述的成本更低,运行速度更快,并且对参与者的负担也更小。
    结论:定性CE访谈被认为是提供更深入了解患者体验的黄金标准。和更强大的数据。然而,研究要求,预算,选择最合适的研究方法时,应考虑可用时间。更多的时间和成本效益的SML和文献综述方法可用于补充定性CE访谈数据,并提供测量概念的早期识别。更多的研究和监管指导进入不太传统的定性方法,然而,需要增加SML和文献综述数据的价值。
    BACKGROUND: To compare the insights obtained about the experience of individuals with presbyopia (age-related impaired near vision) across three different sources of qualitative data: a structured targeted literature review, a social media listening (SML) review, and qualitative concept elicitation (CE) interviews with individuals with presbyopia and healthcare professionals (HCPs). The number of concepts identified, depth of data, cost and time implications, and value of the patient insights generated were explored and compared for each method.
    METHODS: Keyword searches in bibliographic databases and review of abstracts identified 120 relevant publications; in-depth targeted literature review of the qualitative studies identified key symptoms/functioning concepts. SML was conducted using publicly accessible social media sources with focus on ophthalmologic diseases using a pre-defined search string. Relevant posts from individuals with presbyopia (n = 270) were analysed and key concepts identified. Semi-structured CE interviews were conducted with individuals with presbyopia (US n = 30, Germany n = 10, France n = 10), and HCPs (US = 3, France n = 2, Germany n = 1, Japan n = 1) who were experienced in treating presbyopia. Verbatim transcripts were coded using thematic analysis. A conceptual model summarised concepts identified across sources RESULTS: Out of the total of 158 concepts identified across the three sources, qualitative CE interviews yielded the highest number of concepts (n = 151/158, 96%), with SML yielding a third of the concepts (n = 51/158, 32%) and the literature review yielding the fewest concepts (n = 33/158, 21%). Qualitative CE interviews provided greater depth of data than SML and literature reviews. SML and literature reviews were less costly and quicker to run than qualitative CE interviews and also were less burdensome for participants.
    CONCLUSIONS: Qualitative CE interviews are considered the gold standard in providing greater depth of understanding of the patient experience, and more robust data. However, research requirements, budget, and available time should be considered when choosing the most appropriate research method. More time and cost-effective SML and literature review methods can be used to supplement qualitative CE interview data and provide early identification of measurement concepts. More research and regulatory guidance into less traditional qualitative methods, however, are needed to increase the value of SML and literature review data.
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  • 文章类型: Journal Article
    背景:健康相关生活质量(HRQOL)是儿科肿瘤学的一个关键概念。本系统综述旨在更新Anthony等人的概念HRQOL模型。(QualLifeRes23(3):771-789,2014),覆盖物理,情感,社会和一般HRQOL方面,并全面概述癌症儿童的年龄和疾病特异性HRQOL问题。
    方法:Medline,心理信息,Cochrane系统评价数据库(CDSR),并在COSMIN数据库中搜索(最高31.12.2020)使用患者报告的结果测量(PROM)和针对癌症儿童(8-14岁)或其父母的定性研究的出版物.提取项目和报价并将其映射到上述患有癌症的儿童的HRQOL的概念模型上。
    结果:在2038项确定的研究中,221个被包括用于数据提取。我们确定了96个PROMS,包含2641个项目,并从45个定性研究中提取了798个报价。大多数项目和报价(94.8%)可以映射到概念模型上。然而,进行了一些调整,并通过“治疗负担”的(子)域补充了该模型,\“治疗参与\”,和“财务问题”。身体和心理方面比社会问题更频繁地涉及。
    结论:本综述全面概述了儿童癌症患者的HRQOL问题。我们的发现大多支持Anthony等人的HRQOL模型。(QualLifeRes23(3):771-789,2014),但是建议进行一些调整。这篇评论可能被认为是完善我们对癌症儿童HRQOL理解的起点。进一步的定性研究将有助于评估HRQOL模型的全面性及其所包含问题的相关性。
    BACKGROUND: Health-related quality of life (HRQOL) is a key concept in pediatric oncology. This systematic review aims to update the conceptual HRQOL model by Anthony et al. (Qual Life Res 23(3):771-789, 2014), covering physical, emotional, social and general HRQOL aspects, and to present a comprehensive overview of age- and disease-specific HRQOL issues in children with cancer.
    METHODS: Medline, PsychINFO, the Cochrane Database for Systematic Reviews (CDSR), and the COSMIN database were searched (up to 31.12.2020) for publications using patient-reported outcome measures (PROMs) and qualitative studies in children with cancer (8-14-year) or their parents. Items and quotations were extracted and mapped onto the conceptual model for HRQOL in children with cancer mentioned above.
    RESULTS: Of 2038 identified studies, 221 were included for data extraction. We identified 96 PROMS with 2641 items and extracted 798 quotations from 45 qualitative studies. Most items and quotations (94.8%) could be mapped onto the conceptual model. However, some adaptations were made and the model was complemented by (sub)domains for \'treatment burden\', \'treatment involvement\', and \'financial issues\'. Physical and psychological aspects were more frequently covered than social issues.
    CONCLUSIONS: This review provides a comprehensive overview of HRQOL issues for children with cancer. Our findings mostly support the HRQOL model by Anthony et al. (Qual Life Res 23(3):771-789, 2014), but some adaptations are suggested. This review may be considered a starting point for a refinement of our understanding of HRQOL in children with cancer. Further qualitative research will help to evaluate the comprehensiveness of the HRQOL model and the relevance of the issues it encompasses.
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