首页> 外文期刊>Value in health: the journal of the International Society for Pharmacoeconomics and Outcomes Research >Concept Elicitation Within Patient-Powered Research Networks: A Feasibility Study in Chronic Lymphocytic Leukemia
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Concept Elicitation Within Patient-Powered Research Networks: A Feasibility Study in Chronic Lymphocytic Leukemia

机译:患者供电的研究网络中的概念诱导:慢性淋巴细胞白血病的可行性研究

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Objectives: To explore the feasibility of using social media-based patient networks to gather qualitative data on patient-reported outcome (PRO) concepts relevant to chronic lymphocytic leukemia (CLL). Methods: Between August and November 2013, US -residing members of the PatientsLikeMe online CLL patient community completed open-ended web-based surveys designed to elicit descriptions of CLL symptoms, impacts, and treatment-related perceptions. Qualitative telephone follow-up interviews were conducted with a subsample of respondents. Survey responses and interview transcripts were coded for qualitative analysis using Atlas.ti. Results: Fifty survey responses were included in the analyses. Participants were age 60.5 +/- 6.9 years, 54% female, and 96% white. When surveyed, 20% were receiving current treatment, 16% were in remission, and 64% were treatment na ve. Among respondents, 369 descriptions of CLL symptoms were coded. Fatigue-related symptoms were expressed most frequently, with 54% reporting "fatigue," "tiredness," or both in their responses. These concepts were followed by night sweats (38%), swollen lymph nodes (32%), and frequent infections (28%). Among impacts of CLL, worry and fear (66% of respondents), depressed feelings (52%), and work limitations (50%) were noted most frequently. Conclusions: Survey results identified constitutional symptoms of CLL included in existing PRO instruments and the literature. Although the findings suggest that qualitative data obtained through social media applications can be potentially useful in supporting concept identification for newly developed PRO instruments, they also indicate that online approaches alone may not be sufficient to achieve efficient and exhaustive concept elicitation. Further research is needed to identify whether the results can support content validity in the same way as established qualitative research methods. (C) 2016 Published by Elsevier Inc. on behalf of International Society for Pharmacoeconomics and Outcomes Research (ISPOR). This is an open access article under the CC-BY-NC-ND license (http://creativecommons.orgtlicensesiby-nc-nd/1.0/).
机译:目标:探讨使用基于社交媒体的患者网络的可行性,收集与慢性淋巴细胞白血病(CLL)相关的患者报告的结果(Pro)概念的定性数据。方法:2013年8月至11月期间,美国 - 患者患者在线CLL患者社区的成员完成了开放式网络的调查,旨在引发CLL症状,影响和治疗相关的感知的描述。定性电话随访采访是通过受访者的四分代进行的。使用Atlas.ti编码了调查响应和面试成绩单进行定性分析。结果:分析中包含五十次调查响应。参与者年龄为60.5岁+/- 6.9岁,女性54%和96%白色。当调查时,20%正在接受目前的治疗,16%的缓解,64%是治疗Na Ve。在受访者中,编码了369个CLL症状的描述。疲劳相关的症状最常表达,54%报告“疲劳”,“疲劳”或两者兼而有之。这些概念之后是夜间汗水(38%),淋巴结肿大(32%)和频繁感染(28%)。在CLL的影响中,担心和恐惧(66%的受访者),最常常注意到抑郁的感受(52%)和工作限制(50%)。结论:调查结果确定了现有职业工具和文献中包含的CLL的宪法症状。虽然调查结果表明,通过社交媒体应用获得的定性数据可能在支持新开发的Pro仪器的概念识别方面可能是有用的,但他们还表明单独的在线方法可能不足以实现有效和详尽的概念诱因。需要进一步研究以确定结果是否可以以与所建立的定性研究方法相同的方式支持内容有效性。 (c)2016年由elsevier Inc.出版的国际药物经济学和结果研究(ISPOR)。这是CC-BY-NC-ND许可下的开放式访问文章(http://creativecommons.orgtlicenseiby-nc-nd/1.0/)。

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