在英国,CAR - T细胞治疗血癌的患者和护理人员的经验:一项定性研究。

IF 3.1 3区 医学 Q1 HEALTH CARE SCIENCES & SERVICES
Christel McMullan, Melanie J Calvert, Sarah E Hughes, Lester Pyatt, Bernie Kern, Karen L Shaw, Biruk Asfaw, Caroline Besley, Niamh Buckingham, Hayley Ellis, Caitlin Farrow, Maria Mazza, Rachel Miller, David Irvine, Ceri Jones, Emily John, Yasmin Sheikh, Gemma Pugh, Christina Yiallouridou, Olalekan Lee Aiyegbusi
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引用次数: 0

摘要

背景:先进的细胞疗法,包括嵌合抗原受体T细胞(CAR - T细胞)疗法,为晚期血癌如淋巴瘤和白血病的治疗提供了新的机会。然而,由于这些疗法相对较新,关于患者和非正式护理人员的治疗经验的信息有限,这可能会影响这些疗法的采用。本定性研究的目的是探索他们的经验,以促进识别具体问题,应解决积极影响患者的结果和护理经验。方法:我们对来自4个英国CAR - T细胞中心的26名治疗后≥1个月的CAR - T细胞受体和9名护理人员进行了半结构化定性访谈。访谈探讨了参与者对CAR - T细胞治疗的经验和对关键问题的看法。访谈数据采用主题分析进行归纳编码。结果:确定的主题包括(1)信息提供的意见,(2)保护性隔离的经历,(3)疾病和治疗的影响,(4)对需要和接受的支持的反思,以及(5)慈善机构和支持团体的作用。与会者强调需要特别为护理人员提供支持,并为改善未来患者的体验提供切实可行的建议。结论:解决所提出问题的干预措施需要与关键利益相关者共同开发,包括患者、护理人员、医疗保健专业人员、政策制定者和慈善组织。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Patient and Caregiver Experiences of CAR T Cell Therapy for Blood Cancer in the UK: A Qualitative Study.

Background: Advanced cell therapies, including chimeric antigen receptor T cell (CAR T cell) therapies, offer novel opportunities for the treatment of advanced blood cancers such as lymphoma and leukaemia. However, as these therapies are relatively new, there is limited information on the experiences of patients and informal caregivers of the treatment which may influence the uptake of these therapies. The aim of this qualitative study was to explore their experiences to facilitate the identification of specific issues that should be addressed to positively impact patient outcomes and experiences of care.

Methods: We conducted semi-structured qualitative interviews with 26 CAR T cell recipients from four UK CAR T cell centres who were ≥ 1 month post-treatment and nine caregivers. Interviews explored participants' experiences of CAR T cell therapy and perspectives on key issues. Data from the interviews were inductively coded using thematic analysis.

Results: The main themes identified included (1) opinions of information provision, (2) experiences of protective isolation, (3) impacts of illness and treatment, (4) reflections on support needed and received, and (5) role of charities and support groups. Participants highlighted the need for support specifically for caregivers and provided practical suggestions for improving the experiences of future patients.

Conclusions: Interventions to address the issues raised need to be co-developed with key stakeholders, including patients, caregivers, healthcare professionals, policymakers and charitable organisations.

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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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