Development of a Patient-Centered Pathway of Care for Retinoblastoma Patients: A Mixed-Methods Pilot Study.

IF 2.5 3区 医学 Q3 ONCOLOGY Oncology Pub Date : 2024-07-01 DOI:10.1159/000540055
Ivana Ristevski, Kaitlyn Flegg, Mawj Al-Hammadi, Morgan Livingstone, Taline Dorna, Leslie Low, Jill Robert, Alissa Ulster, Stephanie Kletke, Ashwin Mallipatna, Katherine Paton, Helen Dimaras
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Abstract

Introduction Retinoblastoma treatment and follow-up is complex and varies between patients. Pathways of care can enhance quality of care, patient outcomes, safety, satisfaction, and resource optimization. Developing a pathway of care for retinoblastoma was identified as a top research priority by the retinoblastoma community. This study aimed to co-design and pilot a pathway of care called the "Retinoblastoma Journey Map" tailored for caregivers of newly diagnosed children with retinoblastoma. Methods A working group of patients, health professionals and researchers used human-centred design to ideate, prototype and refine the Retinoblastoma Journey Map. Caregivers of affected children were recruited to use and evaluate the Map. Mixed-methods data was collected on feasibility, acceptability, usability and perceived impact on communication, self-efficacy, anxiety, depression, and the quality of physician-patient interaction. Results The Retinoblastoma Journey Map consisted of an illustrated roadmap with 25 child-friendly stickers covering clinical treatment, medical education and milestones. Quantitative analysis revealed that the Map was feasible, acceptable, and usable; however, no significant effect on communication, self-efficacy, anxiety, depression or quality of physician-patient interaction was observed. Qualitative analysis identified 6 themes: Primary Use, Challenges, Impact, Limitations, Feasibility, Acceptability and Usability, and Unmet Needs. Conclusion A pathway of care for retinoblastoma, co-designed by researchers, health professionals and patients, was usable, acceptable, and feasible by caregivers of children with retinoblastoma. While significant effects on communication and physician-patient interaction were not observed, 'legacy building' - documentation of the pathway of care by families for later education of their child - emerged as an unanticipated yet important use of the Retinoblastoma Journey Map.

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为视网膜母细胞瘤患者制定以患者为中心的护理路径:混合方法试点研究。
导言 视网膜母细胞瘤的治疗和随访非常复杂,而且因患者而异。护理路径可以提高护理质量、患者疗效、安全性、满意度和资源优化。视网膜母细胞瘤社区已将开发视网膜母细胞瘤护理路径确定为研究的重中之重。本研究旨在共同设计并试行一种名为 "视网膜母细胞瘤旅程地图 "的护理路径,该地图专为新诊断为视网膜母细胞瘤的儿童患者的护理人员量身定制。方法 由患者、医护人员和研究人员组成的工作组采用以人为本的设计理念,对视网膜母细胞瘤旅程地图进行构思、原型设计和完善。受影响儿童的照顾者被招募来使用和评估该地图。就可行性、可接受性、可用性以及对沟通、自我效能、焦虑、抑郁和医患互动质量的感知影响收集了混合方法数据。结果 视网膜母细胞瘤 "旅程地图 "由一张图文并茂的路线图和 25 张儿童友好贴纸组成,内容涵盖临床治疗、医学教育和里程碑。定量分析显示,该地图是可行的、可接受的和可用的,但对沟通、自我效能感、焦虑、抑郁或医患互动质量没有显著影响。定性分析确定了 6 个主题:主要用途、挑战、影响、局限性、可行性、可接受性和可用性以及未满足的需求。结论 由研究人员、医护人员和患者共同设计的视网膜母细胞瘤护理路径对于视网膜母细胞瘤患儿的护理人员来说是可用的、可接受的和可行的。虽然没有观察到对沟通和医患互动的重大影响,但 "遗产建设"--家庭为日后教育子女而记录护理路径--成为视网膜母细胞瘤旅程图的一个意想不到的重要用途。
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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来源期刊
Oncology
Oncology 医学-肿瘤学
CiteScore
6.00
自引率
2.90%
发文量
76
审稿时长
6-12 weeks
期刊介绍: Although laboratory and clinical cancer research need to be closely linked, observations at the basic level often remain removed from medical applications. This journal works to accelerate the translation of experimental results into the clinic, and back again into the laboratory for further investigation. The fundamental purpose of this effort is to advance clinically-relevant knowledge of cancer, and improve the outcome of prevention, diagnosis and treatment of malignant disease. The journal publishes significant clinical studies from cancer programs around the world, along with important translational laboratory findings, mini-reviews (invited and submitted) and in-depth discussions of evolving and controversial topics in the oncology arena. A unique feature of the journal is a new section which focuses on rapid peer-review and subsequent publication of short reports of phase 1 and phase 2 clinical cancer trials, with a goal of insuring that high-quality clinical cancer research quickly enters the public domain, regardless of the trial’s ultimate conclusions regarding efficacy or toxicity.
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