Perspectives of Lymphoma Survivors and Oncology Care Providers on Survivorship Care: A Qualitative Study.

IF 4.7 3区 医学 Q1 ONCOLOGY
Jeanne M Ferrante, Myneka Macenat, Jenna Howard, Nimi Patel, Jaanvi Mahesh, Meghan Bissett, Jacintha J Peram, Justin D Solleder, Marissa Grosso, Shawna V Hudson, Dena O'Malley, Katie A Devine, Matthew Matasar, Andrew M Evens, Sharon L Manne
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Abstract

Purpose: To explore lymphoma survivors' care experiences and needs post-treatment and to determine optimal information and services for a lymphoma survivorship program from the perspectives of both survivors and oncologists.

Methods: We conducted in-depth semi-structured interviews with 32 lymphoma survivors and 13 lymphoma oncology providers. Interviews were analyzed using a template organizing style and iterative immersion/crystallization analysis of retrieved coded segments. Our thematic analysis focused on identifying commonalities and variations of themes related to lymphoma survivors' post-treatment needs, transition from oncology to primary care, and survivors' and providers' recommendations for improving survivorship care for patients with lymphoma.

Results: Three main themes emerged. (1) A predominant unmet need was how to manage the profound fear of recurrence and anxiety post-treatment. Survivors desired more information about signs and symptoms of recurrence and reassurance from their cancer team. (2) There were diverse views regarding the importance of transition from oncologist to primary care providers. Some survivors and oncologists did not value the importance of transitioning to primary care, whereas others recognized the need for primary care but found difficulty with accessing primary care. (3) Psychosocial support, wellness services, and assistance with financial and employment programs are needed for an ideal survivorship program.

Conclusion: This study provides critical insights into optimal survivorship care for patients with lymphoma. Further research is needed to better understand cost-effective models of care for this unique and complex population of lymphoma survivors.

淋巴瘤幸存者和肿瘤护理人员对幸存者护理的看法:定性研究。
目的:探讨淋巴瘤幸存者的护理经历和治疗后的需求,并从幸存者和肿瘤学家的角度确定淋巴瘤幸存者项目的最佳信息和服务。方法:我们对32名淋巴瘤幸存者和13名淋巴瘤肿瘤提供者进行了深入的半结构化访谈。访谈使用模板组织方式和检索编码片段的迭代浸泡/结晶分析进行分析。我们的主题分析侧重于确定与淋巴瘤幸存者治疗后需求、从肿瘤学到初级保健的过渡以及幸存者和提供者对改善淋巴瘤患者生存护理的建议相关的主题的共性和差异。结果:出现了三个主要主题。(1)一个主要的未满足的需求是如何管理治疗后对复发的深刻恐惧和焦虑。幸存者希望从他们的癌症团队获得更多关于复发症状和体征的信息。(2)关于从肿瘤科医生向初级保健提供者转变的重要性,存在不同的观点。一些幸存者和肿瘤学家不重视向初级保健过渡的重要性,而另一些人认识到初级保健的必要性,但发现难以获得初级保健。(3)理想的生存计划需要社会心理支持、健康服务以及经济和就业计划方面的援助。结论:本研究为淋巴瘤患者的最佳生存护理提供了重要的见解。需要进一步的研究来更好地了解这种独特而复杂的淋巴瘤幸存者群体的成本效益模式。
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
CiteScore
6.40
自引率
7.50%
发文量
518
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