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肿瘤学提供者和非裔美国乳腺癌幸存者对过渡到生存者阶段的情绪体验的看法。

Oncology provider and African-American breast cancer survivor perceptions of the emotional experience of transitioning to survivorship.

机构信息

Division of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington, USA.

Department of Health Services, University of Washington, Seattle, Washington, USA.

出版信息

J Psychosoc Oncol. 2021;39(1):35-53. doi: 10.1080/07347332.2020.1752880. Epub 2020 May 13.

Abstract

PURPOSE

To examine the emotional experience of African American breast cancer survivors (BCS), and the information exchange between providers and patients, during transitioning to post-treatment survivorship.

RESEARCH APPROACH

We conducted a qualitative study using interviews and focus groups.

PARTICIPANTS

We sought perspectives of oncology providers (n = 27) and African-American breast cancer survivors (BCS) (n = 45) who provided and received care in three counties in Washington State.

METHODS

African-American community consultants conducted interviews and focus groups. Thematic coding and constant comparison were applied to identify emergent themes.

FINDINGS

Participants reported emotional health information and support were needed but not consistently provided, resulting in a sense of survivor isolation. Systemic challenges limited providers' ability to deliver emotional support information. Survivors and providers expressed similar understandings of the emotional impact of transition, but each group highlighted different, yet complementary priorities to address emotional needs of African-American BCS.

CONCLUSIONS

There is congruence between African-American BCS and oncology providers perceptions of the emotional experience of transitioning to post-treatment survivorship, but patients are not receiving adequate information and resources to help them adequately address their emotional needs.

IMPLICATIONS FOR POLICY

Improved care continuity, team-based approaches, and partnerships between health systems and community organization partnerships may help patients and providers recognize and address emotional needs during the transition.

摘要

目的

探讨非裔美国乳腺癌幸存者(BCS)在过渡到治疗后生存阶段的情绪体验,以及医患之间的信息交流。

研究方法

我们采用访谈和焦点小组的定性研究方法。

参与者

我们寻求了华盛顿州三个县的肿瘤学提供者(n=27)和非裔美国乳腺癌幸存者(BCS)(n=45)的观点,他们在这些地方提供和接受了治疗。

发现

参与者报告说需要情感健康信息和支持,但这些信息和支持并未得到一致提供,导致幸存者感到孤立。系统挑战限制了提供者提供情感支持信息的能力。幸存者和提供者对过渡对情绪的影响有相似的理解,但每个群体都强调了不同但互补的优先事项,以满足非裔美国 BCS 的情感需求。

结论

非裔美国 BCS 和肿瘤学提供者对过渡到治疗后生存阶段的情绪体验的看法是一致的,但患者没有得到足够的信息和资源来帮助他们充分满足自己的情感需求。

政策启示

改善护理连续性、团队方法以及卫生系统与社区组织之间的伙伴关系,可能有助于患者和提供者在过渡期间识别和满足情感需求。

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