Social support resources in adolescents and young adults with advanced cancer: a qualitative analysis.

IF 2.5 2区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Nancy Lau, Angela Steineck, Casey Walsh, Kaitlyn M Fladeboe, Joyce P Yi-Frazier, Abby R Rosenberg, Krysta Barton
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Abstract

Purpose: Adolescents and Young Adults (AYAs) with cancer are an at-risk group with unique palliative and supportive care needs. Social support in AYAs with cancer is associated with better coping, quality of life, and psychosocial well-being. Here, we extend existing research to examine the sources and types of support received by AYAs with advanced cancer.

Methods: AYAs participated in a semi-structured, 1:1 interview on communication and psychosocial support needs. The present analysis focused on social support experiences for AYAs with advanced cancer. Directed content analysis was used to develop the codebook. Established social support constructs provided a coding framework. We presented our qualitative findings as a code frequency report with quantified frequency counts of all "source of support" and "type of support" codes. We assigned a global "sufficiency of support code" to each AYA.

Results: We interviewed 32 AYAs with advanced cancer (Mage = 18, SDage = 3.2, 41% female). Most AYAs identified family (namely, caregivers) as their primary source of support and stated that family universally provided all types of support: emotional, informational, instrumental, and social companionship. They received informational and emotional support from clinicians, and received emotional support and social companionship from healthy peers, cancer peers, and their existing community. One-third of participants were coded as having "mixed support" and described a lack of support in some domains.

Conclusion: AYAs with advanced cancer described caregivers as their universal source of support, and that other support sources provided support for specific needs. Future research should continue to evaluate social support needs and family-based palliative and supportive care interventions to bolster social support resources in this high-risk group.

癌症晚期青少年的社会支持资源:定性分析。
目的:青少年癌症患者是一个高危群体,他们需要独特的姑息治疗和支持性护理。青少年癌症患者的社会支持与更好的应对能力、生活质量和社会心理健康有关。在此,我们对现有研究进行了扩展,以研究晚期癌症亚裔接受支持的来源和类型:方法:亚裔参加了关于沟通和社会心理支持需求的半结构化 1:1 访谈。本次分析的重点是晚期癌症老年患者的社会支持经历。我们采用了定向内容分析法来编制编码手册。既定的社会支持结构提供了一个编码框架。我们以代码频率报告的形式呈现了定性分析结果,并对所有 "支持来源 "和 "支持类型 "代码进行了量化频率统计。我们为每位亚裔美国人分配了一个总的 "支持充分性代码":我们采访了 32 名患有晚期癌症的亚裔美国人(平均年龄为 18 岁,最小年龄为 3.2 岁,女性占 41%)。大多数青壮年认为家庭(即照顾者)是他们的主要支持来源,并表示家庭普遍提供了各种类型的支持:情感支持、信息支持、工具支持和社会陪伴。他们从临床医生那里获得信息和情感支持,从健康同伴、癌症同伴和现有社区那里获得情感支持和社交陪伴。三分之一的参与者被编码为 "混合支持",并描述在某些领域缺乏支持:结论:患有晚期癌症的亚裔美国人认为,照顾者是他们普遍的支持来源,而其他支持来源则为特定需求提供支持。未来的研究应继续评估社会支持需求以及基于家庭的姑息治疗和支持性护理干预措施,以加强这一高风险群体的社会支持资源。
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
BMC Palliative Care
BMC Palliative Care HEALTH CARE SCIENCES & SERVICES-
CiteScore
4.60
自引率
9.70%
发文量
201
审稿时长
21 weeks
期刊介绍: BMC Palliative Care is an open access journal publishing original peer-reviewed research articles in the clinical, scientific, ethical and policy issues, local and international, regarding all aspects of hospice and palliative care for the dying and for those with profound suffering related to chronic illness.
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