Understanding the Intersection of Identity and Cancer Experience Among Racially, Ethnically, Gender and Sexual Minoritized Adolescents and Young Adults With Cancer.

IF 3.3 2区 医学 Q2 ONCOLOGY Psycho‐Oncology Pub Date : 2024-10-01 DOI:10.1002/pon.70000
Kaitlyn Hanson, Andrew Hatala, Mirha Zohair, Ian Scott, Vinesha Ramasamay, Kristin Wilson, Roxanne van Velzen, Zeba Tayabee, Fiona Schulte, Morgan Stirling, Deepak Louis, Lisa M Lix, Allan Garland, Alyson Mahar, Sapna Oberoi
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Abstract

Objectives: Adolescents and young adults (AYAs, 18-39 years) with cancer identifying as racially/ethnically minoritized or 2SLGBTQIA+ (Two-Spirit, lesbian, gay, bisexual, transgender, queer, intersex, asexual and "+" referring to other queer identities) have been underrepresented in cancer research. This study explores the aspects of identity that hold significance for these minoritized AYAs and how these facets impact their healthcare experiences.

Methods: Eligible participants comprised English-speaking AYAs who self-identified as racially/ethnically minoritized and/or 2SLGBTQIA+, were diagnosed with cancer between the ages of 15-39, currently aged > 18, and had received or were receiving cancer care within Canadian healthcare system. Additionally, four patient partners meeting the same criteria were recruited as research collaborators. Semi-structured one-on-one virtual interviews guided by an interview script were conducted, and qualitative analysis employed a framework approach.

Results: We recruited 23 participants from 4 Canadian provinces (mean age: 28, Range: 20-44); 17 identified as racially/ethnically minoritized, one as sexual/gender minoritized, and five as racially/ethnically and sexually/gender minoritized. Participants emphasized that their culture/ethnicity, religion/spirituality, sexuality, gender, family, career, and being an immigrant are important aspects of their identity, with only one participant recognizing their identity as a "person with cancer". A cancer diagnosis altered the aspects of identity deemed most significant by participants. Both visible and invisible aspects of identity shaped participants' experiences and influenced their level of trust in the healthcare system.

Conclusion: Racially, ethnically, gender, or sexually minoritized AYAs with cancer place considerable importance on aspects of their identity that are shaped by their respective communities. Recognizing and respecting these identities are paramount for healthcare professionals to deliver safe and inclusive care.

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了解在种族、民族、性别和性取向上属于少数群体的青少年和年轻成人癌症患者的身份认同与癌症经历之间的交集。
目标:在癌症研究中,在种族/族裔上属于少数群体或 2SLGBTQIA+(Two-Spirit、女同性恋、男同性恋、双性恋、变性人、同性恋、双性人、无性人,"+"指其他同性恋身份)的青少年和年轻成人(AYAs,18-39 岁)癌症患者的代表性不足。本研究探讨了对这些少数族裔美国青少年具有重要意义的身份方面,以及这些方面如何影响他们的医疗保健经历:符合条件的参与者包括讲英语的亚裔青少年,他们在种族/族裔上自我认同为少数群体和/或 2SLGBTQIA+ ,在 15-39 岁之间被诊断出患有癌症,目前年龄大于 18 岁,在加拿大医疗保健系统中接受过或正在接受癌症治疗。此外,还招募了四名符合相同标准的患者伙伴作为研究合作者。在访谈脚本的指导下,我们进行了半结构化的一对一虚拟访谈,并采用框架方法进行了定性分析:我们招募了来自加拿大 4 个省的 23 名参与者(平均年龄:28 岁,范围:20-44 岁);其中 17 人被认定为种族/族裔少数群体,1 人被认定为性/性别少数群体,5 人被认定为种族/族裔和性/性别少数群体。与会者强调,他们的文化/种族、宗教/灵性、性、性别、家庭、职业和移民身份是他们身份的重要方面,只有一名与会者承认他们的身份是 "癌症患者"。癌症诊断改变了参与者认为最重要的身份方面。身份的可见和不可见方面塑造了参与者的经历,并影响了他们对医疗系统的信任程度:结论:在种族、民族、性别或性取向上属于少数群体的亚裔癌症患者非常重视由其各自社区形成的身份认同。承认并尊重这些身份对于医疗专业人员提供安全、包容的医疗服务至关重要。
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来源期刊
Psycho‐Oncology
Psycho‐Oncology 医学-心理学
CiteScore
6.30
自引率
8.30%
发文量
220
审稿时长
3-8 weeks
期刊介绍: Psycho-Oncology is concerned with the psychological, social, behavioral, and ethical aspects of cancer. This subspeciality addresses the two major psychological dimensions of cancer: the psychological responses of patients to cancer at all stages of the disease, and that of their families and caretakers; and the psychological, behavioral and social factors that may influence the disease process. Psycho-oncology is an area of multi-disciplinary interest and has boundaries with the major specialities in oncology: the clinical disciplines (surgery, medicine, pediatrics, radiotherapy), epidemiology, immunology, endocrinology, biology, pathology, bioethics, palliative care, rehabilitation medicine, clinical trials research and decision making, as well as psychiatry and psychology. This international journal is published twelve times a year and will consider contributions to research of clinical and theoretical interest. Topics covered are wide-ranging and relate to the psychosocial aspects of cancer and AIDS-related tumors, including: epidemiology, quality of life, palliative and supportive care, psychiatry, psychology, sociology, social work, nursing and educational issues. Special reviews are offered from time to time. There is a section reviewing recently published books. A society news section is available for the dissemination of information relating to meetings, conferences and other society-related topics. Summary proceedings of important national and international symposia falling within the aims of the journal are presented.
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