Rady Faculty of Health Sciences, University of Manitoba, Winnipeg, Canada.
Department of Patient and Family Support Services, CancerCare Manitoba, Winnipeg, Canada.
Psychooncology. 2024 Oct;33(10):e70000. doi: 10.1002/pon.70000.
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.
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.
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.
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.
在癌症研究中,少数族裔/少数群体身份认同的青少年和年轻人(18-39 岁)或 2SLGBTQIA+(双性恋、女同性恋、男同性恋、双性恋、变性、酷儿、双性人、无性恋和“+”指其他酷儿身份)的代表性不足。本研究探讨了这些少数族裔青少年和年轻人认同的重要方面,以及这些方面如何影响他们的医疗保健体验。
符合条件的参与者包括讲英语的青少年和年轻人,他们自我认同为少数族裔/少数群体身份认同者和/或 2SLGBTQIA+,在 15-39 岁之间被诊断出患有癌症,年龄超过 18 岁,并且在加拿大医疗保健系统内接受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合作伙伴作为研究合作者。通过访谈脚本进行半结构化的一对一虚拟访谈,采用框架方法进行定性分析。
我们从加拿大的 4 个省招募了 23 名参与者(平均年龄:28 岁,范围:20-44 岁);17 名参与者自我认同为少数族裔/少数群体身份认同者,1 名参与者自我认同为性/性别少数群体身份认同者,5 名参与者自我认同为少数族裔/性/性别少数群体身份认同者。参与者强调,他们的文化/种族、宗教/精神信仰、性取向、性别、家庭、职业以及作为移民是他们身份的重要方面,只有一名参与者认识到自己的身份是“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都塑造了参与者的体验,并影响了他们对医疗保健系统的信任程度。
少数族裔/少数群体身份认同的青少年和年轻人患有癌症,他们非常重视由各自社区塑造的身份方面。承认和尊重这些身份对于医疗保健专业人员提供安全和包容的护理至关重要。