Young Adults with Cancer – How Definitions of Health, Social Determinants, and Multilevel Models of Care Influence Health Care Provision
Young Adults with Cancer: How Definitions of Health, Social Determinants, and Multilevel Models of Care Influence Health Care Provision
Over the past 13 weeks, I, Nicole Freer, have explored several topics related to cancer care. Through this process, I discovered that cancer care in Ontario is influenced by various factors that contribute to inequities in care provision. The Canadian healthcare system is guided by definitions of health established in 1948 by the World Health Organization (WHO). Despite these guiding principles, inequities remain within the Canadian system. Multilevel approaches are used to identify and address these inequities, examining how socioecological factors impact access to cancer care and survivorship support. My focus has been on the young adult population in Ontario and the inequities they face in accessing care.
Defining Health in Canada and its Impact on Cancer Care
Understanding how Canada defines health is essential for understanding the distribution of cancer care services. The Canadian healthcare system, including provincial standards, is based on the WHO’s 1948 definition of health, which views health as “a state of complete physical, mental, and social well-being and not merely the absence of disease or infirmity” (WHO, 1948). This comprehensive definition was designed to address all aspects of health. However, some critics argue that this definition is problematic. For instance, Card (2017), a health policy researcher, suggests that individuals can experience well-being even with a disability or illness, challenging the idea that health requires perfect psychological and physiological conditions. Others oppose the WHO definition, arguing that it leads to overmedicalization, and political decisions focused solely on health (Bircher & Kuruvilla, 2023; Schramme, 2023; Callaham, 2023).
Despite these criticisms, Canada’s healthcare system is still based on WHO principles, which shape our standards of care with the goal of ensuring equal access to healthcare, including cancer care, across provinces. However, disparities in access to care still exist.
The Scope of Cancer and Its Impact
Before delving into the inequities faced by cancer patients, it is important to understand the scope of cancer in Canada. According to the Canadian Cancer Society (2025), in 2024, 247,100 Canadians are expected to be diagnosed with cancer, an increase from 239,100 new cases in 2023, likely due to Canada’s aging population. The number of cancer-related deaths is also expected to rise from 86,700 in 2023 to 88,100 in 2024.
Cancer rates in Ontario are significant, with 556.3 cases per 100,000 people in 2022 (Cancer Care Ontario, 2022). In regions like Hamilton, Haldimand, Brant, and Niagara, cancer rates were 551.5 per 100,000 in 2020. These numbers highlight the widespread impact of cancer diagnoses across Canada. Given the diversity of Canada’s population and its vast geography, there are likely barriers to equal access to care, which are often shaped by social determinants of health.
Social Determinants of Health (DOH)
Social Determinants of Health (DOH) refer to the broad range of personal, social, economic, and environmental factors that influence individual and population health (Government of Canada, n.d.). This aligns with the WHO’s emphasis on a comprehensive approach to healthcare (Schramme, 2023). In Ontario, social determinants are recognized as key factors in determining health outcomes, and include socioeconomic status, employment, job conditions, education, childhood experiences, physical environments, social support, coping skills, healthy behaviors, access to health services, genetics, gender, culture, and race.
Cancer Care Ontario identifies certain populations, including adolescent and young adults (AYA), who are at higher risk for poorer health outcomes due to these determinants. AYAs with cancer face numerous challenges, such as difficulty maintaining employment, attending school, and forming relationships. They also experience financial struggles, limited coping skills, increased side effects from treatment, mental health challenges, and difficulty understanding health information. As a result, AYAs are more likely to miss treatment or not access survivorship support, leading to less comprehensive care and worse long-term outcomes (Berkman et al., 2024). Unlike older cancer patients, young adults face lifelong challenges, including the risk of chronic diseases, body image issues, cancer recurrence, and the development of new cancers. This unique experience calls for a targeted response from healthcare organizations.
Multilevel Frameworks for Addressing Health Disparities
Given the size and diversity of Canada, disparities in cancer care and survivorship vary by region. An ecological multilevel approach considers how multiple socioecological factors—ranging from individual to policy levels—affect overall health and well-being (Baumgartner, 2024). According to Pearson (2021), an ecological model examines individual, interpersonal, institutional, community, and public policy factors. These frameworks help healthcare providers identify specific actions they can take to improve care within their scope of control.
Applying the Ecological Model to AYA Cancer Care
For young adults (AYA), the ecological model is useful in guiding care strategies. AYAs face unique and complex challenges during their cancer treatment, and their struggles continue after treatment. These patients are at risk for chronic disease, mental health issues, body image disturbances, and cancer recurrence. The survivorship quality care model emphasizes the importance of interpersonal, organizational, and community support in addressing these challenges (Berkman et al., 2024).
As a clinical team member, I can collaborate with colleagues to create tailored care plans for AYA patients. Care plans should address personal concerns, provide clear explanations, assess social support, and consider psychological needs. Additionally, healthcare providers should receive ongoing education on the unique needs of AYAs and adopt pediatric strategies when appropriate. The healthcare system can also improve care by prioritizing resources to support these needs, collaborating with community partners, and offering practical support, such as financial and nurse navigators.
The Role of Community Partnerships
Community partnerships are crucial in enhancing cancer care for young adults. These partnerships can provide resources that hospitals may not have, such as transportation and mentorship programs. By connecting with community organizations, oncology units can offer additional layers of support that go beyond active treatment, such as education and emotional support.
Conclusion
By using multilevel frameworks to analyze cancer care for young adults, healthcare providers can better understand and address the barriers posed by social determinants of health. This approach can help improve care delivery and outcomes for the AYA population, ultimately leading to better support during their cancer journey.
References
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