Treatment decision conversations, symptoms, and functional status in older adults with advanced cancer: An exploratory study utilizing mixed methods

Coombs, Lorinda A; Neller, Sarah; Wilson, Christina; Mihas, Paul; Reuland, Daniel; Muss, Hyman B.; Mooney, Kathi

doi:10.1016/j.jgo.2022.12.002

Cited by 1 publication

(1 citation statement)

References 25 publications

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“…[5] Caregivers (i.e., informal/unpaid people who provide care to a friend or family member) of older adults with cancer are increasingly relied upon for complex, intense, and ongoing care, which has contributed to increased caregivingrelated burden. [6] Caregivers help with tasks across the cancer care continuum, which can include long-term management of cancer treatment side effects, symptoms, and adherence; logistical support coordinating services, care, and transportation; clinical treatment decision-making [7] and daily life support through assisting with mobility, nutrition, and hygiene. [8] Both the care that is provided and the health status of the care recipient exert a toll on the caregivers' own health [8]; caregivers are at risk for experiencing their own health problems with anxiety, depression, and cardiovascular disease.…”

Section: Introductionmentioning

confidence: 99%

Inequities Among Cancer Caregivers with Diverse Identities: A Review of the Literature and Future Directions

et al. 2023

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Purpose of ReviewThe number of older adults with cancer relying on support from caregivers continues to increase. Health disparities in older adults with cancer often extend to their caregivers. This review aims to assess the state of cancer caregiving research in historically underrepresented diverse populations and provide recommendations for future research and policy. Recent Findings Research on caregivers of older adults with cancer from diverse backgrounds has primarily been descriptive. Health disparities for historically underrepresented caregivers (LGBTQ + , BIPOC, rural, young adults, youth) exist across several dimensions (e.g., financial, mental, and physical health, and access to caregiver support). Few published studies have closely examined the unique experiences of these caregivers nor provided culturally appropriate tailored interventions. Summary Health equity research within caregiving populations is in its infancy. Priorities for future work should focus on identifying modifiable targets for intervention, changing systems-level processes in acknowledging and supporting caregivers, and creating policies that reduce financial inequities of caregiving.

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