Abstract
In efforts to understand financial distress (FD) associated with advanced cancer care from the perspective of both patients with incurable disease and their spousal caregivers, we assessed FD in both members of the couple, identified symptom and quality of life (QOL) correlates, and examined the potential role of illness communication. Patients undergoing treatment for stage III/IV lung cancer or a grade III/IV primary brain tumor and their spousal caregivers (n = 76 dyads) completed measures of somatic and affective symptoms including FD, physical and mental QOL, and ease of engaging in illness communication. Patients and caregivers additionally rated their perception of each other's symptoms, including FD. FD was endorsed by both patients (any FD 62.7%; high FD 24%) and spousal caregivers (any FD 64.7%; high FD 32.3%). Self-reported FD was significantly correlated (partial r = .52, p < .001) within couples. FD was associated with greater symptoms of anxiety (r = .29, p = .01; r = .31, p = .01), depression (r = 29, p = 01; r = .39, p = .001), and poorer physical QOL(r = - .25, p = .03; r = - .25, p = .001) for patients and caregivers, respectively. For patients, FD was additionally associated with poorer mental QOL(r = - .44, p < .001). Caregivers accurately perceived patient FD, yet patients tended to underreport their caregiver's FD by almost an entire point (t = 2.8, p = .007). A 3-way interaction (FD X role X illness communication) revealed (b = .40, p = .041) that illness communication moderated the association between FD and physical QOL for spouses so that spouses who reported less ease of illness communication demonstrated a stronger association between financial distress and physical QOL (b = - 2.08, p < .001) than those reporting greater ease of engaging in illness communication (b = .49, p = .508). In the advanced cancer setting, FD is prevalent in both patients and their spousal caregivers and associated with psychological distress and poor physical QOL. Results suggest that optimal FD assessment should include patients and spouses, and spouse's ease of engaging with illness communication may be a potential target for future intervention studies.
Highlights
The burden of a cancer is experienced by the patient, and by family members increasingly involved in caregiving roles throughout treatment and at end-of-life
financial distress (FD) was associated with greater anxiety, depression, and poorer physical quality of life (QOL)
FD was associated with poorer mental QOL
Summary
The burden of a cancer is experienced by the patient, and by family members increasingly involved in caregiving roles throughout treatment and at end-of-life. The spouse or romantic partner (hereafter referred to as spouse or spousal caregiver) often serves as the primary source of both instrumental and emotional support to the patient [1]. Physical health is observed to be interdependent in couples [6], yet not all studies find this association in cancer patients [7] This interdependence reaffirms the value of capturing both the patient and spousal caregiver’s perspectives, in that the physical or mental health status of the spousal caregiver may indicate greater risk of psychological distress or poorer physical QOL for their partner and vice versa
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