Hopes, expectations, and informational needs in patients undergoing advanced heart failure therapy evaluations

Abstract

BackgroundPatients undergoing evaluation for advanced heart failure therapies (AHT) are at a critical juncture of their illness. Guidelines recommend shared decision-making with patients and caregivers; however, the approach and content of these discussions is unknown. MethodsPatients referred to a specialty palliative care service during AHT evaluation between October 2018 and September 2022 were identified from electronic healthcare records. Goals of care conversations documented in an advance care planning module were analyzed for participants, content, and timing prior to transplant selection committee meeting. Primary outcomes included prevalence of documented hopes, worries, shared prognostic communication, illness understanding, treatment expectations, and information preferences. Patients were followed for a minimum of six months to evaluate secondary processes and clinical outcomes. Results94 patients (mean age 52.8 years, 76.6% male) met criteria. Most (97.9%, n=92) had illness understanding documented. In initial discussions, 76.3% (n=71) hoped to “live longer” and 67.7% (n=63) to “be independent”; thematic analysis supported these hopes with 91.0% of patients expecting “better functionality”. Most patients preferred multi-modal information and communication. During follow-up, 27.7% (n=26) had treatment decisions deferred at initial committee presentation, and 43.6% (n=41) were reviewed at multiple selection committee meetings. By the end of the study period, 53.2% (n=50) underwent one or more AHT and 24.5% (n=23) had died. ConclusionPatients undergoing the AHT evaluation process face considerable uncertainty. A standardized approach by a specialty palliative care service elicits patients’ illness understanding, hopes, worries, treatment expectations, and information preferences to promote shared decision-making at this critical time.