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Published on: May 11, 2018
Decision-making for destination therapy left ventricular assist devices: implications for caregivers
Colleen K McIlvennan1, Jacqueline Jones2, Larry A Allen2
1From the Section of Advanced Heart Failure and Transplantation, Division of Cardiology (C.K.M., L.A.A., J.L.), Colorado Cardiovascular Outcomes Research Consortium (C.K.M., L.A.A., D.D.M.) and Division of General Internal Medicine (C.N., D.D.M.), University of Colorado School of Medicine, Aurora; University of Colorado School of Nursing, Aurora (J.J.); and Division of General Internal Medicine, Mayo Clinic, Rochester, MN (K.M.S.). colleen.mcilvennan@ucdenver.edu.
Background:
Implanting centers often require the identification of a dedicated caregiver before destination therapy left ventricular assist device (DT LVAD) implantation; however, the caregiver experience surrounding this difficult decision is relatively unexplored.
Methods And Results:
From October 2012 through July 2013, we conducted semistructured, in-depth interviews with caregivers of patients considering DT LVAD. Data were analyzed using a mixed inductive and deductive approach. We interviewed 17 caregivers: 10 caregivers of patients living with DT LVAD, 6 caregivers of patients who had died with DT LVAD, and 1 caregiver of a patient who had declined DT LVAD. The themes identified, which could also be considered dialectical tensions, are broadly interpreted under 3 domains mapping to decision context, process, and outcome: (1) the stark decision context, with tension between hope and reality; (2) the challenging decision process, with tension between wanting loved ones to live and wanting to respect loved ones' wishes; and (3) the downstream decision outcome, with tension between gratitude and burden.
Conclusions:
Decision-making surrounding DT LVAD should incorporate decision support for patients and caregivers. This should include a focus on caregiver burden and the predictable tensions that caregivers experience.
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