Palliative care experience and perceived gaps in training among transplant hepatology fellows: A national survey

• Published in: Hepatology communications 2022-07, Vol.6 (7), p.1680-1688
• Main Authors: Whitsett, Maureen P., Ufere, Nneka N., Patel, Arpan, Shea, Judy A., Jones, Christopher A., Fix, Oren K., Serper, Marina
• Format: Article
• Language: English
• Subjects: Accreditation; Advance directives; Anxiety; Cardiology; Caregivers; Clinical Competence; Curricula; Distance learning; Fellowships and Scholarships; Female; Gastroenterology; Hepatology; Hospice Care; Humans; Liver; Liver cirrhosis; Male; Medical education; Original; Palliative Care; Patients; Quality of life; Training; Transplants & implants
• ISSN: 2471-254X; 2471-254X
• DOI: 10.1002/hep4.1939

Despite the likely benefits of palliative care (PC) for patients with cirrhosis, physician experiences and perspectives about best practices are variable. We aimed to assess PC experience and gaps in training among transplant hepatology fellows. We conducted a national survey of all transplant hepatology fellows enrolled in accredited fellowship programs during the 2020–2021 academic year. We assessed the frequency of PC provision and comfort with physical and psychological symptom management, psychosocial care, communication skills, advance care planning, and end‐of‐life care. A total of 45 of 56 (79%) of transplant hepatology fellows responded to the survey; 50% (n = 22) were female. Most trained at centers performing over 100 transplants per year (67%, n = 29) distributed evenly across geographic regions. Most fellows (69%, n = 31) had a PC or hospice care rotation during residency, and 42% (n = 19) of fellows received education in PC during transplant hepatology fellowship. Fellows reported feeling moderately to very comfortable with communication skills such as breaking bad news (93%, n = 41) and leading family meetings (75%, n = 33), but nearly one‐third (30%, n = 13) reported feeling not very or not at all comfortable assessing and managing anxiety and depression (30%, n = 13) and spiritual distress (34%, n = 15). Nearly one‐quarter (22%, n = 10) had never discussed or documented advance care plans during fellowship. Fellows wished to receive future instruction on the assessment and management of physical symptoms (68%, n = 30) and anxiety and depression (64%, n = 28). Conclusion: Our survey highlights gaps in PC experience and education during transplant hepatology fellowship, lack of comfort in managing psychological distress and advance care planning, and desire to improve skills, particularly in symptom management. Future studies should investigate how to enhance transplant hepatology competencies in these PC domains and whether this impacts clinical care, advance care planning, or patient experience. The aim of this national survey of transplant hepatology fellows was to assess fellows' palliative care educational experience, the frequency of palliative care provision in fellowship, as well as their degree of comfort providing palliative care services to patients. Fellows frequently engage in palliative care provision during their clinical training. While they express a high degree of comfort with communication skills, many fellows did not feel