“…Qualitative studies [30, 36, 40, 42, 45, 48, 54, 61, 71, 72, 74, 77, 80, 83, 88, 104, 110, 117, 119, 131, 137, 138, 142] described a wide range of needs that caregivers felt underprepared for or in need of assistance with, including coping with and managing symptoms; understanding HF and prognosis; handling unplanned hospitalizations and other emergencies; managing medications and devices; providing and receiving emotional and spiritual support; partnering in patients’ self-care; balancing home and work; engaging in their own self-care; having difficult conversations; handing uncertainty about the future and the unpredictably of the disease; communication and care coordination; understanding palliative care services; managing the home; dealing with financial issues; knowing what to expect and how to care for patients at end of life; and leveraging and timely access to formal and informal social support and services. Two quantitative studies both identified handling emergencies as a situation that caregivers’ felt most unprepared for [127, 136].…”