Background: Living with patients of chronic diseases such as heart failure (HF) is a diffi cult situation for the caregivers. This
study explored the Iranian family caregivers’ burden of caregiving for patients with HF.
Materials and Methods: Eighteen family caregivers of the HF patients from two governmental medical training centers in Isfahan,
Iran were recruited using purposive sampling. Data were collected through face-to-face semi-structured interviews. Each interview
was transcribed verbatim and was thematically analyzed concurrently.
Results: Four major themes emerged from the analysis of the transcripts: Lack of care-related knowledge, physical exhaustion,
psychosocial exhaustion, and lack of support. Family caregivers believed that they have little knowledge about the patients’
disease, drugs, and how to perform caregiving roles. They experienced negative physical and psychosocial consequences of
full-time and highly extended caregiving roles, such as musculoskeletal disorder, fatigue, and sleep disturbance, and a high
level of anxiety, stress, and social isolation. Caregivers believed that they receive little familial and organizational support on the
emotional and fi nancial dimensions of caregiving.
Conclusions: The fi ndings of this study can be used by healthcare providers, especially nurses, to provide more effective social,
informational, and professional support for family caregivers
