A family‐centred perspective on the arteriovenous fistula in end‐stage renal disease: Findings from dyadic interviews

Introduction The preservation of a well‐functioning arteriovenous fistula (AVF) is crucial for successful dialysis in patients with end‐stage renal disease (ESRD); nonetheless, complications are frequent which leads to lower quality of life, hospitalisations and death. Self‐care behaviours help to reduce the risk of complications and family caregivers can play an important role as partners for behaviour change. However, the patient and family caregiver's experiences with such an invasive intervention are largely unknown. Aims This study aimed to explore the experiences of patients with ESRD and their family caregivers with the AVF through joint interviews. Methods A qualitative exploratory study was conducted with a purposive sample. Semi‐structured joint interviews were conducted with 14 dyads (28 participants) composed of patients on haemodialysis with AVF and their respective family caregivers. Interviews were audiotaped, transcribed verbatim and submitted to thematic analysis. Findings Four major themes were identified: (i) AVF negative impacts; (ii) (un)presence of self‐care behaviours; (iii) AVF self‐management facilitators and (iv) AVF self‐management barriers. Discussion The findings suggested that more attention needs to be paid to patients’ and their family caregivers’ support needs (e.g. fears, concerns, knowledge, adherence barriers and facilitators) regarding AVF self‐management. The dyads seem to be aware of how to take care of the AVF; however, self‐care behaviours still need to be improved. Conclusion Innovative interventions need to follow an interdisciplinary approach with an educational and support component. The integration of family caregivers should also be considered, since this study evidenced their lack of knowledge and skills, and willingness to participate in these initiatives.