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dc.contributor.authorWalker, Rachael C
dc.contributor.authorHoward, Kirsten
dc.contributor.authorMorton, Rachael L
dc.contributor.authorPalmer, Suetonia C
dc.contributor.authorMarshall, Mark R
dc.contributor.authorTong, Allison
dc.date.accessioned2023-02-09T05:11:30Z
dc.date.available2023-02-09T05:11:30Z
dc.date.issued2015en_AU
dc.identifier.urihttps://hdl.handle.net/2123/29992
dc.description.abstractBackground. Home dialysis can offer improved quality of life and economic benefits compared with facility dialysis. Yet the uptake of home dialysis remains low around the world, which may be partly due to patients’ lack of knowledge and barriers to shared and informed decision-making. We aimed to describe patient and caregiver values, beliefs and experiences when considering home dialysis, to inform strategies to align policy and practice with patients’ needs. Methods. Semi-structured interviews with adult patients with chronic kidney disease Stage 4–5D (on dialysis <1 year) and their caregivers, recruited from three nephrology centres in New Zealand. Transcripts were analysed thematically. Results. In total, 43 patients [ pre-dialysis (n = 18), peritoneal dialysis (n = 13), home haemodialysis (n = 4) and facility haemodialysis (n = 9)] and 9 caregivers participated. We identified five themes related to home dialysis: lacking decisional power (complexity of information, limited exposure to home dialysis, feeling disempowered, deprived of choice, pressure to choose), sustaining relationships (maintaining cultural involvement, family influence, trusting clinicians, minimizing social isolation), reducing lifestyle disruption (sustaining employment, avoiding relocation, considering additional expenses, seeking flexible schedules, creating free time), gaining confidence in choice (guarantee of safety, depending on professional certainty, reassurance from peers, overcoming fears) and maximizing survival. Conclusions. To engage and empower patients and caregivers to consider home dialysis, a stronger emphasis on the development of patient-focused educational programmes and resources is suggested. Pre-dialysis and home dialysis programmes that address health literacy and focus on cultural and social values may reduce fears and build confidence around decisions to undertake home dialysis. Financial burdens may be minimized through provision of reimbursement programmes, employment support and additional assistance for patients, particularly those residing in remote areas.en_AU
dc.language.isoenen_AU
dc.publisherNephrol Dial Transplanten_AU
dc.rightsCopyright All Rights Reserveden_AU
dc.subjecthaemodialysisen_AU
dc.subjecthome haemodialysisen_AU
dc.subjectpatientsen_AU
dc.subjectperitoneal dialysisen_AU
dc.subjectqualitative researchen_AU
dc.titlePatient and caregiver values, beliefs and experiences when considering home dialysis as a treatment option: a semi-structured interview studyen_AU
dc.typeArticleen_AU
dc.identifier.doi10.1093/ndt/gfv330
dc.type.pubtypePublisher's versionen_AU
usyd.facultySeS faculties schools::Faculty of Medicine and Health::NHMRC Clinical Trials Centreen_AU
workflow.metadata.onlyNoen_AU


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