The beliefs and expectations of patients and caregivers about home haemodialysis: an interview study
نویسندگان
چکیده
OBJECTIVES To explore the beliefs and expectations of patients and their caregivers about home haemodialysis in Italy where the prevalence of home haemodialysis is low. DESIGN Semistructured, qualitative interview study with purposive sampling and thematic analysis. SETTING Four dialysis centres in Italy without home haemodialysis services (Bari, Marsala, Nissoria and Taranto). PARTICIPANTS 22 patients receiving in-centre haemodialysis and 20 of their identified caregivers. RESULTS We identified seven major themes that were central to patient and caregiver perceptions of home haemodialysis in regions without established services. Three positive themes were: flexibility and freedom (increased autonomy, minimised wasted time, liberation from strict dialysis schedules and gaining self-worth); comfort in familiar surroundings (family presence and support, avoiding the need for dialysis in hospital) and altruistic motivation to do home haemodialysis as an exemplar for other patients and families. Four negative themes were: disrupting sense of normality; family burden (an onerous responsibility, caregiver uncertainty and panic and visually confronting); housing constraints; healthcare by 'professionals' not 'amateurs' (relinquishing security and satisfaction with in-centre services) and isolation from peer support. CONCLUSIONS Patients without direct experience or previous education about home haemodialysis and their caregivers recognise the autonomy of home haemodialysis but are very concerned about the potential burden and personal sacrifice home haemodialysis will impose on caregivers and feel apprehensive about accepting the medical responsibilities of dialysis. To promote acceptance and uptake of home haemodialysis among patients and caregivers who have no experience of home dialysis, effective strategies are needed that provide information about home haemodialysis to patients and their caregivers, assure access to caregiver respite, provide continuous availability of medical and technical advice and facilitate peer patient support.
منابع مشابه
Survey knowledge of caregivers of patients of schizophrenia about home care in
Introduction: More than ‎‏70%‏‎ of patients with schizophrenia are cared by family at home. ‎Knowledge deficit of caregivers is basically the basic and fundamental problem regarding the ‎signs and symptoms of disease. ‎ Objective: This study was to assess the knowledge level of schizophrenic patients' caregivers ‎referring to Shahid Beheshti hospital in ...
متن کاملClinician beliefs and attitudes about home haemodialysis: a multinational interview study
OBJECTIVES To explore clinician beliefs and attitudes about home haemodialysis in global regions where the prevalence of home haemodialysis is low, and to identify barriers to developing home haemodialysis services and possible strategies to increase acceptance and uptake of home haemodialysis. DESIGN Semistructured interviews, thematic analysis. SETTING 15 dialysis centres in Italy, Portug...
متن کاملAttitude of schizophrenic patients' care givers about their method of patient caring at home
Introduction: Schizophrenia is a type of psychosis which disturbs one's function through its ‎destructive effects on mind, behavior and personal interaction. More than ‎‏70%‏‎ of schizophrenic ‎patients are living with their families. Lack of correct cares of caregivers causes repeated and ‎decreases patient’s physical and mental abilities. Studying the weal po...
متن کاملThe Effect of Roy Adaptation Model-Based Training on Depression, Anxiety and Stress in Home Caregivers of Mental Patients
Background and Aim: Attempts to reduce depression, anxiety and stress of home caregivers of mental patients lead to better results of care givers performance and decrease psychological and physical stress in home caregivers. The purpose of this study was to determine the effect of Roy Adaptation Model-Based training on depression, anxiety and stress in caregivers of chronic psychiatric patients...
متن کاملCare Burden of Home Caregivers of Patients with COVID-19
Background and purpose: Caring for patients with COVID-19 at home is mainly the responsibility of the family which leads to high burden of care. The burden of care refers to psychological pain, physical problems, financial and social pressures, disruption of family relationships, feelings of hopelessness, and other negative consequences of care tasks. The aim of this study was to determine the ...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
دوره 3 شماره
صفحات -
تاریخ انتشار 2013