Nursing Approaches and Perceived Quality of Life in Advanced Stage Huntington's Disease Patients.

BACKGROUND Long-term Huntington's disease (HD) care is offered in specialized inpatient nursing home units with a focus on individually perceived quality of life (QoL). This is shaped in daily care and interaction, which is often abstract and intangible. Furthermore, different perspectives are involved and may vary. OBJECTIVE To explore and describe perceived QoL of HD patients from three perspectives: manifest HD patients, family members, and nursing staff. METHODS 36 patients, 11 family members, and 30 nurses participated in this qualitative study by means of individual interviews and systematic qualitative observations on three units. RESULTS Preservation of identity and autonomy is important for patients. Patients struggle with increasing dependence, and try to cope with the impact, uncertainty, and progressive nature of the disease. All participants emphasize the focus on "being human, not just a patient". Both patients and family members mention the difficulty of dealing with altered behavior and loss of control. Patients are reliant on a relational approach, and an attitude of unconditional acceptance, trust, and understanding support by the nurses. Nursing staff help patients to focus on preserved abilities, and to continue to engage in personalized preferred social activities. Specific qualifications of the nurses were of major influence on QoL for HD patients. CONCLUSION This study shows, from the patient as well as family member and nursing staff perspectives, that caring for HD patients requires specific knowledge and skills. Particular nursing approaches and attitude and qualifications of the nursing staff in residential HD care improves the perceived QoL of patients.

[1]  D. Craufurd,et al.  Illness perceptions, coping styles and psychological distress in adults with Huntington’s disease , 2014, Psychology, health & medicine.

[2]  Jane S. Paulsen,et al.  Psychological well-being in persons affected by Huntington’s disease: A comparison of at-risk, prodromal, and symptomatic groups , 2013, Journal of health psychology.

[3]  E. Giltay,et al.  Psychiatric disorders in Huntington's disease: a 2-year follow-up study. , 2012, Psychosomatics.

[4]  M. Hocaoglu,et al.  The Huntington's Disease health-related Quality of Life questionnaire (HDQoL): a disease-specific measure of health-related quality of life , 2012, Clinical genetics.

[5]  M. Hocaoglu,et al.  Impact of Huntington's across the entire disease spectrum: the phases and stages of disease from the patient perspective , 2011, Clinical genetics.

[6]  R. Roos,et al.  Huntington's disease: a clinical review , 2010, Orphanet journal of rare diseases.

[7]  J. Sanchez-Ramos,et al.  Well-Being of Family Caregivers of Persons with Late-Stage Huntington's Disease: Lessons in Stress and Coping , 2009, Health communication.

[8]  Jane S. Paulsen,et al.  Patient and caregiver quality of life in Huntington's disease , 2008, Movement disorders : official journal of the Movement Disorder Society.

[9]  R. Roos,et al.  Behavioural problems in Huntington's disease using the Problem Behaviours Assessment. , 2008, General hospital psychiatry.

[10]  R. V. D. Mast,et al.  Psychopathology in verified Huntington's disease gene carriers. , 2007, The Journal of neuropsychiatry and clinical neurosciences.

[11]  R. Roos,et al.  Quality of life in couples living with Huntington’s disease: the role of patients’ and partners’ illness perceptions , 2007, Quality of Life Research.

[12]  H. V. van Houwelingen,et al.  Living with Huntington's disease: Illness perceptions, coping mechanisms, and patients' well-being. , 2002, British journal of health psychology.

[13]  A. Kaptein,et al.  Impact of Huntington's disease on quality of life , 2001, Movement disorders : official journal of the Movement Disorder Society.

[14]  Julie S Snowden,et al.  Unawareness of deficits in Huntington's disease. , 2014, Journal of Huntington's disease.