Self-perceived symptoms and care needs of patients with severe to very severe chronic obstructive pulmonary disease, congestive heart failure or chronic renal failure and its consequences for their closest relatives: The research protocol

被引：27
作者：
Janssen D.J.A. [1 ]
Wouters E.F.M. [2 ,3 ]
Schols J.M.G.A. [4 ]
Spruit M.A. [3 ,5 ]
机构：
[1] Central Department of Treatment and Care, Proteion Thuis, Horn
[2] Department of Respiratory Medicine, University Hospital Maastricht, Maastricht
[3] Centre for Integrated Rehabilitation of Organ Failure (CIRO), Horn
[4] Department of General Practice, Faculty of Health Medicine and Life Sciences, University Maastricht, Maastricht
[5] Department of Research, Development and Education, Centre for Integrated Rehabilitation of Organ Failure (CIRO), Horn
来源：
BMC Palliative Care | / 7卷 / 1期
关键词：
Chronic Obstructive Pulmonary Disease; Congestive Heart Failure; Chronic Renal Failure; Caregiver Burden; Severe Chronic Obstructive Pulmonary Disease;
D O I：
10.1186/1472-684X-7-5
中图分类号：
学科分类号：
摘要：
Background. Recent research shows that the prevalence of patients with very severe chronic obstructive pulmonary disease (COPD), congestive heart failure (CHF) and chronic renal failure (CRF) continues to rise over the next years. Scientific studies concerning self-perceived symptoms and care needs in patients with severe to very severe COPD, CHF and CRF are scarce. Consequently, it will be difficult to develop an optimal patient-centred palliative care program for patients with end-stage COPD, CHF or CRF. The present study has been designed to assess the symptoms, care needs, end-of-life care treatment preferences and communication needs of patients with severe to very severe COPD, CHF or CRF. Additionally, family distress and care giving burden of relatives of these patients will be assessed. Methods/design. A cross-sectional comparative and prospective longitudinal study in patients with end-stage COPD, CHF or CRF has been designed. Patients will be recruited by their treating physician specialist. Patients and their closest relatives will be visited at baseline and every 4 months after baseline for a period of 12 months. The following outcomes will be assessed during home visits: self-perceived symptoms and care needs; daily physical functioning; general health status; end-of-life care treatment preferences; end-of-life care communication and care-giver burden of family caregivers. Additionally, end-of-life care communication and prognosis of survival will be assessed with the physician primarily responsible for the management of the chronic organ failure. Finally, if patients decease during the study period, the baseline preferences with regard to life-sustaining treatments will be compared with the real end-of-life care. Discussion. To date, the symptoms, care needs, caregiver burden, end-of-life care treatment preferences and communication needs of patients with very severe COPD, CHF or CRF remain unknown. The present study will increase the knowledge about the self-perceived symptoms, care-needs, caregiver burden, end-of-life care treatment preferences and communication needs from the views of patients, their loved ones and their treating physician. This knowledge is necessary to optimize palliative care for patients with COPD, CHF or CRF. Here, the design of the present study has been described. A preliminary analysis of the possible strengths, weaknesses and clinical consequences is outlined. © 2008 Janssen et al; licensee BioMed Central Ltd.
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