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Open Access Research article

Caregivers' perceived adequacy of support in end-stage lung disease: results of a population survey

David C Currow1*, Morag Farquhar2, Alicia M Ward13, Gregory B Crawford4 and Amy P Abernethy15

Author Affiliations

1 Discipline, Palliative and Supportive Services, Flinders University, Adelaide, Australia

2 General Practice & Primary Care Research Unit, Department of Public Health & Primary Care, University of Cambridge, UK

3 Southern Adelaide Palliative Services, Repatriation General Hospital, Daw Park, South Australia, Australia

4 Discipline of Medicine, University of Adelaide, Adelaide. South Australia, Australia

5 Division of Medical Oncology, Department of Medicine, Duke University Medical Centre, Durham, North Carolina, USA

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BMC Pulmonary Medicine 2011, 11:55  doi:10.1186/1471-2466-11-55

Published: 25 November 2011

Abstract

Background

End-stage lung disease (ESLD) is a frequent cause of death. What are the differences in the supports needed by caregivers of individuals with ESLD at end of life versus other life-limiting diagnoses?

Methods

The South Australian Health Omnibus is an annual, random, face-to-face, cross-sectional survey. In 2002, 2003 and 2005-2007, respondents were asked a range of questions about end-of-life care; there were approximately 3000 survey participants annually (participation rate 77.9%). Responses were standardised for the whole population. The families and friends who cared for someone with ESLD were the focus of this analysis. In addition to describing caring, respondents reported additional support that would have been helpful.

Results

Of 1504 deaths reported, 145 (9.6%) were due to ESLD. The ESLD cohort were older than those with other 'expected' causes of death (> 65 years of age; 92.6% versus 70.6%; p < 0.0001) and were less likely to access specialised palliative care services (38.4% versus 61.9%; p < 0.0001). For those with ESLD, the mean caring period was significantly longer at 25 months (standard deviation (SD) 24) than for 'other diagnoses' (15 months; SD 18; p < 0.0001). Domains where additional support would have been useful included physical care, information provision, and emotional and spiritual support.

Conclusions

Caregiver needs were similar regardless of the underlying diagnosis although access to palliative care specialist services occurred less often for ESLD patients. This was despite significantly longer periods of time for which care was provided.