Back to Search Start Over

Twenty years of home-based palliative care in Malappuram, Kerala, India: a descriptive study of patients and their care-givers.

Authors :
Philip, Rekha Rachel
Philip, Sairu
Prasad Tripathy, Jaya
Manima, Abdulla
Venables, Emilie
Source :
BMC Palliative Care; 2/14/2018, Vol. 17, p1-9, 9p
Publication Year :
2018

Abstract

Background: The well lauded community-based palliative care programme of Kerala, India provides medical and social support, through home-based care, for patients with terminal illness and diseases requiring long-term support. There is, however, limited information on patient characteristics, caregivers and programme performance. This study was carried out to describe: i) the patients enrolled in the programme from 1996 to 2016 and their diagnosis, and ii) the care-giver characteristics and palliative care support from nurses and doctors in a cohort of patients registered during 2013-2015. Methods: A descriptive study was conducted in the oldest community-based palliative clinic in Kerala. Data were collected from annual patient registers from 1996 to 2016 and patient case records during the period 2013--2015. Results: While 91% of the patients registered in the clinic in 1996 had cancer, its relative proportion came down to 32% in 2016 with the inclusion of dementia-related illness (19%) cardiovascular accidents (17%) and severe mental illness (5%).Among patients registered during 2013--15, the median number of home visits from nurses and doctors in 12 months were five and one respectively. In the same cohort, twelve months' post-enrolment, 56% of patients died, 30%wereincontinuinginactivecareand7%optedout.Thosewhooptedoutofcarewerelikelytobeaged<60years, received one or less visit annually from a doctor or have a serious mental illness. 96% of patients had a care-giver at home, 85% of these care-givers being female. Conclusions: The changing dynamics over a 20-year period of this palliative care programme in Kerala, India, highlights the need for similar programmes to remain flexible and adapt their services in response to a growing global burden of Non Communicable Diseases. While a high death rate is expected in this population, the high proportion of patients choosing to stay in the programme suggests that home-based care is valued within this particular group. A diverse range of clinical and psycho-social support skills are required to assist families and their caregivers when caring for a cohort such as this one. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
1472684X
Volume :
17
Database :
Complementary Index
Journal :
BMC Palliative Care
Publication Type :
Academic Journal
Accession number :
128026645
Full Text :
https://doi.org/10.1186/s12904-018-0278-4