Is short-term palliative care cost-effective in multiple sclerosis? A randomized phase II trial.

CONTEXT Palliative care is being advocated for noncancer patients but needs evidence of effectiveness and cost-effectiveness. OBJECTIVE We evaluated the cost-effectiveness of a new palliative care service for people with multiple sclerosis (MS). METHODS We used a randomized fast-track Phase II controlled trial. Patients in South East London who were severely affected by MS were referred by clinicians to the trial. After baseline interview, patients were randomly allocated to either a multiprofessional palliative care team (PCT) immediately (fast track) or the control care group who continued best usual care for three months and then were offered the PCT. Data were collected at baseline, 6, 12, 18, and 26 weeks on use of services, patient symptoms, other outcomes, and caregiver burden. RESULTS Fifty-two patients were randomized: 25 fast track and 21 control patients completed the trial. There was a high level of disability, and mean Expanded Disability Status Scale score was 7.7 (median 8, standard deviation 1.0). At 12 weeks, caregiver burden was 4.47 points lower (95% confidence interval [CI]: 1.05-7.89) in the fast track compared to the control group. Mean service costs, including inpatient care and informal care, over the 0-12-week follow-up were pound1,789 lower for the fast-track group (bootstrapped 95% CI: - pound5,224 to pound1,902). There was a trend toward lower community costs in the fast-track group and no differences in costs to informal caregivers. CONCLUSIONS The trial suggests that short-term palliative care for people severely affected by MS and their caregivers will be cost-effective and warrants further study. The fast-track trial design could be used to assess this.

[1]  D. Torgerson,et al.  Randomisation methods in controlled trials , 1998, BMJ.

[2]  P Lindgren,et al.  Costs and quality of life of patients with multiple sclerosis in Europe , 2006, Journal of Neurology, Neurosurgery & Psychiatry.

[3]  J. Baskerville,et al.  The natural history of multiple sclerosis: a geographically based study. 5. The clinical features and natural history of primary progressive multiple sclerosis. , 1999, Brain : a journal of neurology.

[4]  K. Steinhauser,et al.  What length of hospice use maximizes reduction in medical expenditures near death in the US Medicare program? , 2007, Social science & medicine.

[5]  D. Wade,et al.  Validity and reliability comparison of 4 mobility measures in patients presenting with neurologic impairment. , 2001, Archives of physical medicine and rehabilitation.

[6]  I. Higginson,et al.  Symptom Prevalence and Severity in People Severely Affected by Multiple Sclerosis , 2006, Journal of palliative care.

[7]  J. Borrás,et al.  Resource consumption and costs of palliative care services in Spain: a multicenter prospective study. , 2006, Journal of pain and symptom management.

[8]  B. Lebowitz,et al.  Families, Informal Supports,and Alzheimer's Disease , 1985, Research on aging.

[9]  D. Wade,et al.  The Guy's Neurological Disability Scale in patients with multiple sclerosis: a clinical evaluation of its reliability and validity , 2002, Clinical rehabilitation.

[10]  S. Enguídanos,et al.  Increased Satisfaction with Care and Lower Costs: Results of a Randomized Trial of In‐Home Palliative Care , 2007, Journal of the American Geriatrics Society.

[11]  I. Higginson,et al.  Health and Quality of Life Outcomes , 2004 .

[12]  P. Yates,et al.  Supportive and palliative care needs identified by multiple sclerosis patients and their families. , 2006, International journal of palliative nursing.

[13]  I. Higginson,et al.  What is the best way to help caregivers in cancer and palliative care? A systematic literature review of interventions and their effectiveness , 2003, Palliative medicine.

[14]  L. Kalra,et al.  Training care givers of stroke patients: economic evaluation , 2004, BMJ : British Medical Journal.

[15]  T. Mets,et al.  Patient and caregiver outcomes after 6 ± 1.5-months of rivastigmine therapy for mild-to-moderate Alzheimer's disease:the Belgian FExT study , 2007, Current medical research and opinion.

[16]  Paul McCrone,et al.  Predicting the cost of Parkinson's disease , 2007, Movement disorders : official journal of the Movement Disorder Society.

[17]  J. Baskerville,et al.  The natural history of multiple sclerosis: a geographically based study. 3. Multivariate analysis of predictive factors and models of outcome. , 1991, Brain : a journal of neurology.

[18]  A. Edwards,et al.  Is there evidence that palliative care teams alter end-of-life experiences of patients and their caregivers? , 2003, Journal of pain and symptom management.

[19]  I. Higginson,et al.  Development and validation of a core outcome measure for palliative care: the palliative care outcome scale. Palliative Care Core Audit Project Advisory Group. , 1999, Quality in health care : QHC.

[20]  E. Emanuel,et al.  The economics of dying. The illusion of cost savings at the end of life. , 1994, The New England journal of medicine.

[21]  I. Higginson,et al.  Loss and change: experiences of people severely affected by multiple sclerosis , 2007, Palliative medicine.

[22]  D. Meier,et al.  Cost savings associated with US hospital palliative care consultation programs. , 2008, Archives of internal medicine.

[23]  L. Kristjanson,et al.  Palliative care and support for people with neurodegenerative conditions and their carers. , 2006, International journal of palliative nursing.

[24]  P. Fayers,et al.  A palliative-care intervention and death at home: a cluster randomised trial , 2000, The Lancet.

[25]  P. Reilly,et al.  A primary care-based needs assessment of people with multiple sclerosis. , 2005, The British journal of general practice : the journal of the Royal College of General Practitioners.

[26]  I. Higginson,et al.  The relationship between patient characteristics and carer psychological status in home palliative cancer care , 2003, Supportive Care in Cancer.

[27]  Rachel Burman,et al.  Study protocol: delayed intervention randomised controlled trial within the Medical Research Council (MRC) Framework to assess the effectiveness of a new palliative care service , 2006, BMC Palliative Care.

[28]  D. Molloy,et al.  The Zarit Burden Interview: a new short version and screening version. , 2001, The Gerontologist.

[29]  P. Shekelle,et al.  Evidence for Improving Palliative Care at the End of Life A Systematic Review , 2008, Annals of Internal Medicine.

[30]  I. Higginson,et al.  Randomised controlled trial of a new palliative care service: Compliance, recruitment and completeness of follow-up , 2008, BMC palliative care.

[31]  G. Torrance,et al.  Cost and health related quality of life consequences of multiple sclerosis , 2000, Multiple sclerosis.

[32]  I. Higginson,et al.  Palliative day care: what does it cost to run a centre and does attendance affect use of other services? , 2003, Palliative medicine.