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Economic evaluation of cholinesterase inhibitor therapy for dementia: comparison of Alzheimer's disease and Dementia with Lewy bodies
Author(s) -
Gustavsson Anders,
Van Der Putt Rohan,
Jönsson Linus,
McShane Rupert
Publication year - 2009
Publication title -
international journal of geriatric psychiatry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.28
H-Index - 129
eISSN - 1099-1166
pISSN - 0885-6230
DOI - 10.1002/gps.2223
Subject(s) - dementia with lewy bodies , dementia , medicine , cholinesterase , alzheimer's disease , pediatrics , disease
Objective To assess the cost effectiveness of cholinesterase inhibitor (ChEI) treatment in patients with Alzheimer's disease (AD) and Dementia with Lewy bodies (DLB). Method We used 4‐month open label follow‐up data from routine memory clinic patients. There were 852 patients with AD and 112 with DLB. We applied three predictive models to estimate clinical and economic outcomes at five years, comparing AD and DLB patients with hypothetical untreated controls. Results The mean improvement in MMSE in 852 AD patients was 0.57 (SD 3.4) at 4 months, and in the subgroup with baseline MMSE of 10–20 (moderate) was 1.6 (SD 3.7). Overall, the 112 DLB patients improved by 1.4 (SD 3.7). DLB patients with an MMSE 10–20 improved by 3.1 (SD 4.5) points. These efficacy data were input into the SHTAC, microsimulation and Markov models and produced estimated costs per QALY gained (CQG) for all AD of £194,066, £67,904 and £123,935 respectively. In comparison, the CQGs for all DLB were £46,794, £2,706 and £35,922. For the moderate subgroups only the SHTAC and microsimulation models were applicable. These gave CQG estimates for moderate AD of £39,664 and cost saving respectively. For moderate DLB, both estimates were cost saving. Conclusion The cost per QALY gained of cholinesterase treatment of all patients with DLB (including those with MMSE outside the 10–20 range) is comparable to that of patients with moderate AD, and is probably cost saving. Copyright © 2009 John Wiley & Sons, Ltd.