Primary prevention |
Zhang, Kivipelto [26] |
Hypothetical intervention reducing risk of AD onset in Sweden |
QALYs |
Purpose-built Markov model with 3 health states. 20-year time horizon, 1 year cycles |
CAIDE population based study on risk factors of 1409 individuals [44] |
Hypothetical intervention |
Swedish studies (EQ5D) [41, 57] |
Swedish National Board of Health and Welfare |
Tsiachristas & Smith [32] |
Preventative treatment with B-vitamin supplement for people aged 60 and over with elevated levels of tHcy in the UK |
Life-Years; QALYs |
Stochastic probabilistic decision tree; lifetime horizon. |
Disease progression not modelled. Disease onset based on prevalence data; mortality from life tables. |
Effectiveness of intervention based on a systematic review in lieu of randomised controlled trials [37] |
General population EQ5D survey [36] |
Taken from a UK study [58] |
Secondary prevention |
McMahon [28] |
Functional neuroimaging vs. standard work-up of patients for AD diagnosis at specialised AD clinics in the US |
QALYs |
Markov model based on a previously published study [40]; 6-week cycles, 18-month time horizon. |
Progression within AD and AD mortality from CERAD study [40]. Non-AD mortality from CDC. |
Screening effectiveness from US-based study [59] |
Utility weights obtained from the Neumann et al. [40] |
Primary data from hospital databases; existing literature |
Silverman, Gambhir [31] |
PET vs. standard diagnostic methods in clinical diagnosis of AD in the US |
Number of accurate diagnoses |
Purpose-built decision-tree, unspecified time horizon |
Adapted from a wide range of published data |
Results of PET screening reported in the study |
Not used - CEA |
Defined by Medicare reimbursement rates |
Weimer and Sager [30] |
Early detection and treatment of AD patients in a US (Wisconsin) setting. Two treatments considered. |
MMSE score change |
Monte Carlo model. Lifetime horizon, 1 year cycles |
Adapted from a range of published data and estimates. Data from CVD risk study on 5000 people was used to estimate hazard ratio for death. |
A range of published data and estimates |
Adapted from [40] |
A range of published data and estimates |
Dixon, Ferdinand [35] |
One-off screen of 75 year olds in England and Wales |
Number of additional diagnoses |
Static decision model with lifetime time horizon |
Not provided |
Results of screening based on MMSE (assumed 89% sensitivity, 95.5% specificity) |
Not used – CBA |
A range of published data and estimates |
Saito, Nakamoto [27] |
Community based dementia screening in a US setting |
Dementia diagnosis through MMSE |
Purpose-built Markov model with 6-state 10-year time horizon, 1 year cycles |
Adapted from [46, 48] which investigated 61 and 1145 patients, respectively |
Results of screening program reported in study |
Not used - CEA |
Adapted from a Canadian study [60] |
Tertiary prevention |
McDonnell, Redekop [33] |
A hypothetical intervention which slows cognitive decline in AD patients in the Netherlands |
MMSE score change, care setting, mortality |
Two regression-based simulation models – one modelling MMSE score, another- care setting and mortality. 10-year time horizon, 6 month cycles |
Calculated from a Dutch study [38] with 7528 participants. |
Hypothetical intervention |
Not used – CEA |
From Dutch national data, agencies/ ministries |
Martikainen, Valtonen [29] |
Cognitive-behavioural family intervention to delay admission to nursing home in Finland |
Time to nursing home admission |
Markov model. Adapted from [40]. Model has 4 states, 5-year time horizon, 1 year cycles |
Adapted from the original US-based model (with minor adjustments) – based on longitudinal study with 1145 patients [40] |
Based on a US study of 206 subjects [61] |
From the original US-based model |
From national datasets; some resource utilisation based on expert panel |
Mirsaeedi-Farahani, Halpern [34] |
Deep-brain stimulation therapy for slowing memory loss in AD patients compared to standard treatment |
QALYs |
Purpose-built Markov model with 5 states, 5-year horizon, 1 year cycles |
Adapted from Neumann et al. [46] and Spackman et al. [47] |
Actual success rate of deep brain stimulation is unknown, so was varied from 0 to 100% |
A range of published data |
Costs obtained from [62] |