Heath 2015 - Influenza Vaccine Case Study and Table 1
Summary
A 28-parameter Bayesian cost-effectiveness model of an influenza vaccine, with single-parameter EVPPI computed five ways at willingness to pay . All methods agree to within the Monte Carlo error of the baseline (0.04); and rank highest; nested MC takes about 55 minutes per parameter versus seconds for the rest.
Overview
Model (Sec. 4.1). Two options: vaccine available () or not (). A patient with influenza gets antivirals and often a GP visit; complications include pneumonia and hospitalisation, with indirect costs such as time off work. Costs: drug acquisition, hospital days, GP visits, vaccine. Benefit: QALYs, with each adverse effect contributing negatively. There are 28 key parameters (probability of infection, vaccine risk reduction, complication probabilities, monetary costs, QALY losses); the full parametrisation is in Baio (2012). Draws come from the joint posterior by MCMC.
Main Content
Settings (Sec. 4.2).
- Single-parameter EVPPI for all 28 parameters with all methods.
- Sadatsafavi et al.: visual tool says 23 of 28 parameters change the optimal decision once; the other five have EVPPI by this method.
- Strong-Oakley: chosen as the largest number of subsets with upward bias below 0.1, ranging from 20 down to 2 subsets by parameter.
- Two-step MC: outer loop 1000 posterior samples; inner loop MCMC with 2 chains of 100,000 draws, burn-in 9,500, thinned by 500 to 1000 draws. Monte Carlo error “still quite large”.
- Baseline “current information”: 5,000,000 MCMC draws, burn-in 9,500, thinned to 50,000, MC error about 0.04. Incremental net benefit stored per loop and taken.
- GAM and GP via Strong et al.’s functions with automatic hyper-parameters.
Table 1 - EVPPI values by parameter and method (SO = Strong-Oakley, SAD = Sadatsafavi et al., GP, GAM, MC = two-step Monte Carlo). Group labels are as aligned in the PDF; groupings of follow the printed row labels.
| Parameter | Group | SO | SAD | GP | GAM | MC |
|---|---|---|---|---|---|---|
| Probability of clinical outcomes | 1.15 | 1.17 | 1.11 | 1.11 | 1.06 | |
| same | 0.26 | 0.23 | 0.11 | 0.11 | 0.25 | |
| same | 0.24 | 0.15 | 0.03 | 0.03 | 0.07 | |
| same | 0.14 | 0.13 | 0.08 | 0.09 | 0.05 | |
| same | 0.28 | 0.25 | 0.07 | 0.12 | 0.06 | |
| same | 0.27 | 0.29 | 0.18 | 0.21 | 0.21 | |
| same | 0.35 | 0.40 | 0.30 | 0.30 | 0.25 | |
| Number of drugs prescribed | 0.30 | 0.22 | 0.11 | 0.03 | 0.06 | |
| Probability of taking time off work | 0.11 | 0 | 0.04 | 0 | 0.06 | |
| Probability of receiving drugs | 0.19 | 0.17 | 0.11 | 0.11 | 0.06 | |
| same | 0 | 0 | 0.01 | 0.01 | 0.06 | |
| Number of days off work | 0.41 | 0.44 | 0.41 | 0.43 | 0.43 | |
| Reduction in infection rate due to vaccine | 0.30 | 0.30 | 0.28 | 0.28 | 0.28 | |
| Probability of taking OTC medication | 0.24 | 0.13 | 0.03 | 0.03 | 0.06 | |
| QALY cost for each state | 0.55 | 0.57 | 0.53 | 0.53 | 0.63 | |
| same | 0.20 | 0.23 | 0 | 0 | 0.06 | |
| same | 0.11 | 0.17 | 0.05 | 0.05 | 0.06 | |
| same | 0.18 | 0.16 | 0.12 | 0.12 | 0.13 | |
| same | 0.18 | 0.29 | 0.14 | 0.16 | 0.15 | |
| Vaccine coverage rate | 0.13 | 0 | 0.02 | 0.02 | 0.06 | |
| Cost of resources | 0.17 | 0.17 | 0.13 | 0.13 | 0.07 | |
| same | 0.10 | 0.14 | 0.02 | 0.02 | 0.06 | |
| same | 0.37 | 0.37 | 0.31 | 0.31 | 0.29 | |
| same | 0.46 | 0.52 | 0.35 | 0.35 | 0.42 | |
| same | 0.44 | 0.38 | 0.24 | 0.38 | 0.25 | |
| same | 0.13 | 0.15 | 0.05 | 0.05 | 0.07 | |
| same | 0.20 | 0 | 0 | 0 | 0.07 | |
| same | 0.08 | 0 | 0 | 0 | 0.07 |
Interpretation. The two highest parameters are the same across all five methods (, ); discrepancies in the ordering of the rest are small relative to the 0.04 MC error of the current-information term. The MC column floors near 0.05-0.07 for parameters with no true effect, a signature of the upward bias of nested MC with finite inner samples; the paper attributes variation to “the inherent nature of approximation”. The paper advises reporting EVPPI to 1-2 decimals only.
Figure 1 (EVPI and EVPPI vs willingness to pay, from 0 to 50000). Plotted for EVPI and for and , using Sadatsafavi et al. with one decision change. Both curves peak where the optimal decision changes (“uncertainty is greatest at the point when both strategies are equal”). is near the break-even. Away from break-even, EVPPI values are tiny and MC error would dominate nested-MC estimates.
Figure 2 (mean EVPPI and standard error). Four methods (SO, SAD, GAM, GP; MC excluded) for the four highest-EVPPI parameters (, , , ) show similar standard errors, hence “little difference between the estimation properties of all 4 methods”. (Panel values are plotted only; not tabulated in the text.)
Runtime. Single-parameter methods and GAM: negligible. GP: 2-4 seconds. Nested MC: about 55 minutes for one parameter.
Examples
Reading Table 1 as a decision memo: on every method the infection-risk reduction , the days off work and the QALY cost carry visible value of information (about 0.3-0.6 on the Table’s scale; units are net benefit as scaled in the paper, which this note does not restate), while vaccine coverage and some cost parameters () are worth about nothing on the regression methods. This is the use VoI is advocated for: ranking where more data pays.
Connections
- Methods compared: Heath 2015 - Single-Parameter EVPPI Strong-Oakley and Sadatsafavi, Heath 2015 - Regression-Based EVPPI (GAM and Gaussian Process), Heath 2015 - Nested Monte Carlo and Restrictive EVPPI Approximations.
- Marketing analogue: a ranked EVPPI table for an MMM tells you which saturation or adstock parameter deserves the next lift test.