The two-way sensitivity analysis was conducted on the two main input drivers of the ICER estimate, i.e. the utility in the stable health state and the costs of three health states. The PSA attributed appropriate probability distributions to the input parameters. Results The ICER estimated from the model was –£2782 at the end of 1 year, which means the use of ethyl-EPA as an adjunct therapy for BD is more effective than placebo and
it reduces cost. The main factor contributing toward reduction in cost is the lower transitional probability to manic and depressive episodes for the patients taking ethyl-EPA. This means Inhibitors,research,lifescience,medical that fewer ethyl-EPA-treated patients experienced acute episodes as compared with the placebo group. Hence, service use (such as hospitalization) was lower in the ethyl-EPA group and consequently their treatment costs were lower. The additional drug cost of ethyl-EPA was small (£24) per cycle as compared with the reduction of service use elsewhere. In the Frangou and colleagues [Frangou et al. 2006] trial Inhibitors,research,lifescience,medical no inpatient episode was recorded among the patients allocated to ethyl-EPA adjunct treatment as compared Inhibitors,research,lifescience,medical with, on average, 3 days of inpatient treatment (daily cost of an inpatient episode of £210) in the placebo arm. The number of inpatient episodes in the case of the placebo group is in line with the RR (0.6) of acute episodes
estimated. Two patients in the placebo arm totalled 216 hours
of day centre contacts (DNA Damage antagonist hourly cost of day centre of £9), while no patients in the ethyl-EPA arm had day centre contacts. Lower scores of HRSD Inhibitors,research,lifescience,medical and Young Mania Rating Scale (YMRS) in the ethyl-EPA compared with placebo group at the week 12 assessment support Inhibitors,research,lifescience,medical better quality of life among patients receiving ethyl-EPA, which is estimated in the model as higher number of QALYs. Greater effectiveness and reduced cost contributed toward negative estimate of the ICER, which implies use of ethyl-EPA as an adjunct treatment for BD is a dominant treatment, falling in the dominant quadrant (II) of the cost-effectiveness plane. Although, the data used from the clinical trial covered a very short time period, the model was extended to 5-year time Dichloromethane dehalogenase period, using a discount rate of 3.5% for costs and outcomes, the estimate of 5-year ICER was very close to the 1-year ICER estimate. Sensitivity analysis The tornado diagram in Figure 3 shows how the change (25% increase and 25% decrease) in the value of inputs affect the estimate of ICER. The diagram shows that the main input drivers of the ICER estimate are the utility in the stable health state and the costs of three health states. The tornado diagram also shows that the ICER estimate is negative despite a 25% increase or decrease in the values of most of the inputs. The one-way sensitivity analysis shows that the estimate of ICER was robust.
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