Economic evaluation of culprit lesion only PCI vs. immediate multivessel PCI in acute myocardial infarction complicated by cardiogenic shock: the CULPRIT‑SHOCK trial
Date
2020-10-07Publisher
Springer LinkAuthor
Robles‑Zurita, Jose AntonioBriggs, Andrew
Rana, Dikshyanta
Quayyum, Zahidul
Oldroyd, Keith G.
Zeymer, Uwe
Desch, Stefen
de Waha‑Thiele, Suzanne
Thiele, Holger
Metadata
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Robles-Zurita, J. A., Briggs, A., Rana, D., Quayyum, Z., Oldroyd, K. G., Zeymer, U., . . . Thiele, H. (2020). Economic evaluation of culprit lesion only PCI vs. immediate multivessel PCI in acute myocardial infarction complicated by cardiogenic shock: The CULPRIT-SHOCK trial. European Journal of Health Economics, 21(8), 1197-1209. doi:10.1007/s10198-020-01235-3Abstract
Background The CULPRIT-SHOCK trial compared two treatment strategies for patients with acute myocardial infarction
and multivessel coronary artery disease complicated by cardiogenic shock: (a) culprit vessel only percutaneous coronary
intervention (CO-PCI), with additional staged revascularisation if indicated, and (b) immediate multivessel PCI (MV-PCI).
Methods A German societal and national health service perspective was considered for three diferent analyses. The cost
utility analysis (CUA) estimated costs and quality adjusted life years (QALYs) based on a pre-trial decision analytic model
taking a lifelong time horizon. In addition, a within trial CUA estimated QALYs and costs for 1 year. Finally, the cost
efectiveness analysis (CEA) used the composite primary outcome, mortality and renal failure at 30-day follow-up, and the
within trial costs. Econometric and survival analysis on the trial data was used for the estimation of the model parameters.
Subgroup analysis was performed following an economic protocol.
Results The lifelong CUA showed an incremental cost efectiveness ratio (ICER), CO-PCI vs. MV-PCI, of €7010 per QALY
and a probability of CO-PCI being the most cost-efective strategy>64% at a €30,000 threshold. The ICER for the within
trial CUA was €14,600 and the incremental cost per case of death/renal failure avoided at 30-day follow-up was €9010.
Cost-efectiveness improved with patient age and for those without diabetes.
Conclusions The estimates of cost-efectiveness for CO-PCI vs. MV-PCI have been shown to change depending on the time
horizon and type of economic evaluation performed. The results favoured a long-term horizon analysis for avoiding underestimation of QALY gains from the CO-PCI arm.