Design of clinical cardioprotection trials using CMR: impact of myocardial salvage index and a narrow inclusion window on sample size

Henrik Engblom,Einar Heiberg,David Erlinge,Sigrun Halvorsen,Jean-Luc Dubois-Randé,Håkan Arheden,Marcus Carlsson,Sasha Koul,Dan Atar,Svend Eggert Jensen,Jan Erik Nordrehaug

doi:10.1186/1532-429x-17-s1-p90

Abstract

Background Cardiac magnetic resonance imaging (CMR) can be used to determine both myocardial infarct (MI) size and myocardium at risk (MaR), enabling assessment of myocardial salvage index (MSI). MI size as assessed by hyperenhancement on late gadolinium enhancement (LGE) has been shown to decrease approximately 25% during the first week after infarction. The aim of this study was to determine to what extent assessment of MSI and a narrow inclusion window affect the number of patients needed to reach sufficient statistical power in a clinical CMR cardioprotection trial. Methods Control subjects (n=91) from the recent CHILL-MI 1 and MITOCARE 2 cardioprotection trials, examined by CMR 2-6 days after acute reperfusion therapy, were used to assess the difference in sample size required to reach sufficient statistical power when using MI size alone compared to MSI as outcome variable. In addition, 22 patients undergoing CMR at day 1 and 7 after acute reperfused infarction from a previous follow-up study 3 were included to assess to what extent sample size is affected by the decrease in hyperenhancement seen during the first week after infarction. The variability of MI size by LGE, MaR by contrast-enhanced SSFP and MSI was used to simulate 100.000 clinical trials for different assumed treatment effects to determine the number of patients needed to reach sufficient statistical power. Results

Highlights

Cardiac magnetic resonance imaging (CMR) can be used to determine both myocardial infarct (MI) size and myocardium at risk (MaR), enabling assessment of myocardial salvage index (MSI)
Control subjects (n=91) from the recent CHILL-MI1 and MITOCARE2 cardioprotection trials, examined by CMR 2-6 days after acute reperfusion therapy, were used to assess the difference in sample size required to reach sufficient statistical power when using MI size alone compared to MSI as outcome variable
For an assumed effect of 25 % reduction in MI size by a cardioprotection treatment, the number of patients needed to reach sufficient statistical power can be reduced by 48% (34 patients in each arm versus 65) if using MSI instead of MI size alone as outcome variable (Figure 1)

Summary

Introduction

Cardiac magnetic resonance imaging (CMR) can be used to determine both myocardial infarct (MI) size and myocardium at risk (MaR), enabling assessment of myocardial salvage index (MSI). MI size as assessed by hyperenhancement on late gadolinium enhancement (LGE) has been shown to decrease approximately 25% during the first week after infarction. The aim of this study was to determine to what extent assessment of MSI and a narrow inclusion window affect the number of patients needed to reach sufficient statistical power in a clinical CMR cardioprotection trial

Objectives

Methods

Results

Conclusion