Cardiac T1 mapping in congenital heart disease: bolus vs. infusion protocols for measurements of myocardial extracellular volume fraction

N Al-Wakeel-Marquard, S Rastin, F Muench… - … International Journal of …, 2017 - Springer
N Al-Wakeel-Marquard, S Rastin, F Muench, DO h-Ici, S Yilmaz, F Berger, T Kuehne
The International Journal of Cardiovascular Imaging, 2017Springer
Myocardial extracellular volume fraction (ECV) reflecting diffuse myocardial fibrosis can be
measured with T1 mapping cardiovascular magnetic resonance (CMR) before and after the
application of a gadolinium-based extracellular contrast agent. The equilibrium between
blood and myocardium contrast concentration required for ECV measurements can be
obtained with a primed contrast infusion (equilibrium contrast-CMR). We hypothesized that
equilibrium can also be achieved with a single contrast bolus to accurately measure diffuse …
Abstract
Myocardial extracellular volume fraction (ECV) reflecting diffuse myocardial fibrosis can be measured with T1 mapping cardiovascular magnetic resonance (CMR) before and after the application of a gadolinium-based extracellular contrast agent. The equilibrium between blood and myocardium contrast concentration required for ECV measurements can be obtained with a primed contrast infusion (equilibrium contrast-CMR). We hypothesized that equilibrium can also be achieved with a single contrast bolus to accurately measure diffuse myocardial fibrosis in patients with congenital heart disease (CHD). Healthy controls (n = 17; median age 24.0 years) and patients with CHD (n = 19; 25.0 years) were prospectively enrolled. Using modified Look-Locker inversion recovery T1 mapping before, 15 min after bolus injection, and during constant infusion of gadolinium-DOTA, T1 values were obtained for blood pool and myocardium of the left ventricle (LV), the interventricular septum (IVS), and the right ventricle (RV) in a single midventricular plane in short axis or in transverse orientation. ECV of LV, IVS and RV by bolus-only and bolus-infusion correlated significantly in CHD patients (r = 0.94, 0.95, and 0.74; p < 0.01, respectively) and healthy controls (r = 0.96, 0.89, and 0.64; p < 0.05, respectively). Bland–Altman plots revealed no significant bias between the techniques for any of the analyzed regions. ECV of LV and RV myocardium measured by bolus-only T1 mapping agrees well with bolus-infusion measurements in patients with CHD. The use of a bolus-only approach facilitates the integration of ECV measurements into existing CMR imaging protocols, allowing for assessment of diffuse myocardial fibrosis in CHD in clinical routine.
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