2012 Proceedings - International Tissue Elasticity Conference
2012 Proceedings - International Tissue Elasticity Conference
2012 Proceedings - International Tissue Elasticity Conference
You also want an ePaper? Increase the reach of your titles
YUMPU automatically turns print PDFs into web optimized ePapers that Google loves.
26<br />
Session SAS: Oral Presentations of Finalists for Student Awards Session<br />
Tuesday, October 2 2:30P – 4:30P<br />
011 ELECTROMECHANICAL WAVE IMAGING OF BIOLOGICAL AND ELECTRONIC PACEMAKERS<br />
IN CONSCIOUS DOGS IN VIVO.<br />
Alexandre Costet 1 , Jean Provost 1 , Alok Gambhir 2 , Yevgeniy Bobkov 3 , Gerard J.J. Boink 3 ,<br />
Peter Danilo Jr 3 , Michael R. Rosen 3 , Elisa E. Konofagou 1,4 .<br />
1 Biomedical Engineering Department, 2 Medicine–Cardiology Department, 3 Pharmacology<br />
Department, 4 Radiology Department, Columbia University, New York, NY, USA.<br />
Background: Safe and real–time non–invasive imaging of cardiac electrical activation has been a long<br />
term goal of clinicians and laboratory investigators. Standard methods currently available in the clinic<br />
are all catheter–based and limited to epicardial or endocardial mapping. They are also time consuming<br />
and costly. Electromechanical Wave (EW) Imaging (EWI) is a direct ultrasound–based imaging technique<br />
that can map the transmural electromechanical activation in all four chambers in vivo [1].<br />
Aims: In this study, we assessed the reproducibility of EWI in closed–chest, conscious dogs to determine<br />
EWI’s potential for longitudinal animal studies. In order to show reproducibility in a variety of cases, we<br />
mapped electromechanical activation in conscious animal during normal sinus rhythm (NSR) and during<br />
idioventricular rhythm occurring in dogs in heart block, implanted with electronic and biological<br />
pacemakers (EPM and BPM respectively).<br />
Methods: Six different dogs (n=6) were used in this study. Four dogs underwent AV node ablation to<br />
create heart block and were subsequently implanted with an EPM in the right ventricular (RV)<br />
endocardial apex while two additionally received a BPM at the left ventricular (LV) epicardial base. A<br />
Verasonics system (Verasonics, Redmond, WA) with a 2.5MHz phased array was used to perform EWI<br />
transthoracically in conscious dogs using a flash beam sequence at 2000 frames/s in the apical 2 and<br />
4–chamber views before and 7 days after implantation. In post–implantation animals, EWI was performed<br />
during BPM pacing only and during EPM pacing only. Axial incremental displacements and strains were<br />
estimated using radiofrequency (RF) cross–correlation with a window size of 9.2mm and a window shift of<br />
0.385mm and a least–squares kernel size of 5.0mm, respectively. Isochrones of the electromechanical<br />
activation were then generated in order to assess EWI reproducibility.<br />
Results: During NSR, the EW originated at the right atrium (RA), propagated to the left atrium (LA) and<br />
emerged from multiple sources in both ventricles. During BPM, the EW originated from the LV basal<br />
lateral wall and subsequently propagated throughout the ventricles. During EPM, the EW originated at<br />
the RV apex and propagated throughout both ventricles.<br />
Conclusions: EWI was capable of adequately differentiating BPM from EPM and NSR and identified the<br />
distinct pacing origins transthoracically and in conscious dogs These findings indicate the potential of<br />
EWI to serve as a simple, direct and noninvasive imaging tool for monitoring of pacing therapies.<br />
(a) (b)<br />
Figure 1: EWI isochrones during NSR, biological and electronic pacing. The orgins of the isochrones correspond to the onset of the<br />
P–wave (a) or the QRS (b, c). (a) EWI isochrone of normal sinus rhythm in one dog pre–surgery. Activation at the atria<br />
originates from the RA and propagates to the LA. In the ventricles, arrows indicati the sites of early activation. (b) EWI<br />
isochrone during biological pacing. Early activation is seen in the basal region of the lateral wall in the LV. (c) EWI<br />
isochrone during electronic pacing. Early activation is seen near the apex of the RV.<br />
Acknowledgements: Supported in part by NIH funding (R01EB006042, R01HL094410 and R01HL67101).<br />
References:<br />
[1] Provost J., Lee W–N., et al.: Imaging the Electromechanical Activity of the Heart In–Vivo. Proc. Natl. Acad. Sci.<br />
U.S.A., Vol. 108, No. 21, pp. 8565–8570, 2011.<br />
(<br />
indicates Presenter