Cardiac Arrhythmia Mapping!
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1 Cardiac Arrhythmia Mapping! Challenges and Opportunities" Derek J. Dosdall, Ph.D. 22 October, 2010
2 OUTLINE!! Historical perspective! Current mapping techniques!optical mapping!electrical mapping (Purkinje example)! Future directions and opportunities
3 Noninvasive Electrical Mapping!!Surface ECG was developed by William Einthoven in the early 1900s!Lead I, II, III
4 Noninvasive Electrical Mapping! If 3 leads were good, then 12 leads must be better! And dozens to hundreds of body surface potentials even more useful!
5 Epicardial Mapping!! Initially performed with a limited number of channels on the epicardial surface.! Advances in computing power and storage have allowed for thousands of channels of data to be collected simultaneously.
6 Electrical Epicardial Mapping!! Direct contact with plaques and socks
7 Epicardial & transmural arrays"! Epicardial array Plunge electrodes
8 Electrical Endocardial Mapping! Endocardial baskets Open heart models Plunge needles Endocardial catheter mapping
9 Clinical Endocardial Mapping!! Endovascular catheter mapping reduces invasiveness of mapping techniques! Many clinically available mapping systems with mapping catheters!carto (Biosense-Webster)!EnSite NavX (St. Jude Medical)!Others
10 Invasive Electrical Mapping!
11 Historical Optical Mapping!! Carl Wiggers performed high speed cinematography of VF in the 1930s and 40s! He visualized motion and defined 4 distinct periods of activity during VF
12 Current Optical Mapping!! Voltage sensitive dye binds to cell membrane and fluoresces at a different wavelength when the transmembrane potential (V m ) changes! Other dyes may be used to display intracellular calcium (Ca ++ i ) levels
13 Optical Mapping!! Advantages!Simultaneous V m and Ca ++ i possible!large numbers of pixels and high resolution! Disadvantages!Motion artifact problematic!direct line of site required
14 Panoramic Optical Mapping of Vm!
15 Optrode Recordings!! Fiberoptic bundles arranged in an optical plunge needle configuration
16 Simultaneous V m and Ca i ++ measurements t(s) From Omichi et al.,! Am J Physiol Heart Circ Physiol 286:! H , 2004.!
17 Example of Multiple Mapping Techniques in Research! Role of Purkinje Fibers in Long Duration Ventricular Fibrillation
18 Purkinje Fibers in Sinus Rhythm!
19 Traditional Mechanisms of VF Maintenance! Wandering Wavelets Mother Rotor Reentry
20 Development of Activation Rate!! Several groups have observed an activation rate gradient in LDVF! Present in dogs but not pigs
21 Epicardium" Endocardium"
22 Purkinje Fiber Distribution! In humans, dogs, primates, and rabbits: In pigs, sheep, cows, ungulates, whales:
23
24 Purkinje Potential During VF!
25 V to PF Activation!
26 PF to V Pattern!
27 Focal PF Activation Pattern!
28
29 Lugol s Ablation! Caused VF to terminate after 4.9 min in treated hearts vs 9.2 min in control hearts
30 Eliminated the activation rate gradient
31 3-D Plunge Needle Mapping!
32
33 Intact Endocardial Mapping!
34
35
36 Purkinje in Defibrillation! Sinus SDVF Success LDVF Success SDVF Failure LDVF Failure
37 Purkinje System in LDVF:! 1.! Is a source of rapid activation in VF lasting more than 2-3 minutes 2.! Is the source of first postshock activation following long but not short duration VF
38 What next?!! Optical mapping of the Purkinje system and endocardium during LDVF! Mapping with pharmacological interventions! Pacing of Purkinje system! Mapping of human hearts! Improved modeling
39 Future of Cardiac Mapping!! Electrophysiological mapping combined with anatomical (CT, MRI) or functional imaging (DTI, SPECT or PET)! Electrical and optical mapping of arrythmogenic models (AF, HF, ischemia/reperfusion, pathologic ion channel conditions, genetic conditions, etc.)
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