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J Am Coll Cardiol, 2002; 40:1067-1074
© 2002 by the American College of Cardiology Foundation
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Electromechanical mapping for determination of myocardial contractility and viability

A comparison with echocardiography, myocardial single-photon emission computed tomography, and positron emission tomography

Andreas Keck, MD*, Klaus Hertting, MD*, Yitzhack Schwartz, MD{dagger}, Roland Kitzing, MD*, Michael Weber, MD*, Bernhard Leisner, MD*, Christian Franke, MD{ddagger}, Edda Bahlmann, MD*, Carsten Schneider, MD*, Thomas Twisselmann, MD*, Michael Weisbach, MD*, Robert Küchler, MD* and Karl Heinz Kuck, MD*,*

* St. Georg Hospital, Hamburg, Germany
{dagger} Rambam Medical Center, Haifa, Israel
{ddagger} PET Study Group, Hamburg, Germany



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Figure 1 A zone map demonstrating the transcription of the three-dimensional NOGA map (right anterior oblique view) into a regional bull’s-eye projection. Each of the nine segments is colored differently (i.e., the apical zone is red). A = anterior; L = lateral; P = posterior; S = septal.

 


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Figure 2 A grid composed of rectangles. After an initial flexible distortion, the model was matched to the sampled points and final smoothing was obtained by applying a surface convolution and matching a grid node for each sample and moving that node to the sample location. Each grid point then received a value proportional to its distance from the neighboring points and their values, using color interpolation and smoothing.

 


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Figure 3 Correlation between NOGA parameters and echocardiography (echo). 1 = normokinesia; 2 = hypokinesia; 3 = akinesia; 4 = dyskinesia. Data are expressed as the mean value ± SD. FI = fragmentation index; LLS = linear local shortening; UV = unipolar voltage.

 


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Figure 4 Correlation between NOGA parameters and single-photon emission computed tomography (SPECT) perfusion results. Data are expressed as the mean value ± SD. FI = fragmentation index; LLS = linear local shortening; UV = unipolar voltage.

 


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Figure 5 Analysis of fixed perfusion defects by positron emission tomography (PET). A desired specificity of 90% defines a lower threshold of 4.5 mV for PET and 6 mV for single-photon emission computed tomography (SPECT). Thus, the unipolar voltage can differentiate between viable and non-viable fixed perfusion defects.

 


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Figure 6 A NOGA unipolar voltage (UV) map from a 69-year-old man with an inferior infarction six years ago and an anteroseptal infarction five years ago. The single-photon emission computed tomography (SPECT) images reveal an anteroseptal perfusion defect; the positron emission tomography (PET) polar map shows normal glucose uptake (blue) anteriorly but no glucose uptake (orange) apicoseptally. Viability assessment with the NOGA system (anteroseptal view at a slight craniocaudal angle on the UV map) provided the following information: the territory of the fixed perfusion defect is precisely depicted by voltage values <6 mV. The truly non-viable myocardium, as demonstrated by PET, is characterized by voltage values <4.5 mV; the green zone (4.5–6.0 mV) indicates viable myocardium that may benefit from revascularization.

 




 
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