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1 Physiology, Maastricht University, Maastricht, The Netherlands
2 Cardiology, Otto-von-Guericke-University, Magdeburg, Germany
3 Cardiac Research Management, Guidant Corporation, St. Paul, MN, USA
* To whom correspondence should be addressed. E-mail: frits.prinzen{at}fys.unimaas.nl.
Objective: To explore the use of interventricular asynchrony (interVA) for optimizing cardiac resynchronization therapy (CRT), an idea emerging from a simple pathway model of conduction in the ventricles. Methods: Measurements were performed in 6 dogs with chronic left bundle branch block (LBBB) and in 29 patients of the PATH-CHF-I study. In the dogs intraventricular asynchrony (intraVA) was determined using LV endocardial activation maps. In dogs and patients LVdP/dt|max, pulse pressure (PP) and interVA (time delay between upslope of LV and RV pressure curves) were measured during left (LV), right (RV) and bi-ventricular (BiV) pacing with various atrioventricular (AV-)delays. Results: Measurements in the canine hearts supported the pathway model in that optimal resynchronization occurred at ~50% reduction of intraVA and at an interVA value halfway that during LBBB and LV pacing. In patients with significant hemodynamic response during pacing (n=22) intrinsic interVA and interVA at peak improvement (interVAp) varied widely between patients (from -83ms to -15ms and from -42ms to +31ms, respectively). However, the model predicted individual interVAp accurately (SD ±6ms and ±12 ms for LVdP/dt|max and PP, respectively). At equal interVA, LV and BiV pacing produced equal hemodynamic response, but in 11/22 responders BiV pacing reduced interVA insufficiently to reach the maximum hemodynamic response. LV pacing at short AV-delay proved to result in better hemodynamics than predicted by the model, indicating that additional factors determine hemodynamics during LV pre-excitation. Conclusions: Guided by a simple pathway model, interVA measurements accurately predict optimal hemodynamic performance in individual CRT patients.
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