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Characterizing left ventricular mechanical and electrical activation in patients with normal and impaired systolic function using a non-fluoroscopic cardiovascular navigation system
Authors:Christopher Piorkowski  Arash Arya  Craig D. Markovitz  Hedi Razavi  Chunlan Jiang  Stuart Rosenberg  Ole-A. Breithardt  Sascha Rolf  Silke John  Jedrzej Kosiuk  Yan Huo  Michael Döring  Sergio Richter  Kyungmoo Ryu  Thomas Gaspar  Frits W. Prinzen  Gerhard Hindricks  Philipp Sommer
Affiliation:1.Department of Invasive Electrophysiology,University of Dresden-Heart Center,Dresden,Germany;2.Department of Electrophysiology,University of Leipzig-Heart Center,Leipzig,Germany;3.Abbott,Sylmar,USA;4.Agaplesion Diakonie Kliniken,Kassel,Germany;5.DRK Kliniken Berlin Westend,Berlin,Germany;6.Department of Physiology, Cardiovascular Research Institute Maastricht,Maastricht University,Maastricht,The Netherlands
Abstract:

Purpose

Cardiac disease frequently has a degenerative effect on cardiac pump function and regional myocardial contraction. Therefore, an accurate assessment of regional wall motion is a measure of the extent and severity of the disease. We sought to further validate an intra-operative, sensor-based technology for measuring wall motion and strain by characterizing left ventricular (LV) mechanical and electrical activation patterns in patients with normal (NSF) and impaired systolic function (ISF).

Methods

NSF (n?=?10; ejection fraction?=?62.9?±?6.1%) and ISF (n?=?18; ejection fraction?=?35.1?±?13.6%) patients underwent simultaneous electrical and motion mapping of the LV endocardium using electroanatomical mapping and navigational systems (EnSite? NavX? and MediGuide?, Abbott). Motion trajectories, strain profiles, and activation times were calculated over the six standard LV walls.

Results

NSF patients had significantly greater motion and systolic strains across all LV walls than ISF patients. LV walls with low-voltage areas showed less motion and systolic strain than walls with normal voltage. LV electrical dyssynchrony was significantly smaller in NSF and ISF patients with narrow-QRS complexes than ISF patients with wide-QRS complexes, but mechanical dyssynchrony was larger in all ISF patients than NSF patients. The latest mechanical activation was most often the lateral/posterior walls in NSF and wide-QRS ISF patients but varied in narrow-QRS ISF patients.

Conclusions

This intra-operative technique can be used to characterize LV wall motion and strain in patients with impaired systolic function. This technique may be utilized clinically to provide individually tailored LV lead positioning at the region of latest mechanical activation for patients undergoing cardiac resynchronization therapy.

Clinical trial registration

URL: http://www.clinicaltrials.gov. Unique identifier: NCT01629160.
Keywords:
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