2009
DOI: 10.1515/bmt.2009.013
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Concurrent optimization of timing delays and electrode positioning in biventricular pacing based on a computer heart model assuming 17 left ventricular segments

Abstract: This work proposes a novel non-invasive optimization algorithm to find the best electrode positioning sites and timing delays for BVP in patients with LBBB and MI. This algorithm can be used to plan an optimal therapy for an individual patient.

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Cited by 7 publications
(7 citation statements)
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“…Biophysical models of the heart have been used to optimize AVD, VVD and lead location during CRT simulation (Miri et al, 2008, 2009a,b; Pluijmert et al, 2016; Lee et al, 2017). QRSd, estimated as the difference between the time of the first and last activated cardiac cell (or TAT), have been used as one optimization criterion by Miri and coworkers.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Biophysical models of the heart have been used to optimize AVD, VVD and lead location during CRT simulation (Miri et al, 2008, 2009a,b; Pluijmert et al, 2016; Lee et al, 2017). QRSd, estimated as the difference between the time of the first and last activated cardiac cell (or TAT), have been used as one optimization criterion by Miri and coworkers.…”
Section: Discussionmentioning
confidence: 99%
“…A different criterion suggested in the literature is to place the LV lead in the site corresponding to the shortest QRS registered. Nevertheless, simulation studies that apply this last non-invasive criterion (Miri et al, 2009a,b) estimated QRSd through calculation of the total ventricular activation time (TAT), a parameter not easily accessible in clinical or even experimental settings. In addition, studies such as Potse et al (2012) have observed that biventricular pacing did not change QRS duration but reduced total ventricular activation time when the stimulation was applied in one point of the LV free wall.…”
Section: Introductionmentioning
confidence: 99%
“…The third category considers cardiac output estimated by Swan-Ganz catheterization, thoracic impedance, ultrasonography, and other techniques [55,57,58,[64][65][66][67][68][69][70]. The fourth category eliminates individual optimization and uses a standard value because these methods acknowledge no major differences in VV delay settings [3,35,[71][72][73][74][75][76][77][78][79][80][81][82].…”
Section: Categorization Of Vv Delay Optimization Methodsmentioning
confidence: 99%
“…With a similar goal, cellular automaton models [ 69 ] have also been employed in recent CRT studies [ 70 73 ]. In this model, instead of explicitly solving the complex current flow interaction between the intracellular and extracellular domains, action potentials are pre-calculated based on ionic current equations.…”
Section: Electrophysiology Modelsmentioning
confidence: 99%
“…These models offer the opportunity to carry out non-invasive, automatic optimization of CRT in silico. Briefly, the approach consists of simulating electrical activation in a realistic BiV anatomy for different AVD and VVD as well as several different lead locations and minimizing the error between the obtained activation sequences for each case against a simulated physiological case to determine which combination of AVD, VVD, and lead location yields the best acute response to CRT [ 70 73 , 81 ]. Such models have demonstrated that patient-specific optimization of lead location and AVD and VVD can improve CRT efficacy and impact treatment success [ 31 , 70 , 73 ] and that the use of body surface potential maps can further improve in-silico CRT optimization [ 82 ].…”
Section: Electrophysiology Modelsmentioning
confidence: 99%