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Optimization of CRT programming using non‐invasive electrocardiographic imaging to assess the acute electrical effects of multipoint pacing
Author(s) -
Sieniewicz Benjamin J.,
Jackson Tom,
Claridge Simon,
Pereira Helder,
Gould Justin,
Sidhu Baldeep,
Porter Bradley,
Niederer Steve,
Yao Cheng,
Rinaldi Christopher A.
Publication year - 2019
Publication title -
journal of arrhythmia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.463
H-Index - 21
eISSN - 1883-2148
pISSN - 1880-4276
DOI - 10.1002/joa3.12153
Subject(s) - cardiac resynchronization therapy , medicine , ventricle , cardiology , lead (geology) , heart failure , ejection fraction , geomorphology , geology
Aim Quadripolar lead technology and multi‐point pacing ( MPP ) are important clinical adjuncts in cardiac resynchronization therapy ( CRT ) pacing aimed at reducing the rate of non‐response to therapy. Mixed results have been achieved using MPP and it is critical to identify which patients require this approach and how to configure their MPP stimulation, in order to achieve optimal electrical resynchronization. Methods & Results We sought to investigate whether electrocardiographic imaging ( ECG i), using the CARDIOINSIGHT ™ inverse ECG mapping system, could identify alterations in electrical resynchronization during different methods of device optimization. In no patient did a single form of programming optimization provide the best electrical response. The effects of utilizing MPP were idiosyncratic and highly patient specific. ECG i activation maps were clearly able to discern changes in bulk LV activation during differing MPP programming. In two of the five subjects, MPP resulted in more rapid activation of the left ventricle compared to standard CRT ; however, in the remaining three patients, the use of MPP did not appear to acutely improve electrical resynchronization. Crucially, this cohort showed evidence of extensive LV scarring which was well visualized using both CMR and ECG i voltage mapping. Conclusions Our work suggests a potential role for ECG i in the optimization of non‐responders to CRT , as it allows the fusion of activation maps and scar analysis above and beyond interrogation of the 12 lead ECG .

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