Key result
Pacing with a single population-optimised quadripolar lead design achieved electrical resynchronization with near equivalence to personalised lead designs in both heart failure and reverse remodelled anatomies.
Why the study?
Lead position determines CRT response in dyssynchronous HF, and MPP allows pacing from multiple electrodes, but the design of optimal quadripolar pacing leads across HF and reverse remodelled anatomies remains to be evaluated.
Does multipoint pacing with optimal quadripolar lead designs improve electrical synchrony in virtual cohorts of heart failure and reverse remodelled patients?
Does multipoint pacing with optimal quadripolar lead designs improve electrical synchrony in virtual cohorts of heart failure and reverse remodelled patients?
A single optimal quadripolar lead design provides near-optimal electrical resynchronization across both heart failure and reverse-remodelled anatomies, suggesting patient-specific lead designs may not be necessary if pacing vectors can be reprogrammed.
Answers are grounded in this paper and cite their sources.
May simplify CRT lead selection in models; leaves open human validation of fixed quadripolar designs.
Lead position is an important factor in determining response to Cardiac Resynchronization Therapy (CRT) in dyssynchronous heart failure (HF) patients. Multipoint pacing (MPP) enables pacing from multiple electrodes within the same lead, improving the potential outcome for patients. Virtual quadripolar lead designs were evaluated by simulating pacing from all combinations of 1 and 2 electrodes along the lead in each virtual patient from cohorts of HF (n = 24) and simulated reverse remodelled (RR, n = 20) patients. Electrical synchrony was assessed by the time 90% of the ventricular myocardium is activated (AT090). Optimal 1 and 2 electrode pacing configurations for AT090 were combined to identify the 4-electrode lead design that maximised benefits across all patients. LV pacing in the HF cohort in all possible single and double electrode locations reduced AT090 by 14.48 ± 5.01 ms (11.92 ± 3.51%). The major determinant of reduction in activation time was patient anatomy. Pacing with a single optimal lead design reduced AT090 more in the HF cohort than the RR cohort (12.68 ± 3.29% vs 10.81 ± 2.34%). Pacing with a single combined HF and RR population-optimised lead design achieves electrical resynchronization with near equivalence to personalised lead designs both in HF and RR anatomies. These findings suggest that although lead configurations have to be tailored to each patient, a single optimal lead design is sufficient to obtain near-optimal results across most patients. This study shows the potential of virtual clinical trials as tools to compare existing and explore new lead designs.
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Rodero et al. (2021) studied Dyssynchronous heart failure (n=44). Virtual quadripolar lead pacing (Multipoint pacing) vs. RV pacing alone or personalised lead designs was evaluated on Reduction in time taken to activate 90% of the volume of the biventricular myocardium (AT090) (p=<0.01). Pacing with a single population-optimised quadripolar lead design achieved electrical resynchronization with near equivalence to personalised lead designs in both heart failure and reverse remodelled anatomies.
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