Ventricular force-frequency relationships during biventricular or multisite pacing in congenital heart disease

Congenit Heart Dis. 2019 Mar;14(2):201-206. doi: 10.1111/chd.12684. Epub 2018 Oct 15.

Abstract

Background: Traditional indices to evaluate biventricular (BiV) pacing are load dependent, fail to assess dynamic changes, and may not be appropriate in patients with congenital heart disease (CHD). We therefore measured the force-frequency relationship (FFR) using tissue Doppler-derived isovolumic acceleration (IVA) to assess the dynamic adaption of the myocardium and its variability with different ventricular pacing strategies.

Methods: This was a prospective pilot study of pediatric and young adult CHD patients with biventricular or multisite pacing systems. Color-coded myocardial velocities were recorded at the base of the systemic ventricular free wall. IVA was calculated at resting heart rate and with incremental pacing. FFR curves were obtained by plotting IVA against heart rate for different ventricular pacing strategies.

Results: Ten patients were included (mean: 22 ± 7 years). The FFR identified a best and worst ventricular pacing strategy for each patient, based on the AUC at baseline, submaximal, and peak heart rates (P < .001). However, there was no single best ventricular pacing strategy that was optimal for all patients. Additionally, the best ventricular pacing strategy often differed within the same patient at different heart rates.

Conclusion: This novel assessment demonstrates a wide variability in optimal ventricular pacing strategy. These inherent differences may play a role in the unpredictable clinical response to BiV pacing in CHD, and emphasizes an individualized approach. Furthermore, the optimal ventricular pacing varies with heart rate within individuals, suggesting that rate-responsive ventricular pacing modulation may be required to optimize ventricular performance.

Keywords: biventricular pacing; cardiac resynchronization therapy; congenital heart disease; force-frequency relationship; multisite pacing; ventricular function.

MeSH terms

  • Adolescent
  • Adult
  • Cardiac Pacing, Artificial / methods*
  • Child
  • Cross-Sectional Studies
  • Echocardiography, Doppler
  • Female
  • Follow-Up Studies
  • Heart Defects, Congenital / diagnosis
  • Heart Defects, Congenital / physiopathology
  • Heart Defects, Congenital / therapy*
  • Heart Rate / physiology*
  • Heart Ventricles / diagnostic imaging
  • Heart Ventricles / physiopathology*
  • Humans
  • Male
  • Myocardial Contraction / physiology*
  • Pilot Projects
  • Prospective Studies
  • Time Factors
  • Treatment Outcome
  • Ventricular Function, Left / physiology
  • Young Adult