Echo response and clinical outcome in CRT patients

J van 't Sant1, T P Mast2, M M Bos2

  • 1Department of Cardiology, University Medical Center Utrecht, Heidelberglaan 100, 3584 CX, Utrecht, The Netherlands. j.vantsant@gmail.nl.

Insights

Left ventricular end-systolic volume change (∆LVESV) effectively predicts cardiac resynchronisation therapy (CRT) response in non-ischaemic cardiomyopathy. However, ∆LVESV is less reliable for ischaemic cardiomyopathy, where other markers may be more suitable.

Area of Science:

  • Cardiology
  • Biomedical Engineering
  • Medical Devices

Background:

  • Cardiac resynchronisation therapy (CRT) response is often assessed using changes in left ventricular end-systolic volume (∆LVESV).
  • The efficacy of ∆LVESV as a predictor of favourable outcomes in CRT patients requires further investigation, particularly across different aetiologies of heart failure.

Purpose of the Study:

  • To evaluate ∆LVESV as the optimal surrogate marker for predicting long-term outcomes following CRT.
  • To determine if the predictive value of ∆LVESV differs between patients with ischaemic and non-ischaemic cardiomyopathy.

Main Methods:

  • A cohort of 205 CRT patients underwent baseline and 6-month assessments, including echocardiography, exercise testing, and laboratory measurements.
  • Various parameters, including ∆LVESV, were analysed for their correlation with major adverse cardiac events (MACE) from 6 to 24 months post-CRT.

Main Results:

  • Major adverse cardiac events (MACE) occurred in 19% of patients (13% non-ischaemic, 24% ischaemic).
  • ∆LVESV was the sole significant surrogate marker for CRT response in the overall population (AUC 0.69) and non-ischaemic cardiomyopathy (AUC 0.850).
  • For ischaemic cardiomyopathy, ∆BNP demonstrated the highest predictive value (AUC 0.66).

Conclusions:

  • ∆LVESV is a robust surrogate marker for assessing CRT response and predicting long-term outcomes in patients with non-ischaemic cardiomyopathy.
  • The utility of ∆LVESV is limited in ischaemic cardiomyopathy, highlighting challenges in measuring CRT response in this patient group.
Abstract

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