TY - JOUR
T1 - Long-Term Reverse Remodeling With Cardiac Resynchronization Therapy. Results of Extended Echocardiographic Follow-Up
AU - Verhaert, David
AU - Grimm, Richard A.
AU - Puntawangkoon, Chirapa
AU - Wolski, Kathy
AU - De, Sabe
AU - Wilkoff, Bruce L.
AU - Starling, Randall C.
AU - Tang, W. H Wilson
AU - Thomas, James D.
AU - Popović, Zoran B.
PY - 2010/4/27
Y1 - 2010/4/27
N2 - Objectives: The purpose of this study was to describe the long-term course of left ventricular remodeling induced by cardiac resynchronization therapy (CRT), adjusting for the confounding effect of patient loss due to disease. Background: Reverse remodeling has been identified as the primary mechanism of improved symptoms and outcome in heart failure patients. Methods: A total of 313 consecutive patients who underwent CRT with available baseline echocardiograms and subsequent clinical and echocardiographic follow-up were included in the analysis. Long-term follow-up included all-cause mortality, heart transplantation, and implantation of a left ventricular assist device. Longitudinal data analysis of left ventricular end-systolic volume index (LVESVi) was performed to adjust for the confounding effect of patient loss during follow-up. Results: Patients with uneventful survival had a lower baseline LVESVi (Δ = 8.6 ml/m2, SE = 4.6 ml/m2, p < 0.0001) and a decreased LVESVi by -0.11 ml/m2/day during first 6 months, whereas the LVESVi remained unchanged in patients with adverse events (p < 0.0001). Beyond 6 months, the LVESVi remained unchanged in patients with uneventful survival, whereas the LVESVi continued to increase in those with adverse events at a rate of 0.01 ml/m2/day (p < 0.0001). Predictors of reverse remodeling were nonischemic etiology, female sex, and a wider QRS duration (p < 0.0001, p = 0.014, and p = 0.001, respectively). In the majority of patients, 6 months indicates a break point after which reverse remodeling becomes significantly less pronounced. Conclusions: CRT patients with uneventful survival show a significant decrease in the LVSVi at 6 months and generally maintain this response in the long term. Those with adverse outcomes are characterized by left ventricular dilation despite CRT.
AB - Objectives: The purpose of this study was to describe the long-term course of left ventricular remodeling induced by cardiac resynchronization therapy (CRT), adjusting for the confounding effect of patient loss due to disease. Background: Reverse remodeling has been identified as the primary mechanism of improved symptoms and outcome in heart failure patients. Methods: A total of 313 consecutive patients who underwent CRT with available baseline echocardiograms and subsequent clinical and echocardiographic follow-up were included in the analysis. Long-term follow-up included all-cause mortality, heart transplantation, and implantation of a left ventricular assist device. Longitudinal data analysis of left ventricular end-systolic volume index (LVESVi) was performed to adjust for the confounding effect of patient loss during follow-up. Results: Patients with uneventful survival had a lower baseline LVESVi (Δ = 8.6 ml/m2, SE = 4.6 ml/m2, p < 0.0001) and a decreased LVESVi by -0.11 ml/m2/day during first 6 months, whereas the LVESVi remained unchanged in patients with adverse events (p < 0.0001). Beyond 6 months, the LVESVi remained unchanged in patients with uneventful survival, whereas the LVESVi continued to increase in those with adverse events at a rate of 0.01 ml/m2/day (p < 0.0001). Predictors of reverse remodeling were nonischemic etiology, female sex, and a wider QRS duration (p < 0.0001, p = 0.014, and p = 0.001, respectively). In the majority of patients, 6 months indicates a break point after which reverse remodeling becomes significantly less pronounced. Conclusions: CRT patients with uneventful survival show a significant decrease in the LVSVi at 6 months and generally maintain this response in the long term. Those with adverse outcomes are characterized by left ventricular dilation despite CRT.
KW - cardiac resynchronization therapy
KW - heart failure
KW - remodeling
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U2 - 10.1016/j.jacc.2010.01.022
DO - 10.1016/j.jacc.2010.01.022
M3 - Article
C2 - 20413027
AN - SCOPUS:77950878885
SN - 0735-1097
VL - 55
SP - 1788
EP - 1795
JO - Journal of the American College of Cardiology
JF - Journal of the American College of Cardiology
IS - 17
ER -