Dynamic changes in cardiovascular and systemic parameters prior to sudden cardiac death in heart failure with reduced
Luis E Rohde1,2, Muthiah Vaduganathan1, Brian L Claggett1
1Division of Cardiovascular, Brigham and Women's Hospital, Boston, MA, USA.
Insights
Predicting sudden cardiac death (SCD) is improved by analyzing changes in patient data over time, not just single points. Time-varying factors like heart rate and biomarkers offer better risk assessment in heart failure patients.
Area of Science:
- Cardiology
- Biostatistics
- Medical Prognostics
Background:
- Sudden cardiac death (SCD) prediction models often rely on single time-point data.
- Integrating time-varying covariates can enhance the accuracy of prognostic assessments.
Purpose of the Study:
- To investigate independent predictors of SCD by incorporating time-varying data.
- To assess the impact of temporal changes in patient variables on SCD risk prediction.
Main Methods:
- Analysis of 8399 patients from the PARADIGM-HF trial.
- Utilized time-updated multivariable-adjusted Cox models, CART, and logistic regression.
- Examined temporal profiles of NYHA class, heart rate, and biomarkers.
Main Results:
- Distinct temporal profiles for SCD patients were observed over a year prior to the event.
- Seven time-updated variables independently predicted SCD risk.
- Classification and Regression Tree (CART) analysis identified baseline and time-updated covariates that improved risk stratification, with the highest risk group showing an eightfold increase in SCD hazard.
Conclusions:
- Changes over time in cardiac and systemic variables improve SCD risk prediction in chronic heart failure.
- Temporal data analysis helps differentiate the mode of death, distinguishing SCD from other cardiovascular causes.
Aims:
Prognostic models of sudden cardiac death (SCD) typically incorporate data at only a single time-point. We investigated independent predictors of SCD addressing the impact of integrating time-varying covariates to improve prediction assessment.
Methods And Results:
We studied 8399 patients enrolled in the PARADIGM-HF trial and identified independent predictors of SCD (n = 561, 36% of total deaths) using time-updated multivariable-adjusted Cox models, classification and regression tree (CART), and logistic regression analysis. Compared with patients who were alive or died from non-sudden cardiovascular deaths, patients who suffered a SCD displayed a distinct temporal profile of New York Heart Association (NYHA) class, heart rate and levels of three biomarkers (albumin, uric acid and total bilirubin), with significant differences observed more than 1 year prior to the event (Pinteraction < 0.001). In multivariable models adjusted for baseline covariates, seven time-updated variables independently contributed to SCD risk (incremental likelihood chi-square = 46.2). CART analysis identified that baseline variables (implantable cardioverter-defibrillator use and N-terminal prohormone of B-type natriuretic peptide levels) and time-updated covariates (NYHA class, total bilirubin, and total cholesterol) improved risk stratification. CART-defined subgroup of highest risk had nearly an eightfold increment in SCD hazard (hazard ratio 7.7, 95% confidence interval 3.6-16.5; P < 0.001). Finally, changes over time in heart rate, NYHA class, blood urea nitrogen and albumin levels were associated with differential risk of sudden vs. non-sudden cardiovascular deaths (P < 0.05).
Conclusions:
Beyond single time-point assessments, distinct changes in multiple cardiac-specific and systemic variables improved SCD risk prediction and were helpful in differentiating mode of death in chronic heart failure.
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