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Published on: February 17, 2018
Syncope predicts the outcome of cardiomyopathy patients: analysis of the SCD-HeFT study
Brian Olshansky1, Jeanne E Poole, George Johnson
1University of Iowa, Iowa City, Iowa, USA. brian-olshansky@uiowa.edu
Insights
Syncope in congestive heart failure patients predicts increased mortality risk, regardless of treatment. This finding highlights the importance of evaluating syncope in CHF patients for better outcomes.
Area of Science:
- Cardiology
- Clinical Electrophysiology
- Heart Failure Management
Background:
- The prognostic implications of syncope in congestive heart failure (CHF) patients remain incompletely understood.
- The Sudden Cardiac Death Heart Failure Trial (SCD-HeFT) provides a valuable dataset for investigating syncope in this population.
Purpose of the Study:
- To determine if syncope predicts adverse outcomes in patients with CHF.
- To analyze the association between syncope and mortality in CHF patients within the SCD-HeFT trial.
Main Methods:
- Analysis of data from the SCD-HeFT trial, comparing outcomes and clinical characteristics of patients with and without syncope.
- Statistical analysis including hazard ratios (HR) and 95% confidence intervals (CI) to assess risk factors and outcomes.
Main Results:
- Post-randomization syncope was associated with increased total and cardiovascular mortality (HR 1.41 and 1.55, respectively).
- Syncope predicted appropriate implantable cardioverter-defibrillator (ICD) discharges in the ICD arm (HR 2.91).
- The increased mortality risk associated with syncope did not significantly vary across treatment arms (ICD, amiodarone, placebo).
Conclusions:
- Syncope is associated with an increased risk of mortality in CHF patients, irrespective of treatment with ICD, amiodarone, or placebo.
- In CHF patients with ICDs, syncope correlates with appropriate ICD activations, suggesting its role as a marker for arrhythmic events.
Objectives:
The outcome of congestive heart failure (CHF) patients with syncope is understood incompletely.
Background:
We analyzed data from patients enrolled in the SCD-HeFT (Sudden Cardiac Death Heart Failure Trial) to determine whether syncope predicted outcomes in patients with CHF.
Methods:
We compared outcomes (and associated clinical characteristics) in patients with and without syncope enrolled in SCD-HeFT.
Results:
In SCD-HeFT, 162 (6%) patients had syncope before randomization, 356 (14%) had syncope after randomization (similar incidence in each randomized arm), and 46 (2%) had syncope before and after randomization. A QRS duration >or=120 ms and absence of beta-blocker use predicted syncope during follow-up (hazard ratio [HR] 1.30 and 95% confidence interval [CI] 1.06 to 1.61, p = 0.014 and HR 1.25, 95% CI 1.01 to 1.56, p = 0.048, respectively). Syncope recurrence did not differ by randomization arm. However, in the implantable cardioverter-defibrillator (ICD) arm, syncope, before and after randomization, was associated with appropriate ICD discharges (HR 1.75, 95% CI 1.10 to 2.80, p = 0.019 and HR 2.91, 95% CI 1.89 to 4.47, p = 0.001, respectively). Post-randomization syncope predicted total and cardiovascular death (HR 1.41, 95% CI 1.13 to 1.76, p = 0.002 and HR 1.55, 95% CI 1.19 to 2.02, p = 0.001, respectively). The elevated relative risk of mortality for syncope versus non-syncope patients did not vary significantly across treatment arms (ICD, HR 1.54, 95% CI 1.04 to 2.27; amiodarone, HR 1.33, 95% CI 0.91 to 1.93; and placebo, HR 1.39, 95% CI 0.96 to 2.02, test for difference p = 0.86).
Conclusions:
For CHF patients with ICDs, syncope was associated with appropriate ICD activations. Syncope was associated with increased mortality risk in SCD-HeFT regardless of treatment arm (placebo, amiodarone, or ICD).
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