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Published on: December 11, 2017
Mechanisms underlying improvements in ejection fraction with carvedilol in heart failure
Mathew S Maurer1, Jonathan D Sackner-Bernstein, Lyna El-Khoury Rumbarger
1Division of Cardiology, Columbia Presbyterian Medical Center, New York, NY, USA.
Insights
Beta-blocker therapy with carvedilol improved ejection fraction (EF) in heart failure patients. Heart rate reduction significantly contributed to these EF improvements, alongside increased contractility and reduced afterload.
Area of Science:
- Cardiology
- Pharmacology
Background:
- Beta-blocker therapy is linked to improved ejection fraction (EF) in heart failure.
- The specific mechanisms driving EF improvement (heart rate reduction, inotropism, afterload reduction, reverse remodeling) remain unclear.
Purpose of the Study:
- To quantify the contributions of heart rate (HR) reduction, contractility, and afterload reduction to EF improvements with carvedilol therapy.
Main Methods:
- Serial 3D echocardiography and blood pressure measurements were taken in 29 heart failure patients over 12 months.
- Left ventricular contractility, total peripheral resistance, and arterial elastance were derived from these measurements.
- Changes in EF were correlated with changes in HR, contractility, and peripheral resistance.
Main Results:
- Carvedilol therapy increased EF by 7 percentage points after 6 months (from 25% to 32%).
- This increase was primarily driven by stroke volume, with no significant change in end-diastolic volume.
- EF improvement correlated with decreased HR, increased contractility, and decreased total peripheral resistance.
Conclusions:
- Decreased heart rate accounted for approximately 60% of the EF increase.
- Improved chamber contractility contributed about 30%, and afterload reduction contributed less than 20%.
Background:
Reductions in heart rate (HR) with beta-blocker therapy have been associated with improvements in ejection fraction (EF). However, the relative contributions of HR reduction, positive inotropism, afterload reduction, and reverse remodeling to improvements in EF are unknown.
Methods And Results:
Twenty-nine patients (63+/-12 years old) with New York Heart Association class II-III heart failure underwent serial measurements of left ventricular volumes using 3-dimensional echocardiography and blood pressures by sphygmomanometry at baseline, 2 weeks, 2, 6, and 12 months after initiation of carvedilol. From these parameters, left ventricular contractility (indexed by the end-systolic pressure-volume ratio), total peripheral resistance, and effective arterial elastance (E(a)) were derived. Overall, EF increased by 7-percentage points after 6 months of therapy (from 25+/-9 to 32+/-9, P<0.0001). This change was due to an increase in stroke volume (P<0.001) with no significant change in end-diastolic volume (P=0.15). The EF change correlated with increased contractility, decreased HR and decreased total peripheral resistance (P<0.003 in each case). In those patients whose EF increased at least 5 points, approximately 60% of the increase was due to HR reduction, approximately 30% was due to increased contractility, and <20% was due to the decrease in total peripheral resistance.
Conclusions:
Decreased HR, improved chamber contractility and afterload reduction each contributed significantly to improved EF with carvedilol.
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