AHA 22: Late-Breaker Discussion: The STRONG-HF Trial
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AHA 22: Late-Breaker Discussion: The STRONG-HF Trial
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Late-breaker host Dr Harriette Van Spall (McMaster University, CA) is joined by Prof Alexandre Mebazaa (University Hospitals Saint Louis‐Lariboisière, FR), the primary investigator of the anticipated STRONG-HF Trial.
This study aimed to evaluate the safety and efficacy of rapid-optimization heart failure therapies. 1800 patients were randomized to receive either usual care or high-intensity care; with high-intensity care defined as an intensification of treatment with a beta-blocker, a renin-angiotensin system blocker, and a mineralocorticoid receptor blocker. Safety signals for heart failure were also assessed, and biomarkers and lab measures were frequently measured.
STRONG-HF was terminated early by the data safety monitoring board (DSMB) due to a significantly lower risk of the primary endpoint in the high-intensity care arm as compared to the usual care arm.
Recorded remotely from Hamilton and Paris, 2022.
This content is intended for healthcare professionals only.
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