Why the study?
Current guidelines lack sex-specific treatment recommendations, highlighting the need to emphasize female enrollment in HF trials and explore optimal tailored medication dosages.
Should heart failure medication dosages be tailored based on sex to improve clinical endpoints and quality of life in women with HFrEF?
Should heart failure medication dosages be tailored based on sex to improve clinical endpoints and quality of life in women with HFrEF?
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This review highlights the underrepresentation of women in heart failure trials and advocates for sex-specific tailored dosing to optimize treatment effectiveness and quality of life.
PURPOSE OF THE REVIEW: This narrative review will emphasize the necessity for more female enrollment in heart failure (HF) trials and proposes future investigations regarding optimal dosages. Ultimately, a deeper understanding of the unique pathophysiology and medication responses in both men and women is crucial for effective HF management and may improve the quality of life in women. RECENT FINDINGS: An analysis of 740 cardiovascular studies reveals that women make up only 38.2% of participants on average. Regarding to trials testing the effectiveness of HF medications, women's involvement are as low as 23.1%. While current guidelines lack sex-specific treatment recommendations, emerging research suggests differential medication dosages could be beneficial. Studies indicate that women may achieve comparable outcomes with lower doses of certain medications (angiotensin-receptor blockers) compared to men, signaling potential for more tailored dosing approaches. We advocate that the next step in HF research should prioritize the importance of tailoring treatment for HF patients by taking into account the variations in drug absorption and distribution among women.
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Aydın et al. (2023) studied this question.
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