4.5 Article

Sex- and age-related differences in the management and outcomes of chronic heart failure: an analysis of patients from the ESC HFA EORP Heart Failure Long-Term Registry

Journal

EUROPEAN JOURNAL OF HEART FAILURE
Volume 22, Issue 1, Pages 92-102

Publisher

WILEY
DOI: 10.1002/ejhf.1645

Keywords

Age; Sex; Mortality; Hospitalization; Registry

Funding

  1. Abbott Vascular International
  2. Amgen Cardiovascular
  3. AstraZeneca
  4. Bayer AG
  5. Boehringer Ingelheim
  6. Boston Scientific
  7. Bristol-Myers Squibb
  8. Pfizer Alliance
  9. Daiichi Sankyo Europe GmbH
  10. Eli Lilly & Company Alliance
  11. Edwards
  12. Gedeon Richter
  13. Menarini International Operations
  14. MSD-Merck Co.
  15. Novartis Pharma AG
  16. ResMed
  17. Sanofi
  18. Servier
  19. Vifor

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Aims This study aimed to assess age- and sex-related differences in management and 1-year risk for all-cause mortality and hospitalization in chronic heart failure (HF) patients. Methods and results Of 16 354 patients included in the European Society of Cardiology Heart Failure Long-Term Registry, 9428 chronic HF patients were analysed [median age: 66 years; 28.5% women; mean left ventricular ejection fraction (LVEF) 37%]. Rates of use of guideline-directed medical therapy (GDMT) were high (angiotensin-converting enzyme inhibitors/angiotensin receptor blockers, beta-blockers and mineralocorticoid receptor antagonists: 85.7%, 88.7% and 58.8%, respectively). Crude GDMT utilization rates were lower in women than in men (all differences: P <= 0.001), and GDMT use became lower with ageing in both sexes, at baseline and at 1-year follow-up. Sex was not an independent predictor of GDMT prescription; however, age >75 years was a significant predictor of GDMT underutilization. Rates of all-cause mortality were lower in women than in men (7.1% vs. 8.7%; P = 0.015), as were rates of all-cause hospitalization (21.9% vs. 27.3%; P < 0.001) and there were no differences in causes of death. All-cause mortality and all-cause hospitalization increased with greater age in both sexes. Sex was not an independent predictor of 1-year all-cause mortality (restricted to patients with LVEF <= 45%). Mortality risk was significantly lower in patients of younger age, compared to patients aged >75 years. Conclusions There was a decline in GDMT use with advanced age in both sexes. Sex was not an independent predictor of GDMT or adverse outcomes. However, age >75 years independently predicted lower GDMT use and higher all-cause mortality in patients with LVEF <= 45%.

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