CCS/CHFS Heart Failure Guidelines: Clinical Trial Update on Functional Mitral Regurgitation, SGLT2 Inhibitors, ARNI

Eileen O'Meara1, Michael McDonald2, Michael Chan3

  • 1Institut de Cardiologie de Montréal, Université de Montréal, Montréal, Québec, Canada.

Insights

New heart failure (HF) therapies show promise. Transcatheter mitral valve repair, transthyretin amyloidosis treatment, and sodium-glucose cotransport inhibitors offer improved outcomes for HF patients. Further research is needed for angiotensin receptor-neprilysin inhibitors in HF with preserved ejection fraction.

Area of Science:

  • Cardiology
  • Clinical Trials
  • Pharmacology

Background:

  • Heart failure (HF) management requires updated clinical guidance based on recent evidence.
  • Key therapeutic areas include valvular heart disease, cardiac amyloidosis, and HF with preserved and reduced ejection fraction.
  • Guideline-directed medical therapy and multidisciplinary approaches are crucial for optimal patient care.

Purpose of the Study:

  • To review recent clinical trials (post-2017) on selected HF therapies.
  • To provide evidence-based recommendations for managing patients considered for novel HF treatments.
  • To offer practical tips for healthcare providers treating diverse HF populations.

Main Methods:

  • Systematic review of clinical trials published after 2017 focusing on specific HF interventions.
  • Analysis of evidence for transcatheter mitral valve repair, transthyretin cardiac amyloidosis treatment, ARNI therapy in HFpEF, and SGLT inhibitors in HF.
  • Emphasis on guideline-directed medical therapy and multidisciplinary team roles.

Main Results:

  • Transcatheter mitral valve repair requires optimal guideline-directed medical therapy and multidisciplinary evaluation.
  • Tafamidis is the first agent to demonstrate outcome improvement in transthyretin cardiac amyloidosis.
  • Sacubitril/valsartan may benefit subgroups of HFpEF patients, but further data are needed.
  • Sodium-glucose cotransport inhibitors (e.g., dapagliflozin) reduce HF risk, hospitalizations, and cardiovascular death in patients with and without type 2 diabetes, including those with HF with reduced ejection fraction.

Conclusions:

  • Healthcare providers should consider cardiac amyloidosis in patients with suggestive clinical signs.
  • Tafamidis offers a new therapeutic option for transthyretin cardiac amyloidosis.
  • The role of sacubitril/valsartan in HFpEF requires further investigation.
  • Sodium-glucose cotransport inhibitors are beneficial for HF prevention and treatment across various patient groups, including those with HF with reduced ejection fraction.

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