Effects of Arnica comp.-Heel® on reducing cardiovascular events in patients with stable coronary disease

Massimo Fioranelli1, Maria Bianchi, Maria G Roccia

  • 1G. Marconi University, Rome, Italy - massimo.fioranelli@gmail.com.

Insights

Adding Arnica comp.-Heel® to standard therapy significantly reduced cardiovascular events in stable coronary artery disease patients. This anti-inflammatory treatment shows promise for secondary prevention, lowering event rates effectively.

Area of Science:

  • Cardiology
  • Pharmacology
  • Inflammation Research

Background:

  • Atherosclerotic plaques in stable coronary artery disease (CAD) feature inflammatory cells.
  • Inhibiting inflammation may reduce plaque instability and cardiovascular events.
  • Arnica comp.-Heel® is a low-dose, multi-component medication with anti-inflammatory properties.

Purpose of the Study:

  • To assess the efficacy of daily Arnica comp.-Heel® tablets in reducing cardiovascular events in stable CAD patients.
  • To investigate the anti-inflammatory potential of Arnica comp.-Heel® in cardiovascular disease secondary prevention.

Main Methods:

  • Retrospective observational study of 44 stable CAD patients.
  • Group 1 (n=25): Standard therapy (aspirin/clopidogrel + statins).
  • Group 2 (n=18): Standard therapy + Arnica comp.-Heel® (1 tablet/day).
  • Primary outcome: Incidence of acute coronary syndrome, out-of-hospital cardiac arrest, or ischemic stroke.

Main Results:

  • One cardiovascular event (5.6%) in the Arnica comp.-Heel® group.
  • Four cardiovascular events (16%) in the standard therapy group.
  • A notable reduction in cardiovascular events with the addition of Arnica comp.-Heel®.

Conclusions:

  • Arnica comp.-Heel® (1 tablet/day) combined with standard therapies is effective for secondary prevention in stable CAD.
  • The treatment reduces the incidence of cardiovascular events in patients with stable coronary artery disease.
  • Anti-inflammatory treatment with Arnica comp.-Heel® may improve clinical outcomes in stable CAD.
Abstract

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