Dual vs triple antithrombotic therapy in atrial fibrillation and acute coronary syndrome: An updated meta-analysis of

Enkhtsogt Sainbayar1, Hoang Nhat Pham1, April Olson1

  • 1Department of Medicine, UA College of Medicine, University of Arizona Tucson, Tucson, AZ, USA.

Insights

Dual antithrombotic therapy (DAT) in atrial fibrillation (AF) and acute coronary syndrome (ACS) patients shows reduced bleeding risk compared to triple antithrombotic therapy (TAT). No significant differences were observed in major adverse cardiac events, myocardial infarction, or stroke.

Area of Science:

  • Cardiology
  • Pharmacology
  • Clinical Trials

Background:

  • Managing antithrombotic treatment in patients with both atrial fibrillation (AF) and acute coronary syndrome (ACS) presents a clinical challenge.
  • Comparing dual antithrombotic therapy (DAT) with triple antithrombotic therapy (TAT) is crucial for optimizing patient outcomes.

Purpose of the Study:

  • To compare the efficacy and safety of dual antithrombotic therapy (DAT) versus triple antithrombotic therapy (TAT) in patients with AF and ACS.
  • To evaluate outcomes including major adverse cardiac events (MACE), bleeding, stroke, stent thrombosis, and myocardial infarction (MI).

Main Methods:

  • A systematic review and meta-analysis of randomized controlled trials (RCTs) comparing DAT (DOACs/warfarin + antiplatelets) with TAT (DOACs/warfarin, aspirin, P2Y12 inhibitor).
  • Searched multiple databases from inception to December 17, 2023.
  • Analyzed outcomes using a random-effects model, estimating relative risks and 95% confidence intervals.

Main Results:

  • Ten RCTs involving 6186 patients on TAT and 6800 patients on DAT were included.
  • DAT was associated with significantly lower rates of bleeding events compared to TAT across 3, 6, and 12-month durations (RR 0.69, 0.65, 0.62 respectively).
  • No significant differences were found between DAT and TAT for MACE, MI, stroke, or stent thrombosis.

Conclusions:

  • Dual antithrombotic therapy (DAT) is associated with a reduced risk of bleeding in patients with atrial fibrillation and acute coronary syndrome compared to triple antithrombotic therapy (TAT).
  • DAT offers a favorable safety profile without compromising efficacy regarding major adverse cardiac events, myocardial infarction, or stroke.

Related Concept Videos

Anticoagulant Drugs: Vitamin K Antagonists and Direct Oral Anticoagulants01:18

Anticoagulant Drugs: Vitamin K Antagonists and Direct Oral Anticoagulants

Oral anticoagulants are vital tools in preventing and treating blood clotting disorders. This diverse class of medications can be categorized as vitamin K antagonists, exemplified by warfarin, and direct thrombin inhibitors (DTIs), such as dabigatran, as well as factor Xa inhibitors, including rivaroxaban.
Warfarin, a prominent vitamin K antagonist family member, exerts its effect by inhibiting the enzyme VKORC1 (vitamin K epoxide reductase complex 1). By hindering this enzyme, warfarin...
1.2K
Anticoagulant Drugs: Low-Molecular-Weight Heparins01:30

Anticoagulant Drugs: Low-Molecular-Weight Heparins

Hemostasis is a crucial process that prevents excessive blood loss from damaged blood vessels. It involves various mechanisms such as vasoconstriction, platelet adhesion and activation, and fibrin formation. The importance of each mechanism depends on the type of vessel injury. In contrast, thrombosis is the abnormal formation of a blood clot within the blood vessels, leading to potential complications if the clot obstructs blood flow. Thrombosis can be caused by increased coagulability of the...
659
Antiplatelet Drugs: Prostaglandin Synthesis, P2Y12 and Glycoprotein IIb/IIIa Inhibitors01:20

Antiplatelet Drugs: Prostaglandin Synthesis, P2Y12 and Glycoprotein IIb/IIIa Inhibitors

Antiplatelet drugs emerge as frontline defenders against the insidious threat of thromboembolic diseases, where abnormal clots obstruct vital blood vessels. These drugs stand as bulwarks, inhibiting platelet aggregation and clot formation, thereby mitigating the risk of life-threatening conditions like myocardial infarction, coronary artery disease, and thrombotic strokes.
Prostaglandin synthesis inhibitors, exemplified by the widely known aspirin, wield their power by irreversibly acetylating...
505
Antianginal Drugs: Calcium Channel Blockers and Ranolazine01:25

Antianginal Drugs: Calcium Channel Blockers and Ranolazine

Angina pectoris, a primary symptom of ischemic heart disease, requires careful pharmacological interventions. In this context, calcium channel blockers (CCBs) and ranolazine have emerged as crucial pharmacotherapeutic agents, providing deep insights into the complexities of angina management.
CCBs, a diverse class that includes dihydropyridines (nifedipine) and diphenylalkylamines (verapamil and diltiazem), exert their effect by blocking calcium channels in cardiac and smooth muscle cells. This...
481
Heart Failure Drugs: Inhibitors of Renin-Angiotensin System01:26

Heart Failure Drugs: Inhibitors of Renin-Angiotensin System

The activation of the sympathetic nervous system and the renin-angiotensin-aldosterone system (RAAS) contributes to cardiac remodeling, and inhibiting the RAAS is a pharmacological target in heart failure management. As a result, neurohumoral modulation is a crucial treatment principle for managing heart failure. This approach involves using medications like ACE inhibitors (ACEIs), angiotensin receptor blockers (ARBs), β-blockers, mineralocorticoid receptor antagonists (MRAs), and neutral...
413