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DAPT Duration

Abstract

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Consensus Document ANMCO/ANCE/ARCA/GICR-IACPR/GISE/SICOA: Long-term Antiplatelet Therapy in Patients with Coronary Artery Disease Pooled Analysis of Bleeding, Major Adverse Cardiovascular Events, and All-Cause Mortality in Clinical Trials of Time-Constrained Dual-Antiplatelet Therapy After Percutaneous Coronary Intervention Safety and efficacy of the bioabsorbable polymer everolimus-eluting stent versus durable polymer drug-eluting stents in high-risk patients undergoing PCI: TWILIGHT-SYNERGY Trial Design Principles for Patients at High Bleeding Risk Undergoing PCI: JACC Scientific Expert Panel Global Approach to High Bleeding Risk Patients With Polymer-Free Drug-Coated Coronary Stents: The LF II Study Long-term dual antiplatelet-induced intestinal injury resulting in translocation of intestinal bacteria into blood circulation increased the incidence of adverse events after PCI in patients with coronary artery disease Aspirin-Free Prasugrel Monotherapy Following Coronary Artery Stenting in Patients With Stable CAD: The ASET Pilot Study Ticagrelor Monotherapy Versus Dual-Antiplatelet Therapy After PCI: An Individual Patient-Level Meta-Analysis

Original ResearchVolume 12, Issue 10, May 2019

JOURNAL:JACC Cardiovasc Interv. Article Link

Dual-Antiplatelet Therapy Cessation and Cardiovascular Risk in Relation to Age: Analysis From the PARIS Registry

Joyce LC, Baber U, Mehran R et al. Keywords: DAPT; therapy cessation; PCI; age

ABSTRACT


OBJECTIVES- The aim of this study was to examine the association between dual-antiplatelet therapy (DAPT) cessation and cardiovascular risk after percutaneous coronary intervention in relation to age.

 

BACKGROUND - Examination of outcomes by age after percutaneous coronary intervention is relevant given the aging population.

 

METHODS- Two-year clinical outcomes, incidence, and effect of DAPT cessation on outcomes were compared by ages 55, 56 to 74, and 75 years from the PARIS (Patterns of Non-Adherence to Antiplatelet Regimens in Stented Patients) registry. DAPT cessation included physician-recommended discontinuation, interruption for surgery, and disruption (from noncompliance or bleeding). Clinical endpoints were major adverse cardiac events (MACE) (a composite of cardiac death, definite or probable stent thrombosis, spontaneous myocardial infarction, or clinically indicated target lesion revascularization), a secondary restrictive definition of MACE (MACE2) excluding target lesion revascularization, and bleeding.

 

RESULTS - A total of 1,192 patients (24%) were 55 years, 2,869 (57%) were 56 to 74 years, and 957 (19%) were 75 years of age. Patients 75 years of age had higher DAPT cessation rates and increased risk for MACE2, death, cardiac death, and bleeding compared with younger patients. Discontinuation and interruption were not associated with increased cardiovascular risk across age groups, whereas disruption was associated with increased risk for MACE and MACE2 in younger patients but not in patients 75 years of age (p for trend <0.05).

 

CONCLUSIONS- Nonadherence and outcomes vary by age, with patients 75 years having the highest DAPT cessation rates. We observed no association between outcomes and DAPT cessation in patients 75 years, whereas discontinuation was associated with lower MACE rates and disruption with increased MACE rates in patients <75 years.