Journal Article

Dual-antiplatelet treatment beyond 1 year after drug-eluting stent implantation (ARCTIC-Interruption): a randomised trial

Carrié, Didier, Kerneis, Mathieu, Aubry, Pierre, Monségu, Jacques, Sabouret, Pierre, Vicaut, Eric, Barthélémy, Olivier, Abtan, Jérémie, Cuisset, Thomas, Rangé, Grégoire, Schiele, François, Cayla, Guillaume, Beygui, Farzin, Lhoest, Nicolas, Montalescot, Gilles, Collet, Jean-Philippe, Ohlmann, Patrick, Van Belle, Eric, Elhadad, Simon, Rousseau, Hélène, Silvain, Johanne, O'Connor, Stephen A, Saint-Etienne, Christophe

2014

Overview

Optimum duration of dual antiplatelet treatment (DAPT) after coronary stenting remains uncertain, with an unknown efficacy to safety ratio of extended treatment leading to discrepancies between international guidelines and clinical practice. We assessed whether DAPT continuation beyond 1 year after coronary stenting is beneficial. This analysis was a planned extension of the previously published ARCTIC-Monitoring trial, in which we randomly allocated 2440 patients to a strategy of platelet function testing with antiplatelet treatment adjustment or a conventional strategy after coronary stenting with drug-eluting stent (DES). We recruited patients (aged 18 years or older) scheduled for planned DES implantation at 38 centres in France. After 1 year of follow-up, patients without contraindication to interruption of DAPT were eligible for a second randomisation to this second phase of the study (ARCTIC-Interruption). Using a computer-generated randomisation sequence (1:1; stratified by centre), we allocated patients to a strategy of interruption of DAPT where the thienopyridine was interrupted and single aspirin antiplatelet treatment was maintained (interruption group) or a strategy of DAPT continuation for 6–18 months (continuation group). The primary endpoint was the composite of death, myocardial infarction, stent thrombosis, stroke, or urgent revascularisation, analysed by intention to treat. This trial is registered with ClinicalTrials.gov, number NCT00827411. Between Jan 4, 2011, and March 3, 2012, 1259 eligible patients were randomly allocated to treatment in ARCTIC-Interruption: 624 to the interruption group and 635 to the continuation group. After a median follow-up of 17 months (IQR 15–18), the primary endpoint occurred in 27 (4%) patients in the interruption group and 24 (4%) patients in the continuation group (hazard ratio [HR] 1·17 [95% CI 0·68–2·03]; p=0·58). STEEPLE major bleeding events occurred more often in the continuation group (seven [1%] patients) compared with the interruption group (one [<0·5%] patient; HR 0·15 [0·02–1·20]; p=0·073). Major or minor bleedings were also more common in the continuation group compared with the interruption group (12 [2%] patients vs three [1%] patients; HR 0·26 [0·07–0·91]; p=0·04). Our finding suggests no apparent benefit but instead harm with extension of DAPT beyond 1 year after stenting with DES when no event has occurred within the first year after stenting. No conclusion can be drawn for high-risk patients who could not be randomised. The consistency between findings from all trials of such interruption suggests the need for a reappraisal of guidelines for DAPT after coronary stenting towards shorter duration of treatment. Allies in Cardiovascular Trials Initiatives and Organized Networks (ACTION Study Group), Fondation de France, Sanofi-Aventis, Cordis, Medtronic, Boston Scientific, Fondation SGAM.

• Publisher: Elsevier Ltd,Elsevier,Elsevier Limited
• Subject: Acute coronary syndromes / Adolescent / Adult / Aged / Aspirin / Aspirin - administration & dosage / Aspirin - adverse effects / Aspirin - therapeutic use / Biological and medical sciences / Coronary Artery Disease - therapy / Drug Administration Schedule / Drug therapy / Drug Therapy, Combination / Drug-Eluting Stents / Female / General aspects / Heart attacks / Hemorrhage - chemically induced / Humans / Internal Medicine / Kaplan-Meier Estimate / Male / Medical sciences / Middle Aged / Myocardial infarction / Percutaneous Coronary Intervention - methods / Platelet Aggregation Inhibitors - administration & dosage / Platelet Aggregation Inhibitors - adverse effects / Platelet Aggregation Inhibitors - therapeutic use / Platelet Function Tests - methods / Prospective Studies / Pyridines - administration & dosage / Pyridines - adverse effects / Pyridines - therapeutic use / Stents / Stroke / Studies / Survival analysis / Thromboembolism / Thrombosis / Treatment Outcome / Young Adult