Percutaneous left atrial appendage closure vs warfarin for atrial fibrillation: a randomized clinical trial
| Autor: | Vijay Swarup, Saibal Kar, Petr Neuzil, Jonathan L. Halperin, Brian Whisenant, Investigators, David R. Holmes, Shephal K. Doshi, Nicole Gordon, Vivek Y. Reddy, Kenneth C. Huber, Horst Sievert, Maurice Buchbinder |
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| Rok vydání: | 2014 |
| Předmět: |
Male
medicine.medical_specialty Cardiac Catheterization medicine.medical_treatment Embolism Rate ratio Left atrial appendage occlusion law.invention Prosthesis Implantation Randomized controlled trial law Risk Factors Internal medicine Atrial Fibrillation medicine Humans Atrial Appendage Stroke Aged Aged 80 and over business.industry Hazard ratio Warfarin Anticoagulants Atrial fibrillation Bayes Theorem General Medicine Middle Aged medicine.disease Survival Analysis Treatment Outcome Cardiovascular Diseases Cardiology Female business medicine.drug |
| Zdroj: | JAMA. 312(19) |
| ISSN: | 1538-3598 |
| Popis: | Importance While effective in preventing stroke in patients with atrial fibrillation (AF), warfarin is limited by a narrow therapeutic profile, a need for lifelong coagulation monitoring, and multiple drug and diet interactions. Objective To determine whether a local strategy of mechanical left atrial appendage (LAA) closure was noninferior to warfarin. Design, Setting, and Participants PROTECT AF was a multicenter, randomized (2:1), unblinded, Bayesian-designed study conducted at 59 hospitals of 707 patients with nonvalvular AF and at least 1 additional stroke risk factor (CHADS2score ≥1). Enrollment occurred between February 2005 and June 2008 and included 4-year follow-up through October 2012. Noninferiority required a posterior probability greater than 97.5% and superiority a probability of 95% or greater; the noninferiority margin was a rate ratio of 2.0 comparing event rates between treatment groups. Interventions Left atrial appendage closure with the device (n = 463) or warfarin (n = 244; target international normalized ratio, 2-3). Main Outcomes and Measures A composite efficacy end point including stroke, systemic embolism, and cardiovascular/unexplained death, analyzed by intention-to-treat. Results At a mean (SD) follow-up of 3.8 (1.7) years (2621 patient-years), there were 39 events among 463 patients (8.4%) in the device group for a primary event rate of 2.3 events per 100 patient-years, compared with 34 events among 244 patients (13.9%) for a primary event rate of 3.8 events per 100 patient-years with warfarin (rate ratio, 0.60; 95% credible interval, 0.41-1.05), meeting prespecified criteria for both noninferiority (posterior probability, >99.9%) and superiority (posterior probability, 96.0%). Patients in the device group demonstrated lower rates of both cardiovascular mortality (1.0 events per 100 patient-years for the device group [17/463 patients, 3.7%] vs 2.4 events per 100 patient-years with warfarin [22/244 patients, 9.0%]; hazard ratio [HR], 0.40; 95% CI, 0.21-0.75;P = .005) and all-cause mortality (3.2 events per 100 patient-years for the device group [57/466 patients, 12.3%] vs 4.8 events per 100 patient-years with warfarin [44/244 patients, 18.0%]; HR, 0.66; 95% CI, 0.45-0.98;P = .04). Conclusions and Relevance After 3.8 years of follow-up among patients with nonvalvular AF at elevated risk for stroke, percutaneous LAA closure met criteria for both noninferiority and superiority, compared with warfarin, for preventing the combined outcome of stroke, systemic embolism, and cardiovascular death, as well as superiority for cardiovascular and all-cause mortality. Trial Registration clinicaltrials.gov Identifier:NCT00129545 |
| Databáze: | OpenAIRE |
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