Rate or Rhythm Control for Atrial Fibrillation: Update and Controversies - 23/10/12

Abstract |
Atrial fibrillation is associated with increased mortality and considerable morbidity, including stroke, heart failure, and diminished quality of life. Despite these adverse outcomes, rhythm control has not demonstrated benefit in clinical trials. Antiarrhythmic medications, including recently developed agents, have limited efficacy in achieving durable sinus rhythm and substantial toxicity. A rate-control strategy is therefore more attractive for minimally symptomatic patients, but younger and more symptomatic patients may benefit from restoration of sinus rhythm. Catheter ablation is more effective than medications in preventing arrhythmia recurrence, avoids adverse effects associated with antiarrhythmic drugs, and should be considered early in symptomatic patients when success is likely. However, more definitive data are needed from randomized trials assessing long-term outcomes after ablation, including stroke risk and mortality. Clinical decision tools help select the appropriate management for individual patients. Lenient rate management is easy to achieve and seems reasonably safe for certain patients, although the optimum rate varies with individual comorbidities. Because safer and more effective pharmacologic and interventional therapies are now available, an individualized approach to atrial fibrillation management is essential.
El texto completo de este artículo está disponible en PDF.Keywords : Ablation, Antiarrhythmic drugs, Atrial fibrillation, Rate control, Rhythm control
Esquema
| Funding: None. |
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| Conflict of Interest: JL Halperin has received consulting fees for advisory activities involving the development of new anticoagulant drugs or embolism-prevention devices from Astellas Pharma USA, Atricure/Boston Biomedical Associates, AstraZeneca, Bayer AG HealthCare, Boehringer Ingelheim, Bristol Meyers-Squibb, Daiichi Sankyo, Johnson and Johnson, Pfizer Inc, and Sanofi-Aventis. He received consulting fees from Biotronik as Co-chairman of the Steering Committee for the IMPACT clinical trial. VY Reddy has received consulting fees for advisory activities involving the development of catheter ablation and left atrial appendage closure devices from Biosense-Webster, Boston Scientific, Cardiofocus, Coherex, Endosense, Medtronic, Sentreheart, St Jude Medical, and Voyage Medical. All other authors have no competing interests to disclose. |
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| Authorship: All authors had access to the data and played a role in writing this manuscript. |
Vol 125 - N° 11
P. 1049-1056 - novembre 2012 Regresar al númeroBienvenido a EM-consulte, la referencia de los profesionales de la salud.
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