Antiarrhythmic drug treatment after cardioversion of atrial fibrillation – Authors' reply

Antiarrhythmic drug treatment after cardioversion of atrial fibrillation – Authors' reply

Correspondence colleagues have made an attempt to assess the prevalence of COPD and its correlation with clinical outcomes in various subgroups. Furt...

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Correspondence

colleagues have made an attempt to assess the prevalence of COPD and its correlation with clinical outcomes in various subgroups. Furthermore, because women are reported to have an increased risk of recurrence after cardioversion,3 did Kirchhof and colleagues make an attempt to study the benefits of antiarrhythmic therapy with flecainide in women and compare them with those in men? Kirchhof and colleagues speculate that focal firing from the pulmonary veins could be one of the possible explanations for the noted clinical benefits of flecainide. It would be interesting to know whether catheter ablation was attempted in patients for whom antiarrhythmic therapy failed and whether focal firing or other electrophysiological mechanisms were noted in these patients. We declare that we have no conflicts of interest.

Ajay Vallakati, *Abhishek Sharma, Dhanunjaya Lakkireddy [email protected] KU Cardiovascular Research Institute, University of Kansas Hospital & Medical Center, KS, USA (AV, DL); and Maimonides Medical Center, Brooklyn, NY 11219, USA (AS) 1

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Kirchhof P, Andresen D, Bosch R, et al. Short-term versus long-term antiarrhythmic drug treatment after cardioversion of atrial fibrillation (Flec-SL): a prospective, randomised, open-label, blinded endpoint assessment trial. Lancet 2012; 380: 238–46. Gurevitz OT, Varadachari CJ, Ammash NM, et al. The effect of patient sex on recurrence of atrial fibrillation following successful direct current cardioversion. Am Heart J 2006; 152: e9–13. Okçün B, Yigit Z, Küçükoglu MS, et al. Predictors for maintenance of sinus rhythm after cardioversion in patients with nonvalvular atrial fibrillation. Echocardiography 2002; 19: 351–57.

Authors’ reply We appreciate the thoughtful comments of the correspondents, and would like to briefly provide our view on the different topics. Although verapamil or β blockers might have a true antiarrhythmic effect after cardioversion, the data are ambiguous. Furthermore, pathophysiological insights suggest that mere inhibition of the L-type calcium channel is unlikely 1468

to prevent atrial fibrillation (AF).1 In addition to the studies mentioned, the PAFAC trial2 compared a combination of verapamil and quinidine with d,lsotalol, which combines β blockade and potassium channel inhibition, for prevention of AF after cardioversion. There was no difference in effectiveness, but the verapamil-quinidine combination caused numerically less drug-induced proarrhythmia. Consequently, β blockers and verapamil are recommended for rate control rather than for rhythm control. The patients in the Flec-SL trial received adequate rate control therapy (see original table 1), following current and previous AF guidelines.3 Treatment with angiotensinconverting-enzyme inhibitors or sartans, which were given to about half the Flec-SL trial population, is largely ineffective in preventing recurrent AF in patients without structural heart disease.4 Hence, we would be hesitant to conclude that continued upstream treatment would be clinically mandated in the Flec-SL patient population for whom structural heart disease was rare. In the Flec-SL trial, short-term antiarrhythmic drug therapy was not associated with adverse events, and we designed the trial with a view to reducing complications of antiarrhythmic drug therapy. One previous study,5 referred to in the discussion of our paper, reported that episodic treatment with amiodarone increased treatment-related complications compared with long-term amiodarone treatment. Amiodarone, a multichannel blocker with additional rate-controlling effects, has a biological half-life of several months, rendering it unsuitable for episodic or short-term treatment. The available data hence suggest that short-term antiarrhythmic drug therapy would be a valuable treatment option when agents with a suitable pharmacological profile are used. According to the p values of the adequate interaction tests, female

sex did not affect the outcome of the Flec-SL trial, nor did the presence of chronic obstructive pulmonary disease (COPD). Severe COPD was relatively rare in the population studied in FlecSL (4·6%), hence the study does not provide substantial new information on the question of whether COPD affects recurrence of atrial fibrillation. There were only eight catheter ablations done during the study period and their presence did not alter the treatment effect. Unfortunately, we do not have access to CYP2D6 variant data in this population. We declare that we have no conflicts of interest.

*Paulus Kirchhof, Günter Breithardt, Andras Treszl, Karl Wegscheider [email protected] University of Birmingham, Institute for Biomedical Research, Birmingham B15 2TT, UK (PK); Department of Cardiology and Angiology, Hospital of the University of Münster, Münster, Germany (PK, GB); and Department of Medical Biometry and Epidemiology, University of Hamburg, Hamburg, Germany (AT, KW) 1

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Schotten U, Verheule S, Kirchhof P, Goette A. Pathophysiological mechanisms of atrial fibrillation: a translational appraisal. Physiol Rev 2011; 91: 265–325. Fetsch T, Bauer P, Engberding R, et al. Prevention of atrial fibrillation after cardioversion: results of the PAFAC trial. Eur Heart J 2004; 25: 1385–94. Camm AJ, Lip GY, De Caterina R, et al. 2012 focused update of the ESC guidelines for the management of atrial fibrillation: an update of the 2010 ESC guidelines for the management of atrial fibrillation. Developed with the special contribution of the European Heart Rhythm Association. Europace 2012; 14: 1385–413. Disertori M, Latini R, Barlera S, et al. Valsartan for prevention of recurrent atrial fibrillation. N Engl J Med 2009; 360: 1606–17. Ahmed S, Rienstra M, Crijns HJ, et al. Continuous vs episodic prophylactic treatment with amiodarone for the prevention of atrial fibrillation: a randomized trial. JAMA 2008; 300: 1784–92.

Reconstructive surgery after female genital mutilation The paper by Pierre Foldès and colleagues (July 14, p 134)1 finds that reconstructive surgery after female genital mutilation seems to be associated with reduced pain and www.thelancet.com Vol 380 October 27, 2012