Skip Navigation

European Heart Journal 1996 17(Supplement C):35-40; doi:10.1093/eurheartj/17.suppl_C.35
Copyright © 1996 by the European Society of Cardiology.
This Article
Right arrow FREE Full Text (PDF) Freely available
Right arrow E-letters: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when E-letters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Reimold, S. C.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Reimold, S. C.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

© 1996 1996 The European Society of Cardiology

Clinical challenge I: Control of recurrent symptomatic atrial fibrillation

S. C. Reimold

Cardiovascular Division, Department of Medicine, Brigham and Women's Hospital Boston, Massachusetts, U.S.A.

Correspondence: Sharon C. Reimold, MD, Cardiovascular Division, Brigham and Women's Hospital, 75 Francis St., Boston, MA, U.S.A.

Control of recurrent symptomatic atrial fibrillation should be directed at: (1) alleviation of symptoms associated with atrial fibrillation and (2) reduction of the risk of embolization. Approximately 50–60% of patients treated with conventional agents such as quinidine will develop recurrent atrial fibrillation in the first year of treatment. Because of this relapse rate and the side effects associated with quinidine and other type la antiarrhythmic agents, it is important to investigate the efficacy and safety of newer antiarrhythmic agents such as propafenone and sotalol. In our institution, 100 patients with recurrent symptomatic atrial fibrillation who had failed therapy with at least one type Ia agent were randomized to propafenone or sotalol. Propafenone and sotalol were equally effective in preventing recurrent atrial fibrillation at 6 and 12 months after onset of therapy independent of arrhythmia pattern or left atrial size. Both agents were well tolerated with only 10% of patients discontinuing therapy due to side effects.

We combined data from this randomized study with a stepped care trial of propafenone and sotalol to examine risk factors for the development of recurrent atrial fibrillation. In patients treated with propafenone or sotalol, there was no significant difference in response to therapy based on age, gender, or aetiology of heart disease. Patients with dual-chamber pacing had improved maintenance of sinus rhythm as compared to those individuals without pacemakers. Left atrial size did not significantly influence the likelihood of maintaining sinus rhythm in these trials.

Pharmacological management of the patient with recurrent symptomatic atrial fibrillation remains a difficult problem. Patient symptom severity and the clinical profile should be examined prior to instituting antiarrhythmic therapy in any given patient. These studies indicate that propafenone and sotalol are equally effective when used to maintain sinus rhythm in our population. As more data on the merits and risks of antiarrhythmic therapy for the treatment of atrial fibrillation become available, the role of propafenone and sotalol in the treatment of this disorder will be better understood.

Key Words: Atrial fibrillation • propafenone • sotalol


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?




Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.