Donate Help Contact The AHA Sign In Home
American Heart Association
Circulation
Search: search_blue_button Advanced Search
Circulation. 2008;117:e149
doi: 10.1161/CIRCULATIONAHA.107.736082
This Article
Right arrow Extract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
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 Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ezekowitz, M. D.
Right arrow Articles by Nagarakanti, R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ezekowitz, M. D.
Right arrow Articles by Nagarakanti, R.
Related Collections
Right arrow Arrhythmias, clinical electrophysiology, drugs

(Circulation. 2008;117:e149.)
© 2008 American Heart Association, Inc.


Correspondence

Letter Regarding Article by Connolly et al, "Challenges of Establishing New Antithrombotic Therapies in Atrial Fibrillation"

Michael D. Ezekowitz, MD, PhD; Rangadham Nagarakanti, MD

Lankenau Institute for Medical Research, Main Line Health Heart Center, Wynnewood, Pa

To the Editor:

Dr Connolly and colleagues in the July 24, 2007, issue of Circulation1 have clearly defined the important challenges we face in evaluating antithrombotic drugs for stroke prevention in atrial fibrillation (AF). We are in general agreement with the authors. However, we differ on the advisability of conducting a superiority trial of a new, presumably effective antithrombotic agent against aspirin in patients at high risk for stroke.

The only evidence supporting the benefit of aspirin against the placebo for stroke prevention in AF is from the Stroke Prevention in Atrial Fibrillation (SPAF) I trial.2 The relative risk reduction of stroke and systemic embolism was 42%. The confidence interval was wide (95% confidence interval, 9% to 63%). Other trials, such as the Copenhagen AF, Aspirin, and Anticoagulation Study (AFASAK) and European AF Trial (EAFT), showed a nonsignificant risk reduction of 17% and 11%, respectively. The EAFT included high-risk patients and had an annual stroke rate of 12%, 10%, and 4% in patients assigned to placebo, aspirin, and anticoagulation, respectively.3

The SPAF III trial reported an annual stroke rate of 7.9% and 1.9% in high-risk patients randomized to aspirin plus low-dose warfarin (international normalized ratio, 1.2 to 1.5) and adjusted-dose warfarin (international normalized ratio, 2 to 3), respectively.4 The Birmingham AF Treatment of the Aged (BAFTA) study of high-risk patients reported annual stroke rates of 3.8% and 1.8% in patients assigned to aspirin and warfarin, respectively.5 Thus, with the exception of the SPAF I study, the evidence is overwhelming that stroke rates on aspirin approximate placebo rates in high-risk patients.

A second consideration is the definition of warfarin ineligibility. Definition of warfarin ineligibility in the SPAF I study included patients aged >75 years, now considered a risk factor for stroke prevention and an inclusion factor for current trials. Patients with uncontrolled hypertension or at high risk for bleeds were also excluded. These represent exclusions for any anticoagulant. In the Atrial Fibrillation Clopidogrel Trial With Irbesartan for Prevention of Vascular Events (ACTIVE) A trial, warfarin ineligibility is defined as contraindication to or unwillingness (subjective) to take "oral anticoagulation therapy." ACTIVE A compares reduction in stroke risk between 2 antiplatelet treatment arms. It is difficult to conceive how a patient who is deemed warfarin ineligible can be randomized to another effective anticoagulant unless obvious differences exist such as route of administration or elimination or proven advantages of the drug to be tested. We therefore believe that the known lack of efficacy of aspirin in high-risk patients and the subjectivity of the definition of warfarin ineligibility raise concerns about the trial that Connolly and colleagues propose.


*    Acknowledgments
 
Disclosures

Dr Ezekowitz reports receiving consulting fees from Sanofi-Aventis, Pfizer, Wyeth, Johnson & Johnson, Boehringer Ingelheim, Schering-Plough, and ARYx Therapeutics; lecture fees from Pfizer and Boehringer Ingelheim; and grant support from Boehringer Ingelheim and ARYx Therapeutics. No other potential conflict of interest relevant to this article was reported. Dr Nagarakanti reports no conflicts.


*    References
up arrowTop
*References
 
1. Connolly SJ, Eikelboom J, O’Donnell M, Pogue J, Yusuf S. Challenges of establishing new antithrombotic therapies in atrial fibrillation. Circulation. 2007; 116: 449–455.[Free Full Text]

2. Stroke Prevention in Atrial Fibrillation Investigators. Stroke Prevention in Atrial Fibrillation Study. Circulation. 1991; 84: 527–539.[Abstract/Free Full Text]

3. EAFT (European Atrial Fibrillation Trial) Study Group. Secondary prevention in non-rheumatic atrial fibrillation after transient ischaemic attack or minor stroke. Lancet. 1993; 342: 1255–1262.[Medline] [Order article via Infotrieve]

4. Stroke Prevention in Atrial Fibrillation Investigators. Adjusted-dose warfarin versus low-intensity, fixed-dose warfarin plus aspirin for high-risk patients with atrial fibrillation: Stroke Prevention in Atrial Fibrillation III randomised clinical trial. Lancet. 1996; 348: 633–638.[CrossRef][Medline] [Order article via Infotrieve]

5. Mant J, Hobbs FDR, Fletcher K, Roalfe A, Fitzmaurice D, Lip GYH, Murray E, on behalf of the BAFTA Investigators. Warfarin versus aspirin for stroke prevention in an elderly community population with atrial fibrillation (the Birmingham Atrial Fibrillation Treatment of the Aged Study, BAFTA): a randomised controlled trial. Lancet. 2007; 370: 493–503.[CrossRef][Medline] [Order article via Infotrieve]





This Article
Right arrow Extract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
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 Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ezekowitz, M. D.
Right arrow Articles by Nagarakanti, R.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ezekowitz, M. D.
Right arrow Articles by Nagarakanti, R.
Related Collections
Right arrow Arrhythmias, clinical electrophysiology, drugs