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Scores to Predict Major Bleeding Risk During Oral Anticoagulation Therapy: A Prospective Validation Study - 23/10/12

Doi : 10.1016/j.amjmed.2012.04.005 
Jacques Donzé, MD, MSc a, , Nicolas Rodondi, MD, MAS b, Gérard Waeber, MD c, Pierre Monney, MD d, Jacques Cornuz, MD, MPH e, Drahomir Aujesky, MD, MSc b
a Division of General Internal Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Mass 
b Division of General Internal Medicine, Bern University Hospital, Bern, Switzerland 
c Division of General Internal Medicine, Lausanne University Hospital, Lausanne, Switzerland 
d Division of Cardiology, Lausanne University Hospital, Lausanne, Switzerland 
e Department of Ambulatory Care and Community Medicine, Lausanne University Hospital, Lausanne, Switzerland 

Requests for reprints should be addressed to Jacques Donzé, MD, 1620 Tremont Street, OBC-3-2U, Division of General Internal Medicine, Brigham and Women's Hospital, Boston, MA 02120-1613

Abstract

Background

Clinical scores may help physicians to better assess the individual risk/benefit of oral anticoagulant therapy. We aimed to externally validate and compare the prognostic performance of 7 clinical prediction scores for major bleeding events during oral anticoagulation therapy.

Methods

We followed 515 adult patients taking oral anticoagulants to measure the first major bleeding event over a 12-month follow-up period. The performance of each score to predict the risk of major bleeding and the physician's subjective assessment of bleeding risk were compared with the C statistic.

Results

The cumulative incidence of a first major bleeding event during follow-up was 6.8% (35/515). According to the 7 scoring systems, the proportions of major bleeding ranged from 3.0% to 5.7% for low-risk, 6.7% to 9.9% for intermediate-risk, and 7.4% to 15.4% for high-risk patients. The overall predictive accuracy of the scores was poor, with the C statistic ranging from 0.54 to 0.61 and not significantly different from each other (P=.84). Only the Anticoagulation and Risk Factors in Atrial Fibrillation score performed slightly better than would be expected by chance (C statistic, 0.61; 95% confidence interval, 0.52-0.70). The performance of the scores was not statistically better than physicians' subjective risk assessments (C statistic, 0.55; P=.94).

Conclusion

The performance of 7 clinical scoring systems in predicting major bleeding events in patients receiving oral anticoagulation therapy was poor and not better than physicians' subjective assessments.

El texto completo de este artículo está disponible en PDF.

Keywords : Anticoagulants, Complications, Hemorrhage, Prognosis, Risk factors


Esquema


 Funding: This study was supported by an intramural grant (CardioMet) from the University Hospital Lausanne, Switzerland. Dr Jacques Donzé was supported by grants provided by the Swiss National Science Foundation (PBLAP3-131814 and PBLAP3-136815). The providers of the grants played no role in the design or conduct of the study, or in the collection, management, or interpretation of the data.
 Conflict of Interest: None.
 Authorship: All authors had access to the data and played a role in writing this manuscript.


© 2012  Elsevier Inc. Reservados todos los derechos.
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Vol 125 - N° 11

P. 1095-1102 - novembre 2012 Regresar al número
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