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Predictors of intracranial hemorrhage with fibrinolytic therapy in unselected community patients: a report from the FASTRAK II project - 26/08/11

Doi : 10.1016/j.ahj.2004.02.006 
Thao Huynh, MD a, , Jafna L Cox, MD b, David Massel, MD c, Cheryl Davies, RN d, Joseph Hilbe, PhD e, Wayne Warnica, MD f, Paul A Daly, MD g

FASTRAK II Network

a McGill Health University Center, Montreal, Quebec, Canada 
b Queen Elizabeth II Health Sciences Centre, Halifax, Nova Scotia, Canada, London, United Kingdom 
c London Health Science Center, London, Ontario, Canada 
d Vancouver General Hospital, Vancouver, British Columbia, Canada 
e Arizona State University, Phoenix, Ariz, USA 
f Foothill Hospital, University of Calgary, Calgary, Alberta, Canada 
g Toronto University Health Network, Toronto, Ontario, Canada 

*Reprint requests: Thao Huynh, MD, Montreal General Hospital, McGill University Health Centre, 1650 Cedar Ave, #E5-200, Montreal, Quebec, Canada H3G-1A4.

Abstract

Background

Patients at high risk for intracranial hemorrhage (ICH) are generally excluded from thrombolytic trials. Because the frequency and predictors of ICH reported from these studies may not be widely applicable, we sought to examine this matter further in unselected patients with acute myocardial infarction in the community.

Methods

FASTRAK II is a prospective ongoing registry of acute coronary syndromes involving 111 Canadian hospitals. Trained medical personnel recorded admission, treatment, and discharge data on patients admitted with acute coronary syndromes.

Results

From January 1, 1998, to December 31, 2000, 12,739 patients received fibrinolytic therapy for acute myocardial infarction. Of these, 146 patients (1.15%) sustained strokes and 82 patients (0.65%) had an ICH. Advanced age, female sex, history of cerebrovascular event, and systolic hypertension on arrival (systolic blood pressure >160 mm Hg) were identified with a multivariate logistic regression model to be important independent risks factors for ICH. Patients receiving streptokinase had a lower risk of ICH. Among the patients at high risk for ICH, the ICH rates remained low, ranging from 0.7% to 1.8%.

Conclusion

ICH is an infrequent event after fibrinolytic therapy in ST-elevation MI; this low rate supports broad penetration of this therapy. Simple clinical characteristics are useful in predicting the risk of ICH and allow a clinician to individualize the risk-benefit assessment of this therapy.

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 Supported in part by a grant from Hoffmann-La Roche Limited.
Drs Huynh, Cox, Massel, and Warnica and Ms Davies are members of the FASTRAK II Advisory Board and received honorarium as advisors. Dr Daly is a member of Advisory Board and data manager of the FASTRAK II Project. Dr Hilbe is an independent statistical biostatician under contract with Hoffmann-La Roche Limited.


© 2004  Elsevier Inc. Tutti i diritti riservati.
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Vol 148 - N° 1

P. 86-91 - Luglio 2004 Ritorno al numero
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