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(Stroke. 2006;37:2165.)
© 2006 American Heart Association, Inc.
Research Reports |
From the Department of Neurology, Johann Wolfgang Goethe University, Frankfurt am Main, Germany.
Correspondence to Christian Foerch, MD, Department of Neurology, Johann Wolfgang Goethe University, Schleusenweg 2-16, 60528 Frankfurt am Main, Germany. E-mail foerch{at}em.uni-frankfurt.de
| Abstract |
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Methods Our analysis was based on a large, country-wide stroke registry in Germany. All parameters relevant to this analysis, including age, prehospital status (according to the modified Rankin Scale, mRS), International Classification of Diseasesbased diagnosis, and pretreatment with antiplatelet agents or oral anticoagulants, were recorded prospectively. Main outcome measures were in-hospital mortality rate and functional status at hospital discharge (mRS).
Results Over a 2-year period, 1691 patients with ICH (ICD-10: I61) were documented (48% female; mean age, 72±12 years). At symptom onset, 26% were taking antiplatelet agents, and 12% were taking oral anticoagulants. By univariate logistic regression, pretreatment with antiplatelet drugs or anticoagulants was found to be a significant predictor of in-hospital mortality (odds ratio [OR], 1.42; P=0.008; OR, 1.53; P<0.001) and of an unfavorable functional outcome (defined as mRS >2 or death; OR, 1.33, P=0.039; OR, 1.51; P<0.001). However, after adjustment for age and prehospital status, antiplatelet pretreatment was no longer an independent risk factor of in-hospital death (OR, 1.12; P=0.490) or unfavorable functional outcome (OR, 0.97; P=0.830), whereas the influence of pretreatment with oral anticoagulants remained significant (OR, 1.45; P<0.001; OR, 1.42; P=0.009).
Conclusions In contrast to oral anticoagulants, pretreatment with antiplatelet agents is not an independent risk factor of mortality and unfavorable outcome in patients with ICH.
Key Words: antiplatelet agents cerebral hemorrhage outcome
| Introduction |
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| Subjects and Methods |
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We did not obtain ethics board approval because the registry is a country-wide quality assurance measure based on state law, wherein all inpatients are documented anonymously. Informed consent is not required before enrollment in the registry.
We used t tests and
2 statistics to compare baseline variables (age, prehospital mRS) between patients with and without antithrombotic pretreatment. Univariate and multivariate logistic regression analyses were used to determine the influence of antithrombotic therapy on mortality rate and functional outcome.
| Results |
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2). The corresponding findings for patients without antithrombotic pretreatment compared with patients on oral anticoagulation were similar (70±14 versus 75±7 years, P<0.001; 18% versus 30%, P=0.001).
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In-hospital mortality rates were 21% for patients without antithrombotic pretreatment, 27% for patients using antiplatelet agents, and 38% for patients on oral anticoagulation. The corresponding values for patients having an unfavorable functional outcome (defined as mRS >2 or death) at hospital discharge were 75%, 80%, and 87%, respectively.
By univariate logistic-regression analysis, pretreatment with antiplatelet agents or oral anticoagulation was found to be a significant predictor of in-hospital mortality (odds ratio [OR], 1.42; P=0.008; OR, 1.53; P<0.001) and of an unfavorable functional outcome (OR, 1.33; P=0.039; OR, 1.51; P<0.001). However, after adjustment for age and prehospital mRS, pretreatment with antiplatelet agents was no longer an independent predictor of in-hospital death (OR, 1.12; P=0.490) or unfavorable functional outcome (OR, 0.97; P=0.830), whereas the influence of treatment with oral anticoagulants still remained significant (OR, 1.45; P<0.001; OR, 1.42; P=0.009; see the Figure).
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| Discussion |
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In accordance with previous investigations, our analysis revealed that patients on antiplatelet therapy or oral anticoagulation were older and had a worse prehospital status compared with patients without any antithrombotic treatment.4,5 Our study also confirmed that patients who experienced an ICH while taking oral anticoagulants (mostly phenprocoumon in our cohort) had a significantly worse prognosis compared with patients without pretreatment, independent of age and prehospital functional status.1,2 However, the same did not apply to patients taking antiplatelet agents.
Recently, 2 retrospective studies reported results that are apparently contradictory to our data.4,5 Both studies suggested that previous antiplatelet therapy contributed to an unfavorable outcome in ICH. However, closer analysis of the demographic data of those studies reveals a substantial difference between patients with and without antiplatelet pretreatment in the rate of previous ischemic cerebrovascular events (54% versus 7% and 43% versus 9%, respectively).4,5 Ischemic strokes often lead to relevant functional impairment, and it is therefore likely that patients taking antiplatelet drugs had a worse prehospital status. This hypothesis is supported by our analysis showing that 38% of patients on antiplatelet agents had a prehospital mRS >1 compared with only 18% of patients without pretreatment (P<0.001). Because a reduced prehospital status is a known predictor of an unfavorable prognosis, adjustment for this confounder seems to be essential for determining any independent effect of antiplatelet pretreatment on mortality and functional outcome. In our opinion, both the study by Toyoda et al4 and that by Saloheimo et al5 did not sufficiently control for prehospital status. In view of other negative studies,2,7,8 their results remain questionable.
Surrogate markers of clinical deterioration (eg, hematoma enlargement) may still be significantly different between patients with and without antiplatelet pretreatment, as suggested by the study of Toyoda et al.4 However, considering our data, the influence on the overall prognosis seems to be marginal. In contrast to patients on oral anticoagulation, those on antiplatelet drugs did not show larger hematomas at hospital admission compared with patients without pretreatment. This further strengthens the hypothesis that factors other than antiplatelet therapy may worsen mortality and functional outcome.
In summary, our data do not support an independent effect of previous antiplatelet therapy on mortality and functional outcome in patients with acute ICH and thus, do not justify aggressive measures to revert the effect of antiplatelet agents in the acute setting.
| Acknowledgments |
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None.
Received February 18, 2006; revision received April 2, 2006; accepted May 4, 2006.
| References |
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2. Rosand J, Eckman MH, Knudsen KA, Singer DE, Greenberg SM. The effect of warfarin and intensity of anticoagulation on outcome of intracerebral hemorrhage. Arch Intern Med. 2004; 164: 880884.
3. Roquer J, Rodriguez Campello A, Gomis M, Ois A, Puente V, Munteis E. Previous antiplatelet therapy is an independent predictor of 30-day mortality after spontaneous supratentorial intracerebral hemorrhage. J Neurol. 2005; 252: 412416.[CrossRef][Medline] [Order article via Infotrieve]
4. Toyoda K, Okada Y, Minematsu K, Kamouchi M, Fujimoto S, Ibayashi S. Antiplatelet therapy contributes to acute deterioration of intracerebral hemorrhage. Neurology. 2005; 65: 10001004.
5. Saloheimo P, Ahonen M, Juvela S, Pyhtinen J, Savolainen ER, Hillbom M. Regular aspirin use preceding the onset of primary intracerebral hemorrhage is an independent predictor for death. Stroke. 2006; 37: 129133.
6. Foerch C, Misselwitz B, Sitzer M, Berger K, Steinmetz H, Neumann-Haefelin T. Difference in recognition of right and left hemispheric stroke. Lancet. 2005; 366: 392393.[CrossRef][Medline] [Order article via Infotrieve]
7. Nilsson OG, Lindgren A, Brandt L, Saveland H. Prediction of death in patients with primary intracerebral hemorrhage: a prospective study of a defined population. J Neurosurg. 2002; 97: 531536.[Medline] [Order article via Infotrieve]
8. Flibotte JJ, Hagan N, ODonnell J, Greenberg SM, Rosand J. Warfarin, hematoma expansion, and outcome of intracerebral hemorrhage. Neurology. 2004; 63: 10591064.
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