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From the Department of Neurological Sciences, I Chair of Neurology (Drs. Toni, Fioielli, Sacchetti, Sette, Argentino, and Montinaro), and Chair of Neuroradiology (Drs. Bastianello and Bozzao), University ``La Sapienza,'' Rome, Italy.
Supported in part by Consiglio Nazionale delle Ricerche Grant No. 93051602086.
Received February 24, 1995. Accepted in final form May 31, 1995.
Address correspondence and reprint requests to Dr. Danilo Toni, Department of Neurological Sciences, I Chair of Neurology, University ``La Sapienza'' Viale dell'Universita 30, 00185 Rome, Italy.
Objective: To identify, in the first 5 hours of acute brain infarct, clinical and radiologic predictors of subsequent hemorrhagic transformation (HT), and to evaluate its influence on the clinical course. Background: The identification of early predictors of HT might be important to plan antithrombotic or thrombolytic treatments. Patients: One hundred fifty consecutive patients with cerebral anterior circulation infarct systematically underwent a first CT within 5 hours of onset. During the first week after stroke, we performed a repeat CT or autopsy to look for HT. Outcome measures were early neurologic deterioration within the first week of onset and 30-day case fatality rate and disability. Results: HT was observed in 65 patients (43%): 58 (89%) had a petechial HT and seven (11%) a hematoma. Among initial clinical and CT findings, the only independent predictor of HT was early focal hypodensity. Its presence was associated with subsequent HT in 77% of cases (95% CI, 68 to 86%), whereas its absence predicted the absence of subsequent HT in 94% of cases (95% CI, 89 to 99%). No baseline clinical or CT characteristic differentiated patients with petechial HT from those with hematoma. Antithrombotic and antiplatelet agents did not influence the occurrence of either type of HT. The frequency of early neurologic deterioration and of 30-day death or disability in HT patients was twice as high as in those without HT. However, a large-sized infarct and the presence of mass effect at the repeat CT or autopsy were the only factors independently linked to both the outcome events, irrespective of the development of HT. Clinical evolution of HT patients given antithrombotics was comparable with that of HT patients not receiving these drugs. Conclusions: HT of a brain infarct is a common event that occurs independently of anticoagulation and can be reliably predicted as early as 5 hours from stroke onset by the presence of focal hypodensity at CT. Apart from the infrequent cases of massive hematoma, HT does not influence prognosis, whereas a poor outcome in HT patients is correlated with a higher frequency of large edematous infarcts in this subgroup. The clinical course and final outcome of HT in anticoagulated patients does not differ from that of non-anticoagulated HT patients.
NEUROLOGY 1966;46: 341-345
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