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(Stroke. 2001;32:748.)
© 2001 American Heart Association, Inc.
Original Contributions |
From the Department of Neurosciences, University of California at San Diego School of Medicine, and Department of Neurology, Veterans Administration Medical Center, San Diego, Calif.
Correspondence to Dr Patrick Lyden (127), 3350 La Jolla Village Dr, San Diego, CA 92161. E-mail Plyden{at}ucsd.edu
Background and PurposeTissue plasminogen activator (tPA) is an effective treatment for stroke, but its utility is limited by fear of cerebral hemorrhage. Tenecteplase (TNK), a genetically modified form of wild-type tPA, exhibits a longer biological half-life and greater fibrin specificity, features that could lead to fewer cerebral hemorrhages than wild-type tPA in stroke patients.
MethodsWe injected radiolabeled blood clots into the cerebral circulation of New Zealand White rabbits. One hour later, we administered tPA (n=57), 0.6 mg/kg TNK (n=43), 1.5 mg/kg TNK (n=27), or vehicle control (n=37). A blinded observer examined the brains for macroscopic hemorrhage using a semiquantitative score. We estimated thrombolysis by assessing the amount of radiolabel remaining in the cerebral vessels postmortem.
ResultsBoth wild-type
tPA and TNK caused thrombolysis in most subjects.
Hemorrhage was detected in 26% (6/23) of the control group,
66% (27/41) of the wild-type tPA group, 55% (16/29) in the 0.6-mg/kg
TNK group, and 53% (9/17) in the 1.5-mg/kg TNK group
(P<0.05,
2 test). The tPA group was statistically
significantly different from the control group, but the TNK and tPA
groups did not differ from each other. Neither TNK nor tPA affected the
size of the hemorrhages.
ConclusionsTNK shows comparable rates of recanalization compared with wild-type tPA in a model of embolic stroke. While tPA increases hemorrhage rate, the hemorrhage associated with TNK treatment is not statistically different compared with controls or the tPA group. These findings suggest that TNK shows promise as an alternative thrombolytic treatment for stroke, but we could not demonstrate improved safety compared with wild-type tPA.
Key Words: cerebral embolism hematoma hemorrhage thrombolysis thrombolytic therapy rabbits
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