2008
DOI: 10.2174/157016108783331303
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Platelet GPIIb/IIIa Receptor Antagonists in Human Ischemic Brain Disease

Abstract: The goal of acute stroke therapy is to salvage brain tissue by rapid cerebral artery recanalization to improve microcirculation. A major drawback of fibrinolysis is the activation of platelets leading to a high rate of re-occlusion. Antagonists of the platelet GPIIb/IIIa-receptor inhibit the binding of fibrinogen to platelets counteracting secondary thrombus formation. Also, they were shown to suppress thrombembolus formation and to limit lesion development in cerebral ischemia. We review the literature concer… Show more

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Cited by 27 publications
(25 citation statements)
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References 54 publications
(68 reference statements)
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“…The rationale for this combined treatment is to prevent a downstream re-occlusion subsequent to thrombolysis [10,11]. In fact, the present observations correspond closely to a recanalization of TIMI II or III in about 70% of patients subjected to combined thrombolysis with 20 mg rtPA followed by a continuous infusion of tirofiban [12]. It is beyond the scope of this study to explore whether additional mechanical approaches may be useful in proximal MCA occlusions to enhance rapid recanalization or in patients who do not respond to systemic thrombolysis.…”
Section: Discussionsupporting
confidence: 65%
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“…The rationale for this combined treatment is to prevent a downstream re-occlusion subsequent to thrombolysis [10,11]. In fact, the present observations correspond closely to a recanalization of TIMI II or III in about 70% of patients subjected to combined thrombolysis with 20 mg rtPA followed by a continuous infusion of tirofiban [12]. It is beyond the scope of this study to explore whether additional mechanical approaches may be useful in proximal MCA occlusions to enhance rapid recanalization or in patients who do not respond to systemic thrombolysis.…”
Section: Discussionsupporting
confidence: 65%
“…Patients were subgrouped into a group with recanalization and lacking recanalization after 24 h following thrombolysis (table 1). Thrombolysis was performed with an intravenous bolus of 20 mg rtPA within 3 h after stroke onset followed immediately by an infusion of body weight-adjusted tirofiban (0.4 µg/kg body weight/min for 30 min followed by 0.1 µg/kg body weight/min) [12]. Patients were treated according to their neurological evaluation, the initial MRI, blood serum data including blood sugar and C-reactive protein, as well as continuous blood pressure monitoring.…”
Section: Methodsmentioning
confidence: 99%
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“…645,646 A series of studies evaluated one of these agents, abciximab. These included case reports and small clinical series; in some cases, the agent was given as monotherapy and in others as an adjunct, usually with pharmacological fibrinolysis or mechanical thrombectomy.…”
Section: Intravenous Antiplatelet Agentsmentioning
confidence: 99%
“…The observation that the platelet aggregation and thrombus formation require the binding of fibrinogen to platelet through Glycoprotein (GP) IIb/IIIa receptor prompted a series of studies on intravenously administered platelet GPIIb/IIIa receptor antagonist (eptifibatide, abciximab, tirofiban) aimed at preventing plasminogen bridges between platelets, and disintegrating thrombi 41 . However, fibrinogen binding to this receptor is the last step in platelet aggregation; antagonists can inhibit this process whatever is the agonist.…”
Section: Antiplatelet Therapymentioning
confidence: 99%