Stroke. 2007;38:1113-1114
Published online before print February 1, 2007,
doi: 10.1161/01.STR.0000258356.68323.6d
(Stroke. 2007;38:1113.)
© 2007 American Heart Association, Inc.
Glycoprotein IIb-IIIa Inhibitors for Acute Ischemic Stroke
Alfonso Ciccone, MD;
Iosief Abraha, MD
Ignazio Santilli, MD
From the Stroke Unit, "Niguarda Ca Granda" Hospital (A.C., I.S.), Milan, Italy; and the Epidemiology Department (I.A.), Regional Health Authority of Umbria, Perugia.
Correspondence to Alfonso Ciccone, Stroke Unit, "Niguarda Ca Granda" Hospital, Piazza Ospedale Maggiore 3, Milan, Italy 20162. E-mail alfonso.ciccone{at}ospedaleniguarda.it
Section Editor: Graeme J. Hankey MD, FRCP
Key Words: acute stroke antiplatelet agents antiplatelet drugs brain infarction brain ischemia cerebral infarct cerebrovascular accident platelet inhibitors randomized controlled trials stroke management therapy thrombosis glycoprotein IIb-IIIa inhibitors meta-analysis systematic review
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Introduction
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Glycoprotein (GP) IIb-IIIa inhibitors block the final common
pathway to platelet aggregation antagonizing with receptors
that bind fibrinogen molecules forming bridges between adjacent
platelets. Thus, GP IIb-IIIa inhibitors could favor endogenous
thrombolysis by reducing thrombus growth and prevent thrombus
reformation by competitive inhibition with fibrinogen. Currently
used in clinical practice for acute coronary syndromes and percutaneous
coronary interventions, they could be useful also for patients
with acute ischemic stroke.
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Objective
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To perform a systematic review of controlled clinical trials
in order to assemble all the available data to evaluate the
potential efficacy and safety of GP IIb-IIIa inhibitors in patients
with acute ischemic stroke.
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Search Strategy
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We searched the Cochrane Stroke Group Trials Register (last
searched May 31, 2005). In addition we searched the Cochrane
Central Register of Controlled Trials (CENTRAL; The Cochrane
Library, 2005 Issue 2), MEDLINE (1966 to June 2005) and EMBASE
(1980 to June 2005). In an effort to identify further published,
unpublished and ongoing trials we searched reference lists and
contacted authors and pharmaceutical companies.
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Selection Criteria
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We aimed to analyze unconfounded randomized controlled trials
comparing GP IIb-IIIa inhibitors with placebo in patients with
acute ischemic stroke. Only patients who started the treatment
within 6 hours of stroke onset were included.
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Data Collection and Analysis
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Three reviewers independently selected trials for inclusion,
assessed trial quality and extracted the data.
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Main Results
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Two trials involving 474 patients were included. Only data on
414 patients treated within 6 hours were considered. Patients
were treated with intravenous abciximab or placebo. Treatment
with abciximab was associated with a nonsignificant reduction
of death and dependency combined (OR 0.79; 95% CI, 0.54 to 1.17;
Figure) and of death alone (OR 0.67; 95% CI, 0.36 to 1.25).
Treatment with abciximab was associated with a nonsignificant
increase of symptomatic intracranial hemorrhages (OR 4.13; 95%
CI, 0.86 to 19.67) and of major extracranial hemorrhages (OR
1.51; 95% CI, 0.25 to 9.12).

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Effect of glycoprotein IIb-IIIa inhibitors compared with placebo or open control on death or dependency at end of follow-up (3 months) in patients with ischemic stroke within 6 hours of symptom onset.
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During the preparation of this review, Abciximab in Emergent Stroke Treatment Trial-II (AbESTT-II) stopped recruitment after 808 patients of the 1800 planned had been included, because of an excess of ICH in the treatment group, and an unfavorable risk benefit ratio. These data will be available only with the publication of the full results of the trial. The Safety of Tirofiban in Acute Ischemic Stroke (SaTIS) trial of a different GP IIb-IIIa inhibitor, tirofiban, in 240 patients has also recently been completed and presented, and suggests the agent is safe. A further trial of this agent (SETIS: Study of Efficacy of Tirofiban in acute Ischemic Stroke) is ongoing. As soon as AbESTT-II and SaTIS studies have been published in full, this review will be updated, though clearly the results of the much larger AbESTT-II will predominate.
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Reviewers Conclusions
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There is currently not enough evidence from randomized controlled
trials regarding the efficacy or safety of GP IIb-IIIa inhibitors
therapy in acute ischemic stroke.
The question of whether GP IIb-IIIa inhibitor does more good than harm for acute ischemic stroke will be probably answered soon after the publication of AbESTT-II, SaTIS and SETIS studies. Taking into account the recent and premature interruption of the AbESTT-II trial attributable to high rate of ICH, it seems crucial to see whether the early risk of ICH is offset by a benefit on long-term death and disability.
Note: The full text of this review is available in the Cochrane Library (for subscribers: www.update-software. com/Cochrane). The full article should be cited as: Ciccone A, Abraha I, Santilli I. Glycoprotein IIb-IIIa inhibitors for acute ischemic stroke (Cochrane Review). In: The Cochrane Library, Issue 4, 2006. Oxford: Update Software. © Cochrane Library, John Wiley & Sons Ltd.
Received September 27, 2006;
accepted October 2, 2006.
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