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Randomized Controlled Trial
. 2021 Jun;16(4):476-485.
doi: 10.1177/1747493020946975. Epub 2020 Aug 14.

Prior antiplatelet therapy in patients undergoing endovascular treatment for acute ischemic stroke: Results from the MR CLEAN Registry

Affiliations
Randomized Controlled Trial

Prior antiplatelet therapy in patients undergoing endovascular treatment for acute ischemic stroke: Results from the MR CLEAN Registry

Rob A van de Graaf et al. Int J Stroke. 2021 Jun.

Abstract

Background: Antiplatelet therapy may increase the risk of symptomatic intracranial hemorrhage after endovascular treatment for ischemic stroke but may also have a beneficial effect on functional outcome. The aim of this study is to compare safety and efficacy outcomes after endovascular treatment in patients with and without prior antiplatelet therapy.

Methods: We analyzed patients registered in the MR CLEAN Registry between March 2014 and November 2017, for whom data on antiplatelet therapy were available. We used propensity score nearest-neighbor matching with replacement to balance the probability of receiving prior antiplatelet therapy between the prior antiplatelet therapy and no prior antiplatelet therapy group and adjusted for baseline prognostic factors to compare these groups. Primary outcome was symptomatic intracranial hemorrhage. Secondary outcomes were 90-day functional outcome (modified Rankin Scale), successful reperfusion (extended thrombolysis in cerebral infarction score ≥2B) and 90-day mortality.

Results: Thirty percent (n = 937) of the 3154 patients were on prior antiplatelet therapy, who were matched to 477 patients not on prior antiplatelet therapy. Symptomatic intracranial hemorrhage occurred in 74/937 (7.9%) patients on prior antiplatelet therapy and in 27/477 (5.6%) patients without prior antiplatelet therapy adjusted odds ratio 1.47, 95% confidence interval 0.86-2.49. No associations were found between prior antiplatelet therapy and functional outcome (adjusted common odds ratio 0.87, 95% confidence interval 0.65-1.16), successful reperfusion (adjusted odds ratio 1.23, 95% confidence interval 0.77-1.97), or 90-day mortality (adjusted odds ratio 1.15, 95% confidence interval 0.86-1.54).

Conclusion: We found no evidence of an association of prior antiplatelet therapy with the risk of symptomatic intracranial hemorrhage after endovascular treatment, nor on functional outcome, reperfusion, or mortality. A substantial beneficial or detrimental effect of antiplatelet therapy on clinical outcome cannot be excluded. A randomized clinical trial comparing antiplatelet therapy versus no antiplatelet therapy is needed.

Keywords: Antiplatelet; MR CLEAN Registry; endovascular; stroke; thrombectomy.

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Conflict of interest statement

Declaration of conflicting interests: The author(s) declared the following potential conflicts of interest with respect to the research, authorship, and/or publication of this article: All authors except for S.M.Z. are directly or indirectly involved as investigators for the MR CLEAN-MED (ISRCTN76741621). R.A.v.d.G. has nothing to disclose. S.M.Z. has nothing to disclose. V.C. has nothing to disclose. R.-J.B.G. has nothing to disclose. Amsterdam UMC, University of Amsterdam received compensation from Stryker for consultations by C.B.L.M.M. and Y.B.W.E.M.R. Also, C.B.L.M.M. reports that Amsterdam University Medical Centers, University of Amsterdam received unrestricted grants from CVON/Dutch Heart Foundation, European Commission, TWIN Foundation, and Stryker. C.B.L.M.M. and Y.B.W.E.M.R. are shareholders of Nicolab. Erasmus MC received compensation from Stryker, Medtronic and Bracco Imaging Ltd for activities of A.v.d.L. and D.W.J.D. as a consultant. In addition, A.v.d.L. and D.W.J.D. are the recipients of unrestricted grants from Dutch Heart Foundation, Dutch Brain Foundation, The Netherlands Organisation for Health Research and Development, Health Holland Top Sector Life Science, AngioCare BV, Covidien/EV3®, MEDAC Gmbh/LAMEPRO, Top Medical/Concentric, Thrombolytic Science LLC, Stryker, Medtronic and Penumbra Inc. for the conduct of trials on acute treatment for stroke. H.F.L. has nothing to disclose. A.C.G.M.v.E. has nothing to disclose. B.R. has nothing to disclose.

Figures

Figure 1.
Figure 1.
Flowchart. EVT, endovascular treatment; MR CLEAN, Multicenter randomized clinical trial of endovascular treatment of acute ischemic stroke.
Figure 2.
Figure 2.
mRS distribution for the propensity-score-matched cohort (a) and full cohort (b) for patients on prior antiplatelet therapy and not on prior antiplatelet therapy. Missing values on mRS were handled by multiple imputation in 6.7% of patients. APT, antiplatelet therapy; CI, confidence interval; EVT, endovascular treatment; MR CLEAN, Multicenter randomized clinical trial of endovascular treatment of acute ischemic stroke; mRS, modified Rankin Scale.

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