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Aspirin and extended-release dipyridamole versus clopidogrel for recurrent stroke.

Title: Aspirin and extended-release dipyridamole versus clopidogrel for recurrent stroke.
Authors: SACCO RL; DIENER HC; YUSUF S; COTTON D; OUNPUU S; LAWTON WA; PALESCH Y; MARTIN RH; ALBERS GW; BATH P; BORNSTEIN N; CHAN BP; CHEN ST; CUNHA L; DAHLÖF B; DE KEYSER J; DONNAN GA; ESTOL C; GORELICK P; GU V; HERMANSSON K; HILBRICH L; KASTE M; LU C; MACHNIG T; PAIS P; ROBERTS R; SKVORTSOVA V; TEAL P; VANDERMAELEN C; VOIGT T; WEBER M; YOON BW; TONI, Danilo; LEMBO, Giuseppe; RASURA, Maurizia; SACCHETTI, Maria Luisa
Contributors: Sacco, Rl; Diener, Hc; Yusuf, S; Cotton, D; Ounpuu, S; Lawton, Wa; Palesch, Y; Martin, Rh; Albers, Gw; Bath, P; Bornstein, N; Chan, Bp; Chen, St; Cunha, L; Dahlöf, B; DE KEYSER, J; Donnan, Ga; Estol, C; Gorelick, P; Gu, V; Hermansson, K; Hilbrich, L; Kaste, M; Lu, C; Machnig, T; Pais, P; Roberts, R; Skvortsova, V; Teal, P; Toni, Danilo; Vandermaelen, C; Voigt, T; Weber, M; Yoon, Bw; Lembo, Giuseppe; Rasura, Maurizia; Sacchetti, Maria Luisa
Publication Year: 2008
Collection: Sapienza Università di Roma: CINECA IRIS
Subject Terms: ictu; aspirina; trial clinico
Description: BACKGROUND: Recurrent stroke is a frequent, disabling event after ischemic stroke. This study compared the efficacy and safety of two antiplatelet regimens--aspirin plus extended-release dipyridamole (ASA-ERDP) versus clopidogrel. METHODS: In this double-blind, 2-by-2 factorial trial, we randomly assigned patients to receive 25 mg of aspirin plus 200 mg of extended-release dipyridamole twice daily or to receive 75 mg of clopidogrel daily. The primary outcome was first recurrence of stroke. The secondary outcome was a composite of stroke, myocardial infarction, or death from vascular causes. Sequential statistical testing of noninferiority (margin of 1.075), followed by superiority testing, was planned. RESULTS: A total of 20,332 patients were followed for a mean of 2.5 years. Recurrent stroke occurred in 916 patients (9.0%) receiving ASA-ERDP and in 898 patients (8.8%) receiving clopidogrel (hazard ratio, 1.01; 95% confidence interval [CI], 0.92 to 1.11). The secondary outcome occurred in 1333 patients (13.1%) in each group (hazard ratio for ASA-ERDP, 0.99; 95% CI, 0.92 to 1.07). There were more major hemorrhagic events among ASA-ERDP recipients (419 [4.1%]) than among clopidogrel recipients (365 [3.6%]) (hazard ratio, 1.15; 95% CI, 1.00 to 1.32), including intracranial hemorrhage (hazard ratio, 1.42; 95% CI, 1.11 to 1.83). The net risk of recurrent stroke or major hemorrhagic event was similar in the two groups (1194 ASA-ERDP recipients [11.7%], vs. 1156 clopidogrel recipients [11.4%]; hazard ratio, 1.03; 95% CI, 0.95 to 1.11). CONCLUSIONS: The trial did not meet the predefined criteria for noninferiority but showed similar rates of recurrent stroke with ASA-ERDP and with clopidogrel. There is no evidence that either of the two treatments was superior to the other in the prevention of recurrent stroke. (ClinicalTrials.gov number, NCT00153062.)
Document Type: article in journal/newspaper
File Description: STAMPA
Language: English
Relation: info:eu-repo/semantics/altIdentifier/pmid/18753638; info:eu-repo/semantics/altIdentifier/wos/WOS:000259259900007; volume:359; issue:12; firstpage:1238; lastpage:1251; numberofpages:14; journal:NEW ENGLAND JOURNAL OF MEDICINE; http://hdl.handle.net/11573/224252; http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=000259259900007&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=0c7ff228ccbaaa74236f48834a34396a
DOI: 10.1056/NEJMoa0805002
Availability: http://hdl.handle.net/11573/224252; https://doi.org/10.1056/NEJMoa0805002; http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=000259259900007&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=0c7ff228ccbaaa74236f48834a34396a; http://www.nejm.org/doi/full/10.1056/NEJMoa0805002; http://www.scopus.com/inward/record.url?eid=2-s2.0-51449116270&partnerID=65&md5=e17a55439900d6bb2b3dc79978c282f4
Accession Number: edsbas.B79D0034
Database: BASE