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LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00004509naa a2200445 4500
001oai:DiVA.org:uu-177244
003SwePub
008120704s2012 | |||||||||||000 ||eng|
009oai:prod.swepub.kib.ki.se:124730906
024a https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-1772442 URI
024a https://doi.org/10.1016/S1474-4422(12)70092-32 DOI
024a http://kipublications.ki.se/Default.aspx?queryparsed=id:1247309062 URI
040 a (SwePub)uud (SwePub)ki
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Easton, J. Donald4 aut
2451 0a Apixaban compared with warfarin in patients with atrial fibrillation and previous stroke or transient ischaemic attack :b a subgroup analysis of the ARISTOTLE trial
264 1c 2012
338 a print2 rdacarrier
520 a BackgroundIn the ARISTOTLE trial, the rate of stroke or systemic embolism was reduced by apixaban compared with warfarin in patients with atrial fibrillation (AF). Patients with AF and previous stroke or transient ischaemic attack (TIA) have a high risk of stroke. We therefore aimed to assess the efficacy and safety of apixaban compared with warfarin in prespecified subgroups of patients with and without previous stroke or TIA.MethodsBetween Dec 19,2006, and April 2,2010, patients were enrolled in the ARISTOTLE trial at 1034 clinical sites in 39 countries. 18 201 patients with AF or atrial flutter were randomly assigned to receive apixaban 5 mg twice daily or warfarin (target international normalised ratio 2.0-3.0). The median duration of follow-up was 1.8 years (IQR 1.4-2.3). The primary efficacy outcome was stroke or systemic embolism, analysed by intention to treat. The primary safety outcome was major bleeding in the on-treatment population. All participants, investigators, and sponsors were masked to treatment assignments. In this subgroup analysis, we estimated event rates and used Cox models to compare outcomes in patients with and without previous stroke or TIA. The ARISTOTLE trial is registered with ClinicalTrials.gov, number NTC00412984.FindingsOf the trial population, 3436 (19%) had a previous stroke or TIA. In the subgroup of patients with previous stroke or TIA, the rate of stroke or systemic embolism was 2.46 per 100 patient-years of follow-up in the apixaban group and 3.24 in the warfarin group (hazard ratio [HR] 0.76, 95% CI 0.56 to 1.03); in the subgroup of patients without previous stroke or TLA, the rate of stroke or systemic embolism was 1.01 per 100 patient-years of follow-up with apixaban and 1.23 with warfarin (HR 0.82, 95% CI 0.65 to 1.03; p for interaction=0.71). The absolute reduction in the rate of stroke and systemic embolism with apixaban versus warfarin was 0.77 per 100 patient-years of follow-up (95% CI -0.08 to 1.63) in patients with and 0.22 (-0.03 to 0.47) in those without previous stroke or TIA. The difference in major bleeding with apixaban compared with warfarin was 1.07 per 100 patient-years (95% CI 0.09-2.04) in patients with and 0.93 (0.54-1.32) in those without previous stroke or TIA.InterpretationThe effects of apixaban versus warfarin were consistent in patients with AF with and without previous stroke or TIA. Owing to the higher risk of these outcomes in patients with previous stroke or TIA, the absolute benefits of apixaban might be greater in this population.FundingBristol-Myers Squibb and Pfizer.
700a Lopes, Renato D.4 aut
700a Bahit, M. Cecilia4 aut
700a Wojdyla, Daniel M.4 aut
700a Granger, Christopher B.4 aut
700a Wallentin, Larsu Uppsala universitet,Institutionen för medicinska vetenskaper,Uppsala kliniska forskningscentrum (UCR),kardiologi4 aut0 (Swepub:uu)larswall
700a Alings, Marco4 aut
700a Goto, Shinya4 aut
700a Lewis, Basil S.4 aut
700a Rosenqvist, Martenu Karolinska Institutet4 aut
700a Hanna, Michael4 aut
700a Mohan, Puneet4 aut
700a Alexander, John H.4 aut
700a Diener, Hans-Christoph4 aut
710a Uppsala universitetb Institutionen för medicinska vetenskaper4 org
773t Lancet Neurologyg 11:6, s. 503-511q 11:6<503-511x 1474-4422x 1474-4465
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-177244
8564 8u https://doi.org/10.1016/S1474-4422(12)70092-3
8564 8u http://kipublications.ki.se/Default.aspx?queryparsed=id:124730906

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