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Sökning: WFRF:(Elmér Eskil) > Cyclosporine before...

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FältnamnIndikatorerMetadata
00005725naa a2200901 4500
001oai:lup.lub.lu.se:1ed1e498-272a-41a1-9bd1-af6fddd4a7ae
003SwePub
008160401s2015 | |||||||||||000 ||eng|
024a https://lup.lub.lu.se/record/80774862 URI
024a https://doi.org/10.1056/NEJMoa15054892 DOI
040 a (SwePub)lu
041 a engb eng
042 9 SwePub
072 7a art2 swepub-publicationtype
072 7a ref2 swepub-contenttype
100a Cung, T. -T.4 aut
2451 0a Cyclosporine before PCI in Patients with Acute Myocardial Infarction
264 1c 2015
520 a BACKGROUND Experimental and clinical evidence suggests that cyclosporine may attenuate reperfusion injury and reduce myocardial infarct size. We aimed to test whether cyclosporine would improve clinical outcomes and prevent adverse left ventricular remodeling. METHODS In a multicenter, double-blind, randomized trial, we assigned 970 patients with an acute anterior ST-segment elevation myocardial infarction (STEMI) who were undergoing percutaneous coronary intervention (PCI) within 12 hours after symptom onset and who had complete occlusion of the culprit coronary artery to receive a bolus injection of cyclosporine (administered intravenously at a dose of 2.5 mg per kilogram of body weight) or matching placebo before coronary recanalization. The primary outcome was a composite of death from any cause, worsening of heart failure during the initial hospitalization, rehospitalization for heart failure, or adverse left ventricular remodeling at 1 year. Adverse left ventricular remodeling was defined as an increase of 15% or more in the left ventricular end-diastolic volume. RESULTS A total of 395 patients in the cyclosporine group and 396 in the placebo group received the assigned study drug and had data that could be evaluated for the primary outcome at 1 year. The rate of the primary outcome was 59.0% in the cyclosporine group and 58.1% in the control group (odds ratio, 1.04; 95% confidence interval, 0.78 to 1.39; P = 0.77). Cyclosporine did not reduce the incidence of the separate clinical components of the primary outcome or other events, including recurrent infarction, unstable angina, and stroke. No significant difference in the safety profile was observed between the two treatment groups. CONCLUSIONS In patients with anterior STEMI who had been referred for primary PCI, intravenous cyclosporine did not result in better clinical outcomes than those with placebo and did not prevent adverse left ventricular remodeling at 1 year. (Funded by the French Ministry of Health and NeuroVive Pharmaceutical; CIRCUS ClinicalTrials.gov number, NCT01502774; EudraCT number, 2009-013713-99.)
650 7a MEDICIN OCH HÄLSOVETENSKAPx Klinisk medicinx Kardiologi0 (SwePub)302062 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Clinical Medicinex Cardiac and Cardiovascular Systems0 (SwePub)302062 hsv//eng
700a Morel, O.4 aut
700a Cayla, G.4 aut
700a Rioufol, G.4 aut
700a Garcia-Dorado, D.4 aut
700a Angoulvant, D.4 aut
700a Bonnefoy-Cudraz, E.4 aut
700a Guerin, P.4 aut
700a Elbaz, M.4 aut
700a Delarche, N.4 aut
700a Coste, P.4 aut
700a Vanzetto, G.4 aut
700a Metge, M.4 aut
700a Aupetit, J. -F.4 aut
700a Jouve, B.4 aut
700a Motreff, P.4 aut
700a Tron, C.4 aut
700a Labeque, J. -N.4 aut
700a Steg, P. G.4 aut
700a Cottin, Y.4 aut
700a Range, G.4 aut
700a Clerc, J.4 aut
700a Claeys, M. J.4 aut
700a Coussement, P.4 aut
700a Prunier, F.4 aut
700a Moulin, F.4 aut
700a Roth, O.4 aut
700a Belle, L.4 aut
700a Dubois, P.4 aut
700a Barragan, P.4 aut
700a Gilard, M.4 aut
700a Piot, C.4 aut
700a Colin, P.4 aut
700a De Poli, F.4 aut
700a Morice, M. -C.4 aut
700a Ider, O.4 aut
700a Dubois-Rande, J. -L.4 aut
700a Unterseeh, T.4 aut
700a Le Breton, H.4 aut
700a Beard, T.4 aut
700a Blanchard, D.4 aut
700a Grollier, G.4 aut
700a Malquarti, V.4 aut
700a Staat, P.4 aut
700a Sudre, A.4 aut
700a Elmer, Eskilu Lund University,Lunds universitet,Klinisk neurofysiologi,Sektion IV,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Mitokondriell Medicin,Forskargrupper vid Lunds universitet,Clinical Neurophysiology,Section IV,Department of Clinical Sciences, Lund,Faculty of Medicine,Mitochondrial Medicine,Lund University Research Groups4 aut0 (Swepub:lu)expb-eel
700a Hansson, Magnusu Lund University,Lunds universitet,Klinisk fysiologi, Lund,Sektion V,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Mitokondriell Medicin,Forskargrupper vid Lunds universitet,Clinical Physiology (Lund),Section V,Department of Clinical Sciences, Lund,Faculty of Medicine,Mitochondrial Medicine,Lund University Research Groups4 aut0 (Swepub:lu)expb-mha
700a Bergerot, C.4 aut
700a Boussaha, I.4 aut
700a Jossan, C.4 aut
700a Derumeaux, G.4 aut
700a Mewton, N.4 aut
700a Ovize, M.4 aut
710a Klinisk neurofysiologib Sektion IV4 org
773t New England Journal of Medicineg 373:11, s. 1021-1031q 373:11<1021-1031x 0028-4793
856u http://dx.doi.org/10.1056/NEJMoa1505489y FULLTEXT
8564 8u https://lup.lub.lu.se/record/8077486
8564 8u https://doi.org/10.1056/NEJMoa1505489

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