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dc.contributor.authorSpyropoulos, Alex C.
dc.contributor.authorAgeno, Walter
dc.contributor.authorAlbers, Gregory W.
dc.contributor.authorElliott, C. Gregory
dc.contributor.authorHalperin, Jonathan L.
dc.contributor.authorHiatt, William R.
dc.contributor.authorKaatz, Scott
dc.date.accessioned2020-12-19T19:41:20Z
dc.date.available2020-12-19T19:41:20Z
dc.date.issued2018
dc.identifier.citationSpyropoulos, A. C., Ageno, W., Albers, G. W., Elliott, C. G., Halperin, J. L., Hiatt, W. R., Maynard, G. A., Steg, P. G., Weitz, J. I., Suh, E., Spiro, T. E., Barnathan, E. S., Raskob, G. E., & MARINER Investigators (2018). Rivaroxaban for Thromboprophylaxis after Hospitalization for Medical Illness. The New England journal of medicine, 379(12), 1118–1127. https://doi.org/10.1056/NEJMoa1805090en_US
dc.identifier.issn0028-4793
dc.identifier.issn1533-4406
dc.identifier.urihttps://doi.org/10.1056/NEJMoa1805090
dc.identifier.urihttps://hdl.handle.net/11436/1759
dc.descriptionGrinshtein, Yury/0000-0001-8847-235X; Vyshnyvetskyy, Ivan/0000-0001-7228-3052; Lodigiani, Corrado/0000-0002-9152-9385; Shpagina, Lyubov/0000-0003-0871-7551; Yildiz, Oznur/0000-0002-5379-6829; Weitz, Jeffrey/0000-0002-1092-7550; Nikolaev, Konstantin/0000-0003-4601-6203; Boldueva, Svetlana/0000-0002-1898-084X; Malynovsky, Yaroslav V/0000-0002-9118-1104; Andreev, Denis ?/0000-0002-0276-7374; Prozesky, Hans/0000-0001-9715-3449; Bustillo, Sonia Ruiz/0000-0002-6074-914X; Musial, Jacek/0000-0002-8994-0036; Tsivgoulis, Georgios/0000-0002-0640-3797; Reis, Gilmar/0000-0002-4847-1034; Apartsin, Konstantin A/0000-0003-0577-9001; Zateyshchikov, Dmitry A/0000-0001-7065-2045; Ruzic, Alen/0000-0001-5031-2975; Maslovskyi, Valentyn/0000-0001-5184-1799; Tudoran, Mariana M/0000-0001-8989-5899; Maslovskyi, Valentyn/0000-0001-5184-1799; Marchev, Sotir/0000-0001-9250-510X; Barbarash, Olga/0000-0002-4642-3610; Gallus, Alexander/0000-0001-7347-9989; Giorgi-Pierfranceschi, Matteo/0000-0002-7988-9652; Konstantinides, Stavros/0000-0001-6359-7279; Sanchez Martinez, Rosario/0000-0003-0408-3029; Antonicelli, Roberto/0000-0002-5921-1828; Cuervas-Mons Martinez, Valentin/0000-0003-3086-9463; Karapanayiotides, Theodoros/0000-0002-2357-7967; Lopez Meseguer, Manuel/0000-0003-2650-9238; Ramacciotti, Eduardo/0000-0002-5735-1333; Torbicki, Adam/0000-0003-3475-8832; Zolotaikina, Viktoriia/0000-0002-5265-4861; Baker, Ross/0000-0002-2728-6788; Jara-Palomares, Luis/0000-0002-4125-3376; Koziolkin, Olexandr/0000-0001-9878-5798; Gregorio, Tiago/0000-0002-0131-9430; Repin, Alexey/0000-0001-7123-0645; Khorana, Alok/0000-0002-9509-0998; Kosmacheva, Elena/0000-0001-8600-0199; Apostolovic, Svetlana/0000-0001-9015-297X; Khalafallah, Alhossain/0000-0002-2399-3311; Sala-Llinas, Ernest/0000-0002-6499-1638; Abragamovic, Orest/0000-0001-6862-6809en_US
dc.descriptionWOS: 000445020900006en_US
dc.descriptionPubMed: 30145946en_US
dc.description.abstractBACKGROUND Patients who are hospitalized for medical illness remain at risk for venous thromboembolism after discharge, but the role of extended thromboprophylaxis in the treatment of such patients is a subject of controversy. METHODS in this randomized, double-blind trial, medically ill patients who were at increased risk for venous thromboembolism on the basis of a modified International Medical Prevention Registry on Venous Thromboembolism (IMPROVE) score of 4 or higher (scores range from 0 to 10, with higher scores indicating a higher risk of venous thromboembolism) or a score of 2 or 3 plus a plasma n-dimer level of more than twice the upper limit of the normal range (defined according to local laboratory criteria) were assigned at hospital discharge to either once-daily rivaroxaban at a dose of 10 mg (with the dose adjusted for renal insufficiency) or placebo for 45 days. the primary efficacy outcome was a composite of symptomatic venous thromboembolism or death due to venous thromboembolism. the principal safety outcome was major bleeding. RESULTS of the 12,024 patients who underwent randomization, 12,019 were included in the intention-to-treat analysis. the primary efficacy outcome occurred in 50 of 6007 patients (0.83%) who were given rivaroxaban and in 66 of 6012 patients (1.10%) who were given placebo (hazard ratio, 0.76; 95% confidence interval [CI], 0.52 to 1.09; P=0.14). the prespecified secondary outcome of symptomatic nonfatal venous thromboembolism occurred in 0.18% of patients in the rivaroxaban group and 0.42% of patients in the placebo group (hazard ratio, 0.44; 95% CI, 0.22 to 0.89). Major bleeding occurred in 17 of 5982 patients (0.28%) in the rivaroxaban group and in 9 of 5980 patients (0.15%) in the placebo group (hazard ratio, 1.88; 95% CI, 0.84 to 4.23). CONCLUSIONS Rivaroxaban, given to medical patients for 45 days after hospital discharge, was not associated with a significantly lower risk of symptomatic venous thromboembolism and death due to venous thromboembolism than placebo. the incidence of major bleeding was low.en_US
dc.description.sponsorshipJanssen Research and Development; Daiichi SankyoDaiichi Sankyo Company Limited; Portola; Boehringer IngelheimBoehringer Ingelheim; JanssenJohnson & Johnson USAJanssen Biotech Inc; BayerBayer AG; BMS PfizerPfizer; Aspen; Sanofi; University of Cincinnati and Spectrum Health; PfizerPfizer; ATLAS Group (Colorado Prevention Center); Johnson JohnsonJohnson & Johnson USA; Ortho-McNeil-JanssenJohnson & Johnson USAJanssen Biotech Inc; Bayer/JanssenJohnson & Johnson USAJanssen Biotech IncBayer AG; MerckMerck & Company; AmgenAmgenen_US
dc.description.sponsorshipSupported by Janssen Research and Development.r Dr. Spyropoulos reports receiving advisory board fees from Daiichi Sankyo and Portola, grant support, consulting fees, and advisory board fees from Boehringer Ingelheim and Janssen, consulting fees and advisory board fees from Bayer, and a stipend from ATLAS Group (Colorado Prevention Center); Dr. Ageno, receiving grant support and advisory board fees from Bayer and BMS Pfizer and advisory board fees from Portola, Daiichi Sankyo, Aspen, Boehringer Ingelheim, and Sanofi; Dr. Albers, receiving consulting fees from Bayer; Dr. Elliott, receiving fees for serving on a steering committee from Bayer and lecture fees from the University of Cincinnati and Spectrum Health; Dr. Halperin, receiving consulting fees from Boehringer Ingelheim, Daiichi Sankyo, Pfizer, ATLAS Group (Colorado Prevention Center), Johnson & Johnson, and Ortho-McNeil-Janssen; Dr. Hiatt, receiving grant support from Janssen and Bayer; Dr. Steg, receiving grant support and fees for serving on a steering committee from Bayer/Janssen, grant support and lecture fees from Merck, grant support, consulting fees, lecture fees, and fees for serving as cochair of the ODYSSEY outcomes trial and the SCORED trial from Sanofi, grant support and fees for serving as chair of the CLARIFY registry from Servier, consulting fees and fees for serving on the executive steering committee for the REDUCE IT trial from Amarin, consulting fees and lecture fees from Amgen, consulting fees, lecture fees, and fees for critical event committee work from Bristol-Myers Squibb, fees for serving on the executive steering committee of the REDUAL PCI trial from Boehringer Ingelheim, fees for critical event committee work from Pfizer, consulting fees and fees for serving on the executive steering committee for the PARADISE MI trial from Novartis, consulting fees from Regeneron and Lilly, and consulting fees and fees for serving as cochair of the THEMIS trial from AstraZeneca; Dr. Weitz, receiving consulting fees and honoraria from Bayer, Boehringer Ingelheim, Bristol-Myers Squibb, Daiichi Sankyo, Ionis, Janssen, Merck, Novartis, Pfizer and Portola; Dr. Suh and Dr. Barnathan, being employed by Janssen Research and Development and owning stock in Johnson & Johnson; Dr. Spiro, being employed by and owning shares in Bayer U.S.; and Dr. Raskob, receiving consulting fees from Bayer, BMS, Boehringer Ingelheim, Eli Lilly, Portola, and Novartis and consulting fees and honoraria from Daiichi Sankyo and Pfizer. No other potential conflict of interest relevant to this article was reported.en_US
dc.language.isoengen_US
dc.publisherMassachusetts Medical Socen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleRivaroxaban for thromboprophylaxis after hospitalization for medical illnessen_US
dc.typearticleen_US
dc.contributor.departmentRTEÜ, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümüen_US
dc.contributor.departmentDursun, Adile Berna
dc.contributor.institutionauthorDursun, Adile Berna
dc.identifier.doi10.1056/NEJMoa1805090
dc.identifier.volume379en_US
dc.identifier.issue12en_US
dc.identifier.startpage1118en_US
dc.identifier.endpage1127en_US
dc.ri.editoaen_US
dc.relation.journalNew England Journal of Medicineen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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