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dc.contributor.authorYildiz, Banu Sahin
dc.contributor.authorAkin, Ibrahim
dc.contributor.authorAydin, Ebuzer
dc.contributor.authorYILDIZ, Mustafa
dc.date.accessioned2021-03-04T10:30:42Z
dc.date.available2021-03-04T10:30:42Z
dc.date.issued2014
dc.identifier.citationYildiz B. S. , YILDIZ M., Aydin E., Akin I., "Triple antiplatelet therapy after PCI - should or could it be done?", Cardiovascular and Hematological Disorders - Drug Targets, cilt.14, sa.3, ss.235-239, 2014
dc.identifier.otherav_6d9769fe-a898-4fc3-810f-e07ed08792e9
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/75704
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84924193495&origin=inward
dc.identifier.urihttps://doi.org/10.2174/1871529x14666140825095243
dc.description.abstract© 2014 Bentham Science Publishers.In case of coronary stenting in patients taking long-term oral anticoagulants (OAC), addition of both aspirin and clopidogrel in the drug regimen (so-called triple antiplatelet therapy) is recommended. However such triple therapy increases the risk of serious bleeding events. Comparative data on the efficacy and safety of the triple therapy versus therapy with a single antiplatelet agent and oral anticoagulants in case of coronary stenting are very rare. Most studies show a decreased stroke and myocardial infarction risk, but an increased risk of bleeding events in case of triple therapy. There is general agreement that, when possible, the duration of triple therapy should be shortened followed by clopidogrel and an oral anticoagulant to minimize bleeding risk without increasing other adverse events. In patients with a high risk of bleeding, BMS should be used and triple therapy should be applied for only 1month, followed by one antiplatelet agent and oral anticoagulant. The WOEST study was the first study showing that therapy with clopidogrel and OAC is safe and reduces bleeding and mortality more effectively than triple therapy including aspirin in patients undergoing coronary stenting. Although the risk of bleeding increases with triple therapy as compared to OAC plus a single antiplatelet agent, the second treatment regimen cannot be recommended to all patients. However for those at the highest risk of bleeding it is not unreasonable to consider. Additional randomized studies are needed for the implementation of future treatment guidelines in patients with high risk for bleeding and thrombotic complications.
dc.language.isoeng
dc.subjectYaşam Bilimleri
dc.subjectBiyoteknoloji
dc.subjectTemel Bilimler
dc.subjectMolecular Medicine
dc.subjectLife Sciences
dc.subjectHematology
dc.subjectHealth Sciences
dc.subjectPharmacology
dc.subjectCardiology and Cardiovascular Medicine
dc.subjectKlinik Tıp (MED)
dc.subjectYaşam Bilimleri (LIFE)
dc.subjectKlinik Tıp
dc.subjectFarmakoloji ve Toksikoloji
dc.subjectMikrobiyoloji
dc.subjectCARDIAC ve CARDIOVASCULAR SİSTEMLER
dc.subjectHEMATOLOJİ
dc.subjectFARMAKOLOJİ VE ECZACILIK
dc.subjectBİYOTEKNOLOJİ VE UYGULAMALI MİKROBİYOLOJİ
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectDahili Tıp Bilimleri
dc.subjectİç Hastalıkları
dc.subjectHematoloji
dc.subjectKardiyoloji
dc.subjectEczacılık
dc.subjectTemel Eczacılık Bilimleri
dc.titleTriple antiplatelet therapy after PCI - should or could it be done?
dc.typeMakale
dc.relation.journalCardiovascular and Hematological Disorders - Drug Targets
dc.contributor.departmentKartal Education and Research Hospital , ,
dc.identifier.volume14
dc.identifier.issue3
dc.identifier.startpage235
dc.identifier.endpage239
dc.contributor.firstauthorID2508045


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