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dc.contributor.authorNamal, Esat
dc.contributor.authorSener, Nur
dc.contributor.authorUlas, Turgay
dc.contributor.authorAkcali, Zafer
dc.contributor.authorOztekin, Erkan
dc.contributor.authorBorlu, Fatih
dc.date.accessioned2019-08-13T12:10:23Z
dc.date.accessioned2019-08-13T16:03:54Z
dc.date.available2019-08-13T12:10:23Z
dc.date.available2019-08-13T16:03:54Z
dc.date.issued2011
dc.identifier.issn1302-8723
dc.identifier.urihttps://dx.doi.org/10.5152/akd.2011.192
dc.identifier.urihttp://hdl.handle.net/11446/3192
dc.descriptionWOS: 000298576700009en_US
dc.descriptionPubMed ID: 22088858en_US
dc.description.abstractObjective: The aim of our study was to evaluate the effects of two different statins and a statin/ezetimibe combination on high sensitive C-reactive protein (hsCRP) values, which were given at high doses in the early period of acute coronary syndromes. Methods: A total of 150 patients with non-ST elevation myocardial infarction and unstable angina pectoris were enrolled to our prospective, randomized, single-blind study. Patients were divided into three groups by block randomization method. One group received 20mg/day atorvastatin, one group received 10 mg/day rosuvastatin and the other group received 10 mg/day ezetimibe/simvastatin combination therapy, which was initiated within the first 24 hours of admission. Follow-up duration was 2 months. Biochemical investigations and hsCRP levels (by nephelometric method) were performed with 138 patients evaluated at baseline, 10(th) and 60(th) days of therapy. Decreases of hsCRP levels were analyzed with one-way MANOVA and repeated measures of ANOVA methods. Post-hoc Tukey HSD test was performed for finding the different group, when the difference was detected between the groups. Results: Tenth day hsCRP levels in ezetimibe/simvastatin group was significantly lower than the other groups (p<0.001). Further, after 60 days of follow-up a significant reduction was seen in hsCRP levels in ezetimib/simvastatin group (in ezetimibe/simvastatin group the mean hsCRP was reduced from 38.4 +/- 15.0 mg/L to 2.4 +/- 1.3 mg/L, in atorvastatin group the mean hsCRP was reduced from 27.3 +/- 11.7 mg/L to 4.1 +/- 2.4 mg/L and in rosuvastatin group the mean hsCRP was reduced from 22.0 +/- 6.9 mg/L to 3.6 +/- 1.7 mg/L (F (1.1, 148.2) = 746.9, p<0.01 and the difference between drugs; F (2.2, 148.2) = 32.1, p<0.01). No side effects related to drugs were seen during follow-up in all three treatment groups. Conclusion: This study showed that ezetimibe/simvastatin 10 mg/day combination treatment was superior to atorvastatin 20 mg/day and rosuvastatin 10 mg/day treatment in reducing the inflammatory markers when high dose statins was started in the early period of unstable angina and non ST elevation myocardial infarction. (Anadolu Kardiyol Derg 2011; 11: 703-10)en_US
dc.language.isoturen_US
dc.publisherAVES YAYINCILIKen_US
dc.identifier.doi10.5152/akd.2011.192en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAcute coronary syndromeen_US
dc.subjectstatinsen_US
dc.subjecttreatmenten_US
dc.subjectC - reactive proteinen_US
dc.subjectlipidsen_US
dc.titleEffects of different statins, ezetimibe/simvastatin combination On hsCRP levels in unstable angina pectoris and non-ST elevation myocardial infarction patients: a randomized trialen_US
dc.typearticleen_US
dc.relation.journalANADOLU KARDIYOLOJI DERGISI-THE ANATOLIAN JOURNAL OF CARDIOLOGYen_US
dc.departmentDBÜen_US
dc.identifier.issue8en_US
dc.identifier.volume11en_US
dc.identifier.startpage703en_US
dc.identifier.endpage710en_US
dc.contributor.authorID0000-0003-2473-4431en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.department-temp[Ulas, Turgay] Harran Univ, Tip Fak, Ic Hastaliklan Anabilim Dali, Sanliurfa, Turkey -- [Namal, Esat -- Akcali, Zafer] Bilim Univ, Tip Fak, Tibbi Onkol Bilim Dalt, Istanbul, Turkey -- [Sener, Nur] Kartal Egitim Arastirma Hastanesi, Tibbi Onkol Bilim Dalt, Istanbul, Turkey -- [Oztekin, Erkan] Sisli Etfal Egitim & Arastirma Hastanesi, Istanbul, Turkeyen_US


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