Yayın: Efficacy and safety of extended-release fluvastatin in Turkish patients with hypercholesterolaemia: TULIPS (Turkish Lipid Study)
| dc.contributor.author | İlerigelen, Barış | |
| dc.contributor.author | Üresin, Ali Yağız | |
| dc.contributor.author | Şan, Mustafa | |
| dc.contributor.author | Güneri, Sema | |
| dc.contributor.author | Kültürsay, Hakan | |
| dc.contributor.author | Güleç, Sadi | |
| dc.contributor.author | Pençedemir, H. | |
| dc.contributor.buuauthor | Serdar, Osman Akın | |
| dc.contributor.department | Tıp Fakültesi | |
| dc.contributor.department | Kardiyoloji Ana Bilim Dalı | |
| dc.contributor.researcherid | AAF-5116-2019 | |
| dc.contributor.scopusid | 6507416315 | |
| dc.date.accessioned | 2024-02-27T06:17:56Z | |
| dc.date.available | 2024-02-27T06:17:56Z | |
| dc.date.issued | 2007-03-07 | |
| dc.description | Bu çalışma, 25-29 Haziran 2005 tarihleri arasında Poznan[Polonya]'da düzenlenen 7. Congress of the European Association for Clinical Pharmacology and Therapeutics'da bildiri olarak sunulmuştur. | |
| dc.description.abstract | Objective:The efficacy and safety of extended-release fluvastatin (fluvastatin XL), 80 mg once daily, was assessed in Turkish patients with primary hypercholesterolaemia (low-density lipoprotein cholesterol (LDL-C) 3.37-5.70 mmol/l and triglyceride (TG) < 4.52 mmol/l). Research design: In this open-label, prospective, multi-centre study, 154 patients were given fluvastatin XL 80 mg once daily and lipid levels were assessed after 2 and 12 weeks. Results: Fluvastatin XL 80 mg once daily significantly reduced LDL-C levels by 38.8 and 38.1% at weeks 2 (n = 140) and 12 (n = 116), respectively (p < 0.001 vs. baseline). Treatment with fluvastatin XL for 2 and 12 weeks significantly reduced total cholesterol levels by 30.2 and 27.4%, respectively (p < 0.001 vs. baseline) and reduced TG levels by 14.9 and 7.5%, respectively (p < 0.001 vs. baseline). Following stratification by risk factors for coronary heart disease (CHD) according to the National Cholesterol Education Program Adult Treatment Panel III guidelines, 87.3% of patients with >= 2 risk factors, and 67.4% of patients with existing CHD or CHD risk equivalents achieved target LDL-C levels (< 3.37 mmol/l and < 2.59 mmol/l, respectively) with fluvastatin XL. Fluvastatin XL reduced high-density lipoprotein cholesterol by 8.9 and 4.7% at weeks 2 and 12 weeks, respectively. fluvastatin XL 80 mg once daily was generally well-tolerated. Conclusions: This open-label study indicates fluvastatin XL 80 mg once daily is an effective and well-tolerated lipid-lowering therapy for the reduction of CHD risk in Turkish patients. | |
| dc.description.sponsorship | European Assoc Clin Pharmacol & Therapeut | |
| dc.identifier.citation | İlerigelen, B. vd. (2007). "Efficacy and safety of extended-release fluvastatin in Turkish patients with hypercholesterolaemia: TULIPS (Turkish Lipid Study)". Current Medical Research and Opinion, 23(5), 1093-1102. | |
| dc.identifier.doi | 10.1185/030079907X187847 | |
| dc.identifier.eissn | https://doi.org/10.1185/030079907X187847 | |
| dc.identifier.endpage | 1102 | |
| dc.identifier.issue | 5 | |
| dc.identifier.pubmed | 17519076 | |
| dc.identifier.scopus | 2-s2.0-34249045734 | |
| dc.identifier.startpage | 1093 | |
| dc.identifier.uri | https://www.tandfonline.com/doi/abs/10.1185/030079907X187847 | |
| dc.identifier.uri | https://hdl.handle.net/11452/39979 | |
| dc.identifier.volume | 23 | |
| dc.identifier.wos | 000248757500017 | |
| dc.indexed.wos | SCIE | |
| dc.indexed.wos | CPCIS | |
| dc.language.iso | en | |
| dc.publisher | Taylor & Francis | |
| dc.relation.collaboration | Yurt içi | |
| dc.relation.journal | Current Medical Research and Opinion | |
| dc.relation.publicationcategory | Konferans Öğesi - Uluslararası | |
| dc.rights | info:eu-repo/semantics/closedAccess | |
| dc.subject | Extended-release | |
| dc.subject | Triglycerides | |
| dc.subject | Fluvastatin | |
| dc.subject | Low-density lipoprotein cholesterol | |
| dc.subject | Hypercholesterolaemia | |
| dc.subject | C-reactive protein | |
| dc.subject | Coronary-artery-disease | |
| dc.subject | Cholesterol levels | |
| dc.subject | Statin therapy | |
| dc.subject | Pharmacokinetics | |
| dc.subject | Cardiac events | |
| dc.subject | Atherosclerosis | |
| dc.subject | Risk | |
| dc.subject | Mortality | |
| dc.subject | Prevention | |
| dc.subject.emtree | Adult | |
| dc.subject.emtree | Aged | |
| dc.subject.emtree | Article | |
| dc.subject.emtree | Cardiovascular risk | |
| dc.subject.emtree | Cholesterol blood level | |
| dc.subject.emtree | Clinical feature | |
| dc.subject.emtree | Clinical trial | |
| dc.subject.emtree | Controlled clinical trial | |
| dc.subject.emtree | Controlled drug release | |
| dc.subject.emtree | Controlled study | |
| dc.subject.emtree | Diabetes mellitus | |
| dc.subject.emtree | Diarrhea | |
| dc.subject.emtree | Drug effect | |
| dc.subject.emtree | Drug efficacy | |
| dc.subject.emtree | Drug release | |
| dc.subject.emtree | Drug safety | |
| dc.subject.emtree | Drug tolerability | |
| dc.subject.emtree | Drug withdrawal | |
| dc.subject.emtree | Female | |
| dc.subject.emtree | Human | |
| dc.subject.emtree | Hypercholesterolemia | |
| dc.subject.emtree | Hypertension | |
| dc.subject.emtree | Ischemic heart disease | |
| dc.subject.emtree | Lipid blood level | |
| dc.subject.emtree | Major clinical study | |
| dc.subject.emtree | Male | |
| dc.subject.emtree | Metabolic syndrome x | |
| dc.subject.emtree | Multicenter study | |
| dc.subject.emtree | Nausea | |
| dc.subject.emtree | Patient compliance | |
| dc.subject.emtree | Protein blood level | |
| dc.subject.emtree | Risk factor | |
| dc.subject.emtree | Side effect | |
| dc.subject.emtree | Single drug dose | |
| dc.subject.emtree | Skin manifestation | |
| dc.subject.emtree | Smoking habit | |
| dc.subject.emtree | Unspecified side effect | |
| dc.subject.emtree | Alanine aminotransferase | |
| dc.subject.emtree | Apolipoprotein b | |
| dc.subject.emtree | Aspartate aminotransferase | |
| dc.subject.emtree | Beta adrenergic receptor blocking agent | |
| dc.subject.emtree | C reactive protein | |
| dc.subject.emtree | Creatine kinase | |
| dc.subject.emtree | Diuretic agent | |
| dc.subject.emtree | Fluindostatin | |
| dc.subject.emtree | High density lipoprotein | |
| dc.subject.emtree | Lescol xl | |
| dc.subject.emtree | Low density lipoprotein | |
| dc.subject.emtree | Triacylglycerol | |
| dc.subject.emtree | Unclassified drug | |
| dc.subject.scopus | Hydroxymethylglutaryl-Coa Reductase Inhibitor; Low Density Lipoprotein Cholesterol; Dyslipidemias | |
| dc.subject.wos | Medicine, general & internal | |
| dc.subject.wos | Medicine, research & experimental | |
| dc.title | Efficacy and safety of extended-release fluvastatin in Turkish patients with hypercholesterolaemia: TULIPS (Turkish Lipid Study) | |
| dc.type | Article | |
| dc.type | conferenceObject | |
| dc.type.subtype | Proceedings Paper | |
| dc.wos.quartile | Q1 (Medicine, general & internal) | |
| dc.wos.quartile | Q2 (Medicine, research & experimental) | |
| dspace.entity.type | Publication | |
| local.contributor.department | Tıp Fakültesi/Kardiyoloji Ana Bilim Dalı | |
| local.indexed.at | WOS | |
| local.indexed.at | Scopus | |
| local.indexed.at | PubMed |
