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1.
Int J Cardiol ; 131(2): 285-7, 2009 Jan 09.
Article in English | MEDLINE | ID: mdl-17931721

ABSTRACT

A pilot study was performed to determine the effect of 40,000 IU Epo on myocardial damage in 51 patients with non-ST segment elevation acute coronary syndrome (non-STE ACS). No significant difference in myocardial damage was found, but an increased systolic blood pressure was noticed.


Subject(s)
Acute Coronary Syndrome/drug therapy , Acute Coronary Syndrome/pathology , Erythropoietin/therapeutic use , Myocardial Infarction/drug therapy , Epoetin Alfa , Erythropoietin/administration & dosage , Humans , Injections, Intravenous , Myocardial Infarction/pathology , Pilot Projects , Prospective Studies , Recombinant Proteins
2.
Curr Med Res Opin ; 24(3): 685-94, 2008 Mar.
Article in English | MEDLINE | ID: mdl-18226326

ABSTRACT

OBJECTIVE: To assess the incremental low-density lipoprotein-cholesterol (LDL-C) lowering efficacy of doubling the statin dose or switching to the ezetimibe/simvastatin 10/20 mg combination tablet (EZE/SIMVA) in patients on simvastatin 20 mg or atorvastatin 10 mg not at LDL-C target < 2.5 mmol/L. STUDY DESIGN AND METHODS: Patients with documented coronary heart disease (CHD) and/or type 2 diabetes (DM2) with LDL-C > or = 2.5 and < 5.0 mmol/L despite treatment with atorvastatin 10 mg or simvastatin 20 mg were randomized to (1) double statin dose or (2) switch to ezetimibe/simvastatin 10/20, according to a PROBE study design. LDL-C, lipoprotein subfractions and safety data were assessed during the study. RESULTS: 119 of 178 (67%) patients in the EZE/SIMVA group and 49 of 189 (26%) in the doubling statin group reached target LDL-C < 2.5 mmol/L. The odds ratio of success for EZE/SIMVA versus doubling statin treatment in reaching the LDL-C target of < 2.5 mmol/L was 5.7 (95% CI: 3.7-9.0, p < 0.0001). A reduction in total cholesterol (TC), total/high density lipoprotein (HDL) cholesterol ratio and apolipoprotein B was observed in both groups, but this reduction was significantly more pronounced in the EZE/SIMVA group as compared with the doubling statin dose group. Treatment was well tolerated and no difference was observed between the two groups with regard to adverse effects. CONCLUSIONS: In CHD/DM2 patients treated with simvastatin or atorvastatin with LDL-C persistently > or = 2.5 mmol/L, switching to the EZE/SIMVA was more effective in attaining the LDL-C target of < 2.5 mmol/L than doubling the statin dose.


Subject(s)
Anticholesteremic Agents/therapeutic use , Azetidines/therapeutic use , Cholesterol, LDL/drug effects , Coronary Artery Disease/drug therapy , Heptanoic Acids/therapeutic use , Hydroxymethylglutaryl-CoA Reductase Inhibitors/therapeutic use , Pyrroles/therapeutic use , Simvastatin/therapeutic use , Aged , Anticholesteremic Agents/administration & dosage , Anticholesteremic Agents/adverse effects , Atorvastatin , Azetidines/administration & dosage , Azetidines/adverse effects , Cholesterol, LDL/blood , Diabetes Mellitus, Type 2/blood , Drug Therapy, Combination , Ezetimibe , Female , Heptanoic Acids/administration & dosage , Heptanoic Acids/adverse effects , Humans , Hydroxymethylglutaryl-CoA Reductase Inhibitors/administration & dosage , Hydroxymethylglutaryl-CoA Reductase Inhibitors/adverse effects , Male , Middle Aged , Prospective Studies , Pyrroles/administration & dosage , Pyrroles/adverse effects , Simvastatin/administration & dosage , Simvastatin/adverse effects , Treatment Outcome
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