Efficacy of Zofenopril Compared with Placebo and Other Angiotensin-converting Enzyme Inhibitors in Patients with Acute Myocardial Infarction and Previous Cardiovascular Risk Factors: A Pooled Individual Data Analysis of 4 Randomized, Double-blind, Controlled, Prospective Studies

Autor: Giorgio Reggiardo, Stefano Omboni, Daniela Degli Esposti, Claudio Borghi, Ettore Ambrosioni, Stefano Bacchelli
Přispěvatelé: DIPARTIMENTO DI SCIENZE MEDICHE E CHIRURGICHE, Facolta' di MEDICINA e CHIRURGIA, AREA MIN. 06 - Scienze mediche, Borghi, Claudio, Omboni, Stefano, Reggiardo, Giorgio, Bacchelli, Stefano, Esposti, Daniela Degli, Ambrosioni, Ettore
Jazyk: angličtina
Rok vydání: 2017
Předmět:
Ramipril
Male
cardiovascular risk
medicine.medical_specialty
Captopril
Myocardial Infarction
Angiotensin-Converting Enzyme Inhibitors
Acute myocardial infarction
030204 cardiovascular system & hematology
Placebo
03 medical and health sciences
chemistry.chemical_compound
0302 clinical medicine
Double-Blind Method
Risk Factors
Internal medicine
Medicine
Humans
030212 general & internal medicine
Myocardial infarction
Prospective Studies
Risk factor
Aged
Randomized Controlled Trials as Topic
Retrospective Studies
angiotensinconverting enzyme inhibitors
Pharmacology
business.industry
Hazard ratio
Lisinopril
Middle Aged
medicine.disease
Zofenopril
drug therapy
Cardiology and Cardiovascular Medicine
Treatment Outcome
chemistry
Cardiovascular Diseases
Cardiology
Original Article
Female
Myocardial infarction diagnosis
business
angiotensinconverting enzyme inhibitor
medicine.drug
Zdroj: Journal of Cardiovascular Pharmacology
Popis: none 6 no In the Survival of Myocardial Infarction Long-term Evaluation (SMILE) 1, 3, and 4 studies, early administration of zofenopril in acute myocardial infarction showed to be prognostically beneficial versus placebo or ramipril. The SMILE-2 showed that both zofenopril and lisinopril are safe and showed no significant differences in the incidence of major cardiovascular (CV) complications. In this pooled analysis of individual data of the SMILE studies, we evaluated whether the superior efficacy of zofenopril is maintained also in patients with 1 CV risk factor (CV+, n = 2962) as compared to CV2 (n = 668). The primary study end point was set to 1-year combined occurrence of death or hospitalization for CV causes. The risk of CV events was significantly reduced with zofenopril versus placebo either in the CV+ (237%; hazard ratio: 0.63; 95% confidence interval: 0.51-0.78; P = 0.0001) or in the CV2 group (255%; hazard ratio: 0.45; 0.26-0.78; P = 0.004). Also, the other angiotensinconverting enzyme inhibitors reduced the risk of major CV outcomes, though the reduction was not statistically significant versus placebo (CV+: 0.78; 0.58-1.05; P = 0.107; CV2: 0.71; 0.36-1.41; P = 0.334). The benefit was larger in patients treated with zofenopril than other angiotensin-converting enzyme inhibitors, with a statistically significant difference for CV+ (0.79; 0.63-0.99; P = 0.039) versus CV2 (0.62; 0.37-1.06; P = 0.081). In conclusion, zofenopril administered to patients after acute myocardial infarction has a positive impact on prognosis, regardless of the patient's CV risk profile. none Borghi, Claudio; Omboni, Stefano; Reggiardo, Giorgio; Bacchelli, Stefano; Esposti, Daniela Degli; Ambrosioni, Ettore Borghi, Claudio; Omboni, Stefano; Reggiardo, Giorgio; Bacchelli, Stefano; Esposti, Daniela Degli; Ambrosioni, Ettore
Databáze: OpenAIRE