Abstract
Aims: We aimed to assess the effect of exenatide treatment as an adjunct to primary percutaneous coronary intervention (PCI) on long-term clinical outcome. Methods and results: We performed a post hoc analysis in 334 patients with a first STEMI included in a previous study randomised to exenatide (n=175) or placebo (n=159) as an adjunct to primary PCI. The primary endpoint was a composite of all-cause mortality and admission for heart failure during a median follow-up of 5.2 years (interquartile range: 5.0-5.5). Secondary endpoints were all-cause mortality and admission for heart failure, individually. The primary composite endpoint occurred in 24% in the exenatide group versus 27% in the placebo group, p=0.44 (HR 0.80, p=0.35). Admission for heart failure was lower in the exenatide (11%) compared to the placebo group (20%) (HR 0.53, p=0.042). All-cause mortality occurred in 14% in the exenatide group versus 9% in the placebo group (HR 1.45, p=0.20). Conclusions: In this post hoc analysis of patients with a STEMI, treatment with exenatide at the time of primary PCI did not reduce the primary composite endpoint or the secondary endpoint of all-cause mortality. However, exenatide treatment reduced the incidence of admission for heart failure.
| Originalsprog | Engelsk |
|---|---|
| Sider (fra-til) | 449-455 |
| Antal sider | 7 |
| Tidsskrift | EuroIntervention |
| Vol/bind | 12 |
| Udgave nummer | 4 |
| DOI | |
| Status | Udgivet - jul. 2016 |
| Udgivet eksternt | Ja |
Fingeraftryk
Udforsk hvilke forskningsemner 'A post hoc analysis of long-term prognosis after exenatide treatment in patients with ST-segment elevation myocardial infarction' indeholder.Citationsformater
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