Data on administration of cyclosporine, nicorandil, metoprolol on reperfusion related outcomes in ST-segment Elevation Myocardial Infarction treated with percutaneous coronary intervention

  • Gianluca Campo
  • , Rita Pavasini
  • , Giampaolo Morciano
  • , Michael A. Lincoff
  • , Michael C. Gibson
  • , Masafumi Kitakaze
  • , Jacob Lonborg
  • , Amrita Ahluwalia
  • , Hideki Ishii
  • , Michael Frenneaux
  • , Michel Ovize
  • , Marcello Galvani
  • , Dan Atar
  • , Borja Ibanez
  • , Giampaolo Cerisano
  • , Simone Biscaglia
  • , Brandon J. Neil
  • , Masanori Asakura
  • , Thomas Engstrom
  • , Daniel A. Jones
  • Dana Dawson, Roberto Ferrari, Paolo Pinton, Filippo Ottani

Research output: Contribution to journalArticlepeer-review

16 Citations (Scopus)

Abstract

Mortality and morbidity in patients with ST elevation myocardial infarction (STEMI) treated with primary percutaneous coronary intervention (PCI) are still high [1]. A huge amount of the myocardial damage is related to the mitochondrial events happening during reperfusion [2]. Several drugs directly and indirectly targeting mitochondria have been administered at the time of the PCI and their effect on fatal (all-cause mortality, cardiovascular (CV) death) and non fatal (hospital readmission for heart failure (HF)) outcomes have been tested showing conflicting results [3–16]. Data from 15 trials have been pooled with the aim to analyze the effect of drug administration versus placebo on outcome [17]. Subgroup analysis are here analyzed: considering only randomized clinical trial (RCT) on cyclosporine or nicorandil [3–5,9–11], excluding a trial on metoprolol [12] and comparing trial with follow-up length <12 months versus those with longer follow-up [3–16]. This article describes data related article titled “Clinical Benefit of Drugs Targeting Mitochondrial Function as an Adjunct to Reperfusion in ST-segment Elevation Myocardial Infarction: a Meta-Analysis of Randomized Clinical Trials” [17].

Original languageEnglish
Pages (from-to)197-205
Number of pages9
JournalData in Brief
Volume14
DOIs
Publication statusPublished - 10-2017

All Science Journal Classification (ASJC) codes

  • General

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