Erythropoietin Reduces Post-PCI Arrhythmias in Patients With ST-elevation Myocardial Infarction

BACKGROUND:Arrhythmia is the foremost cause of sudden death after myocardial infarction (MI). Animal models have recently shown that erythropoietin (EPO) can reduce the incidence of arrhythmia after MI. METHODS:We investigated the effects of administrating 33,000 IU EPO on the occurrence of post-MI...

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Veröffentlicht in:Journal of cardiovascular pharmacology 2015-06, Vol.65 (6), p.555-561
Hauptverfasser: Gholamzadeh, Ali, Amini, Sara, Mohammadpour, Amir H, Vahabzadeh, Maryam, Fazelifar, Amir F, Fazlinezhad, Afsoon, Dehghani, Mashalla, Moohebati, Mohsen, Dastani, Mostafa, Malaekeh-Nikouie, Bizhan, Falsoleiman, Homa
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Sprache:eng
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Zusammenfassung:BACKGROUND:Arrhythmia is the foremost cause of sudden death after myocardial infarction (MI). Animal models have recently shown that erythropoietin (EPO) can reduce the incidence of arrhythmia after MI. METHODS:We investigated the effects of administrating 33,000 IU EPO on the occurrence of post-MI arrhythmia in 40 patients with ST-elevation MI who were randomly assigned in either EPO or placebo groups. Arrhythmias were blindly documented using full 12-lead configuration during 24 hours after percutaneous coronary intervention (PCI) by a cardiologist. Afterward, CK-MB, hematologic, and hemodynamic data were examined within 2 weeks after MI. RESULTS:A comparison made between the 2 groups showed significant differences in the incidence of arrhythmias (20% in EPO group and 35% in placebo group, P = 0.043). However, no significant differences in type of arrhythmias were observed between the groups. There was no significant difference between levels of CK-MB in the 2 groups during 24 hours (P = 0.186). Hematologic and hemodynamic data showed no significant changes 2 weeks after PCI. CONCLUSION:High-dose administration of EPO in patients with ST-elevation MI who have been treated by primary PCI and standard antiplatelet therapy reduces the occurrence of arrhythmias. For clinical interpretation of the results, further well-designed trials are required.
ISSN:0160-2446
1533-4023
DOI:10.1097/FJC.0000000000000223