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biomedad.ae. 2024;1(1): 34-41.
doi: 10.34172/bma.06
  Abstract View: 72
  PDF Download: 56
  Full Text View: 16

Original Article

Impact of Allopurinol on early and one-year outcomes of patients with ST-elevation myocardial infarction undergoing primary percutaneous coronary intervention: A randomized controlled trial

Nilgoon Daviran 1 ORCID logo, Amirhosein Ghafouri-Asbagh 1 ORCID logo, Hooman Nateghian 2* ORCID logo, Ahmad Separham 1 ORCID logo, Bahram Sohrabi 1 ORCID logo, Naser Aslanabadi 1 ORCID logo, Mehrdad Raadi 1 ORCID logo

1 Cardiovascular Research Center, Tabriz University of Medical Sciences, Tabriz, Iran
2 Research Center for Evidence‑Based Medicine, Iranian EBM Centre: A Joanna Briggs Institute Affiliated Group, Tabriz University of Medical Sciences, Tabriz, Iran
*Corresponding Author: Hooman Nateghian, Email: Hoomannt@gmail.com

Abstract

Background: Due to the potential benefits of allopurinol in ischemic reperfusion injury, this randomized control trial was performed to evaluate the pretreatment allopurinol effect on major adverse cardiovascular events (MACE) in patients undergoing primary percutaneous coronary intervention (pPCI).

Methods: A randomized controlled trial was performed on 170 firsttime STelevation myocardial infarction (STEMI) patients undergoing pPCI. Before the procedure, patients in intervention group (n=85) received 300 mg dose of allopurinol and control group (n=85) received placebo. Then, for the next 28 days, 100 mg of allopurinol was given to allopurinol group and placebo to the other group. Patients were compared regarding the baseline characteristics, clinical findings and oneyear MACE.

Findings: Our findings showed that patients receiving allopurinol had significantly longer doortoballoon time than the control group (60.76±19.38 vs. 50.06±16.38, P value: 0.001). During one year of followup, heart failure (HF), cerebrovascular event (CVA) and mortality occurred more frequently in allopurinol group but differences were not statistically significant. No significant difference was also seen between the two groups regarding MACE during followup or hospitalization (P=0.179, 0.330 respectively). KaplanMeier curve could not show a significant difference between the two groups in terms of mortality and MACE (P=0.317 and 0.128 respectively).

Conclusion: According to findings of this trial allopurinol had no cardioprotective effect against adverse cardiovascular events or death in patients undergoing pPCI.

Trial Registration: Identifier: IRCT20140512017666N2; https://irct.behdasht.gov.ir/.



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Submitted: 02 Jul 2024
Revision: 27 Aug 2024
Accepted: 10 Sep 2024
ePublished: 01 Oct 2024
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