Evaluating the effects of empagliflozin in preventing myocardial injury in patients undergoing percutaneous coronary intervention: A double-blind, randomized clinical trial
Hossein Behzad, Sina Mashayekhi, Hila Asham, Parvin Sarbakhsh, Taher Entezari-Maleki

TL;DR
This study tested if empagliflozin can prevent heart injury during a common heart procedure, but found no significant benefits.
Contribution
The study provides new evidence on empagliflozin's ineffectiveness in preventing PCI-related myocardial injury.
Findings
Empagliflozin did not reduce cTnI levels at baseline, 8 hours, or 24 hours after PCI.
hs-CRP levels showed no significant differences between the empagliflozin and placebo groups.
No major adverse cardiac events occurred in either group.
Abstract
Percutaneous Coronary Intervention (PCI) is a fundamental procedure for coronary artery disease management, yet the risk of adverse events such periprocedural myocardial injury (PMI) persists. This double-blind, randomized clinical trial aims to assess the efficacy of empagliflozin in preventing myocardial injury during PCI procedure. A total of 90 patients were randomly assigned to two groups A and B; Group A as the intervention group received empagliflozin 25 mg 24 hours before and empagliflozin 10 mg 1-2 hours before coronary intervention and group Bas the control group received placebo at similar intervals. The primary outcome involved comparing baseline, 8-hour, and 24-hour cTnI and baseline and 24-hour hs-CRP levels after PCI in both groups to measure the incidence of periprocedural myocardial injury (PMI) and anti-inflammatory effects of empagliflozin. Baseline cTnI levels with…
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Taxonomy
TopicsDiabetes Treatment and Management · Lipoproteins and Cardiovascular Health · Antiplatelet Therapy and Cardiovascular Diseases
