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DC Field | Value | Language |
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dc.contributor.author | Karim, Birry | - |
dc.contributor.author | Alwi, Idrus | - |
dc.contributor.author | Yamin, Mohammad | - |
dc.contributor.author | Pasaribu, Merci Monica | - |
dc.contributor.author | Harimurti, Kuntjoro | - |
dc.contributor.author | Nafrialdi | - |
dc.date.accessioned | 2025-07-21T01:49:29Z | - |
dc.date.available | 2025-07-21T01:49:29Z | - |
dc.date.issued | 2025-01 | - |
dc.identifier.citation | Original Article | en_US |
dc.identifier.uri | http://localhost:8080/xmlui/handle/123456789/12243 | - |
dc.description.abstract | Background: Inflammation plays a role in ST-segment elevation myocardial infarction (STEMI), especially in reperfusion injury (RI). Colchicine, an anti-inflammatory drug, can suppress inflammation during RI. We assessed the effectiveness of administering colchicine to STEMI patients undergoing primary percutaneous coronary intervention (PPCI) in suppressing RI events. Methods: This study was a randomized, double-blind, placebo-controlled clinical trial conducted in a multicenter manner at two hospitals in Jakarta with IKPP facilities from December 2022 to April 2023. STEMI patients that underwent PPCI received 2 mg of colchicine as a loading dose and a maintenance dose of 0.5 mg every 12 hours for two days or amylum at a similar dose. Patients were observed for RI events (low-flow thrombolysis in myocardial infarction (0–2) during angiography procedure, reperfusion arrhythmia, cardiogenic shock, or persistent chest pain). Results: Seventy-seven STEMI patients with a mean age of 55.2 ± 9.9 years underwent PPCI. Of these patients, 37 received colchicine, and 40 received a placebo. Most subjects were male (77.5%), suffered three-vessel disease (44.15%), and occlusion in left anterior descending coronary artery (53.24%). Colchicine was found to fail to reduce the incidence of ischemia-RI (51.5% vs. 42.4%; p = 0.437). Analysis of comorbidities (hypertension, chronic kidney disease, diabetes mellitus, and obesity) and angiography results (vessel disease, lesion diameter, and culprit artery) failed to demonstrate a statistical difference in RI. Side effects were similar in the colchicine and placebo groups (21.6% vs. 15%). Conclusion: Colchicine administration in STEMI patients undergoing PPCI failed to reduce RI. | en_US |
dc.language.iso | en_US | en_US |
dc.publisher | Acta Medika Indonesia | en_US |
dc.subject | Colchicine, | en_US |
dc.subject | inflammation | en_US |
dc.subject | reperfusion injury | en_US |
dc.subject | PPCI | en_US |
dc.subject | STEMI | en_US |
dc.title | Role of Colchicine in Reducing Reperfusion Injury in STEMI Patients Who Undergo Primary Percutaneous Coronary Intervention: A Randomized Clinical Trial | en_US |
dc.type | Article | en_US |
Appears in Collections: | VOL 57 NO 1 2025 |
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