Colchicine in Acute Coronary Syndrome: A Systematic Review
| Autor: | Ashley H. McKnight, Daniel R Katzenberger, Sara R. Britnell |
|---|---|
| Rok vydání: | 2020 |
| Předmět: |
Acute coronary syndrome
medicine.medical_specialty MEDLINE 030204 cardiovascular system & hematology Coronary artery disease 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Percutaneous Coronary Intervention Internal medicine medicine Colchicine Humans Pharmacology (medical) 030212 general & internal medicine Myocardial infarction Acute Coronary Syndrome Randomized Controlled Trials as Topic business.industry medicine.disease C-Reactive Protein Treatment Outcome chemistry Practice Guidelines as Topic Cardiology business |
| Zdroj: | The Annals of pharmacotherapy. 55(2) |
| ISSN: | 1542-6270 |
| Popis: | Objective: The purpose of this review is to evaluate the efficacy and safety of colchicine after acute coronary syndrome (ACS). Data Sources: English-language searches were made of MEDLINE and EMBASE from database inception through mid-June 2020. Study Selection and Data Extraction: Randomized trials characterizing the effects of colchicine in ACS were considered. Of 627 title and abstracts identified, nine trials were included. Two reviewers extracted data and rated study quality. Data Synthesis: Four studies showed colchicine did not attenuate C-reactive protein production. Colchicine did modulate the NOD-like receptor family pyrin domain containing 3 inflammasome in 3 studies and reduced production of chemokine ligand 2 (CCL2), CCL5, and C-X3-C motif chemokine ligand 1 in 1 study. Major adverse cardiovascular events (MACE) were not significantly different at 30 days in 3 studies, administered as 1.8 mg preprocedurally or scheduled 1 mg daily. One study found a significant reduction in MACE with colchicine 0.5 mg daily over median 22.6 months (hazard ratio = 0.77; 95% CI = 0.61-0.96). Colchicine is associated with increased gastrointestinal adverse events but was generally well tolerated. Relevance to Patient Care and Clinical Practice: Colchicine is likely to reduce MACE in an ACS population if administered for greater than 30 days but does not improve MACE when administered only preprocedurally. Conclusions: Adjunctive colchicine 0.5 mg daily for greater than 30 days is reasonable for an ACS population on guideline-directed medical therapy treated with PCI. Additional studies are needed to validate and determine the durability of these benefits. |
| Databáze: | OpenAIRE |
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