Cost-effectiveness of low-dose colchicine after myocardial infarction in the Colchicine Cardiovascular Outcomes Trial (COLCOT)
Language English Country Great Britain, England Media print
Document type Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't
Grant support
MR/N003403/1
Medical Research Council - United Kingdom
CIHR - Canada
PubMed
32407460
PubMed Central
PMC8445085
DOI
10.1093/ehjqcco/qcaa045
PII: 5837112
Knihovny.cz E-resources
- Keywords
- Colchicine, Cost effectiveness, Myocardial infarction,
- MeSH
- Cost-Benefit Analysis MeSH
- Myocardial Infarction * complications drug therapy MeSH
- Colchicine * therapeutic use MeSH
- Quality-Adjusted Life Years MeSH
- Humans MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Randomized Controlled Trial MeSH
- Geographicals
- Canada epidemiology MeSH
- Names of Substances
- Colchicine * MeSH
AIMS: In the randomized, placebo-controlled Colchicine Cardiovascular Outcomes Trial (COLCOT) of 4745 patients enrolled within 30 days after myocardial infarction (MI), low-dose colchicine (0.5 mg once daily) reduced the incidence of the primary composite endpoint of cardiovascular death, resuscitated cardiac arrest, MI, stroke, or urgent hospitalization for angina leading to coronary revascularization. To assess the in-trial period and lifetime cost-effectiveness of low-dose colchicine therapy compared to placebo in post-MI patients on standard-of-care therapy. METHODS AND RESULTS: A multistate Markov model was developed incorporating the primary efficacy and safety results from COLCOT, as well as healthcare costs and utilities from the Canadian healthcare system perspective. All components of the primary outcome, non-cardiovascular deaths, and pneumonia were included as health states in the model as both primary and recurrent events. In the main analysis, a deterministic approach was used to estimate the incremental cost-effectiveness ratio (ICER) for the trial period (24 months) and lifetime (20 years). Over the in-trial period, the addition of colchicine to post-MI standard-of-care treatment decreased the mean overall per-patient costs by 47%, from $502 to $265 Canadian dollar (CAD), and increased the quality-adjusted life years (QALYs) from 1.30 to 1.34. The lifetime per-patient costs were further reduced (69%) and QALYs increased with colchicine therapy (from 8.82 to 11.68). As a result, both in-trial and lifetime ICERs indicated colchicine therapy was a dominant strategy. CONCLUSION: Cost-effectiveness analyses indicate that the addition of colchicine to standard-of-care therapy after MI is economically dominant and therefore generates cost savings.
ANMCO Research Center Via La Marmora 34 50121 Firenze Italy
Bellevue Medical Center Qanater Zubayda Mansouriyeh Mansourieh Metn District Beirut Lebanon
Cardiovascular Center Na Homolce Hospital Roentgenova 2 150 00 Prague Czech Republic
Estudios Clinicos Latinoamerica Paraguay 160 2000 Rosario Argentina
Fattouma Bourguiba University Hospital 5000 Monastir Tunisia
Logimetrix Inc 3600 Rhodes Drive Windsor Ontario N8W 5A4 Canada
Montreal Heart Institute Université de Montréal 5000 Belanger Street Montréal Québec H1T 1C8 Canada
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