Colchicine in Patients With Acute Coronary Syndrome: The Australian COPS Randomized Clinical Trial.


Journal

Circulation
ISSN: 1524-4539
Titre abrégé: Circulation
Pays: United States
ID NLM: 0147763

Informations de publication

Date de publication:
17 11 2020
Historique:
pubmed: 31 8 2020
medline: 30 9 2021
entrez: 1 9 2020
Statut: ppublish

Résumé

Inflammation plays a crucial role in clinical manifestations and complications of acute coronary syndromes (ACS). Colchicine, a commonly used treatment for gout, has recently emerged as a novel therapeutic option in cardiovascular medicine owing to its anti-inflammatory properties. We sought to determine the potential usefulness of colchicine treatment in patients with ACS. This was a multicenter, randomized, double-blind, placebo-controlled trial involving 17 hospitals in Australia that provide acute cardiac care service. Eligible participants were adults (18-85 years) who presented with ACS and had evidence of coronary artery disease on coronary angiography managed with either percutaneous coronary intervention or medical therapy. Patients were assigned to receive either colchicine (0.5 mg twice daily for the first month, then 0.5 mg daily for 11 months) or placebo, in addition to standard secondary prevention pharmacotherapy, and were followed up for a minimum of 12 months. The primary outcome was a composite of all-cause mortality, ACS, ischemia-driven (unplanned) urgent revascularization, and noncardioembolic ischemic stroke in a time to event analysis. A total of 795 patients were recruited between December 2015 and September 2018 (mean age, 59.8±10.3 years; 21% female), with 396 assigned to the colchicine group and 399 to the placebo group. Over the 12-month follow-up, there were 24 events in the colchicine group compared with 38 events in the placebo group ( The addition of colchicine to standard medical therapy did not significantly affect cardiovascular outcomes at 12 months in patients with ACS and was associated with a higher rate of mortality. Registration: URL: https://www.anzctr.org.au; Unique identifier: ACTRN12615000861550.

Sections du résumé

BACKGROUND
Inflammation plays a crucial role in clinical manifestations and complications of acute coronary syndromes (ACS). Colchicine, a commonly used treatment for gout, has recently emerged as a novel therapeutic option in cardiovascular medicine owing to its anti-inflammatory properties. We sought to determine the potential usefulness of colchicine treatment in patients with ACS.
METHODS
This was a multicenter, randomized, double-blind, placebo-controlled trial involving 17 hospitals in Australia that provide acute cardiac care service. Eligible participants were adults (18-85 years) who presented with ACS and had evidence of coronary artery disease on coronary angiography managed with either percutaneous coronary intervention or medical therapy. Patients were assigned to receive either colchicine (0.5 mg twice daily for the first month, then 0.5 mg daily for 11 months) or placebo, in addition to standard secondary prevention pharmacotherapy, and were followed up for a minimum of 12 months. The primary outcome was a composite of all-cause mortality, ACS, ischemia-driven (unplanned) urgent revascularization, and noncardioembolic ischemic stroke in a time to event analysis.
RESULTS
A total of 795 patients were recruited between December 2015 and September 2018 (mean age, 59.8±10.3 years; 21% female), with 396 assigned to the colchicine group and 399 to the placebo group. Over the 12-month follow-up, there were 24 events in the colchicine group compared with 38 events in the placebo group (
CONCLUSIONS
The addition of colchicine to standard medical therapy did not significantly affect cardiovascular outcomes at 12 months in patients with ACS and was associated with a higher rate of mortality. Registration: URL: https://www.anzctr.org.au; Unique identifier: ACTRN12615000861550.

Identifiants

pubmed: 32862667
doi: 10.1161/CIRCULATIONAHA.120.050771
doi:

Substances chimiques

Colchicine SML2Y3J35T

Banques de données

ANZCTR
['ACTRN12615000861550']

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1890-1900

Commentaires et corrections

Type : CommentIn

Auteurs

David C Tong (DC)

St Vincent's Hospital Melbourne, Fitzroy, Victoria, Australia (D.C.T., R.W., A.W., J.L.).
Cardiology, Department of Medicine, Peninsula Health, Frankston, Victoria, Australia (D.C.T., R.S., N.M.H., J.L.).

Stephen Quinn (S)

Swinburne University of Technology, Department of Health Science and Biostatistics, Hawthorn, Victoria, Australia (S.Q.).

Arthur Nasis (A)

MonashHeart, Monash Health, Clayton, Victoria, Australia (A.N.).

Chin Hiew (C)

Barwon Health, University Hospital Geelong, Victoria, Australia (C.H., J.A.).

Philip Roberts-Thomson (P)

Royal Hobart Hospital, Tasmania, Australia (P.R.-T., H.A.).

Heath Adams (H)

Royal Hobart Hospital, Tasmania, Australia (P.R.-T., H.A.).

Rumes Sriamareswaran (R)

Cardiology, Department of Medicine, Peninsula Health, Frankston, Victoria, Australia (D.C.T., R.S., N.M.H., J.L.).

Nay M Htun (NM)

Cardiology, Department of Medicine, Peninsula Health, Frankston, Victoria, Australia (D.C.T., R.S., N.M.H., J.L.).

William Wilson (W)

Royal Melbourne Hospital, Parkville, Victoria, Australia (W.W.).

Dion Stub (D)

Western Health, St Albans, Victoria, Australia (D.S.).

William van Gaal (W)

Northern Health, Epping, Victoria, Australia (W.v.G.).

Laurie Howes (L)

Gold Coast University Hospital, Southport, Queensland, Australia (L.H.).

Nicholas Collins (N)

John Hunter Hospital, New Lambton Heights, New South Wales, Australia (N.C.).

Andy Yong (A)

Concord Repatriation General Hospital, New South Wales, Australia (A.Y.).

Ravinay Bhindi (R)

Royal North Shore Hospital, St Leonards, New South Wales, Australia (R.B.).

Robert Whitbourn (R)

St Vincent's Hospital Melbourne, Fitzroy, Victoria, Australia (D.C.T., R.W., A.W., J.L.).

Astin Lee (A)

Wollongong Hospital, New South Wales, Australia (A.L.).

Chris Hengel (C)

Ballarat Health Services, Victoria, Australia (C.H.).

Kaleab Asrress (K)

Bankstown-Lidcombe Hospital, Bankstown, New South Wales, Australia (K.A.).

Melanie Freeman (M)

Eastern Health, Box Hill, Victoria, Australia (M.F.).

John Amerena (J)

Barwon Health, University Hospital Geelong, Victoria, Australia (C.H., J.A.).

Andrew Wilson (A)

St Vincent's Hospital Melbourne, Fitzroy, Victoria, Australia (D.C.T., R.W., A.W., J.L.).

Jamie Layland (J)

St Vincent's Hospital Melbourne, Fitzroy, Victoria, Australia (D.C.T., R.W., A.W., J.L.).
Cardiology, Department of Medicine, Peninsula Health, Frankston, Victoria, Australia (D.C.T., R.S., N.M.H., J.L.).
Peninsula Clinical School, Central Clinical School, Monash University, Victoria, Australia (J.L.).

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