Your browser doesn't support javascript.
loading
Colchicine in Patients With Acute Coronary Syndrome: The Australian COPS Randomized Clinical Trial.
Tong, David C; Quinn, Stephen; Nasis, Arthur; Hiew, Chin; Roberts-Thomson, Philip; Adams, Heath; Sriamareswaran, Rumes; Htun, Nay M; Wilson, William; Stub, Dion; van Gaal, William; Howes, Laurie; Collins, Nicholas; Yong, Andy; Bhindi, Ravinay; Whitbourn, Robert; Lee, Astin; Hengel, Chris; Asrress, Kaleab; Freeman, Melanie; Amerena, John; Wilson, Andrew; Layland, Jamie.
Afiliación
  • Tong DC; St Vincent's Hospital Melbourne, Fitzroy, Victoria, Australia (D.C.T., R.W., A.W., J.L.).
  • Quinn S; Cardiology, Department of Medicine, Peninsula Health, Frankston, Victoria, Australia (D.C.T., R.S., N.M.H., J.L.).
  • Nasis A; Swinburne University of Technology, Department of Health Science and Biostatistics, Hawthorn, Victoria, Australia (S.Q.).
  • Hiew C; MonashHeart, Monash Health, Clayton, Victoria, Australia (A.N.).
  • Roberts-Thomson P; Barwon Health, University Hospital Geelong, Victoria, Australia (C.H., J.A.).
  • Adams H; Royal Hobart Hospital, Tasmania, Australia (P.R.-T., H.A.).
  • Sriamareswaran R; Royal Hobart Hospital, Tasmania, Australia (P.R.-T., H.A.).
  • Htun NM; Cardiology, Department of Medicine, Peninsula Health, Frankston, Victoria, Australia (D.C.T., R.S., N.M.H., J.L.).
  • Wilson W; Cardiology, Department of Medicine, Peninsula Health, Frankston, Victoria, Australia (D.C.T., R.S., N.M.H., J.L.).
  • Stub D; Royal Melbourne Hospital, Parkville, Victoria, Australia (W.W.).
  • van Gaal W; Western Health, St Albans, Victoria, Australia (D.S.).
  • Howes L; Northern Health, Epping, Victoria, Australia (W.v.G.).
  • Collins N; Gold Coast University Hospital, Southport, Queensland, Australia (L.H.).
  • Yong A; John Hunter Hospital, New Lambton Heights, New South Wales, Australia (N.C.).
  • Bhindi R; Concord Repatriation General Hospital, New South Wales, Australia (A.Y.).
  • Whitbourn R; Royal North Shore Hospital, St Leonards, New South Wales, Australia (R.B.).
  • Lee A; St Vincent's Hospital Melbourne, Fitzroy, Victoria, Australia (D.C.T., R.W., A.W., J.L.).
  • Hengel C; Wollongong Hospital, New South Wales, Australia (A.L.).
  • Asrress K; Ballarat Health Services, Victoria, Australia (C.H.).
  • Freeman M; Bankstown-Lidcombe Hospital, Bankstown, New South Wales, Australia (K.A.).
  • Amerena J; Eastern Health, Box Hill, Victoria, Australia (M.F.).
  • Wilson A; Barwon Health, University Hospital Geelong, Victoria, Australia (C.H., J.A.).
  • Layland J; St Vincent's Hospital Melbourne, Fitzroy, Victoria, Australia (D.C.T., R.W., A.W., J.L.).
Circulation ; 142(20): 1890-1900, 2020 11 17.
Article en En | MEDLINE | ID: mdl-32862667
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 (P=0.09, log-rank). There was a higher rate of total death (8 versus 1; P=0.017, log-rank) and, in particular, noncardiovascular death in the colchicine group (5 versus 0; P=0.024, log-rank). The rates of reported adverse effects were not different (colchicine 23.0% versus placebo 24.3%), and they were predominantly gastrointestinal symptoms (colchicine, 23.0% versus placebo, 20.8%). 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.
Asunto(s)
Palabras clave

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Colchicina / Angiografía Coronaria / Síndrome Coronario Agudo / Intervención Coronaria Percutánea Tipo de estudio: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged País/Región como asunto: Oceania Idioma: En Año: 2020 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Colchicina / Angiografía Coronaria / Síndrome Coronario Agudo / Intervención Coronaria Percutánea Tipo de estudio: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged País/Región como asunto: Oceania Idioma: En Año: 2020 Tipo del documento: Article