Role of Combination Antiplatelet and Anticoagulation Therapy in Diabetes Mellitus and Cardiovascular Disease: Insights From the COMPASS Trial.


Journal

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

Informations de publication

Date de publication:
09 06 2020
Historique:
pubmed: 1 4 2020
medline: 24 8 2021
entrez: 1 4 2020
Statut: ppublish

Résumé

Patients with established coronary artery disease or peripheral artery disease often have diabetes mellitus. These patients are at high risk of future vascular events. In a prespecified analysis of the COMPASS trial (Cardiovascular Outcomes for People Using Anticoagulation Strategies), we compared the effects of rivaroxaban (2.5 mg twice daily) plus aspirin (100 mg daily) versus placebo plus aspirin in patients with diabetes mellitus versus without diabetes mellitus in preventing major vascular events. The primary efficacy end point was the composite of cardiovascular death, myocardial infarction, or stroke. Secondary end points included all-cause mortality and all major vascular events (cardiovascular death, myocardial infarction, stroke, or major adverse limb events, including amputation). The primary safety end point was a modification of the International Society on Thrombosis and Haemostasis criteria for major bleeding. There were 10 341 patients with diabetes mellitus and 17 054 without diabetes mellitus in the overall trial. A consistent and similar relative risk reduction was seen for benefit of rivaroxaban plus aspirin (n=9152) versus placebo plus aspirin (n=9126) in patients both with (n=6922) and without (n=11 356) diabetes mellitus for the primary efficacy end point (hazard ratio, 0.74, In stable atherosclerosis, the combination of aspirin plus rivaroxaban 2.5 mg twice daily provided a similar relative degree of benefit on coronary, cerebrovascular, and peripheral end points in patients with and without diabetes mellitus. Given their higher baseline risk, the absolute benefits appeared larger in those with diabetes mellitus, including a 3-fold greater reduction in all-cause mortality. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT01776424.

Sections du résumé

BACKGROUND
Patients with established coronary artery disease or peripheral artery disease often have diabetes mellitus. These patients are at high risk of future vascular events.
METHODS
In a prespecified analysis of the COMPASS trial (Cardiovascular Outcomes for People Using Anticoagulation Strategies), we compared the effects of rivaroxaban (2.5 mg twice daily) plus aspirin (100 mg daily) versus placebo plus aspirin in patients with diabetes mellitus versus without diabetes mellitus in preventing major vascular events. The primary efficacy end point was the composite of cardiovascular death, myocardial infarction, or stroke. Secondary end points included all-cause mortality and all major vascular events (cardiovascular death, myocardial infarction, stroke, or major adverse limb events, including amputation). The primary safety end point was a modification of the International Society on Thrombosis and Haemostasis criteria for major bleeding.
RESULTS
There were 10 341 patients with diabetes mellitus and 17 054 without diabetes mellitus in the overall trial. A consistent and similar relative risk reduction was seen for benefit of rivaroxaban plus aspirin (n=9152) versus placebo plus aspirin (n=9126) in patients both with (n=6922) and without (n=11 356) diabetes mellitus for the primary efficacy end point (hazard ratio, 0.74,
CONCLUSIONS
In stable atherosclerosis, the combination of aspirin plus rivaroxaban 2.5 mg twice daily provided a similar relative degree of benefit on coronary, cerebrovascular, and peripheral end points in patients with and without diabetes mellitus. Given their higher baseline risk, the absolute benefits appeared larger in those with diabetes mellitus, including a 3-fold greater reduction in all-cause mortality. Registration: URL: https://www.clinicaltrials.gov; Unique identifier: NCT01776424.

Identifiants

pubmed: 32223318
doi: 10.1161/CIRCULATIONAHA.120.046448
pmc: PMC7314494
doi:

Substances chimiques

Anticoagulants 0
Factor Xa Inhibitors 0
Platelet Aggregation Inhibitors 0
Rivaroxaban 9NDF7JZ4M3
Aspirin R16CO5Y76E

Banques de données

ClinicalTrials.gov
['NCT01776424']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1841-1854

Investigateurs

V Aboyans (V)
M Alings (M)
P Commerford (P)
N Cook-Bruns (N)
G Dagenais (G)
A Dans (A)
G Ertl (G)
C Felix (C)
T Guzik (T)
R Hart (R)
M Hori (M)
A Kakkar (A)
K Keltai (K)
M Keltai (M)
J Kim (J)
A Lamy (A)
F Lanas (F)
Y Liang (Y)
L Liu (L)
E Lonn (E)
P Lopez-Jaramillo (P)
K Metsarinne (K)
P Moayyedi (P)
M O'Donnell (M)
A Parkhomenko (A)
L Piegas (L)
N Pogosova (N)
M Sharma (M)
S Stoerk (S)
A Tonkin (A)
C Torp-Pedersen (C)
J Varigos (J)
P Verhamme (P)
D Vinereanu (D)
K Yusoff (K)
J Zhu (J)

Commentaires et corrections

Type : CommentIn

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Auteurs

Deepak L Bhatt (DL)

Brigham and Women's Hospital Heart and Vascular Center and Harvard Medical School Boston, MA (D.L.B.).

John W Eikelboom (JW)

Population Health Research Institute, McMaster University and Hamilton Health Sciences, Ontario, Canada (J.W.E., S.J.C., S.S.A., J.B., O.S., S.Y.).

Stuart J Connolly (SJ)

Population Health Research Institute, McMaster University and Hamilton Health Sciences, Ontario, Canada (J.W.E., S.J.C., S.S.A., J.B., O.S., S.Y.).

P Gabriel Steg (PG)

Université de Paris and Hôpital Bichat, Assistance Publique-Hôpitaux de Paris, France (P.G.S.).

Sonia S Anand (SS)

Population Health Research Institute, McMaster University and Hamilton Health Sciences, Ontario, Canada (J.W.E., S.J.C., S.S.A., J.B., O.S., S.Y.).

Subodh Verma (S)

Division of Cardiac Surgery, St Michael's Hospital, University of Toronto, Ontario, Canada (S.V.).

Kelley R H Branch (KRH)

University of Washington Medical Centre, Seattle (K.R.H.B., J.P.).

Jeffrey Probstfield (J)

University of Washington Medical Centre, Seattle (K.R.H.B., J.P.).

Jackie Bosch (J)

Population Health Research Institute, McMaster University and Hamilton Health Sciences, Ontario, Canada (J.W.E., S.J.C., S.S.A., J.B., O.S., S.Y.).
School of Rehabilitation Science, Mc-Master University, Hamilton, Ontario, Canada (J.B.).

Olga Shestakovska (O)

Population Health Research Institute, McMaster University and Hamilton Health Sciences, Ontario, Canada (J.W.E., S.J.C., S.S.A., J.B., O.S., S.Y.).

Michael Szarek (M)

State University of New York, Downstate School of Public Health, Brooklyn (M.S.).

Aldo Pietro Maggioni (AP)

ANMCO Research Center, Florence, Italy (A.P.M.).

Petr Widimský (P)

Third Faculty of Medicine, Charles University and University Hospital Kralovske Vinohrady, Prague, Czech Republic (P.W.).

Alvaro Avezum (A)

Hospital Alemão Oswaldo Cruz, São Paulo, Brazil (A.A.).

Rafael Diaz (R)

Estudios Clínicos Latino América, Rosario, Argentina (R.D.).
Instituto Cardiovascular de Rosario, Argentina (R.D.).

Basil S Lewis (BS)

Lady Davis Carmel Medical Centre and the Technion-Israel Institute of Technology, Haifa (B.S.L.).

Scott D Berkowitz (SD)

Bayer US LLC, Whippany, NJ (S.D.B.).

Keith A A Fox (KAA)

Centre for Cardiovascular Science, University of Edinburgh, United Kingdom (K.A.A.F.).

Lars Ryden (L)

Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden (L.R.).

Salim Yusuf (S)

Population Health Research Institute, McMaster University and Hamilton Health Sciences, Ontario, Canada (J.W.E., S.J.C., S.S.A., J.B., O.S., S.Y.).

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