Role of Combination Antiplatelet and Anticoagulation Therapy in Diabetes Mellitus and Cardiovascular Disease: Insights From the COMPASS Trial.
Aged
Anticoagulants
/ administration & dosage
Aspirin
/ administration & dosage
Cardiovascular Diseases
/ blood
Diabetes Mellitus
/ blood
Double-Blind Method
Drug Therapy, Combination
Factor Xa Inhibitors
Female
Humans
Male
Middle Aged
Platelet Aggregation Inhibitors
/ administration & dosage
Rivaroxaban
/ administration & dosage
anticoagulants
coronary artery disease
diabetes mellitus
peripheral artery disease
platelet aggregation inhibitors
Journal
Circulation
ISSN: 1524-4539
Titre abrégé: Circulation
Pays: United States
ID NLM: 0147763
Informations de publication
Date de publication:
09 06 2020
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
1841-1854Investigateurs
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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