Direct oral anticoagulants for extended treatment of venous thromboembolism: insights from the EINSTEIN CHOICE study.
Administration, Oral
Aged
Anticoagulants
/ therapeutic use
Aspirin
/ administration & dosage
Dabigatran
/ administration & dosage
Glycosaminoglycans
/ therapeutic use
Hemorrhage
/ drug therapy
Humans
Middle Aged
Pyrazoles
/ administration & dosage
Pyridones
/ administration & dosage
Recurrence
Risk Factors
Rivaroxaban
/ administration & dosage
Treatment Outcome
Venous Thromboembolism
/ drug therapy
Vitamin K
/ antagonists & inhibitors
Journal
Blood transfusion = Trasfusione del sangue
ISSN: 2385-2070
Titre abrégé: Blood Transfus
Pays: Italy
ID NLM: 101237479
Informations de publication
Date de publication:
01 2020
01 2020
Historique:
received:
28
12
2018
accepted:
15
04
2019
pubmed:
12
6
2019
medline:
14
1
2021
entrez:
12
6
2019
Statut:
ppublish
Résumé
The risk of recurrence of venous thromboembolism (VTE) persists after interruption of the initial anticoagulation therapy. New evidence shows that direct oral anticoagulants are effective for extended treatment of VTE and may reduce the risk of all-cause mortality. The optimal duration of anticoagulation after VTE is, however, controversial and complicated by the need for individualised assessment and balance between thrombosis and bleeding risks. Three direct oral anticoagulants (rivaroxaban, apixaban and dabigatran) have been studied for extended treatment of VTE. Dabigatran was shown to be safer than vitamin K antagonists and similarly effective for the prevention of recurrent VTE. Dabigatran, apixaban and rivaroxaban resulted in significant decreases in the rate of recurrent symptomatic VTE when compared to placebo, without a statistically significant difference in the risk of major bleeding. The latest guidelines of the American College of Chest Physicians suggest the use of low-dose aspirin to prevent VTE recurrence in patients who want to stop anticoagulation. In the randomised, double-blind, phase 3 EINSTEIN CHOICE trial, once-daily rivaroxaban at doses of 20 mg or 10 mg and 100 mg of aspirin were compared in VTE patients for whom there was clinical equipoise for extended anticoagulation. Either a treatment dose (20 mg) or a prophylactic dose (10 mg) of rivaroxaban significantly reduced the risk of VTE recurrence without a significant increase in bleeding risk compared with aspirin. The EINSTEIN CHOICE trial included patients with provoked or unprovoked VTE. Patients with VTE provoked by minor persistent or minor transient risk factors enrolled in this trial had not-negligible VTE recurrence rates. These new findings on extended therapy suggest the possibility of anticoagulation regimens at intensities tailored to the patients' risk profiles and VTE characteristics, with a shift of the risk-benefit balance in favour of extended treatment.
Identifiants
pubmed: 31184579
pii: 2019.0265-18
doi: 10.2450/2019.0265-18
pmc: PMC7053524
doi:
Substances chimiques
Anticoagulants
0
Glycosaminoglycans
0
Pyrazoles
0
Pyridones
0
Vitamin K
12001-79-5
apixaban
3Z9Y7UWC1J
glucuronyl glucosamine glycan sulfate
75HGV0062C
Rivaroxaban
9NDF7JZ4M3
Dabigatran
I0VM4M70GC
Aspirin
R16CO5Y76E
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
49-57Références
N Engl J Med. 2006 Oct 26;355(17):1780-9
pubmed: 17065639
BMJ. 2011 May 24;342:d3036
pubmed: 21610040
Blood Transfus. 2015 Apr;13(2):170-1
pubmed: 25845033
N Engl J Med. 2010 Dec 23;363(26):2499-510
pubmed: 21128814
J Thromb Haemost. 2018 Jul;16(7):1288-1295
pubmed: 29772108
N Engl J Med. 2013 Feb 21;368(8):699-708
pubmed: 23216615
Blood Transfus. 2016 Mar;14(2):175-84
pubmed: 26710352
J Thromb Haemost. 2016 Dec;14(12):2402-2409
pubmed: 27696701
Blood Transfus. 2015 Apr;13(2):181-3
pubmed: 25845035
Blood. 2014 Mar 20;123(12):1794-801
pubmed: 24497538
N Engl J Med. 2012 Nov 22;367(21):1979-87
pubmed: 23121403
Drugs. 2013 Jul;73(11):1171-82
pubmed: 23812923
Circulation. 2014 Sep 23;130(13):1062-71
pubmed: 25156992
N Engl J Med. 1999 Mar 25;340(12):901-7
pubmed: 10089183
Ann Intern Med. 2003 Dec 2;139(11):893-900
pubmed: 14644891
Chest. 2016 Feb;149(2):315-352
pubmed: 26867832
Thromb Haemost. 2014 Sep 2;112(3):511-21
pubmed: 24899092
Eur Heart J. 2014 Nov 14;35(43):3033-69, 3069a-3069k
pubmed: 25173341
Thromb Haemost. 2018 May;118(S 01):S23-S33
pubmed: 29566417
Blood Transfus. 2015 Apr;13(2):178-80
pubmed: 25845034
Haematologica. 2007 Feb;92(2):199-205
pubmed: 17296569
J Thromb Haemost. 2013 Jun;11(6):1053-8
pubmed: 23578305
Arch Intern Med. 2010 Oct 25;170(19):1710-6
pubmed: 20975016
N Engl J Med. 2003 Apr 10;348(15):1425-34
pubmed: 12601075
Circulation. 2015 Nov 17;132(20):1891-7
pubmed: 26408273
N Engl J Med. 2012 May 24;366(21):1959-67
pubmed: 22621626
Ann Intern Med. 2010 May 4;152(9):578-89
pubmed: 20439576
N Engl J Med. 2003 Aug 14;349(7):631-9
pubmed: 12917299
Lancet Haematol. 2016 May;3(5):e228-36
pubmed: 27132697
J Thromb Haemost. 2018 Oct;16(10):1994-2002
pubmed: 30059189
N Engl J Med. 2001 Jul 19;345(3):165-9
pubmed: 11463010
BMJ. 2013 Aug 30;347:f5133
pubmed: 23996149
Thromb Res. 2015 Oct;136(4):732-8
pubmed: 26277682
N Engl J Med. 2017 Mar 30;376(13):1211-1222
pubmed: 28316279
Intern Emerg Med. 2016 Oct;11(7):895-900
pubmed: 27550399
Ann Intern Med. 2003 Jul 1;139(1):19-25
pubmed: 12834314
Blood Adv. 2018 Apr 10;2(7):788-796
pubmed: 29632234
Thromb Res. 2018 Aug;168:121-129
pubmed: 30064683
N Engl J Med. 2013 Feb 21;368(8):709-18
pubmed: 23425163
J Thromb Haemost. 2013 Mar;11(3):435-43
pubmed: 23279158
Blood Transfus. 2018 Sep;16(5):462-470
pubmed: 29106357
Blood. 2014 Sep 18;124(12):1968-75
pubmed: 24963045