Bleeding and thrombotic complications during treatment with direct oral anticoagulants or vitamin K antagonists in venous thromboembolic patients included in the prospective, observational START2-register.
anticoagulation
thromboembolism
vascular medicine
Journal
BMJ open
ISSN: 2044-6055
Titre abrégé: BMJ Open
Pays: England
ID NLM: 101552874
Informations de publication
Date de publication:
27 11 2020
27 11 2020
Historique:
entrez:
28
11
2020
pubmed:
29
11
2020
medline:
7
4
2021
Statut:
epublish
Résumé
The proportion and characteristics of Italian patients affected by venous thromboembolism (VTE) treated with direct oral anticoagulants (DOACs) or vitamin K antagonists (VKAs), and complications occurring during follow-up. A prospective cohort of 2728 VTE patients included in the Survey on anticoagulaTed pAtients RegisTer (START2-Register) from January 2014 to June 2018 was investigated. Characteristics of patients, type of treatment and complications occurring during 2962 years of follow-up were analysed. About 60 Italian anticoagulation and thrombosis centres participated in the observational START2-Register PARTICIPANTS: 2728 adult patients with VTE of a lower limb and/or pulmonary embolism (PE), with a follow-up after the initial phase treatment. Patients could receive DOACs or VKAs; both prescribed by the National and Regional Health Systems for patients with VTE. Efficacy: rate of VTE recurrence (all thrombotic complications were also recorded). the rate of major and clinically relevant non-major bleeding events. Almost 80% of patients were treated with DOACs. The prevalence of symptomatic PE and impaired renal function was higher in patients receiving VKAs. Duration of anticoagulation was >180 days in approximately 70% of patients. Bleeding events were similar in both treatment groups. The overall eventuality of recurrence was significantly higher in DOAC cohorts versus VKA cohorts (HR 2.15 (1.14-4.06), p=0.018); the difference was almost completely due to recurrences occurring during extended treatment (2.73% DOAC vs 0.49% VKA, p<0.0001). All-cause mortality was higher in VKA-treated (5.9%) than in DOAC-treated patients (2.6%, p<0.001). Italian centres treat most patients with VTE with DOACs and prefer VKA for those with more serious clinical conditions. Recurrences were significantly more frequent in DOAC-treated patients due to increased incidence after 180 days of treatment, probably due to reduced adherence to treatment. These results underline the importance of structured surveillance of DOAC-treated patients with VTE to strengthen treatment adherence during extended therapy.
Identifiants
pubmed: 33247017
pii: bmjopen-2020-040449
doi: 10.1136/bmjopen-2020-040449
pmc: PMC7703414
doi:
Substances chimiques
Anticoagulants
0
Vitamin K
12001-79-5
Types de publication
Journal Article
Observational Study
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e040449Investigateurs
Daniela Poli
(D)
Rossella Marcucci
(R)
Niccolò Maggini
(N)
Sophie Testa
(S)
Oriana Paoletti
(O)
Walter Ageno
(W)
Giovanna Colombo
(G)
Benilde Cosmi
(B)
Giuliana Guazzaloca
(G)
Ludovica Migliaccio
(L)
Anna Falanga
(A)
Teresa Lerede
(T)
Luca Barcella
(L)
Vittorio Pengo
(V)
Gentian Denas
(G)
Elisa Bison
(E)
Lucia Ruocco
(L)
Paolo Chiarugi
(P)
Giuliana Martini
(G)
Simona Pedrini
(S)
Federica Bertola
(F)
Lucilla Masciocco
(L)
Pasquale Saracino
(P)
Angelo Benvenuto
(A)
Claudio Vasselli
(C)
Marco Marzolo
(M)
Daniela Mastroiacovo
(D)
Antonietta Piana
(A)
Francesco Cibecchini
(F)
Andrea Toma
(A)
Pietro Barbera
(P)
Antonio Insana
(A)
Carmelo Paparo
(C)
Elvira Grandone
(E)
Donatella Colaizzo
(D)
Domizio Serra
(D)
Pasquale Pignatelli
(P)
Daniele Pastori
(D)
Serena Rupoli
(S)
Giuseppe Malcangi
(G)
Giovanni Nante
(G)
Alberto Tosetto
(A)
Rosella Sangiorgio
(R)
Informations de copyright
© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.
Déclaration de conflit d'intérêts
Competing interests: None declared.
Références
N Engl J Med. 2009 Dec 10;361(24):2342-52
pubmed: 19966341
J Thromb Haemost. 2018 May;16(5):842-848
pubmed: 29532628
N Engl J Med. 2010 Dec 23;363(26):2499-510
pubmed: 21128814
N Engl J Med. 2013 Feb 21;368(8):699-708
pubmed: 23216615
Stroke. 2018 Oct;49(10):2421-2429
pubmed: 30355093
Ann Intern Med. 2007 Oct 16;147(8):573-7
pubmed: 17938396
Semin Hematol. 2014 Apr;51(2):102-11
pubmed: 24861794
Thromb Haemost. 2017 Oct 5;117(10):1840
pubmed: 28862285
Lancet Haematol. 2016 Jan;3(1):e12-21
pubmed: 26765643
Blood Transfus. 2015 Apr;13(2):181-3
pubmed: 25845035
Thromb Haemost. 1993 Mar 1;69(3):236-9
pubmed: 8470047
Nephron. 1976;16(1):31-41
pubmed: 1244564
N Engl J Med. 2012 Apr 5;366(14):1287-97
pubmed: 22449293
J Thromb Haemost. 2015 Nov;13(11):2119-26
pubmed: 26764429
J Chronic Dis. 1987;40(5):373-83
pubmed: 3558716
N Engl J Med. 2013 Oct 10;369(15):1406-15
pubmed: 23991658
Heart. 2020 Jan;106(2):119-126
pubmed: 31601729
Clin Appl Thromb Hemost. 2018 Mar;24(2):241-247
pubmed: 28718296
Thromb Haemost. 2018 Nov;118(11):1951-1961
pubmed: 30357780
N Engl J Med. 2013 Aug 29;369(9):799-808
pubmed: 23808982
PLoS One. 2015 May 22;10(5):e0124719
pubmed: 26001109
Heart. 2019 Apr;105(7):545-552
pubmed: 30327391
Am J Kidney Dis. 2002 Feb;39(2 Suppl 1):S1-266
pubmed: 11904577
J Thromb Haemost. 2005 Apr;3(4):692-4
pubmed: 15842354
Blood. 2014 Sep 18;124(12):1968-75
pubmed: 24963045