Thrombosis recurrence and major bleeding in non-anticoagulated thrombotic antiphospholipid syndrome patients: Prospective study from antiphospholipid syndrome alliance for clinical trials and international networking (APS ACTION) clinical database and repository ("Registry").

Anticoagulant therapy Antiphospholipid antibodies Antiphospholipid syndrome Bleeding Thrombosis

Journal

Seminars in arthritis and rheumatism
ISSN: 1532-866X
Titre abrégé: Semin Arthritis Rheum
Pays: United States
ID NLM: 1306053

Informations de publication

Date de publication:
Apr 2024
Historique:
received: 17 05 2023
revised: 13 11 2023
accepted: 05 12 2023
pubmed: 8 1 2024
medline: 8 1 2024
entrez: 7 1 2024
Statut: ppublish

Résumé

Long-term anticoagulant therapy is generally recommended for thrombotic antiphospholipid syndrome (TAPS) patients, however it may be withdrawn or not introduced in routine practice. To prospectively evaluate the risk of thrombosis recurrence and major bleeding in non-anticoagulated TAPS patients, compared to anticoagulated TAPS, and secondly, to identify different features between those two groups. Using an international registry, we identified non-anticoagulated TAPS patients at baseline, and matched them with anticoagulated TAPS patients based on gender, age, type of previous thrombosis, and associated autoimmune disease. Thrombosis recurrence and major bleeding were prospectively analyzed using Kaplan-Meier method and compared using a marginal Cox's regression model. As of June 2022, 94 (14 %) of the 662 TAPS patients were not anticoagulated; and 93 of them were matched with 181 anticoagulated TAPS patients (median follow-up 5 years [interquartile range 3 to 8]). The 5-year thrombosis recurrence and major bleeding rates were 12 % versus 10 %, and 6 % versus 7 %, respectively (hazard ratio [HR] 1.38, 95 % confidence interval [CI] 0.53 to 3.56, p = 0.50 and HR 0.53; 95 % CI 0.15 to 1.86; p = 0.32, respectively). Non-anticoagulated patients were more likely to receive antiplatelet therapy (p < 0.001), and less likely to have more than one previous thrombosis (p < 0.001) and lupus anticoagulant positivity (p = 0.01). Fourteen percent of the TAPS patients were not anticoagulated at recruitment. Their recurrent thrombosis risk did not differ compared to matched anticoagulated TAPS patients, supporting the pressing need for risk-stratified secondary thrombosis prevention trials in APS investigating strategies other than anticoagulation.

Sections du résumé

BACKGROUND BACKGROUND
Long-term anticoagulant therapy is generally recommended for thrombotic antiphospholipid syndrome (TAPS) patients, however it may be withdrawn or not introduced in routine practice.
OBJECTIVES OBJECTIVE
To prospectively evaluate the risk of thrombosis recurrence and major bleeding in non-anticoagulated TAPS patients, compared to anticoagulated TAPS, and secondly, to identify different features between those two groups.
PATIENTS/METHODS METHODS
Using an international registry, we identified non-anticoagulated TAPS patients at baseline, and matched them with anticoagulated TAPS patients based on gender, age, type of previous thrombosis, and associated autoimmune disease. Thrombosis recurrence and major bleeding were prospectively analyzed using Kaplan-Meier method and compared using a marginal Cox's regression model.
RESULTS RESULTS
As of June 2022, 94 (14 %) of the 662 TAPS patients were not anticoagulated; and 93 of them were matched with 181 anticoagulated TAPS patients (median follow-up 5 years [interquartile range 3 to 8]). The 5-year thrombosis recurrence and major bleeding rates were 12 % versus 10 %, and 6 % versus 7 %, respectively (hazard ratio [HR] 1.38, 95 % confidence interval [CI] 0.53 to 3.56, p = 0.50 and HR 0.53; 95 % CI 0.15 to 1.86; p = 0.32, respectively). Non-anticoagulated patients were more likely to receive antiplatelet therapy (p < 0.001), and less likely to have more than one previous thrombosis (p < 0.001) and lupus anticoagulant positivity (p = 0.01).
CONCLUSION CONCLUSIONS
Fourteen percent of the TAPS patients were not anticoagulated at recruitment. Their recurrent thrombosis risk did not differ compared to matched anticoagulated TAPS patients, supporting the pressing need for risk-stratified secondary thrombosis prevention trials in APS investigating strategies other than anticoagulation.

Identifiants

pubmed: 38185079
pii: S0049-0172(23)00189-0
doi: 10.1016/j.semarthrit.2023.152347
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

152347

Informations de copyright

Copyright © 2023 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest Authors had no conflict of interest to declare.

Auteurs

Cecile M Yelnik (CM)

Univ. Lille, CHU Lille, Département de Médecine Interne et d'Immunologie Clinique, INSERM, UMR 1167, F-59000 Lille, France. Electronic address: cecile.yelnik@chru-lille.fr.

Zeynep Belce Erton (ZB)

Hospital for Special Surgery, New York, NY, USA.

Elodie Drumez (E)

Univ. Lille, CHU Lille, Département de Médecine Interne et d'Immunologie Clinique, INSERM, UMR 1167, F-59000 Lille, France.

Dachi Cheildze (D)

Hospital for Special Surgery, New York, NY, USA; Yale New Haven Hospital, New Haven, CT, USA.

Danieli de Andrade (D)

University of São Paulo, São Paulo, Brazil.

Ann Clarke (A)

University of Calgary, Calgary, Alberta, Canada.

Maria G Tektonidou (MG)

National and Kapodistrian University of Athens, Athens, Greece.

Savino Sciascia (S)

University of Turin, Turin, Italy.

Jose Pardos-Gea (J)

Vall d'Hebron University Hospital Barcelona, Spain.

Vittorio Pengo (V)

Padova University Hospital, Padova, Italy.

Guillermo Ruiz-Irastorza (G)

BioCruces Bizkaia Health Research Institute, Barakaldo, Spain.

H Michael Belmont (HM)

New York University Langone Medical Center, New York, NY, USA.

Chary Lopez Pedrera (CL)

Maimonides Institute for Biomedical Research of Córdoba, Córdoba, Spain.

Paul R Fortin (PR)

Centre ARThrite - CHU de Québec- Université Laval, Quebec, QC, Canada.

Denis Wahl (D)

Université de Lorraine, Inserm DCAC, and CHRU-Nancy, Nancy, France.

Maria Gerosa (M)

University of Milan, Milan, Italy.

Nina Kello (N)

Northwell Health, New Hyde Park, NY, USA.

Flavio Signorelli (F)

Universidade do Estado do Rio de Janeiro, Rio de Janeiro, Brazil.

Tatsuya Atsumi (T)

Hokkaido University Hospital, Sapporo, Japan.

Lanlan Ji (L)

Peking University First Hospital, Beijing, China.

Maria Efthymiou (M)

University College London, London, United Kingdom.

D Ware Branch (DW)

University of Utah and Intermountain Healthcare, Salt Lake City, UT, USA.

Cecilia Nalli (C)

University of Brescia, Brescia, Italy.

Esther Rodriguez-Almaraz (E)

Hospital Universitario 12 de Octubre, Madrid, Spain.

Michelle Petri (M)

Johns Hopkins University School of Medicine, Baltimore, MD, USA.

Ricard Cervera (R)

Hospital Clinic Barcelona, Barcelona, Catalonia, Spain.

Hui Shi (H)

Department of Rheumatology and Immunology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

Yu Zuo (Y)

University of Michigan, Ann Arbor, MI, USA.

Bahar Artim-Esen (B)

Istanbul University School of Medicine, Istanbul, Turkey.

Guillermo Pons-Estel (G)

Centro Regional de Enfermedades Autoinmunes y Reumáticas del Grupo Oroño (GO-CREAR), Rosario, Argentina.

Rohan Willis (R)

University of Texas Medical Branch, Galveston, TX, USA.

Megan R W Barber (MRW)

University of Calgary, Calgary, Alberta, Canada.

Leslie Skeith (L)

University of Calgary, Calgary, Alberta, Canada.

Maria Laura Bertolaccini (ML)

School of Cardiovascular & Metabolic Medicine & Sciences, King's College London, United Kingdom.

Hannah Cohen (H)

University College London, London, United Kingdom.

Robert Roubey (R)

University of North Carolina, Chapel Hill, NC, USA.

Doruk Erkan (D)

Barbara Volcker Center for Women and Rheumatic Disease, Hospital for Special Surgery, Weill Cornell Medicine, New York, NY, USA.

Classifications MeSH