Patent Foramen Ovale Closure among Patients with Hypercoagulable States Maintained on Antithrombotic Therapy.


Journal

Cardiology
ISSN: 1421-9751
Titre abrégé: Cardiology
Pays: Switzerland
ID NLM: 1266406

Informations de publication

Date de publication:
Historique:
received: 04 02 2020
accepted: 28 09 2020
pubmed: 15 2 2021
medline: 1 9 2021
entrez: 14 2 2021
Statut: ppublish

Résumé

Percutaneous device closure was shown to effectively prevent recurrent strokes in patients with patent foramen ovale (PFO). Whether this protective effect is relevant for patients with hypercoagulable states (HCSs) is unknown as they were not represented in prior studies. Data on 136 consecutive patients with a PFO and clinically significant HCS were retrospectively collected. PFO closure and antithrombotic regimen were decided on an individual basis by the treating physicians, and adherence to therapy was routinely evaluated. The outcome was the occurrence of cerebrovascular accident (CVA) or transient ischemic attack (TIA). HCS types consisted of antiphospholipid syndrome (31%), factor-5 Leiden mutation (22%), prothrombin mutation (18%), protein S deficiency (15%), protein C deficiency (7%), methyl-tetra-hydro folate reductase mutation (5%), and essential thrombocytosis (2%). 102 patients (75%) were maintained on anticoagulants and the remaining on antiplatelet therapy. PFO closure was undertaken in 85 (63%); antithrombotic therapy was not interrupted prior to or after the procedures. At a mean follow-up of 46 ± 8 months, 23 patients (17%; 95% confidence interval, 9.3-22%) experienced an outcome event, mainly in the form of CVAs (n = 15, 65%). In multivariable analysis, PFO closure was associated with a 5-fold decrease in the risk of CVA/TIA (p = 0.02). This effect was independent of the type of HCS or antithrombotic therapy. Among patients with HCSs maintained on anticoagulant or antiplatelet therapies, PFO closure was associated with a significantly lower risk of CVA or TIA.

Sections du résumé

BACKGROUND BACKGROUND
Percutaneous device closure was shown to effectively prevent recurrent strokes in patients with patent foramen ovale (PFO). Whether this protective effect is relevant for patients with hypercoagulable states (HCSs) is unknown as they were not represented in prior studies.
METHODS METHODS
Data on 136 consecutive patients with a PFO and clinically significant HCS were retrospectively collected. PFO closure and antithrombotic regimen were decided on an individual basis by the treating physicians, and adherence to therapy was routinely evaluated. The outcome was the occurrence of cerebrovascular accident (CVA) or transient ischemic attack (TIA).
RESULTS RESULTS
HCS types consisted of antiphospholipid syndrome (31%), factor-5 Leiden mutation (22%), prothrombin mutation (18%), protein S deficiency (15%), protein C deficiency (7%), methyl-tetra-hydro folate reductase mutation (5%), and essential thrombocytosis (2%). 102 patients (75%) were maintained on anticoagulants and the remaining on antiplatelet therapy. PFO closure was undertaken in 85 (63%); antithrombotic therapy was not interrupted prior to or after the procedures. At a mean follow-up of 46 ± 8 months, 23 patients (17%; 95% confidence interval, 9.3-22%) experienced an outcome event, mainly in the form of CVAs (n = 15, 65%). In multivariable analysis, PFO closure was associated with a 5-fold decrease in the risk of CVA/TIA (p = 0.02). This effect was independent of the type of HCS or antithrombotic therapy.
CONCLUSIONS CONCLUSIONS
Among patients with HCSs maintained on anticoagulant or antiplatelet therapies, PFO closure was associated with a significantly lower risk of CVA or TIA.

Identifiants

pubmed: 33582661
pii: 000512184
doi: 10.1159/000512184
doi:

Substances chimiques

Fibrinolytic Agents 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

375-383

Informations de copyright

© 2021 S. Karger AG, Basel.

Auteurs

Jonathan Buber (J)

Heart Center, Chaim Sheba Medical Centre, Tel-Hashomer, Israel, yonibuber@gmail.com.
Division of Cardiology, Department of Medicine, University of Washington School of Medicine, Seattle, Washington, USA, yonibuber@gmail.com.

Victor Guetta (V)

Heart Center, Chaim Sheba Medical Centre, Tel-Hashomer, Israel.
Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel.

David Orion (D)

Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
Department of Neurology, Chaim Sheba Medical Centre, Tel-Hashomer, Israel.

Aharon Lubetsky (A)

Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
Coagulation Service, Hematology Department, Chaim Sheba Medical Centre, Tel-Hashomer, Israel.

Sharon Borik (S)

Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel.
Safra International Center for Congenital Heart Disease, Chaim Sheba Medical Centre, Tel-Hashomer, Israel.

Ori Vatury (O)

Heart Center, Chaim Sheba Medical Centre, Tel-Hashomer, Israel.
Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel.

Ariel Israel (A)

Department of Family Medicine, Clalit Health Services, Tel-Aviv, Israel.

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