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Residual pulmonary embolism as a predictor for recurrence after a first unprovoked episode: Results from the REVERSE cohort study

Authors :
Philippe Robin
Marc Carrier
Isabelle Chagnon
David Anderson
Susan R. Kahn
Sadri Bazarjani
Melanie Tan
Susan Solymoss
Wanzhen Zeng
Marc Philip Righini
Grégoire Le Gal
Michael J. Kovacs
Philip S. Wells
Marc A. Rodger
Linda M. Vickars
Richard H. White
Tony Wan
Mark Crowther
Thrombosis Program
University of Ottawa [Ottawa]
Service d'angiologie et d'hémostase (MR)
Hôpital Universitaire de Genève
Section of Vascular Medicine (SVM)
Leiden University Medical Center (LUMC)
Haematology
University of Portsmouth
Department of Medicine
University of Montreal
Department of Medecine [Montréal]
McGill University = Université McGill [Montréal, Canada]
McMaster University [Hamilton, Ontario]
University of Colorado [Colorado Springs] (UCCS)
Department of Medicine (UBC - St Paul Hospital)
University of British Colombia
Groupe d'Etude de la Thrombose de Bretagne Occidentale (GETBO)
Université de Brest (UBO)-Institut Brestois Santé Agro Matière (IBSAM)
Université de Brest (UBO)-Université de Brest (UBO)
CIC Brest
Université de Brest (UBO)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Hôpital de la Cavale Blanche
Source :
Thrombosis Research, Thrombosis Research, Elsevier, 2018, 162, pp.104-109. ⟨10.1016/j.thromres.2017.11.020⟩, Thrombosis Research, Vol. 162 (2018) pp. 104-109
Publication Year :
2018
Publisher :
HAL CCSD, 2018.

Abstract

Background The optimal duration of oral anticoagulant therapy after a first, unprovoked venous thromboembolism is controversial due to tightly balanced risks and benefits of indefinite anticoagulation. Risk stratification tools may assist in decision making. Objectives We sought to determine the relationship between residual pulmonary embolism assessed by baseline ventilation-perfusion scan after completion of 5–7 months of oral anticoagulant therapy and the risk of recurrent venous thromboembolism in patients with the first episode of unprovoked pulmonary embolism. Methods We conducted a multicentre prospective cohort study of participants with a first, unprovoked venous thromboembolism enrolled after the completion of 5–7 months of oral anticoagulation therapy. The participants completed a mean 18-month follow-up. Participants with pulmonary embolism had baseline ventilation-perfusion scan before discontinuation of oral anticoagulant therapy and the percentage of vascular obstruction on baseline ventilation-perfusion scan was determined. During follow-up after discontinuation of oral anticoagulant therapy, all episodes of suspected recurrent venous thromboembolism were independently adjudicated with reference to baseline imaging. Measurements and main results During follow-up, 24 of 239 (10.0%) participants with an index event of isolated pulmonary embolism or pulmonary embolism associated with deep vein thrombosis and central assessment of percentage of vascular obstruction on baseline ventilation-perfusion scan had confirmed recurrent venous thromboembolism. As compared to participants with no residual pulmonary embolism on baseline ventilation-perfusion scan, the hazard ratio for recurrent venous thromboembolism was 2.0 (95% CI 0.5–7.3) for participants with percentage of vascular obstruction of 0.1%–4.9%, 2.1 (95% CI 0.5–7.8) for participants with percentage vascular obstruction of 5.0%–9.9% and 5.3 (95% CI 1.8–15.4) for participants with percentage vascular obstruction greater than or equal to 10%. Conclusions Residual pulmonary embolism assessed by pulmonary vascular obstruction on baseline ventilation-perfusion performed after 5–7 months of oral anticoagulant therapy for the first episode of unprovoked pulmonary embolism was associated with a statistically significant higher risk of subsequent recurrent venous thromboembolism. Percentage of pulmonary vascular obstruction assessment by ventilation-perfusion scans maybe a useful tool to help guide the duration of oral anticoagulant therapy after a first unprovoked pulmonary embolism. Trial registration Registered at www.clinicaltrials.gov identifier: NCT00261014 .

Details

Language :
English
ISSN :
00493848
Database :
OpenAIRE
Journal :
Thrombosis Research, Thrombosis Research, Elsevier, 2018, 162, pp.104-109. ⟨10.1016/j.thromres.2017.11.020⟩, Thrombosis Research, Vol. 162 (2018) pp. 104-109
Accession number :
edsair.doi.dedup.....b7cabaad3fea0ec3e8140a5fcd33efcf
Full Text :
https://doi.org/10.1016/j.thromres.2017.11.020⟩