Long-term risk of postthrombotic syndrome after symptomatic distal deep vein thrombosis: The CACTUS-PTS study.

clinical trial deep vein thrombosis epidemiology; anticoagulant low molecular weight heparin postthrombotic syndrome

Journal

Journal of thrombosis and haemostasis : JTH
ISSN: 1538-7836
Titre abrégé: J Thromb Haemost
Pays: England
ID NLM: 101170508

Informations de publication

Date de publication:
04 2020
Historique:
received: 11 09 2019
revised: 08 12 2019
accepted: 31 12 2019
pubmed: 4 1 2020
medline: 15 5 2021
entrez: 4 1 2020
Statut: ppublish

Résumé

After a proximal lower limb deep vein thrombosis (DVT; involving popliteal veins or above), up to 40% of patients develop postthrombotic syndrome (PTS) as assessed by the Villalta scale (VS). Poor initial anticoagulant treatment is a known risk factor for PTS. The risk of developing PTS after isolated distal DVT (infra-popliteal DVT without pulmonary embolism), and the impact of anticoagulant treatment on this risk, are uncertain. Long-term follow-up of CACTUS double-blind trial comparing 6 weeks of s.c. nadroparin (171 IU/kg/d) versus s.c. placebo for a first symptomatic isolated distal DVT. At least 1 year after randomization, patients had a PTS assessment in clinic or by phone using the VS. After a median follow-up of 6 years, PTS was present in 30% (n = 54) of the 178 patients who had a PTS assessment. PTS was moderate or severe in 24% (n = 13) of cases. There was no statistically significant difference in prevalence of PTS in the nadroparin versus placebo groups (29% versus 32%, P = .6), except in patients without evidence of primary chronic venous insufficiency (9% versus 24%, P = .04). Rates of venous thromboembolism recurrence during follow-up in the nadroparin and placebo groups were, respectively, 8% (n = 7) and 14% (n = 13; P = .2). After a first isolated distal DVT, the risk of PTS is substantial but much lower than that reported after proximal DVT. Anticoagulation with nadroparin doesn't provide any clear benefit to prevent PTS, except in patients without preexisting chronic venous insufficiency. Anticoagulation might be associated with a lower risk of venous thromboembolism recurrence.

Sections du résumé

BACKGROUND
After a proximal lower limb deep vein thrombosis (DVT; involving popliteal veins or above), up to 40% of patients develop postthrombotic syndrome (PTS) as assessed by the Villalta scale (VS). Poor initial anticoagulant treatment is a known risk factor for PTS. The risk of developing PTS after isolated distal DVT (infra-popliteal DVT without pulmonary embolism), and the impact of anticoagulant treatment on this risk, are uncertain.
METHODS
Long-term follow-up of CACTUS double-blind trial comparing 6 weeks of s.c. nadroparin (171 IU/kg/d) versus s.c. placebo for a first symptomatic isolated distal DVT. At least 1 year after randomization, patients had a PTS assessment in clinic or by phone using the VS.
RESULTS
After a median follow-up of 6 years, PTS was present in 30% (n = 54) of the 178 patients who had a PTS assessment. PTS was moderate or severe in 24% (n = 13) of cases. There was no statistically significant difference in prevalence of PTS in the nadroparin versus placebo groups (29% versus 32%, P = .6), except in patients without evidence of primary chronic venous insufficiency (9% versus 24%, P = .04). Rates of venous thromboembolism recurrence during follow-up in the nadroparin and placebo groups were, respectively, 8% (n = 7) and 14% (n = 13; P = .2).
CONCLUSION
After a first isolated distal DVT, the risk of PTS is substantial but much lower than that reported after proximal DVT. Anticoagulation with nadroparin doesn't provide any clear benefit to prevent PTS, except in patients without preexisting chronic venous insufficiency. Anticoagulation might be associated with a lower risk of venous thromboembolism recurrence.

Identifiants

pubmed: 31899848
doi: 10.1111/jth.14728
pii: S1538-7836(22)00279-3
doi:

Substances chimiques

Anticoagulants 0

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

857-864

Subventions

Organisme : The Canadian Institutes of Health Research
ID : MOP-119524
Pays : International
Organisme : The Canadian Institutes of Health Research
ID : CDT-142654
Pays : International

Informations de copyright

© 2020 International Society on Thrombosis and Haemostasis.

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Auteurs

Jean-Philippe Galanaud (JP)

Department of Vascular Medicine, Montpellier University Hospital and University of Montpellier, Montpellier, France.
Department of Medicine, Sunnybrook Health Sciences Centre and University of Toronto, Toronto, ON, Canada.

Marc Righini (M)

Division of Angiology and Hemostasis, Faculty of Medicine, Geneva University Hospital, Geneva, Switzerland.

Lorris Le Collen (L)

Department of Vascular Medicine, Montpellier University Hospital and University of Montpellier, Montpellier, France.

Aymeric Douillard (A)

Clinical Research and Epidemiology Unit, University Hospital, Montpellier, France.

Helia Robert-Ebadi (H)

Division of Angiology and Hemostasis, Faculty of Medicine, Geneva University Hospital, Geneva, Switzerland.

Daniel Pontal (D)

Department of Vascular Medicine, Montpellier University Hospital and University of Montpellier, Montpellier, France.

David Morrison (D)

Department of Medicine and Lady Davis Institute, Jewish General Hospital, Montreal, QC, Canada.

Marie-Thérèse Barrellier (MT)

Vascular Medicine Unit, Caen University Hospital, Caen, France.

Antoine Diard (A)

Vascular Medicine Office, Langoiran, France.

Hervé Guénnéguez (H)

Clinique Mégival, St Aubin sur Scié, France.

Dominique Brisot (D)

Vascular Medicine Unit, Clinique du Parc, Castelnau Le Lez, France.

Pascale Faïsse (P)

Vascular Medicine Physician, Alès, France.

Sandrine Accassat (S)

Clinical Investigation Centre, Saint Etienne University Hospital, Saint Etienne, France.

Myriam Martin (M)

Vascular Medicine Physician, Annecy, France.

Aurélien Delluc (A)

Department of Medicine, Brest University Hospital, Brest, France.
Department of Medicine, Ottawa Hospital Research Institute at the University of Ottawa, Ottawa, ON, Canada.

Susan Solymoss (S)

Division of Hematology, St Mary's Hospital, Montreal, QC, Canada.

Jeannine Kassis (J)

Division of Hematology, Hôpital Rosemont-Maisonneuve, Montréal, QC, Canada.

Marc Carrier (M)

Department of Medicine, Ottawa Hospital Research Institute at the University of Ottawa, Ottawa, ON, Canada.

Isabelle Quéré (I)

Department of Vascular Medicine, Montpellier University Hospital and University of Montpellier, Montpellier, France.

Susan R Kahn (SR)

Vascular Medicine Physician, Alès, France.

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