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  •   University of Thessaly Institutional Repository
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
  • View Item
  •   University of Thessaly Institutional Repository
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
  • View Item
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Treatment of superficial vein thrombosis with intermediate dose of tinzaparin: A real word cohort study – The SeVEN EXTension study

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Author
Karathanos C., Chatzis D., Latzios P., Papakostas I., Goumas K., Giannoukas A.D., on behalf of the SeVEN EXT Collaborators
Date
2021
Language
en
DOI
10.1177/0268355520947300
Keyword
tinzaparin
anticoagulant agent
low molecular weight heparin
tinzaparin
adult
aged
Article
cohort analysis
deep vein thrombosis
disease association
drug efficacy
drug safety
epistaxis
female
human
lung embolism
major clinical study
male
medical history
observational study
postthrombosis syndrome
prospective study
recurrent disease
superficial thrombophlebitis
treatment duration
venous thromboembolism
thrombosis
treatment outcome
vein thrombosis
Anticoagulants
Cohort Studies
Heparin, Low-Molecular-Weight
Humans
Thrombosis
Tinzaparin
Treatment Outcome
Venous Thrombosis
SAGE Publications Ltd
Metadata display
Abstract
Background: To assess the treatment of superficial vein thrombosis (SVT) with intermediate dose of tinzaparin in a setting of real world practice. Methods: Prospective observational study of consecutive patients treated by vascular physicians in the private sector with tinzaparin (131 IU/Kg) once daily. Treatment duration was at the treating physician’s discretion. The outcomes of the study were symptomatic venous thromboembolism, extension of thrombus and bleeding complications. Results: 660 patients were included and followed up for at least 3 months. Median duration of treatment was 30 days (14–120). History of prior deep vein thrombosis (HR 2.77; 95% CI= 1.18–6.49; p = 0.018) and current SVT above the knee (HR1.84; 95% CI = 1.33–3.53; p = 0.0002) were associated with prolonged treatment duration. Primary efficacy outcomes occurred in 20 (3%) patients. The median time to the event was 24 (6–92) days and was not related to treatment duration. Conclusions: Tinzaparin at intermediate dose is an effective and safe treatment for SVT. © The Author(s) 2021.
URI
http://hdl.handle.net/11615/74446
Collections
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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