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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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Recurrence of superficial vein thrombosis in patients with varicose veins

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Συγγραφέας
Karathanos C., Spanos K., Saleptsis V., Tsezou A., Kyriakou D., Giannoukas A.D.
Ημερομηνία
2016
Γλώσσα
en
DOI
10.1177/0268355515596475
Λέξη-κλειδί
antithrombin
protein C
protein S
prothrombin
adult
aged
Article
comorbidity
controlled study
disease association
disease classification
dyslipidemia
female
follow up
gene mutation
high risk patient
human
major clinical study
male
medical history
patient selection
priority journal
prothrombin gene
recurrent disease
risk factor
screening test
superficial vein thrombosis
thrombophilia
varicosis
vein thrombosis
blood clotting disorder
clinical trial
genetics
middle aged
mutation
prospective study
recurrent disease
varicosis
vein thrombosis
very elderly
Adult
Aged
Aged, 80 and over
Blood Coagulation Disorders, Inherited
Female
Follow-Up Studies
Humans
Male
Middle Aged
Mutation
Prospective Studies
Prothrombin
Recurrence
Risk Factors
Varicose Veins
Venous Thrombosis
SAGE Publications Ltd
Εμφάνιση Μεταδεδομένων
Επιτομή
Objective: To investigate which factors other than history of superficial vein thrombosis (SVT) are associated with recurrent spontaneous SVT episodes in patients with varicose veins (VVs). Materials and methods: Patients with a history of spontaneous SVT and VVs were followed up for a mean period of 55 months. Demographics, comorbidities, and thrombophilia screening test were analyzed. Patients were grouped according to the clinical–etiology–anatomy–pathophysiology classification. A multiple logistic regression analysis with the forward likelihood ratio method was undertaken. Results: Thirteen patients out of 97 had a recurrence SVT episode during the follow-up period. All those patients were identified to have a thrombophilia defect. Protein C and S, antithrombin, and plasminogen deficiencies were more frequently present in patients without recurrence. Gene mutations were present in 38% in the nonrecurrence group and 77% in the recurrence group. After logistic regression analysis, patients with dislipidemia and mutation in prothrombin G20210A (FII) had an increased risk for recurrence by 5.4-fold and 4.6-fold, respectively. No deep vein thrombosis or pulmonary embolism occurred. Conclusions: Dislipidemia and gene mutations of F II are associated with SVT recurrence in patients with VVs. A selection of patients may benefit from anticoagulation in the short term and from VVs intervention in the long term. © 2015, © The Author(s) 2015.
URI
http://hdl.handle.net/11615/74454
Collections
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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