2011
DOI: 10.1182/blood-2010-05-286690
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How I treat superficial venous thrombosis

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Cited by 44 publications
(35 citation statements)
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“…Some investigators argue that SVT should not be categorized separately from DVT and PE, but rather be considered as part of the venous thrombotic spectrum. 21 Results from recent studies, including ours, support this view.…”
Section: Discussionsupporting
confidence: 77%
“…Some investigators argue that SVT should not be categorized separately from DVT and PE, but rather be considered as part of the venous thrombotic spectrum. 21 Results from recent studies, including ours, support this view.…”
Section: Discussionsupporting
confidence: 77%
“…The authors of recent studies provide evidence that SVT should be seen as a form of venous thrombosis (VT), together with pulmonary embolism and deep-vein thrombosis. [1][2][3][4][5][6] In a recent clinical trial (Comparison of Arixtra in Lower Limb Superficial Vein Thrombosis with Placebo; CALISTO) investigators showed a symptomatic VT rate of 1.5% within 77 days after the diagnosis of SVT in placebo users. 2 This VT rate was probably positively influenced by the definition of SVT that CALISTO investigators used.…”
Section: Introductionmentioning
confidence: 99%
“…1 Previously called thrombophlebitis, the name suggests that both thrombosis and inflammation play a role in the disease mechanism. The authors of recent studies provide evidence that SVT should be seen as a form of venous thrombosis (VT), together with pulmonary embolism and deep-vein thrombosis.…”
Section: Introductionmentioning
confidence: 99%
“…1 A lthough superficial venous thrombosis was originally perceived as a benign disease with a self-limited clinical course, it is now recognized that this condition is often associated either with concomitant venous thromboembolism or with early development of deep vein thrombosis and pulmonary embolism. [2][3][4][5] Further, Heit et al reported in…”
mentioning
confidence: 98%
“…For example, the isolated C2 domain does not compete with factor VIII for membrane binding and does not interfere with the factor VIIIa-factor IXa complex. 2 Furthermore, factor VIII engineered to lack the C2 domain, retains functional activity, although with a requirement for a higher concentration of phospholipid vesicles with a high density of negative charge. 3 In short, recent biochemical studies suggest that the C2 domain could have only marginal importance.…”
Section: Factor VIII Inhibitor Epitopes and An Enigma ---------------mentioning
confidence: 99%