1996
DOI: 10.1016/s0753-3322(96)89668-5
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Plasmatic parameters of coagulation activation in thrombotic microangiopathy

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Cited by 14 publications
(8 citation statements)
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“…However, profound DIC is a rare complication in the absence of placental abruption. The fall in anti‐thrombin levels seen in pre‐eclampsia is not found in TTP (Sagripanti et al , 1996) and may, therefore, be of diagnostic value.…”
Section: Pre‐eclampsiamentioning
confidence: 96%
See 1 more Smart Citation
“…However, profound DIC is a rare complication in the absence of placental abruption. The fall in anti‐thrombin levels seen in pre‐eclampsia is not found in TTP (Sagripanti et al , 1996) and may, therefore, be of diagnostic value.…”
Section: Pre‐eclampsiamentioning
confidence: 96%
“…However, schistocytes may be absent from the peripheral blood film in the first 24–48 h following clinical presentation. Routine coagulation profiles are usually normal (Monteagudo et al , 1991; Sagripanti et al , 1996; Rock et al , 1998), although slight increases in D‐dimer, fibrin degradation products and thrombin–anti‐thrombin complex (TAT) may be seen (Monteagudo et al , 1991; Sagripanti et al , 1996; Wada et al , 1998). Secondary DIC may, however, arise from prolonged tissue ischaemia and is an ominous prognostic indicator.…”
Section: Laboratory Features and Investigationmentioning
confidence: 99%
“…An acute‐phase response may contribute to a prothrombotic state (Munford 2001) as a result of endothelial perturbation, increased activity of blood coagulation and attenuated fibrinolysis. A prothrombotic state is reflected by the presence of increased concentrations of proteins like von Willebrand factor (vWF) and plasminogen activator inhibitor‐1 (PAI‐1), or protein cleavage products as prothrombin fragment 1+2 (F1+2) and D‐dimer (Sagripanti et al 1996). Indeed, elevated plasma levels of these markers have been associated with a higher risk for recurrent ischaemic events in patients with a history of coronary heart disease or ischaemic stroke (Lindgren et al 1996, Cote et al 2000, Danesh et al 2001, Lowe et al 2001, Barber et al 2004).…”
mentioning
confidence: 99%
“…Previous studies in native kidneys focused on PAI-1, a prothrombotic factor by at least two mechanisms: inhibition of fibrinolysis by inhibiting the tPA-and uPA-mediated activation of plasminogen to plasmin (9) and inactivation of activated protein C (10). Serum studies in HUS (11), TMA (12), and primary and bone marrow transplantYassociated TTP (13) have found elevated PAI-1 serum levels, whereas results in diarrhea-positive HUS were conflicting (14,15). Two tissuebased studies showed increased glomerular PAI-1 compared with normal controls (16) by immunofluorescence and later also by in situ hybridization (17).…”
Section: Discussionmentioning
confidence: 99%