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Potentiation of thrombus instability: a contributory mechanism to the effectiveness of antithrombotic medications
Authors
A Gast
AD Michelson
+65 more
B Labarthe
B Shen
C Patrono
CT Ammollo
D Capodanno
D Gailani
DA Gorog
Diana A. Gorog
DM Coenen
E Álvarez
ER Bates
F Kabirian
F Müller
F Semeraro
G Stephens
H Brogren
HE Speich
HE Speich
HJ Weiss
HJ Weiss
HR Baumgartner
J Zilberman-Rudenko
JD McFadyen
JI Weitz
JM Cosemans
JP Collet
JP Collet
K Hosokawa
K Nagatsuka
KS Sakariassen
L Valerio
LF Brass
M Cattaneo
M Farag
M Humbert
M Larsson
M Li
M Ungerer
MA Bailey
MI Furman
MJ Price
ML Montfoort von
MS Sabatine
P Andre
P Seizer
PA Borne von dem
PP Wadowski
R Hellmuth
R Nergiz-Unal
RA Ajjan
S Goto
S Goto
SA Shaya
SB Larsen
SJ Marciniak
T Heitzer
T Renné
VT Turitto
VT Turitto
WA Schumacher
WS Nesbitt
X Wang
Y Yano
YC Lau
ZM Ruggeri
Publication date
1 March 2018
Publisher
'Springer Science and Business Media LLC'
Doi
Cite
Abstract
© The Author(s) 2018The stability of an arterial thrombus, determined by its structure and ability to resist endogenous fibrinolysis, is a major determinant of the extent of infarction that results from coronary or cerebrovascular thrombosis. There is ample evidence from both laboratory and clinical studies to suggest that in addition to inhibiting platelet aggregation, antithrombotic medications have shear-dependent effects, potentiating thrombus fragility and/or enhancing endogenous fibrinolysis. Such shear-dependent effects, potentiating the fragility of the growing thrombus and/or enhancing endogenous thrombolytic activity, likely contribute to the clinical effectiveness of such medications. It is not clear how much these effects relate to the measured inhibition of platelet aggregation in response to specific agonists. These effects are observable only with techniques that subject the growing thrombus to arterial flow and shear conditions. The effects of antithrombotic medications on thrombus stability and ways of assessing this are reviewed herein, and it is proposed that thrombus stability could become a new target for pharmacological intervention.Peer reviewedFinal Published versio
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info:doi/10.1007%2Fs11239-018-...
Last time updated on 03/12/2019
Supporting member
Spiral - Imperial College Digital Repository
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oai:spiral.imperial.ac.uk:1004...
Last time updated on 27/03/2019
University of Hertfordshire Research Archive
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oai:uhra.herts.ac.uk:7769
Last time updated on 02/07/2025