21
Molding thrombus of an ecmo cannula floating in the right atrium
Morimont P, Lambermont B, Gaspard V, Defraigne JO.
Intensive Care Medicine.
2015;41:1965-1966
This article is a case report of a 23-year-old man was referred to CHU for veno-aerterial extracorporeal membrane oxygenation
(VA ECMO) support as a bridge to heart transplantation.
(tissue pet) vascular metabolic imaging and peripheral plasma biomarkers in the evolution of chronic aortic
dissections
Sakalihasan N, Nienaber CA, Hustinx R, Lovinfosse P, El Hachemi M, Cheramy-Bien JP, Seidel L, Lavigne JP, Quaniers J, Kerstenne
MA, Courtois A, Ooms A, Albert A, Defraigne JO, Michel JB.
European Heart Journal - Cardiovascular Imaging
.
2015;16:626-633
Despite adequate medical management, dissection of the descending aorta (type B) may develop complications, including
aneurysmal progression and eventually rupture. Partial false lumen thrombosis has been identified as a marker of adverse
evolution in chronic dissection. The aim of this study was to test the ability of complementary information, provided by (18)
F-fluorodeoxyglucose ((18)F-FDG) positron emission tomography/computed tomography (PET/CT) and peripheral biomar-
kers, to add pathophysiological significance and a prognostic value to morphological data. We explored serial aortic (18)F-FDG
uptake by PET/CT imaging and plasma biomarkers in a series of 23 patients with type B dissection to predict complications from
initial data and to investigate potential associations with aneurysmal expansion during follow-up. Complications occur-
red in 17 patients. Acute initial characteristics associated with complications were male gender (P = 0.021), arterial hyperten-
sion (P = 0.040), aortic dissection diameter (P = 0.0086), partial thrombosis of the false channel (P = 0.0046), and enhanced
focal (18)F-FDG uptake (P = 0.045). During follow-up (mean 16.7 ± 8.0 months), aneurysmal expansion was associated with false
lumen morphology (P< 0.0001), quantitative (18)F-FDG uptake, (P = 0.0029), elevated plasma concentrations of biomar-
kers of platelets (P-selectin, P = 0.0009) and thrombin activation (TAT complexes, P = 0.0075), and fibrinolysis (PAP complexes,
P < 0.0001; D-dimers, P = 0.0006). Plasma markers of coagulation and fibrinolysis were related to false channel morphology,
suggesting that thrombus biological dynamics may drive progressive expansion of type B dissections. Enhanced FDG uptake may be
considered as a complementary imaging marker associated with secondary complications in type B dissections. During follow-up,
aneurysmal progression is related to PET/CT and biomarkers of thrombus renewal and lysis.
Laboratories
u
Valvular Heart Disorders
Luc Piérard, Patrizio Lancellotti, Cécile Oury
u
Thrombosis Hemostasis
CécileOury, Patrizio Lancellotti, AndréGothot
u
Vascular Wall Disorders
Natzi Sakalihasan, Jean-Olivier Defraigne, Joël
Pincemail
u
Hemodynamics
Bernard Lambermont, Philippe Kohl,
Vincenzo d’Orio, Alexandre Ghuysen,
Philippe Morimont, Thomas Desaive
u
Experimental Surgery
Jean-Olivier Defraigne, Pierre Drion,
François Jouret, Jean-Marie Krzesinski,
Olivier Detry
u
Bioengineering Biophysics
Pierre Dauby, Thomas Desaive
People
15 Scientists
15 Clinician researchers
12 PhD Students
6 Technicians
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