Assessment of coagulation abnormalities in patients with pulmonary arterial hypertension

Doctoral Dissertation uoadl:2816069 450 Read counter

Unit:
Τομέας Κλινικοεργαστηριακός
Library of the School of Health Sciences
Deposit date:
2018-11-02
Year:
2018
Author:
Vrigkou Eleni
Dissertation committee:
Απόστολος Αρμαγανίδης, Καθηγητής, Ιατρική Σχολή, ΕΚΠΑ
Αργυρώ Γιαλεράκη, Αναπληρώτρια Καθηγήτρια, Ιατρική Σχολή, ΕΚΠΑ
Ευάγγελος Γιαμερέλλος - Μπουρμπούλης, Καθηγητής, Ιατρική Σχολή, ΕΚΠΑ
Στυλιανή Κoκκόρη, Επίκουρη Καθηγήτρια, Ιατρική Σχολή, ΕΚΠΑ
Στυλιανός Ορφανός, Καθηγητής, Ιατρική Σχολή, ΕΚΠΑ
Ηρακλής Τσαγκάρης, Αναπληρωτής Καθηγητής, Ιατρική Σχολή, ΕΚΠΑ
Αργύριος Τσαντές, Αναπληρωτής Καθηγητής, Ιατρική Σχολή, ΕΚΠΑ
Original Title:
Διερεύνηση των διαταραχών πήξης σε ασθενείς με πνευμονική αρτηριακή υπέρταση
Languages:
Greek
Translated title:
Assessment of coagulation abnormalities in patients with pulmonary arterial hypertension
Summary:
Introduction: Pulmonary arterial hypertension (PAH) is a progressive and potentially fatal disease characterized by endothelial dysfunction, vasoconstriction and in situ thrombosis, which leads to increased pulmonary artery pressure and, eventually, right heart failure.
Aim: The goal of this study was to evaluate platelet function, coagulation and fibrinolysis in PAH patients at diagnosis, before PAH-specific treatment initiation.
Methods: We enrolled 20 healthy controls and 30 PAH patients (20 with connective tissue disease (CTD-PAH) and 10 idiopathic (iPAH)). None of the participants was on any antiplatelet or anticoagulation therapy. Blood samples from PAH patients were collected during the initial right heart catheterization. All subjects were assessed with platelet function analyzer-100 (PFA-100), epinephrine (Epi) and ADP induced light transmission aggregometry (LTA), thromboelastometry (ROTEM) and endogenous thrombin potential (ETP).
Results: Our results showed that Epi and ADP-LTA values were significantly lower in newly diagnosed PAH patients compared to controls. Disaggregation was present in 73% of patients, a characteristic not seen in healthy individuals. In ROTEM assay, CT and CFT measurements were significantly higher and a angle lower compared to controls. ETP testing revealed significantly reduced outcomes in AUC, Cmax and Tmax. When CTD-PAH and iPAH patient groups were compared, iPAH ADP-LTA values were significantly decreased compared to CTD-PAH.
Conclusion: Newly diagnosed PAH patients presented with decreased platelet aggregation, clot propagation and thrombin generation, along with delayed initiation of the coagulation process. These hemostatic deficits could indicate an “exhaustion” of the coagulation process that could be caused by endothelial dysfunction and chronic activation of the procoagulant pathways.
Main subject category:
Health Sciences
Keywords:
Platelets, Thrombin, Coagulation abnormalities, Pulmonary hypertension
Index:
No
Number of index pages:
0
Contains images:
Yes
Number of references:
169
Number of pages:
116
File:
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Vrigkou Eleni PhD.pdf
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