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CASI CLINICI – Case Reports

Volume:

Biochimica Clinica, 2024; 48(2) e13-e17

Pubblicato on-line:

Marzo 1, 2024

DOI:

10.19186/BC_2024.014

Scarica in PDF:
Autenticazione richiesta

Difetti emostatici in un paziente in trattamento con anticoagulanti orali diretti

AUTORI

Monica Casini1,2, Tiziana Pavia1, Monica Martelloni3, Simone Meini4, Irene Bracalente4, Claudia Cois4, Paola Valentini5, Rossella Marcucci6, Silvia Linari7, Lucia Macchia2,3
1Azienda Ospedaliero Universitaria Pisana- UOC Laboratorio Analisi Chimico Cliniche, Pisa
2Azienda Ospedaliero Universitaria Pisana - Centro Antitrombosi FCSA (Federazione Centri per la diagnosi e la Sorveglianza delle terapie Antitrombotiche) n.281, Pisa
3Azienda Ospedaliero Universitaria Pisana - SOD Patologia Clinica, Pisa
4Presidio Ospedaliero Felice Lotti - UOC Medicina Generale, Pontedera (PI)
5Presidio Ospedaliero Felice Lotti - UOC Laboratorio Analisi Chimico Cliniche VDE (Valdera) e AVC (Alta Val di Cecina), Pontedera (PI)
6Università di Firenze, Dipartimento di Medicina Sperimentale e Clinica, Firenze
7AOU Careggi - SOD Malattie Emorragiche, Firenze

ABSTRACT

Emostatic abnormalities in a patient treated with direct oral anticoagulants

This case report concerns a 68-year-old man with atrial fibrillation who was being treated with edoxaban, a direct oral anticoagulant, to prevent stroke. In the patient’s medical history, two episodes of post-surgical hemorrhagic diathesis were not investigated. He sought First Aid for intense asthenia and dark stool discharge. He presented with severe anemia (hemoglobin 40 g/L) and extended coagulation tests (prothrombin ratio 8.56; activated partial thromboplastin ratio 3.83), antral gastritis, and a gastric ulcer. The prolongation of both coagulation tests suggested a decrease in the activity of one of the common pathway factors.
The subsequent performance of a mixing test, which helps to distinguish clotting time prolongation due to a coagulation factor deficiency rather than to an inhibitor, allowed us to understand that the patient might be suffering from a factor congenital deficiency. Measurements of coagulation factors showed a severe reduction in factor V activity (1.1%). The search for specific inhibitors directed against factor V was negative, confirming the suspicion that it was a congenital deficiency of factor V, a rare autosomal recessive disorder.
Anticoagulant therapy and gastric ulcer made it possible to diagnose a rare congenital disease in an elderly man. The anticoagulant therapy was interrupted and a surgical closure of the left atrial appendage was established.
Before starting anticoagulant therapy, according to consolidated guidelines, a blood count, full coagulation panel, renal, and liver function must be evaluated. Very likely, the patient, affected by congenital factor V deficiency, started the anticoagulant therapy without an adequate evaluation of the hemostasis status.

BIBLIOGRAFIA

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