Chemotherapy and splenectomy are the most frequently used treatments in cases of systemic light-chain amyloidosis with factor X deficiency; although amyloid deposition is reduced and the main site of its absorption is removed, improvement of factor X levels is not observed in all cases. In order to treat or prevent bleeding events, infusions of fresh-frozen plasma, PCC, activated PCC, recombinant activated factor VII or factor X are suggested options in cases with persistent factor X deficiency5. In our experience, PCC infusion at a dosing regimen of 20 U/kg three times a week in factor X deficiency secondary to amyloidosis was effective and followed by a reduction in the frequency and extent of major bleeding requiring hospitalisation, whi...
WOS: 000379715000039PubMed ID: 27197801Introduction: Hereditary factor X (FX) deficiency is a rare b...
Impaired thrombin generation (TG) is seen in patients with acquired coagulopathy, due to a combinati...
The development of inhibitory antibodies to factor (F) VIII and FIX continues to be a major challeng...
Acquired factor X (FX) deficiency is a rare but serious complication of primary amyloidosis, presuma...
Background: Factor X (FX) deficiency is a serious, rare bleeding disorder, with 1 in 500 000 affecte...
Ease of dosing and simplicity of monitoring make new oral anticoagulants an attractive therapy in a ...
Background The lack of an antidote against factor Xa inhibitors in case of major bleeding or need fo...
Factor XI deficiency is a rare autosomally transmitted coagulopathy that is associated with a variab...
Abstract Background The lack of an antidote against factor Xa inhibitors in case of major bleeding o...
Prothrombin complex concentrate (PCC) is a term to describe pharmacological products that contain ly...
Factor X deficiency is a rare coagulation disorder that can be hereditary or acquired. The typology ...
A 70-yr-old woman presented with a severe haemorrhagic diathesis due to an acquired factor X deficie...
What is the correct use of established clotting factors, prothrombin complex concentrates (PCCs), an...
Prothrombin complex concentrates (PCCs) contain vitamin K-dependent clotting factors (II, VII, IX, a...
A new factor VII concentrate, made from ACD plasma by a process involving successive absorptions of ...
WOS: 000379715000039PubMed ID: 27197801Introduction: Hereditary factor X (FX) deficiency is a rare b...
Impaired thrombin generation (TG) is seen in patients with acquired coagulopathy, due to a combinati...
The development of inhibitory antibodies to factor (F) VIII and FIX continues to be a major challeng...
Acquired factor X (FX) deficiency is a rare but serious complication of primary amyloidosis, presuma...
Background: Factor X (FX) deficiency is a serious, rare bleeding disorder, with 1 in 500 000 affecte...
Ease of dosing and simplicity of monitoring make new oral anticoagulants an attractive therapy in a ...
Background The lack of an antidote against factor Xa inhibitors in case of major bleeding or need fo...
Factor XI deficiency is a rare autosomally transmitted coagulopathy that is associated with a variab...
Abstract Background The lack of an antidote against factor Xa inhibitors in case of major bleeding o...
Prothrombin complex concentrate (PCC) is a term to describe pharmacological products that contain ly...
Factor X deficiency is a rare coagulation disorder that can be hereditary or acquired. The typology ...
A 70-yr-old woman presented with a severe haemorrhagic diathesis due to an acquired factor X deficie...
What is the correct use of established clotting factors, prothrombin complex concentrates (PCCs), an...
Prothrombin complex concentrates (PCCs) contain vitamin K-dependent clotting factors (II, VII, IX, a...
A new factor VII concentrate, made from ACD plasma by a process involving successive absorptions of ...
WOS: 000379715000039PubMed ID: 27197801Introduction: Hereditary factor X (FX) deficiency is a rare b...
Impaired thrombin generation (TG) is seen in patients with acquired coagulopathy, due to a combinati...
The development of inhibitory antibodies to factor (F) VIII and FIX continues to be a major challeng...