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1.
Int Angiol ; 39(1): 76-81, 2020 Feb.
Article in English | MEDLINE | ID: mdl-31782283

ABSTRACT

BACKGROUND: Heparin-induced thrombocytopenia (HIT) is the most frequent drug-induced, immune-mediated thrombocytopenia. It is associated with significant morbidity and mortality. Anticoagulation with heparin must be stopped immediately and replaced by some suggested alternative - lepirudin, danaparoid or argatroban. Fondaparinux has been also successfully used in HIT. METHODS: We present a cohort of 10 patients diagnosed with HIT and treated in a university hospital in a period of four years. Diagnosis was based on Keeling´s scoring system, screening immunologic test for HIT (STic EXPERT® HIT) and sandwich ELISA (detection of IgG/heparin-PF4 antibodies). While other alternative anticoagulants are not readily available in our hospital, we used fondaparinux in all cases. RESULTS: From 2014 to 2018, eight males and two females (mean age 67 years, range 46-86 years) were diagnosed with HIT in our hospital. This complication developed in 9 cases after low-molecular-weight heparin and in one after heparin flushes in hemodialysis. A drop-in platelet count developed in all patients, thrombotic complications in 7 and skin necrosis in 2 cases. Fondaparinux was used in all patients, including two cases with severe renal impairment, the dose was chosen individually. We observed complete platelet recovery in all cases. One patient died because of advanced malignancy, others did not have any complication. In 6 cases we switched to oral anticoagulation after platelet recovery. CONCLUSIONS: In our group of 10 HIT patients fondaparinux was shown to be both safe and effective, even in those with severe renal impairment. Additional studies are warranted to confirm this observation.


Subject(s)
Anticoagulants/therapeutic use , Factor Xa Inhibitors/therapeutic use , Fondaparinux/therapeutic use , Heparin, Low-Molecular-Weight/adverse effects , Thrombocytopenia/drug therapy , Aged , Aged, 80 and over , Blood Coagulation/drug effects , Female , Humans , Male , Middle Aged , Platelet Count , Severity of Illness Index , Thrombocytopenia/chemically induced
2.
Vnitr Lek ; 64(5): 559-563, 2018.
Article in English | MEDLINE | ID: mdl-30193526

ABSTRACT

Venous thromboembolism is a multifactorial disease. Inherited thrombophilia is linked with increased risk of VTE and we know about them more than 50 years. Through a robust thrombophilia work-up in the end of millenium, the criteria for testing have significantly gone down. It is associated with increased amount of information about clinical consequence of testing. We discuss current recommendations not only in the literature, but also in our clinic. Key words: criteria for testing - thrombophilia - venous thromboembolism.


Subject(s)
Thrombophilia , Venous Thromboembolism , Humans , Risk Factors , Thrombophilia/congenital , Thrombophilia/diagnosis , Venous Thromboembolism/congenital , Venous Thromboembolism/diagnosis
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