Varfarine bağlı cilt nekrozu: Eski bir soruna yeni bir çözüm
Autor: | Ekrem Güler, Onur Omaygenç, Emir Cantürk, Filiz Kızılırmak, Oguz Karaca |
---|---|
Jazyk: | angličtina |
Rok vydání: | 2014 |
Předmět: |
medicine.medical_specialty
lcsh:Internal medicine lcsh:Diseases of the circulatory (Cardiovascular) system Necrosis lcsh:Medicine skin necrosis Dabigatran medicine cardiovascular diseases lcsh:RC31-1245 medicine.diagnostic_test business.industry lcsh:R Warfarin novel anti-coagulants Atrial fibrillation medicine.disease Thrombosis Discontinuation Surgery warfarin lcsh:RC666-701 Skin biopsy Varfarin Cilt Nekrozu medicine.symptom Cardiology and Cardiovascular Medicine business Protein C medicine.drug |
Zdroj: | Türk Kardiyoloji Derneği Arşivi, Vol 42, Iss 8, Pp 787-787 (2014) |
ISSN: | 1016-5169 |
Popis: | We present two cases of skin necrosis occurring after initiation of warfarin therapy, both of which were safely treated with novel oral anti-coagulants (NOACs). The first case is a 52-year-old male, seen after a transient ischemic event. He had non-valvular atrial fibrillation with a high CHA2DS2-VASc score. The patient was started on warfarin to prevent recurrent ischemic events. On the 3rd day of therapy, the patient developed newonset painful skin lesions in both legs (Figure A). A dermatology consult and skin biopsy revealed non-inflammatory thrombosis with focal necrosis. Warfarin therapy was discontinued and the patient was started on dabigatran 150 mg twice daily. Skin lesions were followed conservatively and seen to disappear in a few days, without any recurrence under dabigatran therapy. A search for genetic mutations in the patient revealed no deficiency of protein C and S. The second case involved a 64-year-old male with acute deep venous thrombosis (DVT). This patient was started on warfarin. In the second week of follow-up, the patient admitted with purpuric and painful lesions in his hands (Figure B) with appropriate INR level. A skin biopsy proved that the lesions were suggestive of warfarin-induced skin necrosis. After termination of warfarin, the patient was started on rivaroxaban 15 mg twice daily for 3 weeks, followed by 20 mg once daily as required. A search for genetic deficiencies of protein C and S revealed no mutations. The lesions diminished with discontinuation of warfarin and did not require debridement. We report two cases of warfarin-associated skin necrosis emphasizing that novel anti-coagulants can be safely used in this relatively rare but serious clinical situation. However, no such complications would have been encountered if NOACs were used as the ‘first choice’ drugs, instead of the ‘old habit’ of preferring warfarin. 787 |
Databáze: | OpenAIRE |
Externí odkaz: |