Key result
Apixaban is linked to severe skin necrosis during pulmonary embolism treatment in a case report.
Why the study?
Skin toxicities are recognized but rare adverse effects of direct oral anticoagulants like apixaban, usually associated with vasculitis, requiring further clinical awareness.
Does apixaban cause skin necrosis in patients treated for pulmonary embolism?
Case Report (n=1)
Does apixaban cause skin necrosis in patients treated for pulmonary embolism?
Apixaban use may be associated with rare but severe skin necrosis, highlighting the need for clinical awareness of this potential adverse effect.
May signal rare apixaban skin necrosis in PE; single case leaves open causality and incidence.
BACKGROUND Apixaban is one of the newer direct oral anticoagulants (DOACs) being used to manage venous thrombosis. Skin toxicities are recognized adverse effects of the new DOACs, but are rare and usually associated with vasculitis. This report is of a 78-year-old man admitted to the hospital with pulmonary thromboembolism, who developed severe and extensive skin necrosis of both forearms 7 days after treatment with apixaban. CASE REPORT A 78-year-old man was admitted for pulmonary embolism and congestive heart failure exacerbation. He was started on therapeutic enoxaparin and diuresis. Later on, enoxaparin was substituted with apixaban. Seven days after starting apixaban, he suddenly developed skin changes that developed into skin necrosis on both forearms and the abdominal wall. A skin biopsy was not performed due to the high risk of bleeding. Skin necrosis was diagnosed based on clinical findings. A review of clinical data and the patient's medication profile did not reveal any other possible etiology or culprit medication. Clinical presentation and lab values were not consistent with infections or autoimmune etiologies. Apixaban was discontinued as it was perceived to be the likely cause of skin necrosis. The skin changes gradually improved within 1 week with supportive wound care, and the patient did not require a skin graft. The patient was discharged safely with subcutaneous low-molecular-weight heparin therapy. CONCLUSIONS This report shows that skin toxicity can be associated with apixaban and that with the increasing use of these newer DOACs, clinicians should be aware of these potential adverse effects.
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Pansuriya et al. (2021) conducted a case report in Pulmonary embolism (n=1). Apixaban was evaluated on Skin necrosis. Treatment with apixaban for pulmonary embolism was associated with the development of severe skin necrosis in a 78-year-old man after 7 days of therapy.
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