Pansuriya Tusharkumar, Nguyen Trung, Sadat Mir Ali, Raza Syed A, Sarva Siva T
Department of Internal Medicine, Hospital Corporation of America (HCA) Houston Healthcare, Kingwood, TX, USA.
Department of Cardiology, Hospital Corporation of America (HCA) Houston Healthcare, Kingwood, TX, USA.
Am J Case Rep. 2021 Jan 25;22:e929002. doi: 10.12659/AJCR.929002.
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.
阿哌沙班是用于治疗静脉血栓形成的新型直接口服抗凝剂(DOACs)之一。皮肤毒性是新型DOACs公认的不良反应,但较为罕见,通常与血管炎有关。本报告介绍了一名78岁因肺血栓栓塞入院的男性患者,其在接受阿哌沙班治疗7天后出现双前臂严重且广泛的皮肤坏死。
一名78岁男性因肺栓塞和充血性心力衰竭加重入院。他开始接受治疗剂量的依诺肝素和利尿治疗。后来,依诺肝素被阿哌沙班替代。开始使用阿哌沙班7天后,他突然出现皮肤改变,双前臂和腹壁发展为皮肤坏死。由于出血风险高,未进行皮肤活检。根据临床表现诊断为皮肤坏死。回顾临床资料和患者用药情况未发现任何其他可能的病因或可疑药物。临床表现和实验室检查结果与感染或自身免疫病因不符。由于认为阿哌沙班可能是皮肤坏死的原因,故停用。通过支持性伤口护理,皮肤改变在1周内逐渐改善,患者无需植皮。患者接受皮下低分子肝素治疗后安全出院。
本报告表明皮肤毒性可能与阿哌沙班有关,并且随着这些新型DOACs的使用增加,临床医生应意识到这些潜在的不良反应。