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Non-Traumatic Spontaneous Spinal Subdural Hematoma in a Patient with Non-Valvular Atrial Fibrillation During Treatment with Rivaroxaban

机译:利伐沙班治疗期间非瓣膜性心房颤动患者的非创伤性自发性硬脊膜硬膜下血肿

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Patient: Male, 69 Final Diagnosis: Spontaneous spinal subdural hematoma Symptoms: Paraplegia Medication: Rivaroxaban Clinical Procedure: — Specialty: General Internal Medicine ? Hospital Medicine ? Cardiology ? Hematology ? Neurology Objective: Diagnostic/therapeutic accidents Background: Spontaneous spinal subdural hematoma (SSDH) is a rare but disabling condition, accounting for only 4.1% of all intraspinal hematomas. Risk factors include arteriovenous malformations, coagulopathy, therapeutic anticoagulation, underlying neoplasms, or following spinal puncture. Vitamin K antagonists, antiplatelet agents, and heparinoids have been associated with SSDHs in prior reports. To the best of our knowledge, no cases have reported this association with the factor Xa inhibitor, rivaroxaban, and SSDHs. Case Report: We report the case of a 69-year-old Honduran man with a 5-year history of symptomatic palpitations due to non-valvular atrial fibrillation. He was initially refractory to pharmacologic therapy. He underwent cardioversion in February 2014. After cardioversion, he remained asymptomatic on flecainide. He was anticoagulated on rivaroxaban 20 mg daily without incident since early 2013 until presentation in August 2014. He presented with sudden onset of excruciating upper and lower back pain after minimal movement. This was immediately followed by bilateral lower extremity paresis rapidly progressing to paraplegia with bowel and bladder dysfunction over 15 minutes. Magnetic resonance imaging demonstrated an acute spinal subdural hematoma extending from T3 inferiorly to the conus medullaris. Six months after undergoing cervical and lumbar drainage procedures, he has not recovered bowel, bladder, or lower extremity neurologic function. Conclusions: Non-traumatic spontaneous spinal subdural hematoma is a rare neurological emergency that may occur during the use of rivaroxaban in patients with non-valvular atrial fibrillation. Physicians should suspect SSDH in patients on rivaroxaban with acute onset of severe back pain and neurologic symptoms to improve the odds of a favorable outcome.
机译:患者:男性,69岁最终诊断:自发性脊髓硬膜下血肿症状:截瘫药物:利伐沙班临床操作:—专长:普通内科药物?医院医学?心脏病学血液学神经内科目的:诊断/治疗事故背景:自发性脊髓硬膜下血肿(SSDH)是一种罕见但致残的疾病,仅占所有椎管内血肿的4.1%。危险因素包括动静脉畸形,凝血障碍,治疗性抗凝,基础肿瘤或脊髓穿刺后。在先前的报道中,维生素K拮抗剂,抗血小板药和类肝素已与SSDH相关。据我们所知,尚无病例报告与Xa因子抑制剂,利伐沙班和SSDHs相关。病例报告:我们报告了一名69岁的洪都拉斯人的病例,该人由于非瓣膜性心房颤动而出现了5年的症状性心history史。最初他对药物治疗无效。他于2014年2月接受了心脏复律。心脏复律后,他继续服用氟卡尼无症状。自2013年初起至2014年8月就诊,他接受利伐沙班每天20 mg的抗凝治疗,直到2014年8月就诊。在突然移动后突然出现剧烈的上背部和下背部疼痛。随后,双侧下肢轻瘫迅速发展为截瘫,并在15分钟内出现肠和膀胱功能障碍。磁共振成像显示急性脊髓硬膜下血肿从T3下延伸至延髓。接受颈腰椎引流手术六个月后,他没有恢复肠,膀胱或下肢的神经功能。结论:非创伤性自发性硬膜下硬膜下血肿是一种罕见的神经系统紧急情况,在非瓣膜性房颤患者使用利伐沙班期间可能发生。医师应怀疑利伐沙班急性发作的严重背痛和神经系统症状的患者出现SSDH,以提高取得有利结果的几率。

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