Mendes Daniel, Veiga Carlos, Machado Rui, Sá-Pinto Pedro, Almeida Rui
Department of Angiology and Vascular Surgery, Centro Hospitalar Universitário de Santo António, Porto, Portugal.
School of Medicine and Biomedical Sciences, University of Porto, Porto, Portugal.
Int J Angiol. 2024 Feb 6;33(3):156-164. doi: 10.1055/s-0044-1779489. eCollection 2024 Sep.
Embolization to multiple arterial beds associated with primary aortic mural thrombus (PAMT) could result in high morbidity and mortality. There are no recommendations to dictate the best management. This study aims to describe our experience in managing this rare disease. A retrospective review of all patients affected by PAMT treated at our institution between January 2015 and December 2021 was performed. Recorded data included demographics, prothrombotic risk factors, imaging findings, clinical presentation, and treatment. Primary outcomes comprised thrombus recurrence, major amputation, and death. Thirteen patients with PAMT have been included. The median age was 52 years (36-68 years), and the male/female ratio was 1:1.6. The diagnosis of PAMT was made by computed tomography angiography (CTA) in all cases. Prothrombotic conditions were identified in 92% of cases, and most patients (92%) had thoracic PAMT. The most common presentation was acute limb ischemia after thrombus embolization (85%), requiring surgical revascularization. Anticoagulation was promptly started in all patients. Two patients developed heparin-induced thrombocytopenia. Recurrence of embolization/thrombosis was observed in 54% of patients; two underwent endovascular thrombus exclusion with a stent graft. We identified one PAMT-related death and one major amputation with a median follow-up time of 39 months (12-64 months). Anticoagulation alone as initial therapy could completely resolve PAMT but is associated with high embolization recurrence. Thoracic endovascular aortic repair is feasible and could prevent additional embolization. However, the criteria for its use as a first-line therapy still need to be defined. Our study highlights the importance of closely monitoring these patients.
与原发性主动脉壁血栓形成(PAMT)相关的多动脉床栓塞可导致高发病率和死亡率。目前尚无关于最佳治疗方案的建议。本研究旨在描述我们在管理这种罕见疾病方面的经验。
对2015年1月至2021年12月在我们机构接受治疗的所有PAMT患者进行了回顾性研究。记录的数据包括人口统计学、血栓形成危险因素、影像学检查结果、临床表现和治疗情况。主要结局包括血栓复发、大截肢和死亡。
纳入了13例PAMT患者。中位年龄为52岁(36 - 68岁),男女比例为1:1.6。所有病例均通过计算机断层扫描血管造影(CTA)诊断为PAMT。92%的病例发现有血栓形成前状态,大多数患者(92%)患有胸段PAMT。最常见的表现是血栓栓塞后急性肢体缺血(85%),需要手术重建血运。所有患者均立即开始抗凝治疗。2例患者出现肝素诱导的血小板减少症。54%的患者观察到栓塞/血栓形成复发;2例接受了带覆膜支架的血管内血栓封堵术。中位随访时间为39个月(12 - 64个月),我们确定了1例与PAMT相关的死亡和1例大截肢。
单独抗凝作为初始治疗可使PAMT完全消退,但与高栓塞复发率相关。胸段血管内主动脉修复是可行的,并且可以防止进一步栓塞。然而,其作为一线治疗的使用标准仍需确定。我们的研究强调了密切监测这些患者的重要性。