Makary Mina S, Fogler Brian D, Dube Priyanka P, Flanders Vince L, Natarajan Kannan, Garcia-Cortes Rafael, Foster Todd, Dowell Joshua D
Division of Vascular and Interventional Radiology, Department of Radiology, The Ohio State University Wexner Medical Center, Columbus, Ohio.
Division of Vascular and Interventional Radiology, St. Vincent Health, 2001 West 86th Street, Indianapolis, IN 46260.
J Vasc Interv Radiol. 2020 Mar;31(3):438-443. doi: 10.1016/j.jvir.2019.11.008. Epub 2020 Jan 22.
To evaluate ultrasound-accelerated, catheter-directed thrombolysis (CDT) for treatment of acute submassive pulmonary embolism (PE).
This single-center, retrospective study included patients who underwent CDT for acute submassive PE (N = 113, 52% men/48% women) from 2013 to 2017. Baseline characteristics included history of deep venous thrombosis (12%), history of PE (6%), and history of cancer (18%). Of cohort patients, 88% (n=99) had a simplified PE severity index score of ≥ 1 indicating a high risk of mortality.
A technical success rate of 100% was achieved with 84% of patients having bilateral catheter placements. Average tissue plasminogen activator (tPA) therapy duration was 20.7 hours ± 1.5, and median tPA dose was 21.5 mg. Three patients (2.6%) experienced minor hemorrhagic complications. Mean hospital length of stay was 6 days. Mean pulmonary arterial pressure decreased from 55 mm Hg on presentation to 37 mm Hg (P < .01) 1 day following initiation of thrombolytic therapy. All-cause mortality rate of 4% (n = 4) was noted on discharge, which increased to 6% (n = 7) at 6 months. At 6-month follow-up compared with initial presentation, symptom improvements (93%), physiologic improvements (heart rate 72 beats/min vs 106 beats/min, P < .01), oxygen requirement improvements (fraction of inspired oxygen 20% vs 28%, P < .01), and right ventricular systolic pressure improvements by echocardiography (30 mm Hg vs 47 mm Hg, P < .01) were observed.
CDT for acute submassive PE was associated with low complications and mortality, decreased right ventricular systolic pressure, high rates of clinical improvement, and improved intermediate-term clinical outcomes.
评估超声加速导管定向溶栓(CDT)治疗急性次大面积肺栓塞(PE)的效果。
这项单中心回顾性研究纳入了2013年至2017年接受CDT治疗急性次大面积PE的患者(n = 113,男性占52%/女性占48%)。基线特征包括深静脉血栓形成病史(12%)、PE病史(6%)和癌症病史(18%)。队列患者中,88%(n = 99)的简化PE严重程度指数评分≥1,表明死亡风险高。
技术成功率达100%,84%的患者进行了双侧导管置入。组织纤溶酶原激活剂(tPA)平均治疗时长为20.7小时±1.5小时,tPA中位剂量为21.5毫克。3例患者(2.6%)出现轻微出血并发症。平均住院时长为6天。溶栓治疗开始1天后,平均肺动脉压从就诊时的55毫米汞柱降至37毫米汞柱(P <.01)。出院时全因死亡率为4%(n = 4),6个月时升至6%(n = 7)。与初始就诊相比,6个月随访时症状改善(93%)、生理指标改善(心率从106次/分钟降至72次/分钟,P <.01)、吸氧需求改善(吸入氧分数从28%降至20%,P <.01)以及超声心动图显示右心室收缩压改善(从47毫米汞柱降至30毫米汞柱,P <.01)。
急性次大面积PE的CDT治疗并发症和死亡率低,右心室收缩压降低,临床改善率高,中期临床结局良好。