Academic Department of Vascular Surgery, School of Cardiovascular Medicine and Sciences, BHF Centre of Excellence and the Biomedical Research Centre at Guy's & St Thomas' NHS Foundation Trust and King's College London, London, UK.
University Hospital Regensburg, Department of Vascular Surgery, Regensburg, Germany.
J Vasc Surg. 2021 Aug;74(2):547-555. doi: 10.1016/j.jvs.2021.01.048. Epub 2021 Feb 15.
To evaluate short term outcomes related to the use of the Zenith TX2 Dissection Endovascular Graft (ZDEG) and the Zenith Dissection Bare stent (ZDES) for the treatment of Stanford type B aortic dissections.
This retrospective multicenter case cohort study collated data from 10 European institutions for patients with both complicated and uncomplicated type B aortic dissection treated with ZDEG and ZDES between 2011 and 2018. The primary end point was mortality at 30 and 90 days. Secondary end points included complications related to TEVAR, such as, type Ia endoleak, stroke, paraparesis, paraplegia, and retrograde type A dissection (RTAD). Statistical analysis was carried out using the t test, or one-way analysis of variance and the χ or Fisher exact tests.
We treated 120 patients (87 male; mean age, 62.7 ± 12.2years) either in the acute 76 (63.3%), subacute 16 (13.3%), or chronic 28 (23.3%) phase. Seven patients (5.8%) died within 30 days after the index procedure and two (1.7%) between 30 and 90 days. There was one instance of postoperative RTAD in a patient treated for rupture. Stroke and paraplegia occurred in three (2.5%) and five (4.2%), patients, respectively. Eight patients (6.7%) had a type Ia endoleak in the perioperative period. There were no instances of paraplegia, no permanent dialysis, and no requirement for adjunctive superior mesenteric or celiac artery stenting in the 33 patients (27.5%) who were treated by concurrent placement of ZDES distal to the ZDEG. The length and distal oversizing of ZDEG components used was less in this group.
The present series demonstrates a low (<1%) RTAD rate and favorable morbidity and mortality. The lower rate of paraplegia, dialysis, and visceral artery stenting in the cohort that had adjunctive use of ZDES is compelling and merits further assessment.
评估使用 Zenith TX2 解剖型血管内移植物(ZDEG)和 Zenith 解剖型裸支架(ZDES)治疗 Stanford 型 B 型主动脉夹层的短期结果。
这是一项回顾性多中心病例队列研究,对 2011 年至 2018 年间,10 家欧洲机构治疗的 120 例复杂和不复杂的 Stanford 型 B 型主动脉夹层患者的数据进行了汇总,这些患者接受了 ZDEG 和 ZDES 治疗。主要终点是 30 天和 90 天的死亡率。次要终点包括与 TEVAR 相关的并发症,如 I 型内漏、中风、截瘫、四肢瘫痪和逆行型 A 型夹层(RTAD)。使用 t 检验、单向方差分析和 χ 或 Fisher 确切检验进行统计学分析。
我们治疗了 120 例患者(87 例男性;平均年龄 62.7±12.2 岁),分别处于急性期 76 例(63.3%)、亚急性期 16 例(13.3%)和慢性期 28 例(23.3%)。7 例(5.8%)患者在指数手术后 30 天内死亡,2 例(1.7%)在 30-90 天内死亡。有 1 例破裂患者发生术后 RTAD。3 例(2.5%)和 5 例(4.2%)患者分别发生中风和四肢瘫痪。8 例(6.7%)患者在围手术期出现 I 型内漏。在同时在 ZDEG 远端放置 ZDES 的 33 例(27.5%)患者中,无截瘫、无永久性透析、无需辅助肠系膜上动脉或腹腔动脉支架。在该组中,ZDEG 组件的长度和远端过度扩张较小。
本系列研究显示,RTAD 发生率较低(<1%),且发病率和死亡率较低。在使用 ZDES 辅助治疗的患者中,截瘫、透析和内脏动脉支架的发生率较低,这一结果令人信服,值得进一步评估。