Ont Health Technol Assess Ser. 2005;5(18):1-59. Epub 2005 Nov 1.
To conduct an assessment on endovascular repair of descending thoracic aortic aneurysm (TAA).
Aneurysm is the most common condition of the thoracic aorta requiring surgery. Aortic aneurysm is defined as a localized dilatation of the aorta. Most aneurysms of the thoracic aorta are asymptomatic and incidentally discovered. However, TAA tends to enlarge progressively and compress surrounding structures causing symptoms such as chest or back pain, dysphagia (difficulty swallowing), dyspnea (shortness of breath), cough, stridor (a harsh, high-pitched breath sound), and hoarseness. Significant aortic regurgitation causes symptoms of congestive heart failure. Embolization of the thrombus to the distal arterial circulation may occur and cause related symptoms. The aneurysm may eventually rupture and create a life-threatening condition. The overall incidence rate of TAA is about 10 per 100,000 person-years. The descending aorta is involved in about 30% to 40% of these cases. The prognosis of large untreated TAAs is poor, with a 3-year survival rate as low as 25%. Intervention is strongly recommended for any symptomatic TAA or any TAA that exceeds twice the diameter of a normal aorta or is 6 cm or larger. Open surgical treatment of TAA involves left thoracotomy and aortic graft replacement. Surgical treatment has been found to improve survival when compared with medical therapy. However, despite dramatic advances in surgical techniques for performing such complex operations, operative mortality from centres of excellence are between 8% and 20% for elective cases, and up to 50% in patients requiring emergency operations. In addition, survivors of open surgical repair of TAAs may suffer from severe complications. Postoperative or postprocedural complications of descending TAA repair include paraplegia, myocardial infarction, stroke, respiratory failure, renal failure, and intestinal ischemia.
Endovascular aortic aneurysm repair (EVAR) using a stent graft, a procedure called endovascular stent-graft (ESG) placement, is a new alternative to the traditional surgical approach. It is less invasive, and initial results from several studies suggest that it may reduce mortality and morbidity associated with the repair of descending TAAs. The goal in endovascular repair is to exclude the aneurysm from the systemic circulation and prevent it from rupturing, which is life-threatening. The endovascular placement of a stent graft eliminates the systemic pressure acting on the weakened wall of the aneurysm that may lead to the rupture. However, ESG placement has some specific complications, including endovascular leak (endoleak), graft migration, stent fracture, and mechanical damage to the access artery and aortic wall. The Talent stent graft (manufactured by Medtronic Inc., Minneapolis, MN) is licensed in Canada for the treatment of patients with TAA (Class 4; licence 36552). The design of this device has evolved since its clinical introduction. The current version has a more flexible delivery catheter than did the original system. The prosthesis is composed of nitinol stents between thin layers of polyester graft material. Each stent is secured with oversewn sutures to prevent migration.
Objectives To compare the effectiveness and cost-effectiveness of ESG placement in the treatment of TAAs with a conventional surgical approachTo summarize the safety profile and effectiveness of ESG placement in the treatment of descending TAAsMeasures of Effectiveness Primary Outcome Mortality rates (30-day and longer term)Secondary Outcomes Technical success rate of introducing a stent graft and exclusion of the aneurysm sac from systemic circulationRate of reintervention (through surgical or endovascular approach)Measures of Safety Complications were categorized into 2 classes: Those specific to the ESG procedure, including rates of aneurysm rupture, endoleak, graft migration, stent fracture, and kinking; andThose due to the intervention, either surgical or endovascular. These include paraplegia, stroke, cardiovascular events, respiratory failure, real insufficiency, and intestinal ischemia.Inclusion Criteria Studies comparing the clinical outcomes of ESG treatment with surgical approachesStudies reporting on the safety and effectiveness of the ESG procedure for the treatment of descending TAAsExclusion Criteria Studies investigating the clinical effectiveness of ESG placement for other conditions such as aortic dissection, aortic ulcer, and traumatic injuries of the thoracic aortaStudies investigating the aneurysms of the ascending and the arch of the aortaStudies using custom-made graftsLiterature Search The Medical Advisory Secretariat searched The International Network of Agencies for Health Technology Assessment and the Cochrane Database of Systematic Reviews for health technology assessments. It also searched MEDLINE, EMBASE, Medline In-Process & Other Non-Indexed Citations, and Cochrane CENTRAL from January 1, 2000 to July 11, 2005 for studies on ESG procedures. The search was limited to English-language articles and human studies. One health technology assessment from the United Kingdom was identified. This systematic review included all pathologies of the thoracic aorta; therefore, it did not match the inclusion criteria. The search yielded 435 citations; of these, 9 studies met inclusion criteria.
Mortality The results of a comparative study found that in-hospital mortality was not significantly different between ESG placement and surgery patients (2 [4.8%] for ESG vs. 6 [11.3%] for surgery).Pooled data from case series with a mean follow-up ranging from 12 to 38 months showed a 30-day mortality and late mortality rate of 3.9% and 5.5%, respectively. These rates are lower than are those reported in the literature for surgical repair of TAA.Case series showed that the most common cause of early death in patients undergoing endovascular repair is aortic rupture, and the most common causes of late death are cardiac events and aortoesophageal or aortobronchial fistula.Technical Success Rate Technical success rates reported by case series are 55% to 100% (100% and 94.4% in 2 studies with all elective cases, 89% in a study with 5% emergent cases, and 55% in a study with 42% emergent cases).Surgical Reintervention In the comparative study, 3 (7.1%) patients in the ESG group and 14 (26.5%) patients in the surgery group required surgical reintervention. In the ESG group, the reasons for surgical intervention were postoperative bleeding at the access site, paraplegia, and type 1 endoleak. In the surgical group, the reasons for surgery were duodenal perforation, persistent thoracic duct leakage, false aneurysm, and 11 cases of postoperative bleeding.Pooled data from case series show that 9 (2.6%) patients required surgical intervention. The reasons for surgical intervention were endoleak (3 cases), aneurysm enlargement and suspected infection (1 case), aortic dissection (1 case), pseudoaneurysm of common femoral artery (1 case), evacuation of hematoma (1 case), graft migration (1 case), and injury to the access site (1 case).Endovascular Revision In the comparative study, 3 (7.1%) patients required endovascular revision due to persistent endoleak.Pooled data from case series show that 19 (5.3%) patients required endovascular revision due to persistent endoleak.Graft Migration Two case series reported graft migration. In one study, 3 proximal and 4 component migrations were noted at 2-year follow-up (total of 5%). Another study reported 1 (3.7%) case of graft migration. Overall, the incidence of graft migration was 2.6%.Aortic Rupture In the comparative study, aortic rupture due to bare stent occurred in 1 case (2%). The pooled incidence of aortic rupture or dissection reported by case series was 1.4%.Postprocedural Complications In the comparative study, there were no statistically significant differences between the ESG and surgery groups in postprocedural complications, except for pneumonia. The rate of pneumonia was 9% for those who received an ESG and 28% for those who had surgery (P = .02). There were no cases of paraplegia in either group. The rate of other complications for ESG and surgery including stroke, cardiac, respiratory, and intestinal ischemia were all 5.1% for ESG placement and 10% for surgery. The rate for mild renal failure was 16% in the ESG group and 30% in the surgery group. The rate for severe renal failure was 11% for ESG placement and 10% for surgery.POOLED DATA FROM CASE SERIES SHOW THE FOLLOWING POSTPROCEDURAL COMPLICATION RATES IN THE ESG PLACEMENT GROUP: paraplegia (2.2%), stroke (3.9%), cardiac (2.9%), respiratory (8.7%), renal failure (2.8%), and intestinal ischemia (1%).Time-Related Outcomes The results of the comparative study show statistically significant differences between the ESG and surgery group for mean operative time (ESG, 2.7 hours; surgery, 5 hours), mean duration of intensive care unit stay (ESG, 11 days; surgery, 14 days), and mean length of hospital stay (ESG, 10 days; surgery, 30 days).The mean duration of intensive care unit stay and hospital stay derived from case series is 1.6 and 7.8 days, respectively. ONTARIO-BASED ECONOMIC ANALYSIS: In Ontario, the annual treatment figures for fiscal year 2004 include 17 cases of descending TAA repair procedures (source: Provincial Health Planning Database). Fourteen of these have been identified as "not ruptured" with a mean hospital length of stay of 9.23 days, and 3 cases have been identified as "ruptured," with a mean hospital length of stay of 28 days. However, because one Canadian Classification of Health Interventions code was used for both procedures, it is not possible to determine how many were repaired with an EVAR procedure or with an open surgical procedure. (ABSTRACT TRUNCATED)
对降主动脉瘤(TAA)的血管内修复进行评估。
动脉瘤是胸主动脉最常见的需要手术治疗的疾病。主动脉瘤被定义为主动脉的局限性扩张。大多数胸主动脉瘤无症状,是偶然发现的。然而,TAA往往会逐渐增大并压迫周围结构,引起胸痛、背痛、吞咽困难、呼吸困难、咳嗽、喘鸣(一种粗糙、高音调的呼吸声)和声音嘶哑等症状。严重的主动脉瓣关闭不全可导致充血性心力衰竭的症状。血栓栓塞至远端动脉循环可能发生并引起相关症状。动脉瘤最终可能破裂,造成危及生命的情况。TAA的总体发病率约为每10万人年10例。降主动脉受累约占这些病例的30%至40%。未经治疗的大型TAA预后较差,3年生存率低至25%。强烈建议对任何有症状的TAA或任何直径超过正常主动脉两倍或直径为6 cm或更大的TAA进行干预。TAA的开放手术治疗包括左胸切开术和主动脉移植物置换。与药物治疗相比,手术治疗已被证明可提高生存率。然而,尽管进行此类复杂手术的技术有了显著进步,但优秀中心的择期手术死亡率在8%至20%之间,急诊手术患者的死亡率高达50%。此外,TAA开放手术修复的幸存者可能会出现严重并发症。降主动脉瘤修复的术后或术后并发症包括截瘫、心肌梗死、中风、呼吸衰竭、肾衰竭和肠缺血。
使用支架移植物进行血管内主动脉瘤修复(EVAR),即所谓的血管内支架移植物(ESG)置入术,是传统手术方法的一种新替代方案。它的侵入性较小,多项研究初步结果表明,它可能降低降主动脉瘤修复相关的死亡率和发病率。血管内修复的目标是将动脉瘤排除在体循环之外,防止其破裂,因为破裂会危及生命。支架移植物的血管内置入消除了作用于可能导致破裂的动脉瘤薄弱壁上的体循环压力。然而,ESG置入有一些特定并发症,包括血管内漏(内漏)、移植物移位、支架断裂以及对入路动脉和主动脉壁的机械损伤。Talent支架移植物(由美敦力公司制造,明尼阿波利斯,明尼苏达州)在加拿大被许可用于治疗TAA患者(4类;许可证36552)。自临床应用以来,该装置的设计不断改进。当前版本的输送导管比原始系统更灵活。假体由聚酯移植物材料薄层之间的镍钛诺支架组成。每个支架用缝扎线固定以防止移位。
目的比较ESG置入术与传统手术方法治疗TAA的有效性和成本效益总结ESG置入术治疗降主动脉瘤的安全性和有效性有效性指标主要结局死亡率(30天及长期)次要结局引入支架移植物的技术成功率以及将动脉瘤囊排除在体循环之外的成功率再次干预率(通过手术或血管内途径)安全性指标并发症分为两类:ESG手术特有的并发症,包括动脉瘤破裂、内漏、移植物移位、支架断裂和扭结的发生率;以及手术或血管内干预引起的并发症。这些包括截瘫、中风、心血管事件、呼吸衰竭、肾衰竭和肠缺血。纳入标准比较ESG治疗与手术方法临床结局的研究报告ESG手术治疗降主动脉瘤安全性和有效性的研究排除标准研究ESG置入术治疗其他疾病(如主动脉夹层、主动脉溃疡和胸主动脉创伤性损伤)的临床有效性研究升主动脉和主动脉弓动脉瘤的研究使用定制移植物的研究文献检索医学咨询秘书处检索了国际卫生技术评估机构网络和Cochrane系统评价数据库中的卫生技术评估。它还检索了2000年1月1日至2005年7月11日期间的MEDLINE、EMBASE、Medline在研及其他未索引引文和Cochrane CENTRAL中关于ESG手术的研究。搜索仅限于英文文章和人体研究。确定了一篇来自英国的卫生技术评估。该系统评价包括胸主动脉的所有病变;因此,它不符合纳入标准。搜索产生了435条引文;其中9项研究符合纳入标准。
死亡率一项比较研究的结果发现,ESG置入组和手术组的住院死亡率无显著差异(ESG组为2例[4.8%],手术组为6例[11.3%])。平均随访时间为12至38个月的病例系列汇总数据显示,30天死亡率和晚期死亡率分别为3.9%和5.5%。这些比率低于文献中报道的TAA手术修复的比率。病例系列显示,血管内修复患者早期死亡的最常见原因是主动脉破裂,晚期死亡的最常见原因是心脏事件和主动脉食管或主动脉支气管瘘。技术成功率病例系列报告的技术成功率为55%至100%(两项所有病例均为择期的研究中分别为100%和94.4%,一项有5%急诊病例的研究中为89%,一项有42%急诊病例的研究中为55%)。手术再次干预在比较研究中,ESG组3例(7.1%)患者和手术组14例(26.5%)患者需要手术再次干预。在ESG组,手术干预的原因是入路部位术后出血、截瘫和I型内漏。在手术组,手术原因是十二指肠穿孔、胸导管持续渗漏、假性动脉瘤以及11例术后出血。病例系列汇总数据显示,9例(2.6%)患者需要手术干预。手术干预的原因是内漏(3例)、动脉瘤增大和疑似感染(1例)、主动脉夹层(1例)、股总动脉假性动脉瘤(1例)、血肿清除(1例)、移植物移位(1例)和入路部位损伤(1例)。血管内翻修在比较研究中,3例(7.1%)患者因持续性内漏需要血管内翻修。病例系列汇总数据显示,19例(5.3%)患者因持续性内漏需要血管内翻修。移植物移位两个病例系列报告了移植物移位。一项研究在2年随访时发现3例近端移位和