Early and Midterm Results of a Novel Stented Graft for Patients with Stanford Type A Aortic Dissection

医学 临床试验 主动脉夹层 外科 解剖(医学) 梅德林 入射(几何) 主动脉瘤 普通外科 疾病
作者
Jue Yang,Jia Hu,Yan Yang,Yong Cao,Jinlin Wu,Jianfang Luo,Tucheng Sun,Changjiang Yu,Xin Li,Yucheng Peng,Yuan Liu,Ruixin Fan
出处
期刊:European Journal of Cardio-Thoracic Surgery [Oxford University Press]
卷期号:67 (12) 被引量:1
标识
DOI:10.1093/ejcts/ezaf401
摘要

OBJECTIVES: The objective of this study was to assess the feasibility and effectiveness of the novel stented graft in treating Stanford type A aortic dissection (TAAD). METHODS: This research was a prospective, multicentre, single-arm study that enrolled patients with Stanford TAAD at high risk for open aortic repair. Primary end-points included aorta-related mortality or reintervention at 1 month. Secondary end-points comprised type Ia and III endoleak, major adverse cardiovascular and cerebrovascular events at 1 month, 6 months, and 12 months. RESULTS: Fifty-three patients were enrolled with a mean age of 63.3 years (range 30-81), of whom 44 (83.0%) were male. Forty-six (86.8%) patients presented with retrograde Stanford TAAD, while the remainder had DeBakey type II aortic dissection. Forty-eight patients (90.6%) were in the acute phase. Carotid-to-subclavian artery bypass was performed in 17(32.1%) patients. The stented graft was successfully delivered via the femoral artery in all cases. Follow-up occurred at 1 month, 6 months, and 12 months. The median follow-up was 6 months (range 1-24). The all-cause mortality was 3.8% (2/53) and the aorta-related mortality was 1.9% (1/53). Six(11.3%) patients required open surgery due to left ventricular rupture (1 patient), retrograde progression of aortic dissection (3 patients), and severe type Ia endoleak (2 patients). Mild type Ia endoleak was observed in 1 patient and 1 patient suffered from cerebral infarction. CONCLUSIONS: The early and midterm results of the first-in-man evaluation of the new stented graft for Stanford TAAD were satisfactory, achieving 100% technical success and 1.9% aorta-related mortality. CLINICAL TRIAL REGISTRATION NUMBER: This clinical trial was registered in the Chinese Clinical Trial Registry under the identifier ChiCTR2200057706 (Chinese Clinical Trial Register (ChiCTR)-The world health organization international clinical trials registered organization registered platform).
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