Acute Aortic Syndrome
Conditions
Brief summary
The objective of this study to evaluate the safety and effectiveness of the Castor single branch stent graft for endovascular repair of acute aortic syndrome patients without an inadequate proximal landing zone (\<15mm)
Detailed description
The goal of this observational, ambispective, and multicenter cohort study is to evaluate efficacy and safety of the Castor single branch stent graft. 205 patients who received thoracic endovascular aortic repair by meant of the Castor single branch stent graft from June 2018 to June 2022 were enrolled in our study. All enrolled patients have an inadequate proximal landing zone (\<15mm) , and they underwent routine follow-up after thoracic endovascular aortic repair at 1-month, 6-months, and 1-year for the following, but not limited to assessment: physical examination, laboratory test and the CT angiography. Meanwhile, the enrolled patients will come for continuous follow-up at 2-years, 3-years, and annually to 10-years post-procedure.
Interventions
DEVICEthe Castor single branch stent graft
Participants who received thoracic endovascular aortic repair by meant of the Castor single branch stent graft from June 2018 to June 2022 were enrolled in our study.
Sponsors
Hanzhong Central Hospital
Affiliated Hospital of Gansu Medical College
The Second Affiliated Hospital of Shaanxi University of Chinese Medicine
Xianyang Hospital of Yan'an University
Baoji Central Hospital
General Hospital of Ningxia Medical University
People's Hospital of Ningxia Hui Autonomous Region
Qinghai Red Cross Hospital
Hanzhong People's Hospital
First Affiliated Hospital Xi'an Jiaotong University
Study design
Observational model
COHORT
Time perspective
OTHER
Eligibility
Sex/Gender
ALL
Age
18 Years to 95 Years
Healthy volunteers
No
Inclusion criteria
* Patients with acute Stanford type B aortic syndrome who received thoracic endovascular aortic repair by meant of Castor single branch stent graft from June 2018 to June 2022
Exclusion criteria
* Patients with acute type B aortic syndrome with an adequate proximal landing zone (≥15mm) * Previous endovascular repair of the aorta * Patients with missing data and loss of follow-up
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Immediate post-operative technique success | immediately post operation | Immediate technical success is defined as successful delivery of the aortic and branching stent graft conveyors to their predetermined position, accurate positioning and successful deployment of the stent, safe removal of the delivery device outside the body, absence of Type I and III endoleaks on angiography at the end of the procedure, and patent branch stents. |
| All-cause mortality and major | 1-year post operation | All-cause mortality includes aortic mortality, non-aortic mortality, and mortality from unknown causes. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Major device/procedure-related adverse events of post-operation as assessed by computer tomography angiography | 1-month, 6-months, 1-year, and annually to 10-years post operation | Major device or procedure related major adverse events as assessed by computer tomography angiography included: death, dissection or aneurysm rupture, new myocardial infarction requiring intervention (percutaneous transluminal coronary angioplasty, bypass), retrograde type A aortic dissection, endoleaks, new disabling stroke, paraplegia, new hepatic infarction, new chronic renal insufficiency/renal failure requiring dialysis, lower limb ischemia (increase in Rutherford classification), access vessel thrombosis or rupture, conversion to open surgery, and stent migration, fracture or migration, stent graft infection, stent graft-induced new entry tear. |
| Aortic remodeling results as assessed by computer tomography angiography (the size of the true and false lumen of aorta, and the thrombosis degree of the false lumen of aorta) | 1-month, 6-months, 1-year, and annually to 10-years post operation | Compare the results of computer tomography angiography before operation and on the first-, 6th- and 12th-month post operation, the expansion of the true lumen and the thrombosis of the false lumen at the coverage of the stent graft to determine whether the blood vessel is successfully remodeled |
| Re-intervention during follow-up | 1-month, 6-months, 1-year, and annually to 10-years post operation | Re-intervention result from device/procedure-related adverse events. |
Countries
China
Contacts
Primary ContactHongyan Tian, MD
Backup ContactMengyang Kang, MD
Outcome results
None listed