Aortic arch chronic dissection following ascending aorta prosthetic replacement for acute Stanford A dissection Circulatory System
Conditions
Interventions
Endovascular repair of aortic arch chronic dissection with a custom made branched endograft (Cook Medical, Bloomington, In, USA).
Endografts includes 2 branched (one for the brachiocep
Sponsors
Centre Chirurgical Marie Lannelongue
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Patients aged 18 or older 2. With prior ascending aorta prosthetic replacement for Stanford A acute dissection 3. With chronic dissection of the aortic arch with arch dilatation 4. Treated with a custom-made branched endograft (Cook Medical, Bloomington, In, USA)
Exclusion criteria
Exclusion criteria: Does not meet inclusion criteria
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Rates of in-hospital mortality and stroke, measured during the postoperative course (between surgical procedure and postoperative day 30) | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Technical success, defined as successful delivery of the endograft without type 1 endoleak and evaluated on the preoperative angiogram, without death during the first 24 postoperative hours. Measured during the beginning of the surgical procedure and postoperative hour 24 2. Early complications, measured using evaluation of the presence of cardiac (troponin elevation with electrocardiogram modification), renal (elevation of creatinin level requiring extracorporeal epuration) or respiratory (hypoxemia, pneumoniae or reintubation) failure or necessity of secondary surgical procedure. Measured before postoperative day 30 3. Late complications, measured using the same measurement as early complications 4. Re-intervention and mortality rates measured during follow up (between postoperative day 30 and the most recent news) | — |
Countries
Brazil, France, Germany, Hong Kong, Netherlands, Poland, Sweden, United Kingdom, United States of America
Outcome results
None listed