Aortic Dissection
Conditions
Keywords
Aorta, Aorta-Stent-Graft, Surgical operation, Aortic dissection
Brief summary
The aims of the aorta-stent-Registry are: • participating hospitals (with audit) document all consecutive patients diagnosed with a disease of the distal thoracal aorta that receive one of the following therapies:
Detailed description
1. Endovascular Aorta-Stent-Graft 2. Surgical operation of the distal thoracal aorta * Documentation of the indications, the procedural results and the clinical short- and long-term results of the endovascular and chirurgical treatment in day to day hospital routine. * Documentation of the operational risk (Euroscore) * Documentation of the technical enforcement of the procedure as well as the result of the intervention * Documentation of the hospital lethality and the non-fatal serious complications (Spinal Cord Ischemia, SCI, Stroke, TIA, high blood loss etc.) * Documentation of medication at hospital discharge * Documentation of long-term lethality and non-fatal serious complications (SCI, Stroke, TIA, major bleeding etc.) as well as hospitalization, re-intervention rates and medicinal drug therapy after 30 days, 1, 3 & 5 years.
Interventions
None listed
Sponsors
Stiftung Institut fuer Herzinfarktforschung
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Healthy volunteers
No
Inclusion criteria
* Patients with significant illness of the distal thoracal aorta (distal Aortic-dissection; TAA; penetrated ulcer; covered perforation; traumatically transection of the distal thoracal aorta) including those that receive an endovascular stent or an open surgical operation.
Exclusion criteria
* Missing signed informed consent
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| ◦Documentation of the indications, the procedural results and the clinical short- and long-term results of the endovascular and chirurgical treatment in day to day hospital routine | Hospital-stay |
Countries
Germany
Outcome results
None listed