Skip to content

Surgical Management of the Aortic Root and Long-term Outcomes For Acute Type A Aortic Dissection

Surgical Management of the Aortic Root and Long-term Outcomes For Acute Type A Aortic Dissection

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05346497
Enrollment
1600
Registered
2022-04-26
Start date
2005-01-01
Completion date
2021-11-01
Last updated
2022-04-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Type A Aortic Dissection

Keywords

Type A Aortic Dissection, Aortic Root Surgery

Brief summary

The investigators focus on the patients who underwent aortic root surgery for acute type A aortic dissection between 2005.01-2021.11. The patients are divided into 3 groups according to the different aortic root surgical methods(Bentall,David and root reconstruction). Clinical data including age, gender, comorbidities, surgical informations and perioperative informations will be collected. All patients will receive follow-ups in hospital or by telephone. All the informations will be analyzed by SPSS to show the difference of both perioperative and long-term results among different surgical strategies.

Detailed description

Acute type A aortic dissection (ATAAD) is a rare but life threatening situation requiring immediate intervention. Regarding emergency operation for ATAAD, an important principle is to reconstruct the afflicted aorta to prevent fatal rupture. For aortic root dissection, the Bentall procedure has been the standard operation and has been proven simple and effective. However, the requirement for lifelong anticoagulation therapy is associated with increased risk of thromboembolic and bleeding complications. Valve sparing aortic root reimplantation (David reimplantation), which has been proven effective in root aneurysm with satisfactory safety and long-term outcomes, is an appealing alternative to preserve native aortic valve, especially for younger patients with intact valve function. Aortic root reconstruction without valve surgery is also a well-used strategy for aortic root dissection, but the long-term outcome is still controversial. The investigators focus on the patients who underwent aortic root surgery for acute type A aortic dissection between 2005.01-2021.11. The patients are divided into 3 groups according to the different aortic root surgical methods(Bentall,David and root reconstruction). Clinical data including age, gender, comorbidities, surgical informations and perioperative informations will be collected. All patients will receive follow-ups in hospital or by telephone. All the informations will be analyzed by SPSS to show the difference of both perioperative and long-term results among different surgical strategies.

Interventions

PROCEDUREDavid

David procedure: include replacement of aortic root and aortic valvuloplasty

PROCEDUREARR

Aortic root reconstruction: reconstruction instead of replacement of aortic root, without surgery of the valve. include sandwich procedure, adventitia invertion procedure, etc.

PROCEDUREBentall

Bentall procedure: include replacement of both aortic valve and root

Sponsors

Shanghai Zhongshan Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients who were followed up at our hospital for aortic lesions or who underwent aortic root surgery (including the Bentall procedure, the David procedure, and other aortic root angioplasty or replacement procedures) * Patients older than 18 years of age, no specific gender requirement * Patients who are compliant and able to complete follow-up * Patients who understand the purpose of the study, voluntarily participate, and have signed the Biospecimen and Health-Related Information Donation Form by themselves or their legal representative. * Patients who understand the purpose of the study, voluntarily participate and have signed the informed consent form for donation of biological samples and health-related information by themselves or their legal representative

Exclusion criteria

* Patients who are unable or unwilling to participate in the study and sign the informed consent form * Patients with poor compliance and unable to complete follow-up * Patients with severe organ insufficiency

Design outcomes

Primary

MeasureTime frameDescription
Death for any reasonFrom date of surgery until the date of death for any reason, up to 20 yearsDeath for any reason

Secondary

MeasureTime frameDescription
Redo aortic surgeryFrom date of surgery until the date of redo aortic surgery for any reason, up to 20 yearsPatients underwent aortic surgery again for any reason

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026