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Updated: May 25, 2026

Standardized Technique of Aortic Valve Re-implantation for Valve-sparing Aortic Root Replacement
Published on: December 11, 2017
Expanding the indications for the David V aortic root replacement: early results
Bradley G Leshnower1, Robert A Guyton, Richard J Myung
1Clinical Research Unit, Division of Cardiothoracic Surgery, Joseph B Whitehead Department of Surgery, Emory University School of Medicine, Atlanta, GA, USA.
The David V valve-sparing aortic root replacement is safe and effective for complex cases like aortic dissection and severe aortic insufficiency (AI) in selected patients. This procedure shows excellent short-term valve function and durability with low complications.
Area of Science:
- Cardiovascular Surgery
- Thoracic Surgery
- Aortic Surgery
Background:
- The David V procedure is a type of valve-sparing aortic root replacement.
- Expanded use of the David V procedure in higher-risk patients requires evaluation.
Purpose of the Study:
- To assess the early outcomes of the David V valve-sparing aortic root replacement in patients with aortic dissection, severe aortic insufficiency (AI), or those undergoing reoperative cardiac surgery.
Main Methods:
- A retrospective review of 150 David V procedures from 2005-2011.
- Comparison of 78 patients in an expanded, higher-risk group with 72 patients in a traditional, elective group.
- Follow-up data were 88% complete with a mean follow-up of 19 months.
Main Results:
- Overall 6-year survival was 95%, with 3 operative deaths (2.2%) in the expanded group.
- Freedom from moderate AI was 93%, and freedom from aortic valve replacement was 98% at follow-up.
- No significant difference in freedom from moderate AI between expanded (91%) and traditional (95%) groups.
Conclusions:
- The David V procedure is safe and effective for selected patients with expanded indications, including aortic dissection, severe AI, and reoperative surgery.
- Excellent short-term valve function and durability were observed.
- The procedure demonstrated a low rate of valve-related complications in this cohort.
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