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Antegrade Cardioplegia Decannulation Made Simple With the Cor-Knot System: Technique and Tips After 20 Consecutive
Aristotelis Panos1,2,3, Kyriakos Mpellos2, Sylvio Vlad2
1537314 Cardiovascular Surgery, La Tour Hospital, Meyrin/Geneva, Switzerland.
Innovations (Philadelphia, Pa.)
|September 1, 2020
Summary
A modified Cor-Knot system effectively closes the cardioplegia cannulation site in minimally invasive cardiac surgery, preventing bleeding and erosion. This technique offers a safe and efficient solution for hemostasis in video-assisted procedures.
Area of Science:
- Cardiovascular Surgery
- Minimally Invasive Techniques
- Medical Device Innovation
Background:
- Closing the cardioplegia cannulation site is a challenge in minimally invasive cardiac surgery.
- The Cor-Knot system is efficient for valve sutures but carries a risk of erosion to adjacent structures.
- A need exists for a safe method to achieve hemostasis at the aortic root cannulation site.
Purpose of the Study:
- To evaluate the safety and efficacy of a modified Cor-Knot system for closing the cardioplegia cannulation site.
- To prevent erosion of the aorta or right atrium during minimally invasive cardiac surgery.
- To assess the hemostatic capability of the modified device.
Main Methods:
- A single-arm prospective study involving 20 consecutive patients undergoing video-assisted minimally invasive cardiac surgery.
- A modified Cor-Knot system was used to secure a Teflon-felt band over the cardioplegia site.
- Suture placement and protection of the right atrial appendage were performed to prevent sharp end exposure.
Main Results:
- Hemostasis was successfully achieved in all 20 patients without additional sutures.
- No bleeding complications were observed.
- No instances of aortic or right atrial erosion were reported at the 6-month follow-up.
Conclusions:
- The modified Cor-Knot system provides a safe and effective method for off-label closure of the cardioplegia cannulation site in minimally invasive cardiac surgery.
- This technique demonstrates potential for preventing complications associated with cannulation site closure.
- Further investigation into this modified device is warranted based on initial positive outcomes.
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