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A Steerable and Electromagnetically Tracked Catheter: Navigation Performance Compared With Image Fusion in a Swine
Erik Nypan1,2, Geir Arne Tangen1,2,3, Reidar Brekken2,3
1Department of Circulation and Medical Imaging, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology, Trondheim, Norway.
A new steerable catheter with electromagnetic (EM) tracking offers similar navigation performance to image fusion for visceral vessel cannulation during endovascular aortic repair, potentially reducing radiation and contrast doses.
Area of Science:
- Vascular Surgery
- Medical Device Technology
- Interventional Radiology
Background:
- Cannulating visceral vessels is crucial for fenestrated and branched endovascular aortic repair.
- Reducing radiation and contrast dye exposure during these procedures is a significant clinical goal.
Purpose of the Study:
- To evaluate the cannulation performance of a novel electromagnetically (EM) trackable and manually steerable catheter.
- To compare EM tracking navigation against conventional image fusion guidance in a preclinical swine model.
Main Methods:
- Seven operators performed cannulations of visceral arteries (renal, SMA, celiac trunk) in three pigs.
- Cannulation attempts were made using 3D image navigation with EM tracking and subsequently with image fusion.
- Success rates, procedure times, and radiation exposure were recorded.
Main Results:
- Both EM tracking and image fusion achieved similar cannulation rates on the first attempt (79%).
- No statistically significant differences were observed in cannulation rates or procedure times between the two navigation methods.
- Image fusion achieved a 97% success rate when multiple attempts were permitted.
Conclusions:
- The steerable and EM trackable catheter demonstrated feasibility for 3D image navigation in visceral vessel cannulation.
- EM tracking navigation performance was comparable to image fusion, suggesting potential for reduced radiation and contrast use.
- Further clinical studies are warranted to validate its utility in patients undergoing endovascular aortic repair.
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