Abstract

This study presents a case of a successful severed femoral sheath recapture during transfemoral transcatheter aortic valve replacement (TAVR). During skin tunneling with a scalpel, the discontinuity of the femoral sheath occurred. Grasping of the distal sheath with the surgical hemostat was attempted unsuccessfully. A proximal part of the severed sheath was removed and Medtronic Sentrant introducer sheath (14 French) was then placed over the existing Confida wire which permanently remained in position, followed by the introduction of the Amplatz Left 2 (AL2) catheter which pushed the severed sheath in the ascending aorta over the Confida wire. The crucial maneuver was the entanglement of the severed sheath in the aortic non-coronary cusp which allowed for its entrapment by the AL2 catheter. This allowed for the coronary guidewire BMW Universal (0.014″) placement and a slow balloon retrieval (SeQuent NEO 2.5 × 25 mm2) of the severed sheath into the introducer sheath. The guidewire/balloon catheter was then exchanged for the support wire (0.035″) followed by the removal of the introducer sheath, AL2 catheter and the severed sheath. In conclusion, sheath severing is a complex accidental event during TAVR, which can be solved by intra-aortic recapture and retraction.

Highlights

  • Transcatheter aortic valve replacement (TAVR) is increasingly utilized for the treatment of severe aortic stenosis (AS) [1]

  • Sheath severing is a complex accidental event during TAVR, which can be solved by intra-aortic recapture and retraction

  • Who have a prohibitive risk for surgical aortic valve replacement (SAVR) with a predicted post-TAVR survival of >12 months, or those who are older than 80 years or for younger patients with a life expectancy of

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Summary

Introduction

Transcatheter aortic valve replacement (TAVR) is increasingly utilized for the treatment of severe aortic stenosis (AS) [1]. According to the latest guidelines of the American College of Cardiology, TAVR is primarily recommended for symptomatic patients with severe AS who have a prohibitive risk for surgical aortic valve replacement (SAVR) with a predicted post-TAVR survival of >12 months, or those who are older than 80 years or for younger patients with a life expectancy of

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