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Pacing the Atrium to Confirm or Exclude Pacemaker Indication in TAVI (PACE-TAVI)

A

AZ Sint-Jan AV

Status

Enrolling

Conditions

Aortic Valve Stenosis

Treatments

Procedure: RAP TAVI

Study type

Observational

Funder types

Other

Identifiers

NCT05278585
version 1 21/02/2022

Details and patient eligibility

About

The current observational registry aims to evaluate in patients undergoing TAVI implantation:

  1. the positive and negative predictive value for PPM post TAVI of Wenckebach phenomenona (WB) during RAP during the TAVI procedure,
  2. baseline and procedural characteristics of TAVI-implantation associated with new conduction abnormalities and need for PPM implantation,
  3. peri-procedural safety, in-hospital and 1-month outcomes after TAVI implantation.

Full description

The persistent growth in transcatheter aortic valve implantation (TAVI) calls for optimized early discharge programs to handle the increasing patient load. While access site bleeding and stroke rate have decreased with improved technologies and operators' experience, acquired conduction abnormalities necessitating prolonged rhythm-monitoring and permanent pacemaker (PPM) implantation have remained largely unchanged, and even up to 39.9% for some TAVI platforms. Prompt identification of patients necessitating PPM implantation leads to optimal patient care and use of resources. Conversely, prompt identification of patients with low -to no- risk for PPM post TAVI shortens their hospitalization and facilitates early and safe discharge.

Several baseline characteristics such as age, preexistent right bundle branch block (RBBB) and the use of self-expanding valves are associated with post-TAVI PPM implantation, but more practical and clinically more relevant parameters are needed with high negative and positive predictive values that could support clinical decision-making.

En passant rapid atrial pacing (RAP) immediately following TAVI has recently been reported to be a valuable tool in PPM risk stratification. The absence of Wenckebach phenomena post implantation at RAP up to 120/' has a negative predictive value for PPM of 98.7%.2 First use of RAP in routine practice at AZ Sint Jan Brugge can confirm these first results (unpublished data). This technique improves our clinical assessment and identification of low-risk patients for PPM suitable for safe early discharge, as well as high-risk patients requiring further rhythm monitoring and eventual PPM implantation.

The current observational registry aims to evaluate in patients undergoing TAVI implantation:

  1. the positive and negative predictive value for PPM post TAVI of Wenckebach phenomenona (WB) during RAP during the TAVI procedure,
  2. baseline and procedural characteristics of TAVI-implantation associated with new conduction abnormalities and need for PPM implantation,
  3. peri-procedural safety, in-hospital and 1-month outcomes after TAVI implantation.

Enrollment

500 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All patients in sinus rhythm with TAVI

Exclusion criteria

  • Patients in atrial fibrillation at the time of the implantation
  • Patients with pre-existent pacemaker

Trial design

500 participants in 1 patient group

RAP TAVI group
Description:
All patients in sinus rhythm with TAVI
Treatment:
Procedure: RAP TAVI

Trial contacts and locations

12

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Central trial contact

Emma Christiaen, Msc; Ian Buysschaert, MD, PhD

Data sourced from clinicaltrials.gov

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