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Left Bundle Branch Block (LBBB) After IntuityTM

P

Public Assistance-Hospitals of Marseille (AP-HM)

Status

Completed

Conditions

Aortic Valve Disease

Study type

Observational

Funder types

Other

Identifiers

NCT04897659
CIL 2019-48 bis

Details and patient eligibility

About

This study aimed to evaluate incidence, prognosis and predictive factors of new-onset of persistent left bundle branch block (LBBB) after rapid-deployment aortic valve replacement (RD-AVR) with the IntuityTM bioprosthesis.

It was an observational, retrospective and single-center study. Two hundred and seventy-four consecutive patients without any baseline ventricular conduction disorder or previous permanent pacemaker or defibrillator implantation who underwent RD-AVR with the IntuityTM valve were included. Twelve-lead electrocardiogram and transthoracic echocardiography were performed preoperatively, postoperatively, at discharge, 1-month, and 1-year. Incidence, prognosis and predictive factors of new-onset of persistent LBBB were evaluated.

Enrollment

274 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • rapid-deployment aortic valve replacement (RD-AVR) with the Edwards Intuity™ bioprosthesis for severe aortic valve stenosis
  • between July 2012 and May 2018

Exclusion criteria

  • preoperative permanent pacemaker or defibrillator,
  • complete intraventricular conductive disorder defined by a QRS width ≥ 120 ms.
  • absence of patient's authorization for anonymous publication of their clinical data for research purposes.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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