Comprehensive analysis of substernal lead removal: experience from EV ICD Pilot, Pivotal, and Continued Access Studies.

Extravascular ICD explant extraction lead removal substernal

Journal

Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology
ISSN: 1532-2092
Titre abrégé: Europace
Pays: England
ID NLM: 100883649

Informations de publication

Date de publication:
30 Aug 2024
Historique:
received: 18 07 2024
revised: 20 08 2024
accepted: 29 08 2024
medline: 31 8 2024
pubmed: 31 8 2024
entrez: 30 8 2024
Statut: aheadofprint

Résumé

The extravascular implantable cardioverter-defibrillator (EV ICD) has been shown to be safe and effective for patients at risk of sudden cardiac death, but little is known about EV ICD lead removal in humans. This analysis aimed to characterize the EV ICD lead removal experience thus far. This was a retrospective analysis of lead removals from the EV ICD Pilot, Pivotal, and Continued Access Studies. Patients with a successful EV ICD implant who underwent lead removal were included. The main objective was lead removal success. Ancillary objectives included characterizing technique used, procedure complications, and reimplantation status. An EV ICD system was successfully implanted in 347 patients across the 3 studies (25.9% female; 53.4±13.3 years; LVEF: 39.7±15.9). Of these patients, 29 (8.4%) underwent lead removal with a mean lead dwell time of 12.6±14.3 months (0.2-58.4). The main reason for lead removal was lead dislodgement (n=9, 31.0%). Lead removal was successful in 27/29 (93.1%) cases [100% (19/19) success rate <1 year and 80% (8/10) success rate >1-year post-implant]. Simple traction was used in 22/26 (84.6%) and extraction tools in 4/26 (15.4%) successful cases where technique was known. No complications were reported for any of the removal procedures. All 11 EV ICD reimplant attempts were successful. Complete removal of the EV ICD lead was successful in 93.1% of cases and simple traction was sufficient in most instances. Based on these results, lead removal from the substernal space was safe and achievable up to 3 years post-implant.

Sections du résumé

BACKGROUND AND AIMS OBJECTIVE
The extravascular implantable cardioverter-defibrillator (EV ICD) has been shown to be safe and effective for patients at risk of sudden cardiac death, but little is known about EV ICD lead removal in humans. This analysis aimed to characterize the EV ICD lead removal experience thus far.
METHODS METHODS
This was a retrospective analysis of lead removals from the EV ICD Pilot, Pivotal, and Continued Access Studies. Patients with a successful EV ICD implant who underwent lead removal were included. The main objective was lead removal success. Ancillary objectives included characterizing technique used, procedure complications, and reimplantation status.
RESULTS RESULTS
An EV ICD system was successfully implanted in 347 patients across the 3 studies (25.9% female; 53.4±13.3 years; LVEF: 39.7±15.9). Of these patients, 29 (8.4%) underwent lead removal with a mean lead dwell time of 12.6±14.3 months (0.2-58.4). The main reason for lead removal was lead dislodgement (n=9, 31.0%). Lead removal was successful in 27/29 (93.1%) cases [100% (19/19) success rate <1 year and 80% (8/10) success rate >1-year post-implant]. Simple traction was used in 22/26 (84.6%) and extraction tools in 4/26 (15.4%) successful cases where technique was known. No complications were reported for any of the removal procedures. All 11 EV ICD reimplant attempts were successful.
CONCLUSIONS CONCLUSIONS
Complete removal of the EV ICD lead was successful in 93.1% of cases and simple traction was sufficient in most instances. Based on these results, lead removal from the substernal space was safe and achievable up to 3 years post-implant.

Identifiants

pubmed: 39210643
pii: 7745550
doi: 10.1093/europace/euae225
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of the European Society of Cardiology.

Auteurs

Venkata Sagi (V)

Baptist Heart Specialists, Jacksonville, Florida, US.

Francis Murgatroyd (F)

King's College Hospital, London, UK.

Lucas V A Boersma (LVA)

Cardiology Departments of St. Antonius Hospital Nieuwegein and Amsterdam University Medical Center, NL.

Jaimie Manlucu (J)

London Health Sciences Centre, London, ON, CA.

Bradley P Knight (BP)

Northwestern University, Chicago, IL, US.

Christophe Leclercq (C)

CHU de Rennes - Hôpital Pontchaillou, Rennes, FR.

Anish Amin (A)

Riverside Methodist Hospital, Columbus, OH, US.

Ulrika Maria Birgersdotter-Green (UM)

University of California San Diego (UCSD), San Diego, CA, US.

Joseph Yat Sun Chan (JYS)

Prince of Wales Hospital, Chinese University of Hong Kong, Hong Kong.

Henri Roukoz (H)

Cardiology Division, Electrophysiology Section, University of Minnesota, Minneapolis, MN, US.

Mauro Biffi (M)

IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, IT.

Haris Haqqani (H)

St. Vincent's Private Hospital Northside, Chermside, QLD, AU.

Russell Denman (R)

St. Vincent's Private Hospital Northside, Chermside, QLD, AU.

Christopher Wiggenhorn (C)

Medtronic Inc., Mounds View, MN, US.

Thomas R Holmes (TR)

Medtronic Inc., Mounds View, MN, US.

Thomas Lulic (T)

Medtronic Inc., Mounds View, MN, US.

Paul Friedman (P)

Mayo Clinic, Rochester, MN, US.

Ian Crozier (I)

Christchurch Hospital, Christchurch, NZ.

Classifications MeSH