Perioperative Safety and Early Patient and Device Outcomes Among Subcutaneous Versus Transvenous Implantable Cardioverter Defibrillator Implantations : A Randomized, Multicenter Trial.


Journal

Annals of internal medicine
ISSN: 1539-3704
Titre abrégé: Ann Intern Med
Pays: United States
ID NLM: 0372351

Informations de publication

Date de publication:
12 2022
Historique:
pubmed: 8 11 2022
medline: 22 12 2022
entrez: 7 11 2022
Statut: ppublish

Résumé

Implantable cardioverter defibrillators (ICDs) improve survival in patients at risk for cardiac arrest, but are associated with intravascular lead-related complications. The subcutaneous ICD (S-ICD), with no intravascular components, was developed to minimize lead-related complications. To assess key ICD performance measures related to delivery of ICD therapy, including inappropriate ICD shocks (delivered in absence of life-threatening arrhythmia) and failed ICD shocks (which did not terminate ventricular arrhythmia). Randomized, multicenter trial. (ClinicalTrials.gov: NCT02881255). The ATLAS trial. 544 eligible patients (141 female) with a primary or secondary prevention indication for an ICD who were younger than age 60 years, had a cardiogenetic phenotype, or had prespecified risk factors for lead complications were electrocardiographically screened and 503 randomly assigned to S-ICD (251 patients) or transvenous ICD (TV-ICD) (252 patients). Mean follow-up was 2.5 years (SD, 1.1). Mean age was 49.0 years (SD, 11.5). The primary outcome was perioperative major lead-related complications. There was a statistically significant reduction in perioperative, lead-related complications, which occurred in 1 patient (0.4%) with an S-ICD and in 12 patients (4.8%) with TV-ICD (-4.4%; 95% CI, -6.9 to -1.9; At present, the ATLAS trial is underpowered to detect differences in clinical shock outcomes; however, extended follow-up is ongoing. The S-ICD reduces perioperative, lead-related complications without significantly compromising the effectiveness of ICD shocks, but with more early postoperative pain and a trend for more inappropriate shocks. Boston Scientific.

Sections du résumé

BACKGROUND
Implantable cardioverter defibrillators (ICDs) improve survival in patients at risk for cardiac arrest, but are associated with intravascular lead-related complications. The subcutaneous ICD (S-ICD), with no intravascular components, was developed to minimize lead-related complications.
OBJECTIVE
To assess key ICD performance measures related to delivery of ICD therapy, including inappropriate ICD shocks (delivered in absence of life-threatening arrhythmia) and failed ICD shocks (which did not terminate ventricular arrhythmia).
DESIGN
Randomized, multicenter trial. (ClinicalTrials.gov: NCT02881255).
SETTING
The ATLAS trial.
PATIENTS
544 eligible patients (141 female) with a primary or secondary prevention indication for an ICD who were younger than age 60 years, had a cardiogenetic phenotype, or had prespecified risk factors for lead complications were electrocardiographically screened and 503 randomly assigned to S-ICD (251 patients) or transvenous ICD (TV-ICD) (252 patients). Mean follow-up was 2.5 years (SD, 1.1). Mean age was 49.0 years (SD, 11.5).
MEASUREMENTS
The primary outcome was perioperative major lead-related complications.
RESULTS
There was a statistically significant reduction in perioperative, lead-related complications, which occurred in 1 patient (0.4%) with an S-ICD and in 12 patients (4.8%) with TV-ICD (-4.4%; 95% CI, -6.9 to -1.9;
LIMITATION
At present, the ATLAS trial is underpowered to detect differences in clinical shock outcomes; however, extended follow-up is ongoing.
CONCLUSION
The S-ICD reduces perioperative, lead-related complications without significantly compromising the effectiveness of ICD shocks, but with more early postoperative pain and a trend for more inappropriate shocks.
PRIMARY FUNDING SOURCE
Boston Scientific.

Identifiants

pubmed: 36343346
doi: 10.7326/M22-1566
doi:

Banques de données

ClinicalTrials.gov
['NCT02881255']

Types de publication

Randomized Controlled Trial Multicenter Study Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1658-1665

Investigateurs

Jeff S Healey (JS)
Blandine Mondesert (B)
Andrew D Krahn (AD)
Jamil Bashir (J)
Tim Stivland (T)
Mark Mosley (M)
Peter Aitkins (P)
John Sapp (J)
William F McIntyre (WF)
Jason D Roberts (JD)
Amir Janmohamed (A)
Guy Amit (G)
Francois Philippon (F)
Andrew Epstein (A)
John Cairns (J)
Kevin Thorpe (K)
Darryl P Leong (DP)
Naif Saad (N)
Harry Klimis (H)
Felipe Cirne (F)
Osama Eltebi (O)
Aditya Khetan (A)
Tais Araujo (T)
Hisham Dokainish (H)
Guy Amit (G)
Bernice Tsang (B)
Jacqueline Joza (J)
Derek V Exner (DV)
David H Birnie (DH)
Mouhannad Sadek (M)
Chris Lane (C)
Marc Dubuc (M)
Vidal Essebag (V)
Darryl Leong (D)
Markus Sikkel (M)
Victoria Korley (V)
Benoît Plourde (B)
Bernard Thibault (B)
John Sapp (J)
Christian Steinberg (C)
Amir Janmohamed (A)
Jean-Francois Roux (JF)
Danna Spears (D)
Eugene Crystal (E)
Zachary Laksman (Z)
Tom Hruczkowski (T)
Angie Djuric (A)
Kim Simek (K)
Roberta Napoleoni (R)
Brook Snider (B)
Shun Fu Lee (SF)
Gloria Wong (G)
Kailey Howell (K)
Lauren Christmas (L)
Svetlana Stoyanova-Brennecke (S)
Kiran Qamar (K)
Francois Lemarbre (F)
Julie Lefebvre (J)
Faye McCarthy (F)
Ambreen Syeda (A)
Nancy Page (N)
Marina Sanchez (M)
Marie-Christine Cote (MC)
Annette Nath (A)
Pei Ying (P)
Caitlin Patterson (C)
Elisa Ramser (E)
Nadia Vachon (N)
Rebecca Cairns (R)
Marta Gadacz (M)
Melissa Braga Gomes (MB)

Auteurs

Jeff S Healey (JS)

Population Health Research Institute, Hamilton, Ontario, Canada (J.S.H., W.F.M., D.P.L., S.F.L., G.W., A.D., S.J.C.).

Andrew D Krahn (AD)

Centre for Cardiovascular Innovation, University of British Columbia, Vancouver, British Columbia, Canada (A.D.K., J.B.).

Jamil Bashir (J)

Centre for Cardiovascular Innovation, University of British Columbia, Vancouver, British Columbia, Canada (A.D.K., J.B.).

Guy Amit (G)

McMaster University, Hamilton, Ontario, Canada (G.A.).

François Philippon (F)

Institut Universitaire de Cardiologie et de Pneumologie de Québec, Laval University, Quebec City, Quebec, Canada (F.P.).

William F McIntyre (WF)

Population Health Research Institute, Hamilton, Ontario, Canada (J.S.H., W.F.M., D.P.L., S.F.L., G.W., A.D., S.J.C.).

Bernice Tsang (B)

Southlake Regional Hospital, Newmarket, Ontario, Canada (B.T.).

Jacqueline Joza (J)

McGill University, Montreal, Quebec, Canada (J.J.).

Derek V Exner (DV)

University of Calgary, Calgary, Alberta, Canada (D.V.E.).

David H Birnie (DH)

University of Ottawa, Ottawa, Ontario, Canada (D.H.B., M.S.).

Mouhannad Sadek (M)

University of Ottawa, Ottawa, Ontario, Canada (D.H.B., M.S.).

Darryl P Leong (DP)

Population Health Research Institute, Hamilton, Ontario, Canada (J.S.H., W.F.M., D.P.L., S.F.L., G.W., A.D., S.J.C.).

Markus Sikkel (M)

University of Victoria, Victoria, British Columbia, Canada (M.S.).

Victoria Korley (V)

University of Toronto, Toronto, Ontario, Canada (V.K., E.C.).

John L Sapp (JL)

Dalhousie University and QEII Health Sciences Centre, Halifax, Nova Scotia, Canada (J.L.S.).

Jean-Francois Roux (JF)

University of Sherbrooke, Sherbrooke, Quebec, Canada (J.R.).

Shun Fu Lee (SF)

Population Health Research Institute, Hamilton, Ontario, Canada (J.S.H., W.F.M., D.P.L., S.F.L., G.W., A.D., S.J.C.).

Gloria Wong (G)

Population Health Research Institute, Hamilton, Ontario, Canada (J.S.H., W.F.M., D.P.L., S.F.L., G.W., A.D., S.J.C.).

Angie Djuric (A)

Population Health Research Institute, Hamilton, Ontario, Canada (J.S.H., W.F.M., D.P.L., S.F.L., G.W., A.D., S.J.C.).

Danna Spears (D)

University Health Network, University of Toronto, Toronto, Ontario, Canada (D.S.).

Sandra Carroll (S)

Population Health Research Institute, Hamilton, and School of Nursing, McMaster University, Hamilton, Ontario, Canada (S.C.).

Eugene Crystal (E)

University of Toronto, Toronto, Ontario, Canada (V.K., E.C.).

Tom Hruczkowski (T)

University of Alberta, Edmonton, Alberta, Canada (T.H.).

Stuart J Connolly (SJ)

Population Health Research Institute, Hamilton, Ontario, Canada (J.S.H., W.F.M., D.P.L., S.F.L., G.W., A.D., S.J.C.).

Blandine Mondesert (B)

Montreal Heart Institute, Montreal, Quebec, Canada (B.M.).

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