Driving Restrictions and Early Arrhythmias in Patients Receiving a Secondary Prevention Implantable Cardioverter-Defibrillator (DREAM-ICD-II study)

Author:

Steinberg Christian1ORCID,Dognin Nicolas1ORCID,Sodhi Amit2,Champagne Catherine1,Staples John A.3ORCID,Champagne Jean1ORCID,Laksman Zachary2ORCID,Sarrazin Jean-François1ORCID,Bennett Matthew2,Plourde Benoit1,Deyell Marc W.2ORCID,Andrade Jason G.4,Roy Karine1,Yeung-Lai-Wah John A.2,Hawkins Nathaniel M.2ORCID,Mondésert Blandine5,Blier Louis1,Nault Isabelle1,O'Hara Gilles1,Krahn Andrew D.2ORCID,Philippon François1,Chakrabarti Santabhanu2ORCID

Affiliation:

1. Institut universitaire de cardiologie et pneumologie de Québec (IUCPQ−UL), Québec, Canada

2. Centre for Cardiovascular Innovation, Division of Cardiology, University of British Columbia, Vancouver, Canada; Department of Medicine, University of British Columbia, Vancouver, Canada

3. Department of Medicine, University of British Columbia, Vancouver, Canada; Centre for Clinical Epidemiology & Evaluation (C2E2), Vancouver, Canada

4. Centre for Cardiovascular Innovation, Division of Cardiology, University of British Columbia, Vancouver, Canada; Department of Medicine, University of British Columbia, Vancouver, Canada; Montreal Heart Institute, Department of Medicine, Université de Montréal, Montreal, Quebec, Canada

5. Montreal Heart Institute, Department of Medicine, Université de Montréal, Montreal, Quebec, Canada

Abstract

Background: Regulatory authorities of most industrialized countries recommend 6-months of private driving restriction after implantation of a secondary prevention ICD. These driving restrictions result in significant inconvenience and social implications. The purpose of this study was to assess the incidence rate of appropriate device therapies in contemporary recipients of a secondary prevention ICD. Methods: A retrospective study at three Canadian tertiary care centers enrolling consecutive patients with new secondary prevention ICD implants between 2016-2020. Results: 721 patients were followed for a median of 760 days (324, 1190). The risk of recurrent ventricular arrhythmia was highest during the first three months after device insertion (34.4%), and decreased over time (10.6% between 3−6 months, 11.7% between 6-12 months). The corresponding incidence rate per 100 patient-days was 0.48 (95% CI 0.35-0.64) at 90 days, 0.28 (95% CI 0.18−0.48) at 180 days and 0.20 (95% CI 0.13−0.31) between 181-365 days after ICD insertion (p<0.001). The cumulative incidence of arrhythmic syncope resulting in sudden cardiac incapacitation was 1.8% within the first 90 days and subsequently dropped to 0.4% between 91-180 days (p<0.001) after ICD insertion. Conclusions: The incidence rate of appropriate therapies resulting in sudden cardiac incapacitation in contemporary recipients of a secondary prevention ICD is much lower than previously reported, and significantly declines after the first three months. Lowering driving restrictions to three months after the index cardiac event seems safe and revision of existing guidelines recommending should be considered in countries still adhering to a 6-months period. Existing restrictions for private driving after implantation of a secondary prevention ICD should be reconsidered.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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