Inappropriate shock incidence in patients with subcutaneous implantable cardioverter‐defibrillators with concomitant cardiac implantable electronic devices: A single‐center cohort study

Author:

Okazaki Makiko12ORCID,Sahashi Yuki3ORCID,Nagase Takahiko4ORCID,Inoue Kanki4,Sekiguchi Yukio4,Nitta Junichi4,Shinoda Satoru5,Shimizu Sayuri2,Kuroki Makoto2,Isobe Mitsuaki6,Mihara Takahiro2ORCID

Affiliation:

1. Department of Clinical Engineering Sakakibara Heart Institute Fuchu‐shi Tokyo Japan

2. Department of Health Data Science Yokohama City University Graduate School of Data Science Yokohama‐shi Kanagawa Japan

3. Department of Cardiology Gifu University Graduate School of Medicine Gifu‐shi Japan

4. Department of Cardiology Sakakibara Heart Institute Fuchu‐shi Tokyo Japan

5. Department of Biostatistics School of Medicine Yokohama City University Yokohama‐shi Kanagawa Japan

6. Sakakibara Heart Institute Fuchu‐shi Tokyo Japan

Abstract

AbstractBackgroundSubcutaneous implantable cardioverter defibrillators (S‐ICDs) are occasionally used in combination with other cardiac implantable electronic devices (CIEDs). However, whether the incidence of inappropriate shock increases in patients with S‐ICDs and concomitant CIEDs remains unclear. This study aimed to investigate the association between the concomitant use of CIEDs and the incidence of inappropriate shock in patients with current‐generation S‐ICDs.MethodsA total of 127 consecutive patients received an S‐ICD. Patients were assigned to two groups depending on concomitant use of CIEDs at the time of S‐ICD implantation: patients without other CIEDs (non‐combined group, 106 patients) and patients with other CIEDs (combined group, 21 patients). CIEDs included pacemakers, implantable cardioverter defibrillators, cardiac resynchronization therapy pacemakers, and cardiac resynchronization therapy defibrillators. The primary outcome was inappropriate shock, defined as a shock other than ventricular arrhythmia. Hazard ratios and 95% confidence intervals were calculated using a time‐varying Cox proportional hazards model which was adjusted for age because age differed between the groups and could be a confounder.ResultsDuring a median follow‐up period of 2.2 years (interquartile range, 1.0–3.4 years), inappropriate shock events occurred in 17 (16%) and five (19%) patients of the non‐combined and combined groups, respectively. While the age‐adjusted hazard ratio for inappropriate shock was 24% higher in the combined than in the non‐combined group (hazard ratio = 1.24, 95% confidence interval, 0.39–3.97), this difference was insignificant (p = .71).ConclusionThe incidence of inappropriate shock did not differ between patients with and without concomitant use of CIEDs, suggesting that S‐ICDs could potentially be combined with other CIEDs without increasing the number of inappropriate shocks. Further studies are warranted to confirm the safety and feasibility of concomitant use of S‐ICDs and CIEDs.

Publisher

Wiley

Subject

Cardiology and Cardiovascular Medicine,General Medicine

Reference21 articles.

1. 2017 AHA/ACC/HRS guideline for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: a report of the American College of Cardiology/American Heart Association Task Force on Clinical Practice Guidelines and the Heart Rhythm Society;Al‐Khatib SM;Circulation,2018

2. Subcutaneous Versus Transvenous Implantable Defibrillator Therapy

3. Effectiveness of Implantation of a Subcutaneous Implantable Cardioverter-Defibrillator in a Patient With Complete Heart Block and a Pacemaker

4. Subcutaneous implantable cardioverter-defibrillator: First single-center experience with other cardiac implantable electronic devices

5. Implant and Midterm Outcomes of the Subcutaneous Implantable Cardioverter-Defibrillator Registry

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