The wearable defibrillator: a most affordable vest

Neth Heart J The wearable defibrillator: a most affordable vest J. R. de Groot 0 1 0 Heart Center, Department of Cardiology, Academic Medical Center, University of Amsterdam , Amsterdam , The Netherlands 1 J. R. de Groot - Published online: 13 April 2017 © The Author(s) 2017. This article is available at SpringerLink with Open Access. The implantable cardioverter-defibrillator (ICD) has become a cornerstone in the prevention of sudden cardiac death in patients with ischaemic and non-ischaemic cardiomyopathy, as well as in survivors of idiopathic ventricular arrhythmias and carriers of a genetic arrhythmia syndrome. Current guidelines recommend ICD implantation in patients with a left ventricular ejection fraction 35%, despite optimal medical treatment for 3 months, and at least 40 days after myocardial infarction or revascularisation [ 1 ]. These delays have been implemented because ejection fraction may improve over time upon treatment, and ICD implantation shortly after myocardial infarction has been demonstrated futile, mainly due to death as a consequence of pump failure. As physicians, we can accept this. However, the fact that our patients nonetheless have a high risk of preventable arrhythmic death in the meantime, is harder to accept. The same risk applies to patients in whom an infected ICD system has been extracted, who face long-term antibiotic treatment during which no new device can be implanted. That is why several strategies are employed to overcome the issue of unprotected arrhythmia risk, among which monitored hospitalisation and the temporary use of a wearable cardioverter-defibrillator (WCD). In a European Heart Rhythm Association (EHRA) survey of WCD use in European countries, Lenarczyk et al. describe that less than 50% of the centres responding used the WCD [ 2 ]. The most important barriers were reimbursement issues, followed by patient compliance, and only 55% of centres reported a patient compliance of >90% per day. In this issue of the Netherlands Heart Journal, Quast and colleagues report on the experience with a wearable defibrillator in two high-volume Dutch centres [ 3 ]. The report follows the initial description of the first experience with this technology in the Netherlands [ 4 ]. The majority of the patients Quast et al. report on are patients with newly diagnosed cardiomyopathy without a sufficiently long duration of optimal medical therapy, whereas in the remainder the WCD was used as a bridge to implantation in patients with a contraindication for immediate implantation due to infection or planned radiotherapy. During a median wearing time of 79 days, compliance was excellent with 23.3 h/day. Two patients received an appropriate shock, and one an inappropriate shock (all with ischaemic cardiomyopathy). This translated into an annual appropriate and inappropriate shock rate of 13.6 and 6.7%, respectively. There were no unsuccessful treatment episodes. Can the description of a relatively low number of patients, with an established therapeutic intervention, contribute to our understanding? And what do the real-life data from the Netherlands tell us? In an era of limited health-care system funds on the one hand, and indications for ICD implantation, particularly driven by low ejection fractions (irrespective of the cause), on the other, the data that Quast and colleagues present teach us two important lessons. First, the patients concerned were indeed at a very high risk of sudden arrhythmic death. Not only was the reported annual rate of appropriate therapy for ventricular fibrillation considerably higher than in most contemporary studies, but also one of the three patients who refused ICD implantation after WCD treatment subsequently died from sudden cardiac death during follow-up (median follow-up was 1.6 years). These numbers justify any form of protection against arrhythsubcutaneous ICDs, the appropriate shock rate was considerably lower than in the patients Quast et al. describe [ 5 ]. This does not imply that the indication criteria for ICD implantation were less strict in those patients, nor can it be concluded that all patients awaiting ICD implantation are at similar risk of having arrhythmias as the patients described by Quast et al. Postponing ICD implantation beyond the guideline-directed time periods, however, clearly prevents unnecessary implantations and with that, future device-related complications. It seems safe to conclude, therefore, that the WCD is an effective and affordable bridge to destination therapy. Funding ZonMw (NL) (016.146.310) Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http:// creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 1. Priori SG , Blomstrom-Lundqvist C , Mazzanti A , et al. ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death: The Task Force for the Management of Patients with Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death of the European Society of Cardiology (ESC). Endorsed by: Association for European Paediatric and Congenital Cardiology (AEPC) . Eur Heart J . 2015 ; 2015 (36): 2793 - 867 . 2. Lenarczyk R , Potpara TS , Haugaa KH , et al. The use of wearable cardioverter-defibrillators in Europe: results of the European Heart Rhythm Association survey . Europace . 2016 ; 18 : 146 - 50 . 3. Quast AF , van Dijk VF , Wilde AA , et al. Outpatient treatment with the wearable cardioverter defibrillator: clinical experience in two Dutch centres . Neth Heart J . 2017 ; 25 doi:10.1007/s12471-017- 0957-4. 4. Knops RE , Kooiman KM , Ten Sande JN , et al. First experience with the wearable cardioverter defibrillator in the Netherlands . Neth Heart J . 2012 ; 20 : 77 - 81 . 5. Brouwer TF , Yilmaz D , Lindeboom R , et al. Long-Term Clinical Outcomes of Subcutaneous Versus Transvenous Implantable Defibrillator Therapy . JACC . 2016 ; 68 : 2047 - 55 .