Literature DB >> 32123786

Undetected displacement of a subcutaneous implantable cardioverter-defibrillator lead. importance of performing a chest X-ray during the first weeks post-implant: a case report.

Jose Apolo1, Rodolfo San Antonio1,2, Lluís Mont1,2,3, José María Tolosana1,2,3.   

Abstract

BACKGROUND: In recent years, subcutaneous implantable cardioverter-defibrillator (S-ICD) implants have progressively increased and have been shown to be safe and highly successful, affording low reintervention rates regardless of the technique used. CASE
SUMMARY: We present a case of S-ICD implantation in a patient diagnosed with idiopathic ventricular fibrillation. In the first follow-up consultation the patient showed appropriate detection parameters in the three configurations. However, chest X-ray revealed lead displacement with a tip migration from the manubrium area of the sternum to the xiphoid process. DISCUSSION: This case highlights the importance of performing at least one chest X-ray during the first weeks after S-ICD implantation, allowing the detection of a problem such as lead displacement, which can lead to undersensing of ventricular arrhythmias or S-ICD oversensing.
© The Author(s) 2019. Published by Oxford University Press on behalf of the European Society of Cardiology.

Entities:  

Keywords:  Cardiac devices; Case report; S-ICD; X-ray

Year:  2019        PMID: 32123786      PMCID: PMC7042129          DOI: 10.1093/ehjcr/ytz189

Source DB:  PubMed          Journal:  Eur Heart J Case Rep        ISSN: 2514-2119


Learning points

Lead dislodgement after subcutaneous implantable cardioverter-defibrillator (S-ICD) implantation is a rare complication. Routine device checks may be not sufficient to ensure adequate S-ICD performance. A chest X-ray within the first weeks after implantation is needed to assess correct lead position and complement device revision.

Introduction

Subcutaneous implantable cardioverter-defibrillators (S-ICDs) are alternatives to transvenous implantable cardioverter-defibrillators (ICDs) for preventing sudden cardiac death in patients who do not require bradycardia or antitachycardia pacing. These devices were developed to eliminate the primary risks of transvenous ICDs, such as lead dysfunction or device infection, both associated with increased morbi-mortality., The S-ICD implant procedure has been shown to be safe and the implant success rate high, accompanied by low reintervention rates regardless the technique used., In addition, the design of high-pass filters (SMARTpass filtering) has drastically reduced T-wave oversensing.

Case presentation

A 29-year-old man with no previous history of cardiovascular disease (weight 76 kg; height 177 cm; body mass index 24) presented with out-of-hospital cardiac arrest. The rhythm initially recorded was ventricular fibrillation. He was admitted to another centre where a complete cardiac study (echocardiogram, cardiac magnetic resonance, ajmaline test, and coronary angiography) was performed. The specific cause of cardiac arrest was not identified. According to European Society of Cardiology (ESC) guidelines, implantable cardioverter-defibrillator (ICD) implantation is recommended for survivors of idiopathic ventricular fibrillation (Class of recommendation I; Level of evidence B); therefore, an S-ICD (EMBLEM; Boston Scientific) was implanted using the two-incision technique. The secondary vector (distal-tip-to-can) was the chosen configuration, and the SMARTPass sensing filter was also activated. The patient was discharged and referred to our centre 13 days later for device and clinical follow-up. At this 13-day follow-up, no clinical complications were revealed. Assessment of the S-ICD electrograms revealed unremarkable results (Figure ). Neither arrhythmias nor oversensing episodes were identified, and the secondary vector continued as the configuration of choice to obtain adequate signal amplitude. The SMARTPass filter remained activated (Figure ). Subcutaneous electrocardiogram detected by the device at first follow-up. Thirteen days post-implant. Device interrogation does not show alerts; the SMARTPass is activated. According to our institutional protocol, a chest X-ray was performed, which surprisingly revealed an important inferior lead displacement (by about 9 cm). This lead dislodgement had not been previously detected during device interrogation, because the distal electrode moved to the proximal electrode position, so the detection of the device remained unchanged (Figure ). Posteroanterior and lateral chest X-ray showing lead displacement from its original position (red arrow) to the lower parasternal region (black arrows). The heart did not interpose between the coil and the ICD generator; therefore, the lead was replaced. During reintervention, an S-ICD lead was found to be stitched without sufficient firmness at the xiphoid level, allowing displacement of the distal electrode 2 cm above the xiphoid appendage. To reduce the risk of displacement of the new lead, the three-incision technique was performed, fixing the lead tip to the underlying fascia and muscle at the manubriosternal junction, 1 cm left of the midline. Further dislodgement was not subsequently observed (Figure ). Position of the subcutaneous implantable cardioverter-defibrillator electrode after the three-incision technique.

Discussion

This case shows that S-ICD lead displacement can occur without detection by remote device monitoring (Latitude) or routine device revision. This should be kept in mind because important lead displacement can have important repercussions in the treatment of ventricular arrhythmias. Proper functioning of the S-ICD is directly related to the position of its components (device-electrode) in the thorax and their relationships with the heart in the presence of malignant arrhythmias. The displacement of an S-ICD lead is a rare complication (0.8–1.7%), and its primary aetiology is inadequate fixation of the suture olive in the muscular plane. This migration usually manifests itself by producing inappropriate discharges as a result of extracardiac detection signals. Three circumstances necessitate intraoperative S-ICD lead repositioning: (i) when the defibrillation threshold is not met (failure of a defibrillation test); (ii) when sensing fails in the three vectors; and (iii) when the myocardium does not interpose between the coil and the generator. In this case, the secondary configuration (tip-electrode-to-can) likely acted as a primary configuration (proximal-electrode-to-can), given that the distal electrode of the lead was placed where the proximal electrode had previously been. The excellent signal obtained in both positions did not produce inappropriate shocks, and the SMARTPass filter remained activated. However, in ventricular arrhythmia, the shock could have been ineffective, given that the coil was in a low position, thus excluding the cardiac structure between it and the can. Since its initial description, the two-incision technique has been shown to provide technical and aesthetic advantages over the three-incision technique (Table ); however, it has not been shown to reduce the frequency of electrode displacement. In our case, the three-incision technique was chosen at reintervention to provide greater distal support to the electrode. Comparison between S-ICD implant techniques Shorter procedure time. Greater comfort; aesthetically superior. Poor distal lead support. Distal lead support. Longer procedure time. The high sternal wound is associated with superficial infections and discomfort. In the S-ICD System IDE Clinical Investigation, device interrogations and chest X-rays were performed at hospital discharge and at 30, 90, and 180 days after implantation. However, in other studies performed in a real-world setting, no information about performing chest X-rays during follow-up was provided.,,, Our protocol specifies two X-rays during follow-up (at 4 weeks and again between the 6th and 12th months).

Conclusions

This case highlights the importance of performing at least one chest X-ray during the first weeks after implantation of an S-ICD, allowing detection of a problem such as lead displacement, which can lead to undersensing ventricular arrhythmias or S-ICD oversensing. Real-world, multicentre registries are needed to better explore the causes and best management of S-ICD complications.

Lead author biography

Jose Apolo is a cardiologist and EP fellow of the arrhythmia section of Hospital Clinic-Barcelona, he has worked in training and research programmes at the Álvaro Cunqueiro Hospital-Vigo and Clinico San Carlos Hospital-Madrid, currently, he is focused on the cardiac devices and atrial fibrillation research.

Supplementary material

Supplementary material is available at European Heart Journal - Case Reports online. Slide sets: A fully edited slide set detailing this case and suitable for local presentation is available online as Supplementary data. Consent: The author/s confirm that written consent for submission and publication of this case report including image(s) and associated text has been obtained from the patient in line with COPE guidance. Conflict of interest: none declared. Click here for additional data file.
DayHourEvent
0Subcutaneous implantable cardioverter-defibrillator (S-ICD) implant after aborted sudden death and normal cardiovascular studies.
1310:30First follow-up consultation and detection of electrode displacement.
1608:30Reintervention for S-ICD implant with the three incisions technique.
1710:00Device and X-ray control, patient discharge.
4510:00Follow-up consultation demonstrating normal functioning of the S-ICD.
Table 1

Comparison between S-ICD implant techniques

AdvantagesDisadvantages
Two incisions

Shorter procedure time.

Greater comfort; aesthetically superior.

Poor distal lead support.

Three incisions

Distal lead support.

Longer procedure time.

The high sternal wound is associated with superficial infections and discomfort.

  13 in total

1.  Safety and efficacy of a totally subcutaneous implantable-cardioverter defibrillator.

Authors:  Raul Weiss; Bradley P Knight; Michael R Gold; Angel R Leon; John M Herre; Margaret Hood; Mayer Rashtian; Mark Kremers; Ian Crozier; Kerry L Lee; Warren Smith; Martin C Burke
Journal:  Circulation       Date:  2013-08-27       Impact factor: 29.690

2.  Safety and Efficacy of the Totally Subcutaneous Implantable Defibrillator: 2-Year Results From a Pooled Analysis of the IDE Study and EFFORTLESS Registry.

Authors:  Martin C Burke; Michael R Gold; Bradley P Knight; Craig S Barr; Dominic A M J Theuns; Lucas V A Boersma; Reinoud E Knops; Raul Weiss; Angel R Leon; John M Herre; Michael Husby; Kenneth M Stein; Pier D Lambiase
Journal:  J Am Coll Cardiol       Date:  2015-04-28       Impact factor: 24.094

3.  Implantation of the Subcutaneous Implantable Cardioverter-Defibrillator: An Evaluation of 4 Implantation Techniques.

Authors:  Tom F Brouwer; Marc A Miller; Anne-Floor B E Quast; Chandrasekar Palaniswamy; Srinivas R Dukkipati; Vivek Reddy; Arthur A Wilde; Jonathan M Willner; Reinoud E Knops
Journal:  Circ Arrhythm Electrophysiol       Date:  2017-01

4.  Follow-up of the first patients with a totally subcutaneous ICD in Germany from implantation till battery depletion.

Authors:  Markus Bettin; Benjamin Rath; Christian Ellermann; Patrick Leitz; Florian Reinke; Julia Köbe; Lars Eckardt; Gerrit Frommeyer
Journal:  Clin Res Cardiol       Date:  2018-06-12       Impact factor: 5.460

5.  Implantation and follow-up of totally subcutaneous versus conventional implantable cardioverter-defibrillators: a multicenter case-control study.

Authors:  Julia Köbe; Florian Reinke; Christian Meyer; Dong-In Shin; Eimo Martens; Stefan Kääb; Andreas Löher; Susanne Amler; Artur Lichtenberg; Joachim Winter; Lars Eckardt
Journal:  Heart Rhythm       Date:  2012-09-29       Impact factor: 6.343

6.  2015 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).

Authors:  Silvia G Priori; Carina Blomström-Lundqvist; Andrea Mazzanti; Nico Blom; Martin Borggrefe; John Camm; Perry Mark Elliott; Donna Fitzsimons; Robert Hatala; Gerhard Hindricks; Paulus Kirchhof; Keld Kjeldsen; Karl-Heinz Kuck; Antonio Hernandez-Madrid; Nikolaos Nikolaou; Tone M Norekvål; Christian Spaulding; Dirk J Van Veldhuisen
Journal:  Eur Heart J       Date:  2015-08-29       Impact factor: 29.983

7.  Two-incision technique for implantation of the subcutaneous implantable cardioverter-defibrillator.

Authors:  Reinoud E Knops; Louise R A Olde Nordkamp; Joris R de Groot; Arthur A M Wilde
Journal:  Heart Rhythm       Date:  2013-05-21       Impact factor: 6.343

8.  Shock efficacy of subcutaneous implantable cardioverter-defibrillator for prevention of sudden cardiac death: initial multicenter experience.

Authors:  Ali Aydin; Friederike Hartel; Michael Schlüter; Christian Butter; Julia Köbe; Martin Seifert; Nils Gosau; Boris Hoffmann; Matthias Hoffmann; Eik Vettorazzi; Iris Wilke; Karl Wegscheider; Hermann Reichenspurner; Lars Eckardt; Daniel Steven; Stephan Willems
Journal:  Circ Arrhythm Electrophysiol       Date:  2012-08-23

9.  Failure-free survival of the Riata implantable cardioverter-defibrillator lead after a very long-term follow-up.

Authors:  Rodolfo San Antonio; Eduard Guasch; Fredy Chipa-Ccasani; José Apolo; Margarida Pujol-López; Hael Fernández; Omar Trotta; Mireia Niebla; Roger Borràs; Emilce Trucco; Elena Arbelo; Ivo Roca-Luque; Josep Brugada; Lluís Mont; José María Tolosana
Journal:  Indian Pacing Electrophysiol J       Date:  2019-02-19

10.  SMART pass will prevent inappropriate operation of S-ICD.

Authors:  Motomi Tachibana; Nobuhiro Nishii; Kimikazu Banba; Shinpei Fujita; Etsuko Ikeda; Keisuke Okawa; Hiroshi Morita; Hiroshi Ito
Journal:  J Arrhythm       Date:  2018-11-20
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