Literature DB >> 25093004

Electromagnetic interference with implantable cardioverter defibrillators causing inadvertent shock: case report and review of current literature.

Muhammad Akhtar1, Tariq Bhat1, Mohmad Tantray2, Chris Lafferty3, Saiful Faisal1, Sumaya Teli4, Hilal Bhat5, Muhammad Raza2, Mariam Khalid2, Soad Biekht1.   

Abstract

As the number of patients having implantable cardioverter defibrillator (ICD) devices is increasing, it is important for the physicians and patients to be aware of situations and conditions that can result in interference with normal functioning of these devices. There are multiple cases of malfunction of ICDs reported in literature and it may be of great significance to have an overview of these incidents for appropriate recognition and future prevention. Here we are reviewing the available literature as well as reporting an interesting case of electromagnetic interference (EMI) resulting from leak of current in pool water causing firing of ICD.

Entities:  

Keywords:  defibrillator; electromagnetic interference; inadvertent shock

Year:  2014        PMID: 25093004      PMCID: PMC4116377          DOI: 10.4137/CMC.S10990

Source DB:  PubMed          Journal:  Clin Med Insights Cardiol        ISSN: 1179-5468


Introduction

Implantable cardioverter defibrillators (ICDs) are a proven therapy for secondary and primary prevention of sudden cardiac death.1,2 Because of their effectiveness, the number of patients having these devices is increasing by the day.3 So, it is important for the primary care physicians, cardiologists, and the patients alike to be aware of the common problems that can be encountered. Electromagnetic interference (EMI) is one of the inappropriate causes of firing of automatic ICDs (AICDs). We are reporting a case of AICD firing due to EMI resulting from leakage of electric current in the pool.

Case Report

This is a case of a 76-year-old male with past medical history of gout, diabetes mellitus, coronary artery disease, and ischemic cardiomyopathy with ejection fraction of 30%. His past surgical history is significant for coronary artery bypass grafting. Patient had an AICD which was implanted in July 2006. The device was EnTrust D154ATG made by Medtronic. The atrial lead was 5594 CapSure SP Novus, made by Medtronic and implanted in July 2006 while right ventricle/superior vena cava (RV/SVC) lead was 6947 Sprint Quattro Secure, made by Medtronic and implanted in March 2009. On his current presentation, he came to see his cardiologist after being shocked by his ICD three times. The patient was swimming in his pool when he felt these shocks. He denied any chest pain, palpitations, headache, lightheadedness, or dizziness before being shocked. As soon as he felt shocks, he came out of the pool and did not get any further shocks after coming out of water. The patient was taking subcutaneous insulin, aspirin, clopidogrel, metoprolol, candesartan, simvastatin, furosemide, famotidine, allopurinol, and colchicine at home. The patient was allergic to penicillin and social history was significant for smoking half a pack of cigarettes per day for 40 years. The physical examination was normal. From the ICD interrogation done in his cardiologist’s office, the device was programmed to detect ventricular fibrillation (VF) at > 188 bpm and ventricular tachycardia (VT) between 162–188 bpm. Sensitivity was programmed to 0.3 mV. Pacing lead impedance was 272 ohms and defibrillator lead impedance was 39 ohms for RV and 52 ohms for SVC. Stored intra-cardiac electrograms recorded during this event showed high frequency undulating noise consistent with 60 Hz alternating current (Fig. 1). This was interpreted by ICD as VF and was shocked three times (Fig. 2). The pool was examined by a certified electrician who found a small leak into the pool from a lamp. The problem was fixed. Patient was counseled to be careful handling electrical equipment.
Figure 1

Intra-cardiac electrocardiograms recorded by the device during the event showing, high frequency electromagnetic interference in the background of normal QRS morphology (White Arrows), shocks delivers during this event (marked as stars), black arrow denotes the time when patient came out of pool and shows disappearance of EMI with no further shocks.

Figure 2

Intra-cardiac electrocardiograms recorded by the device during the event showing, high frequency electromagnetic interference in the background of normal QRS morphology (White Arrows), shocks delivers during this event (marked as stars), black arrow denotes the time when patient came out of pool and shows disappearance of EMI with no further shocks.

Discussion

EMI, also called radio frequency interference (RFI) when in high frequency or radio frequency, is a disturbance that affects an electrical circuit due to either electromagnetic induction or electromagnetic radiation emitted from an external source. The disturbance may interrupt, obstruct, or otherwise degrade or limit the effective performance of the circuit. For the normal functioning of an ICD, appropriate detection of myocardial action potentials is needed. EMI resulting in ICD malfunction is a well-known phenomenon.4 Source of EMI may be a normally functioning device including electronic article surveillance systems, hand-held radiofrequency remote controls, slot machines, abdominal muscle stimulators, etc. EMI may also be due to leakage of alternating electrical current from different devices such as a washing machine, refrigerator, swimming pool, and shower, among many others. If the radiofrequency signal is strong enough, it can be detected by the ICD. The detection of these signals depend on various factors including the strength of signal, distance of the device from the source of EMI, path of the current through the body, and the size of receiver.5 ICDs have built-in algorithms for detection of ventricular dysrhythmias. It is difficult for these algorithms to differentiate EMI from true ventricular arrhythmia; thus EMI may be detected and interpreted by an ICD as a shockable rhythm leading to inappropriate shock delivery. Inappropriate shock delivery from ICD in an awake patient is not only painful and frightening but also pro-arrhythmic.6 Currently, there are few cases reported in the literature where EMI resulted in an inappropriate ICD shock (Table 1).
Table 1

Reported cases of EMI related ICD malfunction.

NO.AUTHORSCAUSE OF EMI LEADING TO ICD FIRING
1Stelios P. et al.7Electrical current leakage from the electrical switch that was not grounded in the bathroom
2Ali M et al.5Accidental contact with AC power line during work
3Ashok G. et al.4Shower with minimal electrical leak
4Sung L. et al.8Swimming in a pool with minimal electrical leak
5Ayman A et al.9Refrigerator with unearth power supply
6Ngai C. et al.10• Outdoor use of power drill in rain• Washing machine
Our case, along with the other cases reported, illustrate some potential environmental hazards in patients with an ICD. Diagnosis of an inappropriate ICD shock depends on history and device interrogation. These patients typically deny any symptoms such as dizziness, lightheadedness, or syncope before the shock delivery. Interrogation of ICD reveals high frequency background noise (resulting from EMI) superimposed on patient’s baseline rhythm. Management of such inappropriate shock includes educating the patients about potential sources of EMI and their avoidance (Table 2). At the same time, efforts should be made to improve the ICDs, which includes better shielding of the devices and improving the software algorithms in order for EMIs to be differentiated from real cardiac dysrhythmias.
Table 2

Following can be used as example to educate patients about safety of ICDs.

• Patients should Stay away from:
 • High-voltage power lines
 • Large Magnets
• Cell phones should be used with caution
• Following devices at least 12 in. (30.5 cm) away from the pace-maker or ICD:
 • Radio transmitters
 • Magnets
 • Arc welders
 • Battery-powered cordless power tools
 • Industrial power generators
  10 in total

1.  Inadvertent detection of 60-Hz alternating current by an implantable cardioverter defibrillator.

Authors:  Sung W Lee; Jeffrey P Moak; Brian Lewis
Journal:  Pacing Clin Electrophysiol       Date:  2002-04       Impact factor: 1.976

2.  Inappropriate ICD therapy due to electrical interference: external alternating current leakage.

Authors:  Stelios Paraskevaidis; Kostas P Polymeropoulos; George Louridas
Journal:  J Invasive Cardiol       Date:  2004-06       Impact factor: 2.022

3.  Trends in use of implantable cardioverter-defibrillator therapy among patients hospitalized for heart failure: have the previously observed sex and racial disparities changed over time?

Authors:  Sana M Al-Khatib; Anne S Hellkamp; Adrian F Hernandez; Gregg C Fonarow; Kevin L Thomas; Hussein R Al-Khalidi; Paul A Heidenreich; Stephen Hammill; Clyde Yancy; Eric D Peterson
Journal:  Circulation       Date:  2012-01-27       Impact factor: 29.690

4.  Detection of refrigerator-associated 60 Hz alternating current as ventricular fibrillation by an implantable defibrillator.

Authors:  Ayman S Al Khadra; Abdulaziz Al Jutaily; Salem Al Shuhri
Journal:  Europace       Date:  2006-01-05       Impact factor: 5.214

5.  Alternating current electrocution detection and termination by an implantable cardioverter defibrillator.

Authors:  A Mehdirad; C Love; S Nelson; S Schaal; J Collins; K Huffman
Journal:  Pacing Clin Electrophysiol       Date:  1997-07       Impact factor: 1.976

6.  Prophylactic implantation of a defibrillator in patients with myocardial infarction and reduced ejection fraction.

Authors:  Arthur J Moss; Wojciech Zareba; W Jackson Hall; Helmut Klein; David J Wilber; David S Cannom; James P Daubert; Steven L Higgins; Mary W Brown; Mark L Andrews
Journal:  N Engl J Med       Date:  2002-03-19       Impact factor: 91.245

7.  Inappropriate implantable cardioverter-defibrillator shock due to external alternating current leak: report of two cases.

Authors:  Ngai Yin Chan; Lillian Wai-Ling Ho
Journal:  Europace       Date:  2005-03       Impact factor: 5.214

8.  A comparison of antiarrhythmic-drug therapy with implantable defibrillators in patients resuscitated from near-fatal ventricular arrhythmias.

Authors: 
Journal:  N Engl J Med       Date:  1997-11-27       Impact factor: 91.245

Review 9.  The proarrhythmic potential of implantable cardioverter-defibrillators.

Authors:  S L Pinski; G J Fahy
Journal:  Circulation       Date:  1995-09-15       Impact factor: 29.690

10.  Inappropriate implantable cardioverter defibrillator discharge from sensing of external alternating current leak.

Authors:  Ashok Garg; Manish Wadhwa; Keith Brown; Cathy Luckett; Tim Vaughn; Ulrika Birgersdotter-Green; Gregory Feld
Journal:  J Interv Card Electrophysiol       Date:  2002-10       Impact factor: 1.900

  10 in total
  1 in total

1.  Assessment of Electromagnetic Interference with Active Cardiovascular Implantable Electronic Devices (CIEDs) Caused by the Qi A13 Design Wireless Charging Board.

Authors:  Tobias Seckler; Kai Jagielski; Dominik Stunder
Journal:  Int J Environ Res Public Health       Date:  2015-05-27       Impact factor: 3.390

  1 in total

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