A Challenging Case of Electrical Storm in an Implantable Cardioverter Defibrillator Patient.

Implantable cardioverter defibrillators (ICD) have become indispensable in managing life-threatening ventricular arrhythmias. On average, 50%-70% of the patients receive a device-based therapy within the first two years post implantation. A few patients experience the electrical storm (ES). ES is a syndrome of recurrent ventricular tachycardia or fibrillation occurring two or more times in a 24-hour period, calling for the need of electrical cardioversion or defibrillation to stabilize the patient. We present the case of a patient with severe cardiomyopathy who presented with resistant ES after failing to respond initially to conventional medications like amiodarone and lidocaine. Propofol infusion was not an option due to his severe cardiomyopathy and hypotensive shock state. Aggressive treatment with intravenous medications stabilized his ES and he was eventually transferred to an outside facility for ventricular tachycardia ablation.

Introduction

Studies have shown that 50% to 70% of implantable cardioverter defibrillator (ICD) patients receive appropriate device therapy within the first two years of implantation [1]. While the total number of delivered discharges remains low, some patients receive multiple appropriate shocks during a short period of time consequent to recurrent or incessant ventricular tachycardia (VT) or ventricular fibrillation (VF); either of these conditions is termed an arrhythmic or electrical storm (ES). This has been observed in 10% to 20% of ICD patients [2]. While the prognostic outcome is still unclear with some initial studies clearly not reporting an increased mortality rate, some recent trials have strongly linked ES with consequent fatal events [3].

With the increased prevalence of coronary artery disease and heart failure, ICD implantations continue to rise significantly. This substantiates the need for better understanding and hence management (and prophylaxis) of the ES.

A thorough search for, and hence management of, triggering factors such as electrolyte imbalance or recurrent ischemia becomes of utmost importance. Early and prompt management of any possible triggering factors may abort/hinder the occurrence of the ES without needing to resort to antiarrhythmics [4]. However, a study by Gatzoulis et al., in which a majority (28 of the 32) of patients presenting with ES had no evident precipitating factor [5], showed that reversible triggers appear to be present in only a minority of the patients.

The antiarrhythmic medication regimen is tailored accordingly. Despite its poor side effect profile, amiodarone remains the cornerstone for treatment, with one study showing promising outcomes if given intravenously during resuscitation [6]. Variable success rates were reported using Class 1 with perhaps better outcomes with polymorphic arrhythmias. With close monitoring and careful titration in heart failure patients, beta-blockers have also proven their efficiency, mostly due to the underestimation of the sympathetic nervous system influence [7]. Adequate sedation, and in extremely refractory cases even general anesthesia, may prove to be life-saving. Monomorphic arrhythmias respond well to cathetar ablation which also seems promising for VF [8]. Hemodynamic support or even heart transplantation may be an option if all methods have failed. Unfortunately, most patients are not suitable candidates for the latter because of their age or comorbidity.

Case presentation

A male patient with a past medical history of acute myocardial infarction status post coronary stenting, ischemic cardiomyopathy with reduced ejection fraction status post-ICD placement, and dyslipidemia initially presented to our hospital with dizziness, presyncope and two episodes of ICD firing. During his initial hospital course stay on the medical floor, he had six episodes of sustained ventricular tachycardia over a period of 2 hours that required immediate termination from the ICD.

Blood work showed troponin of 0.04 ng/dL that was stable on follow-up, serum potassium of 4.5 mmol/L, and magnesium of 2.0 mg/dL. The rest of his blood work was unremarkable.

Initial electrocardiogram (EKG) on admission showed a paced rhythm with frequent premature ventricular contractions (PVCs) (Figure 1). During his hospital stay, he had multiple episodes of ventricular tachycardia that was terminated with ICD firing (Figures 2-3). He was transferred emergently to the ICU, initially received loading amiodarone bolus of 150 mg over 30 minutes intravenously followed by amiodarone drip but then he developed multiple PVCs and received three ICD shocks within 6 minutes. A bolus of IV lidocaine 80 mg was given and the patient was started on lidocaine intravenous drip. Another sustained ventricular tachycardia episode followed with subsequent ICD firing and yet another 150 mg intravenous bolus of amiodaron. His blood pressure dropped to 60/30 mmHg, deeming the option to sedate the patient with propofol infusion inapplicable.

Figure 1

Electrocardiogram showing atrial sensed V-paced rhythm with premature ventricular beats

Figure 2

First episode of ventricular tachycardia requiring shock from the implantable cardioverter defibrillator (ICD) device

Figure 3

Another episode of ventricular tachycardia ending in implantable cardioverter defibrillator (ICD) shock

Emergent echocardiogram showed ejection fraction of 10%-15% with severe global hypokinesia.

Patient was started on phenylephrine as a vasopressor with slight improvement of PVCs with amiodarone and lidocaine intravenous drips. The plan was to transfer the patient to an outside facility for urgent intervention and possible ventricular tachycardia ablation followed by left ventricular assist device placement.

Discussion

ES, which has been shown to be an independent predictor of death, might indicate a more severely diseased myocardium [9]. This is clearly evident in the Antiarrhythmics Versus Implantable Defibrillators (AVID) trial, where ES incidence was much higher in patients who have received an ICD for secondary prevention than in those who had an ICD implanted for primary prevention.

In another study patients with ischemic cardiomyopathy and low left ventricular ejection fraction (LVEF) who received ICDs for primary prophylaxis had a relatively low incidence of ES [10]. Verma and colleagues studied various cases of ES and have reached the conclusion that fatality rate is much higher in ES patients than the control group of ICD patients without the ES [11].

A clear cause for the development of ES in the majority of patients, however, was not found in several studied cases. 26% of the patients observed by Credner et al. have been reported to have at least one of the triggering factors: acute heart failure, acute myocardial infarction, and/or hypokalemia [12]. ES patients were less likely to have received a revascularization procedure as per Exner et al. [13]. The SHIELD trial (Supporting Patients Undergoing HIgh-Risk PCI Using a High-Flow Percutaneous Left Ventricular Support Device) revealed a precipitating factor in only 13% of patients. A probable cause of ES (heart failure, diarrhea, hypokalemia, fever of psychological stress) was found in 65% of Bänsch et al. [14].

While ES seems to be directly related to the interplay between various elements, any predisposing factors or underlying imbalances need to be closely studied and corrected. Reduction of the elevated sympathetic tone by beta‐blockers. frequently combined with benzodiazepines is essential [15]. Treatment with IV amiodarone has also been successful in cessation of the arrythmia. Since electrolyte disturbances play an important role particularly in caes of prolonged QT interval; any imbalances of magnesium and potassium should be corrected. While certain pathophysiologies can not be reversed (e.g tissue scarring, ischemia, and increased left ventricular dimensions in progressive heart failure), every measure to manage the existing heart failure and avoiding further deterioration in the cardiac state should be taken. Amiodarone-refractory ES reponds well to cathetar ablation [16]. Last but not least, fast VT episodes can be minimalized through anti-tachycardia pacing of the ICD [17].

Conclusions

In the era of increased ICD placement both for primary and secondary prevention, there is undeniably an increased risk for ES. ES needs to be further studied taking into consideration the various comorbidities that might hinder the successful management and treatment of ICD storm. Physicians need to be made aware of the potential risk of developing ES in their patients and be well equipped to deal with it if and when it happens.