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Published on: February 28, 2012
Implantable cardioverter-defibrillator in patients with inherited arrhythmia syndromes: A systematic review
Paulo Medeiros1, Maria Santos2, Carina Arantes1
1Department of Cardiology, Braga Hospital, Rua das comunidades Lusíadas 133, Braga 4710-243, Portugal.
Insights
Implantable cardioverter-defibrillator (ICD) therapy for inherited arrhythmia syndromes has a 20% rate of inappropriate therapies and 22% complication rate. Individualized decisions are crucial, considering patient risk and potential ICD complications.
Area of Science:
- Cardiology
- Electrophysiology
- Medical Devices
Background:
- Implantable cardioverter-defibrillator (ICD) therapy is recognized for its benefit in inherited arrhythmia syndromes.
- However, ICD implantation carries risks, including inappropriate therapies and device-related complications.
Approach:
- A systematic review analyzed 36 studies with 2750 patients diagnosed with inherited arrhythmia syndromes.
- Data on appropriate and inappropriate ICD therapies and complications were extracted from PubMed and Embase.
- Follow-up averaged 69 months, assessing outcomes in Brugada Syndrome, CPVT, ERS, LQTS, and SQTS.
Key Points:
- Appropriate ICD therapies occurred in 21% of patients, while inappropriate therapies affected 20%.
- Overall ICD-related complications were observed in 22% of patients, with lead malfunction (46%) and infections (13%) being most common.
- Recent publications indicate a trend toward lower rates of inappropriate therapies.
Conclusions:
- ICD-related complications are significant, particularly in younger individuals with longer exposure times.
- Subcutaneous ICD (S-ICD) presents a viable alternative to transvenous ICD for preventing sudden cardiac death.
- Individualized patient assessment, considering risk and complication potential, is essential for optimal ICD implantation decisions.
Background:
The potential benefit of implantable cardioverter-defibrillator (ICD) therapy in individuals with inherited arrhythmia syndromes is well known. However, it is not deprived of morbidity, in the form of inappropriate therapies and other ICD-related complications.
Objective:
The aim of this systematic review is to estimate the rate of appropriate and inappropriate therapy, as well as other ICD-related complications, in individuals with inherited arrhythmia syndromes.
Methods:
A systematic review was performed, regarding appropriate and inappropriate therapy, and other ICD-related complications, in individuals with inherited arrhythmia syndromes (Brugada Syndrome, Catecholaminergic Polymorphic Ventricular Tachycardia, Early Repolarization Syndrome, Long QT Syndrome and Short QT syndrome). Studies were identified by searching published papers in PubMed and Embase up to August 23rd, 2022.
Results:
From data gathered of 36 studies, with a total of 2750 individuals, during a mean follow-up time of 69 months, appropriate therapies occurred in 21% of the individuals and inappropriate therapies in 20% of the individuals. Concerning the other ICD-related complications, 456 complications were observed, amongst 2084 individuals (22%), with the most frequent being lead malfunction (46%), followed by infectious complications (13%).
Conclusions:
ICD-related complications are not uncommon, especially when one considers the exposure time of young individuals. The incidence of inappropriate therapies was 20%, although lower rates were reported in recent publications. S-ICD is an effective alternative to transvenous ICD for sudden death prevention. The decision to implant an ICD should be individualized, taking into account the risk profile of each patient, as well as the possibility of complications.
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