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Implantation of Total Artificial Heart in Congenital Heart Disease
Published on: July 18, 2014
[The implantable cardioverter-defibrillator and hypertrophic cardiomyopathy. Experience at three centers]
Francisco Marín1, Juan R Gimeno, Eduardo Payá
1Servicio de Cardiología, Hospital General de Alicante, Pintor Baeza s/n, 03002 Alicante, Spain. fcomarino@hotmail.com
Insights
Implantable cardioverter-defibrillators (ICDs) show variable use in hypertrophic cardiomyopathy (HCM) patients in Spain. Appropriate ICD therapy is common for secondary prevention, particularly in those with prior ventricular arrhythmias.
Area of Science:
- Cardiology
- Electrophysiology
- Genetics
Background:
- Implantable cardioverter-defibrillators (ICDs) are recommended for high-risk hypertrophic cardiomyopathy (HCM) patients.
- However, there is no consensus on their general use, and data from Spain is limited.
Purpose of the Study:
- To describe HCM patients receiving ICDs in Spain.
- To analyze implantation indications and follow-up outcomes.
Main Methods:
- Retrospective evaluation of 726 HCM patients across three Spanish hospitals.
- Analysis of risk factors for sudden death and ICD therapy appropriateness during follow-up.
Main Results:
- 45 (6.2%) patients received ICDs; implantation rates varied significantly between centers.
- Primary prevention was the indication in 27 patients, secondary in 18.
- Appropriate ICD therapy occurred in 22.0% of patients during a median 32-month follow-up, with higher rates for secondary prevention (11.1% annually) vs. primary (1.6% annually). History of sustained ventricular tachycardia/fibrillation predicted appropriate therapy.
Conclusions:
- ICD implantation rates in Spanish HCM patients are highly variable, likely due to differing selection criteria.
- ICD therapy is frequently appropriate for secondary prevention in HCM, especially in patients with prior ventricular arrhythmias.
Introduction And Objectives:
Although implantable cardioverter-defibrillators (ICDs) are recommended for high-risk patients with hypertrophic cardiomyopathy (HCM), there is no agreement on their general use. Moreover, little information is available on ICD use in this setting in Spain. Our aims were to describe the characteristics of HCM patients who received ICDs at three hospitals in Spain, and to study indications for device implantation and the results of follow-up in device users.
Methods:
We evaluated risk factors for sudden death in HCM patients with ICDs, including family history of sudden death, recurrent syncope, maximum wall thickness > or =30 mm, left ventricular outflow pressure gradient >30 mmHg, abnormal blood pressure response to exercise, and nonsustained ventricular tachycardia. During regular follow-up, appropriate and inappropriate administration of ICD therapy was recorded.
Results:
Of 726 HCM patients, 45 (6.2%) had an ICD (mean age 43 [20] years). The proportion of patients with ICDs at the three centers studied was highly variable despite patients' clinical characteristics being similar. The indication for implantation was primary prevention in 27 patients and secondary prevention in 18. During follow-up (median 32 months), ICD therapy was administered appropriately in 10 (22.0%) patients (in nine, as secondary prevention and, in one, as primary prevention). The annual appropriate ICD therapy rate was 11.1% for secondary prevention and 1.6% for primary prevention. Two patients received an ICD to treat ventricular fibrillation and eight, to treat sustained ventricular tachycardia. The only significant predictor of appropriate ICD therapy was a history of sustained ventricular tachycardia or ventricular fibrillation (hazard ratio =13.3, P=.014).
Conclusions:
The percentage of HCM patients undergoing ICD implantation at Spanish hospitals was highly variable, possibly due to different selection criteria. When used as secondary prevention, ICD therapy was administered appropriately in a high proportion of cases (50% in 3 years).
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