Implantable cardioverter-defibrillator therapy in hypertrophic cardiomyopathy: A SIMPLE substudy

Mate Vamos1, Jeff S Healey2, Jia Wang3

  • 1University Hospital Frankfurt, Goethe University, Frankfurt, Germany.

Heart Rhythm
|November 22, 2017
PubMed

Insights

Defibrillation testing (DT) in hypertrophic cardiomyopathy (HCM) patients undergoing implantable cardioverter-defibrillator (ICD) insertion showed no significant difference in outcomes compared to other cardiomyopathies. DT did not improve shock efficacy in HCM patients.

Area of Science:

  • Cardiology
  • Electrophysiology
  • Medical Devices

Background:

  • Hypertrophic cardiomyopathy (HCM) patients face higher risks for defibrillation issues and complications with implantable cardioverter-defibrillators (ICDs).
  • Assessing the necessity and impact of defibrillation testing (DT) in these high-risk patients is crucial for optimizing ICD therapy.

Purpose of the Study:

  • To evaluate the value of defibrillation testing (DT) in patients with hypertrophic cardiomyopathy (HCM) undergoing implantable cardioverter-defibrillator (ICD) implantation.
  • To compare DT efficacy, perioperative complications, and long-term outcomes in HCM patients versus those with ischemic cardiomyopathy (ICM) or dilated cardiomyopathy (DCM).

Main Methods:

  • The study analyzed data from the SIMPLE trial, comparing HCM patients with ICM/DCM patients who underwent ICD insertion.
  • Outcomes including defibrillation thresholds, perioperative complications, and long-term mortality were assessed.
  • HCM patients were further analyzed based on randomization to DT or no DT groups.

Main Results:

  • Defibrillation safety margins were similar between HCM (88.5%) and ICM/DCM (90.5%) patients.
  • Perioperative complications were comparable across HCM with DT (1.9%), ICM/DCM with DT (6.4%), and HCM without DT (7.1%).
  • Long-term outcomes such as all-cause mortality, arrhythmic events, and shock complications did not significantly differ between HCM and ICM/DCM groups, nor between HCM patients with or without DT.

Conclusions:

  • Defibrillation testing (DT) did not demonstrate a significant benefit in improving intraoperative or clinical shock efficacy in hypertrophic cardiomyopathy (HCM) patients.
  • No significant differences were observed in intraoperative defibrillation efficacy, perioperative complications, or long-term outcomes between HCM and other cardiomyopathy groups (ICM/DCM).
Abstract

Related Concept Videos

Cardiomyopathy III: Hypertrophic Cardiomyopathy01:29

Cardiomyopathy III: Hypertrophic Cardiomyopathy

Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
540
Cardiomyopathy V: Interprofessional Care01:29

Cardiomyopathy V: Interprofessional Care

Managing cardiomyopathy involves addressing underlying or precipitating causes, treating heart failure with medications, and implementing dietary changes and a balanced exercise and rest regimen.Lifestyle ModificationsCardiomyopathy patients should adopt a low-sodium diet to reduce fluid retention and manage heart failure. A personalized exercise and rest plan helps maintain physical fitness without overstraining the heart. Avoiding alcohol and tobacco is essential to prevent further damage to...
493
Cardiomyopathy II: Dilated Cardiomyopathy01:30

Cardiomyopathy II: Dilated Cardiomyopathy

Dilated cardiomyopathy, or DCM, is a progressive myocardial disorder characterized by ventricular chamber dilation and contractile dysfunction.EtiologyVarious factors can cause DCM, including hypertension and heavy alcohol intake, which contribute to the weakening and enlargement of the heart muscle. Viral infections, such as Coxsackievirus B, adenoviruses, and influenza, can lead to DCM by causing inflammation and damage to heart tissue. Certain chemotherapeutic agents, including daunorubicin,...
608
Heart Failure VI: Adjunct Therapies01:22

Heart Failure VI: Adjunct Therapies

Additional therapies for treating patients with heart failure (HF) may include procedural interventions, supplemental oxygen, the management of sleep disorders, and nutritional therapy.Procedural InterventionsImplantable Cardioverter-Defibrillator: For patients at risk of life-threatening arrhythmias due to severe left ventricular dysfunction, an Implantable Cardioverter-Defibrillator (ICD) can detect and terminate these arrhythmias, preventing sudden cardiac death and improving survival rates.
417
Cardiomyopathy IV: Restrictive Cardiomyopathy01:29

Cardiomyopathy IV: Restrictive Cardiomyopathy

Restrictive cardiomyopathy (RCM) is a rare heart muscle disease characterized by impaired ventricular filling due to stiffened ventricular walls, leading to significant diastolic dysfunction.EtiologyRestrictive cardiomyopathy can arise from both inherited and acquired diseases, many of which are systemic. It is categorized into four main types: infiltrative, storage, non-infiltrative, and endomyocardial diseases.Infiltrative diseases, such as amyloidosis, lead to RCM by depositing amyloid...
616