Atrial Antitachycardia Pacing in Complex Congenital Heart Disease: A Case Series

Collin C Kramer1, Jennifer R Maldonado2, Mark D Olson2

  • 1University of Iowa Carver College of Medicine, Iowa City, IA, USA.

Insights

Atrial antitachycardia pacing (ATP) effectively treats tachycardia in congenital heart disease (CHD) patients. However, success rates vary by individual anatomy and compliance, with challenges in complex cases.

Area of Science:

  • Cardiology
  • Electrophysiology
  • Congenital Heart Disease

Background:

  • Intra-atrial reentrant tachycardia (IART) is a frequent complication in congenital heart disease (CHD) patients, increasing morbidity and mortality.
  • Atrial antitachycardia pacing (ATP) via atrial antitachycardia devices (ATDs) is a treatment for IART, but data on its efficacy in CHD is limited.
  • Comparisons of ATP effects across different CHD subtypes are lacking.

Observation:

  • This study reviewed three complex CHD patients with ATDs: systemic left ventricle, systemic right ventricle, and single ventricle.
  • Data included ATP success rates, medications, DC cardioversions, and ATD-related complications.
  • ATP success rates were 73% (systemic left ventricle), 96% (systemic right ventricle), and 97% (single ventricle).

Findings:

  • Patients with biventricular physiology (systemic left and right ventricles) reduced or eliminated the need for DC cardioversions post-ATD implantation.
  • The single-ventricle patient required DC cardioversions due to noncompliance and IART episodes with 1:1 conduction or low rates.
  • ATP efficacy in CHD varies based on arrhythmia substrate, cardiac anatomy, and patient compliance.

Implications:

  • ATP is a viable treatment option for IART across diverse CHD anatomies.
  • Individualized patient management and monitoring are crucial for optimizing ATP outcomes in CHD.
  • Further research is needed to address IART detection challenges in highly complex CHD cases.

Related Concept Videos

Dysrhythmias II: Classification of Tachyarrhythmias01:28

Dysrhythmias II: Classification of Tachyarrhythmias

Tachyarrhythmias are a type of dysrhythmia where the heart rate exceeds 100 beats per minute. Here are some common types of tachyarrhythmias:Sinus TachycardiaSinus tachycardia originates from increased impulses from the sinus node, leading to an elevated heart rate. It is often triggered by stress, fever, or exercise.Patients may experience palpitations, a sensation of a racing heart, dizziness, and chest discomfort.Causes and Risk Factors: Common causes include physical exertion, emotional...
378
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...
216
Dysrhythmias VI: Management of Dysrhythmias01:25

Dysrhythmias VI: Management of Dysrhythmias

Dysrhythmia management involves a multifaceted approach, incorporating pharmacological treatments, medical procedures, surgical interventions, lifestyle modifications, and patient education.Pharmacological ManagementAntiarrhythmic Drugs:Class I (Sodium Channel Blockers): This class includes quinidine and procainamide, which reduce the speed of impulse conduction in the heart, stabilize the cardiac membrane, and control arrhythmias. Quinidine and procainamide are Class IA agents that prolong the...
305
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,...
329
Dysrhythmias IV: Characteristics of Bradyarrhythmias01:18

Dysrhythmias IV: Characteristics of Bradyarrhythmias

Bradyarrhythmias are cardiac rhythm disorders characterized by a slower-than-normal heart rate, typically defined as fewer than 60 beats per minute. Some of which are discussed here:Sinus BradycardiaSinus bradycardia presents a heart rate lower than 60 beats per minute, with a regular rhythm originating from the SA node. The ECG typically shows normal P waves preceding each QRS complex, a normal PR interval (0.12 to 0.20 seconds), and a normal QRS duration (0.06 to 0.10 seconds).First-Degree AV...
376
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...
277