Incidence and predictors of super-response to cardiac resynchronization therapy

Manoj Kumar Rohit1, Darshan Krishnappa2

  • 1Department of Cardiology, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

Indian Heart Journal
|November 30, 2019
PubMed

Insights

Cardiac resynchronization therapy (CRT) benefits heart failure patients. Super-responders, with over 30% LVESV decrease, were identified, with dilated cardiomyopathy predicting a better response.

Area of Science:

  • Cardiology
  • Heart Failure Management
  • Medical Devices

Background:

  • Cardiac resynchronization therapy (CRT) improves outcomes in heart failure with reduced ejection fraction (HFrEF).
  • A subset of patients, termed

Purpose of the Study:

  • To determine the prevalence and clinical characteristics of CRT super-responders in an Indian and Asian population.
  • To identify predictors of super-response to CRT in HFrEF patients.

Main Methods:

  • Retrospective analysis of 58 patients undergoing CRT implantation.
  • Assessment of ejection fraction and LVESV changes one year post-implantation.
  • Stratification into non-responders, responders (>15% LVESV decrease), and super-responders (>30% LVESV decrease).

Main Results:

  • Super-responders constituted 27.6% of the study cohort.
  • Predictors of super-response included dilated cardiomyopathy (vs. ischemic), prior RV apical pacing, and absence of prior MI.
  • Dilated cardiomyopathy was present in 93.7% of super-responders (p=0.01).

Conclusions:

  • 27.6% of patients achieved super-response to CRT.
  • Dilated cardiomyopathy, prior RV apical pacing, and no history of MI predict super-response.
  • These findings aid in identifying Asian patients likely to benefit most from CRT.
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...
325
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,...
405
Acute Coronary Syndrome III: Diagnostic Studies01:30

Acute Coronary Syndrome III: Diagnostic Studies

Diagnosing acute coronary syndrome or ACS begins with a thorough patient history. Notable symptoms include central, crushing chest pain radiating to the left arm, neck, jaw, or back, along with shortness of breath, sweating (diaphoresis), nausea, vomiting, dizziness, and palpitations.It is crucial to note any history of cardiac illnesses and assess risk factors, including age, gender, smoking, hypertension, diabetes, hyperlipidemia, and a sedentary lifestyle.During physical examination, vital...
173
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...
402
Heart Failure II: Pathophysiology01:29

Heart Failure II: Pathophysiology

Systolic Heart Failure and Compensatory MechanismsSystolic heart failure (also termed HFrEF, Heart Failure with Reduced Ejection Fraction) is the most prevalent type of heart filure. It results in a decreased volume of blood being pumped from the ventricle. The aortic arch and carotid sinuses have baroreceptors that detect reduced blood pressure, triggering the sympathetic nervous system (SNS) to release epinephrine and norepinephrine. Initially, this response aims to boost heart rate and...
624
Heart Failure IV: Classification and Diagnostic Evaluation01:30

Heart Failure IV: Classification and Diagnostic Evaluation

Heart failure can be classified in various ways, with the most common classifications based on physical activity limitations, disease progression, severity, and treatment strategies.The Functional Classification of Heart Failure divides patients into four categories based on physical activity limitation due to symptom burden.Class I: Patients in this class have cardiac disease but no physical activity limitations. Ordinary activities like walking, climbing stairs, or routine tasks do not cause...
261