Procedural Volume and Outcomes After Septal Reduction Therapies in Hypertrophic Obstructive Cardiomyopathy

Nirav Patel1, Naman S Shetty2,3, Mokshad Gaonkar1

  • 1Division of Cardiovascular Disease University of Alabama at Birmingham Birmingham AL.

Insights

Lower volume septal reduction therapies for hypertrophic cardiomyopathy are linked to worse patient outcomes. High-volume centers and experienced operators are crucial for better results in septal myectomy and alcohol septal ablation.

Area of Science:

  • Cardiology
  • Interventional Cardiology
  • Health Services Research

Background:

  • Septal reduction therapies, including septal myectomy and alcohol septal ablation (ASA), treat symptomatic obstructive hypertrophic cardiomyopathy.
  • Operator and hospital procedural volume may impact patient outcomes, but current data are limited.

Purpose of the Study:

  • To investigate the association between operator and hospital volume and outcomes for septal reduction therapies.
  • To analyze 30-day mortality and 90-day readmission rates based on procedural volume.

Main Methods:

  • Retrospective cohort study using the Vizient Clinical Data Base (2016-2022).
  • Identified patients undergoing septal myectomy or ASA using ICD-10-CM codes.
  • Stratified patients into low-, medium-, and high-volume groups by operator and hospital annual volume.
  • Analyzed 30-day in-hospital mortality and 90-day readmission using multivariable logistic and Cox models.

Main Results:

  • Low-volume operators for septal myectomy showed higher 30-day mortality and 90-day readmission risk.
  • Medium-volume operators and hospitals for septal myectomy had increased 30-day mortality.
  • Low-volume hospitals for septal myectomy had a greater risk of 90-day readmission.
  • Low- and medium-volume operators for ASA had increased 30-day mortality; hospital volume did not significantly impact ASA outcomes.

Conclusions:

  • Lower operator and hospital volumes are associated with adverse outcomes in septal reduction therapies.
  • Referral of hypertrophic cardiomyopathy patients to high-volume centers with experienced operators is recommended for improved outcomes.
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...
Mitral Stenosis I: Introduction01:22

Mitral Stenosis I: Introduction

Mitral Valve Stenosis (MVS) is a heart condition where the mitral valve narrows, impeding blood circulation from the left atrium to the left ventricle. The etiology and pathophysiology of this condition are multifaceted, leading to a cascade of cardiovascular complications.Causes of Mitral Valve StenosisRheumatic Heart Disease: It is the main cause of mitral valve stenosis, particularly in developing nations. This condition arises from rheumatic fever, an inflammatory illness resulting from...
2
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...
1
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,...
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.
1