Myocardial apoptosis predicts postoperative course after aortic valve replacement in patients with severe left

Mario Gaudino1, Amedeo Anselmi, Antonio Abbate

  • 1Department of Cardiac Surgery, Catholic University of the Sacred Heart, Rome, Italy.

Insights

Myocardial apoptosis in patients undergoing aortic valve replacement (AVR) for severe aortic stenosis is linked to worse postoperative outcomes, including longer intensive care unit (ICU) stays and renal issues. Identifying these patients may improve surgical risk assessment.

Area of Science:

  • Cardiology
  • Cardiac Surgery
  • Cellular Biology

Background:

  • Myocardial apoptosis is implicated in heart failure and post-infarct remodeling.
  • Delayed aortic valve replacement in severe aortic stenosis correlates with poor outcomes.
  • The study investigates cardiomyocyte apoptosis in patients undergoing aortic valve replacement (AVR).

Purpose of the Study:

  • To evaluate the impact of cardiomyocyte apoptosis on the postoperative course after AVR for severe aortic stenosis.
  • To identify predictors of adverse outcomes in patients with severe left ventricular hypertrophy (LVH) undergoing AVR.

Main Methods:

  • Myocardial biopsies were obtained from the left ventricle of 11 patients with severe LVH during elective AVR.
  • Apoptosis rates in myocardial samples were analyzed.

Main Results:

  • The mean apoptotic rate was 10.4 +/- 3.7 per thousand.
  • Apoptotic rate correlated with NYHA class, ICU stay, renal insufficiency, and troponin T levels.
  • Apoptotic rate and LVH were independent predictors of prolonged ICU stay.
  • Apoptotic rate predicted duration of postoperative renal insufficiency.

Conclusions:

  • Myocardial apoptosis is associated with poorer postoperative outcomes in patients with severe LVH undergoing AVR.
  • Non-invasive correlates of apoptosis could identify high-risk patients.
  • Anti-apoptotic strategies may improve surgical results for AVR.
Abstract

Related Concept Videos

Cardiomyopathy VII: Pre and Post Operative Nursing Management01:28

Cardiomyopathy VII: Pre and Post Operative Nursing Management

Patients with hypertrophic cardiomyopathy (HCM) and left ventricular outflow tract (LVOT) obstruction who remain symptomatic despite optimal medical therapy may undergo a septal myectomy (Morrow procedure). This procedure involves excising a portion of the hypertrophied septum below the aortic valve using a heart-lung machine to improve blood flow through the LVOT. Effective preoperative and postoperative nursing management ensures successful patient outcomes, minimizes complications, and...
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...
Aortic Regurgitation III: Medical Management01:25

Aortic Regurgitation III: Medical Management

Aortic regurgitation (AR) is when the aortic valve does not close or seal properly, leading to backward blood circulation from the aorta into the left ventricle during diastole. Common causes of AR include rheumatic heart disease, congenital valve defects, and aortic root dilation. Managing AR requires a multifaceted approach to alleviate symptoms, preserve left ventricular function, and address the underlying cause of the regurgitation. Patients with symptomatic AR or significant left...
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...
Aortic Regurgitation II: Clinical Features and Diagnostic Tests01:22

Aortic Regurgitation II: Clinical Features and Diagnostic Tests

Aortic valve regurgitation (AR) occurs when the aortic valve fails to close properly, allowing blood to flow backward from the aorta into the left ventricle. This backflow can result in two distinct clinical presentations: acute and chronic AR, each characterized by its own set of symptoms and physical findings.Acute Aortic RegurgitationAcute AR presents with a sudden onset of severe symptoms. Patients typically experience profound dyspnea (shortness of breath), chest pain, and signs of left...
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,...