Coronary anomalies in Pakistani children with tetralogy of Fallot

Ijaz Hussain1, Najma Patel, Abdul Ghaffar

  • 1Department of Paediatric Cardiology, The National Institute of Cardiovascular Diseases, Karachi. ijazpaeds@yahoo.com

Insights

Coronary artery anomalies in Tetralogy of Fallot (TOF) were found in 8.4% of Pakistani children. The most common anomaly was a single origin coronary artery, impacting surgical planning for these congenital heart defects.

Area of Science:

  • Pediatric Cardiology
  • Congenital Heart Disease
  • Cardiac Imaging

Background:

  • Tetralogy of Fallot (TOF) is a complex congenital heart defect.
  • Coronary artery anomalies can affect surgical outcomes in TOF patients.
  • Understanding local prevalence of these anomalies is crucial for surgical planning.

Purpose of the Study:

  • To determine the frequency and types of coronary artery anomalies in Pakistani children diagnosed with Tetralogy of Fallot.
  • To assess the diagnostic utility of angiography in identifying these anomalies.

Main Methods:

  • A case series study was conducted at the National Institute of Cardiovascular Diseases, Karachi, Pakistan.
  • Eighty-three children under 15 with echocardiographic diagnosis of TOF underwent pre-operative cardiac catheterization and angiography.
  • Coronary arteries were visualized using nonselective aortic root angiograms.

Main Results:

  • Out of 83 patients, 8.4% exhibited coronary artery anomalies.
  • The most frequent anomaly was a single origin coronary artery (57.14% of anomalous cases).
  • Anomalous origin of the left anterior descending artery from the right coronary artery was observed in 42.86% of anomalous cases.

Conclusions:

  • Coronary artery anomalies are present in a notable percentage of Pakistani children with Tetralogy of Fallot.
  • Single origin coronary artery is the predominant anomaly in this cohort.
  • Angiographic evaluation is essential for identifying coronary variations in TOF patients prior to surgical intervention.
Abstract

Related Concept Videos

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...
Imaging Studies for Cardiovascular System V: CT01:28

Imaging Studies for Cardiovascular System V: CT

Cardiac computed tomography (CT) scanning is an advanced cardiac imaging technique that utilizes CT technology, with or without intravenous (IV) contrast, to produce accurate cross-sectional virtual slices of specific areas of the heart, coronary circulation, and major blood vessels such as the aorta, pulmonary veins, and arteries. The computer processes these slices to generate three-dimensional images. Multidetector CT (MDCT) is a rapid form of CT scanning that captures multiple slices...
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...
Aneurysm I: Introduction01:30

Aneurysm I: Introduction

An aortic aneurysm is a localized outpouching or dilation at a weak point in the artery wall. It may involve different parts of the aorta, such as the abdominal aorta, aortic arch, or thoracic aorta.Etiological factorsSeveral disorders are associated with aortic aneurysms.Congenital causes, such as primary connective tissue disorders like Marfan syndrome, impact the integrity and strength of connective tissues, notably affecting the aorta. Marfan syndrome is a genetic disorder that specifically...
Mitral Stenosis II: Clinical features and Diagnostic Tests01:23

Mitral Stenosis II: Clinical features and Diagnostic Tests

Mitral stenosis is a heart condition in which the mitral valve, which allows blood to flow from the left atrium to the left ventricle, becomes narrowed or stenotic. This narrowing hinders blood flow and leads to clinical symptoms requiring specific medical evaluations and management strategies. The following overview outlines the clinical symptoms, assessments, diagnostic findings, prevention methods, and treatments for mitral stenosis.Clinical ManifestationsDyspnea (shortness of breath): This...
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...