Adult congenital heart diseases (ACHD), in addition to complex heart defect diagnosed in childhood, also include very simple singular heat defects that are diagnosed only in adulthood due to their minor hemodynamic influence and severity. The indicators of simple ACHD on the left side of the heart and the aorta are signs the left ventricle (LV) has been remodeled by volume, pathological morphology of the valve (most commonly bicuspid aortic valve (BAV) disease and myxomatous mitral valve disease), and coarctation of the aorta. Volume load of the LV due to increased inflow into the left side of the heart leads to eccentric hypertrophy of the LV (normal wall thickness, increased volume, and ball-like shape) proportionate to the severity of the hemodynamic defect – the greater the regurgitation or shunt volume, the greater the dilation of the heart. Dilatation of the ascending aorta is also common in BAV. Volume load on the LV causes concentric hypertrophy (low systolic and diastolic volume, thickened walls). The most common natural causes of volume load on the LV are: congenital aortic stenosis, subaortic stenosis (isolated subaortic fibrous ring and subaortic membrane), coarctation of the aorta (more often associated with BAV), and conditions after previous surgical procedures. Other than the size of the cavities and the thickness of the walls and the left and right heart, the dynamic relationship of pressure changes during the cardiac cycle is important as well. When this relationship is disrupted, the ventricular or inter-atrial septum is displaced towards the area of lower pressure. Pressure load of the right ventricle (RV) causes the septum to be displaced towards the left in the systole and create a so-called D-shaped left ventricle. Volume load of the RV causes the septum to be displaced to the left in the diastole, causing a so-called D-shaped left ventricle in the diastole. In conclusion, we can group the echocardiographic indicators of simple and less severe ACHD into 5 basic categories: 1) size and morphology of the LV; 2) size of the right atrium, position of the inter-atrial septum; 3) size and morphology of the RV; 4) pulmonary hypertension; 5) flow pressure gradient across the aortic and pulmonary valve (AV/LVOT and PV/RVOT). Finding any of these indicators (with or without accompanying cardiologic signs and symptoms) should raise suspicion of the existence of ACHD, which should then be established or eliminated from the differential diagnosis.
Adult congenital heart diseases (ACHD) represent a special clinical problem in cardiology that is typically seen as including complex morphological and multiple functional defects, which are fully or partially operable in childhood. (
A female patient presented with shortness of breath during exertion a year before admission, in class I of the New York Heart Association (NYHA) Functional Classification. Medical documentation showed that a systolic murmur over the base of the heart had been found at an earlier point, but not mentioned again. Since her issues kept progressing, repeated examinations were performed (dynamic electrocardiogram, exercise stress test, and transthoracic echocardiography in two laboratories, as well as a pulmonology exam) but did not identify the cause of the dyspnea. Repeating the echocardiographic imaging established moderate dilation of the right atrium and mild dilation of the right ventricle with signs of volume hemodynamic load. While actively searching for the volume load of the right side of the heart, broad communication was found at the level of the inter-atrial septum (
Broad communication at the level of the inter-atrial septum (arrow) – atrial septal opening in an apical 4 chamber view (L). A significant left-to-right shunt at the atrial level in color Doppler imaging, with small turbulence at the opening.
This example illustrates several important principles in the clinical assessment and diagnosis of simple ACHD.
Examining patient complaints in detail and a clinical examination focusing on auscultation of the heart should be integral and primary elements of echocardiography examinations. If we fail to find the most important issues and cardiac signs during the first contact with the patient, we can be led astray into long and ineffective diagnostic processing. After patient history and physical examination, a tentative diagnosis or clinical question should be put forward, i.e. whether a heart defect is suspected in the adult patient.
Echocardiography is the primary imaging method used in diagnostic procedures to answer the suspicions and clinical questions we are dealing with.
Clinical echocardiography will be fit for purpose if we are guided by the following basic principles.
Contrasting with the complexities of echocardiography is the so called FOCUS (focused cardiac ultrasound) examination. It is used as a simple, surface look at the heart for emergency services. It is an orientation examination used to eliminate heart disease as a cause of the emergency. The examination gives a clear yes/no answer to several questions (e.g. systolic dysfunction – yes/no; pericardial effusion – yes/no; valvular defect – yes/no). Simple, palm-sized devices with low imagining power are used. These examinations are very useful in patients with known ACHD that present to emergency service with cardiac issues. (
ACHD indicators in the left heart and the aorta are signs of volume and pressure remodeling of the left ventricle (LV), the pathologic morphology of the valve (usually a bicuspid aortic valve and myxomatous mitral valve), and coarctation of the aorta. If isolated, dilation of the left atrium (LA) is usually not specific to ACHD.
Increased inflow to the left heart leads to eccentric hypertrophy of the LV (normal wall thickness, increase volume, ball-shaped) in proportion to the severity of the hemodynamic defect – greater regurgitation volume or a larger shunt leads to more dilation of the ventricle. In milder and simpler ACHD that can lead to volume load, the systolic and diastolic functions of the LV stay undamaged for a long time, and patients have very few issues. Thus it is important to assess the hemodynamic load and function during echocardiographic examination and monitoring, and make timely treatment decisions to avoid missing opportunities for full myocardial remodelling. (
Aortic regurgitation (congenital morphologic pathology of the aortic valve)
Mitral regurgitation (myxomatous mitral valve disease, unrecognized atrioventricular channel)
Ductus Botalli (the connection between the descending aorta and the left pulmonary artery/pulmonary trunk when a small to medium shunt creates load to LV and LA).
Mitral valve prolapse with regurgitation is easy to diagnose and is rarely a diagnostic problem. However, a bicuspid valve must be actively searched for if it is causing volume load and aortic regurgitation. Special care should be taken to look for signs of ductus Botalli (the unexplained dilation of the LV with normal function and systolic-diastolic murmur). Parasternal transverse section over the base of the heart should be used in checking for the turbulent flow of the systolic-to-diastolic shunt in the pulmonary truncus or its branching. This is established by continuous wave Doppler imaging with ceiling velocities in the systole and lower velocities in the diastole (which is characteristic of smaller connections that do not lead to pulmonary hypertension). (
Apical views of the several planes are needed to establish the presence of three leaflets, but also the way they open. Often only the shape of the open leaflets confirms the suspected bicuspid aortic valve (BAV). Namely, an open bicuspid valve makes an ellipsoid opening directed longitudinally, with two points of origin from the commissures (
Tricuspid aortic valve open during systole – triangular opening (L), bicuspid aortic valve open during systole – ellipsoid opening (R). Cross section at the base of the heart using the parasternal view.
Special attention should be given to discovering possible dilation of the ascending aorta and its monitoring in follow-up. The ascending aorta is measured with the aortic arch long axis (LAX) view, in which the axis of measurement must be perpendicular to both walls so as to avoid overestimated measurements due to the diagonal cross section. It should also be noted that the direction of the ascending aorta is in some cases not parallel to the image and the measurements can be incorrect. They should thus be verified using at least two views (using short axis and jugular views in addition to LAX). If there are no significant dilation and hemodynamic defects, follow-up every 2-3 years is sufficient. (
A pressure-loaded LV undergoes concentric hypertrophy remodeling (low volume in the systole and diastole, thickened walls).
The most common congenital causes of pressure load to the LV that should be suspected are:
Congenital aortic stenosis (most commonly BAV) (see above)
Subaortic stenosis (an isolated subaortic fibrous ring, subaortic membrane)
Coarctation of the aorta (often associated with BAV)
The result of previous surgical procedures
Subaortic stenosis should be suspected when the turbulent systolic flow is below the aortic valve. This is demonstrated by high velocities in the systole, measured in the apical view of five chambers by continuous Doppler in the left ventricular outflow tract (LVOT). When assessing the severity of the stenosis, we must also take into consideration the assessment of the aortic valve, since multiple stenoses are possible. (
Coarctation of the aorta diagnosed only in adulthood is usually a less severe stenosis of the descending aorta or has significant constriction but abundant collateral circulation. Coarctation should be suspected in patients with arterial hypertension and signs of poor peripheral perfusion and volume load to the LV. Other manifestations can be the dissection of the aorta, endocarditis, and hemorrhagic stroke. Constriction of the descending aorta most commonly is seen at the joint of the arterial ductus (below the subclavian artery) and includes various forms of constriction (hypoplastic descending part of the arch or pre-, para-, and postductal constriction). It can be seen on the suprasternal, i.e. jugular view, which shows the morphological location and type of constriction as well as the turbulent flow. (
When examining a patient suspected or being screened for simple ACHD, the right heart should receive special attention. Indicators of pressure or volume load (e.g. dilated cavity of the RA or RV, RV hypertrophy, etc.) indicate a defect that should be examined further.
In addition to cavity size and wall thickness in the left and right heart, the dynamic relationship of the pressure differential during the cardiac cycle is important as well. When it is disturbed, the ventricular or interatrial septum is displaced towards the cavity with the lower pressure. (
Pressure load to the right heart. Concentric hypertrophy of the right ventricle (L), systolic flattening of the interventricular septum, D– systolic shape of the left ventricle (R).
Hypertrophy of the right ventricle. Wall thickness measurement in the right ventricle at the level of the chords of the tricuspid valve, in subcostal view in the diastole. Wall thickness >0.5mm RA = right atrium; RV = right ventricle
Common causes of pressure load to the right heart in ACHD cases include:
Pulmonary stenosis (subvalvular, valvular, and supravalvular) (including stenosis of prosthetics and implants)
Obstruction of the outflow tract of the right ventricle (RVOT) (e.g. after tetralogy of Fallot (TOF) repair)
Atrial switch procedure for the transposition of the great arteries (TGA)
Congenitally corrected transposition of the great arteries (ccTGA)
Peripheral stenosis of the pulmonary artery
Volume load to the right ventricle with diastolic flattening of the interventricular septum; D-shape in the diastole (L); septum is normalized in the systole (R).
In cases of significant dilation of the RV and RA, the tricuspid ring can expand with consequent functional tricuspid regurgitation. The velocity of the regurgitation flow and the pressure differentials are low, PAP≤40 mmHg.
The most common causes of volume load to the RV in adult patients with no previously diagnosed ACHD can be:
Anomalous pulmonary venous return
Sinus venosus (an opening at the superior or inferior vena cava)
Atrial septal defect (ASD)
Pulmonary regurgitation
Primary tricuspid regurgitation (all forms of Ebstein’s anomaly)
The most common causes of isolated dilation of the right atrium are found in anomalous pulmonary venous, small ASD, and congenital tricuspid valve disease. (
In conclusion, we can say that echocardiographic indicators for simple and less complex ACHD can be divided into five basic categories:
LV size and morphology
Size of the right atrium, position of the interatrial septum
RV size and morphology
Pulmonary hypertension
AV/LVOT and PV/RVOT pressure gradients
The presence of any of the above indicators with or without cardiologic symptoms or signs should make us suspect ACHD, which should then be established or eliminated.