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Congenital Heart Diseases Charles University of Prague 2ndFaculty of Medicine Filip Koubek
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CHD – Epidemiology 600-700/100 000 (live newborn in CR) ~ 6-7/1000 30-40% of all CHD - Ventricular Septal Defect (VSD) - most common CHD Bicuspid Aortic Valve – 1-2% of General Population Atrial Septal Defect – Most common CHD diagnosed in adulthood No exact evidence – Complex CHD (e.g.TGA+VSD) Prevalence ~ 2800 CHD adults / 1mil. people
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Most of CHD diagnosed in newborn and early childhood (VSD, AVSD, ToF, TGA, CoA, PA, etc.) Some of them can be diagnosed in adults: ASD (only smaller), CoA, ccTGA, Ebstein disease of TV, etc. (generally less serious forms) CHD - diagnosing
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CHD – diagnosing/follow-up History Symptoms and Signs ECG, pulse oximetry Cardiopulmonary exercise testing - especially for timing of (re)intervention Holter ECG (24-hours monitor) Echocardiography Chest X-ray Cardiac CT and MRI (precise anatomy of heart and big vessels, assessment of RV volume and function, quantification of valvular regurgitation etc.) Invasive testing – catheterization – haemodynamics (shunt quantification, pulmonary pressure/resistance measurement etc.) or electrophysiology testing (assessment of arrhythmias)
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CHD – general problems Heart failure (valvular defect, shunts, volume and/or preasure overloading of ventricles, RV in systemic position) Pharmacotherapy (ACEi, BB, diuretics) CRT (Cardiac resynchronisation therapy) – biventricular stimulation in case of uneffective (dyssynchronic) contraction Heart transplantation Arrythmias and SCD (sudden cardiac death) More difficult issue than in normal heart Risk stratification, investigation, and choice of treatment are often different from those applied to the normally formed heart (drugs poorly tolerated, side effects) – EP and ablation is prefer Onset of arrhythmias may be a signal of haemodynamic decompensation SCD – especially in: ToF, TGA, ccTGA, aortic stenosis (AS), and UVHs – various risk factors - ICD
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CHD – general problems Infectious endocarditis High risk particularly in: Cyanotic CHD without surgical repair, residual defects, palliative shunts Prostetic valves Residual defects (generally) after surgical or cath. closure Patients with previous IE
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CHD – general problems Pregnancy Generally well tolerated but Extremely High risk (high mortality 30-50%): Severe pulmonary art. hypertension (Eisenmenger sy) High risk Cyanosis (esp. SpO2 <85%) Stenotic left valve disease (AS, MS) Poor EF LV (<40%) NYHA II< Aortic roof dilation (Marfan sy) Arrhythmias
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CHD – general problems Recurrence rate of CHD in offspring 2-50% Higher risk when the mother has CHD Highest recurrence risks in single gene disorders and/or chromosomal abnormalities (Marfan, Noonan, and 22q11 deletion syndromes - DiGeorge, Holt – Oram syndrome) Others defects recurrence rate 2-4% Aortic stenose 13–18% VSD 6 – 10%
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Atrial septal defect Different anatomic types: Secundum ASD (80% of ASDs; located in the region of the fossa ovalis and its surrounding) Primum ASD (15%, synonym: partial atrioventricular septal defect (AVSD), located near the crux, AV valves are typically malformed resulting in various degrees of regurgitation (esp. Mitral) Superior sinus venosus defect (5%, located near the superior vena cava (SVC) entry, associated with partial or complete connection of right pulmonary veins to SVC/right atrium (RA) Inferior sinus venosus defect (1%, located near the inferior vena cava (IVC) entry) Unroofed coronary sinus (1%, separation from the left atrium can be partially or completely missing)
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Atrial septal defect
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Atrial septal defect - echocardiography
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Atrial septal defect - pathophysiology Naturally L to R shunt (higher BP in LA) Volume overloading of RV – dilation RA+RV Arrhythmias (Atrial fibrillation, flutter) (5th decade) Increase of transpulmonary flow – reactive higher pulmonary vascular resistance severe PAH (only in 5%) and bidirectional shunt (Eisenmenger physiology) Paradoxical embolism (thrombus from lower limb veins through ASD to systemic circulation e.g. CNS)
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Atrial septal defect - diagnosing Symptoms – exertional shortness of breath, fatigue, palpitation Signs – fixed splitting of the second heart sound, systolic pulmonary flow murmur, ECG – iRBBB, right axis deviation and/or Symptoms and signs connected with paradoxical embolism
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Atrial septal defect - treatment Surgical or Percutaneous closure Only significant defects: Symptoms, Arrhythmias Dilation of RV (volume overloading sign) Significant shunt – Qp/Qs >1,5 Paradoxical embolism (Planned pregnancy) – prevention of paradoxical embolism Eisenmenger sy (severe PAH with high pulmonary vascular resistance) – contraindication of closure
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Atrial septal defect - treatment ASD secundum – (if possible catheterisation device closure is prefer)
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Atrial septal defect - treatment ASD primum – connected with cleft of anterior mitral leaflet with mitral regurgitation (mostly significant) - surgical treatment usually necessary
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Atrial septal defect - treatment ASD sinus venosus superior – connected with partial anomalous pulmonary venous connection – PAPVC (mostly right upper pulmonary vein to RA) – L-R shunt Only surgical treatment Big ASD generally operated in childhood (3-5y)
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Ventricular septal defect
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Ventricular septal defect - pathophysiology Naturally L to R shunt (much higher BP in LV) If significant defect: Volume overloading of LV – dilation Pressure overloading of RV – hypertrophy Increase of transpulmonary flow and blood pressure in AP – reactive increase pulmonary vascular resistance severe PAH and bidirectional shunt (Eisenmenger physiology) is developed early (within 1st year) (Infants are operated in 3-5months)
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Ventricular septal defect - echocardiography
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Ventricular septal defect - echocardiography
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Ventricular septal defect - treatment Insignificant (restrictive) defect (with loud systolic murmur and high pressure gradient) Conservative, only observation, IE prophylaxis Significant (unrestrictive) – (prefer) surgical closure Symptoms Signs of LV volume overloading (dilation) History of IE Significant shunt (Qp/Qs >1,5) and no severe PAH and vascular resistance Progressive Aortic regurgitation due to prolapse of aortic valve cusp (suck to defect)
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Tetralogy of Fallot non-restrictive VSD overriding aorta (but <50%) RVOTO which may be infundibular, valvular, or (usually) a combination of both, with or without supravalvular or branch PA stenosis RV hypertrophy 10% of CHD Surgical treatment – VSD closure + relief of RVOTO (with resection of the infundibulum and pulmonary valvotomy) Common complication in adulthood (after repair) : Pulmonary regurgitation, Residual RVOTO, Aortic root dilation with valve regurgitation, RV dilation and dysfunction, Residual VSD All patients should be followed-up in specialized GUCH centers
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Tetralogy of Fallot after repair
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Tetralogy of Fallot after repair
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Transposition of the Great Arteries (TGA) Counts ~ 5% of CHD Ventriculo-arterial discordance + (Atrio-ventricular concordance) 45% Complex TGA – TGA + VSD (45%), LVOTO (25%), CoA (5%) Male predominance 2:1 Simple TGA is critical CHD (incompatible with life without shunts) – repair in early newborn age 1st degree – palliative atrioseptostomy (Rashkind procedure) 2nd degree – definitive repair
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Transposition of the Great Arteries (TGA)
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Transposition of the Great Arteries (TGA) 2 types of repair: Atrial switch (Senning or Mustard procedure) Older type of repair - developed and first performed by Senning in 1957, method of first choice till the turn of the 80s and 90s Creation of atrial baffle/conduit channeling blood from the superior and inferior vena cava towards the mitral valve (LV) and blood from pulmonary veins towards tricuspid valve (RV) (anatomically) RV is in systemic position!
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Transposition of the Great Arteries (TGA)
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Transposition of the Great Arteries (TGA) 2 types of repair: Arterial switch (Jatene procedure) Newer type of repair - developed and first performed by Jatene in 1975 (in common practice since 90s) Change (reimplantation) of great arteries to corresponding ventricles, coronary arteries also reimplanted to “neoaorta” Result of this procedure – physiological circulation
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Transposition of the Great Arteries (TGA)
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Transposition of the Great Arteries (TGA) Complications after Atrial switch: RV failure (progressive dilation, dysfunction) TV regurgitation Sinus node dysfunction (symptomatic bradycardia) Tachyarrhythmias (SVT – AF, VT with risk of sudden death) Intra-atrial tunnel stenosis (systemic vein or pulmonary vein with corresponding symptoms) Progressive heart failure is the most severe complication requiring Heart Tx
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TGA after Senning procedure
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Transposition of the Great Arteries (TGA) Complications after Arterial switch: Coronary artery stenosis (after reimplantation) with LV ischemia – systolic dysfunction, ventricular arrhythmias Dilation of ascending aorta with AR Pulmonary stenosis (supravalvular and branches) Large majority of pts. after arterial switch are long term without complication
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Coarctation of Aorta (CoA) Accounts 5-8% of CHD Circumscript narrowing typically located in the area where the ductus arteriosus inserts (rare occurs ectopically ( asc., desc., abd.) Often associated with: Bicuspid aortic valve (85%), subvalvular, valvular, or supravalvular AS, mitral valve stenosis or complex congenital heart defects, Turner sy
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Coarctation of Aorta
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Coarctation of Aorta - pathophysiology Narrowing causes significant afterload on the LV, resulting in increased wall stress, compensatory LVH, LV dysfunction, and the development of arterial collaterals Fibrosis in the ascending and descending aorta, resulting in an increased stiffness of the aorta and carotid arteries Accelerated atherosclerosis in part circulation in front of stenosis with higher pressure (including coronary arteries)
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Coarctation of Aorta - diagnosing Mild forms detected in adulthood Symptoms: headache, nosebleeds, dizziness, tinnitus, shortness of breath, abdominal angina, leg claudication, exertional leg fatigue, and cold feet Sings: upper body systolic hypertension, lower body hypotension, a blood pressure gradient (20 mmHg) is significant CoA radio-femoral pulse delay suprasternal thrill, vascular murmur in the back, or continuous murmurs (due to collateral vessels). chest X-ray findings may include rib notching of the third and fourth ribs from collaterals, ectatic ascending aorta, kinking or double contouring in the descending aorta (‘figure 3’ sign), widening of the left subclavian artery
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Coarctation of Aorta - treatment Surgery (end-to-end anastomosis, resection and extended end-to-end anastomosis, prosthetic patch aortoplasty, subclavian flap aortoplasty, interposition of (tube) graft, and bypass tube (jump) grafts) – usually in native CoA in childhood and in adults if anatomy is not attractive for angioplasty X Catheterization (angioplasty with or without stent) – if anatomy convenient, more often used in reCoA after surgery
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Coarctation of Aorta – indication for intervention non-invasive pressure difference >20 mmHg between upper and lower limbs upper limb hypertension (>140/90 mmHg in adults) pathological blood pressure response during exercise significant LVH patients with ≥50% aortic narrowing relative to the aortic diameter at the diaphragm level (on cMRI, CT, or invasive angiography)
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Coarctation of Aorta - surgery
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Other rarer CHDs (for interested of you - next time) Univentricular Heart (with Fontan circulation) Pulmonary atresia (with or without VSD) Ebstein’s anomaly of tricuspid valve Eisenmenger sy (reactive severe and irreversible pulmonary hypertension) …
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Thank you for your attention!!!