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Approach to a patient with
congenital heart disease
Guide : Dr.Vijay G.Somannavar
Introduction
• Congenital heart diseases or Congenital
heart anomalies are defects in the
structure of the heart and great vessels
which are present at birth.
• CHD are the leading cause of birth defect-
related deaths.
D E F I N I T I O N
When to suspect CHD
•-Cyanosis
-Respiratory distress
-Poor peripheral perfusion
-Decreased pulsations
-Difference in pulses (arm
vs. leg)
-Single 2nd heart sound
-Abnormally loud 2nd heart
sound
-Prominent heart murmur
-Hyperactive precordium
F I N D I N G S T H A T S H O U L D A L E R T O N E T O T H E P O S S I B I L I T Y O F C H D
Incidence
• 1 in 10 stillborn infants have a cardiac anomalies.
• 8 out of 1000 live born children have significant cardiac
malformations.
• Every year 1,80,000 children are born with heart defects in India.
Lesions % of all Lesions
- Ventricular septal defect 25-30
- Atrial septal defect (Secundum) 10
- Patent ductus arteriosus 10
- Coarctation of aorta 7
- Tetralogy of Fallot 6
- Pulmonary Valve Stenosis 5-7
- Aortic Valve Stenosis 4-7
- Transposition of great arteries 4
- 0thers 20
Classification
CHD
Acyanotic Cyanotic
Left-to-right
shunts
Outflow
obstruction
- Ventricular Septal
Defect (VSD)
- Patent Ductus
Arteriosus (PDA)
- Atrial Septal Defect
(ASD
- Pulmonary
Stenosis
- Aortic Stenosis
-Coarctation of
aorta
• Teralogy of fallot
• Tricuspid atresia
• Transposition of
great vessels
• Truncus arteriosus
• Total anomalous
pulmonary venous
return (TAPVR)
• Ebstein’s anomaly
Etiology
Maternal
disorders
• Rubella infection
(30-35%)
• PDA, pulmonary
stenosis
• DM (2%)
Maternal drugs
• Fetal alcohol
syndrome (25%)
• ASD, VSD,
tetralogy of
Fallot
• Anti seizure drugs
• Thalidomide
• isotretinoin
Chromosomal
abnormality
• Down’s syndrome
(30%)
• Atrioventricular
septal defect, VSD
• Turner’s syndrome
(15%)
• Aortic valve stenosis,
coarctation of the aorta
• Edward’s and
Patau’s syndrome
(60-80%)
Left to right shunts
• L to R shunts are characterised by RV
enlargement and RV failure.
• Usually present with recurrent chest
infections.
• They are not typically cyanotic.
Ventricular Septal Defect (VSD)
• Most common congenital cardiac lesion.
• Accounts for 25% of all CHDs.
• Defect may be –
perimembranous(adjacent to tricuspid
valve) or muscular(surrounded by muscle)
• Spontaneous closure occurs by 10 years.
Peri membranous
Muscular
Clinical features
• Children with small defects will remain asymptomatic .
• Infants with moderate to large defects will become
symptomatic within the first few weeks of life.
.
S I G N S A N D S Y M P T O M S V A R Y W I T H T H E S I Z E O F T H E D E F E C T
Small VSDs
– Symptoms
• Asymptomatic
– Physical signs
• Thrills at lower sternal edge
• Loud pansystolic murmur at lower left sternal edge
• Quiet second heart sound (P2)
Large VSDs
– Symptoms
• Breathlessness and failure to thrive.
• Recurrent chest infections
– Physical signs
• Prominence of the left precordium
• Soft pansystolic murmur
• Mid-diastolic murmur at the apex
• Loud pulmonary second sound (P2)
Investigations
– Chest X-ray
• Cardiomegaly
• Enlarged pulmonary arteries
• Pulmonary vascular
markings
• Pulmonary oedema
– ECG
• Biventricular hypertrophy and
signs of pulmonary HTN 
right ventricular enlargement
and hypertrophy
– Echocardiography
• Demonstrates the anatomical
defect, haemodynamic
effects and severity of
pulmonary HTN.
Atrial Septal Defect(ASD)
• Seen in 10% of all CHDs
• Females > males.
• It is an abnormal opening between
the atria
• Spontaneous closure ocurrs with in
1st year of life.
Clinical features
Symptoms :
• Fatigue and SOB
• Palpitations
• Recurrent respiratory infections
Physical signs :
• Ejection Systolic murmur
• Diastolic murmur (large
shunts).
• Wide fixed split S2
• Tachypnea, tachycardia and
enlarged liver from heart failure
M O S T I N F A N T S A N D C H I L D R E N A R E A S Y M P T O M A T I C .
Diagnostic tests
- CXR – enlarged
heart,increased
pulmonary vascular
markings
- ECG- Ostium
secundum:Right axis
deviation with Right
bundle branch block.
- 2D echo – show pattern
of blood flow through the
septal opening
Patent Ductus Arteriousus
(PDA)
• PDA occurs in 6-11 % of all children with
CHD
• It is a connection between the aorta and
the pulmonary artery
• Most babies have a closed ductus
arteriosus by 72 hours after birth.
Clinical features
• Fatigue
• Sweating
• Tachypnea
• Shortness of breath
Physical examination
• Widened pulse pressure
• Collapsing/ bounding pulse
• Left infraclvicular/upper left sternal edge continuos machinery murmur
• Differential cyanosis (cyanosis of lower limb but upper limb pink)
Coarctation of aorta
• Accounts for 7 % of all CHD.
• is narrowing of the aorta at varying points
anywhere from the transverse arch to the
iliac bifurcation.
• 98% of coarctations are juxtaductal.
Clinical presentation
• In older children:
– Leg discomfort with
exercise
– Headache
– Epistaxis
• Systolic hypertension of
upper extremities.
• Ejection systolic murmur
at upper sternal edge
• Diminished lower
extremity pulses
– Radio-femoral delay:
• blood bypassing the
obstruction via collateral
vessels in the chest wall
Right to Left Shunts
• R  L shunts cause hypoxia and central
cyanosis.
• Blood is shunted from the R to the L side
of the heart w/o passing through the
lungs for oxygenation.
• Unoxygenated blood circulates in
arteries  cyanosis
Tetrology of fallot
Components
• Ventricular septal defect
• Pulmonary stenosis
• Overriding of aorta
• RVH
M O S T C O M M O N C Y A N O T I C H E A R T D I S E A S E
Clinical features
– Cyanosis
– Shortness of breath
– Rapid breathing
– Loss of consciousness
– Clubbing of fingers and toes
– Restless and agitated
– Poor weight gain
S Y M P T O M A T I C A N Y T I M E A F T E R B I R T H
Posture
– It is a compensatory
mechanism
– Squatting increases the
peripheral vascular
resistance, diminishes the
right-to-left shunt and
increases pulmonary
blood flow.
S I T T I N G P O S T U R E O R S Q U A T T I N G
• Chest X-ray
– Normal sized, boot
shaped heart
– Concavity of Left heart
border
– Oligaemic lung fields
• ECG
– At birth normal
– Older: Right axis
deviation and RVH
• Echocardiography
– Degree of stenosis
– Coronary anomalies(5%
in TOF)
Thank You

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Approach to patient with congenital heart disease

  • 1. Approach to a patient with congenital heart disease Guide : Dr.Vijay G.Somannavar
  • 2. Introduction • Congenital heart diseases or Congenital heart anomalies are defects in the structure of the heart and great vessels which are present at birth. • CHD are the leading cause of birth defect- related deaths. D E F I N I T I O N
  • 3. When to suspect CHD •-Cyanosis -Respiratory distress -Poor peripheral perfusion -Decreased pulsations -Difference in pulses (arm vs. leg) -Single 2nd heart sound -Abnormally loud 2nd heart sound -Prominent heart murmur -Hyperactive precordium F I N D I N G S T H A T S H O U L D A L E R T O N E T O T H E P O S S I B I L I T Y O F C H D
  • 4. Incidence • 1 in 10 stillborn infants have a cardiac anomalies. • 8 out of 1000 live born children have significant cardiac malformations. • Every year 1,80,000 children are born with heart defects in India.
  • 5. Lesions % of all Lesions - Ventricular septal defect 25-30 - Atrial septal defect (Secundum) 10 - Patent ductus arteriosus 10 - Coarctation of aorta 7 - Tetralogy of Fallot 6 - Pulmonary Valve Stenosis 5-7 - Aortic Valve Stenosis 4-7 - Transposition of great arteries 4 - 0thers 20
  • 6. Classification CHD Acyanotic Cyanotic Left-to-right shunts Outflow obstruction - Ventricular Septal Defect (VSD) - Patent Ductus Arteriosus (PDA) - Atrial Septal Defect (ASD - Pulmonary Stenosis - Aortic Stenosis -Coarctation of aorta • Teralogy of fallot • Tricuspid atresia • Transposition of great vessels • Truncus arteriosus • Total anomalous pulmonary venous return (TAPVR) • Ebstein’s anomaly
  • 7. Etiology Maternal disorders • Rubella infection (30-35%) • PDA, pulmonary stenosis • DM (2%) Maternal drugs • Fetal alcohol syndrome (25%) • ASD, VSD, tetralogy of Fallot • Anti seizure drugs • Thalidomide • isotretinoin Chromosomal abnormality • Down’s syndrome (30%) • Atrioventricular septal defect, VSD • Turner’s syndrome (15%) • Aortic valve stenosis, coarctation of the aorta • Edward’s and Patau’s syndrome (60-80%)
  • 8. Left to right shunts • L to R shunts are characterised by RV enlargement and RV failure. • Usually present with recurrent chest infections. • They are not typically cyanotic.
  • 9. Ventricular Septal Defect (VSD) • Most common congenital cardiac lesion. • Accounts for 25% of all CHDs. • Defect may be – perimembranous(adjacent to tricuspid valve) or muscular(surrounded by muscle) • Spontaneous closure occurs by 10 years.
  • 11. Clinical features • Children with small defects will remain asymptomatic . • Infants with moderate to large defects will become symptomatic within the first few weeks of life. . S I G N S A N D S Y M P T O M S V A R Y W I T H T H E S I Z E O F T H E D E F E C T
  • 12. Small VSDs – Symptoms • Asymptomatic – Physical signs • Thrills at lower sternal edge • Loud pansystolic murmur at lower left sternal edge • Quiet second heart sound (P2)
  • 13. Large VSDs – Symptoms • Breathlessness and failure to thrive. • Recurrent chest infections – Physical signs • Prominence of the left precordium • Soft pansystolic murmur • Mid-diastolic murmur at the apex • Loud pulmonary second sound (P2)
  • 14. Investigations – Chest X-ray • Cardiomegaly • Enlarged pulmonary arteries • Pulmonary vascular markings • Pulmonary oedema – ECG • Biventricular hypertrophy and signs of pulmonary HTN  right ventricular enlargement and hypertrophy – Echocardiography • Demonstrates the anatomical defect, haemodynamic effects and severity of pulmonary HTN.
  • 15. Atrial Septal Defect(ASD) • Seen in 10% of all CHDs • Females > males. • It is an abnormal opening between the atria • Spontaneous closure ocurrs with in 1st year of life.
  • 16. Clinical features Symptoms : • Fatigue and SOB • Palpitations • Recurrent respiratory infections Physical signs : • Ejection Systolic murmur • Diastolic murmur (large shunts). • Wide fixed split S2 • Tachypnea, tachycardia and enlarged liver from heart failure M O S T I N F A N T S A N D C H I L D R E N A R E A S Y M P T O M A T I C .
  • 17. Diagnostic tests - CXR – enlarged heart,increased pulmonary vascular markings - ECG- Ostium secundum:Right axis deviation with Right bundle branch block. - 2D echo – show pattern of blood flow through the septal opening
  • 18. Patent Ductus Arteriousus (PDA) • PDA occurs in 6-11 % of all children with CHD • It is a connection between the aorta and the pulmonary artery • Most babies have a closed ductus arteriosus by 72 hours after birth.
  • 19.
  • 20. Clinical features • Fatigue • Sweating • Tachypnea • Shortness of breath Physical examination • Widened pulse pressure • Collapsing/ bounding pulse • Left infraclvicular/upper left sternal edge continuos machinery murmur • Differential cyanosis (cyanosis of lower limb but upper limb pink)
  • 21. Coarctation of aorta • Accounts for 7 % of all CHD. • is narrowing of the aorta at varying points anywhere from the transverse arch to the iliac bifurcation. • 98% of coarctations are juxtaductal.
  • 22.
  • 23. Clinical presentation • In older children: – Leg discomfort with exercise – Headache – Epistaxis • Systolic hypertension of upper extremities. • Ejection systolic murmur at upper sternal edge • Diminished lower extremity pulses – Radio-femoral delay: • blood bypassing the obstruction via collateral vessels in the chest wall
  • 24. Right to Left Shunts • R  L shunts cause hypoxia and central cyanosis. • Blood is shunted from the R to the L side of the heart w/o passing through the lungs for oxygenation. • Unoxygenated blood circulates in arteries  cyanosis
  • 25. Tetrology of fallot Components • Ventricular septal defect • Pulmonary stenosis • Overriding of aorta • RVH M O S T C O M M O N C Y A N O T I C H E A R T D I S E A S E
  • 26. Clinical features – Cyanosis – Shortness of breath – Rapid breathing – Loss of consciousness – Clubbing of fingers and toes – Restless and agitated – Poor weight gain S Y M P T O M A T I C A N Y T I M E A F T E R B I R T H
  • 27.
  • 28. Posture – It is a compensatory mechanism – Squatting increases the peripheral vascular resistance, diminishes the right-to-left shunt and increases pulmonary blood flow. S I T T I N G P O S T U R E O R S Q U A T T I N G
  • 29. • Chest X-ray – Normal sized, boot shaped heart – Concavity of Left heart border – Oligaemic lung fields • ECG – At birth normal – Older: Right axis deviation and RVH • Echocardiography – Degree of stenosis – Coronary anomalies(5% in TOF)

Editor's Notes

  1. Perimemb 80% supracristal/infracristal
  2. Palpitatns:atrial arrhytmias;resp inf:large pulm flow