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Fetal Circulation and
Approach to CHD
Dr Tushar Jagzape,
Pediatrics ,
AIIMS, Raipur
Learning objectives:
• At the end of this lecture, the learner should be able
to:
• Describe fetal circulation and changes that occur at birth.
• Highlight the salient differences between fetal and
neonatal circulation.
• Describe the classification of CHD.
• Enlist common acyanotic and cyanotic congenital heart
diseases.
• Approach to a child with suspected CHD.
• Describe the hemodynamics of Lt to Rt shunts
Fetal circulation and difference between fetal
and neonatal circulation.
• Parallel vs series circulation.
• Structures responsible for parallel circulation.
• Ductus venosus
• Foramen ovale
• Ductus arteriosus.
413-1-15 4
30-35 mm of
Hg
26-28 mm of
Hg
12-14 mm of
Hg
• After birth
• Lung expansion -- ↓ in pulmonary pressure.
• Increase in paO2 of blood.
• Loss of low pressure placental circulation.
• Functional closure of foramen ovale.
• Closure of ductus venosus and arteriosus.
• Series circulation.
Heart diseases in children:
• Heart, Pericardium, blood vessels.
• Congenital or acquired.
• Isolated or as a part of other systemic diseases.
Prevalence
• Congenital
• Cyanotic: 22%
• Acyanotic: 68%
• VSD 25%
• ASD 6%
• PDA 6%
• TOF 5%
• PS 5%
• AS 5%
• Acquired
• Kawasaki disease
• Rheumatic
• Tubercular
• Collagen
• Viral myocardidits
• Storage disorders
• Myopathies.
• Iron overload
• Infective endocarditis
8
Congenital Heart Diseases:-
• Incidence and prevalence:-
-Initial estimate 6-8 per 1000 live births.
-Recent estimate1/100 live births.
-Accounts to 15-20% of cardiac cases.
Etiology:-
-90% cases etiology not known.
-Both sexes are equally affected.
-Rt. Sided lesions common in female and left sided in male.
10
• Heredity
• Environmental factors
• Maternal diseases or factors
• Intrauterine infections:- TORCH group
• Drugs like thalidomide
• Metabolic factors like idiopathic hypercalcemia.
• Genetic diseases:- Marfan syndrome, Ehlers-Danlos syndrome,
Hurler syndrome
• Chromosomal aberrations:- Turner, Down and other trisomy
syndromes.
Presenting complaints/signs
• Failure to thrive
• Exercise intolerence
• Easy fatigability
• Chest indrawing
• Sweating during feeding
• Bluish spells
• Fever with rigor
• Palpitation
• Convulsion
• Fast breathing
• Oedema
• Hepatomegaly,
• spleenomegaly
• Clubbing
• Cyanosis
• Focal neurological lesion
• Other organ defects
• Chromosomal anomalies
12
Nadas` Criteria:-
• Major
i. Systolic murmur grade
III or more specially
with a thrill.
ii. Diastolic murmur
iii. Cyanosis
iv. Congestive cardiac
failure
• Minor
i. Systolic murmur less
than grade III
ii. Abnormal S2
iii. Abnormal ECG
iv. Abnormal X ray
v. Abnormal BP
Cyanosis: is it a cardiac cause or lung cause
• Hyperoxia test
• Neonates with cyanotic congenital heart disease usually do not have
significantly raised arterial Pao2 during administration of 100% oxygen.
Classification
Acyanotic
ASD
VSD
PDA
Cyanotic
TOF
TGA
Tru Art
TAPVC
Tri Atresia
Obstructive
PS
AS
COA
Approach to CHD
• History
• Physical examination
• Investigations
Left To Right Shunt
• Acyanotic CHD
Acyanotic heart disease ( VSD / ASD /PDA )
COMMON FINDING
• Frequent chest infections (6-8 attacks 1st year of life)
• Increased sweating / Perspiration / FTT
• Precordial bulge / Hyperkinetic precordium
• Loud S2 / Murmur +
• X-ray: Plethoric + Cardiomegaly
Cyanotic heart disease with increase
pulmonary flow.
• Clinical features similar to acyanotic heart diseases with left to right
shunt. In addition the patient is cyanosed.
Cyanotic heart disease with decreased blood
flow:
• Cyanosis
• Age of onset or age at which cyanosis noticed.
• Cyanotic spells or squatting episodes.
• Exertional dyspnea.
• Clubbing.
• Precordium silent
• Single second heart sound.
• Murmur of collaterals.
Some common chromosomal diseases
associated with CHD.
Which is the commonest CHD
associated with Down syndrome?
CHD associated with Turner syndrome?
Pulmonary oligemia Pulmonary plethora
Approach to a Patient with Congenital Heart Disease
Suspected CHD
Cyanosis
Present Absent
Repeated RTI Repeated RTI
Present PresentAbsent Absent
Obstructive/
Regurgitant
lesions
R
-Coarctation
of Aorta
-Aortic
Stenosis
-Mitral
Stenosis
-Aortic
Regurgitaion
-Mitral
Regurgitation
Left to Right
Shunt
Second
Heart Sound
Wide &
Variable
Wide &
Fixed
Not
Applicable
VSD ASD PDA
Cyanotic
Heart
Disease with
Increased
Pulmonary
Flow
Cyanotic
Heart
Disease with
Decreased
Pulmonary
Flow
-TGA
-TAPVC
-TA
-TOF
-Tricuspid
atresia
-Pulmonary
atresia
Summary
• Fetal circulation – parallel which becomes series after birth.
• Heart diseases – congenital , acquired
• CHD : acyanotic, cyanotic or obstructive.
• Nadas criteria helpful.
• Proper history and clinical examination helps to reach diagnosis.

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Fetal ciruclation and approach to chd

  • 1. Fetal Circulation and Approach to CHD Dr Tushar Jagzape, Pediatrics , AIIMS, Raipur
  • 2. Learning objectives: • At the end of this lecture, the learner should be able to: • Describe fetal circulation and changes that occur at birth. • Highlight the salient differences between fetal and neonatal circulation. • Describe the classification of CHD. • Enlist common acyanotic and cyanotic congenital heart diseases. • Approach to a child with suspected CHD. • Describe the hemodynamics of Lt to Rt shunts
  • 3. Fetal circulation and difference between fetal and neonatal circulation. • Parallel vs series circulation. • Structures responsible for parallel circulation. • Ductus venosus • Foramen ovale • Ductus arteriosus.
  • 4. 413-1-15 4 30-35 mm of Hg 26-28 mm of Hg 12-14 mm of Hg
  • 5. • After birth • Lung expansion -- ↓ in pulmonary pressure. • Increase in paO2 of blood. • Loss of low pressure placental circulation. • Functional closure of foramen ovale. • Closure of ductus venosus and arteriosus. • Series circulation.
  • 6. Heart diseases in children: • Heart, Pericardium, blood vessels. • Congenital or acquired. • Isolated or as a part of other systemic diseases.
  • 7. Prevalence • Congenital • Cyanotic: 22% • Acyanotic: 68% • VSD 25% • ASD 6% • PDA 6% • TOF 5% • PS 5% • AS 5% • Acquired • Kawasaki disease • Rheumatic • Tubercular • Collagen • Viral myocardidits • Storage disorders • Myopathies. • Iron overload • Infective endocarditis
  • 8. 8 Congenital Heart Diseases:- • Incidence and prevalence:- -Initial estimate 6-8 per 1000 live births. -Recent estimate1/100 live births. -Accounts to 15-20% of cardiac cases.
  • 9. Etiology:- -90% cases etiology not known. -Both sexes are equally affected. -Rt. Sided lesions common in female and left sided in male.
  • 10. 10 • Heredity • Environmental factors • Maternal diseases or factors • Intrauterine infections:- TORCH group • Drugs like thalidomide • Metabolic factors like idiopathic hypercalcemia. • Genetic diseases:- Marfan syndrome, Ehlers-Danlos syndrome, Hurler syndrome • Chromosomal aberrations:- Turner, Down and other trisomy syndromes.
  • 11. Presenting complaints/signs • Failure to thrive • Exercise intolerence • Easy fatigability • Chest indrawing • Sweating during feeding • Bluish spells • Fever with rigor • Palpitation • Convulsion • Fast breathing • Oedema • Hepatomegaly, • spleenomegaly • Clubbing • Cyanosis • Focal neurological lesion • Other organ defects • Chromosomal anomalies
  • 12. 12 Nadas` Criteria:- • Major i. Systolic murmur grade III or more specially with a thrill. ii. Diastolic murmur iii. Cyanosis iv. Congestive cardiac failure • Minor i. Systolic murmur less than grade III ii. Abnormal S2 iii. Abnormal ECG iv. Abnormal X ray v. Abnormal BP
  • 13. Cyanosis: is it a cardiac cause or lung cause • Hyperoxia test • Neonates with cyanotic congenital heart disease usually do not have significantly raised arterial Pao2 during administration of 100% oxygen.
  • 15. Approach to CHD • History • Physical examination • Investigations
  • 16. Left To Right Shunt • Acyanotic CHD
  • 17. Acyanotic heart disease ( VSD / ASD /PDA ) COMMON FINDING • Frequent chest infections (6-8 attacks 1st year of life) • Increased sweating / Perspiration / FTT • Precordial bulge / Hyperkinetic precordium • Loud S2 / Murmur + • X-ray: Plethoric + Cardiomegaly
  • 18. Cyanotic heart disease with increase pulmonary flow. • Clinical features similar to acyanotic heart diseases with left to right shunt. In addition the patient is cyanosed.
  • 19. Cyanotic heart disease with decreased blood flow: • Cyanosis • Age of onset or age at which cyanosis noticed. • Cyanotic spells or squatting episodes. • Exertional dyspnea. • Clubbing. • Precordium silent • Single second heart sound. • Murmur of collaterals.
  • 20. Some common chromosomal diseases associated with CHD. Which is the commonest CHD associated with Down syndrome?
  • 21. CHD associated with Turner syndrome?
  • 22.
  • 24. Approach to a Patient with Congenital Heart Disease Suspected CHD Cyanosis Present Absent Repeated RTI Repeated RTI Present PresentAbsent Absent Obstructive/ Regurgitant lesions R -Coarctation of Aorta -Aortic Stenosis -Mitral Stenosis -Aortic Regurgitaion -Mitral Regurgitation Left to Right Shunt Second Heart Sound Wide & Variable Wide & Fixed Not Applicable VSD ASD PDA Cyanotic Heart Disease with Increased Pulmonary Flow Cyanotic Heart Disease with Decreased Pulmonary Flow -TGA -TAPVC -TA -TOF -Tricuspid atresia -Pulmonary atresia
  • 25. Summary • Fetal circulation – parallel which becomes series after birth. • Heart diseases – congenital , acquired • CHD : acyanotic, cyanotic or obstructive. • Nadas criteria helpful. • Proper history and clinical examination helps to reach diagnosis.