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Normal Heart
ANATOMY
ASD
Diagram of ASD
Clinical Features
Symptoms
Most infants : asymptomatic ..undetected
The first present at age 6 to 8 weeks with a soft
murmur and possibly a fixed and somewhat widely
split S2
Infant with large ASD may present with poor
growth, recurrent lower respiratory tract
infection and heart failure
Lungs
LV
LA
AO
PA
RV
RA
Qp > Qs
Systemic
RA
RV
RA
LA
RV
LV
LA
LV
Diagnosis Differential
Primary Atrial Septal Defect
ECG : LAD
Partial Anomalous Pulmonary Vein
Drainage
Pulmonary Stenosis
Innocent Murmur
Management
Surgery : Preschool age
Recent treatment: transcatheter closure using
ASO (Amplatzer septal occluder)
ASD
Large Shunt
Small Shunt
Observation
Evaluation
At age 5-8 yrs
Cath
FR<1.5
Heart
Failure (-)
Children/Adults
PH (-)
Heart
Failure (+)
PVD
(-)
Anti failure
Success
FR>1.5
Conservative
Infants
Age >1yrs
W >10kg
PH (+)
PVD
(+)
Hyperoxia
Fail
Surgical
Closure
Reactive
Non
reactive
Conservative
VSD
Lungs
LV
LA
AO
PA
RA
RV
Qp > Qs
Systemic
RA
RV
LA
LV
RA
LA
RV
LV
Clinical findings
Day 1st after birth: murmur (-)
After 2-6 weeks : murmur (+)
Murmur : pansystolic grade 3/6 or higher
at LSB 3
Small muscular defect: early systolic murmur
Significant defect: Mid diastolic murmur at apex
Murmur: pansystolic
grade 3/6 or higher at
LSB 3
Small VSD
Large VSD
Cardiomegaly
Apex down ward
Prominence pulmonary
artery segment
Increased pulmonary vascular
marking
Diagnosis Differential
PDA with PH
Tetralogy Fallot non cyanotic
Inoscent murmur
Management:
Definitive : VSD closure
Surgery
Transcatheter closure
DSV
Heart failure (+)
Anti failure
Aortic valve
prolaps
Fail
Infundibular
stenosis
PVD(-)
Success
PAB
Evaluate
in 6 mths
PH Spontaneous
closure
Cath
PVD(+)
Cath
Reactive
Smaller
Cath
FR<1.5 FR>1.5
Nonreactive
Conservative
Anatomy
Fetus: ductus arteriosus connects PA and aorta
If ductus does not closs Patent Ductus arteriosus
PDA
RA
RV
LA
LV
RA
LA
RV
LV
Lungs
LV
LA
AO
PA
RA
RV
Qp > Qs
Systemic
Clinical findings
Small defect:
Symptom (-)
Growth and development normal
Moderate and large defect:
Decreased exercise tolerant
Weigh gained not good
Frequent URTI
DIAGNOSIS
Chest X-Ray
Large PDA:
Prominence of the left
atrium,
left ventricle, ascending
aorta,
Pulmonary vascular
marking
ECG
Diagnosis Differential
AP-window
Arterio-venous fistulae
Management
premature: ibuprofen
PDA closure : surgery
transcatheter closure
MANAGEMENT
Medical treatment : prostaglandin synthesis
inhibitor
Preterm neonates : usefull
Aterm neonates : useless
TRANSCATHETER CLOSURE
Tetralogy Fallot
Incidence
5-8% from all CHD
Anatomy
Cause: Left-anterior deviation of infundibular septum
Sindroma consist of 4 items:
VSD
pulmonary stenosis
aortic over-riding
RVH
Tetralogy Fallot
Central cyanosis
Central cyanosis
Pathophysiology
Cyanosis is a bluish discoloration of the
skin and mucous membranes resulting
from an increased concentration of
reduced hemoglobin
Clinical cyanosis occurs when the amount
of reduced hemoglobin in the cutaneous
vein may result 5 g/100ml
The critical level of reduced hemoglobin in
the cutaneous vein may result from either
desaturation of arterial blood or increased
extraction of oxygen by peripheral tissue
Diagnosis
Clinically : cyanosis
Single 2nd HS, ejection systolic murmur
X Ray : Boot Shaped
ECG: RAD, RVH
Tetralogy Fallot
CXR :
Boot-shaped
Concave pulmonary segment
Apex upturned
Decreased pulmonary blood flow
Tetralogy Fallot
Tetralogy Fallot
Diagnosis Differential
Pulmonary Atresia
Double outlet right ventricle and pulmonary stenosis
Transposisi of great arteri and pulmonary stenosis
Management
Paliative treatment: Blalock-Taussig shunt
Definitive: total correction
clinically
ECG
Tetralogy of Fallot
< 1 yr
> 1 yr
spell (+)
propranolol
spell (-)
age 1 yr
failed
CXR
echo
succeed
cath
BTS
evaluation
cath
BTS/
PDA Stent
small PA
total correction
good sized PA