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VENTRICULAR SEPTAL
DEFECT (VSD)
VSD – TYPES ( location )
• Location of the defect:
• Type I: Subarterial (outlet, subpulmonic,
supracristal or infundibular)
• Type II: Perimembranous (subaortic)
• Type III: Inlet
• Type IV: Muscular
VSD – TYPES (SIZE )
• Large (nonrestrictive):
• Diameter of the defect is approximately equal to diameter of the
aortic orifice
• Right ventricular systolic pressure is systemic
• Degree of left to right shunt depends on pulmonary vascular
resistance
• Moderate (restrictive):
• Diameter of the defect is less than that of the aortic orifice
• Right ventricular pressure is half to two third systemic
• Left to right shunt is >2:1
• Small (restrictive):
• Diameter of the defect is less than one third the size of the aortic
orifice
• Right ventricular pressure is normal
• left to right shunt is <2:1
VSD ‐ HEMODYNAMICS
CLINICAL FEATURES
SYMPTOMS
• Feeding difficulty
• Suck rest suck cycle (dyspnea on exertion)
• Recurrent respiratory tract infection
• Congestive cardiac failure- breathlessness, feeding difficulty, sweating
• Failure to thrive
SIGNS
• Tachypnea
• CHF- Tachypnea, tachycardia, dependent edema, hepatomegaly & raised
JVP
• Wide pulse pressure
• Cardiomegaly –shifted apex
• Hyperkinetic precordium with a systolic thrill at left sternal border
• Pansystolic murmur at left sternal border
• The murmur is characteristically loud, harsh or blowing
• S1 and S2 masked by PSM at left sternal border
• Widely split & variable S2 with accentuated P2
• S3 at the apex may be audible
• ESM at pulmonary wall (flow murmur)
• Mid diastolic murmur at apex (flow murmur)
Clinical assessment of size of defect
• Small size VSD: normal growth of the child; no cardiomegaly; no cardiac
failure
• Medium size VSD : there will be cardiomegaly & may develop cardiac failure,
when there is associated respiratory infection. MDM at apex implies
significant shunt (>2:1 shunt)
• Large size VSD: there will be heart failure, growth failure & frequent
respiratory tract infection.
MODE OF DIAGNOSIS
• Physical examination
• ECG
• X‐ray chest
• Echocardiography
INVESTIGATIONS
• In small asymptomatic VSD- ECG & X-ray are likely to be normal
• In symptomatic medium & large sized VSDs:
• X-ray: cardiomegaly, pulmonary vascular markings are increased,
prominent pulmonary artery segment seen, left atrial enlargement
(shadow in shadow on the right side of cardiac shadow)
• ECG: left ventricular enlargement of volume overload type, evidence of
right ventricular hypertrophy & enlargement of left atrium
• Echocardiography –assess location & size of VSD & blood flow across it
NATURAL HISTORY
• About 10% of large nonrestrictive VSDs die in first year, primarily due
to congestive heart failure.
• Spontaneous closure is uncommon in large VSDs.
• 30%‐40% of moderate or small defects (restrictive) close
spontaneously, majority by 3‐5 years of age.
• Decrease in size of VSD is seen in 25%.
COMPLICATIONS
• Congestive heart failure
• Pulmonary arterial hypertension
• Eisenmenger’s syndrome
• Right ventricular outflow tract obstruction
• Aortic regurgitation
• Infective endocarditis
TREATMENT
• Medical management
• Maintain nutrition – adequate calories
• Prevent or manage anaemia
• Treatment of respiratory infections
• Infection prevention- immunization with H.influenza type B,
streptococcus pneumonia whenever possible
• Treatment of CHF - Diuretics (furosemide & thiazide), Inotropes, ACE
inhibitors
• Surgical
• Indications
• CCF
• Large left to right shunt
• VSD associated with pulmonary stenosis, pulmonary arterial
hypertension , aortic regurgitation
VSD ‐ MODE OF CLOSURE
• Surgical closure.
• Device closure for muscular VSD in those weighing >15 Kg & For
Perimembranous VSD
• Pulmonary artery banding is indicated for multiple (Swiss cheese) , or
very large VSD, almost single ventricle , infants with low weight (<2
Kg), and those with associated co‐morbidity like chest infection .
Thank you

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Ventricular septal defect (vsd)

  • 2.
  • 3. VSD – TYPES ( location ) • Location of the defect: • Type I: Subarterial (outlet, subpulmonic, supracristal or infundibular) • Type II: Perimembranous (subaortic) • Type III: Inlet • Type IV: Muscular
  • 4. VSD – TYPES (SIZE ) • Large (nonrestrictive): • Diameter of the defect is approximately equal to diameter of the aortic orifice • Right ventricular systolic pressure is systemic • Degree of left to right shunt depends on pulmonary vascular resistance
  • 5. • Moderate (restrictive): • Diameter of the defect is less than that of the aortic orifice • Right ventricular pressure is half to two third systemic • Left to right shunt is >2:1
  • 6. • Small (restrictive): • Diameter of the defect is less than one third the size of the aortic orifice • Right ventricular pressure is normal • left to right shunt is <2:1
  • 8.
  • 9. CLINICAL FEATURES SYMPTOMS • Feeding difficulty • Suck rest suck cycle (dyspnea on exertion) • Recurrent respiratory tract infection • Congestive cardiac failure- breathlessness, feeding difficulty, sweating • Failure to thrive
  • 10. SIGNS • Tachypnea • CHF- Tachypnea, tachycardia, dependent edema, hepatomegaly & raised JVP • Wide pulse pressure • Cardiomegaly –shifted apex • Hyperkinetic precordium with a systolic thrill at left sternal border • Pansystolic murmur at left sternal border • The murmur is characteristically loud, harsh or blowing
  • 11. • S1 and S2 masked by PSM at left sternal border • Widely split & variable S2 with accentuated P2 • S3 at the apex may be audible • ESM at pulmonary wall (flow murmur) • Mid diastolic murmur at apex (flow murmur)
  • 12. Clinical assessment of size of defect • Small size VSD: normal growth of the child; no cardiomegaly; no cardiac failure • Medium size VSD : there will be cardiomegaly & may develop cardiac failure, when there is associated respiratory infection. MDM at apex implies significant shunt (>2:1 shunt) • Large size VSD: there will be heart failure, growth failure & frequent respiratory tract infection.
  • 13.
  • 14. MODE OF DIAGNOSIS • Physical examination • ECG • X‐ray chest • Echocardiography
  • 15. INVESTIGATIONS • In small asymptomatic VSD- ECG & X-ray are likely to be normal • In symptomatic medium & large sized VSDs: • X-ray: cardiomegaly, pulmonary vascular markings are increased, prominent pulmonary artery segment seen, left atrial enlargement (shadow in shadow on the right side of cardiac shadow) • ECG: left ventricular enlargement of volume overload type, evidence of right ventricular hypertrophy & enlargement of left atrium • Echocardiography –assess location & size of VSD & blood flow across it
  • 16. NATURAL HISTORY • About 10% of large nonrestrictive VSDs die in first year, primarily due to congestive heart failure. • Spontaneous closure is uncommon in large VSDs. • 30%‐40% of moderate or small defects (restrictive) close spontaneously, majority by 3‐5 years of age. • Decrease in size of VSD is seen in 25%.
  • 17. COMPLICATIONS • Congestive heart failure • Pulmonary arterial hypertension • Eisenmenger’s syndrome • Right ventricular outflow tract obstruction • Aortic regurgitation • Infective endocarditis
  • 18. TREATMENT • Medical management • Maintain nutrition – adequate calories • Prevent or manage anaemia • Treatment of respiratory infections • Infection prevention- immunization with H.influenza type B, streptococcus pneumonia whenever possible • Treatment of CHF - Diuretics (furosemide & thiazide), Inotropes, ACE inhibitors
  • 19. • Surgical • Indications • CCF • Large left to right shunt • VSD associated with pulmonary stenosis, pulmonary arterial hypertension , aortic regurgitation
  • 20. VSD ‐ MODE OF CLOSURE • Surgical closure. • Device closure for muscular VSD in those weighing >15 Kg & For Perimembranous VSD • Pulmonary artery banding is indicated for multiple (Swiss cheese) , or very large VSD, almost single ventricle , infants with low weight (<2 Kg), and those with associated co‐morbidity like chest infection .