Ventricular septal defect: Difference between revisions
(Created page with "==Background== ==Clinical Features== ==Differential Diagnosis== ==Evaluation== ==Management== ==Disposition== ==See Also== ==External Links== ==References== <r...") |
|||
| Line 1: | Line 1: | ||
==Background== | ==Background== | ||
*A defect in the septum of the heart which separates the left and right ventricles | |||
*Second most common congenital heart defect | |||
*These defects can be isolated, due to chromosomal abnormalities (5%), or coexist with other heart defects such as Tetrology of Fallot | |||
*Clinical presentation will vary depending on comorbid conditions | |||
==Clinical Presentation== | |||
==Clinical | *Small VSDs | ||
**Will generally be asymptomatic | |||
*Moderate Size VSDs | |||
**May be asymptomatic | |||
**May develop heart failure symptoms in childhood or early adulthood | |||
**VSD may decrease in size without intervention as patient ages | |||
*Large VSDs | |||
**Left-to-right shunts causing heart failure in infancy | |||
**may present with cyanosis, dyspnea, poor feeding, or failure to thrive | |||
*VSD murmurs are best heard over the lower left sternal boarder | |||
**Characterized as a holosystolic murmur | |||
**Often, the small the defect, the louder the murmur | |||
==Differential Diagnosis== | ==Differential Diagnosis== | ||
*Pulmonary stenosis | |||
*Patent ductus arteriosis | |||
*Tetrology of Fallot | |||
*Aortic stenosis | |||
*Tricuspid regurgitation | |||
*Mitral Regurgitation | |||
*Hypertrophic Cardiomyopathy | |||
==Evaluation== | ==Evaluation== | ||
*Echocardiogram | |||
**This is the most important clinical test | |||
**High detection rate for VSD | |||
**Allows operator to visualize the defect and assess how much bloodflow is crossing the defect by using color flow Doppler | |||
**Allows for detection of other possible structural defects | |||
*Electrocardiogram (EKG) | |||
**most patients with VSDs will have a normal EKG | |||
**conduction delay or RBBB may be seen in large defects | |||
*Chest X Ray | |||
**typically normal in patients with VSDs | |||
**may show cardiomegaly with enlarged left ventricle and atrium | |||
==Management== | ==Management== | ||
*40-60% of these defects require no intervention an will spontaneously close in early childhood | |||
*Surgical closure (often done percutaneously) is the definitive treatment for defects that do not close on their own and cause significant disability | |||
*Patient's with unrepaired VSDs are at increased risk for | |||
**endocarditis | |||
**Arrhythmias | |||
***Premature Ventricular Beats (PVCs) | |||
***Ventricular tachyarrhythmias | |||
***Sudden death | |||
***Congestive heart failure | |||
***Aortic regurgitation | |||
***COPD | |||
***Pulmonary Hypertension | |||
*Treatment is aimed at reducing the complications associated with the VSD, as highlighted above | |||
==Disposition== | |||
*Suspected VSDs require workup by a cardiologist | |||
*Once surgery becomes an option, surgical consultation is recommended | |||
==Disposition== | ==Disposition== | ||
| Line 21: | Line 67: | ||
==External Links== | ==External Links== | ||
*Ventricular septal defects | circulation Retrieved 8/18/2017, 2017, from http://circ.ahajournals.org/content/114/20/2190 | |||
*Du ZD, Roguin N, Wu XJ. Spontaneous closure of muscular ventricular septal defect identified by echocardiography in neonates. Cardiol Young 1998; 8:500. | |||
==References== | ==References== | ||
Revision as of 01:07, 19 August 2017
Background
- A defect in the septum of the heart which separates the left and right ventricles
- Second most common congenital heart defect
- These defects can be isolated, due to chromosomal abnormalities (5%), or coexist with other heart defects such as Tetrology of Fallot
- Clinical presentation will vary depending on comorbid conditions
Clinical Presentation
- Small VSDs
- Will generally be asymptomatic
- Moderate Size VSDs
- May be asymptomatic
- May develop heart failure symptoms in childhood or early adulthood
- VSD may decrease in size without intervention as patient ages
- Large VSDs
- Left-to-right shunts causing heart failure in infancy
- may present with cyanosis, dyspnea, poor feeding, or failure to thrive
- VSD murmurs are best heard over the lower left sternal boarder
- Characterized as a holosystolic murmur
- Often, the small the defect, the louder the murmur
Differential Diagnosis
- Pulmonary stenosis
- Patent ductus arteriosis
- Tetrology of Fallot
- Aortic stenosis
- Tricuspid regurgitation
- Mitral Regurgitation
- Hypertrophic Cardiomyopathy
Evaluation
- Echocardiogram
- This is the most important clinical test
- High detection rate for VSD
- Allows operator to visualize the defect and assess how much bloodflow is crossing the defect by using color flow Doppler
- Allows for detection of other possible structural defects
- Electrocardiogram (EKG)
- most patients with VSDs will have a normal EKG
- conduction delay or RBBB may be seen in large defects
- Chest X Ray
- typically normal in patients with VSDs
- may show cardiomegaly with enlarged left ventricle and atrium
Management
- 40-60% of these defects require no intervention an will spontaneously close in early childhood
- Surgical closure (often done percutaneously) is the definitive treatment for defects that do not close on their own and cause significant disability
- Patient's with unrepaired VSDs are at increased risk for
- endocarditis
- Arrhythmias
- Premature Ventricular Beats (PVCs)
- Ventricular tachyarrhythmias
- Sudden death
- Congestive heart failure
- Aortic regurgitation
- COPD
- Pulmonary Hypertension
- Treatment is aimed at reducing the complications associated with the VSD, as highlighted above
Disposition
- Suspected VSDs require workup by a cardiologist
- Once surgery becomes an option, surgical consultation is recommended
Disposition
See Also
External Links
- Ventricular septal defects | circulation Retrieved 8/18/2017, 2017, from http://circ.ahajournals.org/content/114/20/2190
- Du ZD, Roguin N, Wu XJ. Spontaneous closure of muscular ventricular septal defect identified by echocardiography in neonates. Cardiol Young 1998; 8:500.
