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Related Subjects: |Congenital Acyanotic Heart Disease |Congenital Cyanotic Heart Disease |Cardiac Embryology |Cyanosis - Central and Peripheral |Down's syndrome (Trisomy 21) |Tetralogy of Fallot |Patent Foramen Ovale (PFO) |Ventricular Septal defect (VSD)
Small VSD's may produce loud murmurs and large VSD's may produce no murmur at all but will cause heart failure usually at 6+ weeks. Many smaller VSD's close without any treatment
Type of VSD | Description | Comments |
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Perimembranous VSD | The most common type, located in the membranous portion of the ventricular septum, near the tricuspid and aortic valves. | Can vary in size and often associated with aortic valve prolapse or insufficiency. It may close spontaneously, especially in smaller defects. |
Muscular VSD | Occurs in the muscular portion of the septum, lower in the ventricular septum, away from the valves. | Often referred to as "Swiss cheese" VSD when multiple small defects are present. These defects have a high chance of spontaneous closure. |
Inlet (Atrioventricular Canal) VSD | Located near the tricuspid and mitral valves, in the area where the blood enters the ventricles from the atria. | Commonly associated with atrioventricular septal defects (AVSD) and Down syndrome. Surgical intervention is often required. |
Outlet (Supracristal or Subarterial) VSD | Located near the outflow tracts of the right and left ventricles, beneath the pulmonary and aortic valves. | Less common, more frequent in Asian populations. Associated with aortic valve prolapse, which may necessitate early surgical repair. |
Gerbode VSD | Rare type of VSD that involves a direct communication between the left ventricle and the right atrium. | This type of defect is unusual and often requires surgical correction due to the significant left-to-right shunt it causes. |
Management Option | Description | Comments |
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Observation | Close Monitoring of the VSD without immediate intervention. Small defects are likely to close spontaneously without intervention. | Small muscular VSDs, particularly in infants, as these defects frequently close on their own. |
Medications | Use of drugs such as IV/PO diuretics, ACEi, and digoxin to manage fluid overload/heart failure. | Can alleviate symptoms, prior to definitive surgery. Use when surgery delayed or not immediately necessary. |
Surgical Repair | Open-heart surgery to close the VSD using a patch or sutures. | Indicated for large defects causing significant symptoms, failure to thrive, or increased pulmonary blood flow. Surgery is often performed in early childhood. |
Transcatheter Device Closure | A minimally invasive procedure where a device is inserted through a catheter to close the VSD. | Typically used for muscular VSDs or residual VSDs after surgery. It’s less invasive than open-heart surgery and involves a shorter recovery time. |
Endocarditis Prophylaxis | Antibiotic therapy to prevent infective endocarditis, particularly in patients with certain types of VSD or after surgical repair. | Recommended for individuals with VSD who have a history of endocarditis or those who have undergone VSD repair with residual defects. |
Long-term Follow-up | Regular cardiac evaluations to monitor for complications such as residual defects, arrhythmias, or pulmonary hypertension. | Essential for all patients with a history of VSD, regardless of whether they have undergone surgical or transcatheter repair. |