Ventricular septal defect differential diagnosis: Difference between revisions

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CHF:
 
diuretics and vasodilator such as captopril
 
digoxin (controversial)
 
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Revision as of 14:18, 26 February 2020

Ventricular septal defect Microchapters

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Overview

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Pathophysiology

Causes

Differentiating Ventricular Septal Defect from other Diseases

Epidemiology and Demographics

Risk Factors

Natural History, Complications and Prognosis

Diagnosis

History and Symptoms

Physical Examination

Electrocardiogram

Chest X Ray

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Echocardiography

Cardiac Catheterization

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Medical Therapy

Surgery

Ventricular septal defect post-surgical prognosis

ACC/AHA Guidelines for Surgical and Catheter Intervention Follow-Up

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1], Leida Perez, M.D. Associate Editor(s)-In-Chief: Keri Shafer, M.D. [2], Priyamvada Singh, MBBS

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Differentiating Ventricular Septal Defect from other Disorders



Disease Signs and Symptoms Association Lab finding Diagnostic modality Management Prognosis
VSD
  • Shortness of breath
  • Tachypnea
  • Palpitation
  • Paleness
  • Failure to gain weight
  • Sweating while feeding
  • Frequent respiratory infections
  • Fainting
  • Chest pain
  • Cyanosis
  • Echocardiogram
  • Electrocardiogram (ECG)
  • Chest X-ray
  • Cardiac catheterization
  • Pulse oximetry
  • Small VSD: Observe, symptomatic treatment until spontaneous closure.
  • Surgical repair:
  • During first year of life
  • Immediately if severe symptoms present
  • Small VSD to prevent complications related to their locations, such as heart valves damage
  • Nutritional support or tubal feeding if VSD causing tiredness of the infant during feeding
  • Surgical repair
  • Catheter procedure
  • Hybrid procedure (surgical and catheter-based techniques)
  • Small VSD usually closes spontaneously by 18 months. Up to 75% are closed by the age of 10.
  • Medium to large VSDs often become smaller but remain patent and allow shunting of blood and eventual development of Eisenmenger’s syndrome and heart failure.
  • If large defects are not corrected before pulmonary hypertension develops the prognosis is poor.
  • Patients with the Eisenmenger’s syndrome have an average life expectancy of 33 years.
  • Surgical correction provide a better outcome.
Atrioventricular septal defect[2]
  • cyanosis mild or absent
  • congestive cardiac failure
  • right ventricular impulse
  • increased pulmonic component second heart sound
  • variable ejection systolic murmur, apical mid‐diastolic murmur (in large left to right shunt), pansystolic murmur (with atrioventricular valve regurgitation)
  • Subaortic stenosis
  • Ventricular hypoplasia
  • Tetralogy of Fallot
  • Atrial isomerism
  • Antenatal ultrasound anomaly scanning (four‐chamber view)
  • Postnatal diagnosis:
  • ECG
  • Chest radiograph
  • Echocardiogram
  • Magnetic resonance imaging
  • Angiography
Medical treatment

CHF:

diuretics and vasodilator such as captopril

digoxin (controversial)

Atrial septal defect
Patent Ductus Arteriosus (PDA)
Infundibular Pulmonary Stenosis

References

  1. LAMBERT EC, KELSCH JV, VLAD P (1963). "Differential diagnosis of ventricular septal defect in infancy: a common problem". Am J Cardiol. 11: 447–51. doi:10.1016/0002-9149(63)90003-1. PMID 13928242.
  2. Craig B (2006). "Atrioventricular septal defect: from fetus to adult". Heart. 92 (12): 1879–85. doi:10.1136/hrt.2006.093344. PMC 1861295. PMID 17105897.

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