Cardiology Flashcards
In utero, this structure allows 50% of umbilical venous blood to go directly to the IVC, bypassing the liver
Ductus venosus
Pulmonary vascular obstructive disease usually seen in VSDs that may cause pulmonary hypertension
Eisenmenger’s syndrome
In fetal transitional circulation, after birth, the interruption of blood supply of umbilical cord results in:
1) increase in SVR (due to removal of placenta)
2) closure of ductus venosus (due to cut blood supply from placenta)
In fetal circulation, less oxygenated blood from the pulmonary artery flows through this structure that opens directly to the descending aorta and then to the placenta for oxygenation
Ductus arteriosus
Acyanotic infant with systolic ejection murmur at 2nd left ICS with widely split S2; on PE, right-sided enlargement; leads to CHF and Pulmonary hypertension if left untreated
Atrial septal defect (Ostium Secundum type most common)
In fetuses, around 1/3 of blood from fetal Inferior Vena Cava is directed to the left atrium directly via this structure:
Foramen Ovale (other 2/3 enters right ventricle then pulmonary artery)
Acyanotic infant with systolic regurgitant murmur at the left lower sternal border with loud S2 heard (unsplit); left-sided enlargement with biventricular hypertrophy if with Eisenmenger’s Syndrome (pulmonary vascular obstructive disease); this defect may usually present with recurrent pulmonary infections and delayed growth and development
Ventricular Septal Defect (most common congenital heart disease)
Acyanotic infant with a continuous “machinery-like” murmur heard at the 2nd left infraclavicular area; on PE, patient has hyperactive precordium, bounding pulses with wide pulse pressure.
Patent Ductus Arteriosus (patency between left pulmonary artery and descending aorta)
Most common cause of cyanotic congenital heart disease in newborns; patient has single, loud S2 with hypoxemia unresponsive to oxygen inhalation; on CXR, an egg-shaped cardiac silhouette with a narrow, superior mediastinum.
Transposition of the Great Arteries (aorta arises from right ventricle, pulmonary artery arises from left ventricle)
Cyanotic condition in infant with pulmonary stenosis, right ventricular hypertrophy, ventricular septal defect and the aorta overriding this defect; patient may present with a systolic ejection murmur at 2nd upper left sternal border. On CXR, boot-shaped heart seen.
Hypoxic spells (paroxysm of hyperpnea, irritability, prolonged crying, increasing cyanosis, decreasing intensity of murmur after crying, feeding or defecation)
Tetralogy of Fallot
Palliative surgical management of Tranposition of Great Arteries wherein the objective is to create an interatrial communication to avoid progressive hypoxemia
Balloon atrial septostomy (Rashkind procedure) and surgical atrial septostomy (Blalock-Hanlon procedure)
Definitive surgical repair for TGA wherein objective is to switch right and left-sided blood
1) Atrial level repair (Senning or Mustard)
2) Ventricular level repair (Rastelli)
3) Great Artery level repair (Jatene)
General management of hypoxic spells in TOF:
1) Knee-chest position (decrease systemic venous return from legs)
2) Morphine sulfate (suppress respiratory center)
3) NaHCO3
4) Oxygen (improve arterial oxygenation)
5) Phenylephrine (raise SVR)
6) Propranolol (stabilize vascular reactivity of systemic arteries to prevent drops in SVR)
7) Ketamine (raise SVR)
Surgical management options for Tetralogy of Fallot:
Bloalock-Taussig (for >3 months old) and Gore-Tex Shunt (for
What are the components of Tricuspid Atresia?
1) Atretic tricuspid valve (missing valve)
2) Hypoplastic Right Ventricle
3) Ventricular Septal Defect
4) Atrial Septal Defect
5) Pulmonary Stenosis