Congenital Module 3
Jatene procedure
- arterial switch method - Involves transection of the aorta and PAs about the valve sinuses (including removal of the coronaries) - great arteries are switched. - The coronaries are sewn into the new aorta (formerly the PA) - Very difficult. - Advantages: LV is systemic ventricle, and no conduit to go bad.
Transannular Patch Repair
- relieve PS/sub PS - RVOT incision - pericardial/synthetic patch - enlarged outflow tract - results in free PR
D-Transposition
1 of the 2 most common cyanotic CHD
large unrestrictive VSD, RVOT obstruction, large, overriding aorta, RV hypertrophy
4 characteristics of Tetralogy of Fallot
right aortic arch, secundum ASD, LSVC, coronary artery abnormalities
4 most common associated cardiac defects with Truncus arteriosus
valvular
80-90% of patients with RVOTO at this level
Tet Spell
A child with Tetralogy of Fallot (TOF) responds to this by squatting, which will increase blood flow back to the heart. It is a period of cyanosis. hold baby in knee-chest position
D-Transposition of the Great Arteries
An anomaly where the RA connects to the RV but the RV connects to the aorta and the LA connects to the LV but the LV connects to the pulmonary artery - lethal congenital malformation
double-chambered RV
Can occur when infundibular stenosis is so severe that the RV is divided into a low-pressure (distal or infundibulum and apical) and a high-pressure chamber (proximal or inflow) - usually with a membranous VSD
VSD (most common), coronary artery anomalies, PS or subpulmonic outflow tract obstruction, AS or subaortic stenosis, coarctation of the aorta
D-TGA associated lesions (most common is this)
McGoon & Rastelli
Truncus Arteriosus surgical repair: VSD closure, detach PA's and repair aorta, possible trruncal valve repair, possible aortic arch repair
Noonan syndrome
Webbed neck Pectus excavatum Short stature shield chest Pulmonary stenosis - 25% - thickened, myxomatous PV - DO NOT respond well to balloon angioplasty
L-looping
abnormal twisting of the heart tube to the left and results in the RV to the left
thickened leaflets, fusion along free edge cusp, domed, fixed central orifice, dysplastic valve, hypoplastic annulus, bicuspid pulmonary valve
anatomic features seen on valvular RVOTO
anterior and leftward
aorta orientation in CCTGA
PFO/ASD, additional VSD, AV canal defect, persistent LSVC, right Ao arch, anomalous coronary arteries
associated lesions with TOF
sinus node dysfunction, RV dysfunction, TR, LVOTO
atrial switch complications
Senning procedure
atrial switch procedure that uses native atrial tissue
Mustard procedure
atrial switch procedure that uses prosthetic material
double switch
atrial-level re-routing procedure (Mustard or Senning) and either an arterial switch or a Rastelli type ventricular level re-routing procedure
PLAX
best view to assess aortic override, aortic root size, infundibular and pulmonary valve narrowing
PSAX
best view to assess relationship of VSD to inlet, outlet, and trabecular septum, RVOTO, PV morphology, coronary arteries, pulmonary arteries
dyspnea, fatigue, tachy/brady arrhythmias/ complete HB, CHF
clinical features of CCTGA
VSD, LVOTO, subpulmonary stenosis, unusual anatomical location of AV node and Bundle of His (complete heart block)
common associated anomalies with CCTGA
higher risk in young child, transannular patch to enlarge RVOT results in increase PR leading to RVE and heart failure
cons of early surgical repair of TOF
infundibular septum
displacement of _________ _________ crowds RVOT and fails to occupy space above ventricular septum resulting in VSD shunt
truncus arteriosus
failure of septum formation, resulting in a single vessel that comes off of the ventricles - uncommon CHD - conotruncal abnormalitiy
common arterial trunk, single truncal valve, outlet VSD, pulmonary artery anatomy, aortic arch, coronary arteries
features and assessment of truncus arteriosus
relieve RVOTO and close VSD
goals of complete surgical TOF repair
discordance
in CCTGA there is atrioventricular and ventriculoarterial _________
corrected
in CCTGA there is hemodynamically ______ circulation
right and anterior
in D-TGA the aorta is described as
parallel
in D-TGA the great arteries are _______ to one another
concordant, discordant
in D-TGA there are ________ atrioventricular connections and ________ ventriculoarterial connections resulting in 2 parallel circuits
coronary arteries, pulmonary arteries, systemic arteries
in truncus arteriosus the single vessel coming off of the ventricle gives rise to this arteries
asymptomatic, dyspnea, fatigue
mild PS clinical features
cyanosis, CHF, syncope, sudden death
moderate-severe PS clinical features
- TV inserts more apically - TV/RV has chrodal attachments to ventricular septum - RV has moderator band, pyramidal shape, trabeculated endocardial surface
morphological TV/RV will have these anatomic qualities
Tetralogy of Fallot
most common cyanotic congenital heart defect
severe pulmonary regurgitation (symptoms, RVE/dysfunction)
most common reason for repeat surgical repair
RVOT obstruction
obstruction of blood flow from the RV to the pulmonary artery (valvular, subvalvular, supravalvular)
systemic, pulmonic
post-op assessment of atrial switch looks at ventricular function. The RV is the _______ ventricle and LV is the _______ ventricle
decrease RVH, myocardial fibrosis and frequency of late arrhythmia
pros of early surgical repair in TOF
atrial switch
pulmonary veins rerouted to right heart which is connected to Aorta and body. SVC/IVC rerouted to left heart which is connected to PV and lungs
cyanosis
right-to-left shunting at ventricular level through VSD and aorta rather than to the lungs - timing of presentation and degree is dependent on severity of obstruction
parallel
semilunar valves are in ______ and seen in same imaging plane (aorta typically anterior and rightward)
tricuspid
single (semilunar) truncal valve has this anatomy
infundibular
subvalvular RVOTO also referred to as this
pulmonary atresia
the absence of the pulmonary valve, which in turn prohibits blood flow from the right ventricle into the pulmonary artery and essentially to the lungs
PA trunk, PA bifurcation, proximal right and left branches
three locations of supravalvular RVOTO
repair or replace left AV valve, afterload reduction - RV dysfunction, transplant
treatment for CCTGA
regurgitation
truncal valve will more commonly have this problem with it
conotruncal septation
truncus arteriosus anomaly results from the failure of this to form
subpulmonary, infundibulum stenosis
type of RVOTO that is almost ALWAYS present in TOF
congenitally corrected transposition of the great arteries
uncommon, ventricles are switched - morphologic RV is the systemic ventricle on the left side of heart - morphologic LV is the sub pulmonary ventricle on right side of heart
central cyanosis
usually occurs due to right-left shunt through foramen ovale or small ASD
2/3
when RV pressure is _____ systemic = surgery
asymptomatic, no cyanosis, not diagnosed until late adulthood
without any associated lesions the patient is usually these things