Congenital Heart Disease

Congenital Heart Disease

Congenital heart disease (CHD)
occurs in 1/125 live births.
most common birth defect
occur during the 1st 8 wks. of fetal
development
majority have no known cause
 Factors Contributing to CHD
85 to 90 % of cases, there is no identifiable cause for the
heart defect generally considered to be caused by
multifactorial inheritance.
factors are usually both genetic and environmental, where a
combination of genes from both parents, in addition to unknown
environmental factors, produce the trait or condition.
Maternal Factors:
seizure disorders w/ intake of anti-seizure medications
intake of lithium for depression
uncontrolled IDDM
lupus
german measles (rubella) 1st trimester of pregnancy
 Factors Contributing to CHD
Family History:
risk increases when either parent has CHD, or when another
sibling was born w/ CHD
If you have had one child with CHD, the chance that another child will
be born with CHD ranges from 1.5 to 5 %, depending on the type of CHD
in the first child.
If you have had two children with CHD, then the risk to 5 to 10 %, to
have another child with CHD.
If the mother has CHD, the risk for a child to be born with CHD ranges
from 2.5 to 18 percent, with an average risk of 6.7 percent.
Chromosome abnormalities:
5 to 8 % of all babies with CHD have a chromosome abnormality
includes Down syndrome, trisomy 18 and trisomy 13, Turners
syndrome, Cri-du-chat syndrome
Fetal circulation:
Blood flows from
the placenta
IVC
RA
through the FO
LA
LV
ascending aorta
head & upper
extremities
returns via the
SVC
Fetal circulation:
From the SVC
RA
RV
pulm artery
through the PDA
descending
aorta
lower extremities
and placenta
Fetal circulation:
Only a very small amount
of blood is directed
through the right and
left pulmonary
arteries to the lungs.
 Blood circulation after birth:

The transformation from fetal to neonatal

circulation involves two major changes:
1. A marked increase in systemic resistance.
caused by loss of the low-resistance
placenta.
2. A marked decrease in pulmonary resistance.
caused by pulmonary artery dilation with the
neonates first breaths.
Fetal Circulation 8 Hours old 24-72 hrs
 Blood circulation after birth:

With the first breaths of air the baby takes at birth, the
fetal circulation changes. A larger amount of blood is sent to
the lungs to pick up oxygen.
Because the ductus arteriosus (the normal connection
between the aorta and the pulmonary valve) is no longer
needed, it begins to wither and close off. (72 hrs.)
The circulation in the lungs increases and more blood flows
into the left atrium of the heart pressure causes the
foramen ovale to close and blood circulates normally
 Acyanotic Congenital Heart Defects

Pink Baby (L R shunt)

L R shunts cause CHF and pulmonary hypertension.

This leads to RV enlargement, RV failure
These babies present with CHF and respiratory
distress.
They are not typically cyanotic
Examples: Patent Ductus Arteriosus (PDA)
Ventricular Septal Defect (VSD)
Atrial Septal Defect (ASD)
Coarctation of the Aorta
 Cyanotic Congenital Heart Defects

Blue Baby (R L shunt)

R L shunts cause hypoxia and central cyanosis.
Venous blood is shunted from the R to the L side of
the heart w/o passing through the lungs to be
oxygenated
Unoxygenated blood circulates in arteries
cyanosis
Examples:
Tetralogy of Fallot (TOF)
Transposition of the Great Arteries (TGA)
Truncus Arteriosus (TA)
Tricuspid Atresia
 Atrial Septal Defect (ASD)
an opening in the atrial septum
An atrial septal defect allows oxygenated (red) blood to pass from
the left atrium, through the opening in the septum, and then mix
with unoxygenated (blue) blood in the right atrium
During fetal heart devt. the partitioning process does not occur
completely, leaving an opening in the atrial septum
occur in 4-10% of all infants w/ CHD

EFFECTS: When blood passes through the ASD from the left
atrium to the right atrium a larger volume of blood than normal
must be handled by the right side of the heart extra blood then
passes through the pulmonary artery into the lungs pulmonary
hypertension and pulmonary congestion
Atrial Septal Defect (ASD)
 Atrial Septal Defect (ASD)
Signs and Symptoms
child tires easily when playing
infant tires easily when feeding
fatigue
sweating
tachypnea, tachycardia
shortness of breath, crackles
poor growth
murmur
Diagnostic tests:
- CXR enlarged heart
- ECG
- 2D echo show pattern of blood flow through the septal
opening, det. how large the opening
 Atrial Septal Defect (ASD)

20% of atrial septal defects will close spontaneously in the

first year of life.
atrial septal defects may close spontaneously as a child
grows
Usually, an ASD will be repaired if it has not closed on its
own by the time the child starts school - to prevent lung
problems that will develop from long-time exposure to extra
blood flow
pulmonary arteries become thickened and obstructed due to
increased flow, from left to right for many years (pulmonary
vascular obstructive disease)
 Treatment
medical management
digoxin - helps strengthen the heart muscle, enabling it to
pump more efficiently.
diuretics relieve pulmonary congestion
infection control
- prophylactic antibiotics to prevent bacterial endocarditis before
dental procedures and other invasive procedures
surgical repair
- the patient is placed on cardiopulmonary bypass (the heart-lung
machine), the right atrium is then opened to allow access to the
atrial septum below
- defect may be closed with stitches or a special patch.
- the material utilized for patch closure of ASDs may be the
patients own pericardium, commercially available bovine
pericardium, or synthetic material (Gore-Tex, Dacron)
Treatment

Transcatheter management
This technique involves implantation
of one of several devices (basically
single or double wire frames covered
by fabric) using cardiac
catheterization
cardiac catheterization - involves
slowly moving a catheter (a long, thin,
flexible, hollow tube) into the heart.
The catheter is initially inserted into
a large vein through a small incision
made usually in the inner thigh (groin
area) and then is advanced into the
heart
 An ASD closure device is
moved through the catheter
to the heart and specifically
to the location of the heart
wall defect
Within a few days, the bodys
own tissue will begin to grow
over the device. By 3 to 6
months, the device is
completely covered by heart
tissue and at that point
becomes a part of the wall of
the patients heart.
Example of Closure Device

Amplatzer Septal Occluder

Example of Closure Device

CardioSEAL Occluder
 Coarctation of the Aorta
Narrowing of the aorta
can occur anywhere, but is most likely to happen in the segment just
after the aortic arch. This narrowing restricts the amount of blood
to the lower part of the body
occurs in about 8-11 % of all children with CHD
EFFECTS:
The left ventricle has to work harder to try to move blood through
the narrowing in the aorta left-sided heart failure
BP is higher above the narrowing, and lower below the narrowing.
Older children may have headaches from too much pressure in the
vessels in the head, or cramps in the legs or abdomen from too
little blood flow in that region.
The walls of the arteries may become weakened by high pressure
spontaneous tears cause a stroke or uncontrollable bleeding.
risk for bacterial endocarditis.
 Signs and Symptoms

irritability
pale skin
sweating
heavy and/or rapid breathing
poor feeding
poor weight gain
cold feet and/or legs
diminished or absent pulses in the feet
BP in the arms significantly greater than the BP in the legs
Mild narrowing may not cause symptoms at all. Often, a school-
aged child or adolescent is simply noted to have high BP or a
heart murmur on a physical examination. Some may complain of
headaches or cramps in the lower sections of the body.
 Treatment
interventional cardiac catheterization
- During the procedure, the child is sedated and a small, thin,
flexible tube (catheter) is inserted into a blood vessel in the groin
and guided to the inside of the heart
- once the catheter is in the heart, the cardiologist will pass an
inflated balloon through the narrowed section of the aorta to
stretch the area open.
- A small device, called a stent, may also be placed in the narrowed
area after the balloon dilation to keep the aorta open.
surgical repair
Your child's coarctation of the aorta may be repaired surgically in
an operating room. The surgical repair is performed under GA. The
narrowed area is either surgically removed, or made larger with
the help of surrounding structures or a patch.
 Patent Ductus Arteriosus (PDA)
characterized by a connection between the aorta and the
pulmonary artery
All babies are born with a ductus arteriosus.
As the baby takes the first breath, the blood vessels in the
lungs open up, and blood begins to flow the ductus
arteriosus is not needed to bypass the lungs
Most babies have a closed ductus arteriosus by 72 hours
after birth.
In some babies, however, the ductus arteriosus remains open
(patent) .
The opening between the aorta and the pulmonary artery
allows oxygenated blood to pass back through the blood
vessels in the lungs.
PDA occurs in 6-11 % of all children with CHD
 Patent Ductus Arteriosus (PDA)
In many children, there is no known reason for the ductus
arteriosus remaining open. However, PDA is seen more often
in the following:
premature infants
infants born to a mother who had rubella during the first
trimester of pregnancy
EFFECTS:
PDA oxygenated blood passes from the aorta to the
pulmonary artery & mixes w/ the unoxygenated blood w/c
goes to the lungs blood volume to the lungs
pulmonary hypertension & congestion
Further, because blood is pumped at high pressure through
the PDA, the lining of the pulmonary artery will become
irritated and inflamed. Bacteria in the bloodstream can
easily infect this injured area bacterial endocarditis.
Signs and Symptoms

fatigue
sweating
tachypnea
shortness of breath
congested breathing
disinterest in feeding, or tiring while feeding
poor weight gain
murmur
increase systolic BP
bounding pulse
 Treatment
Medical Management
Indomethacin IV (prostaglandin inhibitor) may help close a PDA.
- works by stimulating the muscles inside the PDA to
constrict, thereby closing the connection
Digoxin
Diuretics
adequate nutrition
(premature infants or those infants with a large PDA may become
tired when feeding, and are not able to eat enough to gain weight)
high-calorie formula or breast milk
Special nutritional supplements may be added to formula or
pumped breast milk that increase the number of calories in each
ounce, thereby allowing your baby to drink less and still consume
enough calories to grow properly.
Treatment

supplemental tube feedings

- infants who can drink part of their bottle, but not all, may
be fed the remainder through the feeding tube
- infants who are too tired to bottle-feed may receive their
formula or breast milk through the feeding tube alone.
PDA surgical repair or closure
- Repair is usually indicated in infants younger than 6 months
of age who have large defects that are causing
symptoms, such as poor weight gain and rapid breathing
- Transcatheter coil closure of the PDA
- PDA ligation
- involves closing the open PDA with stitches or the
vessel connecting the aorta and pulmonary artery may
be cut and cauterized
 Ventricular Septal Defect (VSD)

an opening in the ventricular septum

allows oxygenated blood to pass from the left ventricle,
through the opening in the septum, and then mix with
unoxygenated blood in the right ventricle.
VSDs are the most commonly occurring type of congenital
heart defect, occurring in 14-17 % of babies born each year.
occur when the partitioning process does not occur
completely, leaving an opening in the ventricular septum.
 Ventricular Septal Defect (VSD)

EFFECTS:
When blood passes through the VSD from the left ventricle
to the right ventricle a larger volume of blood than
normal must be handled by the right side of the heart
extra blood then passes through the pulmonary artery into
the lungs pulmonary hypertension and pulmonary
congestion pulmonary arteries become thickened and
obstructed due to increased pressure
If VSD is not repaired, and lung disease begins to occur
pressure in the right side of the heart will eventually exceed
pressure in the left R to L shunt cyanosis
Due to high pressure --- tissue damage may eventually occur
in the right ventricle bacteria in the bloodstream can
easily infect this injured area bacterial endocarditis.
Signs and Symptoms

fatigue
sweating
tachypnea
murmur
heavy breathing
congested breathing
disinterest in feeding, or tiring while feeding
poor weight gain
The larger the opening, the greater the amount of blood
that passes through and overloads the right ventricle and
lungs.
Treatment

Medical management
- digoxin
- diuretics
Adequate nutrition
- high-calorie formula or breast milk
- supplemental tube feedings
Prophylactic antibiotics to prevent bacterial endocarditis
Surgical repair VSD will be closed w/ stitches or special
patch
Interventional cardiac catheterization Septal occluder
 Tetralogy of Fallot (TOF)
a complex condition of several congenital defects that occur due
to abnormal devt. of the fetal heart during the first 8 weeks of
pregnancy. These problems include the following:
1. ventricular septal defect (VSD)
2. Pulmonary valve stenosis
3. overriding aorta - The aorta sits above both the left and right
ventricles over the VSD, rather than just over the left
ventricle. As a result, oxygen poor blood from the right
ventricle can flow directly into the aorta instead of into the
pulmonary artery to the lungs.
4. Right ventricular hypertrophy - The muscle of the right
ventricle is thicker than usual because of having to work harder
than normal.
 Tetralogy of Fallot (TOF)
EFFECTS:
If the right ventricle obstruction is severe, or if the
pressure in the lungs is high a large amount of oxygen-
poor (blue) blood passes through the VSD, mixes with the
oxygen-rich (red) blood in the left ventricle, and is pumped
to the body cyanosis
The more blood that goes through the VSD, the less blood
that goes through the pulmonary artery to the lungs
oxygenated blood to the left side of the heart.
Soon, nearly all the blood in the left ventricle is oxygen-poor
(blue). This is an emergency situation, as the body will not
have enough oxygen to meet its needs.
Signs and Symptoms

Cyanosis (blue color of the skin, lips, and nail beds) that
occurs with such activity as crying or feeding
Some babies do not have noticeable cyanosis, but may
instead be very irritable or lethargic due to a decreasing
amount of oxygen available in the bloodstream.
Murmur
Tachycardia
Irritability
Syncope
Clubbing of fingers
 Treatment
Tetralogy of Fallot is treated by surgical repair of the defects.
A team of cardiac surgeons performs the surgery, usually
before an infant is 1 year old. In many cases, the repair is made
at around 6 months of age, or even a little earlier. Repairing the
heart defects will allow oxygen-poor (blue) blood to travel its
normal route through the pulmonary artery to receive oxygen.
The operation is performed under general anesthesia, and
involves the following:
The ventricular septal defect is closed with a patch.
The obstructed pathway between the right ventricle and the
pulmonary artery is opened and enlarged with a patch. If the
pulmonary valve is small, it may be opened as well.
 Transposition of the Great Arteries (TGA)
the aorta is connected to the right ventricle, and the pulmonary
artery is connected to the left ventricle
Oxygen-poor (blue) blood returns to the right atrium from the
body passes through the right atrium and ventricle, into
the misconnected aorta back to the body.
Oxygen-rich (red) blood returns to the left atrium from the
lungs passes through the left atrium and ventricle, into the
pulmonary artery and back to the lungs.
Other heart defects are often associated with TGA
- atrial or ventricular septal defect
- may be necessary in order for the infant with TGA to survive
- Allow mixing of blood providing at least smaller amounts of
oxygen to the body
 Signs and Symptoms

Cyanosis soon after delivery

rapid breathing
labored breathing
rapid heart rate
murmur
cool, clammy skin
 Treatment
admitted to the NICU, placed on oxygen, and possibly even on a
ventilator, IV medications to help the heart and lungs function
more efficiently.
a cardiac catheterization procedure will usually be performed to
evaluate the defect(s) and the amount of blood that is mixing.
as part of the cardiac catheterization, a balloon atrial septostomy
may be performed to improve mixing of oxygen-rich (red) and
oxygen-poor (blue) blood.
A catheter with a balloon in the tip is used to create an opening in
the atrial septum
The catheter is guided through the foramen ovale (a small opening
present in the atrial septum that closes shortly after birth) and into
the left atrium.
The balloon is inflated.
The catheter is quickly pulled back through the hole, into the right
atrium, enlarging the hole, allowing blood to mix between the atria.
 Treatment
An IV prostaglandin E1 is given to keep the ductus arteriosus from
closing.
Within the first 1 to 2 weeks of age, TGA is surgically repaired.
The switch operation is performed under GA, and involves the ff:
The aorta is moved from the right ventricle to its normal position
over the left ventricle.
The pulmonary artery is moved from the left ventricle to its
normal position over the right ventricle.
The coronary arteries are moved so they will originate from the
aorta and take oxygen-rich (red) blood to the heart muscle.
Other defects, such as atrial or ventricular septal defects or a
patent ductus arteriosus, are commonly closed.
 Truncus Arteriosus
The aorta and pulmonary artery start as a single blood vessel,
which eventually divides and becomes two separate arteries.
Truncus arteriosus occurs when the single great vessel fails to
separate completely, leaving a connection between the aorta and
pulmonary artery.
Usually accompanied by a ventricular septal defect
EFFECTS:
oxygen-poor (blue) and oxygen-rich (red) blood mix back and forth
through the ventricular septal defect.
This mixed blood then flows through the common truncal vessel.
Some of it will flow to pulmonary artery and on to the lungs, and
some of the mixed blood will go into the aortic branch and to the
body.
The mixed blood that goes to the body does not have as much
oxygen as normal, and will cause varying degrees of cyanosis
Signs and Symptoms

cyanosis
fatigue
sweating
pale skin
cool skin
rapid breathing
heavy breathing
rapid heart rate
congested breathing
disinterest in feeding, or tiring while feeding
poor weight gain
 Treatment
Truncus arteriosus must be treated by surgical repair of the
defects. However, medical support may be necessary until the
best time for the operation to take place.
medical management
Digoxin
Diuretics
ACE (angiotensin-converting enzyme) inhibitors - dilates the
blood vessels, making it easier for the heart to pump blood
forward into the body.
adequate nutrition
high-calorie formula or breast milk
supplemental tube feedings
Treatment

surgical repair
Surgery is usually performed after the infant is 2 weeks old,
but before the blood vessels in the lungs are overwhelmed
by extra blood flow and become diseased.

The operation is performed under general anesthesia, and

involves the following:
The pulmonary arteries are detached from the common
artery (truncus arteriosus) and connected to the right
ventricle using a homograft (a section of pulmonary
artery with its valves intact from a tissue donor).
The ventricular septal defect is closed with a patch.
 Tricuspid Atresia

In this condition, there is no tricuspid valve, therefore, no

blood flows from the right atrium to the right ventricle.
Blood in right atrium foramen ovale left atrium and
left ventricle aorta
Tricuspid atresia defect is characterized by the following:
a small right ventricle
a large left ventricle
Small VSD and PDA
diminished pulmonary circulation
cyanosis - bluish color of the skin and mucous membranes
caused from a lack of oxygen.
A surgical shunting procedure is often necessary to increase
the blood flow to the lungs.