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Obstruction of Blood Flow
Obstruction of Blood Flow
a. PULMONARY STENOSIS
Narrowing of the pulmonary valve or the pulmonary artery just distal to the valve
10% of congenital anomalies
Inability of the right ventricle to evacuate blood by way of the pulmonary artery because
of the obstruction leads to right ventricular hypertrophy.
Assessment:
Cyanosis – if narrowing is severe
Due to inability of the blood to reach the lungs for oxygenation or there is right-left shunting
across the foramen ovale-------this happens because of the increase pressure at the right side
of the heart
Systolic ejection murmur ( grade IV or V crescendo-decresendo in quality) loudest at the
upper left sterna border radiating to the suprasternal border.
Thrill- from the upper left sterna border or at suprasternal notch.
Widely split of the 2nd heart sound ------because of late closure f the pulmonary valve.
Diagnosis:
ECG/ echocardiography- reveal ventricular hypertrophy
Cardiac catheterization – used for interventional enlargement of the stenosed valve
Therapeutic Management:
Balloon angioplasty – procedure of choice
A catheter with an uninflated balloon at its tip is inserted and passed through the heart into the
stenosed valve
As the balloon is inflated, it breaks the valve adhesions and relieves the stenosis.
Children may have residual heart murmur
Can expect a normal life span
b. AORTIC STENOSIS
Stenosis or stricture of the aortic valve prevents blood from passing freely from the left
ventricle of the heart into the aorta.
Because the heart cannot force blood through the stricture valve
increased pressure and hypertrophy of the left ventricle occur
if the left ventricular pressure become acute----- increase
pressure in the left atrium back pressure in pulmonary veins pulmonary edema
Assessment:
Asymptomatic
Murmur- can be transmitted to the right shoulder, clavicle and up the vessels of the neck, heart
apex
Rough systolic sound heard loudest in the 2 nd right interspace ( aortic space)
Thrill- at suprs sterna notch
Decreased cardiac output - if severe
Faint pulses
Hypotension
Tachycardia
Inability to suck for long periods
Chest pain similar to angina
Because the coronary arteries receive inadequate amount of oxygen needed by the heart
muscle on exertion far exceeds what is available
Diagnosis
ECG/echocardiography – reveal left ventricular hypertrophy
Therapeutic Management:
Beta-blocker/calcium channel blocker---to reduce cardiac hypertrophy before the defect is
corrected
Balloon valvuloplasty – treatment of choice
Dividing the stenotic valve r dilating an accompanying constrictive aortic ring
May lead to aortic valve insufficiency later in life—further surgery may be needed
Some children will need artificial valve replacement for correction
If prosthetic valve is used---- continue to receive anticoagulation or antiplatelet therapy and
antibiotic prophylaxis against endocarditis
Children need exercise testing before participating in competitive sports if an artificial valve is
in place.
c. COARCTATION OF AORTA
Narrowing of the lumen of the aorta due to constricting band
Occurs most frequently in boys than in girls
Leading cause of congestive heart failure in the first few months of life.
2 Locations:
Preductal – the constriction occurs between the subclavian artery and the ductus arteriosus
Postductal – constriction is distal to the ductus arteriosus
Difficult for blood to pass through the narrowed lumen of the aorta
Blood pressure increases proximal to the coarctation decreases distal
Increased BP in the heart and upper portions of the body as pressure in the subclavian
artery increases
headache, vertigo
epistaxis (nose bleed)
cerebrovascular accident
Assessment:
Absence of palpable femoral pulses- slight coarctation
Always include evaluation of femoral pulses in all initial newborn assessment and admission
inspections
Absent brachial pulses – those with an obstruction proximal to the left subclavian artery
Lower BP in the lower extremities
Leg pain on exertion
Because of diminished blood supply to the lower extremities
Cold feet
Muscle spasms
Pulse is weak, delayed or even absent
Collateral arteries enlargement
Seen on the ribs as obvious nodules as the child grows older
Soft, moderately loud systolic murmur – from the base of the heart and transmitted to the left
interscapular area
BP is higher in upper extremities---because of the pull of gravity
Headache
Epistaxis
Pulse in the upper extremities will be rapid and bounding
Diagnosis:
BP in the arms will be at least 20mmHg higher than in the legs
Echocardiography
ECG – reveal left-sided heart enlargement from
MRI – back pressure and also notching of the
X-ray – ribs from the enlarge collateral vessels.
Therapeutic Management:
Interventional angiography ( balloon catheter)/surgery
The narrowed portion of the aorta is removed and the new ends of aorta are anastomosed
A graft of transplanted subclavian artery may be necessary if the narrowed section is so
extensive than an anastomosis cannot be accomplished readily
Digoxin – given before the time of surgery
Diuretics – aims to reduce the severity of congestive heart failure
from hypertension
PLANNING IS IMPORTANT:
It would be ideal if children could achieve the greater part of their adult height before surgical
correction, preventing strain on the incision site as they grow
In terms of self-image – correction is best done before children begin to think of themselves as
chronically ill or before they develop complications such as chronic hypertension.
Girls must have the defect repaired before childbearing age –or the extra blood volume during
pregnancy can cause heart failure
Surgical repair is scheduled by 2 years of age
After operation – abdominal vessels receives more blood resulting to abdominal pain or
generalized abdominal discomfort
Some may have elevated upper body hypertension after the repair
Need continual treatment with antihypertensive agents
Some may require repeat balloon angioplasty at adolescence to re-enlarge the aortic lumens
and help reduce this upper body hypertension.