CONGENITAL HEART DISEASE
- Acyanotic diseases
• Pulmonary circulation and systemic circulation are not connected
• If there is a connection, the pressure is higher in the left side than in the
right side
PATENT DUCTUS ARTERIOSUS
• Most common congenital heart defect
• Symptoms depend on size of the vessel and age of the child
• May have no symptoms; indication may be a murmur
• Increasing dyspnea, full bounding pulse, wide pulse pressure
• Spontaneous closure after infancy rarely occurs
• Without treatment – life expectancy short
ATRIAL SEPTAL DEFECTS
• 10% of all forms of congenital heart disease
• Allows oxygenated blood returning from the lungs to pass into the right
atrium
VENTRICULAR SEPTAL DEFECT
• constitute 20% of all forms of CHD
• allows systemic venous and oxygenated arterial blood to mix
• may produce no symptoms at all
• require no specific treatment and often close spontaneously
COARCTATION OF THE AORTA
• narrowing of the lumen of the aorta
• may be an isolated defect or associated with other cardiac malformation
• Assessment: measure BP in both arms and a leg and to assess the pulse
in both upper and lower extremities
• surgical repair – only permanent treatment; usually deferred until 3 years
of age
PULMONIC VALVE STENOSIS
• usually do not produce symptoms; typical murmur
AORTIC VALVE STENOSIS
• mild to moderate asymptomatic; typical murmur
CYANOTIC DISEASES
TETRALOGY OF FALLOT
- VSD
- Overriding of the aorta
- Pulmonary valve stenosis
- Enlarged right ventricular wall
Assessment:
• Primary sign – cyanosis
• Hypoxic spells – usually initiated by crying
• Fainting – due to cerebral hypoxia
• Stunted growth, clubbed fingers and toes
• Squatting position – characteristic position to relieve dyspnea
Implementation
• Decrease hypoxic spells – do not permit child to cry
• Place in knee chest position
• O2 as needed
TRANSPOSITION OF THE GREAT VESSELS
• aorta arises from the right ventricle
• degree of cyanosis depends on the abnormal connections
Assessment:
• cyanotic at birth
• develop polycythemia à risk for emboli and thromboses
• may develop CHF or pulmonary vascular obstructive
Implementation:
• require emergency medical treatment
• cardiac catheterization
• ballool atrial septostomy
TRICUSPID ATRESIA
• condition in which tricuspid valve did not form
• no opening between the right atrium and right ventricle
• 2% of congenital heart defects
• profound cyanosis and dyspnea at birth
• emergency catheterization with balloon atrial septotomy
TOTAL ANOMALOUS VENOUS RETURN
• condition in which all the pulmonary venous blood returns to the heart
• cyanosis and severe respiratory distress
• emergency surgical intervention
TRUNCUS ARTERIOSUS
• single vessel arising from the ventricles just above a large VSD
• retarded growth; enlarged liver and heart
• usually infants die within the first year
CARDIOVASCULAR DEFECTS
• Monitor vital signs closely
• Monitor respiratory status
• Auscultate breath sounds for crackles, ronchi or rales
• if respiratory effort is increased, place child in reverse Trendelenburg
position
• administer humidified oxygen
• Monitor for hypercyanotic spells:
- Place infant in a knee chest position
- Administer 100% oxygen by mask
- Administer morphine as ordered
- IVF as prescribed
• Assess for signs of CHF
• Assess peripheral pulses
• Keep child stress free as possible; allow maximal rest
CARDIAC SURGERY
Postoperatively:
• monitor for signs of discomfort
• monitor for signs of sepsis (fever, lethargy, diaphoresis, altered LOC)
• Monitor lines, tubes or catheters ; remove promptly
• administer pain medications; note effectiveness
• encourage rest periods
• facilitate parent-child contact as soon as possible
Home Care
• omit activities in which child could fall for 2-4 weeks
• avoid crowds for 2 weeks after discharge
• no added salt diet
• do not put creams, lotions or powders on the incision site
• child may return to school 3rd week after discharge
• no physical education for 2 months
• follow up after 2 weeks
• avoid immunizations, invasive procedure and dental visits for 2 months
• advise parents regarding importance of dental visit every 6 months
• inform dentist of cardiac problem
• instruct parents to call MD if with coughing, tachypnea, cyanosis, diarrhea
CONGESTIVE HEART FAILURE
• inability of the heart to pump sufficiently to meet the metabolic demands
of the body
• infants – most commonly caused by congenital heart defects
• combination of both left sided and right sided heart failure
• goal of treatment: to improve cardiac function, remove accumulated fluid
and sodium, decrease cardiac demands, improve tissue oxygenation
Assessment:
• tachycardia
• tachypnea
• profuse scalp sweating especially in infants
• fatigue and irritability
• sudden weight gain
• respiratory distress
Implementation:
• monitor vital signs closely and for early signs of CHF
• monitor for respiratory distress
• monitor I and O; weigh diapers
• Monitor daily weight to assess for fluid retention; weight gain of 0.5 kg
( 1 lb /day)
• monitor for facial or peripheral edema , auscultate lung sounds
• elevate HOB
• maintain neutral thermal environment to prevent cold stress in infants
• administer cool, humidified oxygen
• organize nursing activities to allow uninterrupted sleep
• maintain adequate nutritional status
• provide rest; decrease environmental stimuli
• feed when hungry and soon after awakening
• infant should be well rested before feeding
• provide small, frequent feedings
• administer sedation
• administer digoxin
• check with physician parameters for witholding digoxin
• Note that infants rarely receive more than 1 mL (50 ug or 0.05 mg) of digoxin
• Administer diuretics; monitor for hypokalemia
• administer potassium supplements
• monitor serum electrolytes
• restrict fluid in acute stages
• check with physician regarding sodium restriction; infant formulas have slightly
more sodium than does breast milk
Home care Instructions for Administering Digoxin
• administer 1 hr before or 2 hrs after feeding
• do not mix medication with food or drink
• if the child vomits, do not administer a second dose
• if more than 2 consecutive doses have been missed, notify MD; do not
increase or double the dose for missed doses
• keep the medication in a locked cabinet
• if the child becomes ill, notify MD
RHEUMATIC FEVER
• an inflammatory autoimmune disease
• affects connective tissue of the heart, joints, subcutaneous tissues and
blood vessels of the CNS
• most serious complication – RHD affecting the cardiac valves
• presents 2-6 weeks following an untreated Group A beta hemolytic strep
• Jones criteria
Asssessment:
• signs of carditis: SOB, edema of the face, abdomen or ankles, precordial pain
• signs of polyarthritis: edema, inflammation of the large joints, joint pain
• erythema marginatum: macular rash on trunk and extremities
• subcutaneous nodules
• fever
• elevated ASO
• elevated ESR
• elevated CRP
Implementation:
• Assess vital signs
• Control joint pain and inflammation with massage
• Febrile phase – provide bed rest
• limit physical exercise in child with carditis
• Administer antibiotics (penicillin) as prescribed
• administer salicylates and anti-inflammatory agents
• Instruct parents about the importance of follow up and need for
antibiotic prophylaxis for dental work, infection, invasive procedures
• advise child to inform the parents if anyone in school develops a
strep throat infection
KAWASAKI DISEASE
• known as mucocutaneous lymph node syndrome
• acute systemic inflammatory illness
• unknown cause
• cardiac involvement – most serious complication
Assessment:
• fever
• conjunctival injection
• red throat
• Swollen hands, rash, enlargement of the cervical lymph nodes
Implementation:
• monitor temperature frequently
• assess heart sounds and rhythm
• assess extremities for edema, redness, desquamation
• monitor mucus membrane for inflammation
• weigh daily
• administer IV immune globulin
• instruct parents in the administration of prescribed meds
aspirin – need to monitor bleeding
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