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Monday, 29 August 2011

Cardio Pediatrics



CONGENITAL HEART DISEASE

  1. 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
  1. VSD
  2. Overriding of the aorta
  3. Pulmonary valve stenosis
  4. 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:
  1. Place infant in a knee chest position
  2. Administer 100% oxygen by mask
  3. Administer morphine as ordered
  4. 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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