Complications of Congenital Heart Disease
·
Definition: inability of
myocardium to meet metabolic needs of the body
·
Causes:
o Congential Heart disease:
§ Lesions with left to right shunt: Large VSD (® blood to pump ® overloaded heart), AV canal defect, Patent ductus
§ Left outflow obstruction: Hypoplastic left heart, Coarctation of the
aorta, aortic stenosis
o Arrhythmia: usually SVT
o Cardiomyopathy: Usually ischaemic, due to birth asphyxia
·
Incidence by age:
o Infants: congential heart lesions, rarely arrhythmias (eg SVT)
o > 1 year: cardiomyopathy, right heart disease, dysrhythmias
·
Symptoms of heart failure: respiratory
effort, sweating, poor feeding (no energy to suck), failure to thrive
(hypermetabolic state and poor feeding due to breathlessness)
·
Signs of heart failure:
Tachycardia (160 in infants), tachypnoea (intercostal indrawing, wheeze), gallop
rhythm, hepatomegaly
·
Features not found in children:
o JVP
o Peripheral oedema
o Crepitations in lung fields
·
Key differential to acute onset
is sepsis
·
Treatment:
o Rest
o Diuretics
o Digoxin
o O2
o Adequate calories: fortified feeds
o Treatment of underlying cause (arrhythmias, infections, anaemia, etc)
·
Sequalae of large L ® R shunt
with untreated VSD, PDA or ASD. Rare –
as there usually corrected
·
Usually present in 3rd to 4th decade
·
Pulmonary flow ® oversupply of blood ® pulmonary capillary hypertrophy ® resistance ® pulmonary
hypertension ®:
o Reversal of shunt (R ® L) ® development of cyanosis
o RH hypertrophy and failure
·
Also abnormal flow ® mural
thrombosis ® endocarditis (as in most congenital defects)
·
Clinical:
o Signs of pulmonary hypertension: RV heave, loud P2, hepatomegaly
o Little or no murmur
o Cyanosis, clubbing
·
Prognosis:
o Arrhythmias and sudden cardiac death
o Hb due to
cyanosis (polycythaemia) ® viscosity ® clotting problems
o Risk of
systemic emboli (lungs don‟t act as a filter for emboli)
o Haemoptysis due to pulmonary infarct/haemorrhage
·
Treatment: Supportive or
heart-lung transplant
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