new presentation notes for chd

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    Cyanosis

    What is cyanosis and how you would identify it?

    Porth, (2002:1449) says that cyanosis is a bluish discolouration,

    especially to the skin and mucous membranes, caused by an excess of

    deoxygenated haemoglobin in the blood.

    It is important for the nurse to distinguish between cardiopulmonary and

    respiratory causes ensures effective management.

    Hypoxemia test can be instigated

    Administer 100% high-pressured oxygen for ten minutes. If the infant

    responds and its colour becomes pink then cardiopulmonary causes are

    discounted (McConnell & Elixson, 2002). In addition to this, arterial

    blood gases should be monitored.

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    Transposition of the great vessels

    The great vessels of the heart include the aorta and the pulmonary artery.

    In the transposition of the great vessels the aorta and pulmonary artery are

    reversed (McConnell & Elixson, 2002). Hence:

    The pulmonary artery is connected to the left ventricle instead of

    the right ventricle.

    The aorta is connected to the right ventricle instead of the left

    ventricle.

    This means two things:

    That unoxygenatated blood returning from the body to the heart

    misses out on getting oxygenated and gets pumped directly into the

    system via the aorta what would happen?

    Oxygenated blood returning from the lungs gets pumped back to

    the lungs again what may happen with this?

    In the infant with transposition of the great arteries Reddy (2002) claim

    that the closure of the patent ductus arteriosus will cause a rapid onset of

    cyanosis and tachypnoea. It is an emergency. Infants with the

    transposition of the great vessels will not survive unless there is another

    defect in the form of a patent ductus arteriosus (Muscari).

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    What is a patent ductus arteriosis?

    The initial breath at birth induces the circulatory switch from placental to

    pulmonary oxygenation of blood. Prior to this, blood in the foetal heartbypasses the lungs and flows across the left and right ventricles to the

    systemic circulation via openings called the ductus arteriosus and the

    foramen ovale (Porth, 2002:522).

    Within the first 24 to 72 hours of life, the switch to pulmonary

    oxygenation of blood causes these openings to close, thereby separating

    the ventricles into the pulmonary and systemic circulations (Porth,

    2002:524).

    Emergency medical care for infants with the transposition of the great

    arteries is focused on maintaining the patent ductus arteriosus by

    administering intravenous Prostaglandin E.

    This procedure may cause apnoea. Hence the nurse must prepare for an

    intubation procedure (McConnell & Elixson, 2002).

    Surgical treatment is arterial switch. Preferably performed within the

    first two weeks of life. If conditions do not permit this, then an atrial

    switch is performed, however, this operation has a much higher long-term

    morbidity rate (Porth, 2002:528).

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    Tetralogy of Fallot

    The tetralogy of Fallot is the most common cyanotic heart defect (Pretre

    et al., 2001).

    It is a complex congenital heart disorder that consists offour linked

    congenital heart defects.

    These include,

    A ventricular septal defect,

    Right ventricular hypertrophy causing right to left shunting of

    unoxygenated blood. Which leads to cyanosis and hypoxemia.

    Obstruction of the pulmonary outflow channel including

    pulmonary stenosis. Also leads to decreasing oxygenated blood.

    An aorta overriding the ventricular defect.

    What happens?

    The obstruction of the pulmonary outflow and pulmonary stenosis

    causes the right ventricle to work harder (Porth, 2002:527).

    This leads to hypertrophy of the right ventricle.

    Right to left shunting through the ventricles causes mixing of

    oxygenated blood and unoxygenated blood. This causes decrease inoxygenated blood to systemic circulation.

    Also decrease in pulmonary blood, which causes hypoxemia and

    cyanosis (Suddaby, 2001).

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    Signs and Symptoms of Tetralogy of Fallot

    Infants with the tetralogy of Fallot will display some cyanosis at birth.

    As pulmonary obstruction and ventricular hypertrophy increase, cyanosis

    will become more severe, and they will experience hypercyanotic or tet

    spells

    These will be evident in the infants first months of life and continue into

    childhood. Pfleiger, (2005).

    What are tet spells?

    Activities that increase oxygen requirements such as crying, feeding,

    defaecating

    Increase pulmonary vascular resistance.

    Right to left shunting

    Decreases pulmonary blood flow.

    What signs and symptoms do we see?

    Child becomes acutely cyanotic.

    Hyperpneic (increase to rate of breath in proportion to rate of

    metabolism)

    Irritable

    Diaphoretic

    As spell progresses child will become limp and may lose consciousness.

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    What do we do?

    Place child in knee to chest position increases vascular systemic

    resistance and increases pulmonary blood flow.

    Older children may naturally assume these positions.

    Surgical Management of Tetralogy of Fallot

    Palliative surgery designed to increase pulmonary blood flow and

    decrease hypoxemia. A shunt to increase pulmonary blood flow called

    Blalock-Taussig shunt

    Corrective surgery carried out later on in childhood is cardiopulmonary bypass and

    aortic cross-clamping will be necessary.