Sickle Cell Anaemia Flashcards

1
Q

What type of disorder is SCA?

A

Autosomal recessive

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2
Q

What is the main risk factor?

A

African descent

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3
Q

What happens in SCA?

A

There is an amino acid substitution in the beta chain resulting in a change from glu to val. This means HbS is produced

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4
Q

How does HbS cause sickling?

A

It polymerises when deoxygenated causing deformation

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5
Q

How do sickle cells cause problems?

A

They’re fragile, haemolyse and block small vessels

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6
Q

Where do vaso-occlusive crises often affect?

A

Bone marrow

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7
Q

What can trigger a vaso-occlusive crisis?

A

Cold, dehydration, infection, hypoxia

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8
Q

What is a sequestration crisis?

A

Pooling of blood in the spleen (and sometimes liver) that leads to severe anaemia and shock

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9
Q

What should you do if your patient is having a sequestration crisis?

A

Urgent transfusion

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10
Q

What investigations could you do?

A

Blood film, Sickle solubility test, Hb electrophoresis, blood count

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11
Q

What does Hb electrophoresis tell you?

A

It confirms diagnosis

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12
Q

What drug would you give if your patient has frequent crises?

A

Hydroxycarbamide

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13
Q

What are signs and symptoms of a crises?

A

Pain in hands and feet, long bone pain, cognitive defects in children, PH and chronic lung disease, splenic sequestration

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14
Q

What would the blood count be?

A

Hb 60-80g per L

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15
Q

Is sickle solubility test positive or negative?

A

Positive

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16
Q

How do you manage general SCA?

A

Folic acid, possible blood transfusions, stem cell transplant

17
Q

How do you treat acute attacks?

A

IV fluids, analgesia, oxygen