Sickle Cell Flashcards

1
Q

What is sickle cell disease?

A

Sickle cell mutliorgan disorder
Chronic vasular disease
Ongoing vaso-occlusion
Self perpetuating cycle of vaso-occlusion and vaso-occlusive crises (VOCs)

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2
Q

How does sickle cell affect the CNS?

A

•Acute Pain is the number one cause of hospital admissions4
•Cerebrovascular accident
–Transient ischemic attack occurs in ~4%5
–Overt stroke occurs in ~16%5
–Silent cerebral infarction occurs in ~20% of children6
–Screen for vascular disease and stroke starting at age 2 years and continuing until at least age 16 years7
•Retinopathy occurs in ~23%5
•Seizures occur in ~12%5

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3
Q

How does SCD affect muscoskeletal?

A
  • Bone pain crisis (~30%) is the most common complication of vaso-occlusive pain, and can lead to bone or bone marrow infarction and osteonecrosis8,9
    • Avascular necrosis: 21%1
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4
Q

How does SCD affect cardiopulmonary ?

A
  • Acute chest syndrome(ACS) occurs in ~75%5
    • Pulmonary hypertensionoccurs in ~20%6
    • Left-sided heart diseaseoccurs in ~13%6
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5
Q

How does SCD affect reticuloendothelial?

A

Splenic sequestration, which occurs in ~50% of patients who survive their first episode and can worsen anemia

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6
Q

How does SCD affect Gastrointestinala and urogential?

A

Gastrointestinal
•Cholelithiasis, acute cholecystitis, biliary sludge, and acute choledocholithiasis are common7
•Gallstones occur in ~75%7
Urogenital
•Renal dysfunction begins at an early age, and ~30% experience chronic renal failure6
•Priapism occurs in ~35% of men1

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7
Q

What are social impacts of SCD?

A

Can experience PTSD, axiety, depression
Missed work/school/education
Stay at home os lose social interactions, not feeling like fit in
Overt and/or silent stroke may affect cognitive function e.g. memory impairment, communication skills Hospitalisation
ER visits

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8
Q

What are other impacts of SCD and how many are affected?

A
SCD (African Caribbean): sepsis, organ failure, vomit, temperature 
Diarrhoea vomiting fever 
15,000 in UK 
Pain and wait 
Staff shortages so not getting care
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9
Q

What are some symptoms of SCD?

A
  • Anemia
  • Repeated infections
  • Periodic episodes of pain
  • Frequent hospitalisation
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10
Q

What is the blood like in SCD?

A

Sickle shaped cells not flexible and so stick to vessel walls causing blockage and so oxygen unable to reach nearby tissues
Affects haemoglobin
Cells break down prematurely
High bp

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11
Q

What are causes of SCD?

A
  • Mutation in HBB gene

- beta globin mutation HbS (at least one beta globin subunits replaced with HbS for sickle cell both are replaced

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12
Q

What is there bone crisis in SCD?

A
  • Bone marrow ischemia or infraction of synovium
  • with acute bone pair crisis, fever, leukocytosis and warmth and tenderness around affected joints
  • Vaso-occlusive bone pain (when circulation of blood vessels obstructed causing iscoemic injuries
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13
Q

Why is there visual loss in SCD?

A
  • Blockage in small blood vessels in inner lining of retina of the eyes
  • deprive eye of oxygen
  • Sickle retinopathy
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14
Q

Why is there a stroke in SCD?

A
  • Blockage of arteries in brain - overtime damage lining and affect big ones
  • Form collaterals to compensate but these are fryable, leaky susceptible to damage and not as good as the OG - they “by[pass” area of narrowing and help to restore blood flow
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15
Q

What is ischaemia?

A

an inadequate blood supply to an organ or part of the body, especially the heart muscles.

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16
Q

What is infraction?

A

obstruction of the blood supply to an organ or region of tissue, typically by a thrombus or embolus, causing local death of the tissue.