EXAM 3: Sickle Cell Disease Flashcards

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1
Q

What is sickle cell disease? How does sickle cell disease affect red blood cells?

A

Genetic, multisystem and progressive disease. Causes abnormal, sickled red blood cells (abnormal hemoglobin form strands that cause sickle shape)

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2
Q

What are the complications of sickle cell disease? Most/least common?

A
  • Most common - Pain (sickled cells get stuck when moving through small blood vessels, this can block blood flow)
  • Pulmonary and cardiac complications (acute chest syndrome)
  • Strokes/central nervous system complications (symptomatic stroke, silent stroke)
  • Weakened bones + joints
  • Vision Loss
  • Fertility and pregnancy issues
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3
Q

How does sickle cell disease affect the central nervous system?

A

It affects the central nervous system by causing strokes

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4
Q

What are the recommended lifestyle changes to help manage sickle cell disease?

A
  • Drinking Water (8-10 glasses/day)
  • Avoid getting too hot/cold
  • Avoid high attitudes (e.g., flying)
  • Avoid exposure to low oxygen levels (extreme exercise)
  • Does the prevalence of sickle cell disease vary by race? In what racial group does sickle cell disease most commonly occur?
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5
Q

What psychological functions does sickle cell anemia often effect?

A
  • Low executive function, attention, and processing speed
  • Lower academic achievement
  • Higher sxs of depression + anxiety
  • Lower self-esteem and decreased social activities
  • Lower health-related quality-of-life (HRQol)
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6
Q

What does treatment for sickle cell disease look like?

A
  • Lifestyle/Behavior Change
  • Medical Interventions (Vaccines, antibiotics)
  • Frequent blood transfusions
  • Hydroxyurea
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7
Q

How does sickle cell disease affect red blood cells?

A

Abnormal Hemoglobin forms strands that cause sickle shape

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8
Q

How does sickle cell disease affect acute and chronic pain?

A
  • Acute pain (blockage in blood flow)
  • Chronic (damage from repeated restricted blood flow to tissues
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9
Q

What is transition of care? How does transition of care often effect health for people with sickle cell?

A
  • Transition (18-30) is often difficult
  • Characterized by increasing response + independence (communicating with healthcare providers, making medication decisions, responsiblities for self-care)
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