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Sickle Cell Disease

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Sickle cell disease (SCD) is a serious, genetic (inherited) condition affecting the blood and various organs in the body. It affects the red blood cells, causing them to change shape, known as 'sickling' or 'crisis', producing episodes of pain and other symptoms.

6 Modules1 hour
$169$0
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Sickle Cell Disease
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Learning Outcomes

What you'll learn

  • Describe how SCD is caused
  • Identify common symptoms of SCD
  • Describe how sickling occurs
  • Recognise the similarities and differences between sickle cell disease and sickle cell trait
  • Explain how to prevent crisis
  • Describe common treatments for SCD
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Modules

  • What is Sickle Cell Disease?
  • What Causes SCD?
  • Symptoms
  • Treatment
  • Living With SCD
  • Summary
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Frequently Asked Questions

Sickle cell disease (SCD) is an inherited blood disorder that causes red blood cells to become rigid and sickle-shaped, potentially leading to anaemia, pain and other complications.

Common symptoms include episodes of severe pain, fatigue, anaemia, swelling of the hands and feet, jaundice and increased risk of infections.

Sickle cell disease can cause significant health problems, while sickle cell trait usually does not cause symptoms. This course explores the key differences between the two.

Following an individual care plan, staying hydrated, avoiding known triggers and taking prescribed treatments can help reduce the risk of sickle cell crises.

Management may include pain relief, medicines, vaccinations, infection prevention and other treatments based on individual needs. Australian healthcare workers should follow clinical guidance and care plans.