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Physiological AdaptationPlatelets <100k, autoimmune

Immune Thrombocytopenic PurpuraNCLEX cheat sheet

Immune (idiopathic) thrombocytopenic purpura is an autoimmune disorder in which antibodies destroy platelets, leading to a low platelet count and increased bleeding risk.

26 key facts 3 practice questions Reviewed Oct 2026
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Mechanism

  • Autoantibodies destroy platelets
  • Often post-viral in kids

Signs

  • Petechiae, purpura, ecchymoses
  • Epistaxis, gum/mucosal bleeding

Report

  • Intracranial bleed = fatal risk
  • Platelets <20k → high bleed risk

Do

  • Corticosteroids, IVIG first-line
  • Bleed precautions, no NSAIDs
  • Splenectomy if refractory
Red flag to remember

Headache, confusion, or neurologic changes may indicate intracranial hemorrhage, the most feared complication; report immediately.

Before you read

Test yourself first: 3 questions

Question 1 of 3

The nurse reviews a white blood cell count of 22,000/microliter. Which condition is most consistent with this result?

What is immune thrombocytopenic purpura?

It often follows a viral infection in children (usually self-limiting) and is more chronic in adults. The spleen sequesters and destroys the antibody-coated platelets. Hallmark findings are petechiae, purpura, easy bruising, and mucosal bleeding.

Key points to remember

  • Autoantibodies coat platelets, which are then destroyed by the spleen, dropping the platelet count.
  • Skin findings include petechiae, purpura, and ecchymoses; mucosal bleeding (gums, nose) is common.
  • Platelet count is low (often <50,000, sometimes <20,000); PT and aPTT are normal.
  • First-line treatment includes corticosteroids and IV immunoglobulin (IVIG); anti-D may be used in Rh-positive clients.
  • Splenectomy is considered for chronic or refractory disease because the spleen is the main site of platelet destruction.
  • Bleeding risk rises sharply as platelets fall, with spontaneous bleeding likely below about 20,000/mm3.

Signs & symptoms

  • Petechiae, purpura, ecchymoses
  • Epistaxis, gum/mucosal bleeding

Nursing priorities

  1. Implement bleeding precautions: soft toothbrush, electric razor, no IM injections, fall prevention.
  2. Monitor platelet counts and assess skin and mucous membranes for new petechiae, purpura, or active bleeding.
  3. Administer corticosteroids or IVIG as prescribed and monitor response.
  4. Apply prolonged pressure to puncture sites and avoid invasive procedures when possible.
  5. Assess for signs of internal bleeding, including neurologic changes suggesting intracranial hemorrhage.

Labs & values

Platelet count: decreased (often <50,000/mm3; normal 150,000-400,000)
PT and aPTT: normal
Bleeding time: prolonged
Hemoglobin/hematocrit: may be low if bleeding
Platelet antibody testing: may be positive

Patient teaching

  • Avoid aspirin, NSAIDs, and activities with a high injury risk; use acetaminophen for pain.
  • Use a soft toothbrush and electric razor; blow the nose gently and avoid straining.
  • Report any new bruising, petechiae, bleeding, black stools, blood in urine, or headache.
  • If taking corticosteroids, do not stop abruptly and watch for infection and elevated glucose.
  • Wear medical alert identification and prevent falls and bumps.

Red flags: report now

  • Headache, confusion, or neurologic changes may indicate intracranial hemorrhage, the most feared complication; report immediately.
  • Never give aspirin, NSAIDs, or other antiplatelet/anticoagulant medications.
  • Active or uncontrolled bleeding with a very low platelet count requires urgent intervention.

References

Clinical references for this topic

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