NURS 6501: Final Exam:
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In a pediatric patient with severe immune thrombocytopenic purpura (ITP) and a platelet count below 10,000/µL, why are intravenous immunoglobulin (IVIG) and steroids typically given, while platelet transfusions are reserved for life-threatening bleeding?
Group of answer choices
- Platelets are almost immediately destroyed by the autoimmune process.
- Platelet transfusions can worsen the thrombocytopenia.
- IVIG and steroids directly increase platelet production.
- Platelets can induce an allergic reaction.
- IVIG:
- Blocks Fc receptors in the spleen/liver, preventing platelet destruction.
- Provides a rapid but temporary rise in platelet count (within 24–48 hours).
- Steroids (e.g., prednisone):
- Suppress antibody production and reduce splenic clearance of platelets.
- Slower onset but more sustained effect than IVIG.
- Platelet transfusions:
- Not first-line because transfused platelets are quickly destroyed by the same autoimmune process.
- Reserved for severe bleeding (e.g., intracranial hemorrhage).
- "Platelet transfusions worsen thrombocytopenia": Incorrect—they don’t exacerbate the disease but are ineffective due to rapid destruction.
- "IVIG/steroids directly increase production": No—they reduce destruction (bone marrow production is usually normal in ITP).
- "Platelets induce allergic reactions": Rare and unrelated to ITP pathophysiology.
