Nelson Textbook of Pediatrics 22nd Edition | Hyposplenism/functional asplenia: sickle cell disease (by age 5 years), celiac disease, inflammatory bowel disease, congenital asplenia (Ivemark syndrome). Labs: Howell-Jolly bodies, pits on RBCs. Overwhelming post-splenectomy infection (OPSI): encapsulated bacteria (S. pneumoniae, H. influenzae type b, N. meningitidis). Prevention: vaccinations (PCV13, PPSV23, MenACWY, MenB, Hib) + prophylactic penicillin. Splenic trauma: non-operative management (NOM) in 80-90% of children. Splenectomy indications: severe trauma, refractory immune cytopenias, hereditary spherocytosis (severe), hypersplenism.
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