Sepsis is an important cause of pediatric morbidity and mortality. Improvin
g the outcome of pediatric sepsis requires diverse efforts, including preve
ntion, early recognition, improvements in early management and transport, a
nd physiology-directed care. Awareness that septic shock represents a patho
physiologic host response to infection has prompted investigation of immune
mediators and coagulation factors as potential targets for anti-sepsis the
rapies. Advancements thus far include: the potential prevention of neonatal
sepsis with granulocyte colony-stimulating factor; recognition of clindamy
cin as a potential inhibitor of endotoxin release; improved outcome from me
ningococcal disease in children treated with bactericidal/permeability-incr
easing protein (rBPI(21)); and improved outcome from sepsis in premature in
fants treated with pentoxifylline. Further randomized controlled studies of
immunomodulatory agents are indicated and a few are in progress. Current s
tudies on genetic propensities in cytokine and coagulation protein expressi
on may explain variability in patient outcomes and eventually lead to genom
ics-based therapeutics. Curr Opin Infect Dis 13:253-258. (C) 2000 Lippincot
t Williams & Wilkins.