Multiple trauma often leads to systemic inflammatory reaction and mult
iple organ dysfunction. Modulation of this response may be promising.
Several pharmacologic approaches, such as antioxidants (e.g. superoxid
edismutase), calcium channel blockers (e.g. diltiazem), cytokines (e.g
. interferone gamma), and modulators of intracellular signal transduct
ion pathways (e.g. pentoxiphylline) have been shown to improve outcome
in experimental models and/or in clinical pilot studies. However, up
to now no defintive evidence has been provided in prospective, randomi
zed, and blinded ''intention to treat'' trials that these agents are a
ble to reduce mortality and morbidity of the traumatized patient. Henc
e, supportive care of failing organs, treatment of hypoxemia and maint
enance of an appropriate systemic blood pressure remain the mainstay o
f critical care therapy. Widely accepted therapeutic measures are (i)
immediate treatment of hypoxia by administration of oxygen and ventila
tory support, if needed, to maintain an oxygen tension of 60 mmHg or h
igher (ii) maintenance of adequate oxygen content by transfusion of re
d packed cells in order to restore a hematocrit of 23-30% (iii) treatm
ent of hypovolemia by infusion of crystalloids, colloids and blood pro
ducts (iv) normoventilation and restoration of a normal or elevated bl
ood pressure in patients with severe head injury (v) immobilisation an
d early administration of methylprednisolone in patients with spinal c
ord injury (vi) analgesia by administration of opioids, non-steroidal
antiinflammatory drugs, or ketamine (vii) sedation with benzodiazepine
s, gamma-hydroxbutyrate or propofol (viii) early enteral nutrition (ix
); antibiotic therapy of infections (x) pessure controlled ventilation
in patients with acute lung injury (xi) continuous veno-venous hemofi
ltration in patients developing acute renal failure and (xii) early su
rgical interventions to control bleeding and/or to evacuate intracereb
ral hematomas.