Dm. Alspaugh et al., Prehospital resuscitation with phenylephrine in uncontrolled hemorrhagic shock and brain injury, J TRAUMA, 48(5), 2000, pp. 851-863
Background: Hypotension doubles the adverse outcome of severe brain injury
(BT), This finding is thought to be due to secondary ischemia caused by cer
ebral hypoperfusion, Aggressive prehospital fluid resuscitation in BI is ad
vocated to maintain mean arterial pressure (MAP). Increasing MAP by prehosp
ital fluid resuscitation before control of hemorrhage is thought to increas
e blood loss and reduce survival. We hypothesized that vasoconstrictor trea
tment of uncontrolled hemorrhage would increase MAP, reduce hemorrhage volu
me, and decrease the extent of BI compared with delayed fluid resuscitation
(DR) or resuscitation with Ringer's lactate (RL).
Methods: Swine were randomly assigned to a control group or an experimental
group: splenic laceration (uncontrolled hemorrhage) and cryogenic BI. The
experimental group received one of three prehospital resuscitation regimens
: DR, RL, or phenylephrine (Phen) to maintain baseline MAP. Variables were
measured at baseline and at 20, 50, and 120 minutes during the simulated "p
rehospital and early hospital" phases and at 2 and 8 hours after surgical c
ontrol of the uncontrolled hemorrhage. After killing, biopsies of the brain
, liver, kidney, and gut mere evaluated for histologic evidence of ischemia
and compared between groups.
Results: Hemorrhage volume was similar in the experimental groups. Mortalit
y was lowest in the Phen group (11%) compared with DR (40%) and RL (33%) gr
oups. Phen increased MAP and cerebral perfusion pressure. RL infusion incre
ased cerebral blood flow and resulted in less secondary injury than either
Phen or DR.
Conclusion: Phen improves MAP and systemic and cerebral perfusion pressure
in the prehospital phase but does not reduce secondary neuronal ischemia, R
L restores cerebral blood flow earlier and is associated with less secondar
y ischemia than either Phen or DR in this model. These data suggest that pr
ehospital infusion of RL in patients with BI and shock is warranted and dec
reases secondary ischemia.