Objectives: Using a new fluorescence-quenching optode which, unlike ea
rlier oximeters, neither consumes oxygen nor generates heat, we sought
to determine the effects of hemorrhage and resuscitation on subcutane
ous Po-2. Additionally, we compared the effects of resuscitation with
diaspirin crosslinked hemoglobin, an oxygen-carrying solution, on subc
utaneous Po-2 to that of traditional resuscitative fluids. We also com
pared mean arterial pressure and central venous oxygen saturation, ind
irect indices of perfusion, to subcutaneous Po-2, a direct index of pe
rfusion. Design: Prospective trial, randomized for selection of treatm
ent regimen. Setting: Shock-trauma laboratory of a medical university.
Subjects: Male Sprague-Dawley rats, weighing 260 to 380 g. Interventi
ons: Rats were bled 22 mL/kg and resuscitated, 1 min later, with eithe
r 66 mL/kg of lactated Ringer's solution, 22 mL/kg of human serum albu
min, 22 mL/kg of blood, or 22 mL/kg of diaspirin crosslinked hemoglobi
n. A fifth group of animals was not resuscitated after hemorrhage. Sub
cutaneous Po-2 and mean arterial pressure were monitored continuously
throughout the experiment, while central venous oxygen saturation was
measured intermittently. Measurements and Main Results: Subcutaneous P
o-2 decreased in response to hemorrhage and, although it did increase
after resuscitation with each fluid, no treatment was able to restore
subcutaneous Po-2 to baseline within 2 hrs postresuscitation. Subcutan
eous Po-2 continued to decrease after hemorrhage in the unresuscitated
animals. In contrast, mean arterial pressure was restored to baseline
values in only blood- and diaspirin crosslinked hemoglobin-treated an
imals, although this effect was lost within 30 mins in the blood-treat
ed group. Only blood restored the central venous oxygen saturation to
baseline values in the early postresuscitation period. Conclusions: Th
e fluorescence-quenching optode consistently followed changes in subcu
taneous Po-2 during hemorrhage and after resuscitation. Diaspirin cros
slinked hemoglobin performed as well as blood in restoring peripheral
perfusion, as measured by subcutaneous Po-2, while both of these fluid
s were superior to either lactated Ringer's solution or albumin. Both
whole blood and diaspirin crosslinked hemoglobin restored mean arteria
l pressure to baseline, although the effect of the latter was of a lon
ger duration. The presser effect of the crosslinked hemoglobin did not
affect peripheral perfusion, as reflected by the values for subcutane
ous Po-2. Subcutaneous Po-2 is a useful adjunct in assessment of the a
dequacy of peripheral perfusion and may help redefine targets for resu
scitation.