J. Van Bommel et al., Critical hematocrit in intestinal tissue oxygenation during severe normovolemic hemodilution, ANESTHESIOL, 94(1), 2001, pp. 152-160
Citations number
39
Categorie Soggetti
Aneshtesia & Intensive Care","Medical Research Diagnosis & Treatment
Background: A critical point in oxygen supply for microvascular oxygenation
during normovolemic hemodilution has not been identified. The relation bet
ween organ microvascular oxygen partial pressure (mu Po-2) and organ oxygen
consumption ((V) over dot O-2) during a decreasing oxygen delivery (Do(2))
is not well understood. The present study was designed to determine the sy
stemic hematocrit and organ Do(2) values below which organ mu Po-2 and (V)
over dot O-2, cannot be preserved by regulatory mechanisms during normovole
mic hemodilution.
Methods: Eighteen male Wistar rats were randomized between an experimental
group (n = 12), in which normovolemic hemodilution was performed with paste
urized protein solution (PPS), and a control group (n = 6). Systemic hemody
namic and intestinal oxygenation parameters were monitored. Intestinal mu P
o-2 was measured using the oxygen-dependent quenching of palladium-porphyri
n phosphorescence.
Results: Baseline values in hemodilution and control group were similar, He
modilution decreased hematocrit to 6.2 +/- 0.8% (mean +/- SD). Constant cen
tral venous pressure measurements suggested maintenance of isovolemia. Desp
ite an increasing mesenteric blood flow, intestinal Do(2) decreased immedia
tely. Initially, mu Po-2 was preserved, whereas mesenteric venous Po-2 (P(m
v)o(2)) decreased; below a hematocrit of 15%, mu Po-2 decreased significant
ly below P(mv)o(2). Critical Do(2) was 1.5 +/- 0.5 ml . kg(-1) . min(-1) fo
r (V) over dot O-2, and 1.6 +/- 0.5 ml . kg(-1) . min(-1) for mu Po-2. Crit
ical hematocrit values for (V) over dot O-2 and mu Po-2 were 15.8 +/- 4.6%
and 16.0 +/- 3.5%, respectively.
Conclusions: Intestinal mu Po-2 and (V) over dot O-2 were limited by a crit
ical decrease in Do(2) and hematocrit at the same time. Beyond these critic
al points not only shunting of oxygen from the microcirculation could be de
monstrated, but also a significant correlation between intestinal mu Po-2 a
nd (V) over dot O-2.