Critical hematocrit in intestinal tissue oxygenation during severe normovolemic hemodilution

Citation
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
Journal title
ANESTHESIOLOGY
ISSN journal
00033022 → ACNP
Volume
94
Issue
1
Year of publication
2001
Pages
152 - 160
Database
ISI
SICI code
0003-3022(200101)94:1<152:CHIITO>2.0.ZU;2-4
Abstract
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.