TY - JOUR
T1 - New generation of hemoglobin-based oxygen carriers evaluated for oxygenation of critically ischemic hamster flap tissue
AU - Contaldo, Claudio
AU - Plock, Jan
AU - Sakai, Hiromi
AU - Takeoka, Shinji
AU - Tsuchida, Eishun
AU - Leunig, Michael
AU - Banic, Andrej
AU - Erni, Dominique
PY - 2005/4/1
Y1 - 2005/4/1
N2 - Objectives: The aim of this study was to investigate and compare the effects of a traditionally formulated, low-viscosity, right-shifted polymerized bovine hemoglobin solution and a highly viscous, left-shifted hemoglobin vesicle solution (HbV-HES) on the oxygenation of critically ischemic peripheral tissue. Design: Randomized, prospective study. Setting: University laboratory. Subject: A total of 40 male golden Syrian hamsters. Interventions: Island flaps were dissected from the back skin of anesthetized hamsters. The flap included a critically ischemic, hypoxic area that was perfused via a collateralized vasculature. One hour after completion of the preparation, the animals received a 33% blood exchange with 6% hydroxyethyl starch 200/ 0.5 (HES, n = 9), HbV suspended in HES (HbV-HES, n = 8), or polymerized bovine hemoglobin solution (n = 9). Measurements and Main Results: Three hours after the blood exchange, microcirculatory blood flow (laser-Doppler flowmetry) was increased to 262% of baseline for HbV-HES (p < .01) and 197% for polymerized bovine hemoglobin solution (p < .05 vs. baseline and HbV-HES). Partial tissue oxygen tension (bare fiber probes) was only improved after HbV-HES (9.4 torr to 14.2 torr, p < .01 vs. baseline and other groups). The tissue lactate/pyruvate ratio (microdialysis) was elevated to 51 in the untreated control animals, and to 34 ± 8 after HbV-HES (p < .05 vs. control) and 38 ± 11 after polymerized bovine hemoglobin solution (not significant). Conclusions: Our study suggests that in critically ischemic and hypoxic collateralized peripheral tissue, oxygenation may be improved by normovolemic hemodilution with HbV-HES. We attributed this improvement to a better restoration of the microcirculation and oxygen delivery due to the formulation of the solution.
AB - Objectives: The aim of this study was to investigate and compare the effects of a traditionally formulated, low-viscosity, right-shifted polymerized bovine hemoglobin solution and a highly viscous, left-shifted hemoglobin vesicle solution (HbV-HES) on the oxygenation of critically ischemic peripheral tissue. Design: Randomized, prospective study. Setting: University laboratory. Subject: A total of 40 male golden Syrian hamsters. Interventions: Island flaps were dissected from the back skin of anesthetized hamsters. The flap included a critically ischemic, hypoxic area that was perfused via a collateralized vasculature. One hour after completion of the preparation, the animals received a 33% blood exchange with 6% hydroxyethyl starch 200/ 0.5 (HES, n = 9), HbV suspended in HES (HbV-HES, n = 8), or polymerized bovine hemoglobin solution (n = 9). Measurements and Main Results: Three hours after the blood exchange, microcirculatory blood flow (laser-Doppler flowmetry) was increased to 262% of baseline for HbV-HES (p < .01) and 197% for polymerized bovine hemoglobin solution (p < .05 vs. baseline and HbV-HES). Partial tissue oxygen tension (bare fiber probes) was only improved after HbV-HES (9.4 torr to 14.2 torr, p < .01 vs. baseline and other groups). The tissue lactate/pyruvate ratio (microdialysis) was elevated to 51 in the untreated control animals, and to 34 ± 8 after HbV-HES (p < .05 vs. control) and 38 ± 11 after polymerized bovine hemoglobin solution (not significant). Conclusions: Our study suggests that in critically ischemic and hypoxic collateralized peripheral tissue, oxygenation may be improved by normovolemic hemodilution with HbV-HES. We attributed this improvement to a better restoration of the microcirculation and oxygen delivery due to the formulation of the solution.
KW - Arterial occlusive diseases
KW - Blood substitutes
KW - Collateral circulation
KW - Energy metabolism
KW - Microcirculation
KW - Surgical flaps
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U2 - 10.1097/01.CCM.0000159195.12111.CE
DO - 10.1097/01.CCM.0000159195.12111.CE
M3 - Article
C2 - 15818109
AN - SCOPUS:17044387058
SN - 0090-3493
VL - 33
SP - 806
EP - 812
JO - Critical Care Medicine
JF - Critical Care Medicine
IS - 4
ER -