Volume expansion with modified hemoglobin solution, colloids, or crystalloid after hemorrhagic shock in rabbits: Effects in skeletal muscle oxygen pressure and use versus arterial blood velocity and resistance

被引:49
作者
Boura, C
Caron, A
Longrois, D
Mertes, PM
Labrude, P
Menu, P
机构
[1] Univ Nancy 1, Fac Pharm, Lab Hematol & Physiol, F-54000 Nancy, France
[2] Univ Nancy 1, Fac Med, Lab Les Reparat Remodelage Cardiaque & Arteriel, F-54000 Nancy, France
[3] CHU Brabois, Dept Anesthesie Reanimat Chirurg, Nancy, France
来源
SHOCK | 2003年 / 19卷 / 02期
关键词
hypoxia; resuscitation; plasma expanders; microdialysis; lactate; oxygen sensor;
D O I
10.1097/00024382-200302000-00015
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Therapeutic goals for hemorrhagic shock resuscitation are the increase of cardiac output and oxygen delivery. The possibility exists that because of microcirculatory effects, different volume expanders result in different tissue oxygen delivery and oxygen use. In a rabbit model of resuscitation from hemorrhagic shock (500% blood loss), we compared the effects of an hemoglobin-based O-2-carrying solution (HbOC) with those elicited by albumin, hydroxyethyl starch (HES), or saline on systemic hemodynamics, skeletal muscle O-2 pressure (PtiO(2)), and interstitial concentration of lactate (LACi) through the combined implantation of a microdialysis probe and a sensitive O-2 electrode into the hind limb. Hemorrhagic shock induced a 500%. decrease in mean arterial pressure (MAP), femoral artery blood flow (BF), and PtiO(2). After resuscitation, there were statistically significant differences among the volume expanders. The increase in MAP was faster with HbOC and colloids, and slower with saline, mainly obtained by vasoconstriction for HbOC and by increased BF with albumin and HES. The maximum MAP values were significantly higher for HbOC compared with the other volume expanders. HbOC; and colloids induced a faster increase in PtiO(2) as compared with saline, but maximum PtiO(2) values were not different among the volume expanders. Tissue oxygen use as estimated by LACi increased transiently at the beginning of volume expansion with similar maximum values. Animals resuscitated with saline had significantly higher LACi concentrations after the onset of volume expansion as compared with HbOC but not with colloids. Our mutts demonstrate that there are measurable differences in MAP and BF upon resuscitation with the four different solutions and there is a slower increase in tissue PtiO(2) with saline than With colloids associated with significantly increased LACi consistent with delayed reoxygenation upon resuscitation with saline.
引用
收藏
页码:176 / 182
页数:7
相关论文
共 28 条
[1]  
BAUE AE, 1993, PATHOPHYSIOLOGY SHOC, P1004
[2]   IMMEDIATE VERSUS DELAYED FLUID RESUSCITATION FOR HYPOTENSIVE PATIENTS WITH PENETRATING TORSO INJURIES [J].
BICKELL, WH ;
WALL, MJ ;
PEPE, PE ;
MARTIN, RR ;
GINGER, VF ;
ALLEN, MK ;
MATTOX, KL .
NEW ENGLAND JOURNAL OF MEDICINE, 1994, 331 (17) :1105-1109
[3]   Cardiovascular and hemorheological effects of three modified human hemoglobin solutions in hemodiluted rabbits [J].
Caron, A ;
Menu, P ;
Faivre-Fiorina, B ;
Labrude, P ;
Alayash, AI ;
Vigneron, C .
JOURNAL OF APPLIED PHYSIOLOGY, 1999, 86 (02) :541-548
[4]   Systemic and renal hemodynamics after moderate hemodilution with HbOCs in anesthetized rabbits [J].
Caron, A ;
Menu, P ;
Faivre-Fiorina, B ;
Labrude, P ;
Alayash, A ;
Vigneron, C .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2000, 278 (06) :H1974-H1983
[5]   Hemoglobin solutions - Not just red blood cell substitutes [J].
Creteur, J ;
Sibbald, W ;
Vincent, JL .
CRITICAL CARE MEDICINE, 2000, 28 (08) :3025-3034
[6]   Site-specific modifications and toxicity of blood substitutes - The case of diaspirin cross-linked hemoglobin [J].
D'Agnillo, F ;
Alayash, AI .
ADVANCED DRUG DELIVERY REVIEWS, 2000, 40 (03) :199-212
[7]   Pharmacology of hemoglobin therapeutics [J].
Gulati, A ;
Barve, A ;
Sen, AP .
JOURNAL OF LABORATORY AND CLINICAL MEDICINE, 1999, 133 (02) :112-119
[8]  
HAGSTROMTOFT E, 1997, AM J PHYSIOL, V273, pD584
[9]  
Halmaja Hillman K, 1997, BAILLIERE CLIN ANAES, V11, P1
[10]  
HARRIS AG, 1997, AM J PHYSIOL, V271, pH2388