Continuous infusion of pyridoxalated hemoglobin polyoxyethylene conjugate in hyperdynamic septic sheep

被引:24
作者
Bone, HG
Fischer, SR
Schenarts, PJ
McGuire, R
Traber, LD
Traber, DL [1 ]
机构
[1] Univ Texas, Med Branch, Dept Anesthesiol, Galveston, TX 77555 USA
[2] Univ Texas, Med Branch, Dept Physiol, Galveston, TX 77555 USA
[3] Univ Texas, Med Branch, Dept Biophys, Galveston, TX 77555 USA
[4] Shriners Burns Inst, Galveston, TX 77555 USA
[5] Univ Munster, Department Anesthesiol & Intens Care Medicine, D-4400 Munster, Germany
来源
SHOCK | 1998年 / 10卷 / 01期
关键词
D O I
10.1097/00024382-199807000-00012
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Cell-free hemoglobin solutions can scavenge nitric oxide and therefore increase mean arterial pressure (MAP), The present study investigated the effects of a continuous low-dose infusion of modified hemoglobin during ovine hyperdynamic sepsis. 13 sheep received a continuous infusion of live Pseudomonas aeruginosa bacteria for 48 h. Animals that survived the first 24 h of sepsis (n = 12) were randomly assigned either to a treatment group that received 20 mg.kg(-1).h(-1) pyridoxalated hemoglobin polyoxyethylene conjugate (PHP) for 20 h or to a control group that received the same volume of the vehicle for 20 h, MAP increased in the treatment group during 4 h of PHP infusion 12.7 +/- 1.7 mmHg (p < .05) and after 20 h of PHP infusion MAP was still 12.4 +/- 2.1 mmHg above the MAP before starting PHP (p < .05). MAP in the control group did not change significantly from 24 h to 48 h of sepsis, No differences in regional blood flow were seen between groups. Bacterial counts in the spleen and kidney were lower in the treatment group than in the control group. Continuous low-dose infusion of PHP can normalize systemic vascular resistance and MAP for long periods without deterioration of regional blood flow or bacterial clearance.
引用
收藏
页码:69 / 76
页数:8
相关论文
共 32 条
[1]  
ALAYASH AI, 1994, ANN NY ACAD SCI, V738, P378
[2]   Effect of human hemoglobin on systemic and regional hemodynamics in a porcine model of endotoxemic shock [J].
Aranow, JS ;
Wang, HL ;
Zhuang, J ;
Fink, MP .
CRITICAL CARE MEDICINE, 1996, 24 (05) :807-814
[3]   FEEDBACK INHIBITION OF NITRIC-OXIDE SYNTHASE ACTIVITY BY NITRIC-OXIDE [J].
ASSREUY, J ;
CUNHA, FQ ;
LIEW, FY ;
MONCADA, S .
BRITISH JOURNAL OF PHARMACOLOGY, 1993, 108 (03) :833-837
[4]  
Booke M, 1995, New Horiz, V3, P123
[5]   Nitric oxide synthase inhibition versus norepinephrine in ovine sepsis: Effects on regional blood flow [J].
Booke, M ;
Hinder, F ;
McGuire, R ;
Traber, LD ;
Traber, DL .
SHOCK, 1996, 5 (05) :362-370
[6]  
CROWLEY JP, 1993, CIRC SHOCK, V41, P144
[7]   Blood substitutes: Fluids, drugs, or miracle solutions? [J].
Dietz, NM ;
Joyner, MJ ;
Warner, MA .
ANESTHESIA AND ANALGESIA, 1996, 82 (02) :390-405
[8]  
EVANS T, 1993, CIRC SHOCK, V41, P77
[9]   HEMOGLOBIN-BASED BLOOD SUBSTITUTES AND SEPSIS [J].
GRIFFITHS, E ;
CORTES, A ;
GILBERT, N ;
STEVENSON, P ;
MACDONALD, S ;
PEPPER, D .
LANCET, 1995, 345 (8943) :158-160
[10]   Role of endothelin in the cardiovascular effects of diaspirin crosslinked and stroma reduced hemoglobin [J].
Gulati, A ;
Sharma, AC ;
Singh, G .
CRITICAL CARE MEDICINE, 1996, 24 (01) :137-147