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首页> 外文期刊>American Journal of Physiology >Isovolemic exchange transfusion with increasing concentrations of low oxygen affinity hemoglobin solution limits oxygen delivery due to vasoconstriction.
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Isovolemic exchange transfusion with increasing concentrations of low oxygen affinity hemoglobin solution limits oxygen delivery due to vasoconstriction.

机译:随着低氧亲和力血红蛋白溶液浓度的增加,等渗交换输血由于血管收缩而限制了氧的输送。

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摘要

O2-carrying fluids based on hemoglobin (Hb) are in various stages of clinical trials to determine their suitability as O2-carrying plasma expanders. Polymerized Hb solutions are characterized by their vasoactivity, low O2 affinity, oncotic effect, prolonged shelf life, and stability. Physiological responses to facilitated O2 transport after exchange transfusion with polymerized bovine Hb (PBH) were studied in the hamster window chamber model during acute moderate anemia to determine how PBH affects microvascular perfusion and tissue oxygenation. The anemic state [29% hematocrit (Hct)] was induced by hemodilution with a plasma expander (70 kDa dextran). After hemodilution, animals were randomly assigned to different exchange transfusion groups. Study groups were based on the concentration of PBH used, namely: PBH at 13 g Hb/dl [PBH13], PBH diluted to 8 (PBH8) or 4 (PBH4) g Hb/dl in albumin solution at matching colloidal osmotic pressure (COP), and no PBH (only albumin solution) at matching COP (PBH0). Measurement of systemic parameters, microvascular hemodynamics, capillary perfusion, and intravascular and tissue O2 levels was performed at 18% Hct. Restitution of O2-carrying capacity with PBH13 increased arterial pressure and triggered vasoconstriction, low perfusion, and high peripheral resistance. PBH4 and PBH0 exhibited lower arterial pressures compared with PBH13. Exchange transfused animals with PBH8 and PBH4 better maintained perfusion and functional capillary density than PBH13. Blood gas parameters and acid-base balance were recovered proportional to microvascular perfusion. Arterial O2 tensions were improved with PBH4 and PBH8 by preventing O2 precapillary release and increasing O2 reserve. Further studies to establish PBH optimal dosage, efficacy, safety, and its effect on outcome are indicated before Hb-based O2-carrying blood substitutes are implemented in routine practice.
机译:基于血红蛋白(Hb)的含O2的流体正处于临床试验的各个阶段,以确定它们是否适合作为含O2的血浆膨胀剂。聚合的Hb溶液的特征在于它们的血管活性,低的O2亲和力,溶血作用,延长的保存期限和稳定性。在急性中度贫血期间,在仓鼠窗室模型中研究了用聚合牛血红蛋白(PBH)交换输血后对促进O2转运的生理反应,以确定PBH如何影响微血管灌注和组织氧合。贫血状态[29%血细胞比容(Hct)]是通过血浆稀释剂(70 kDa右旋糖酐)血液稀释引起的。血液稀释后,将动物随机分为不同的交换输血组。研究组基于使用的PBH浓度,即:PBH浓度为13 g Hb / dl [PBH13],在匹配的胶体渗透压(COP)下将白蛋白溶液中的PBH稀释至8(PBH8)或4(PBH4)g Hb / dl ),并且在匹配的COP(PBH0)时没有PBH(仅白蛋白溶液)。在18%Hct下测量全身参数,微血管血流动力学,毛细血管灌注以及血管内和组织中的O2水平。 PBH13恢复O2携带能力会增加动脉压并触发血管收缩,低灌注和高外周阻力。与PBH13相比,PBH4和PBH0表现出较低的动脉压。与PBH13相比,用PBH8和PBH4交换输血的动物能更好地保持灌注和功能性毛细血管密度。血气参数和酸碱平衡与微血管灌注成正比。 PBH4和PBH8可通过防止O2毛细血管前释放和增加O2储备来改善动脉O2张力。在常规操作中使用基于Hb的O2替代血液替代品之前,需要进行进一步研究以确定PBH的最佳剂量,疗效,安全性及其对结果的影响。

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