Pearson T C, Grimes A J, Slater N G, Wetherley-Mein G
Br J Haematol. 1981 Sep;49(1):123-7. doi: 10.1111/j.1365-2141.1981.tb07205.x.
An in vitro study of the effect of red-cell changes due to iron deficiency on whole-blood viscosity has been made on samples from patients with polycythaemia treated by venesection. When the PCV of the samples was adjusted to a standard value of 0.45, whole-blood viscosity was unrelated to decreasing MCH. In contrast, when samples were adjusted to a standard Hb concentration of 14 g/dl, whole-blood viscosity rose exponentially with decreasing MCH. This increase in whole-blood viscosity was shown to be a function of the increasing PCV that accompanies the falling MCH at this standard Hb value. It is suggested that in polycythaemia not due to hypoxia, hyperviscosity can be satisfactorily corrected by venesection controlled by monitoring the PCV alone. Other consideration may apply in hypoxic polycythaemia and these are discussed.
对通过放血治疗的真性红细胞增多症患者的样本进行了一项体外研究,以探讨缺铁引起的红细胞变化对全血粘度的影响。当将样本的血细胞比容调整到0.45的标准值时,全血粘度与平均红细胞血红蛋白含量(MCH)的降低无关。相反,当将样本调整到14 g/dl的标准血红蛋白浓度时,全血粘度随MCH的降低呈指数上升。结果表明,在该标准血红蛋白值下,全血粘度的这种增加是伴随MCH下降而增加的血细胞比容的函数。有人提出,在非缺氧性真性红细胞增多症中,通过仅监测血细胞比容来控制放血,可以令人满意地纠正高粘滞血症。对于缺氧性真性红细胞增多症可能需要考虑其他因素,本文对此进行了讨论。