Severinghaus J W, Astrup P B
J Clin Monit. 1985 Oct;1(4):259-77. doi: 10.1007/BF02832819.
Electrometric measurement of the hydrogen ion concentration was discovered by Wilhelm Ostwald in Leipzig about 1890 and described thermodynamically by his student Walther Nernst, using the van't Hoff concept of osmotic pressure as a kind of gas pressure, and the Arrhenius concept of ionization of acids, both of which had been formalized in 1887. Hasselbalch, after adapting the pH nomenclature of Sørensen to the carbonic-acid mass equation of Henderson, made the first actual blood pH measurements (with a hydrogen electrode) and proposed that metabolic acid-base imbalance be quantified as the "reduced" pH of blood after equilibration to a carbon dioxide tension (PCO2) of 40 mm Hg. This good idea, coming 40 years before simple blood pH measurements at 37 degrees C became widely available, was never adopted. Instead, Van Slyke developed a concept of acid-base chemistry that depended on measuring plasma CO2 content with his manometric apparatus, a standard method until the 1960s, when it was displaced by the three-electrode method of blood gas analysis. The 1952 polio epidemic in Copenhagen stimulated Astrup to develop a glass electrode in which pH could be measured in blood at 37 degrees C before and after equilibration with known PCO2. He introduced the interpolative measurement of PCO2 and bicarbonate level (later base excess) using only pH measurements and, with Siggaard-Andersen, developed clinical acid-base chemistry. Controversy arose when blood base excess was noted to be altered by acute changes in PCO2 and when abnormalities of base excess were called metabolic acidosis or alkalosis, even when they represented compensation for respiratory abnormalities in PCO2. In the 1970s it became clear that "in-vivo" or "extracellular fluid" base excess (measured at an average extracellular fluid hemoglobin concentration of 5 g) eliminated the error caused by acute changes in PCO2. Base excess is now almost universally used as the index of nonrespiratory acid-base imbalance.
氢离子浓度的电动测量法是1890年左右由莱比锡的威廉·奥斯特瓦尔德发现的,他的学生瓦尔特·能斯特从热力学角度对其进行了描述,能斯特采用了范特霍夫的渗透压概念(一种气体压力)以及阿伦尼乌斯的酸电离概念,这两个概念在1887年已被形式化。哈塞尔巴尔赫在将索伦森的pH命名法应用于亨德森的碳酸质量方程后,首次实际测量了血液pH值(使用氢电极),并提议将代谢性酸碱失衡量化为血液在二氧化碳分压(PCO2)为40 mmHg时平衡后的“降低”pH值。这个好想法在37摄氏度下简单的血液pH测量广泛可用的40年前就已出现,但从未被采用。相反,范斯莱克提出了一种酸碱化学概念,该概念依赖于用他的测压装置测量血浆CO2含量,这是直到20世纪60年代的标准方法,后来被血气分析的三电极法所取代。1952年哥本哈根的小儿麻痹症流行促使阿斯图普开发了一种玻璃电极,可在37摄氏度下测量血液在与已知PCO2平衡前后的pH值。他引入了仅使用pH测量来插值测量PCO2和碳酸氢盐水平(后来是碱剩余)的方法,并与西格gaard - 安德森一起发展了临床酸碱化学。当发现血液碱剩余会因PCO2的急性变化而改变,并且当碱剩余异常被称为代谢性酸中毒或碱中毒时,即使它们代表对PCO2呼吸异常的代偿,争议也随之出现。在20世纪70年代,人们清楚地认识到“体内”或“细胞外液”碱剩余(在平均细胞外液血红蛋白浓度为5 g时测量)消除了由PCO2急性变化引起的误差。碱剩余现在几乎被普遍用作非呼吸性酸碱失衡的指标。