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Am J Physiol Renal Physiol 294: F1009-F1031, 2008. First published January 9, 2008; doi:10.1152/ajprenal.00475.2007
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INVITED REVIEW

Acid-base analysis: a critique of the Stewart and bicarbonate-centered approaches

Ira Kurtz,1 Jeffrey Kraut,2 Vahram Ornekian,1 and Minhtri K. Nguyen1

1Division of Nephrology, David Geffen School of Medicine at UCLA, and 2Medical and Research Services, Veterans Health Administration Greater Los Angeles (VHAGLA) Healthcare System, and Division of Nephrology, VHAGLA Healthcare System, David Geffen School of Medicine at UCLA, Los Angeles, California

When approaching the analysis of disorders of acid-base balance, physical chemists, physiologists, and clinicians, tend to focus on different aspects of the relevant phenomenology. The physical chemist focuses on a quantitative understanding of proton hydration and aqueous proton transfer reactions that alter the acidity of a given solution. The physiologist focuses on molecular, cellular, and whole organ transport processes that modulate the acidity of a given body fluid compartment. The clinician emphasizes the diagnosis, clinical causes, and most appropriate treatment of acid-base disturbances. Historically, two different conceptual frameworks have evolved among clinicians and physiologists for interpreting acid-base phenomena. The traditional or bicarbonate-centered framework relies quantitatively on the Henderson-Hasselbalch equation, whereas the Stewart or strong ion approach utilizes either the original Stewart equation or its simplified version derived by Constable. In this review, the concepts underlying the bicarbonate-centered and Stewart formulations are analyzed in detail, emphasizing the differences in how each approach characterizes acid-base phenomenology at the molecular level, tissue level, and in the clinical realm. A quantitative comparison of the equations that are currently used in the literature to calculate H+ concentration ([H+]) is included to clear up some of the misconceptions that currently exist in this area. Our analysis demonstrates that while the principle of electroneutrality plays a central role in the strong ion formulation, electroneutrality mechanistically does not dictate a specific [H+], and the strong ion and bicarbonate-centered approaches are quantitatively identical even in the presence of nonbicarbonate buffers. Finally, our analysis indicates that the bicarbonate-centered approach utilizing the Henderson-Hasselbalch equation is a mechanistic formulation that reflects the underlying acid-base phenomenology.

acid-base; SID; bicarbonate; kidney; lung



Address for reprint requests and other correspondence: I. Kurtz, Div. of Nephrology, David Geffen School of Medicine at UCLA, 10833 Le Conte Ave., Rm. 7–155 Factor Bldg., Los Angeles, California 90095 (e-mail: ikurtz{at}mednet.ucla.edu)







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