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Updated: Jun 4, 2025

Measurement and Analysis of Extracellular Acid Production to Determine Glycolytic Rate
Published on: December 12, 2015
Understanding the Acid-Base Response to Respiratory Derangements: Finding, and Clinically Applying, the In Vivo Base
Micah L A Heldeweg1,2, Kenrick Berend3, Patrick Schober1
1Department of Anesthesiology, Amsterdam University Medical Centers, Amsterdam, The Netherlands.
The body's base excess response to acute changes in carbon dioxide varies significantly between individuals. A buffer power coefficient of 12.1 may be more appropriate for clinical use than the standard 16.2.
Area of Science:
- Physiology
- Acid-Base Balance
- Respiratory Medicine
Background:
- Understanding in vivo acid-base regulation is crucial for clinical management.
- Existing models for calculating base excess may not accurately reflect physiological responses to carbon dioxide fluctuations.
Purpose of the Study:
- To evaluate the in vivo base excess response to acute changes in arterial carbon dioxide.
- To determine an appropriate buffer power coefficient for clinical application.
Main Methods:
- Secondary analysis of data from three experimental studies involving canine and human subjects.
- Eighty-nine carbon dioxide exposure experiments were analyzed using linear regression.
- Arterial carbon dioxide levels were manipulated via environmental chambers or mechanical ventilation.
Main Results:
- Significant individual variations in base excess response to carbon dioxide were observed.
- The standard buffer power coefficient of 16.2 showed different baselines and slopes across studies.
- A buffer power coefficient of 12.1 (95% CI, 9.1-15.1) demonstrated a more appropriate in vivo base excess equation.
Conclusions:
- In vivo carbon dioxide changes elicit clinically relevant base excess variations in individual patients.
- The buffer power coefficient of 16.2 may be inappropriate for in vivo calculations and requires validation.
- A revised coefficient of 12.1 warrants further investigation for general clinical use.
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