期刊
CRITICAL CARE MEDICINE
卷 28, 期 8, 页码 2932-2936出版社
LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/00003246-200008000-00041
关键词
accuracy; base excess; CO(2) invariance; in vitro assessment; lactic acidosis; standard base excess; Van Slyke equation
Objectives: To evaluate the precision, bias and CO(2) invariance of base excess as determined by the Van Slyke equation over a wide PCO(2) range at normal and low hemoglobin concentrations. Design: Prospective in vitro study. Setting: University research laboratory. Subjects: Normal human blood, both undiluted and diluted with plasma. Interventions: Two experiments were conducted. In the first, blood unmodified or after adding HCl or sodium bicarbonate was rendered hypercarbic (PCO(2) >70 torr) by gas equilibration. Rapid PCO(2) reduction in greater than or equal to 10 steps to a final PCO(2) less than or equal to 20 torr was then performed. In the second experiment, blood unmodified or diluted to a hemoglobin concentration of similar to 4 G% was mixed anaerobically (9:1, vol:vol) with varying concentrations of lactic acid in saline (0-250 mmol/L). Measurements and Main Results: In the first experiment, blood gas analysis at each step during the progressive PCO(2) reduction revealed that base excess remained nearly constant (SD all specimens less than or equal to 0.6 mmol/L) whereas PCO(2) changed by >80 torr. In the second experiment, simultaneous blood gas and plasma lactate analyses showed that changes in base excess correlated closely with changes in both plasma and whole blood lactate concentrations (r(2) greater than or equal to 0.91) despite concurrent PCO(2) elevations as great as 200 torr. Quantification by base excess of change in whole blood lactate concentration was precise with slight negative bias (mean negative bias, 1.1 +/- 1.9 mmol/L) in both diluted and undiluted blood. There was significant underestimation of change in plasma lactate concentration in undiluted blood, presumably because base excess is a whole blood variable. Conclusions:Base excess calculated using the Van Slyke equation accurately quantifies metabolic (nonrespiratory) acidbase status in blood in vitro. This accuracy is little affected by large simultaneous alterations in PCO(2), or by very low hemoglobin concentrations similar to that used to calculate standard base excess.
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