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1 Department of Surgery (Geriatric Surgery) and 2 Consiglio Nazionale delle Ricerche Center for the Study of Pathophysiology of Shock, Catholic University School of Medicine, I-00168 Rome, Italy; and 3 Intensive Care Unit, Hospital das Clinicas, University of Campinas School of Medicine, 13100 Campinas, SP, Brazil
Adequate assessment of circulatory and gas-exchange interactions may involve the quantification of the Haldane effect (HE) and of the changes in blood PCO2 mediated by changes in Hb-O2 saturation and O2-linked CO2 binding. This is commonly prevented by the complexity of the involved calculations. To simplify the task, a large series of patient measurements has been processed by regression analysis, thus developing an accurate fit for this quantification
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0.001), where
(v-a)PCO2 HE
is the reduction in venous PCO2
(PvCO2, Torr) allowed by the chemical
binding of CO2 in blood due to the
HE (Torr), (a-v)HbO2 is the
arteriovenous difference in Hb-bound
O2 (ml/dl), and Hct is hematocrit
fraction. Values of
(v-a)PCO2 HE
estimated by this expression compared well with the results of
previously published experiments. This formula is useful in assessing
the impact of HE on PvCO2 and
venoarterial PCO2 gradient and the
survival advantage offered by HE in extreme conditions. Use may be
extended to all investigative and clinical settings in which changes in blood O2 saturation and
O2-linked
CO2 binding must be converted into
the corresponding changes in dissolved
CO2 and
PCO2.
carbon dioxide exchange; circulatory failure; respiratory failure; shock; venous hypercapnia; sepsis
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