Am J Perinatol 2019; 36(14): 1481-1484
DOI: 10.1055/s-0039-1677800
Original Article
Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

Validation of the Siggaard–Andersen Acid–Base Nomogram for Hemoglobin F: Implications for Fetal Cord Blood Gas Analysis

Megan Whitham
1   Department of Obstetrics and Gynecology, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas
2   Department of Pathology, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas
,
Jayson Pagaduan
1   Department of Obstetrics and Gynecology, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas
2   Department of Pathology, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas
,
Steven L. Clark
1   Department of Obstetrics and Gynecology, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas
2   Department of Pathology, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas
,
Ila Singh
1   Department of Obstetrics and Gynecology, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas
2   Department of Pathology, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas
,
Michael Belfort
1   Department of Obstetrics and Gynecology, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas
2   Department of Pathology, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas
,
Sridevi Devaraj
1   Department of Obstetrics and Gynecology, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas
2   Department of Pathology, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas
,
Jing Cao
1   Department of Obstetrics and Gynecology, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas
2   Department of Pathology, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas
,
Anil Shetty
1   Department of Obstetrics and Gynecology, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas
2   Department of Pathology, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas
,
Shweta Pai
1   Department of Obstetrics and Gynecology, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas
2   Department of Pathology, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas
,
Karin Fox
1   Department of Obstetrics and Gynecology, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas
2   Department of Pathology, Texas Children's Hospital, Baylor College of Medicine, Houston, Texas
› Author Affiliations
Further Information

Publication History

31 July 2018

11 December 2018

Publication Date:
23 January 2019 (online)

Abstract

Objective The calculation of HCO3 and base excess in current blood gas analysis is based on the Siggaard–Andersen equation. One of the constants in this equation is dependent on the known buffering capacity of hemoglobin A. We sought to investigate differences in buffering capacity between adult hemoglobin A and fetal hemoglobin F as a potential explanation for the observed poor correlation between calculated base excess in umbilical cord blood and newborn outcomes. Such differences would influence a key constant in the Van Slyke/Siggaard–Andersen equation used to calculate HCO3 and base excess and could be an explanation of these observations.

Study Design This was a prospective observational study. We analyzed umbilical cord blood bicarbonate levels both as calculated values from a traditional blood gas analyzer and as measured values in 20 women giving birth at term. Since the calculated value is dependent upon the concentration and known buffering capacity of hemoglobin A, significant differences in these two analyses would imply differences in the buffering capacity of hemoglobins A and F.

Results The mean calculated HCO3 value was 25 mEq/L (25.3 ± 1.9) compared with a mean measured value of 25 mEq/L (24.6 ± 1.7) over a range of pH levels of 7.16 to 7.42. This difference was not significant (p = 0.07).

Conclusion The buffering capacity of hemoglobin F, for clinical purposes, is not different than that of hemoglobin A and is not an explanation for the recognized poor correlation between base excess and neonatal outcome.

 
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