The Bilirubin Binding Panel: A Henderson-Hasselbalch Approach to Neonatal Hyperbilirubinemia.

Ahlfors, Charles E · Pediatrics · 2016

review · Level V

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Abstract

Poor plasma bilirubin binding increases the risk of bilirubin neurotoxicity in newborns with hyperbilirubinemia. New laboratory tests may soon make it possible to obtain a complete bilirubin binding panel when evaluating these babies. The 3 measured components of the panel are the plasma total bilirubin concentration (B<sub>Total</sub>), which is currently used to guide clinical care; the bilirubin binding capacity (BBC); and the concentration of non-albumin bound or free bilirubin (B<sub>Free</sub>). The fourth component is the bilirubin-albumin equilibrium dissociation constant, K<sub>D</sub>, which is calculated from B<sub>Total</sub>, BBC, and B<sub>Free</sub> The bilirubin binding panel is comparable to the panel of components used in the Henderson-Hasselbalch approach to acid-base assessment. Bilirubin binding population parameters (not prospective studies to determine whether the new bilirubin binding panel components are better predictors of bilirubin neurotoxicity than B<sub>Total</sub>) are needed to expedite the clinical use of bilirubin binding. At any B<sub>Total</sub>, the B<sub>Free</sub> and the relative risk of bilirubin neurotoxicity increase as the K<sub>D</sub>/BBC ratio increases (ie, bilirubin binding worsens). Comparing the K<sub>D</sub>/BBC ratio of newborns with B<sub>Total</sub> of concern with that typical for the population helps determine whether the risk of bilirubin neurotoxicity varies significantly from the inherent risk at that B<sub>Total</sub> Furthermore, the bilirubin binding panel individualizes care because it helps to determine how aggressive intervention should be at any B<sub>Total</sub>, irrespective of whether it is above or below established B<sub>Total</sub> guidelines. The bilirubin binding panel may reduce anxiety, costs, unnecessary treatment, and the likelihood of undetected bilirubin neurotoxicity.

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