Hemoglobin Bonn
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Very rare. Abnormality of hemoglobin due to a mutation of the HBA1 gene resulting in the replacement of histidine by aspartic acid in position 87 on the α chain of hemoglobin .
This mutation results in:
- microcytic anemia with moderate hemolysis
- a peak absorbance of light by oxyhemoglobin Bonn at 668 nm, close to the absorbance of light by oxyhemoglobin A at 660 nm, one of the wavelengths used by the pulse oximeters: SpO2 is therefore artificially low
Anesthetic implications:
erroneously low measurement of SpO2 (pulse oximetry): maximum value at 91% in pure oxygen; monitoring by measurement of transcutaneous paO2 or the blood gases.
References:
Updated: August 2017