Screening for glucose-6-phosphate dehydrogenase deficiency in neonates: A comparison between cord and peripheral blood samples

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Abstract

Background: The use of cord blood in the neonatal screening for glucose-6-phosphate dehydrogenase (G6PD) deficiency is being done with increasing frequency but has yet to be adequately evaluated against the use of peripheral blood sample which is usually employed for confirmation. We sought to determine the incidence and gender distribution of G6PD deficiency, and compare the results of cord against peripheral blood in identifying G6PD DEFICIENCY neonates using quantitative enzyme activity assay. Methods: We carried out a retrospective and cross-sectional study employing review of primary hospital data of neonates born in a tertiary care center from January to December 2008. Results: Among the 8139 neonates with cord blood G6PD assays, an overall incidence of 2% for G6PD deficiency was computed. 79% of these were males and 21% were females with significantly more deficient males (p

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AlSaif, S., Ponferrada, M. B., AlKhairy, K., AlTawil, K., Sallam, A., Ahmed, I., … AlBalwi, M. (2017). Screening for glucose-6-phosphate dehydrogenase deficiency in neonates: A comparison between cord and peripheral blood samples. BMC Pediatrics, 17(1). https://doi.org/10.1186/s12887-017-0912-y

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