Galactosemia among Positive-screened Patients who Underwent Lactose Challenge: A Review of Records of the Newborn Screening Program
- PMID: 39483312
- PMCID: PMC11522362
- DOI: 10.47895/amp.vi0.8179
Galactosemia among Positive-screened Patients who Underwent Lactose Challenge: A Review of Records of the Newborn Screening Program
Abstract
Background: Newborns screened positive for Galactosemia through Expanded Newborn Screening (ENBS) with borderline levels undergo lactose challenge that requires interruption of breastfeeding temporarily then shifting to soy-based formula.
Objective: To determine the percentage of Classical Galactosemia (CGal), Non-classical Galactosemia (NCGal), probable mild variant form, and negative Galactosemia among newborns screened positive for Galactosemia who underwent lactose challenge.
Methods: This is a retrospective study. NBS records were reviewed and data were collected from January 2015 to December 2020.
Results: Out of the 117 newborns screened positive for Galactosemia, 58 underwent lactose challenge. Majority were male, term with a birth weight of 2500-4000g and received a final disposition in 4-6 months. Fifteen patients underwent 1-week lactose challenge wherein six reached a resolution on first challenge. Majority, 35 (60.3%) were negative for Galactosemia, six (10.3%) probable mild variant Galactosemia, three (5.2%) NCGal, and no CGal were observed. Fourteen suspected cases (24.1%) are pending final disposition.
Conclusion: This study describes the demographics of newborns flagged for Galactosemia who underwent lactose challenge. A 1-week lactose challenge may be recommended to further detect patients who are negative for Galactosemia.
Keywords: ENBS; galactosemia; lactose challenge.
© 2024 Acta Medica Philippina.
Conflict of interest statement
Both authors declared no conflicts of interest.
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References
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- Asghar A, Shabanova V, Mercurio MR, Bizzarro MJ. A high rate of false positive newborn screening results in the neonatal intensive care unit. J Child Adolesc Health. 2019;3(1):7-11.
-
- Serving the family from birth to the medical home . Newborn screening: a blueprint for the future - a call for a national agenda on state newborn screening programs. Pediatrics. 2000. Aug;106(2 Pt 2): 389-422. PMID: 10947682. - PubMed
-
- Padilla CD. Enhancing case detection of selected inherited disorders through Expanded Newborn Screening in the Philippines. Acta Med Philipp. 2012;46(4)-2013;47(1):24-30. doi: 10.47895/amp.v47i1.1429. - DOI
-
- PhilHealth Circular No. 34, s-2006 . PhilHealth Newborn Care Package [Internet]. [cited 2020 Jul 2]. Available from: https://www.philhealth.gov.ph/circulars/2006/circ34_2006.pdf
-
- Pyhtila BM, Shaw KA, Neumann SE, Fridovich-Keil JL. Newborn screening for galactosemia in the United States: looking back, looking around, and looking ahead [published correction appears in JIMD Rep. 2015;15:133]. JIMD Rep. 2015;15: 79-93. doi: 10.1007/8904_2014_302. PMID: 24718839. PMCID: . - DOI - PMC - PubMed
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