Literature DB >> 28320216

A neurologic dysfunction scoring protocol for jaundiced neonates requiring exchange transfusion.

Bolajoko O Olusanya1, Folashade B Osibanjo1, Adeniyi A Ajiboye2, Oluwafemi E Ayodele2, Adebanke A Odunsi2, Serah M Olaifa2, Abieyuwa A Emokpae2.   

Abstract

AIM: To evaluate the performance of a neurologic assessment protocol among jaundiced infants requiring exchange transfusion (ET).
METHODS: We identified infants in a referral children's hospital who received ET and those who met the American Academy of Pediatrics (AAP) criteria for ET based on total serum bilirubin (TSB) levels. The performance of a bilirubin-induced neurologic dysfunction (BIND-M) scoring protocol for acute bilirubin encephalopathy (ABE) in detecting infants treated with ET in both groups was investigated by logistic regression analysis and c-statistic.
RESULTS: A total of 438 late-preterm and term infants were enrolled, out of which 141 (32.2%) received ET, and 155 (35.4%) met AAP criteria for ET. Infants with BIND-M scores of 3-6 (intermediate ABE) or 7-12 (advanced ABE) were significantly associated with ET in both groups, but not scores of 1-2 (mild ABE), with or without adjustment for confounding neurotoxicity risk factors. However, the discriminatory ability of BIND-M regression models was modestly satisfactory (c-statistic range: 0.693-0.791).
CONCLUSIONS: Our findings suggest that BIND-M is a potentially useful decision-making tool for ET and support current recommendation for immediate ET for infants with intermediate-to-advanced stages of ABE regardless of the TSB levels.

Entities:  

Keywords:  Acute bilirubin encephalopathy; exchange transfusion; late presentation; neurological examination; newborn care

Mesh:

Substances:

Year:  2017        PMID: 28320216      PMCID: PMC6166872          DOI: 10.1080/14767058.2017.1300650

Source DB:  PubMed          Journal:  J Matern Fetal Neonatal Med        ISSN: 1476-4954


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1.  Amplitude-integrated electroencephalography improves the predictive ability of acute bilirubin encephalopathy.

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