AI Article Synopsis

  • The study aimed to assess the clinical features of bilirubin encephalopathy in preterm infants in Japan by conducting a nationwide survey.
  • A total of 41 pBE infants were identified, with 30 providing clinical data, showing severe motor impairments but some preserved manual skills and communication abilities.
  • MRI scans revealed specific brain changes in most patients, and auditory brainstem response tests indicated hearing issues in a subset, helping to improve diagnosis of pBE.

Article Abstract

Objectives: To determine the clinical features of bilirubin encephalopathy in preterm infants (pBE) in Japan.

Methods: We performed a retrospective, nationwide questionnaire-based survey. The initial survey determined the number of children with pBE who were born after 2000. Using a structured questionnaire, the second survey clarified the clinical manifestations and characteristics of children with pBE, including demographic data, neurological symptoms, and MRI and auditory brainstem response (ABR) findings.

Results: The initial survey identified 41 pBE infants from 18 institutions. After exclusion of patients included in previous studies, clinical information was collected from 30 patients (21 boys and 9 girls) during the secondary survey. The median gestational age was 26 weeks and the median birthweight was 846 g. Chronic lung disease and symptomatic patent ductus arteriosus were common neonatal complications. Head control was observed in 63% and functional gait in 17% of patients. Purposeful hand use was seen in 57% and verbal communication in 50% of patients. MRI showed T2 hyperintensities in the globus pallidus of 29 of 30 patients. ABR abnormalities were present in 11 of 15 patients. None of the variables were significantly different between the 2017 and 2021 surveys.

Conclusions: The pBE infants had severely impaired gross motor function and relatively preserved manual function and verbal communication. MRI and ABR findings aid in the diagnosis of pBE.

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Source
http://dx.doi.org/10.1016/j.braindev.2023.08.009DOI Listing

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