The Neurodevelopmental Outcome of Severe Neonatal Hemolytic and Nonhemolytic Hyperbilirubinemia

Journal Title: The Journal of Pediatric Research - Year 2020, Vol 7, Issue 2

Abstract

Aim: Neonatal bilirubin-induced neurologic dysfunction can present with a wide spectrum of symptoms from mild neurologic impairment to severe acute bilirubin encephalopathy. In this study, we aimed to determine the risk factors of unconjugated hyperbilirubinemia among hospitalized infants with serum total bilirubin levels ≥25 mg/dL and evaluate the effects of high serum bilirubin levels due to hemolysis on neurodevelopmental outcome at postnatal between 18 and 24 months. Materials and Methods: Thirty-six term infants were enrolled in the study. The patients were divided into two groups according to their condition of either hemolytic or nonhemolytic hyperbilirubinemia. Neurodevelopmental assessment with The Bayley scale of Infant Development-II at postnatal between 18 and 24 months was performed on all infants. Results: Fourteen infants (38.9%) were in the nonhemolytic group, while 22 (61.1%) were in the hemolytic group and there was no statistically significant difference between the groups in terms of the measured mean Mental Developmental index and Psychomotor Developmental index scores. All 4 patients who underwent exchange transfusion had subgroup incompatibility and their Psychomotor Developmental index scores were significantly lower (p<0.05). Conclusion: In our study, we found that subgroup incompatibility was an important risk factor for hemolytic indirect hyperbilirubinemia and that the mean psychomotor neurodevelopmental score associated with high hyperbilirubinemia may be lower in these patients. We believe that larger case series studies are needed to discuss the relationship between subgroup nonconformity and neurodevelopmental outcomes.

Authors and Affiliations

Rüya Çolak, Şebnem Çalkavur, Ezgi Yangın Ergon, Kıymet Çelik, Senem Alkan Özdemir, Özgür Olukman, Zeynep Üstünyurt

Keywords

Related Articles

Evaluation of Six Patients with Chromosome 18 Structural Anomalies and Novel Findings

Aim: Structural chromosome 18 anomalies are characterized by multiple congenital anomalies and intellectual disability. In this study, 6 cases with structural anomalies of chromosome 18 diagnosed by using conventional an...

Evaluation of Patients Diagnosed with Brain Death in Paediatric Critical Care

Aim: We aimed to investigate the rate of brain death (BD) determinations and organ donations in our tertiary pediatric intensive care unit (PICU), and to report the data on demographic pattern and supplementary descripti...

A Case of Late-onset Hyperinsulinemic Hypoglycemia: HNF4A Mutation

Hyperinsulinemic hypoglycemia is a rare disease affecting infants and children. The frequency of HNF4A mutation is the third most common type following ABCC8 and KCNJ11 mutations. HNF4A inactivating mutations may cause h...

The Effect of a Nurse Education Program on Infiltration and Extravasation in Pediatric Patients at a University Hospital

Aim: Prevention of infiltration/extravasation (I/E) in pediatric patients is important. This study has examined the effect of an education program, which aims to prevent and manage pediatric I/E, on I/E rates in pediatri...

Frequency of Nail Abnormalities in Children and Adolescents Admitted to a Dermatology Outpatient Clinic

Aim: The incidence and spectrum of nail abnormalities in children differ from adults. The aim of this study is to investigate the frequency and spectrum of nail abnormalities in children and adolescents admitted to a der...

Download PDF file
  • EP ID EP685488
  • DOI 10.4274/jpr.galenos.2019.16779
  • Views 172
  • Downloads 0

How To Cite

Rüya Çolak, Şebnem Çalkavur, Ezgi Yangın Ergon, Kıymet Çelik, Senem Alkan Özdemir, Özgür Olukman, Zeynep Üstünyurt (2020). The Neurodevelopmental Outcome of Severe Neonatal Hemolytic and Nonhemolytic Hyperbilirubinemia. The Journal of Pediatric Research, 7(2), -. https://europub.co.uk/articles/-A-685488