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Hyperbilirubinemia and Follow-up Auditory Brainstem Responses in Preterm Infants
OBJECTIVES. Neonatal hyperbilirubinemia is considered one of the most common causative factors of hearing loss. Preterm infants are more vulnerable to neuronal damage caused by hyperbilirubinemia. This study aimed to evaluate the effect of hyperbilirubinemia on hearing threshold and auditory pathway...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Korean Society of Otorhinolaryngology-Head and Neck Surgery
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6453789/ https://www.ncbi.nlm.nih.gov/pubmed/30404412 http://dx.doi.org/10.21053/ceo.2018.00899 |
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author | Nam, Gi-Sung Kwak, Sang Hyun Bae, Seong Hoon Kim, Sung Huhn Jung, Jinsei Choi, Jae Young |
author_facet | Nam, Gi-Sung Kwak, Sang Hyun Bae, Seong Hoon Kim, Sung Huhn Jung, Jinsei Choi, Jae Young |
author_sort | Nam, Gi-Sung |
collection | PubMed |
description | OBJECTIVES. Neonatal hyperbilirubinemia is considered one of the most common causative factors of hearing loss. Preterm infants are more vulnerable to neuronal damage caused by hyperbilirubinemia. This study aimed to evaluate the effect of hyperbilirubinemia on hearing threshold and auditory pathway in preterm infants by serial auditory brainstem response (ABR). In addition, we evaluate the usefulness of the unconjugated bilirubin (UCB) level compared with total serum bilirubin (TSB) on bilirubin-induced hearing loss. METHODS. This study was conducted on 70 preterm infants with hyperbilirubinemia who failed universal newborn hearing screening by automated ABR. The diagnostic ABR was performed within 3 months after birth. Follow-up ABR was conducted in patients with abnormal results (30 cases). TSB and UCB concentration were compared according to hearing threshold by ABR. RESULTS. The initial and maximal measured UCB concentration for the preterm infants of diagnostic ABR ≥40 dB nHL group (n=30) were statistically higher compared with ABR ≤35 dB nHL group (n=40) (P=0.031 and P=0.003, respectively). In follow-up ABR examination, 13 of the ABR ≥40 dB nHL group showed complete recovery, but 17 had no change or worsened. There was no difference in bilirubin level between the recovery group and non-recovery group. CONCLUSION. UCB is a better predictor of bilirubin-induced hearing loss than TSB in preterm infants as evaluated by serial ABR. Serial ABR testing can be a useful, noninvasive methods to evaluate early reversible bilirubin-induced hearing loss in preterm infants. |
format | Online Article Text |
id | pubmed-6453789 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Korean Society of Otorhinolaryngology-Head and Neck Surgery |
record_format | MEDLINE/PubMed |
spelling | pubmed-64537892019-05-01 Hyperbilirubinemia and Follow-up Auditory Brainstem Responses in Preterm Infants Nam, Gi-Sung Kwak, Sang Hyun Bae, Seong Hoon Kim, Sung Huhn Jung, Jinsei Choi, Jae Young Clin Exp Otorhinolaryngol Original Article OBJECTIVES. Neonatal hyperbilirubinemia is considered one of the most common causative factors of hearing loss. Preterm infants are more vulnerable to neuronal damage caused by hyperbilirubinemia. This study aimed to evaluate the effect of hyperbilirubinemia on hearing threshold and auditory pathway in preterm infants by serial auditory brainstem response (ABR). In addition, we evaluate the usefulness of the unconjugated bilirubin (UCB) level compared with total serum bilirubin (TSB) on bilirubin-induced hearing loss. METHODS. This study was conducted on 70 preterm infants with hyperbilirubinemia who failed universal newborn hearing screening by automated ABR. The diagnostic ABR was performed within 3 months after birth. Follow-up ABR was conducted in patients with abnormal results (30 cases). TSB and UCB concentration were compared according to hearing threshold by ABR. RESULTS. The initial and maximal measured UCB concentration for the preterm infants of diagnostic ABR ≥40 dB nHL group (n=30) were statistically higher compared with ABR ≤35 dB nHL group (n=40) (P=0.031 and P=0.003, respectively). In follow-up ABR examination, 13 of the ABR ≥40 dB nHL group showed complete recovery, but 17 had no change or worsened. There was no difference in bilirubin level between the recovery group and non-recovery group. CONCLUSION. UCB is a better predictor of bilirubin-induced hearing loss than TSB in preterm infants as evaluated by serial ABR. Serial ABR testing can be a useful, noninvasive methods to evaluate early reversible bilirubin-induced hearing loss in preterm infants. Korean Society of Otorhinolaryngology-Head and Neck Surgery 2019-05 2018-11-09 /pmc/articles/PMC6453789/ /pubmed/30404412 http://dx.doi.org/10.21053/ceo.2018.00899 Text en Copyright © 2019 by Korean Society of Otorhinolaryngology-Head and Neck Surgery This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Nam, Gi-Sung Kwak, Sang Hyun Bae, Seong Hoon Kim, Sung Huhn Jung, Jinsei Choi, Jae Young Hyperbilirubinemia and Follow-up Auditory Brainstem Responses in Preterm Infants |
title | Hyperbilirubinemia and Follow-up Auditory Brainstem Responses in Preterm Infants |
title_full | Hyperbilirubinemia and Follow-up Auditory Brainstem Responses in Preterm Infants |
title_fullStr | Hyperbilirubinemia and Follow-up Auditory Brainstem Responses in Preterm Infants |
title_full_unstemmed | Hyperbilirubinemia and Follow-up Auditory Brainstem Responses in Preterm Infants |
title_short | Hyperbilirubinemia and Follow-up Auditory Brainstem Responses in Preterm Infants |
title_sort | hyperbilirubinemia and follow-up auditory brainstem responses in preterm infants |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6453789/ https://www.ncbi.nlm.nih.gov/pubmed/30404412 http://dx.doi.org/10.21053/ceo.2018.00899 |
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