Relation between serum bilirubin levels ≥450 μmol/L and bilirubin encephalopathy; a Danish population-based study
Aim: Describe the relation between levels of total serum bilirubin (TsB) ≥450 μmol/L and acute intermediate, acute advanced and chronic bilirubin encephalopathy. Material and methods: All infants born at gestational age ≥35 weeks in Denmark between 2000 and 2007 with a TsB ≥450 μmol/L according to...
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Published in: | Acta Paediatrica Vol. 101; no. 4; pp. 384 - 389 |
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Abstract | Aim: Describe the relation between levels of total serum bilirubin (TsB) ≥450 μmol/L and acute intermediate, acute advanced and chronic bilirubin encephalopathy.
Material and methods: All infants born at gestational age ≥35 weeks in Denmark between 2000 and 2007 with a TsB ≥450 μmol/L according to the national laboratory information system. Infants diagnosed with bilirubin encephalopathy were found in the Danish National Registry of Patients.
Results: 502 766 infants at gestational age ≥35 weeks were identified. Two hundred twenty‐four developed a TsB ≥450 μmol/L, equivalent to an incidence of 45/100 000/year, and it increased during the period. Incidence of infants with peak TsB of 450–499, 500–599 and 600–1000 μmol/L were 29.6, 12.7 and 2.2 per 100 000, respectively. Three infants had acute advanced bilirubin encephalopathy and got severe sequelae, whereas the two infants with acute intermediate encephalopathy developed normally. Their peak TsB was ≥544 μmol/L. Having a peak TsB 600–1000 μmol/L, the risk of acute advanced and chronic bilirubin encephalopathy was 27% (95% CI 6;61), and the incidence of these conditions was 0.6 (95% CI 0.1;1.7) per 100 000.
Conclusion: The incidence of infants with TsB ≥450 μmol/L was 45/100 000/year. Infants with a TsB ≥600 μmol/L had a substantial risk of developing acute advanced and chronic bilirubin encephalopathy, and the incidence of these conditions was 0.6 per 100 000. |
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AbstractList | AIMDescribe the relation between levels of total serum bilirubin (TsB) ≥450 μmol/L and acute intermediate, acute advanced and chronic bilirubin encephalopathy.MATERIAL AND METHODSAll infants born at gestational age ≥35 weeks in Denmark between 2000 and 2007 with a TsB ≥450 μmol/L according to the national laboratory information system. Infants diagnosed with bilirubin encephalopathy were found in the Danish National Registry of Patients.RESULTS502,766 infants at gestational age ≥35 weeks were identified. Two hundred twenty-four developed a TsB ≥450 μmol/L, equivalent to an incidence of 45/100,000/year, and it increased during the period. Incidence of infants with peak TsB of 450-499, 500-599 and 600-1000 μmol/L were 29.6, 12.7 and 2.2 per 100,000, respectively. Three infants had acute advanced bilirubin encephalopathy and got severe sequelae, whereas the two infants with acute intermediate encephalopathy developed normally. Their peak TsB was ≥544 μmol/L. Having a peak TsB 600-1000 μmol/L, the risk of acute advanced and chronic bilirubin encephalopathy was 27% (95% CI 6;61), and the incidence of these conditions was 0.6 (95% CI 0.1;1.7) per 100,000.CONCLUSIONThe incidence of infants with TsB ≥450 μmol/L was 45/100,000/year. Infants with a TsB ≥600 μmol/L had a substantial risk of developing acute advanced and chronic bilirubin encephalopathy, and the incidence of these conditions was 0.6 per 100,000. Aim: Describe the relation between levels of total serum bilirubin (TsB) ≥450 μmol/L and acute intermediate, acute advanced and chronic bilirubin encephalopathy. Material and methods: All infants born at gestational age ≥35 weeks in Denmark between 2000 and 2007 with a TsB ≥450 μmol/L according to the national laboratory information system. Infants diagnosed with bilirubin encephalopathy were found in the Danish National Registry of Patients. Results: 502 766 infants at gestational age ≥35 weeks were identified. Two hundred twenty‐four developed a TsB ≥450 μmol/L, equivalent to an incidence of 45/100 000/year, and it increased during the period. Incidence of infants with peak TsB of 450–499, 500–599 and 600–1000 μmol/L were 29.6, 12.7 and 2.2 per 100 000, respectively. Three infants had acute advanced bilirubin encephalopathy and got severe sequelae, whereas the two infants with acute intermediate encephalopathy developed normally. Their peak TsB was ≥544 μmol/L. Having a peak TsB 600–1000 μmol/L, the risk of acute advanced and chronic bilirubin encephalopathy was 27% (95% CI 6;61), and the incidence of these conditions was 0.6 (95% CI 0.1;1.7) per 100 000. Conclusion: The incidence of infants with TsB ≥450 μmol/L was 45/100 000/year. Infants with a TsB ≥600 μmol/L had a substantial risk of developing acute advanced and chronic bilirubin encephalopathy, and the incidence of these conditions was 0.6 per 100 000. Aim: Describe the relation between levels of total serum bilirubin (TsB) ≥450 μmol/L and acute intermediate, acute advanced and chronic bilirubin encephalopathy. Material and methods: All infants born at gestational age ≥35 weeks in Denmark between 2000 and 2007 with a TsB ≥450 μmol/L according to the national laboratory information system. Infants diagnosed with bilirubin encephalopathy were found in the Danish National Registry of Patients. Results: 502 766 infants at gestational age ≥35 weeks were identified. Two hundred twenty‐four developed a TsB ≥450 μmol/L, equivalent to an incidence of 45/100 000/year, and it increased during the period. Incidence of infants with peak TsB of 450–499, 500–599 and 600–1000 μmol/L were 29.6, 12.7 and 2.2 per 100 000, respectively. Three infants had acute advanced bilirubin encephalopathy and got severe sequelae, whereas the two infants with acute intermediate encephalopathy developed normally. Their peak TsB was ≥544 μmol/L. Having a peak TsB 600–1000 μmol/L, the risk of acute advanced and chronic bilirubin encephalopathy was 27% (95% CI 6;61), and the incidence of these conditions was 0.6 (95% CI 0.1;1.7) per 100 000. Conclusion: The incidence of infants with TsB ≥450 μmol/L was 45/100 000/year. Infants with a TsB ≥600 μmol/L had a substantial risk of developing acute advanced and chronic bilirubin encephalopathy, and the incidence of these conditions was 0.6 per 100 000. Describe the relation between levels of total serum bilirubin (TsB) ≥450 μmol/L and acute intermediate, acute advanced and chronic bilirubin encephalopathy. All infants born at gestational age ≥35 weeks in Denmark between 2000 and 2007 with a TsB ≥450 μmol/L according to the national laboratory information system. Infants diagnosed with bilirubin encephalopathy were found in the Danish National Registry of Patients. 502,766 infants at gestational age ≥35 weeks were identified. Two hundred twenty-four developed a TsB ≥450 μmol/L, equivalent to an incidence of 45/100,000/year, and it increased during the period. Incidence of infants with peak TsB of 450-499, 500-599 and 600-1000 μmol/L were 29.6, 12.7 and 2.2 per 100,000, respectively. Three infants had acute advanced bilirubin encephalopathy and got severe sequelae, whereas the two infants with acute intermediate encephalopathy developed normally. Their peak TsB was ≥544 μmol/L. Having a peak TsB 600-1000 μmol/L, the risk of acute advanced and chronic bilirubin encephalopathy was 27% (95% CI 6;61), and the incidence of these conditions was 0.6 (95% CI 0.1;1.7) per 100,000. The incidence of infants with TsB ≥450 μmol/L was 45/100,000/year. Infants with a TsB ≥600 μmol/L had a substantial risk of developing acute advanced and chronic bilirubin encephalopathy, and the incidence of these conditions was 0.6 per 100,000. |
Author | Ebbesen, Finn Vandborg, Pernille K Bjerre, Jesper V |
Author_xml | – sequence: 1 givenname: Finn surname: Ebbesen fullname: Ebbesen, Finn organization: Department of Paediatrics, Aalborg Hospital, Aarhus University Hospital, Aalborg, Denmark – sequence: 2 givenname: Jesper V surname: Bjerre fullname: Bjerre, Jesper V organization: Department of Paediatrics, Aarhus University Hospital, Aarhus, Denmark – sequence: 3 givenname: Pernille K surname: Vandborg fullname: Vandborg, Pernille K organization: Department of Paediatrics, Aalborg Hospital, Aarhus University Hospital, Aalborg, Denmark |
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Cites_doi | 10.1016/B978-1-4160-3995-2.10013-5 10.1542/peds.107.5.1075 10.1093/tropej/fmp142 10.1136/adc.2006.105361 10.1016/j.jpeds.2004.01.054 10.1111/j.1651-2227.2008.00879.x 10.1503/cmaj.060328 10.1097/00005176-199208000-00030 10.1542/peds.111.6.1303 10.1542/peds.2007-2915 10.1111/j.1442-200X.1992.tb01024.x 10.1056/NEJMoa054244 10.1038/sj.jp.7210629 10.1111/j.1552-6909.2006.00044.x 10.1111/j.1651-2227.2000.tb00738.x 10.1038/jp.2008.211 |
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Keywords | Human Bilirubin encephalopathy Pediatrics Neonates Nervous system diseases Hyperbilirubinaemia Bilirubin Statistical study Cerebral disorder Relation Hyperbilirubinemia Newborn Encephalopathy Population-based survey Central nervous system disease Clinical biology Danish Public health |
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References_xml | – volume: 354 start-page: 1889 year: 2006 end-page: 900 article-title: Outcomes among newborns with serum bilirubin levels of 25 mg per deciliter or more publication-title: N Engl J Med – volume: 92 start-page: F342 year: 2007 end-page: 6 article-title: Prospective surveillance study of severe hyperbilirubinaemia in the newborn in the UK and Ireland publication-title: Arch Dis Child Fetal Neonatal Ed – volume: 111 start-page: 303 year: 2003 end-page: 11 article-title: Infants with bilirubin levels of 30 mg/dL or more in a large managed care organization publication-title: Pediatrics – volume: 34 start-page: 642 year: 1992 end-page: 7 article-title: Determination of serum unbound bilirubin for prediction of kernicterus in low birthweight infants publication-title: Acta Paediatr Jpn – volume: 97 start-page: 1030 year: 2008 end-page: 4 article-title: Surveillance of extreme hyperbilirubinaemia in Denmark. A method to identify the newborn infants publication-title: Acta Paediatr – volume: 144 start-page: 626 year: 2004 end-page: 31 article-title: Adverse events associated with neonatal exchange transfusion in the 1990s publication-title: J Pediatr – volume: 35 start-page: 444 year: 2006 end-page: 55 article-title: A system approach for neonatal hyperbiliruninemia in term and near‐term newborns publication-title: J Obstet Gynecol Neonatal Nurse – volume: 89 start-page: 1213 year: 2000 end-page: 7 article-title: Recurrence of kernicterus in term and near‐term infants in Denmark publication-title: Acta Paediatr – volume: 21 start-page: S25 issue: Suppl. 1 year: 2001 end-page: 9 article-title: Breast feeding and jaundice publication-title: J Perinatol – start-page: 619 year: 2008 end-page: 51 – volume: 175 start-page: 587 year: 2006 end-page: 90 article-title: Incidences and causes of severe hyperbilirubinemia in Canada publication-title: CMAJ – volume: 99 start-page: 1689 year: 2010 end-page: 94 article-title: Reversibility of acute intermediate phase bilirubin encephalopathy publication-title: Acta Paediatr – volume: 29 start-page: 525 year: 2009 end-page: 45 article-title: Clinical report from the Pilot USA Kernicterus Registry publication-title: J Perinatol – volume: 56 start-page: 333 year: 2010 end-page: 6 article-title: Neurodevelopmental outcome of acute bilirubin encephalopathy publication-title: J Trop Pediatr – volume: 15 start-page: 220 year: 1992 end-page: 1 article-title: Direct bilirubin measurements in term newborns – a waste of timeand money? publication-title: J Pediatr Gastroenterol Nutr – volume: 107 start-page: 1075 year: 2001 end-page: 80 article-title: Developmental follow‐up of breastfed term and near‐term infants with hyperbilirubinemia publication-title: Pediatrics – volume: 123 start-page: 524 year: 2009 end-page: 32 article-title: Trends in hospitalizations for neonatal jaundice and kernicterus in the United States, 1988‐ 2005 publication-title: Pediatrics – start-page: 619 volume-title: Neurology of the newborn year: 2008 ident: e_1_2_8_2_2 doi: 10.1016/B978-1-4160-3995-2.10013-5 contributor: fullname: Volpe JJ – ident: e_1_2_8_15_2 doi: 10.1542/peds.107.5.1075 – ident: e_1_2_8_16_2 doi: 10.1093/tropej/fmp142 – ident: e_1_2_8_10_2 doi: 10.1136/adc.2006.105361 – volume: 99 start-page: 1689 year: 2010 ident: e_1_2_8_12_2 article-title: Reversibility of acute intermediate phase bilirubin encephalopathy publication-title: Acta Paediatr contributor: fullname: Hansen TWR – ident: e_1_2_8_14_2 doi: 10.1016/j.jpeds.2004.01.054 – ident: e_1_2_8_4_2 doi: 10.1111/j.1651-2227.2008.00879.x – ident: e_1_2_8_8_2 doi: 10.1503/cmaj.060328 – ident: e_1_2_8_5_2 doi: 10.1097/00005176-199208000-00030 – ident: e_1_2_8_9_2 doi: 10.1542/peds.111.6.1303 – ident: e_1_2_8_17_2 doi: 10.1542/peds.2007-2915 – ident: e_1_2_8_18_2 doi: 10.1111/j.1442-200X.1992.tb01024.x – ident: e_1_2_8_7_2 doi: 10.1056/NEJMoa054244 – ident: e_1_2_8_6_2 doi: 10.1038/sj.jp.7210629 – ident: e_1_2_8_11_2 doi: 10.1111/j.1552-6909.2006.00044.x – ident: e_1_2_8_3_2 doi: 10.1111/j.1651-2227.2000.tb00738.x – ident: e_1_2_8_13_2 doi: 10.1038/jp.2008.211 |
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Snippet | Aim: Describe the relation between levels of total serum bilirubin (TsB) ≥450 μmol/L and acute intermediate, acute advanced and chronic bilirubin... Describe the relation between levels of total serum bilirubin (TsB) ≥450 μmol/L and acute intermediate, acute advanced and chronic bilirubin encephalopathy.... Aim: Describe the relation between levels of total serum bilirubin (TsB) ≥450 μmol/L and acute intermediate, acute advanced and chronic bilirubin... AIMDescribe the relation between levels of total serum bilirubin (TsB) ≥450 μmol/L and acute intermediate, acute advanced and chronic bilirubin... |
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SubjectTerms | Bilirubin - blood Bilirubin encephalopathy Biological and medical sciences Denmark - epidemiology Female Follow-Up Studies General aspects Humans Hyperbilirubinaemia Incidence Infant, Newborn Infant, Premature Infant, Premature, Diseases - epidemiology Kernicterus - epidemiology Male Medical sciences Miscellaneous Neonates Public health. Hygiene Public health. Hygiene-occupational medicine Registries Risk Assessment |
Title | Relation between serum bilirubin levels ≥450 μmol/L and bilirubin encephalopathy; a Danish population-based study |
URI | https://api.istex.fr/ark:/67375/WNG-8646F72N-C/fulltext.pdf https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fj.1651-2227.2011.02565.x https://www.ncbi.nlm.nih.gov/pubmed/22176133 https://search.proquest.com/docview/926509121 |
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