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Updated: Mar 26, 2026

Biochemical Measurement of Neonatal Hypoxia
Published on: August 24, 2011
Severe Neonatal Hyperbilirubinemia Decreased after the 2007 Canadian Guidelines
Michael Sgro1, Sharmilaa Kandasamy2, Vibhuti Shah3
1Keenan Research Center of the Li Ka Shing Knowledge Institute, St. Michael's Hospital, Toronto, Ontario, Canada; Department of Pediatrics, St. Michael's Hospital, Toronto, Ontario, Canada; Division of Neonatology, Department of Pediatrics, University of Toronto, Toronto, Ontario, Canada.
Insights
Severe neonatal hyperbilirubinemia incidence in Canada decreased significantly after 2007 guideline implementation. The minimum estimated incidence is now 1 in 8352 live births, a notable improvement in infant health outcomes.
Area of Science:
- Neonatal Medicine
- Pediatrics
- Public Health
Background:
- Severe neonatal hyperbilirubinemia poses significant health risks to newborns.
- The Canadian Pediatric Society (CPS) established guidelines in 2007 to manage hyperbilirubinemia.
- Previous incidence rates in Canada were reported at 1 in 2480.
Purpose of the Study:
- To estimate the incidence of severe neonatal hyperbilirubinemia in Canada between 2011 and 2013.
- To assess the impact of the 2007 CPS guidelines on hyperbilirubinemia rates.
Main Methods:
- Prospective surveillance of term infants (≤ 60 days) with peak serum total bilirubin > 425 μmol/L or exchange transfusion.
- Exclusion criteria included rhesus isoimmunization and prematurity (< 35 weeks gestation).
- Data collected via the Canadian Pediatric Surveillance Program from 2011-2013.
Main Results:
- Ninety-one cases of severe neonatal hyperbilirubinemia were confirmed.
- The incidence was estimated at a minimum of 1 in 8352 live births.
- Infants were 3.5 times less likely to be diagnosed with severe hyperbilirubinemia compared to 2002-2004.
Conclusions:
- The incidence of severe neonatal hyperbilirubinemia in Canada has substantially decreased.
- Implementation of CPS guidelines and increased physician awareness are likely contributors to this decline.
- This trend suggests improved management and outcomes for neonatal hyperbilirubinemia in Canada.
Objectives:
To estimate the incidence of severe neonatal hyperbilirubinemia in Canada from 2011-2013 following the implementation of the Canadian Pediatric Society's published guidelines on the management of hyperbilirubinemia in 2007. Our previously reported incidence of hyperbilirubinemia in Canada was 1 in 2480.
Study Design:
Term infants ≤ 60 days of age, with a peak serum total bilirubin level > 425 μmol/L or who had an exchange transfusion were followed prospectively through the Canadian Pediatric Surveillance Program from 2011-2013. Infants with rhesus isoimmunization or born < 35 weeks gestation were excluded.
Results:
Ninety-one cases of severe neonatal hyperbilirubinemia were confirmed. Sixty-nine infants (76%) were readmitted to hospital, 47 (52%) of them within 6 days of age. The remaining 22 infants (24%) were identified with severe neonatal hyperbilirubinemia before they were discharged from the hospital. The mean reported peak bilirubin level was 484 μmol/L (range 181-788; SD ± 92). An etiology was identified in 57 (63%) cases, with ABO incompatibility (n = 35) and glucose-6-phosphate dehydrogenase deficiency (n = 11) being the most common. An infant was 3.5 times more likely to be diagnosed with severe neonatal hyperbilirubinemia from 2002-2004 compared with 2011-2013 (95% CI 2.72-4.47).
Conclusions:
The minimum estimated incidence of severe neonatal hyperbilirubinemia in Canada is 1 in 8352 live births. Introduction of the Canadian Pediatric Society guidelines and improved physician awareness of severe neonatal hyperbilirubinemia in the last 10 years likely made positive contributions to this trend.
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