Newborn screening for biliary atresia using direct bilirubin: An implementation science study.

Objective: Biliary atresia (BA) is a liver disease of infancy characterized by obstruction of the biliary tree. Infants with BA have the best outcomes when identified early and the Kasai portoenterostomy is performed before 45 days of life (DoL). In our hospital system, the average age at Kasai was...

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Publicado en:Journal of Medical Screening Vol. 32; no. 2; pp. 61 - 67
Autores principales: Rabbani, Tebyan, Shah, Jay
Formato: research tables/charts Journal Article
Publicado: Sage Publications Inc. Jun2025
Acceso en línea:Ver este registro en EBSCOhost
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      jtl: Journal of Medical Screening
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      dt: Jun2025
      vid: 32
      iid: 2
      pid: 344
      pub: Sage Publications Inc.
      place: Thousand Oaks, California
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        10.1177/09691413241284243
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        atl: Newborn screening for biliary atresia using direct bilirubin: An implementation science study.
      aug:
        au:
          Rabbani, Tebyan
          Shah, Jay
        affil: 24349Lucile Salter Packard Children's Hospital at Stanford, Palo Alto, CA, USA
      sug:
        subj:
          Biliary Atresia Diagnosis
          Health Screening Methods
          Neonatal Assessment
          Bilirubin Blood
          Human
          Infant, Newborn
          Texas
          Academic Medical Centers
          Biliary Atresia Surgery
          Anastomosis, Surgical Methods
          Implementation Science
          Health Policy
          Gastroenterology Care
          Descriptive Statistics
          Infant, Newborn: birth-1 month
      ab: Objective: Biliary atresia (BA) is a liver disease of infancy characterized by obstruction of the biliary tree. Infants with BA have the best outcomes when identified early and the Kasai portoenterostomy is performed before 45 days of life (DoL). In our hospital system, the average age at Kasai was 60 DoL. To address the problem of late presentation, we implemented a two-stage BA screening strategy utilizing direct bilirubin (DB). Methods: New institutional policies were established that all newborns were tested at 24–48 h of life, and those with levels ≥0.5 mg/dL were followed further. The infant's primary care provider was contacted to recommend a repeat DB at 2 weeks of life. If the repeat DB was ≥1.0 mg/dL, the patient was evaluated by gastroenterology. Results: Over the 16 months, 3880 infants were born and 3861 (99.5%) were screened; 53 infants (1.3%) had DB levels ≥0.5 mg/dL initially. Upon repeat testing at 2 weeks, there were three groups of infants: not retested (n = 1), retested <1.0 mg/dL (n = 40), and retested ≥1.0 mg/dL (n = 12). The average time to be seen by gastroenterology was 4.3 days or 18.3 DoL. Discussion: The screening included a series of steps that needed to be implemented effectively. Screening had a net false positive rate of 0.3% (12 out of 3861) and identified causes of cholestasis other than BA. BA was excluded by 28 DoL on average. Our results can provide a template for other institutions interested in implementing a BA screening protocol in their practice.
      pubtype: Academic Journal
      doctype:
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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