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Patients with biliary atresia have elevated direct/conjugated bilirubin levels shortly after birth
Sanjiv Harpavat1, Milton J Finegold, Saul J Karpen
1Department of Pediatrics, BaylorCollege of Medicine, Houston,TX, USA.
Insights
Biliary atresia (BA) infants show elevated direct/conjugated bilirubin (DB/CB) levels shortly after birth, even with normal total bilirubin. Early screening of DB/CB levels, not just ratios, can improve detection and outcomes for newborns with BA.
Area of Science:
- Neonatal Medicine
- Pediatric Gastroenterology
- Bilirubin Metabolism
Background:
- Biliary atresia (BA) is a serious neonatal liver disease.
- Early diagnosis of BA is crucial for improved patient outcomes.
- Current diagnostic approaches may miss early signs of BA.
Purpose of the Study:
- To determine the earliest detectable time for biliary atresia (BA).
- To investigate direct/conjugated bilirubin (DB/CB) levels in newborns with BA shortly after birth.
- To hypothesize that newborns may not have acquired the disease immediately after birth.
Main Methods:
- Retrospective analysis of newborn DB/CB levels from birth hospitals.
- Inclusion of BA patients born between 2007-2010 and treated at Texas Children's Hospital.
- Exclusion of patients with BA splenic malformation syndrome or prematurity; controls were healthy term newborns.
Main Results:
- 56% of 61 BA subjects had measured newborn DB/CB levels, all exceeding norms.
- BA infants had significantly higher mean DB levels at 24-48 hours (1.4 ± 0.43 mg/dL) vs. controls (0.19 ± 0.075 mg/dL).
- Most BA patients (79%) had normal DB:TB ratios (≤0.2) despite elevated DB/CB.
Conclusions:
- Elevated DB/CB levels are present shortly after birth in infants with BA.
- Screening all newborns for elevated DB/CB levels, irrespective of jaundice appearance, is recommended.
- Follow-up of all newborns with elevated DB/CB levels, not solely those with high DB:TB ratios, may enhance early BA detection.
Objectives:
Healthy infants are thought to acquire biliary atresia (BA) in the first weeks of life. Because those diagnosed earlier have better outcomes, we were interested in determining the earliest time BA could be detected. We started by examining the immediate postnatal period, hypothesizing that newborns would not yet have acquired disease and still have normal direct/conjugated bilirubin (DB/CB) levels.
Patients And Methods:
Newborn DB/CB levels were obtained retrospectively from birth hospitals. Subjects with BA were born between 2007 and 2010 and cared for at Texas Children's Hospital. Those with BA splenic malformation syndrome or born prematurely were excluded. Control subjects were term newborns who later never developed neonatal liver disease.
Results:
Of the 61 subjects with BA, 56% had newborn DB/CB levels measured. All DB/CB levels exceeded laboratory norms and rose over time. At 24 to 48 hours of life, subjects with BA had mean DB levels significantly higher than those of controls (1.4 ± 0.43 vs. 0.19 ± 0.075 mg/dL, P < .0001), even while their mean total bilirubin (TB) levels remained below phototherapy limits. Finally, despite the elevated DB/CB levels, the majority of patients (79%) had normal DB:TB ratios ≤ 0.2.
Conclusions:
Patients with BA have elevated DB/CB levels shortly after birth. To detect affected infants earlier and improve outcomes, the results suggest two possibilities: (1) screen all newborns for elevated DB/CB levels, rather than just those who appear jaundiced; and then (2) follow all newborns with elevated DB/CB levels, rather than just those with DB:TB ratios >0.2.
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