Hepatology Program

Part of the Division of Pediatric Gastroenterology, Hepatology and Nutrition, the Hepatology Program offers consultative services and comprehensive care for children with a wide range of liver and hepatobiliary disorders. Among the services provided at the Hepatology Program are:

  • Inpatient and outpatient consultation
  • Diagnosis using a variety of serologic, metabolic, molecular, histologic, radiographic and endoscopic examinations
  • Comprehensive therapeutic plans and consultations including, but not limited to:
    • Viral hepatitis
    • Cholestasis
    • Autoimmune liver disease
    • Portal hypertension
    • Metabolic liver disease
    • Wilson disease
    • Cirrhosis and its complications
  • Collaborative consultation and care with the Hillman Center for Pediatric Transplantation and the Division of Pediatric Surgery for liver transplantation, hepatobiliary surgery (biliary atresia, biliary cysts, liver tumors, portosystemic shunts, etc.) and other innovative surgical approaches to liver disease in children.
  • Care plan coordination
  • Long-term follow-up care
  • State-of-the-art clinical research
  • Biliary atresia
  • Cholestatic liver disease
  • Acute liver failure

Referral Requirements

Referrals are not required from primary care physicians or other Children’s Hospital of Pittsburgh specialty services. Referrals for patients enrolled in managed care insurance plans may require authorization from the insurance provider and primary care physician.

All necessary referral and authorization forms must be received before the patient’s visit. Prior submission of medical records, imaging studies and biopsy slides are recommended for optimal consultation.

Doctors

Locations

Clinical Studies

  • Hepatology

    Children's Hospital of Pittsburgh of UPMC
    4401 Penn Avenue
    Floor 3
    Pittsburgh, PA 15224
    412-692-5180
  • Alpha-1 Antitrypsin Deficiency Study – Phase II

    A Preliminary Study of the Efficacy and Safety of Carbamazepine in Severe Liver Disease Due to Alpha-1-Antitrypsin Deficiency

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    Cholestasis Long-term Observation: The LOGIC Study

    Longitudinal Study of Genetic Causes of Intrahepatic Cholestasis (LOGIC)

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    Mitochondrial Hepatopathies Long-term Observation: The MITOHEP Study

    Longitudinal Study of Mitochondrial Hepatopathies

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