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Normal Gamma Glutamyl Transferase Levels at Presentation Predict Poor Outcome in Biliary Atresia.
Shankar, Sahana; Bolia, Rishi; Foo, Hee Wei; D'Arcy, Colleen E; Hardikar, Natasha; Wensing, Martin; Hardikar, Winita.
Affiliation
  • Shankar S; Department of Gastroenterology and Clinical Nutrition, Royal Children's Hospital, Melbourne, Australia.
  • Bolia R; Division of Paediatric Gastroenterology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Foo HW; Department of Gastroenterology and Clinical Nutrition, Royal Children's Hospital, Melbourne, Australia.
  • D'Arcy CE; Department of Anatomical Pathology, Royal Children's Hospital, Melbourne, Australia.
  • Hardikar N; Department of Gastroenterology and Clinical Nutrition, Royal Children's Hospital, Melbourne, Australia.
  • Wensing M; Department of Gastroenterology and Clinical Nutrition, Royal Children's Hospital, Melbourne, Australia.
  • Hardikar W; Department of Gastroenterology and Clinical Nutrition, Royal Children's Hospital, Melbourne, Australia.
J Pediatr Gastroenterol Nutr ; 70(3): 350-355, 2020 03.
Article in En | MEDLINE | ID: mdl-31738295
ABSTRACT

OBJECTIVES:

Gamma-glutamyl transferase levels (GGT) are typically elevated in biliary atresia (BA), but normal GGT levels have been observed. This cohort of "normal GGT" BA has neither been described nor has the prognostic value of GGT level on outcomes in BA. We aimed to describe outcomes of a single-centre Australian cohort of infants with BA and assess the impact of GGT level at presentation on outcomes in BA.

METHODS:

Infants diagnosed with BA between 1991 and 2017 were retrospectively analysed. Outcomes were defined as survival with native liver, liver transplantation (LT), and death. Patients were categorized into normal (<200I U/L) or high GGT groups based on a mean of 3 consecutive GGT values done before Kasai portoenterostomy (KPE). Baseline parameters, age at surgery, clearance of jaundice (COJ), and outcomes were compared between the 2 groups.

RESULTS:

One hundred thirteen infants underwent KPE at median 61 (30-149) days. At a median follow-up of 14.2 (0.9-26.3) years, 35% (39/113) patients were surviving with native liver, 55% (62/113) underwent LT and 11% (12/113) died pretransplant. 12.3% (14/113) patients had normal GGT. Age at KPE and time to COJ were similar between normal and high GGT groups. Normal GGT group had shorter time from KPE to LT (11 vs 18 months, P = 0.02), underwent LT at a younger age (14 vs 20 months, P = 0.04), and had poorer transplant-free survival (P = 0.04) than high GGT group.

CONCLUSIONS:

12.3% of infants with BA had normal GGT levels at diagnosis. Low GGT levels at presentation in BA was associated with a poorer outcome.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biliary Atresia Type of study: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans / Infant Country/Region as subject: Oceania Language: En Journal: J Pediatr Gastroenterol Nutr Year: 2020 Document type: Article Affiliation country: Australia

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biliary Atresia Type of study: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Humans / Infant Country/Region as subject: Oceania Language: En Journal: J Pediatr Gastroenterol Nutr Year: 2020 Document type: Article Affiliation country: Australia