Medical Status of 219 children with biliary atresia surviving long-term with their native livers: Results from a North American multicenter consortium

Vicky Lee Ng, Barbara H. Haber, John C. Magee, Alexander Miethke, Karen F. Murray, Sonia Michail, Saul J. Karpen, Nanda Kerkar, Jean Molleston, Rene Romero, Philip Rosenthal, Kathleen B. Schwarz, Benjamin L. Shneider, Yumirle P. Turmelle, Estella M. Alonso, Averell H. Sherker, Ronald J. Sokol

Research output: Contribution to journalArticle

30 Citations (Scopus)

Abstract

Objectives To examine the medical status of children with biliary atresia (BA) with their native livers after hepato- portoenterostomy (HPE) surgery. Study design The Childhood Liver Disease Research and Education Network database was utilized to examine subjects with BA living with their native livers 5 or more years after HPE and to describe the prevalence of subjects with BA with an "ideal" outcome, defined as no clinical evidence of chronic liver disease, normal liver biochemical indices (aspartate aminotransferase, alanine aminotransferase, γ-glutamyl transpeptidase, platelet count, total bilirubin, international normalized ratio, and albumin), and normal health-related quality of life 5 or more years after HPE. Results Children with BA (n = 219; 43% male) with median age 9.7 years were studied. Median age at HPE was 56 (range 7-125) days. Median age- and sex-adjusted height and weight z-scores at 5-year follow-up were 0.487 (IQR -0.27 to 1.02) and 0.00 (IQR -0.74 to 0.70), respectively. During the 12 preceding months, cholangitis and bone fractures occurred in 17% and 5.5%, respectively. Health-related quality of life was reported normal by 53% of patients. However, only 1.8% met the study definition of "ideal" outcome. Individual tests of liver synthetic function (total bilirubin, albumin, and international normalized ratio) were normal in 75%, 85%, and 73% of the study cohort. Conclusion Cholangitis and fractures in long-term survivors underscore the importance of ongoing medical surveillance. Over 98% of this North American cohort of subjects with BA living with native livers 5 or more years after HPE have clinical or biochemical evidence of chronic liver disease.

Original languageEnglish
JournalJournal of Pediatrics
Volume165
Issue number3
DOIs
StatePublished - 2014

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Biliary Atresia
Liver
Liver Diseases
Cholangitis
International Normalized Ratio
Bilirubin
Albumins
Chronic Disease
Quality of Life
gamma-Glutamyltransferase
Liver Function Tests
Bone Fractures
Aspartate Aminotransferases
Alanine Transaminase
Platelet Count
Survivors
Cohort Studies
Databases
Education
Weights and Measures

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health
  • Medicine(all)

Cite this

Medical Status of 219 children with biliary atresia surviving long-term with their native livers : Results from a North American multicenter consortium. / Ng, Vicky Lee; Haber, Barbara H.; Magee, John C.; Miethke, Alexander; Murray, Karen F.; Michail, Sonia; Karpen, Saul J.; Kerkar, Nanda; Molleston, Jean; Romero, Rene; Rosenthal, Philip; Schwarz, Kathleen B.; Shneider, Benjamin L.; Turmelle, Yumirle P.; Alonso, Estella M.; Sherker, Averell H.; Sokol, Ronald J.

In: Journal of Pediatrics, Vol. 165, No. 3, 2014.

Research output: Contribution to journalArticle

Ng, VL, Haber, BH, Magee, JC, Miethke, A, Murray, KF, Michail, S, Karpen, SJ, Kerkar, N, Molleston, J, Romero, R, Rosenthal, P, Schwarz, KB, Shneider, BL, Turmelle, YP, Alonso, EM, Sherker, AH & Sokol, RJ 2014, 'Medical Status of 219 children with biliary atresia surviving long-term with their native livers: Results from a North American multicenter consortium', Journal of Pediatrics, vol. 165, no. 3. https://doi.org/10.1016/j.jpeds.2014.05.038
Ng, Vicky Lee ; Haber, Barbara H. ; Magee, John C. ; Miethke, Alexander ; Murray, Karen F. ; Michail, Sonia ; Karpen, Saul J. ; Kerkar, Nanda ; Molleston, Jean ; Romero, Rene ; Rosenthal, Philip ; Schwarz, Kathleen B. ; Shneider, Benjamin L. ; Turmelle, Yumirle P. ; Alonso, Estella M. ; Sherker, Averell H. ; Sokol, Ronald J. / Medical Status of 219 children with biliary atresia surviving long-term with their native livers : Results from a North American multicenter consortium. In: Journal of Pediatrics. 2014 ; Vol. 165, No. 3.
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abstract = "Objectives To examine the medical status of children with biliary atresia (BA) with their native livers after hepato- portoenterostomy (HPE) surgery. Study design The Childhood Liver Disease Research and Education Network database was utilized to examine subjects with BA living with their native livers 5 or more years after HPE and to describe the prevalence of subjects with BA with an {"}ideal{"} outcome, defined as no clinical evidence of chronic liver disease, normal liver biochemical indices (aspartate aminotransferase, alanine aminotransferase, γ-glutamyl transpeptidase, platelet count, total bilirubin, international normalized ratio, and albumin), and normal health-related quality of life 5 or more years after HPE. Results Children with BA (n = 219; 43{\%} male) with median age 9.7 years were studied. Median age at HPE was 56 (range 7-125) days. Median age- and sex-adjusted height and weight z-scores at 5-year follow-up were 0.487 (IQR -0.27 to 1.02) and 0.00 (IQR -0.74 to 0.70), respectively. During the 12 preceding months, cholangitis and bone fractures occurred in 17{\%} and 5.5{\%}, respectively. Health-related quality of life was reported normal by 53{\%} of patients. However, only 1.8{\%} met the study definition of {"}ideal{"} outcome. Individual tests of liver synthetic function (total bilirubin, albumin, and international normalized ratio) were normal in 75{\%}, 85{\%}, and 73{\%} of the study cohort. Conclusion Cholangitis and fractures in long-term survivors underscore the importance of ongoing medical surveillance. Over 98{\%} of this North American cohort of subjects with BA living with native livers 5 or more years after HPE have clinical or biochemical evidence of chronic liver disease.",
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T2 - Results from a North American multicenter consortium

AU - Ng, Vicky Lee

AU - Haber, Barbara H.

AU - Magee, John C.

AU - Miethke, Alexander

AU - Murray, Karen F.

AU - Michail, Sonia

AU - Karpen, Saul J.

AU - Kerkar, Nanda

AU - Molleston, Jean

AU - Romero, Rene

AU - Rosenthal, Philip

AU - Schwarz, Kathleen B.

AU - Shneider, Benjamin L.

AU - Turmelle, Yumirle P.

AU - Alonso, Estella M.

AU - Sherker, Averell H.

AU - Sokol, Ronald J.

PY - 2014

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N2 - Objectives To examine the medical status of children with biliary atresia (BA) with their native livers after hepato- portoenterostomy (HPE) surgery. Study design The Childhood Liver Disease Research and Education Network database was utilized to examine subjects with BA living with their native livers 5 or more years after HPE and to describe the prevalence of subjects with BA with an "ideal" outcome, defined as no clinical evidence of chronic liver disease, normal liver biochemical indices (aspartate aminotransferase, alanine aminotransferase, γ-glutamyl transpeptidase, platelet count, total bilirubin, international normalized ratio, and albumin), and normal health-related quality of life 5 or more years after HPE. Results Children with BA (n = 219; 43% male) with median age 9.7 years were studied. Median age at HPE was 56 (range 7-125) days. Median age- and sex-adjusted height and weight z-scores at 5-year follow-up were 0.487 (IQR -0.27 to 1.02) and 0.00 (IQR -0.74 to 0.70), respectively. During the 12 preceding months, cholangitis and bone fractures occurred in 17% and 5.5%, respectively. Health-related quality of life was reported normal by 53% of patients. However, only 1.8% met the study definition of "ideal" outcome. Individual tests of liver synthetic function (total bilirubin, albumin, and international normalized ratio) were normal in 75%, 85%, and 73% of the study cohort. Conclusion Cholangitis and fractures in long-term survivors underscore the importance of ongoing medical surveillance. Over 98% of this North American cohort of subjects with BA living with native livers 5 or more years after HPE have clinical or biochemical evidence of chronic liver disease.

AB - Objectives To examine the medical status of children with biliary atresia (BA) with their native livers after hepato- portoenterostomy (HPE) surgery. Study design The Childhood Liver Disease Research and Education Network database was utilized to examine subjects with BA living with their native livers 5 or more years after HPE and to describe the prevalence of subjects with BA with an "ideal" outcome, defined as no clinical evidence of chronic liver disease, normal liver biochemical indices (aspartate aminotransferase, alanine aminotransferase, γ-glutamyl transpeptidase, platelet count, total bilirubin, international normalized ratio, and albumin), and normal health-related quality of life 5 or more years after HPE. Results Children with BA (n = 219; 43% male) with median age 9.7 years were studied. Median age at HPE was 56 (range 7-125) days. Median age- and sex-adjusted height and weight z-scores at 5-year follow-up were 0.487 (IQR -0.27 to 1.02) and 0.00 (IQR -0.74 to 0.70), respectively. During the 12 preceding months, cholangitis and bone fractures occurred in 17% and 5.5%, respectively. Health-related quality of life was reported normal by 53% of patients. However, only 1.8% met the study definition of "ideal" outcome. Individual tests of liver synthetic function (total bilirubin, albumin, and international normalized ratio) were normal in 75%, 85%, and 73% of the study cohort. Conclusion Cholangitis and fractures in long-term survivors underscore the importance of ongoing medical surveillance. Over 98% of this North American cohort of subjects with BA living with native livers 5 or more years after HPE have clinical or biochemical evidence of chronic liver disease.

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