Growth failure and outcomes in infants with biliary atresia: A report from the biliary atresia research consortium

Hepatology

Volumn 46, Issue 5, 2007, Pages 1632-1638

  DeRusso, Patricia A ^a,b   Ye, Wen ^c   Shepherd, Ross ^d   Haber, Barbara A ^e   Shneider, Benjamin L ^f   Whitington, Peter F ^g   Schwarz, Kathleen B ^a   Bezerra, Jorge A ^h   Rosenthal, Philip ⁱ   Karpen, Saul ^j   Squires, Robert H ^k   Magee, John C ^c,n   Robuck, Patricia R ^l   Sokol, Ronald J ^m  

^a JOHNS HOPKINS CHILDREN S CENTER   (United States)

^b PFIZER INC   (United States)

^c UNIVERSITY OF MICHIGAN   (United States)

^d ST LOUIS CHILDREN S HOSPITAL   (United States)

^e CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^f MOUNT SINAI SCHOOL OF MEDICINE   (United States)

^g CHILDREN'S MEMORIAL HOSPITAL   (United States)

^h CINCINNATI CHILDREN'S HOSPITAL MEDICAL CENTER   (United States)

ⁱ UNIVERSITY OF CALIFORNIA   (United States)

^j BAYLOR COLLEGE OF MEDICINE   (United States)

^k CHILDREN S HOSPITAL OF PITTSBURGH   (United States)

^l NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES   (United States)

^m UNIVERSITY OF COLORADO SCHOOL OF MEDICINE   (United States)

ⁿ UNIVERSITY OF MICHIGAN HEALTH SYSTEM   (United States)

more..

Author keywords

[No Author keywords available]

Indexed keywords

BILIRUBIN;

ARTICLE; BILE DUCT ATRESIA; CHILD GROWTH; CONTROLLED STUDY; FEMALE; GROWTH CURVE; GROWTH DISORDER; HUMAN; INFANT; INFANT MORTALITY; LIVER TRANSPLANTATION; MAJOR CLINICAL STUDY; MALE; MEDICAL RESEARCH; OUTCOME ASSESSMENT; PORTOENTEROSTOMY; PRIORITY JOURNAL; SCORING SYSTEM; AGE; BILIARY TRACT SURGERY; BILIRUBIN BLOOD LEVEL; BODY WEIGHT; DIET SUPPLEMENTATION; ENTEROSTOMY; GROWTH RATE; HEPATOPORTOENTEROSTOMY; PEDIATRIC HOSPITAL; RETROSPECTIVE STUDY;

BILIARY ATRESIA; BILIRUBIN; COHORT STUDIES; FEMALE; GROWTH DISORDERS; HUMANS; INFANT; INFANT, NEWBORN; LIVER TRANSPLANTATION; MALE; PARENTERAL NUTRITION; RETROSPECTIVE STUDIES; RISK FACTORS; TREATMENT OUTCOME; UNITED STATES;

EID: 36348983232     PISSN: 02709139     EISSN: None     Source Type: Journal    
DOI: 10.1002/hep.21923     Document Type: Article

References (20)

1. Sokol RJ, Mack D, Narkewicz MR, Karrer FM. Pathogenesis and outcome of biliary atresia: Current concepts. J Pediatr Gastroenterol Nutr 2003;37:4-21.
2. Perlmutter DH, Shepherd RW. Extrahepatic biliary atresia: A disease or a phenotype? HEPATOLOGY 2002;35:1297-1304.
3. Karrer FM, Bensard DD. Neonatal cholestasis. Semin Pediatr Surg 2000;9:166-169.
4. Chardot C, Carton M, Spire-Bendelac N, Le Pommelet C, Golmard JL, Auvert B. Epidemiology of biliary atresia in France: a national study 1986-96. J Hepatol 1999;31:1006-1013.
5. Karrer FM, Price MR, Bensard DD, Sokol RJ, Narkewicz MR, Smith DJ, et al. Long-term results with Kasai operation for biliary atresia. Arch Surg 1996;131:493-496.
6. Shneider BL, Brown MB, Haber B, Whitington PF, Schwarz K, Squires R, et al. A multi-center study of the outcome of biliary atresia in the United States, 1997-2000. J Pediatr 2006;148:467-474.
7. McDiarmid SV, Anand R, Lindblad AS. Development of a pediatric end-stage liver disease score to predict poor outcome in children awaiting liver transplantation. Transplantation 2002;74:173-181.
8. Pierro A, Koletzko B, Camielli V, Superina RA, Roberts EA, Filler RM, et al. Resting energy expenditure is increased in infants and children with extrahepatic biliary atresia. J Pediatr Surg 1989;24:534-538.
9. Greer R, Lehnert M, Lewindon P, Cleghorn GJ, Shepherd RW. Body composition and components of energy expenditure in children with end-stage liver disease. J Pediatr Gastroenterol Nutr 2003;36:358-363.
10. Chin SE, Shepherd RW, Thomas BJ, Cleghorn GJ, Patrick MK, Wilcox JA, et al. The nature of malnutrition in children with end-stage liver disease awaiting orthotopic liver transplantation. Am J Clin Nutr 1992;56:164-168.
11. Sokol RJ, Stall C. Anthropometric evaluation of children with chronic liver disease. Am J Clin Nutr 1990;52:203-208.
12. Utterson EC, Shepherd RW, Sokol RJ, Bucuvalas J, Magee JC, McDiarmid SV, et al. Biliary atresia: Clinical profiles, risk factors, and outcomes of 755 patients listed for liver transplantation. J Pediatr 2005;147:180-185.
13. Shepherd RW, Chin SE, Cleghorn GJ, Patrick M, Ong TH, Lynch SV, et al. Malnutrition in children with chronic liver disease accepted for liver transplantation: clinical profile and effect on outcome. J Paediatr Child Health 1991;27:295-299.
14. Chin SE, Shepherd RW, Thomas BJ, Cleghorn GJ, Patrick MK, Wilcox JA, et al. Nutritional support in children with end-stage liver disease: a randomized crossover trial of a branched-chain amino acid supplement. Am J Clin Nutr 1992;56:158-163.
15. Chin SE, Shepherd RW, Cleghorn GJ, Patrick M, Ong TH, Wilcox J, et al. Pre-operative nutritional support in children with end-stage liver disease accepted for liver transplantation: an approach to management. J Gastroenterol Hepatol 1990;5:566-572.
16. Holt RI, Miell JP, Jones JS, Mieli-Vergani B, Baker AJ. Nasogastric feeding enhances nutritional status in paediatric liver disease but does not alter circulating levels of IGF-I and IGF binding proteins. Clin Endocrinol 2000;52:217-224.
17. Zhang D, Lin X, Raz J, Sowers M. Semiparametric stochastic mixed models for longitudinal data. J Amer Statistical Assoc 1998;93:710-719.
18. Ohhama Y, Shinkai M, Fujita S, Nishi T, Yamamoto H. Early prediction of long-term survival and the timing of liver transplantation after the Kasai operation. J Pediatr Surg 2000;35:1031-1034.
19. Arvay JL, Zemel BS, Gallagher PR, Rovner AJ, Mulberg AE, Stallings VA, et al. Body composition of children age 1 to 12 years with biliary atresia or alagille syndrome. J Pediatr Gastroenterol Nutr 2005;40:146-150.
20. Hadzic N, Davenport M, Tizzard S, Singer J, Howard ER, Mieli-Vergani G. Long-term survival following Kasai portoenterostomy: Is chronic liver disease inevitable? J Pediatr Gastroenterol Nutr 2003;37:430-433.