62
Views
0
CrossRef citations to date
0
Altmetric
Reviews

Improving treatment outcomes in patients with biliary atresia

, FRCS (Paeds) (Senior Clinical Fellow) & , ChM FRCS (Paeds) (Professor of Paediatric Surgery)

Bibliography

  • Kasai M, Suzuki S. A new operation for “non-correctable” biliary atresia: hepatic portoenterostomy. Shujutsu 1959;13:733-9
  • Starzl TE, Marchioro TL, Vonkaulla KN, et al. Homotransplantation of the liver in humans. Surg Gynecol Obstet 1963;117:659-76
  • Davenport M, Savage M, Mowat AP, Howard ER. Biliary atresia splenic malformation syndrome: an etiologic and prognostic subgroup. Surgery 1993;113:662-8
  • Davenport M, Tizzard SA, Underhill J, et al. The biliary atresia splenic malformation syndrome: a 28-year single-center retrospective study. J Pediatr 2006;149:393-400
  • Caponcelli E, Knisely AS, Davenport M. Cystic biliary atresia: an etiologic and prognostic subgroup. J Pediatr Surg 2008;43:1619-24
  • Petersen C. Biliary atresia: the animal models. Semin Pediatr Surg 2012;21:185-91
  • Takamizawa S, Zaima A, Muraji T, et al. Can biliary atresia be diagnosed by ultrasonography alone? J Pediatr Surg 2007;42:2093-6
  • Shneider BL, Brown MB, Haber B, et al. A multicenter study of the outcome of biliary atresia in the United States, 1997 to 2000. J Pediatr 2006;148:467-74
  • Grieve A, Makin E, Davenport M. Aspartate Aminotransferase-to-Platelet ratio index (APRi) in infants with biliary atresia: prognostic value at presentation. J Pediatr Surg 2013;48:789-95
  • Davenport M, Puricelli V, Farrant P, et al. The outcome of the older (≥100 days) infant with biliary atresia. J Pediatr Surg 2004;39:575-81
  • McKiernan PJ, Baker AJ, Kelly D. The frequency and outcome of biliary atresia in the UK and Ireland. Lancet 2000;355(9197):25-9
  • Esteves E, Clemente Neto E, Ottaiano Neto M, et al. Laparoscopic Kasai portoenterostomy for biliary atresia. Pediatr Surg Int 2002;18:737-40
  • Martinez-Ferro M, Esteves E, Laje P. Laparoscopic treatment of biliary atresia and choledochal cyst. Semin Pediatr Surg 2005;14:206-15
  • Lee H, Hirose S, Bratton B, Farmer D. Initial experience with complex laparoscopic biliary surgery in children: biliary atresia and choledochal cyst. J Pediatr Surg 2004;39:804-7
  • Liem NT, Son TN, Quynh TA, Hoa NP. Early outcomes of laparoscopic surgery for biliary atresia. J Pediatr Surg 2010;45:1665-7
  • Yamataka A, Lane GJ, Cazares J. Laparoscopic surgery for biliary atresia and choledochal cyst. Semin Pediatr Surg 2012;21:201-10
  • Chan KW, Lee KH, Wong HY V, et al. From laparoscopic to open Kasai portoenterostomy: the outcome after reintroduction of open Kasai portoenterostomy in infant with biliary atresia. Pediatr Surg Int 2014;30:605-8
  • Ure BM, Kuebler JF, Schukfeh N, et al. Survival with the native liver after laparoscopic versus conventional Kasai portoenterostomy in infants with biliary atresia: a prospective trial. Ann Surg 2011;253:826-30
  • Wong KK, Chung PH, Chan K-L, et al. Should open Kasai portoenterostomy be performed for biliary atresia in the era of laparoscopy? Pediatr Surg Int 2008;24:931-3
  • Laje P, Clark FH, Friedman JR, Flake AW. Increased susceptibility to liver damage from pneumoperitoneum in a murine model of biliary atresia. J Pediatr Surg 2010;45:1791-6
  • Sullivan JS, Sundaram SS, Pan Z, Sokol RJ. Parenteral nutrition supplementation in biliary atresia patients listed for liver transplantation. Liver Transpl 2012;18:120-8
  • Pierro A, Koletzko B, Carnielli V, et al. Resting energy expenditure is increased in infants and children with extrahepatic biliary atresia. J Pediatr Surg 1989;24:534-8
  • Sokol RJ, Heubi JE, Iannaccone S, et al. Mechanism causing vitamin E deficiency during chronic childhood cholestasis. Gastroenterology 1983;85:1172-82
  • DeRusso PA, Ye W, Shepherd R, et al. Growth failure and outcomes in infants with biliary atresia: a report from the Biliary Atresia Research Consortium. Hepatology 2007;46:1632-8
  • Utterson EC, Shepherd RW, Sokol RJ, et al. Biliary atresia: clinical profiles, risk factors, and outcomes of 755 patients listed for liver transplantation. J Pediatr 2005;147:180-5
  • Carter-Kent C, Radhakrishnan K, Feldstein AE. Increasing calories, decreasing morbidity and mortality: is improved nutrition the answer to better outcomes in patients with biliary atresia? Hepatology 2007;46:1329-31
  • McDiarmid S V, Anand R, Lindblad AS. Development of a pediatric end-stage liver disease score to predict poor outcome in children awaiting liver transplantation. Transplantation 2002;74:173-81
  • Sokol RJ, Shepherd RW, Superina R, et al. Screening and outcomes in biliary atresia: summary of a National Institutes of Health workshop. Hepatology 2007;46:566-81
  • Chin SE, Shepherd RW, Cleghorn GJ, 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;5:566-72
  • Chin SE, Shepherd RW, Thomas BJ, 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(1):158-63
  • Holt RI, Miell JP, Jones JS, et al. Nasogastric feeding enhances nutritional status in paediatric liver disease but does not alter circulating levels of IGF-I and IGF binding proteins. Clin Endocrinol (Oxf) 2000;52:217-24
  • Shneider BL, Magee JC, Bezerra JA, et al. Efficacy of fat-soluble vitamin supplementation in infants with biliary atresia. Pediatrics 2012;130:e607-14
  • Sokol RJ. Fat-soluble vitamins and their importance in patients with cholestatic liver diseases. Gastroenterol Clin North Am 1994;23:673-705
  • Midgley DE, Bradlee TA, Donohoe C, et al. Health-related quality of life in long-term survivors of pediatric liver transplantation. Liver Transpl 2000;6:333-9
  • Howard ER, MacLean G, Nio M, et al. Survival patterns in biliary atresia and comparison of quality of life of long-term survivors in Japan and England. J Pediatr Surg 2001;36:892-7
  • Ohya T, Fujimoto T, Shimomura H, Miyano T. Degeneration of intrahepatic bile duct with lymphocyte infiltration into biliary epithelial cells in biliary atresia. J Pediatr Surg 1995;30:515-18
  • Petersen C, Davenport M. Aetiology of biliary atresia: what is actually known? Orphanet J Rare Dis 2013;8:128
  • Davenport M, Gonde C, Redkar R, et al. Immunohistochemistry of the liver and biliary tree in extrahepatic biliary atresia. J Pediatr Surg 2001;36:1017-25
  • Narayanaswamy B, Gonde C, Tredger JM, et al. Serial circulating markers of inflammation in biliary atresia – evolution of the post-operative inflammatory process. Hepatology 2007;46:180-7
  • Elenkov IJ. Glucocorticoids and the Th1/Th2 balance. Ann N Y Acad Sci 2004;1024:138-46
  • Miner PB, Gaito JM. Bile flow in response to pharmacologic agents. Hepatic DNA as a reference standard. Biochem Pharmacol 1979;28:1063-6
  • Tatekawa Y, Muraji T, Tsugawa C. Glucocorticoid receptor alpha expression in the intrahepatic biliary epithelium and adjuvant steroid therapy in infants with biliary atresia. J Pediatr Surg 2005;40:1574-80
  • Karrer FM, Lilly JR. Corticosteroid therapy in biliary atresia. J Pediatr Surg 1985;20:693-5
  • Dillon PW, Owings E, Cilley R, et al. Immunosuppression as adjuvant therapy for biliary atresia. J Pediatr Surg 2001;36:80-5
  • Meyers RL, Book LS, O’Gorman MA, et al. High-dose steroids, ursodeoxycholic acid, and chronic intravenous antibiotics improve bile flow after Kasai procedure in infants with biliary atresia. J Pediatr Surg 2003;38:406-11
  • Davenport M, Stringer MD, Tizzard SA, et al. Randomized, double-blind, placebo-controlled trial of corticosteroids after Kasai portoenterostomy for biliary atresia. Hepatology 2007;46:1821-7
  • Davenport M, Parsons C, Tizzard S, Hadzic N. Steroids in biliary atresia: single surgeon, single centre, prospective study. J Hepatol 2013;59:1054-8
  • Bezerra J, Spino C, Magee JC, et al. Use of Corticosteroids after hepatoportoenterostomy for bile drainage in infants with biliary atresia. JAMA 2014;311:1750-9
  • Jimenez-Rivera C, Jolin-Dahel KS, Fortinsky KJ, et al. International incidence and outcomes of biliary atresia. J Pediatr Gastroenterol Nutr 2013;56:344-54
  • Kelly D, Davenport M. Current management of biliary atresia. Arch Dis Child 2007;92:1132-5
  • Muraji T, Higashimoto Y. The improved outlook for biliary atresia with corticosteroid therapy. J Pediatr Surg 1997;32:1103-6
  • Muraji T, Nio M, Ohhama Y, et al. Postoperative corticosteroid therapy for bile drainage in biliary atresia – a nationwide survey. J Pediatr Surg 2004;39:1803-5
  • Nio M, Muraji T. Multicenter randomized trial of postoperative corticosteroid therapy for biliary atresia. Pediatr Surg Int 2013;29:1091-5
  • Santos JL, Carvalho E, Bezerra JA. Advances in biliary atresia: from patient care to research. Braz J Med Biol Res 2010;43:522-7
  • Wildhaber BE. Biliary atresia: 50 years after the first Kasai. ISRN Surg 2012;2012:132089
  • Stringer MD, Davison SM, Rajwal SR, McClean P. Kasai portoenterostomy: 12-year experience with a novel adjuvant therapy regimen. J Pediatr Surg 2007;42:1324-8
  • Sarkhy A, Schreiber RA, Milner RA, Barker CC. Does adjuvant steroid therapy post-Kasai portoenterostomy improve outcome of biliary atresia? Systematic review and meta-analysis. Can J Gastroenterol 2011;25:440-4
  • Dong R, Song Z, Chen G, et al. Improved outcome of biliary atresia with postoperative high-dose steroid. Gastroenterol Res Pract 2013;2013:902431
  • Lao OB, Larison C, Garrison M, et al. Steroid use after the Kasai procedure for biliary atresia. Am J Surg 2010;199:680-4
  • Ernest van Heurn LW, Saing H, Tam PKH. Cholangitis after hepatic portoenterostomy for biliary atresia: a multivariate analysis of risk factors. J Pediatr 2003;142:566-71
  • Ogasawara Y, Yamataka A, Tsukamoto K, et al. The intussusception antireflux valve is ineffective for preventing cholangitis in biliary atresia: a prospective study. J Pediatr Surg 2003;38:1826-9
  • Houben C, Phelan S, Davenport M. Late-presenting cholangitis and Roux loop obstruction after Kasai portoenterostomy for biliary atresia. J Pediatr Surg 2006;41:1159-64
  • Wong KKY, Fan AH, Lan LCL, et al. Effective antibiotic regime for postoperative acute cholangitis in biliary atresia – an evolving scene. J Pediatr Surg 2004;39:1800-2
  • Bu L-N, Chen H-L, Chang C-J, et al. Prophylactic oral antibiotics in prevention of recurrent cholangitis after the Kasai portoenterostomy. J Pediatr Surg 2003;38:590-3
  • Luo Y, Zheng S. Current concept about postoperative cholangitis in biliary atresia. World J Pediatr 2008;4:14-19
  • Lee JY, Lim LTK, Quak SH, et al. Cholangitis in children with biliary atresia: health-care resource utilisation. J Paediatr Child Health 2014;50:196-201
  • Rothenberg SS, Schroter GP, Karrer FM, Lilly JR. Cholangitis after the Kasai operation for biliary atresia. J Pediatr Surg 1989;24:729-32
  • Ecoffey C, Rothman E, Bernard O, et al. Bacterial cholangitis after surgery for biliary atresia. J Pediatr 1987;111:824-9
  • Mones RL, DeFelice a R, Preud’Homme D. Use of neomycin as the prophylaxis against recurrent cholangitis after Kasai portoenterostomy. J Pediatr Surg 1994;29:422-4
  • Koga H, Wada M, Nakamura H, et al. Factors influencing jaundice-free survival with the native liver in post-portoenterostomy biliary atresia patients: results from a single institution. J Pediatr Surg 2013;48:2368-72
  • Endo M, Masuyama H, Hirabayashi T, et al. Effects of invaginating anastomosis in Kasai hepatic portoenterostomy on resolution of jaundice, and long-term outcome for patients with biliary atresia. J Pediatr Surg 1999;34:415-19
  • Lilly JR, Karrer FM, Hall RJ, et al. The surgery of biliary atresia. Ann Surg 1989;210:289-94
  • Ohya T, Miyano T, Kimura K. Indication for portoenterostomy based on 103 patients with Suruga II modification. J Pediatr Surg 1990;25:801-4
  • Karrer FM, Lilly JR, Stewart BA, Hall RJ. Biliary atresia registry, 1976 to 1989. J Pediatr Surg 1990;25:1076-80
  • Tsao K, Rosenthal P, Dhawan K, et al. Comparison of drainage techniques for biliary atresia. J Pediatr Surg 2003;38:1005-7
  • Matsuo S, Suita S, Kubota M, et al. Hazards of hepatic portocholecystostomy in biliary atresia. Eur J Pediatr Surg 2001;11:19-23
  • Beuers U, Boyer JL, Paumgartner G. Ursodeoxycholic acid in cholestasis: potential mechanisms of action and therapeutic applications. Hepatology 1998;28:1449-53
  • Yamashiro Y, Ohtsuka Y, Shimizu T, et al. Effects of ursodeoxycholic acid treatment on essential fatty acid deficiency in patients with biliary atresia. J Pediatr Surg 1994;29:425-8
  • Willot S, Uhlen S, Michaud L, et al. Effect of ursodeoxycholic acid on liver function in children after successful surgery for biliary atresia. Pediatrics 2008;122:e1236-41
  • Kotb MA. Review of historical cohort: ursodeoxycholic acid in extrahepatic biliary atresia. J Pediatr Surg 2008;43:1321-7
  • Iinuma Y, Kubota M, Yagi M, et al. Effects of the herbal medicine inchinko-to on liver function in postoperative patients with biliary atresia—a pilot study. J Pediatr Surg 2003;38:1607-11
  • Tamura T, Kobayashi H, Yamataka A, et al. Inchin-ko-to prevents medium-term liver fibrosis in postoperative biliary atresia patients. Pediatr Surg Int 2007;23:343-7
  • Vajro P, Couturier M, Lemonnier F, Odièvre M. Effects of postoperative cholestyramine and phenobarbital administration on bile flow restoration in infants with extrahepatic biliary atresia. J Pediatr Surg 1986;21:362-5
  • McClement JW, Howard ER, Mowat AP. Results of surgical treatment for extrahepatic biliary atresia in United Kingdom 1980-2. Survey conducted on behalf of the British Paediatric Association Gastroenterology Group and the British Association of Paediatric Surgeons. Br Med J (Clin Res Ed) 1985;290(6465):345-7
  • Davenport M, De Ville de Goyet J, Stringer MD, et al. Seamless management of biliary atresia in England and Wales (1999-2002). Lancet 2004;363(9418):1354-7
  • Davenport M, Ong E, Sharif K, et al. Biliary atresia in England and Wales: results of centralization and new benchmark. J Pediatr Surg 2011;46:1689-94
  • Kvist N, Davenport M. Thirty-four years’ experience with biliary atresia in Denmark: a single center study. Eur J Pediatr Surg 2011;21:224-8
  • Lampela H, Ritvanen A, Kosola S, et al. National centralization of biliary atresia care to an assigned multidisciplinary team provides high-quality outcomes. Scand J Gastroenterol 2012;47:99-107
  • Chardot C, Buet C, Serinet M-O, et al. Improving outcomes of biliary atresia: french national series 1986-2009. J Hepatol 2013;58:1209-17
  • Schreiber RA, Barker CC, Roberts E, et al. Biliary atresia: the Canadian experience. J Pediatr 2007;151:659-65
  • Hadzić N, Davenport M, Tizzard S, et al. Long-term survival following Kasai portoenterostomy: is chronic liver disease inevitable? J Pediatr Gastroenterol Nutr 2003;37:430-3
  • Czaja AJ. Hepatic inflammation and progressive liver fibrosis in chronic liver disease. World J Gastroenterol 2014;20:2515-32
  • Hofmann AF. Pharmacology of ursodeoxycholic acid, an enterohepatic drug. Scand J Gastroenterol Suppl 1994;204:1-15
  • Serinet M-O, Broué P, Jacquemin E, et al. Management of patients with biliary atresia in France: results of a decentralized policy 1986-2002. Hepatology 2006;44:75-84
  • Superina R, Magee JC, Brandt ML, et al. The anatomic pattern of biliary atresia identified at time of Kasai hepatoportoenterostomy and early postoperative clearance of jaundice are significant predictors of transplant-free survival. Ann Surg 2011;254:577-85

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.