Comprehensive managements after Kasai portoenterostomy for biliary atresia

References:

1 Couturier L,Jarvis C,Rousseau H,et al.Biliary atresia[J].Can Fam Physician,2015,61(11):965-968.
2 Shen WJ,Chen G,Wang M,et al.Liver fibrosis in biliary atresia[J].World J Pediatr,2019,15(2):117-123.DOI:10.1007/s12519-018-0203-1.
3 Feldman AG,Mack CL.Biliary atresia:clinical lessons learned[J].J Pediatr Gastroenterol Nutr,2015,61(2):167-175.DOI:10.1097/MPG.0000000000000755.
4 Kasai M,Suzuki S.A new operation for noncorrectable biliary atresia-hepatic portoenterostomy[J].Shujutsu,1959,13:733-739.
5 Kelay A,Davenport M.Long-term outlook in biliary atresia[J].Semin Pediatr Surg,2017,26(5):295-300.DOI:10.1053/j.sempedsurg.2017.09.003.
6 Lee WS,Ong SY,Foo HW,et al.Chronic liver disease is universal in children with biliary atresia living with native liver[J].World J Gastroenterol,2017,23(43):7776-7784.DOI:10.3748/wjg.v23.i43.7776.
7 Parolini F,Boroni G,Milianti S,et al.Biliary atresia:20-40-year follow-up with native liver in an Italian center[J].J Pediatr Surg,2019,54(7):1440-1444.DOI:10.1016/j.jpedsurg.2018.10.060.
8 Nio M,Wada M,Sasaki H,et al.Risk factors affecting late-presenting liver failure in adult patients with biliary atresia[J].J Pediatr Surg,2012,47(12):2179-2183.DOI:10.1016/j.jpedsurg.2012.09.003.
9 Nio M,Ohi R,Miyano T,et al.Five-and 10-year survival rates after surgery for biliary atresia:a report from the Japanese Biliary Atresia Registry[J].J Pediatr Surg,2003,38(7):997-1000.DOI:10.1016/s0022-3468(03)00178-7.
10 Ramos-Gonzalez G,Elisofon S,Dee EC,et al.Predictors of need for liver transplantation in children undergoing hepatoportoenterostomy for biliary atresia[J].J Pediatr Surg,2019,54(6):1127-1131.DOI:10.1016/j.jpedsurg.2019.02.051.
11 贾金富,詹江华.Kasai术后胆汁酸增高研究进展[J].中华小儿外科杂志,2019,40(9):862-865.DOI:10.3760/cma.j.issn.0253-3006.2019.09.020. Jia JF,Zhan JH,Research advances in an elevation of bile acid after Kasia procedure[J].Chin J Pediatr Sur,2019,40(9):862-865.DOI:10.3760/cma.j.issn.0253-3006.2019.09.020.
12 卢雪心,郑珊.胆道闭锁Kasai术后类固醇辅助治疗的现状和研究进展[J].中华小儿外科杂志,2016,37(4):310-314.DOI:10.3760/cma.j.issn.0253-3006.2016.04.017. Lu XX,Zheng S.Biliary atresia:an overview of adjuvant steroid therapy post-kasai portoenterostomy[J].Chin J Pediatr Surg,2016,37(4):310-314.DOI:10.3760/cma.j.issn.0253-3006.2016.04.017.
13 Davenport M.Adjuvant therapy in biliary atresia:hopelessly optimistic or potential for change?[J].Pediatr Surg Int,2017,33(12):1263-1273.DOI:10.1007/s00383-017-4157-5.
14 Kumar R,Lal BB,Sood V,et al.Predictors of successful Kasai portoenterostomy and survival with native liver at 2 years in infants with biliary atresia[J].J Clin Exp Hepatol,2019,9(4):453-459.DOI:10.1016/j.jceh.2018.09.008.
15 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].J Pediatr Surg,2003,38(3):406-411.DOI:10.1053/jpsu.2003.50069.
16 Alonso EM,Ye W,Hawthorne K,et al.Impact of steroid therapy on early growth in infants with biliary atresia:the multicenter steroids in biliary atresia randomized trial[J].J Pediatr,2018,202(11):179-185.DOI:10.1016/j.jpeds.2018.07.002.
17 中华医学会小儿外科分会新生儿外科学组,小儿肝胆外科学组.中国大陆地区胆道闭锁诊断及治疗(专家共识)[J].中华小儿外科杂志,2013,34(9):700-705.DOI:10.3760/cma.j.issn.0253-3006.2013.09.014. Groups of Neonatal Surgery & Pediatric Hepatobiliary Surgery,Branch of Pediatric Surgery,Chinese Medical Association:Expert Consensus on Diagnosing & Treating Biliary Atresia in mainland China)[J].Chin J Pediatr Sur,2013,34(9):700-705.DOI:10.3760/cma.j.issn.0253-3006.2013.09.014.
18 Simental-Mendía M,Sánchez-García A,Simental-Mendía LE.Effect of ursodeoxycholic acid on liver markers:A systematic review and meta-analysis of randomized placebo-controlled clinical trials[J].Br J Clin Pharmacol,2020,86(8):1476-1488.DOI:10.1111/bcp.14311.
19 刘小舟,郑珊.胆道闭锁婴儿脂溶性维生素缺乏的现状与治疗[J].中华实用儿科临床杂志,2018,33(9):718-720.DOI:10.3760/cma.j.issn.2095-428X.2018.09.016. Liu XZ,Zheng S.Current situation and treatment of fat-soluble vitamins deficiency in infants with biliary atresia[J].Chin J Appl Clin Pediatr,2018,33(9):718-720.DOI:10.3760/cma.j.issn.2095-428X.2018.09.016.
20 Li D,Chen X,Fu K,et al.Preoperative nutritional status and its impact on cholangitis after Kasai portoenterostomy in biliary atresia patients[J].Pediatr Surg Int,2017,33(8):901-906.DOI:10.1007/s00383-017-4118-z.
21 詹江华.婴幼儿胆汁淤积性黄疸的外科诊疗决策[J].临床小儿外科杂志,2016,15(1):1-3.DOI:10.3969/j.issn.1671-6353.2016.01.001. Zhan JH.Surgical decision-making in the diagnosis and treatment of bile static jaundice in infants and toddlers[J].J Clin Ped Sur,2016,15(1):1-3.DOI:10.3969/j.issn.1671-6353.2016.01.001.
22 Shiga C,Ohi R,Chiba T,et al.Assessment of nutritional status of postoperative patients with biliary atresia[J].Tohoku J Exp Med,1997,181(1),217-23.DOI:10.1620/tjem.181.217.
23 Maharjana MA,Suyasa IK,Kawiyana IKS,et al.Pathological fracture of the femur in Alagille Syndrome:A case report[J].J Clin Orthop Trauma,2020,11(2):298-301.DOI:10.1016/j.jcot.2019.12.009.
24 Peng CH,Lee HC,Jiang CB,et al.Serum vitamin D level is inversely associated with liver fibrosis in post Kasai’s portoenterostomy biliary atresia patients living with native liver[J].PLoS One,2019,14(6):e0218896.DOI:10.1371/journal.pone.0218896.
25 Yeh YT,Lin NC,Yeh YC,et al.Vitamin A can ameliorate fibrosis of liver in an established rat model of biliary atresia and Kasai portoenterostomy[J].J Pediatr Surg,2018,53(12):2416-2422.DOI:10.1016/j.jpedsurg.2018.08.033.
26 Wang J,Qian T,Jiang J,et al.Gut microbial profile in biliary atresia:a case-control study[J].J Gastroenterol Hepatol,2020,35(2):334-342.DOI:10.1111/jgh.14777.
27 Zheng X,Huang F,Zhao A,et al.Bile acid is a significant host factor shaping the gut microbiome of diet-induced obese mice[J].BMC Biol,2017,15(1):120.DOI:10.1186/s12915-017-0462-7.
28 Lien TH,Bu LN,Wu JF,et al.Use of Lactobacillus casei rhamnosus to prevent cholangitis in biliary atresia after Kasai operation[J].J Pediatr Gastroenterol Nutr,2015,60(5):654-658.DOI:10.1097/MPG.0000000000000676.
29 Liu J,Dong R,Chen G,et al.Risk factors and prognostic effects of cholangitis after Kasai procedure in biliary atresia patients:A retrospective clinical study[J].J Pediatr Surg,2019,54(12):2559-2564.DOI:10.1016/j.jpedsurg.2019.08.026.
30 Baek SH,Kang JM,Ihn K,et al.The epidemiology and etiology of cholangitis after Kasai portoenterostomy in patients with biliary atresia[J].J Pediatr Gastroenterol Nutr,2020,70(2):171-177.DOI:10.1097/MPG.0000000000002555.
31 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].J Pediatr Surg,2013,48(12):2368-2372.DOI:10.1016/j.jpedsurg.2013.08.007.
32 Chung PHY,Tam PKH,Wong KKY.Does the identity of the bacteria matter in post-Kasai cholangitis? A comparison between simple and the intractable cholangitis[J].J Pediatr Surg,2018,53(12):2409-2411.DOI:10.1016/j.jpedsurg.2018.08.028.
33 王培,冯杰雄.胆道闭锁术后胆管炎抗生素分级治疗的多中心研究方案[J].临床小儿外科杂志,2019,18(11):922-926.DOI:10.3969/j.issn.1671-6353.2019.11.006. Wang P,Feng JX.Antibiotics treatment of cholangitis Post-Kasai portoenterostomy:A multi-center study protocol[J].J Clin Ped Sur,2019,18(11):922-926.DOI:10.3969/j.issn.1671-6353.2019.11.006.
34 张志波.影响胆道闭锁预后的原因及其争议[J].临床外科杂志,2019,27(6):465-468.DOI:10.3969/j.issn.1005-6483.2019.06.006. Zhang ZB.Causes and controversies of prognostic factors for biliary atresia[J].Journal of Clinical Surgery,2019,27(6):465-468.DOI:10.3969/j.issn.1005-6483.2019.06.006.
35 Chen SY,Lin CC,Tsan YT,et al.Number of cholangitis episodes as a prognostic marker to predict timing of liver transplantation in biliary atresia patients after Kasai portoenterostomy[J].BMC Pediatr,2018,18(1):119.DOI:10.1186/s12887-018-1074-2.
36 Wu ET,Chen HL,Ni YH,et al.Bacterial cholangitis in patients with biliary atresia:impact on short-term outcome[J].Pediatr Surg Int,2001,17(5-6):390-395.DOI:10.1007/s003830000573.
37 Bu LN,Chen HL,Chang CJ,et al.Prophylactic oral antibiotics in prevention of recurrent cholangitis after the Kasai portoenterostomy[J].J Pediatr Surg,2003,38(4):590-593.DOI:10.1053/jpsu.2003.50128.
38 Ginstr?m DA,Hukkinen M,Kivisaari R,et al.Biliaryatresia-associated cholangitis:the central role and effective management of bile lakes[J].J Pediatr Gastroenterol Nutr,2019,68(4):488-494.DOI:10.1097/MPG.0000000000002243.
39 Watanabe M,Hori T,Kaneko M,et al.Intrahepatic biliary cysts in children with biliary atresia who have had a Kasai operation[J].J Pediatr Surg,2007,42(7):1185-1189.DOI:10.1016/j.jpedsurg.2007.02.035.
40 Takahashi A,Tsuchida Y,Suzuki N,et al.Intrahepatic biliary cysts in biliary atresia in the era of liver transplantation[J].J Pediatr Gastroenterol Nutr,2003,36(5):608-612.DOI:10.1097/00005176-200305000-00003.
41 Lykavieris P,Chardot C,Sokhn M,et al.Outcome in adulthood of biliary atresia:a study of 63 patients who survived for over 20 years with their native liver[J].Hepatology,2005,41(2):366-371.DOI:10.1002/hep.20547.
42 Jain V,Burford C,Alexander EC,et al.Prognostic markers at adolescence in patients requiring liver transplantation for biliary atresia in adulthood[J].J Hepatol,2019,71(1):71-77.DOI:10.1016/j.jhep.2019.03.005.
43 Fang CK,Ong C,Low Y,et al.Non-invasive predictors for the first variceal hemorrhage in children with biliary atresia after Kasai portoenterostomy[J].J Clin Exp Hepatol,2019,9(5):581-587.DOI:10.1016/j.jceh.2019.03.005.
44 Hukkinen M,Lohi J,Heikkil? P,et al.Noninvasive evaluation of liver fibrosis and portal hypertension after successful portoenterostomy for biliary atresia[J].Hepatol Commun,2019,3(3):382-391.DOI:10.1002/hep4.1306.
45 Kasahara M,Umeshita K,Sakamoto S,et al.Liver transplantation for biliary atresia:a systematic review[J].Pediatr Surg Int,2017,33(12),1289-1295.DOI:10.1007/s00383-017-4173-5.
46 Sundaram SS,Mack CL,Feldman AG,et al.Biliary atresia:Indications and timing of liver transplantation and optimization of pretransplant care[J].Liver Transpl,2017,23(1):96-109.DOI:10.1002/lt.24640.
47 Anand R,Utterson EC,Sokol RJ,et al.Biliary atresia:clinical profiles,risk factors,and outcomes of 755 patients listed for liver transplantation[J].J Pediatr,2005,147(2):180-185.DOI:10.1016/j.jpeds.2005.04.073.
48 陈士凤,王梅,刘红燕.基于微信平台的延续护理模式在TIPS术后出院患者中的应用[J].齐鲁护理杂志,2020,26(11):20-23.DOI:10.3969/j.issn.1006-7256.2020.11.006. Chen SF,Wang M,Liu HY.Application of transitional care model based in WeChat platform in patients discharged after TIPS surgery[J].Journal of Qilu Nursing,2020,26(11):20-23.DOI:10.3969/j.issn.1006-7256.2020.11.006.
49 池益强,马姗姗,郑惠能,等.疫苗使用说明书禁忌症分析与探讨[J].海峡预防医学杂志,2014,20(5):76-77. Chi YQ,Ma SS,Zheng HN,et al.Analysis and explorations of contraindications for vaccine package insert[J].Strait Journal of Preventive Medicine,2014,20(5):76-77.
50 唐莹,李春龙,肖雷,等.先天性胆道闭锁儿童的预防接种[J].中国疫苗和免疫,2019,25(5):589-592. Tang Y,Li CL,Xiao L,et al.Vaccination of children with congenital biliary atresia[J].Chinese Journal of Vaccines & Immunization,2019,25(5):589-592.
51 Ng VL,Sorensen LG,Alonso EM,et al.Neurodevelopmental outcome of young children with biliary atresia and native liver:results from the ChiLDReN study[J].J Pediatr,2018,196:139-147.e3.DOI:10.1016/j.jpeds.2017.12.048.