用户名: 密码: 验证码:
Design and validation of an early scoring system for predicting early outcomes of type III biliary atresia after Kasai’s operation
详细信息    查看全文
  • 作者:Chen Zhen ; Qiao Guoliang ; Ma Lishuang ; Zhang Zhen…
  • 关键词:Early scoring system ; Logistic model ; Biliary atresia ; Prognosis ; Kasai’s operation
  • 刊名:Pediatric Surgery International
  • 出版年:2015
  • 出版时间:June 2015
  • 年:2015
  • 卷:31
  • 期:6
  • 页码:535-542
  • 全文大小:479 KB
  • 参考文献:1.Chiu CY, Chen PH, Chan CF, Chang MH, Wu TC (2013) Biliary atresia in preterm infants in Taiwan: a nationwide survey. J Pediatr 163:100-03View Article PubMed
    2.Gallo A, Esquivel CO (2013) Current options for management of biliary atresia. Pediatr Transplant 17:95-8View Article PubMed
    3.Kelly DA, Davenport M (2007) Current management of biliary atresia. Arch Dis Child 92:1132-135View Article PubMed Central PubMed
    4.Kasai M, Suzuki S (1959) A new operation for “non-correctable-biliary atresia: hepatic portoenterostomy. Shujjutsu 13:733
    5.Lykavieris P, Chardot C, Sokhn M, Gauthier F, Valayer J et al (2005) Outcome in adulthood of biliary atresia: a study of 63 patients who survived for over 20?years with their native liver. Hepatology 41:366-71View Article PubMed
    6.Shneider BL, Brown MB, Haber B, Whitington PF, Schwarz K et al (2006) A multicenter study of the outcome of biliary atresia in the United States, 1997 to 2000. J Pediatr 148:467-74View Article PubMed
    7.Ohi R (1998) Surgical treatment of biliary atresia in the liver transplantation era. Surg Today 28:1229-232View Article PubMed
    8.Tomita H, Masugi Y, Hoshino K, Fuchimoto Y, Fujino A et al (2014) Long-term native liver fibrosis in biliary atresia: development of a novel scoring system using histology and standard liver tests. J Hepatol 60:1242-248View Article PubMed
    9.Nio M, Ohi R, Shimaoka S, Iwami D, Sano N (1997) The outcome of surgery for biliary atresia and the current status of long-term survivors. Tohoku J Exp Med 181:235-44View Article PubMed
    10.de Vries W, Homan-Van DVJ, Hulscher JB, Hoekstra-Weebers JE, Houwen RH et al (2011) Twenty-year transplant-free survival rate among patients with biliary atresia. Clin Gastroenterol Hepatol 9:1086-091View Article PubMed
    11.Hartley JL, Davenport M, Kelly DA (2009) Biliary atresia. Lancet 374:1704-713View Article PubMed
    12.Shinkai M, Ohhama Y, Take H, Kitagawa N, Kudo H et al (2009) Long-term outcome of children with biliary atresia who were not transplanted after the Kasai operation: >20-year experience at a children’s hospital. J Pediatr Gastroenterol Nutr 48:443-50View Article PubMed
    13.Sullivan LM, Massaro JM, D’Agostino RS (2004) Presentation of multivariate data for clinical use: the Framingham Study risk score functions. Stat Med 23:1631-660View Article PubMed
    14.Hashimoto T, Otobe Y, Shimizu Y, Suzuki T, Nakamura T et al (1997) A modification of hepatic portoenterostomy (Kasai operation) for biliary atresia. J Am Coll Surg 185:548-53View Article PubMed
    15.Yamada G (2004) Histopathological characteristics and clinical significance of New Inuyama Classification in chronic hepatitis B. Nihon Rinsho 62(Suppl 8):290-92PubMed
    16.Bedossa P, Poynard T (1996) An algorithm for the grading of activity in chronic hepatitis C. The METAVIR Cooperative Study Group. Hepatology 24:289-93View Article PubMed
    17.Tabac Hni Ck BG, LS FD (1996) Using multivariate statistics. HarperCollins, New York
    18.Rodeck B, Becker AC, Gratz KF, Petersen C (2007) Early predictors of success of Kasai operation in children with biliary atresia. Eur J Pediatr Surg 17:308-12View Article PubMed
    19.Koga H, Wada M, Nakamura H, Miyano G, Okawada M et al (2013) Factors influencing jaundice-free survival with the native liver in post-portoenterostomy biliary atresia patients: results from a single institution. J Pediatr Surg 48:2368-372View Article PubMed
    20.Gupta L, Gupta SD, Bhatnagar V (2012) Extrahepatic biliary atresia: correlation of histopathology and liver function tests with surgical outcomes. J Indian Assoc Pediatr Surg 17:147-52View Article PubMed Central PubMed
    21.Venerito M, Fry LC, Rickes S, Malfertheiner P, Monkemuller K (2009) Cholangitis as a late complication of choledochoduodenostomy: the sump syndrome. Endoscopy 41(Suppl 2):E142–E143View Article PubMed
    22.Nio M, Sano N, Ishii T, Sasaki H, Hayashi Y et al (2004) Cholangitis as a late complication in long-term survivors after surgery for biliary atresia. J Pediatr Surg 39:1797-799View Article PubMed
    23.Bu LN, Chen HL, Ni YH, Peng S, Jeng YM et al (2002) Multiple intrahepatic biliary cysts in children with biliary atresia. J Pediatr Surg 37:1183-187View Article PubMed
    24.Hung PY, Chen CC, Chen WJ, Lai HS, Hsu WM et al (2006) Long-term prognosis of patients with biliary atresia: a 25?year summary. J Pediatr Gastroenterol Nutr 42:190-95View Article PubMed
    25.Chitsaz E, Schreiber RA, Collet JP, Kaczorowski J (2009) Biliary atresia: the timing needs a changin- Can J Public Health 100:475-77PubMed
    26.Chen G, Zheng S, Sun S, Xiao X, Ma Y et al (2012) Early surgical outcomes and pathological scoring values of older infants (?0?days old) with biliary atresia. J Pediatr Surg 47:2184-188View Article PubMed
    27.Oh M, Hobeldin M, Chen T, Thomas DW, Atkinson JB (1995) The Kasai procedure in the treatment of biliary atresia. J Pediatr Surg 30(1077-080):1080-08
  • 作者单位:Chen Zhen (1) (2)
    Qiao Guoliang (1)
    Ma Lishuang (1)
    Zhang Zhen (1)
    Wang Chen (1)
    Zhang Jun (1)
    Liu Shuli (1)
    Guan Kaoping (1)
    Liu Chao (1)
    Yang Xuan (1)
    Li Long (1)

    1. Department of Pediatric Surgery, Capital Institute of Pediatrics-Peking University Teaching Hospital, Yabao Road 2#, Chaoyang, Beijing, 100021, People’s Republic of China
    2. Medical Department, Peking University, Beijing, 100000, People’s Republic of China
  • 刊物类别:Medicine
  • 刊物主题:Medicine & Public Health
    Pediatrics
    Surgery
    Pediatric Surgery
  • 出版者:Springer Berlin / Heidelberg
  • ISSN:1437-9813
文摘
Background/purpose The purpose of this study was to determine reliable predictors of outcome of biliary atresia (BA) after Kasai’s operation. Patients and methods This study included two consecutive stages of infants with biliary atresia. First stage, 200 BA cases who underwent Kasai’s operation at our institution between May 2006 and May 2010 were retrospectively reviewed. In the first stage, we wanted to calculate a clinical scoring system by logistic regression. For cut-off determination, receiver operating characteristic (ROC) analysis was employed. Second stage (validation of scoring system), we used our scoring system to prospectively predict the outcomes of patients underwent a Kasai operation from inspecting the accuracy of our system. Results Early cholangitis, age at operation, JC time, post-operative TB, DB, AST, ALT and surgical method entered into our scoring system. The most reliable cut-offs determined by ROC analysis were 7.71 (sensitivity: 86.0?%, specificity: 98.0?%). We used our scoring system to predict the prognosis of the 15 BA patients and found that 13 of 15 patients were correctly predicted at the cut-off value of 7.71. Conclusion Our scoring system is considered to be a reliable and useful predictor of the prognosis of biliary atresia.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700