Wu Xiaoxia,Ren Hongxia,Jin Yuanyuan,et al.Risk factors of native liver survival time under 2 years after Kasai operation for biliary atresia[J].Journal of Clinical Pediatric Surgery,2021,20(02):114-118.[doi:10.12260/lcxewkzz.2021.02.003]
胆道闭锁Kasai手术后自体肝生存时间小于2年的危险因素分析
- Title:
- Risk factors of native liver survival time under 2 years after Kasai operation for biliary atresia
- Keywords:
- Biliary Atresia/SU; Prognosis; Native Liver Survival; Risk Factors
- 分类号:
- R657.4+4 R726.1
- 摘要:
- 目的 探讨胆道闭锁(biliary atresia,BA)Kasai手术后自体肝生存(native liver survival,NLS)时间小于2年的危险因素。方法 回顾性分析山西省儿童医院2009年1月至2017年6月行Kasai手术的BA患者临床资料及随访资料。根据术后NLS时间是否小于2年分为死亡组(n=78)和生存组(n=46)。将BA分型、性别、巨细胞病毒(cytomegalovirus,CMV)感染、手术年龄、术后使用抗生素方案、术后使用激素方案、是否合并早期胆管炎及术后黄疸是否消退作为自变量,采用Kaplan-Meier法绘制生存曲线并进行Log-rank检验,采用Cox比例风险模型(逐步前进法)筛选BA患者Kasai手术后NLS时间小于2年的危险因素。结果 共纳入124例BA患者,其中生存组46例,死亡组78例,2年NLS率为37.1%。单因素分析结果显示合并早期胆管炎及术后黄疸消退是影响BA患者术后2年NLS率的因素(P<0.05)。Cox比例风险模型分析结果显示术后3个月内黄疸未消退为BA患者Kasai手术后NLS时间小于2年的独立危险因素,术后3个月内黄疸未消退组患者NLS时间小于2年的风险是黄疸消退患者的5.65(95%CI:2.45~13.04)倍。结论 BA患者Kasai手术后3个月内黄疸未消退是NLS时间小于2年的危险因素。
- Abstract:
- Objective To explore the risk factors of native liver survival (NLS) time under 2 years after Kasai operation for biliary atresia (BA).Methods Clinical and follow-up data were retrospectively analyzed for all children undergoing Kasai operation for BA from January 2009 to June 2017.According to whether or not NLS time was under 2 years,they were divided into survival and death groups.BA classification,gender,cytomegalovirus (CMV) infection,age at Kasai,postoperative antibiotic and hormone regimens,postoperative early cholangitis and jaundice clearance were independent variables.Kaplan-Meier survival analysis was employed for plotting the survival curves of two groups and log-rank test performed for assessing the inter-group difference.Cox proportional hazard models were constructed for assessing the risk factors of native liver survival time under 2 years.Within 3 months,the risk of NLS time under 2 years for non-clearing group was 5.65 folds of that for clearing group (95%CI:2.45-13.04).Results There were 46 cases in survival group and 78 in death group.And 2-year NLS rate was 37.1%.Univariate analysis showed that statistically significant difference existed in survival curve between two variables associated with postoperative early cholangitis and jaundice clearance (P<0.05).COX proportional risk model analysis indicated that failure of jaundice clearance within 3 months after Kasai operation was an independent risk factor for NLS time <2 years.Conclusion Failure of jaundice clearance within 3 months is a risk factor for NLS time under 2 years after Kasai operation for biliary atresia.
参考文献/References:
1 詹江华,陈亚军.肝移植时代如何看待胆道闭锁的诊治[J].中华小儿外科杂志,2014,35(4):245-247.DOI:10.3760/cma.j.issn.0253-3006.2014.04.003. Zhan JH,Chen YJ.Diagnosing and treating biliary atresia in the era of liver transplantation[J].Chin J Pediatr Surg,2014,35(4):245-247.DOI:10.3760/cma.j.issn.0253-3006.2014.04.003.
2 Shneider BL,Mazariegos GV.Biliary atresia:a transplant perspective[J].Liver Transpl,2007,13(11):1482-1495.DOI:10.1002/lt.21303.
3 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.
4 Ferreira AR,Queiroz TCN,Vidigal PVT,et al.Multivariate analysis of biliary flow-related factors and post-Kasai survival in biliary atresia patients[J].Arq Gastroenterol,2019,56(1):71-78.DOI:10.1590/S0004-2803.201900000-18.
5 Witt M,van Wessel DBE,de Kleine RHJ,et al.Prognosis of biliary atresia after 2-year survival with native liver:a nationwide cohort analysis[J].J Pediatr Gastroenterol Nutr,2018,67(6):689-694.DOI:10.1097/MPG.0000000000002130.
6 中华医学会小儿外科学分会肝胆外科学组,中国医师协会器官移植医师分会儿童器官移植学组.胆道闭锁诊断及治疗指南(2018版)[J].中华小儿外科杂志,2019,40(5):392-398. Section of Hepatobiliary Surgery,Branch of Pediatric Surgery,Chinese Medical Association;Section of Pediatric Hepatic Transplantation,Branch of Organ Transplantation,Chinese Medical Doctor Association:Guidelines for Diagnosing & Treating Biliary Atresia (2018 Edition)[J].Chin J Pediatr Surg,2019,40(5):392-398.
7 Davenport M.Biliary atresia:clinical aspects[J].Semin Pediatr Surg,2012,21(3):175-184.DOI:10.1053/j.sempedsurg.2012.05.010.
8 Parolini F,Boroni G,Milianti S,et al.Biliary atresia:20-40-year follow-up with native liver in an Italian centre[J].J Pediatr Surg,2019,54(7):1440-1444.DOI:10.1016/j.jpedsurg.2018.10.060.
9 Davenport M,Ong E,Sharif K,et al.Biliary atresia in England and Wales:results of centralization and new benchmark[J].J Pediatr Surg,2011,46(9):1689-1694.DOI:10.1016/j.jpedsurg.2011.04.013.
10 Nio M.Japanese Biliary Atresia Registry[J].Pediatr Surg Int,2017,33(12):1319-1325.DOI:10.1007/s00383-017-4160-x.
11 Wang Z,Chen Y,Peng C,et al.Five-year native liver survival analysis in biliary atresia from a single large Chinese center:The death/liver transplantation hazard change and the importance of rapid early clearance of jaundice[J].J Pediatr Surg,2019,54(8):1680-1685.DOI:10.1016/j.jpedsurg.2018.09.025.
12 Serinet MO,Wildhaber BE,Broué P,et al.Impact of age at Kasai operation on its results in late childhood and adolescence:a rational basis for biliary atresia screening[J].Pediatrics,2009,123(5):1280-1286.DOI:10.1542/peds.2008-1949.
13 Obayashi J,Kawaguchi K,Manabe S,et al.Prognostic factors indicating survival with native liver after Kasai procedure for biliary atresia[J].Pediatr Surg Int,2017,33(10):1047-1052.DOI:10.1007/s00383-017-4135-y.
14 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.
15 Tyraskis A,Parsons C,Davenport M.Glucocorticosteroids for infants with biliary atresia following Kasai portoenterostomy[J].Cochrane Database Syst Rev,2018,5(5):CD008735.DOI:10.1002/14651858.CD008735.pub3.
16 Fabris L,Spirli C,Cadamuro M,et al.Emerging concepts in biliary repair and fibrosis[J].Am J Physiol Gastrointest Liver Physiol,2017,313(2):G102-G116.DOI:10.1152/ajpgi.00452.2016.
17 Chan KWE,Lee KH,Wong HYV,et al.Ten-year native liver survival rate after laparoscopic and open kasai portoenterostomy for biliary atresia[J].J Laparoendosc Adv Surg Tech A,2019,29(1):121-125.DOI:10.1089/lap.2018.0350.
18 葛亮,詹江华.胆道闭锁肝纤维化与自体肝生存关系的研究进展[J].临床小儿外科杂志,2020,19(2):171-175.DOI:10.3969/j.issn.1671-6353.2020.02.016. Ge L,Zhan JH.Relationship between liver fibrosis and native liver survival in infants with biliary atresia[J].J Clin Ped Sur,2020,19(2):171-175.DOI:10.3969/j.issn.1671-6353.2020.02.016.
19 Hukkinen M,Kerola A,Lohi J,et al.Very low bilirubin after portoenterostomy improves survival of the native liver in patients with biliary atresia by deferring liver fibrogenesis[J].Surgery,2019,165(4):843-850.DOI:10.1016/j.surg.2018.10.032.
20 Chung PH,Wong KK,Tam PK.Predictors for failure after Kasai operation[J].J Pediatr Surg,2015,50(2):293-296.DOI:10.1016/j.jpedsurg.2014.11.015.
21 Ernest van Heurn LW,Saing H,Tam PK.Cholangitis after hepatic portoenterostomy for biliary atresia:a multivariate analysis of risk factors[J].J Pediatr,2003,142(5):566-571.DOI:10.1067/mpd.2003.195.
22 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.
23 Nio M,Sano N,Ishii T,et al.Cholangitis as a late complication in long-term survivors after surgery for biliary atresia[J].J Pediatr Surg,2004,39(12):1797-1799.DOI:10.1016/j.jpedsurg.2004.08.021.
相似文献/References:
[1]潘静,郑永钦,佘锦标,等.胆道闭锁术后肝内胆管囊性扩张的诊治[J].临床小儿外科杂志,2008,7(04):0.
[2]马力,钟微,余家康,等.新生儿肠穿孔危重评分及预后分析[J].临床小儿外科杂志,2007,6(04):10.
[3]金龙 俞钢 陈丹 朱小春 葛午平 林炎坤. 产前诊断脐膨出胎儿80例结局分析[J].临床小儿外科杂志,2011,10(03):199.
[J].Journal of Clinical Pediatric Surgery,2011,10(02):199.
[4]方炜 丁力 张峰 胡英超 陈雨青. 婴幼儿法乐四联症手术治疗近期疗效的影响因素[J].临床小儿外科杂志,2011,10(06):403.
[J].Journal of Clinical Pediatric Surgery,2011,10(02):403.
[5]詹江华 管志伟 罗喜荣 包国强 刘谊 王栋. I型胆管闭锁的外科治疗[J].临床小儿外科杂志,2012,11(01):10.
[6]吴德华,田红娟,唐达星,等.AR基因突变雄激素不敏感综合征相关因素在性别分配中的作用分析[J].临床小儿外科杂志,2019,18(05):387.[doi:10.3969/j.issn.1671-6353.2019.05.010]
Wu Dehua,Tian Hongjuan,Tang Daxing,et al.Preliminary study on gender assignments and related predictors of androgen insensitivity syndrome with AR gene mutation[J].Journal of Clinical Pediatric Surgery,2019,18(02):387.[doi:10.3969/j.issn.1671-6353.2019.05.010]
[7]蔡元霞,武志祥,王奕,等.CDC5L表达对神经母细胞瘤临床及预后评估的意义[J].临床小儿外科杂志,2019,18(06):472.[doi:10.3969/j.issn.1671-6353.2019.06.008]
Cai Yuanxia,Wu Zhixiang,Wang Yi,et al.Expression of CDC5L in neuroblastoma and its clinical and prognostic significance[J].Journal of Clinical Pediatric Surgery,2019,18(02):472.[doi:10.3969/j.issn.1671-6353.2019.06.008]
[8]彭宇明,司中州,袁妙贤,等.儿童肝移植20例诊治分析[J].临床小儿外科杂志,2019,18(08):681.[doi:10.3969/j.issn.1671-6353.2019.08.013]
Peng Yuming,Si Zhongzhou,Yuan Miaoxian,et al.Diagnoses and treatments of hepatic transplantation in 20 children[J].Journal of Clinical Pediatric Surgery,2019,18(02):681.[doi:10.3969/j.issn.1671-6353.2019.08.013]
[9]陈籽荣,厉亚坤,万锋.儿童神经肿瘤临床和病理特点[J].临床小儿外科杂志,2019,18(09):723.[doi:10.3969/j.issn.1671-6353.2019.09.003]
Chen Zirong,Li Yakun,Wan Feng.Clinicopathological features of children with neurological tumors[J].Journal of Clinical Pediatric Surgery,2019,18(02):723.[doi:10.3969/j.issn.1671-6353.2019.09.003]
[10]李军亮,许新科,陈程,等.Galen静脉动脉瘤样畸形6例诊治及预后分析[J].临床小儿外科杂志,2019,18(09):744.[doi:10.3969/j.issn.1671-6353.2019.09.007]
Li Junliang,Xu Xinke,Chen Cheng,et al.Diagnosis and treatment of Galen venous aneurysmal malformation: a report of 6 cases[J].Journal of Clinical Pediatric Surgery,2019,18(02):744.[doi:10.3969/j.issn.1671-6353.2019.09.007]
[11]刘钢高昕刘树立黄柳明王伟邵培侯文英张军李龙.胆道闭锁葛西手术后肝内胆管扩张的治疗与预后分析[J].临床小儿外科杂志,2010,9(03):0.
LIU Gang,GAO Xin,LIU Shu-li,et al.The managements and prognosis of intrahepatic biliary dilatation with biliary atresia after Kasai procedure[J].Journal of Clinical Pediatric Surgery,2010,9(02):0.
[12]沈淳,郑珊,王玮,等.手术年龄对胆道闭锁Kasai手术后预后影响的研究[J].临床小儿外科杂志,2007,6(03):6.
[13]张金山 李龙 侯文英 刘树立. Ⅲ型胆道闭锁不同亚型与预后关系的探讨[J].临床小儿外科杂志,2012,11(04):244.
[J].Journal of Clinical Pediatric Surgery,2012,11(02):244.
[14]庞文博,陈亚军,张廷冲,等.胆道闭锁Kasai术后胆管炎的诊治及预后研究[J].临床小儿外科杂志,2022,21(01):41.[doi:10.3760/cma.j.cn.101785-202006073-008]
Pang Wenbo,Chen Yajun,Zhang Tingchong,et al.Diagnosis,management and prognosis of post-Kasai cholangitis[J].Journal of Clinical Pediatric Surgery,2022,21(02):41.[doi:10.3760/cma.j.cn.101785-202006073-008]
[15]徐琛,汤悦,郑珊,等.Kasai术中肝脏吲哚菁绿显像特点与胆道闭锁患儿早期预后的关系探索[J].临床小儿外科杂志,2022,21(08):738.[doi:10.3760/cma.j.cn101785-202111058-007]
Xu Chen,Tang Yue,Zheng shan,et al.Study of real-time imaging with indocyanine green during hepatoportoenterostomy as a prognostic factor in children with biliary atresia[J].Journal of Clinical Pediatric Surgery,2022,21(02):738.[doi:10.3760/cma.j.cn101785-202111058-007]
备注/Memo
收稿日期:2020-05-06。
基金项目:山西省重点研发计划项目(编号:201803D31181);山西省儿童医院院内课题(编号:201928);山西省儿童医院院内课题(编号:201943)
通讯作者:任红霞,Email:renhongxia100@sina.com