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胆管炎发作次数作为预测Kasai肝门空肠吻合术后胆道闭锁患者肝移植时机的预后标志物。

Number of cholangitis episodes as a prognostic marker to predict timing of liver transplantation in biliary atresia patients after Kasai portoenterostomy.

作者信息

Chen Szu-Ying, Lin Chieh-Chung, Tsan Yu-Tse, Chan Wei-Cheng, Wang Jiaan-Der, Chou Yi-Jung, Lin Ching-Heng

机构信息

Division of Pediatric Gastroenterology and Hepatology, Department of Pediatrics, Taichung Veterans General Hospital, 1650 Taiwan Boulevard Sect. 4, 40705, Taichung, Taiwan, Republic of China.

Wuri Lin Shin Hospital, Taichung, Taiwan.

出版信息

BMC Pediatr. 2018 Apr 2;18(1):119. doi: 10.1186/s12887-018-1074-2.

DOI:10.1186/s12887-018-1074-2
PMID:29606115
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5880092/
Abstract

BACKGROUND

Cholangitis may affect liver failure of biliary atresia (BA) patients after Kasai portoenterostomy (KP). We examined whether the number of cholangitis episodes could be a prognostic marker for liver transplant (LT) in children with BA after Kasai portoenterostomy (KP).

METHODS

Data for BA patients born after 1998 and undergoing KP were obtained from National Health Insurance Research Database (NHIRD), Taiwan. Patients were followed up until the end of 2011. Incidence and the number of cholangitis episodes were recorded and compared between patients based on LT status.

RESULTS

Ninety-six (26.8%) of the 366 BA patients underwent LT. More patients who underwent KP at < 60 days of age survived with their native liver (P = 0.007). The mean age at first cholangitis was 0.9 years and 0.8 years in the LT and non-LT groups, respectively (P = 0.868). The cumulative incidence of cholangitis within 2 years after KP did not differ between the groups (hazard ratio 1.2; 95% CI 0.9-1.6). However, the total number of cholangitis episodes was higher in the LT group within 2 years after KP (P < 0.001).

CONCLUSIONS

Cholangitis occurrence was not related to LT in the first 2 years after KP in BA patients, but the number of cholangitis episodes could be a prognostic marker for future LT.

摘要

背景

胆管炎可能影响肝门空肠吻合术(KP)后胆道闭锁(BA)患者的肝衰竭情况。我们研究了胆管炎发作次数是否可作为肝门空肠吻合术(KP)后BA患儿肝移植(LT)的预后标志物。

方法

从台湾国民健康保险研究数据库(NHIRD)获取1998年后出生并接受KP的BA患者数据。对患者进行随访至2011年底。记录胆管炎的发病率和发作次数,并根据LT状态在患者之间进行比较。

结果

366例BA患者中有96例(26.8%)接受了LT。60日龄前接受KP的患者中,更多患者存活且肝脏未移植(P = 0.007)。LT组和非LT组首次发生胆管炎的平均年龄分别为0.9岁和0.8岁(P = 0.868)。KP后2年内胆管炎的累积发病率在两组之间无差异(风险比1.2;95%置信区间0.9 - 1.6)。然而,KP后2年内LT组的胆管炎发作总数更高(P < 0.001)。

结论

BA患者在KP后的前2年,胆管炎的发生与LT无关,但胆管炎发作次数可能是未来LT的预后标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4740/5880092/2b04636f9bd1/12887_2018_1074_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4740/5880092/49035ed531cd/12887_2018_1074_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4740/5880092/501a66c58a58/12887_2018_1074_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4740/5880092/2b04636f9bd1/12887_2018_1074_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4740/5880092/49035ed531cd/12887_2018_1074_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4740/5880092/501a66c58a58/12887_2018_1074_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4740/5880092/2b04636f9bd1/12887_2018_1074_Fig3_HTML.jpg

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2
Validation of acute myocardial infarction cases in the national health insurance research database in taiwan.台湾全民健康保险研究数据库中急性心肌梗死病例的验证
J Epidemiol. 2014;24(6):500-7. doi: 10.2188/jea.je20140076. Epub 2014 Aug 30.
3
Medical status of 219 children with biliary atresia surviving long-term with their native livers: results from a North American multicenter consortium.
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Am J Transl Res. 2024 Aug 15;16(8):3822-3831. doi: 10.62347/CPFT4246. eCollection 2024.
4
Retrospective analysis of the standardized BARD criteria for acute cholangitis in biliary atresia patients.对胆道闭锁患者急性胆管炎的标准化BARD标准进行回顾性分析。
JPGN Rep. 2024 Apr 12;5(3):309-316. doi: 10.1002/jpr3.12071. eCollection 2024 Aug.
5
Early bile drainage improves native liver survival in biliary atresia without cholangitis.早期胆汁引流可提高无胆管炎的胆道闭锁患儿的自体肝存活率。
Front Pediatr. 2023 Jul 12;11:1189792. doi: 10.3389/fped.2023.1189792. eCollection 2023.
6
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Korean J Radiol. 2023 May;24(5):465-475. doi: 10.3348/kjr.2022.0586. Epub 2023 Mar 30.
7
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Pediatr Surg Int. 2022 Dec;38(12):1881-1885. doi: 10.1007/s00383-022-05230-y. Epub 2022 Sep 14.
8
Comprehensive Analysis of Gut Microbiota and Fecal Bile Acid Profiles in Children With Biliary Atresia.胆道闭锁患儿肠道微生物群和粪便胆汁酸谱的综合分析。
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Pediatr Surg Int. 2022 Feb;38(2):193-199. doi: 10.1007/s00383-021-05047-1. Epub 2021 Dec 2.
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4
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J Pediatr Surg. 2013 Dec;48(12):2368-72. doi: 10.1016/j.jpedsurg.2013.08.007.
5
Risk factors affecting late-presenting liver failure in adult patients with biliary atresia.影响成人胆道闭锁患者迟发性肝功能衰竭的危险因素。
J Pediatr Surg. 2012 Dec;47(12):2179-83. doi: 10.1016/j.jpedsurg.2012.09.003.
6
Twenty-year transplant-free survival rate among patients with biliary atresia.胆道闭锁患者 20 年无移植存活率。
Clin Gastroenterol Hepatol. 2011 Dec;9(12):1086-91. doi: 10.1016/j.cgh.2011.07.024. Epub 2011 Aug 4.
7
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Pharmacoepidemiol Drug Saf. 2011 Mar;20(3):236-42. doi: 10.1002/pds.2087. Epub 2010 Dec 29.
8
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Pediatr Surg Int. 2010 Aug;26(8):825-30. doi: 10.1007/s00383-010-2637-y. Epub 2010 Jun 30.
9
Biliary atresia in Canada: the effect of centre caseload experience on outcome.加拿大的胆道闭锁:中心病例量经验对结果的影响。
J Pediatr Gastroenterol Nutr. 2010 Jul;51(1):61-5. doi: 10.1097/MPG.0b013e3181d67e5e.
10
Long-term outcome of children with biliary atresia who were not transplanted after the Kasai operation: >20-year experience at a children's hospital.接受葛西手术后未接受移植的胆道闭锁患儿的长期预后:一家儿童医院的20多年经验
J Pediatr Gastroenterol Nutr. 2009 Apr;48(4):443-50. doi: 10.1097/mpg.0b013e318189f2d5.