Peri-Operative Liver Fibrosis and Native Liver Survival in Pediatric Patients with Biliary Atresia: A Systematic Review and Meta-Analysis.

IF 1.3 Q3 PEDIATRICS
Ashkan Jahangirnia, Irina Oltean, Youssef Nasr, Nayaar Islam, Arielle Weir, Joseph de Nanassy, Ahmed Nasr, Dina El Demellawy
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引用次数: 0

Abstract

No systematic review to date has examined histopathological parameters in relation to native liver survival in children who undergo the Kasai operation for biliary atresia (BA). A systematic review and meta-analysis is presented, comparing the frequency of native liver survival in peri-operative severe vs. non-severe liver fibrosis cases, in addition to other reported histopathology parameters. Records were sourced from MEDLINE, Embase, and CENTRAL databases. Studies followed the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guidelines and compared native liver survival frequencies in pediatric patients with evidence of severe vs. non-severe liver fibrosis, bile duct proliferation, cholestasis, lobular inflammation, portal inflammation, and giant cell transformation on peri-operative biopsies. The primary outcome was the frequency of native liver survival. A random effects meta-analysis was used. Twenty-eight observational studies were included, 1,171 pediatric patients with BA of whom 631 survived with their native liver. Lower odds of native liver survival in the severe liver fibrosis vs. non-severe liver fibrosis groups were reported (odds ratio [OR], 0.16; 95% confidence interval [CI], 0.08-0.33; I2 =46%). No difference in the odds of native liver survival in the severe bile duct destruction vs. non-severe bile duct destruction groups were reported (OR, 0.17; 95% CI, 0.00-63.63; I2 =96%). Lower odds of native liver survival were documented in the severe cholestasis vs. non-severe cholestasis (OR, 0.10; 95% CI, 0.01-0.73; I2 =80%) and severe lobular inflammation vs. non-severe lobular inflammation groups (OR, 0.02; 95% CI, 0.00-0.62; I2 =69%). There was no difference in the odds of native liver survival in the severe portal inflammation vs. non-severe portal inflammation groups (OR, 0.03; 95% CI, 0.00-3.22; I2 =86%) or between the severe giant cell transformation vs. non-severe giant cell transformation groups (OR, 0.15; 95% CI, 0.00-175.21; I2 =94%). The meta-analysis loosely suggests that the presence of severe liver fibrosis, cholestasis, and lobular inflammation are associated with lower odds of native liver survival in pediatric patients after Kasai.

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胆道闭锁儿科患者术后肝纤维化与原肝存活率:系统回顾与元分析》。
迄今为止,还没有系统性综述研究过接受葛西手术治疗胆道闭锁(BA)的儿童原肝存活率的相关组织病理学参数。本文介绍了一项系统综述和荟萃分析,比较了围手术期严重肝纤维化与非严重肝纤维化病例的原肝存活率,以及其他已报道的组织病理学参数。研究记录来自 MEDLINE、Embase 和 CENTRAL 数据库。研究遵循PRISMA(系统综述和荟萃分析首选报告项目)指南,比较了围手术期活检中出现严重与非严重肝纤维化、胆管增生、胆汁淤积、小叶炎症、门脉炎症和巨细胞转化的儿科患者的原肝存活率。主要结果是原肝存活率。研究采用随机效应荟萃分析法。共纳入了 28 项观察性研究,1,171 名儿童 BA 患者,其中 631 人的原肝存活。据报道,严重肝纤维化组与非严重肝纤维化组的原肝存活几率较低(几率比 [OR],0.16;95% 置信区间 [CI],0.08-0.33;I2 =46%)。严重胆管破坏组与非严重胆管破坏组的原肝存活率无差异(OR,0.17;95% CI,0.00-63.63;I2 =96%)。重度胆汁淤积组与非重度胆汁淤积组(OR,0.10;95% CI,0.01-0.73;I2 =80%)和重度小叶炎症组与非重度小叶炎症组(OR,0.02;95% CI,0.00-0.62;I2 =69%)的原肝存活几率较低。重度门静脉炎症组与非重度门静脉炎症组(OR,0.03;95% CI,0.00-3.22;I2 =86%)或重度巨细胞转化组与非重度巨细胞转化组(OR,0.15;95% CI,0.00-175.21;I2 =94%)的原肝存活几率没有差异。荟萃分析粗略地表明,严重肝纤维化、胆汁淤积和肝小叶炎症的存在与卡塞术后儿科患者较低的原肝存活率有关。
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来源期刊
CiteScore
3.90
自引率
0.00%
发文量
43
期刊介绍: Pediatric Gastroenterology, Hepatology and Nutrition (Pediatr Gastroenterol Hepatol Nutr), an official journal of The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition, is issued bimonthly and published in English. The aim of Pediatr Gastroenterol Hepatol Nutr is to advance scientific knowledge and promote child healthcare by publishing high-quality empirical and theoretical studies and providing a recently updated knowledge to those practitioners and scholars in the field of pediatric gastroenterology, hepatology and nutrition. Pediatr Gastroenterol Hepatol Nutr publishes review articles, original articles, and case reports. All of the submitted papers are peer-reviewed. The journal covers basic and clinical researches on molecular and cellular biology, pathophysiology, epidemiology, diagnosis, and treatment of all aspects of pediatric gastrointestinal diseases and nutritional health problems.
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