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Twenty-first Century Trends in the Global Epidemiology of Pediatric-Onset Inflammatory Bowel Disease: Systematic Review.21世纪儿童期起病的炎症性肠病全球流行病学趋势:系统评价
Gastroenterology. 2022 Apr;162(4):1147-1159.e4. doi: 10.1053/j.gastro.2021.12.282. Epub 2022 Jan 5.
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Diagnostic Delay Is Associated With Complicated Disease and Growth Impairment in Paediatric Crohn's Disease.诊断延迟与儿科克罗恩病的复杂疾病和生长障碍有关。
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[Expert consensus on the diagnosis and management of pediatric inflammatory bowel disease].[儿童炎症性肠病诊断与管理专家共识]
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4
Current global trends in the incidence of pediatric-onset inflammatory bowel disease.当前儿科炎症性肠病发病的全球趋势。
World J Gastroenterol. 2018 Jul 7;24(25):2741-2763. doi: 10.3748/wjg.v24.i25.2741.
5
Diagnostic delay in Canadian children with inflammatory bowel disease is more common in Crohn's disease and associated with decreased height.加拿大炎症性肠病患儿的诊断延误在克罗恩病中更为常见,且与身高降低有关。
Arch Dis Child. 2018 Apr;103(4):319-326. doi: 10.1136/archdischild-2017-313060. Epub 2017 Aug 9.
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Anemia in a population-based IBD cohort (ICURE): still high prevalence after 1 year, especially among pediatric patients.基于人群的炎症性肠病队列(ICURE)中的贫血:1年后患病率仍很高,尤其是在儿科患者中。
Inflamm Bowel Dis. 2014 Dec;20(12):2266-70. doi: 10.1097/MIB.0000000000000191.
7
Early-onset Crohn's disease is a risk factor for smaller final height.早发性克罗恩病是最终身高较矮的一个风险因素。
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8
Natural history of pediatric-onset inflammatory bowel disease: a systematic review.儿科炎症性肠病的自然史:系统评价。
J Clin Gastroenterol. 2012 Aug;46(7):581-9. doi: 10.1097/MCG.0b013e318247c32f.
9
Prevalence and management of anemia in children, adolescents, and adults with inflammatory bowel disease.炎症性肠病患儿、青少年和成人贫血的患病率及处理。
Inflamm Bowel Dis. 2012 Mar;18(3):513-9. doi: 10.1002/ibd.21740. Epub 2011 May 20.
10
Slow hematological recovery in children with IBD-associated anemia in cases of "expectant management".在“期待治疗”的情况下,IBD 相关贫血儿童的血液学恢复缓慢。
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[新诊断炎症性肠病患儿的营养状况及其影响因素]

[Nutritional status and its influencing factors in children with newly diagnosed inflammatory bowel disease].

作者信息

Zhou Juan, Xiao Xiong, Xia Yu, You Jie-Yu, Zhao Hong-Mei

机构信息

Department of Gastroenterology and Nutrition, Hunan Children's Hospital, Changsha 410007, China.

出版信息

Zhongguo Dang Dai Er Ke Za Zhi. 2023 Jul 15;25(7):745-750. doi: 10.7499/j.issn.1008-8830.2212066.

DOI:10.7499/j.issn.1008-8830.2212066
PMID:37529958
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10414168/
Abstract

OBJECTIVES

To investigate the nutritional status and its influencing factors in children with newly diagnosed inflammatory bowel disease (IBD).

METHODS

A retrospective analysis was conducted on the clinical data of children who were diagnosed with IBD for the first time in Hunan Children's Hospital from January 2015 to December 2021. Diagnostic delay was defined as the time from the symptom onset to IBD diagnosis being in the upper quartile (-) of all IBD children in the study. Multivariate logistic regression analysis was used to explore the risk factors for emaciation and growth retardation.

RESULTS

A total of 125 children with newly diagnosed IBD were included, with Crohn's disease being the main type (91.2%). The rates of emaciation and growth retardation were 42.4% (53 cases) and 7.2% (9 cases), respectively, and the rate of anemia was 77.6% (97 cases). Diagnostic delay was noted in 31 children (24.8%), with the time from the symptom onset to IBD diagnosis of 366 to 7 211 days. Multivariate logistic regression analysis showed that diagnostic delay was a risk factor for emaciation and growth retardation (=2.73 and =4.42, respectively; <0.05) and that age was positively associated with emaciation (=1.30, <0.05).

CONCLUSIONS

Children with newly diagnosed IBD have poor nutritional status, and the rates of anemia, emaciation, and growth retardation are high. Diagnostic delay is associated with malnutrition in children with IBD.

摘要

目的

探讨新诊断的炎症性肠病(IBD)患儿的营养状况及其影响因素。

方法

对2015年1月至2021年12月在湖南省儿童医院首次诊断为IBD的患儿的临床资料进行回顾性分析。诊断延迟定义为从症状出现到IBD诊断的时间处于本研究中所有IBD患儿的上四分位数(-)。采用多因素logistic回归分析探讨消瘦和生长发育迟缓的危险因素。

结果

共纳入125例新诊断的IBD患儿,以克罗恩病为主(91.2%)。消瘦和生长发育迟缓的发生率分别为42.4%(53例)和7.2%(9例),贫血发生率为77.6%(97例)。31例患儿(24.8%)存在诊断延迟,从症状出现到IBD诊断的时间为366至7211天。多因素logistic回归分析显示,诊断延迟是消瘦和生长发育迟缓的危险因素(分别为=2.73和=4.42;<0.05),年龄与消瘦呈正相关(=1.30,<0.05)。

结论

新诊断的IBD患儿营养状况较差,贫血、消瘦和生长发育迟缓的发生率较高。诊断延迟与IBD患儿的营养不良有关。