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患有先天性巨结肠症及伴有认知功能障碍综合征的儿童:临床表现、治疗及预后

Children with Hirschsprung's Disease and Syndromes with Cognitive Dysfunction: Manifestations, Treatment, and Outcomes.

作者信息

Hedbys Josefine, Hasserius Johan, Granéli Christina, Arnbjörnsson Einar, Hagelsteen Kristine, Stenström Pernilla

机构信息

Department of Clinical Sciences, Lund University, Lund, Sweden.

Department of Pediatric Surgery, Skåne University Hospital, Lund, Sweden.

出版信息

Surg J (N Y). 2019 Sep 4;5(3):e103-e109. doi: 10.1055/s-0039-1696730. eCollection 2019 Jul.

DOI:10.1055/s-0039-1696730
PMID:31508491
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6727023/
Abstract

To assess differences in initial symptoms, treatments, and bowel function between children with Hirschsprung's disease (HD) with or without a cognitive dysfunction (CD).  The study included children with HD who underwent transanal endorectal pull-through. A retrospective chart review was performed to collect data on patient characteristics, diagnosis, and treatment. Data on bowel symptoms in children older than 4 years without a colostomy were compiled during a cross-sectional, patient-reported follow-up.  Fifty-three children with HD were included; of these, 12 (23%) had CD. The median birth weight was lower, frequency of vomiting as the presenting symptom was lower, and time until the first contact with a pediatric surgeon was higher in children with CD than in those without (3,295 vs. 3,623 g,  = 0.013; 28 vs. 66%,  = 0.02; and 4 days vs. 1 day,  = 0.048, respectively). At follow-up, 5 (15%) of 33 children aged over 4 years had CD. More children without CD had some ability to hold back defecation and sense the urge to defecate than those with CD (  = 0.002 and  = 0.001, respectively).  HD children who have CD present with different initial symptoms, have a delay in the first consultation with a pediatric surgeon, and experience poorer bowel function outcomes than HD children without CD. Therefore, HD children with CD should receive special attention in both clinical practice and research.

摘要

评估患有或不患有认知功能障碍(CD)的先天性巨结肠(HD)患儿在初始症状、治疗方法和肠道功能方面的差异。

该研究纳入了接受经肛门直肠拖出术的HD患儿。通过回顾性病历审查收集患者特征、诊断和治疗的数据。在横断面、患者报告的随访期间收集4岁以上无结肠造口术患儿的肠道症状数据。

共纳入53例HD患儿;其中12例(23%)患有CD。CD患儿的出生体重中位数较低,以呕吐作为首发症状的频率较低,与未患CD的患儿相比,首次接触小儿外科医生的时间更长(分别为3295 vs. 3623g,P = 0.013;28% vs. 66%,P = 0.02;4天 vs. 1天,P = 0.048)。随访时,33例4岁以上患儿中有5例(15%)患有CD。与患有CD的患儿相比,更多未患CD的患儿有一定的控制排便能力和排便冲动感知能力(分别为P = 0.002和P = 0.001)。

患有CD的HD患儿表现出不同的初始症状,首次咨询小儿外科医生的时间延迟,并且肠道功能结局比未患CD的HD患儿更差。因此,患有CD的HD患儿在临床实践和研究中都应受到特别关注。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47f4/6727023/25106cb38d77/10-1055-s-0039-1696730-i1800075oa-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47f4/6727023/e4a1357a9e9f/10-1055-s-0039-1696730-i1800075oa-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47f4/6727023/25106cb38d77/10-1055-s-0039-1696730-i1800075oa-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47f4/6727023/e4a1357a9e9f/10-1055-s-0039-1696730-i1800075oa-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/47f4/6727023/25106cb38d77/10-1055-s-0039-1696730-i1800075oa-2.jpg

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