hirschsprung disease

先天性巨结肠病
  • 文章类型: Journal Article
    目的:患有肛门直肠畸形(ARM)和先天性巨结肠病(HD)的患者即使在成年期也受到这些疾病的长期影响。我们的目标是探索物理,这些疾病对青少年和年轻人的社会和情感影响,以制定过渡护理的最佳做法。
    方法:我们对在四个三级转诊中心接受手术的年龄≥11岁的ARM和HD患者进行了一对一的深入访谈。所有访谈都是录音和逐字转录的。我们分析了反复出现的主题的抄本,并收集数据直至达到数据饱和。三名研究人员使用主题分析方法独立编码主要主题的成绩单。
    结果:我们在2022年10月至2023年4月期间采访了16名参与者(11名男性)。年龄从11岁到26岁不等。出现了五个主要主题:(1)个人影响(子主题:身体,情绪和心理健康,社会,School),(2)对家庭的影响,(3)对他们未来的看法(次主题:关系,职业,健康状况),(4)支持来源(子主题:家庭,同行,partner),和(5)过渡护理(次主题:关注,期望)。只有女性对未来的生育率表示担忧。
    结论:这项研究强调了患有ARM和HD的青少年和年轻人所面临的不断发展的问题,特别是针对特定性别的问题。我们的发现可以为提供个性化护理的努力提供信息。
    OBJECTIVE: Patients with anorectal malformation (ARM) and Hirschsprung\'s disease (HD) live with long-term impact of these diseases even into adulthood. We aimed to explore the physical, social and emotional impact of these diseases in adolescents and young adults to develop best practices for transition care.
    METHODS: We conducted one-on-one in-depth interviews with ARM and HD patients aged  ≥ 11 years who had undergone surgery at four tertiary referral centers. All interviews were audio-recorded and transcribed verbatim. We analyzed transcripts for recurring themes, and data were collected until data saturation was reached. Three researchers independently coded the transcripts for major themes using thematic analysis approach.
    RESULTS: We interviewed 16 participants (11 males) between October 2022 and April 2023. Ages ranged from 11 to 26 years. Five major themes emerged: (1) personal impact (subthemes: physical, emotional and mental health, social, school), (2) impact on family, (3) perceptions of their future (subthemes: relationships, career, state of health), (4) sources of support (subthemes: family, peers, partner), and (5) transition care (subthemes: concerns, expectations). Only females expressed concerns regarding future fertility.
    CONCLUSIONS: This study highlights the evolving problems faced by adolescents and young adults with ARM and HD, especially gender-specific concerns. Our findings can inform efforts to provide individualized care.
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  • 文章类型: Journal Article
    目的:探讨先天性巨结肠相关性小肠结肠炎(post-HAEC)术后对远期预后的影响,并确定HAEC后的危险因素。
    方法:回顾了304例符合诊断为先天性巨结肠病(HSCR)的患者的病历。我们分析了HAEC后的临床特征及其对长期结局的影响。此外,早期和复发HAEC的危险因素被分别确定.
    结果:术后HAEC的总发生率为29.9%(91/304)。我们将早期HAEC分类为术后3个月内发生(n=39),复发性HAEC分类为术后6个月内发生≥3次发作(n=25)。早期HAEC患者更有可能经历更差的营养状况,排便功能,和生活质量与晚期或无发作者相比(P<0.05)。同样,复发HAEC对这些结局的不利影响也显著(P<0.05).早期HAEC的危险因素包括术前营养不足,长段HSCR,术后30天内发生3-4级并发症。对于复发性HAEC,危险因素为术前营养不良,非父母照顾者,长段HSCR,术后30天内发生3-4级并发症。
    结论:根据首次发作时间和频率对HAEC后进行分类是必要的。早期或更频繁的后HAEC发作对长期结果有不利影响。此外,早期和复发HAEC的危险因素不同.
    OBJECTIVE: To explore the influence of postoperative Hirschsprung-associated enterocolitis (post-HAEC) on long-term outcomes and to identify risk factors of post-HAEC.
    METHODS: The medical records of 304 eligible patients diagnosed with Hirschsprung\'s disease (HSCR) were reviewed. We analyzed the clinical characteristics of post-HAEC and its influence on long-term outcomes. Furthermore, risk factors for early and recurrent HAEC were identified separately.
    RESULTS: The overall incidence of post-HAEC was 29.9% (91/304). We categorized early HAEC as occurring within postoperative 3 months (n = 39) and recurrent HAEC as occurring ≥ 3 episodes within postoperative 6 months (n = 25). Patients with early HAEC were more likely to experience worse nutritional status, defecation function, and quality of life compared to those with late or no episodes (P < 0.05). Similarly, the adverse influences of recurrent HAEC on these outcomes were also significant (P < 0.05). The risk factors for early HAEC included preoperative undernutrition, long-segment HSCR, and postoperative Grade 3-4 complications within 30 days. For recurrent HAEC, risk factors were preoperative malnutrition, non-parental caregivers, long-segment HSCR, and postoperative Grade 3-4 complications within 30 days.
    CONCLUSIONS: Classification of post-HAEC based on the first episode time and frequency was necessary. The earlier or more frequent episodes of post-HAEC have detrimental influences on long-term outcomes. Furthermore, risk factors for early and recurrent HAEC were different.
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  • 文章类型: Journal Article
    一些研究指出了肠道微生物群(GM)及其代谢产物在先天性巨结肠病(HSCR)发病机理中的关键作用。然而,GM和HSCR之间的详细因果关系仍然未知.
    在这项研究中,我们使用双样本孟德尔随机化(MR)分析来研究GM和HSCR之间的因果关系,基于MiBioGen联盟的全基因组关联研究(GWAS)和GWAS目录的HSCR数据。随后进行反向MR分析,和敏感性分析,Cochran的Q检验,MR多效性残差总和,异常值(MR-PRESSO),MR-Egger截距用于分析异质性或水平多效性。开发16SrDNA测序和靶向质谱用于初步验证。
    在正向MR分析中,逆方差加权(IVW)估计表明Eggerthella(OR:2.66,95CI:1.23-5.74,p=0.01)是HSCR的危险因素,而肽球菌(OR:0.37,95CI:0.18-0.73,p=0.004),Ruminococus2(OR:0.32,95CI:0.11-0.91,p=0.03),梭菌1(OR:0.22,95CI:0.06-0.78,p=0.02),MollicutesRF9(OR:0.27,95CI:0.09-0.8,p=0.02),Ruminocycaceae(OR:0.16,95CI:0.04-0.66,p=0.01),和Paraprevotella(OR:0.45,95CI:0.21-0.98,p=0.04)是HSCR的保护因素,没有异质性或水平多效性。然而,反向MR分析显示,HSCR(OR:1.02,95CI:1-1.03,p=0.049)是Eggerthella的危险因素。此外,上述一些微生物群和短链脂肪酸(SCFA)在HSCR中发生了变化,显示出相关性。
    我们的分析建立了特定GM和HSCR之间的关系,确定特定细菌作为保护或危险因素。HSCR中重要的微生物群和SCFA发生了变化,强调进一步研究的重要性,并为发病机制和治疗提供新的见解。
    UNASSIGNED: Several studies have pointed to the critical role of gut microbiota (GM) and their metabolites in Hirschsprung disease (HSCR) pathogenesis. However, the detailed causal relationship between GM and HSCR remains unknown.
    UNASSIGNED: In this study, we used two-sample Mendelian randomization (MR) analysis to investigate the causal relationship between GM and HSCR, based on the MiBioGen Consortium\'s genome-wide association study (GWAS) and the GWAS Catalog\'s HSCR data. Reverse MR analysis was performed subsequently, and the sensitivity analysis, Cochran\'s Q-test, MR pleiotropy residual sum, outlier (MR-PRESSO), and the MR-Egger intercept were used to analyze heterogeneity or horizontal pleiotropy. 16S rDNA sequencing and targeted mass spectrometry were developed for initial validation.
    UNASSIGNED: In the forward MR analysis, inverse-variance weighted (IVW) estimates suggested that Eggerthella (OR: 2.66, 95%CI: 1.23-5.74, p = 0.01) was a risk factor for HSCR, while Peptococcus (OR: 0.37, 95%CI: 0.18-0.73, p = 0.004), Ruminococcus2 (OR: 0.32, 95%CI: 0.11-0.91, p = 0.03), Clostridiaceae1 (OR: 0.22, 95%CI: 0.06-0.78, p = 0.02), Mollicutes RF9 (OR: 0.27, 95%CI: 0.09-0.8, p = 0.02), Ruminococcaceae (OR: 0.16, 95%CI: 0.04-0.66, p = 0.01), and Paraprevotella (OR: 0.45, 95%CI: 0.21-0.98, p = 0.04) were protective factors for HSCR, which had no heterogeneity or horizontal pleiotropy. However, reverse MR analysis showed that HSCR (OR: 1.02, 95%CI: 1-1.03, p = 0.049) is the risk factor for Eggerthella. Furthermore, some of the above microbiota and short-chain fatty acids (SCFAs) were altered in HSCR, showing a correlation.
    UNASSIGNED: Our analysis established the relationship between specific GM and HSCR, identifying specific bacteria as protective or risk factors. Significant microbiota and SCFAs were altered in HSCR, underlining the importance of further study and providing new insights into the pathogenesis and treatment.
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  • 文章类型: Journal Article
    先天性巨结肠病(HSCR)是一种病因不明的先天性疾病,影响肠神经系统(ENS)。由于ENS的早期妊娠发育依赖于产前母体的代谢环境,这项初步研究的目的是探讨特定母体血浆代谢物在HSCR病因中的作用.
    在这项横断面研究中,我们从被诊断患有HSCR的儿童的母亲(n=7)和年龄匹配的正常儿童的母亲(n=6)获得出生后(作为产前替代)血浆样本.通过超高压液相色谱和质谱分析血浆代谢组。使用CompoundDiscoverer软件通过mzCloud鉴定代谢物。使用非目标代谢组学工作流程,确定了代谢产物与病例组和对照组的差异。
    在母体血浆中鉴定并注释了总共268种独特的血浆代谢物。其中,57例病例组与对照组差异有统计学意义(P<0.05,t检验)。使用10%的错误发现率校正截止值来调整多重比较,19种代谢物在HSCR病例中有显著差异,包括肉碱,中链脂肪酸,还有谷氨酸.受影响的途径是氨基酸和脂质代谢。
    产前代谢途径紊乱可能与胎儿发育中HSCR的病因有关。这是评估HSCR中母体血浆代谢组学的第一项研究。
    UNASSIGNED: Hirschsprung disease (HSCR) is a congenital disorder of unknown etiology affecting the enteric nervous system (ENS). Since the early gestational development of the ENS is dependent on the prenatal maternal metabolic environment, the objective of this pilot study was to explore the role of specific maternal plasma metabolites in the etiology of HSCR.
    UNASSIGNED: In this cross-sectional study, postnatal (as a surrogate for prenatal) plasma samples were obtained from mothers of children diagnosed with HSCR (n = 7) and age-matched mothers of normal children (n = 6). The plasma metabolome was analyzed by ultra-high-pressure liquid chromatography and mass spectrometry. Metabolites were identified by mzCloud using Compound Discoverer software. Using an untargeted metabolomics workflow, metabolites with case versus control group differences were identified.
    UNASSIGNED: A total of 268 unique plasma metabolites were identified and annotated in maternal plasma. Of these, 57 were significantly different between case and control groups (P < 0.05, t-test). Using a false discovery rate corrected cutoff of 10% to adjust for multiple comparisons, 19 metabolites were significantly different in HSCR cases, including carnitines, medium-chain fatty acids, and glutamic acid. Pathways affected were for amino acid and lipid metabolism.
    UNASSIGNED: Disordered prenatal metabolic pathways may be involved in the etiopathogenesis of HSCR in the developing fetus. This is the first study to assess maternal plasma metabolomics in HSCR.
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  • 文章类型: Journal Article
    目前对先天性巨结肠的诊断通常是具有挑战性和侵入性的。本研究旨在研究表面肠电图是否可以非侵入性地辨别健康受试者与患有先天性巨结肠病的受试者。9名健康受试者(7名儿童,两名成人)和11名患有未经手术治疗的先天性巨结肠病的受试者(9名儿童,两名成年人)接受了肠电图检查。该程序包括超声引导在腹部上放置表面电极,覆盖结肠的所有部分,空腹和两次20分钟的肠电图测量由一餐分开。主导频率,比较两组之间结肠活动的大小和相对增加(餐前到餐后)。结果显示,在儿科组中,优势频率没有显著差异,对照组和患者之间观察到结肠活动和相对功率增加。成年患者显示结肠运动性下降,最靠近远端结肠的电极的相对功率增加,当与对照中的相同电极和它们自身的更近端的电极相比时。最后,幼儿的肠电图测量具有挑战性,但在成人中的研究结果表明,这些测量结果可以区分对照组和赫氏弹簧患者。因此,优化幼儿的肠电图测量是必要的。
    Current diagnostics in Hirschsprung\'s disease are often challenging and invasive. This study aims to investigate whether surface electroenterography can non-invasively discern healthy subjects from subjects suffering from Hirschsprung\'s disease. Nine healthy subjects (seven children, two adults) and eleven subjects suffering from surgically untreated Hirschsprung\'s disease (nine children, two adults) underwent an electroenterography procedure. This procedure consisted of ultrasound-guided placement of surface electrodes on the abdomen covering all parts of the colon, fasting and two 20-min electroenterography measurements separated by a meal. The dominant frequency, magnitude and relative increase (pre- to postprandial) of colonic activity were compared between both groups. The results showed that in the pediatric group, no significant differences in dominant frequency, colonic activity and relative power increase were observed between controls and patients. The adult patients showed decreased colonic motility and relative power increase in the electrodes closest to the distal colon, both when compared to the same electrodes in controls and to the more proximal electrodes of themselves. To conclude, electroenterography measurements in young children is challenging, but the results in adults demonstrate that these measurements can possibly distinguish between controls and Hirschsprung\'s patients. Therefore, optimization of electroenterography measurements in young children is necessary.
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  • 文章类型: Journal Article
    背景:在低收入和中等收入国家,先天性巨结肠(HD)的外科治疗通常是分阶段进行的,需要多次住院和就诊,增加了家庭经济负担。目前,关于寻求手术干预的先天性巨结肠患儿看护者承担的费用的信息有限。这项研究旨在衡量乌干达西部Hirschsprung病手术治疗的成本和经济负担。
    方法:对2017年1月至2021年12月在乌干达西部的两家医院完成HD手术治疗的看护者进行了一项使用成本分析的横断面研究。计算了在公立和私立医院就诊的护理人员产生的平均直接和间接成本。
    结果:共有69名患者(M:F=7:1)纳入研究。儿童诊断时的中位年龄为60.5(IQR3-151.25)天,并且两阶段拉出手术是常见的手术。治疗的平均总成本为960美元(SD=720美元),大部分费用来自直接医疗费用。近一半(48%)的参与者求助于困境融资来资助他们孩子的手术护理。绝大多数患者(n=64,93%)在HD手术的总费用中产生了灾难性的支出,97%的参与者在治疗完成时低于国际贫困线。
    结论:尽管政府医院和非营利服务提供了“免费护理”,这项研究发现,先天性巨结肠的外科治疗给患有先天性巨结肠的患者家庭带来了巨大的费用负担.
    BACKGROUND: Surgical management of Hirschsprung disease (HD) in low- and middle-income countries is typically a staged procedure, necessitating multiple hospitalizations and clinic visits increasing family financial burden. Currently, there is limited information on the costs borne by caretakers of children with Hirschsprung disease seeking surgical intervention. This study seeks to measure the costs and economic burden of surgical treatment for Hirschsprung disease in western Uganda.
    METHODS: A cross-sectional study using cost analysis was conducted among caretakers of patients who completed surgical treatment of HD between January 2017 and December 2021 at two hospitals in western Uganda. The average direct and indirect costs incurred by caretakers presenting at a public and private hospital were computed.
    RESULTS: A total of 69 patients (M: F = 7:1) were enrolled in the study. The median age at diagnosis was 60.5 (IQR 3-151.25) days for children and two-staged pull-through procedure was the common surgery performed. The mean overall cost for treatment was US $960 (SD = $720), with the majority of costs coming from direct medical costs. Nearly half (48%) of participants resorted to distress financing to finance their child\'s surgical care. The overwhelming majority of patients (n = 64, 93%) incurred catastrophic expenditure from the total costs of surgery for HD, and 97% of participants fell below the international poverty line at the time treatment was completed.
    CONCLUSIONS: Despite the availability of \'free care\' from government hospital and non-profit services, this study found that surgical management of Hirschsprung disease imposed substantial cost burden on families with Hirschsprung disease patients.
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  • 文章类型: Journal Article
    本研究旨在探讨在进行家庭反流灌肠的先天性巨结肠婴儿护理中的照顾者负担经验。研究结果将为制定有针对性的有效护理干预措施提供依据。
    采用了现象学研究方法。2022年10月至2023年1月,对福建省某三级儿科医院12名接受家庭反流灌肠的先天性巨结肠患儿照顾者进行半结构式深度访谈。使用Colaizzi的7步分析方法对收集的数据进行分析和组织,导致确定关键主题。
    该分析得出了三个主要主题,这些主题涉及先天性巨结肠婴儿家庭反流灌肠护理中的照顾者负担经验:疾病相关知识不足,在护理过程中存在多种压力,以及对更大支持的渴望。
    这项研究对12名先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性先天性对出院后在家进行反流灌肠的患儿看护人的感受也有了深刻的理解。建议实施基于PERMA模式的积极心理干预,并融入"互联网+协同护理",为护理人员提供专业知识,解决他们的压力和需求,在提高护理能力的同时促进他们的福祉。
    UNASSIGNED: This study aims to explore the caregiver burden experience in the care of infants with congenital megacolon undergoing home reflux enema. The findings will provide a basis for developing targeted and effective nursing interventions.
    UNASSIGNED: A phenomenological research approach was employed. From October 2022 to January 2023, semi-structured in-depth interviews were conducted with 12 caregivers of infants with congenital megacolon undergoing home reflux enema in a tertiary paediatric hospital in Fujian Province. The collected data were analysed and organized using the Colaizzi\'s 7-step analysis method, leading to the identification of key themes.
    UNASSIGNED: The analysis yielded three major themes concerning the caregiver burden experience in the care of infants with congenital megacolon undergoing home reflux enema: inadequate disease-related knowledge, presence of multiple pressures during the caregiving process, and a desire for greater support.
    UNASSIGNED: This study employed qualitative interviews with the caregivers of 12 children with congenital Hirschsprung\'s disease undergoing home reflux enema, and the feelings of caregivers of children with reflux enema at home after discharge were deeply understood. It is recommended to implement positive psychological interventions based on the PERMA model and incorporate \"Internet + collaborative nursing\" to provide caregivers with professional knowledge, address their pressures and needs, and promote their well-being while enhancing nursing abilities.
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  • 文章类型: Journal Article
    背景:机器人辅助手术越来越多地用于儿童。虽然机器人辅助儿童手术已被证明是安全可行的,在婴儿中使用是有争议的。这项研究的目的是提出机器人辅助腹部手术在儿童<5个月的研究。
    方法:回顾性分析2020年4月至2022年12月在我院行腹部手术的111例<5月龄患者。数据包括临床信息,操作细节,和术后结果。
    结果:在这111名患者中,67例接受了机器人辅助手术,44例接受了腹腔镜辅助手术,机器人辅助组包括40例先天性巨结肠病患者,20例胆总管囊肿,和7例肠重复患者,腹腔镜辅助组包括26例先天性巨结肠患者,胆总管囊肿9例,肠重复9例。对于先天性巨结肠病,机器人辅助组手术时间明显长于腹腔镜辅助组(P=0.013),术中出血量明显少于腹腔镜辅助组(P=0.000).胆总管囊肿,机器人辅助组180分钟的中位手术时间与腹腔镜辅助手术组160分钟相比无明显延长(P=0.153).对于肠道重复,机器人辅助组手术时间明显长于腹腔镜辅助组(P=0.002).对于这三种疾病,机器人辅助组住院费用明显高于腹腔镜辅助组(P<0.05),并发症没有显着差异,两组患者术后禁食时间(P>0.05)。
    结论:机器人辅助腹部手术在5月龄以下的儿童中是安全可行的。这项研究表明,达芬奇机器人系统在儿童中的手术适应症可以扩展到婴儿。
    BACKGROUND: Robot-assisted surgery is increasingly used in children. While robot-assisted surgery in children has been proved to be safe and feasible, use in infants is controversial. The purpose of this study was to present a study of robot-assisted abdominal surgery in children less than5 months of age.
    METHODS: A retrospective analysis of 111 patients less than 5 months of age who underwent abdominal surgery from April 2020 to December 2022 in our hospital. The data included clinical information, operative details, and postoperative outcomes.
    RESULTS: Among these 111 patients, 67 underwent robot-assisted surgery and 44 underwent laparoscopic-assisted surgery, the robot-assisted group includes 40 patients with Hirschsprung disease, 20 patients with choledochal cysts, and 7 patients with intestinal duplication, the laparoscopic-assisted group includes 26 patients with Hirschsprung disease, 9 patients with choledochal cysts, and 9 patients with intestinal duplication. For Hirschsprung disease, the operation time was significantly longer ( P =0.013) and the intraoperative bleeding was significantly less ( P =0.000) in the robot-assisted group than the laparoscopic assisted group. For choledochal cysts, the median operation time of 180 mins for the robot-assisted group was not significantly longer than the laparoscopic assisted surgery group at 160 mins ( P =0.153). For intestinal duplication, the operation time was significantly longer ( P =0.002) in the robot-assisted group than the laparoscopic assisted group. For these three diseases, the hospitalization expense was significantly higher ( P <0.05) in the robot-assisted group than the laparoscopic assisted group, there were no significant differences in complications, and postoperative fasting time between two groups ( P >0.05).
    CONCLUSIONS: Robot-assisted abdominal surgery in children less than 5 months of age is safe and feasible. This study showed that the surgical indications for the Da Vinci robot system in children can be extended to infants.
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  • 文章类型: Multicenter Study
    背景:全结肠神经节病(TCA)是Hirschsprung病(HD)的一种罕见变种,其中结肠和远端回肠部分缺乏神经节细胞。大多数儿科使用直回肠(Swenson或Yancey-Soave)或短Duhamel牵拉法进行TCA。没有大型研究比较这些技术。我们旨在比较这些方法之间的短期和中期结果。
    方法:对2001年至2019年在三家大型儿童医院接受原发性Duhamel或Swenson牵拉的TCA儿童进行了回顾性研究。接受重做的患者和小肠神经节病大于30%的患者被排除在外。我们收集了人口统计数据,手术入路,和结果,两个,还有三年.连续变量采用t检验,分类变量采用卡方检验或Fisher检验。
    结果:共有54例患者,26人(48%)接受Duhamel,28人(52%)接受Swenson牵拉。性别没有差异,年龄,医疗合并症,或操作细节,包括穿越的年龄,腹腔镜与开放,受累小肠的长度,和手术时间。住院时间和术后并发症没有差异。穿越三年后,接受Duhamel治疗的患者每天大便较少(1-3次大便69.6%vs14.3%,p=0.003),并且不太可能处方纤维补充剂(4.2%vs43.8%,p=0.003)。灌溉没有差异,肉毒杆菌毒素给药,洛哌丁胺,或HD招生。
    结论:Duhamel和直拉法对治疗TCA都是安全的,具有可接受的短期和中期结果。有必要对患者报告的结果进行进一步研究,以检查长期差异。
    方法:III.
    BACKGROUND: Total colonic aganglionosis (TCA) is a rare variant of Hirschsprung disease (HD) where the colon and portion of distal ileum lack ganglion cells. Most pediatric use either a straight ileoanal (Swenson or Yancey-Soave) or a short Duhamel pull-through for TCA. There are no large studies comparing these techniques. We aimed to compare short-and medium-term outcomes between these approaches.
    METHODS: A retrospective review was performed among children with TCA from 2001 to 2019 undergoing a primary Duhamel or Swenson pull-through across three large children\'s hospitals. Patients undergoing redo and patients with greater than 30 % small bowel aganglionosis were excluded. We gathered data on demographics, operative approach, and outcomes at one, two, and three years. Continuous variables were analyzed with t-tests and categorical variables with Chi square or Fisher\'s tests.
    RESULTS: There were 54 patients, with 26 (48 %) undergoing Duhamel and 28 (52 %) undergoing Swenson pull-through. There were no differences in sex, age, medical comorbidities, or operative details, including age at pull-through, laparoscopic vs open, length of involved small bowel, and operative time. Length of stay and post-operative complications were not different. Three years after pull-through, patients undergoing Duhamel had fewer stools per day (1-3 stools 69.6 % vs 14.3 %, p = 0.003) and were less likely to be prescribed fiber supplementation (4.2 % vs 43.8 %, p = 0.003). There were no differences in irrigations, botulinum toxin administration, loperamide, or HD admissions.
    CONCLUSIONS: Both Duhamel and straight pull-throughs are safe for treatment of TCA, with acceptable short- and medium-term outcomes. Further studies on patient-reported outcomes are necessary to examine long-term differences.
    METHODS: III.
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  • 文章类型: Observational Study
    背景:已知炎症性肠病(IBD)与先天性巨结肠病(HSCR)相关。大多数病例以克罗恩病(CD)为代表,发生在总结肠神经节病(TCSA)患者中,估计患病率约为2%。基于这些考虑和属于我们消化疾病中心的一些临时数据,我们开发了一项旨在描述表型的单中心横断面观察研究,基因型,所有TCSA和克罗恩样病变患者的病理学和宏基因组学。
    结果:在一系列62名合格的TCSA患者中,48人符合纳入标准,并被纳入研究。10名患者由于不遵守或撤回同意而未完成研究,随后被退出。共有38名患者完成了研究。通过粪便钙卫汀(FC)或隐匿性粪便血(OFB)的组合对所有患者进行了慢性肠道炎症测试,并进行了粪便宏基因组学。十九(50%)的FC检测呈阳性,OFB,或两者兼而有之,随后行逆行回肠镜检查。14例(36.8%)患者出现克罗恩样病变,发生在手术后中位数11.5年(范围8个月-21.5年)。在人口统计方面没有统计学上的显着差异,表型和基因型进行观察,比较有和没有病变的患者,除了在有病变的患者中需要更频繁的输血。病变患者(不是看护者)的粪便微生物组生物多样性较低,其特征是拟杆菌减少,和过量的变形杆菌。FC在3/14的病变患者中检测为阴性(21%)。
    结论:我们的研究表明,TCSA中慢性炎症的发生率高10倍。多达50%的患者术后可能发展为IBD样病变。尽管如此,我们未能确定用于实施预防策略的特定风险因素.根据我们的研究结果,我们建议对所有TCSA患者行逆行回肠镜检查,无论FC/OFB值如何.内窥镜评估的频率和FC/OFB筛查在提示内窥镜检查中的作用尚待确定。
    BACKGROUND: Inflammatory Bowel Diseases (IBD) are known to occur in association with Hirschsprung disease (HSCR). Most of cases are represented by Crohn Disease (CD) occurring in patients with Total Colonic Aganglionosis (TCSA) with an estimated prevalence of around 2%. Based on these considerations and on a number of provisional data belonging to our Center for Digestive Diseases, we developed a unicentric cross-sectional observational study aimed at describing phenotype, genotype, pathology and metagenomics of all patients with TCSA and Crohn-like lesions.
    RESULTS: Out of a series of 62 eligible TCSA patients, 48 fulfilled inclusion criteria and were enrolled in the study. Ten patients did not complete the study due to non-compliance or withdrawal of consent and were subsequently dropped out. A total of 38 patients completed the study. All patients were tested for chronic intestinal inflammation by a combination of fecal calprotectine (FC) or occult fecal blood (OFB) and underwent fecal metagenomics. Nineteen (50%) tested positive for FC, OFB, or both and subsequently underwent retrograde ileoscopy. Fourteen patients (36.8%) presented Crohn-like lesions, occurring after a median of 11.5 years after surgery (range 8 months - 21.5 years). No statistically significant differences regarding demographic, phenotype and genotype were observed comparing patients with and without lesions, except for need for blood transfusion that was more frequent in those with lesions. Faecal microbiome of patients with lesions (not that of caregivers) was less biodiverse and characterized by a reduction of Bacteroidetes, and an overabundance of Proteobacteria. FC tested negative in 3/14 patients with lesions (21%).
    CONCLUSIONS: Our study demonstrated an impressive 10-folds higher incidence of chronic inflammation in TCSA. Up to 50% of patients may develop IBD-like lesions postoperatively. Nonetheless, we failed in identifying specific risk factors to be used to implement prevention strategies. Based on the results of our study, we suggest screening all TCSA patients with retrograde ileoscopy regardless of FC/OFB values. The frequency of endoscopic assessments and the role of FC/OFB screening in prompting endoscopy is yet to be determined.
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