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新冠病毒病(COVID-19)急性后期的儿科胃肠道结局

Pediatric Gastrointestinal Tract Outcomes During the Postacute Phase of COVID-19.

作者信息

Zhang Dazheng, Stein Ronen, Lu Yiwen, Zhou Ting, Lei Yuqing, Li Lu, Chen Jiajie, Arnold Jonathan, Becich Michael J, Chrischilles Elizabeth A, Chuang Cynthia H, Christakis Dimitri A, Fort Daniel, Geary Carol R, Hornig Mady, Kaushal Rainu, Liebovitz David M, Mosa Abu S M, Morizono Hiroki, Mirhaji Parsa, Dotson Jennifer L, Pulgarin Claudia, Sills Marion R, Suresh Srinivasan, Williams David A, Baldassano Robert N, Forrest Christopher B, Chen Yong

机构信息

The Center for Health AI and Synthesis of Evidence, University of Pennsylvania, Philadelphia.

Department of Biostatistics, Epidemiology and Informatics, Perelman School of Medicine at the University of Pennsylvania, Philadelphia.

出版信息

JAMA Netw Open. 2025 Feb 3;8(2):e2458366. doi: 10.1001/jamanetworkopen.2024.58366.


DOI:10.1001/jamanetworkopen.2024.58366
PMID:39918822
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11806396/
Abstract

IMPORTANCE: The profile of gastrointestinal (GI) tract outcomes associated with the postacute and chronic phases of COVID-19 in children and adolescents remains unclear. OBJECTIVE: To investigate the risks of GI tract symptoms and disorders during the postacute (28-179 days after documented SARS-CoV-2 infection) and the chronic (180-729 days after documented SARS-CoV-2 infection) phases of COVID-19 in the pediatric population. DESIGN, SETTING, AND PARTICIPANTS: This retrospective cohort study was performed from March 1, 2020, to September 1, 2023, at 29 US health care institutions. Participants included pediatric patients 18 years or younger with at least 6 months of follow-up. Data analysis was conducted from November 1, 2023, to February 29, 2024. EXPOSURES: Presence or absence of documented SARS-CoV-2 infection. Documented SARS-CoV-2 infection included positive results of polymerase chain reaction analysis, serological tests, or antigen tests for SARS-CoV-2 or diagnosis codes for COVID-19 and postacute sequelae of SARS-CoV-2. MAIN OUTCOMES AND MEASURES: GI tract symptoms and disorders were identified by diagnostic codes in the postacute and chronic phases following documented SARS-CoV-2 infection. The adjusted risk ratios (ARRs) and 95% CI were determined using a stratified Poisson regression model, with strata computed based on the propensity score. RESULTS: The cohort consisted of 1 576 933 pediatric patients (mean [SD] age, 7.3 [5.7] years; 820 315 [52.0%] male). Of these, 413 455 patients had documented SARS-CoV-2 infection and 1 163 478 did not; 157 800 (13.6%) of those without documented SARS-CoV-2 infection had a complex chronic condition per the Pediatric Medical Complexity Algorithm. Patients with a documented SARS-CoV-2 infection had an increased risk of developing at least 1 GI tract symptom or disorder in both the postacute (8.64% vs 6.85%; ARR, 1.25; 95% CI, 1.24-1.27) and chronic (12.60% vs 9.47%; ARR, 1.28; 95% CI, 1.26-1.30) phases compared with patients without a documented infection. Specifically, the risk of abdominal pain was higher in COVID-19-positive patients during the postacute (2.54% vs 2.06%; ARR, 1.14; 95% CI, 1.11-1.17) and chronic (4.57% vs 3.40%; ARR, 1.24; 95% CI, 1.22-1.27) phases. CONCLUSIONS AND RELEVANCE: In this cohort study, the increased risk of GI tract symptoms and disorders was associated with the documented SARS-CoV-2 infection in children or adolescents during the postacute or chronic phase. Clinicians should note that lingering GI tract symptoms may be more common in children after documented SARS-CoV-2 infection than in those without documented infection.

摘要

重要性:与儿童和青少年新冠病毒感染后急性期及慢性期相关的胃肠道(GI)道结局情况仍不明确。 目的:调查儿科人群在新冠病毒感染后急性期(记录的新冠病毒2感染后28 - 179天)和慢性期(记录的新冠病毒2感染后180 - 729天)出现胃肠道症状和疾病的风险。 设计、背景和参与者:这项回顾性队列研究于2020年3月1日至2023年9月1日在美国29家医疗机构进行。参与者包括18岁及以下且至少随访6个月的儿科患者。数据分析于2023年11月1日至2024年2月29日进行。 暴露因素:是否有记录的新冠病毒2感染。记录的新冠病毒2感染包括新冠病毒聚合酶链反应分析、血清学检测或抗原检测的阳性结果,或新冠病毒感染及新冠病毒2感染后急性期后遗症的诊断编码。 主要结局和测量指标:通过记录的新冠病毒2感染后急性期和慢性期的诊断编码确定胃肠道症状和疾病。使用分层泊松回归模型确定调整后的风险比(ARR)和95%置信区间(CI),分层基于倾向评分计算。 结果:该队列包括1576933名儿科患者(平均[标准差]年龄,7.3[5.7]岁;820315名[52.0%]为男性)。其中,413455名患者有记录的新冠病毒2感染,1163478名没有;根据儿科医疗复杂性算法,在没有记录的新冠病毒2感染的患者中,157800名(13.6%)患有复杂慢性病。与没有记录感染的患者相比,有记录的新冠病毒2感染的患者在急性期(8.64%对6.85%;ARR,1.25;95%CI,1.24 - 1.27)和慢性期(12.60%对9.47%;ARR,1.28;95%CI,1.26 - 1.30)出现至少1种胃肠道症状或疾病的风险增加。具体而言,新冠病毒感染阳性患者在急性期(2.54%对2.06%;ARR,1.14;95%CI,1.11 - 1.17)和慢性期(4.57%对3.40%;ARR,1.24;95%CI,1.22 - 1.27)出现腹痛的风险更高。 结论和意义:在这项队列研究中,胃肠道症状和疾病风险增加与儿童或青少年在新冠病毒感染后急性期或慢性期有记录的新冠病毒2感染有关。临床医生应注意,有记录的新冠病毒2感染后的儿童持续存在胃肠道症状可能比未感染的儿童更常见。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30ad/11806396/e8c6dc928bec/jamanetwopen-e2458366-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30ad/11806396/7b23973172fa/jamanetwopen-e2458366-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30ad/11806396/a9801d93c47b/jamanetwopen-e2458366-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30ad/11806396/e8c6dc928bec/jamanetwopen-e2458366-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30ad/11806396/7b23973172fa/jamanetwopen-e2458366-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30ad/11806396/a9801d93c47b/jamanetwopen-e2458366-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/30ad/11806396/e8c6dc928bec/jamanetwopen-e2458366-g003.jpg

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引用本文的文献

[1]
Risk of neuropsychiatric and related conditions associated with SARS-CoV-2 infection: a difference-in-differences analysis.

Nat Commun. 2025-7-24

[2]
COVID-19-associated multiple colonic perforations in a 6-month-old infant: a rare case report.

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[3]
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[4]
Reinfection with SARS-CoV-2 in the Omicron Era is Associated with Increased Risk of Post-Acute Sequelae of SARS-CoV-2 Infection: A RECOVER-EHR Cohort Study.

medRxiv. 2025-3-30

本文引用的文献

[1]
Impact of preexisting digestive problems on the gastrointestinal symptoms of patients with omicron variant of SARS-CoV-2 infection.

PLoS One. 2024

[2]
Body Mass Index and Postacute Sequelae of SARS-CoV-2 Infection in Children and Young Adults.

JAMA Netw Open. 2024-10-1

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Real-World Effectiveness of BNT162b2 Against Infection and Severe Diseases in Children and Adolescents.

Ann Intern Med. 2024-2

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Dig Dis Sci. 2024-2

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