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Challenges in Diagnosis of Congenital Toxoplasmosis on Postimplementation of Minas Gerais Screening Program. 米纳斯吉拉斯州筛查计划实施后先天性弓形虫病诊断的挑战。
IF 2.2 4区 医学 Q3 IMMUNOLOGY Pub Date : 2026-02-01 Epub Date: 2025-09-11 DOI: 10.1097/INF.0000000000004990
Ericka Viana Machado Carellos, Elisa Maria Silva Vieira, Daniel Vitor Vasconcelos-Santos, Danuza Oliveira Machado, Roberta Maia Castro Romanelli, Luciana Macedo Resende, Ana Lívia Libardi, Jose Nélio Januário, Gláucia Manzan Queiroz Andrade

Background: Congenital toxoplasmosis is both prevalent and severe in Brazil. The Minas Gerais Congenital Toxoplasmosis Control Program (PCTC-MG) used prenatal and neonatal screening to identify neonates at risk for congenital toxoplasmosis. This study aimed to evaluate the clinical and laboratory parameters used to diagnose the disease in this population.

Methods: This retrospective cohort study included children with suspected congenital toxoplasmosis who participated in the PCTC-MG between 2013 and 2020.

Results: A total of 347 children participated in the study; 228 had confirmed toxoplasmosis and 119 were excluded. The majority (314/347; 90.5%) underwent neonatal screening for IgM in filter paper (FP). Among these, 269/314 (85.7%) had positive or indeterminate results, with 186 (69.1%) confirmed infections, while 45/314 (14.3%) had nonreactive results, with 17 confirmed infections. There was an association between treatment during pregnancy (45/227; 19.8%) and a lower number of reagent IgM results in FP ( P = 0.002) and serum ( P = 0.001). A higher gestational age was associated with a higher proportion of IgM in the FP ( P = 0.001) and serum ( P = 0.004). Retinochoroiditis (73.2%; 167/228) and neurologic changes (36.9%; 75/203) were frequent in the infected children. The treatment decision was based on the presence of IgM/IgA (176/226; 77.9%), retinochoroiditis (45/226; 19.9%) or persistence/increase in IgG levels (4/226; 1.8%).

Conclusions: Screening with specific and sensitive serology identified most, but not all, children with congenital toxoplasmosis. Ophthalmologic evaluations and neuroimaging are mandatory in this context. The absence of IgM in the FP did not exclude the diagnosis.

背景:先天性弓形虫病在巴西既普遍又严重。米纳斯吉拉斯州先天性弓形虫病控制项目(PCTC-MG)使用产前和新生儿筛查来识别有先天性弓形虫病风险的新生儿。本研究旨在评估用于诊断该人群疾病的临床和实验室参数。方法:本回顾性队列研究纳入2013 - 2020年参与PCTC-MG的疑似先天性弓形虫病儿童。结果:共有347名儿童参与研究;确诊弓形虫病228例,排除119例。大多数(314/347,90.5%)接受了新生儿滤纸IgM筛查(FP)。其中,269/314例(85.7%)结果阳性或不确定,确诊感染186例(69.1%);45/314例(14.3%)结果无反应,确诊感染17例。妊娠期治疗与FP (P = 0.002)和血清(P = 0.001)中较低的试剂IgM结果之间存在相关性(45/227;19.8%)。胎龄越高,卵磷脂(P = 0.001)和血清中IgM的比例越高(P = 0.004)。视网膜脉络膜炎(73.2%,167/228)和神经系统改变(36.9%,75/203)在感染儿童中较为常见。治疗决定基于IgM/IgA(176/226; 77.9%)、视网膜脉络膜炎(45/226;19.9%)或IgG水平持续/升高(4/226;1.8%)的存在。结论:特异性和敏感的血清学筛查可识别大多数,但不是全部先天性弓形虫病患儿。在这种情况下,眼科评估和神经成像是强制性的。FP中IgM的缺失并不能排除诊断。
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引用次数: 0
Cryptococcal Granulomatous Inflammation in Immunocompetent Pediatric Patients Presenting as Hepatic Space-occupying Lesions. 免疫功能正常儿童的隐球菌性肉芽肿性炎症表现为肝脏占位性病变。
IF 2.2 4区 医学 Q3 IMMUNOLOGY Pub Date : 2026-02-01 Epub Date: 2025-09-17 DOI: 10.1097/INF.0000000000005007
Ke Cao, Xiaojuan Luo, Wenhong Ye, Defa Li, Xueyan Chen
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引用次数: 0
Black Hairy Tongue on Second Line Antituberculous Therapy: Don't Forget Linezolid Induced Lingua Villosa Nigra. 二线抗结核治疗的黑毛舌:不要忘记利奈唑胺诱导的黑舌。
IF 2.2 4区 医学 Q3 IMMUNOLOGY Pub Date : 2026-02-01 Epub Date: 2025-09-10 DOI: 10.1097/INF.0000000000004974
Suhani Jain, Reepa Agrawal, Ira Shah
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引用次数: 0
Papillon-Lefèvre Syndrome Unmasked by Atypical Cat Scratch Disease. 非典型猫抓病揭示的乳头状瘤-左侧病变综合征。
IF 2.2 4区 医学 Q3 IMMUNOLOGY Pub Date : 2026-02-01 Epub Date: 2025-09-17 DOI: 10.1097/INF.0000000000005002
Rohan Grotra, Ashwin Varadarajan, Rajni Yadav, Sanchita Gupta, Rohan Malik
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引用次数: 0
Fusobacterium on the Rise: A Decade of Otogenic and Beyond. 扶桑杆菌的崛起:十年的耳源性和超越。
IF 2.2 4区 医学 Q3 IMMUNOLOGY Pub Date : 2026-02-01 Epub Date: 2025-09-11 DOI: 10.1097/INF.0000000000004982
Sraya Kraus, Goni Peleg, Maayan Shachor, Yotam Dizitzer Hillel, Haim Ben Zvi, Ori Snapiri, David Levy, Efraim Bilavsky, Nimrod Sachs

Background: Fusobacterium has become increasingly recognized pediatric pathogen, responsible for a wide spectrum of infections, including otogenic, oropharyngeal, intra-abdominal and soft tissue infections. However, large-scale studies remain limited.

Objective: This study aimed to assess the incidence, clinical features, complications and outcomes of pediatric Fusobacterium infections.

Methods: Retrospective cohort study of children (0-18 years) diagnosed with Fusobacterium infections at a tertiary pediatric hospital between 2010 and 2023.

Results: A total of 195 cases were identified, with a 10-fold increase in incidence over 13 years. Linear regression demonstrated a significant annual rise in Fusobacterium isolations [β = 2.25, 95% confidence interval (CI): 1.99-2.60, P < 0.01], affecting both otologic (β = 0.65, 95% CI: 0.19-1.11, P < 0.01) and nonotologic sources (β = 1.58, 95% CI: 1.23-1.94, P < 0.001). Infections were primarily otogenic (50.2%), followed by skin and soft tissue, intra-abdominal and pharyngeal infections. Patients with otogenic infections were significantly younger (mean 2.6 vs. 10.3 years, P < 0.001). Hospitalization was required in 80.5%, and complications occurred in 37%. No mortality was observed.

Conclusions: Pediatric Fusobacterium infections are rising, with significant clinical complexity and complications. While often otogenic, these infections affect multiple body systems. Awareness of their evolving epidemiology is crucial for optimizing diagnosis and management.

背景:梭杆菌已成为越来越多的儿童病原体,负责广泛的感染,包括耳源性,口咽,腹腔内和软组织感染。然而,大规模的研究仍然有限。目的:探讨小儿梭杆菌感染的发生率、临床特点、并发症及转归。方法:回顾性队列研究2010 - 2023年在某三级儿科医院诊断为梭杆菌感染的儿童(0-18岁)。结果:共发现195例,13年来发病率增加了10倍。线性回归显示,梭杆菌分离菌的数量逐年显著上升[β = 2.25, 95%可信区间(CI): 1.99-2.60, P < 0.01],影响耳部(β = 0.65, 95% CI: 0.19-1.11, P < 0.01)和非耳部来源(β = 1.58, 95% CI: 1.23-1.94, P < 0.001)。感染以耳源性感染为主(50.2%),其次为皮肤和软组织感染、腹腔感染和咽部感染。耳源性感染患者明显更年轻(平均2.6岁vs 10.3岁,P < 0.001)。80.5%的患者需要住院治疗,37%的患者出现并发症。未观察到死亡。结论:儿童梭杆菌感染呈上升趋势,具有明显的临床复杂性和并发症。虽然通常是耳源性的,但这些感染会影响多个身体系统。了解其不断变化的流行病学对优化诊断和管理至关重要。
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引用次数: 0
Neonatal Enterovirus and Parechovirus Infections: National Enterovirus Surveillance System, United States, 2004-2023. 新生儿肠道病毒和Parechovirus感染:美国国家肠道病毒监测系统,2004-2023。
IF 2.2 4区 医学 Q3 IMMUNOLOGY Pub Date : 2026-02-01 Epub Date: 2025-09-17 DOI: 10.1097/INF.0000000000004983
Miranda J Delahoy, Randall English, Halle Getachew, Terry Fei Fan Ng, Sarah Kidd

Background: Enteroviruses (EVs)-including echoviruses (Es) and coxsackieviruses-and parechoviruses (PeVs) can cause severe illness among neonates. Recent data on which EV and PeV infections are most reported among US neonates are limited.

Methods: The National Enterovirus Surveillance System (NESS) is a US laboratory-based national surveillance system that collects reports of EV and PeV typing results from patients of all ages. We analyzed NESS data on EV and PeV infections from specimens collected during 2004-2023, including mortality data from 2014 to 2023.

Results: During 2004-2023, 11,065 EV and PeV infections were reported to NESS: 823/9393 (9%) of infections with reported age occurred among neonates. Among 690 neonatal infections with identified virus type, Coxsackievirus type B5 (CV-B5, n = 90; 13%), CV-B4 (70; 10%), CV-B3 (68; 10%), PeV-A3 (63; 9%) and E-11 (56; 8%) were reported most frequently overall, with the top virus types varying from year to year. During 2014-2023, 85/503 neonates with EV or PeV infections had reported outcome (17%), of whom 18/85 (21%) died.

Conclusions: This analysis utilized 2 decades of surveillance data to identify top EV and PeV virus types reported among US neonates. Mortality data emphasize that EV and PeV infections can be severe among neonates and result in death. The variety of enteroviruses observed highlights the need for strengthened surveillance and further research to improve the current understanding of neonatal enteroviral disease and inform future development of prevention and treatment strategies.

背景:肠病毒(ev)——包括埃可病毒(Es)和柯萨奇病毒——和parechovirus (pev)可引起新生儿严重疾病。最近关于美国新生儿中报告的EV和PeV感染最多的数据有限。方法:国家肠道病毒监测系统(NESS)是美国一个以实验室为基础的国家监测系统,收集来自所有年龄段患者的EV和PeV分型结果报告。我们分析了2004-2023年收集的标本中EV和PeV感染的NESS数据,包括2014 -2023年的死亡率数据。结果:2004-2023年,全国共报告EV和PeV感染11065例,其中823/9393(9%)为新生儿。在690例已确定病毒类型的新生儿感染中,柯萨奇病毒B5型(CV-B5, n = 90; 13%)、CV-B4型(70;10%)、CV-B3型(68;10%)、PeV-A3型(63;9%)和E-11型(56;8%)的报告频率最高,每年的最高病毒类型有所不同。2014-2023年期间,85/503例EV或PeV感染的新生儿报告了结果(17%),其中18/85(21%)死亡。结论:该分析利用了20年的监测数据来确定美国新生儿中报告的EV和PeV病毒的主要类型。死亡率数据强调,EV和PeV感染在新生儿中可能很严重并导致死亡。观察到的各种肠道病毒突出了加强监测和进一步研究的必要性,以提高目前对新生儿肠道病毒疾病的认识,并为未来预防和治疗策略的发展提供信息。
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引用次数: 0
First Reported Pediatric Case of Mycobacterium obuense Peritonitis Associated With Continuous Ambulatory Peritoneal Dialysis. 首次报道的儿童结核分枝杆菌腹膜炎与持续动态腹膜透析相关的病例。
IF 2.2 4区 医学 Q3 IMMUNOLOGY Pub Date : 2026-02-01 Epub Date: 2025-09-03 DOI: 10.1097/INF.0000000000004972
Yoshiaki Cho, Kotaro Araki, Nao Ogura, Iku Kaneko, Masatsugu Uehara, Tomoo Kise
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引用次数: 0
Severe Presentations and Outcomes in Hospitalized Pediatric Patients With Parvovirus B19 Infection During the 2024 Outbreak: A Multicenter Prospective Study in Italy. 2024年意大利爆发期间感染细小病毒B19的住院儿科患者的严重表现和结局:一项多中心前瞻性研究
IF 2.2 4区 医学 Q3 IMMUNOLOGY Pub Date : 2026-02-01 Epub Date: 2025-10-15 DOI: 10.1097/INF.0000000000005014
Elisabetta Venturini, Agnese Maria Tamborino, Giusy Arrichiello, Federica Attaianese, Francesca Ippolita Calò Carducci, Claudio Cafagno, Désirée Caselli, Maia De Luca, Valeria Garbo, Vania Giacomet, Cecilia Liberati, Laura Lancella, Amelia Licari, Marco Maglione, Fabio Midulla, Cristina Moracas, Maria Moriondo, Marco Poeta, Claudia Rossini, Alfredo Guarino, Luisa Galli

Background: Since March 2024, the European Center for Disease Prevention and Control has reported increased Parvovirus B19 (B19V) infections across 14 European countries. While often self-limiting in healthy children, B19V may cause severe disease in vulnerable populations.

Methods: This multicenter prospective study aimed to characterize the clinical presentation of B19V infection in hospitalized children and identify risk factors for severe outcomes. Data were collected through the INF-ACT pediatric surveillance system, as part of the National Recovery and Resilience Plan. Children hospitalized with confirmed B19V infection were enrolled from January to December 2024 in 10 Italian INF-ACT centers.

Results: A total of 135 children were included (median age 7.6 years, interquartile range 4.4-9.9), with 78.5% of cases occurring between April and July 2024. Acute myocarditis (20.7%) and neurologic complications (17.8%) were the most frequent severe manifestations. Myocarditis was significantly associated with younger age ( P < 0.001), longer hospital stays (median 19.5 vs. 6.5 days; P = 0.0018) and higher intensive care unit (ICU) admission rates (71.4% vs. 20.8%; P < 0.001). Multivariate analysis showed myocardial involvement increased the risk of ICU admission over 20-fold ( P < 0.001).

Conclusions: Although often mild, B19V infection can cause severe complications in children, particularly myocarditis and neurologic involvement. Prompt recognition is essential, even in the absence of classic features like erythema infectiosum, to ensure timely monitoring and management of potentially life-threatening outcomes.

背景:自2024年3月以来,欧洲疾病预防控制中心报告了14个欧洲国家细小病毒B19 (B19V)感染的增加。虽然B19V病毒在健康儿童中往往具有自限性,但它可能在脆弱人群中引起严重疾病。方法:本多中心前瞻性研究旨在描述住院儿童B19V感染的临床表现,并确定严重后果的危险因素。作为国家恢复和复原力计划的一部分,通过INF-ACT儿科监测系统收集数据。2024年1月至12月,在意大利10个INF-ACT中心招募了确诊感染B19V的住院儿童。结果:共纳入135例患儿(中位年龄7.6岁,四分位数范围4.4 ~ 9.9),78.5%的病例发生在2024年4月~ 7月。急性心肌炎(20.7%)和神经系统并发症(17.8%)是最常见的严重表现。心肌炎与年龄较小(P < 0.001)、住院时间较长(中位19.5天对6.5天,P = 0.0018)和重症监护病房(ICU)住院率较高(71.4%对20.8%,P < 0.001)显著相关。多因素分析显示心肌受累使ICU住院风险增加20倍以上(P < 0.001)。结论:虽然B19V感染通常是轻微的,但在儿童中可引起严重的并发症,特别是心肌炎和神经系统受累。即使在没有传染性红斑等典型特征的情况下,及时识别也是至关重要的,以确保及时监测和管理可能危及生命的后果。
{"title":"Severe Presentations and Outcomes in Hospitalized Pediatric Patients With Parvovirus B19 Infection During the 2024 Outbreak: A Multicenter Prospective Study in Italy.","authors":"Elisabetta Venturini, Agnese Maria Tamborino, Giusy Arrichiello, Federica Attaianese, Francesca Ippolita Calò Carducci, Claudio Cafagno, Désirée Caselli, Maia De Luca, Valeria Garbo, Vania Giacomet, Cecilia Liberati, Laura Lancella, Amelia Licari, Marco Maglione, Fabio Midulla, Cristina Moracas, Maria Moriondo, Marco Poeta, Claudia Rossini, Alfredo Guarino, Luisa Galli","doi":"10.1097/INF.0000000000005014","DOIUrl":"10.1097/INF.0000000000005014","url":null,"abstract":"<p><strong>Background: </strong>Since March 2024, the European Center for Disease Prevention and Control has reported increased Parvovirus B19 (B19V) infections across 14 European countries. While often self-limiting in healthy children, B19V may cause severe disease in vulnerable populations.</p><p><strong>Methods: </strong>This multicenter prospective study aimed to characterize the clinical presentation of B19V infection in hospitalized children and identify risk factors for severe outcomes. Data were collected through the INF-ACT pediatric surveillance system, as part of the National Recovery and Resilience Plan. Children hospitalized with confirmed B19V infection were enrolled from January to December 2024 in 10 Italian INF-ACT centers.</p><p><strong>Results: </strong>A total of 135 children were included (median age 7.6 years, interquartile range 4.4-9.9), with 78.5% of cases occurring between April and July 2024. Acute myocarditis (20.7%) and neurologic complications (17.8%) were the most frequent severe manifestations. Myocarditis was significantly associated with younger age ( P < 0.001), longer hospital stays (median 19.5 vs. 6.5 days; P = 0.0018) and higher intensive care unit (ICU) admission rates (71.4% vs. 20.8%; P < 0.001). Multivariate analysis showed myocardial involvement increased the risk of ICU admission over 20-fold ( P < 0.001).</p><p><strong>Conclusions: </strong>Although often mild, B19V infection can cause severe complications in children, particularly myocarditis and neurologic involvement. Prompt recognition is essential, even in the absence of classic features like erythema infectiosum, to ensure timely monitoring and management of potentially life-threatening outcomes.</p>","PeriodicalId":19858,"journal":{"name":"Pediatric Infectious Disease Journal","volume":" ","pages":"e37-e42"},"PeriodicalIF":2.2,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145293376","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Epidemiology and Clinical Impact of Mycoplasma pneumoniae in an Italian Pediatric Center: An Observational Study from 2017 to 2024. 意大利儿科中心肺炎支原体的流行病学和临床影响:2017年至2024年的观察性研究
IF 2.2 4区 医学 Q3 IMMUNOLOGY Pub Date : 2026-02-01 Epub Date: 2025-09-17 DOI: 10.1097/INF.0000000000004993
Marco Bianchi, Mara Pisani, Lara Ricotta, Carmen D'Amore, Anna Chiara Vittucci, Sebastian Cristaldi, Anna Maria Musolino, Paola Bernaschi, Velia Chiara Di Maio, Venere Cortazzo, Claudio Cherchi, Renato Cutrera, Federica Pellizzoni, Alessia Arduini, Maria Antonietta Barbieri, Andrea Campana, Martina Di Giuseppe, Umberto Raucci, Laura Lancella, Marta Luisa Ciofi Degli Atti, Carlo Federico Perno, Alberto Villani

Background: Mycoplasma pneumoniae (MP) is a common cause of lower respiratory tract infections in children. During the COVID-19 pandemic, a marked decline in MP infections was observed, with a delayed resurgence reported in some European countries. This study aimed to assess the epidemiologic trends and clinical features of MP infections in a pediatric tertiary care academic hospital in Italy from 2017 to 2024.

Methods: We conducted a retrospective, single-center study including immunocompetent patients 30 days to 17 years of age, hospitalized with confirmed MP infection. Clinical, laboratory, and radiologic data were analyzed across 3 periods: prepandemic (2017-2019), pandemic (2020-2022) and postpandemic (2023-2024). Statistical analyses were performed to compare incidence and clinical characteristics over time.

Results: Of 303 included patients, 130 were hospitalized prepandemic and 148 postpandemics. The proportion of MP among acute respiratory infection hospitalizations nearly doubled, from 3.2% in 2019 to 6.1% in 2024. Despite the higher incidence, the need for respiratory support remained stable (25.7% overall; P = 0.3), the pediatric intensive care admissions were rare and unchanged (2.0% vs. 2.0%, P = 1.0) and median hospital stay was consistent across both periods (5 days, interquartile range 4-8; P = 0.803).

Conclusions: MP incidence increased significantly postpandemic, and clinical severity remained comparable to prepandemic levels. Ongoing epidemiologic surveillance is essential to better understand infection dynamics and to guide effective clinical management strategies.

背景:肺炎支原体(Mycoplasma pneumoniae, MP)是儿童下呼吸道感染的常见病因。在2019冠状病毒病大流行期间,观察到脊髓炎感染显著下降,但在一些欧洲国家报告出现了延迟复发。本研究旨在评估意大利某儿科三级专科医院2017 - 2024年MP感染的流行病学趋势和临床特征。方法:我们进行了一项回顾性的单中心研究,纳入了30天至17岁的免疫功能正常的住院确诊MP感染患者。临床、实验室和放射学数据分3个时期进行分析:大流行前(2017-2019)、大流行前(2020-2022)和大流行后(2023-2024)。进行统计分析,比较发病率和临床特征随时间的变化。结果:纳入的303例患者中,大流行前住院130例,大流行后住院148例。急性呼吸道感染住院患者中MP的比例几乎翻了一番,从2019年的3.2%增至2024年的6.1%。尽管发病率较高,但对呼吸支持的需求保持稳定(总体为25.7%,P = 0.3),儿科重症监护入院率很少且未发生变化(2.0%对2.0%,P = 1.0),两个时期的住院时间中位数一致(5天,四分位数间距为4-8,P = 0.803)。结论:MP发病率在大流行后显著增加,临床严重程度保持与大流行前水平相当。持续的流行病学监测对于更好地了解感染动态和指导有效的临床管理策略至关重要。
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引用次数: 0
Epidemiology and Risk Factors of Pediatric Clostridioides difficile Infection: A Nationwide Claims-based Comparison With Adults in Japan. 儿童艰难梭菌感染的流行病学和危险因素:日本全国范围内与成人的比较
IF 2.2 4区 医学 Q3 IMMUNOLOGY Pub Date : 2026-02-01 Epub Date: 2025-09-12 DOI: 10.1097/INF.0000000000004992
Daisuke Yamasaki, Yoshiki Kusama, Shiho Ito, Masaki Tanabe

Background: Pediatric Clostridioides difficile infection (CDI) is a growing concern, yet nationwide data from Japan are scarce. Current guidelines often discourage CDI testing in infants due to a presumed low incidence of clinical disease. We aimed to characterize the epidemiology and risk factors of pediatric CDI in Japan, focusing on age-specific patterns and community-onset cases.

Methods: We performed a retrospective analysis using the Japan Medical Data Center claims database from 2013 to 2022. CDI cases were defined by the presence of both diagnostic testing and anti-CDI treatment within 7 days. Episodes that relapsed within 8 weeks were excluded. CDI onset setting was classified according to CDC/NHSN criteria. Risk factors were evaluated by age and onset setting.

Results: Of the 4090 CDI cases, 284 were pediatric. The incidence in children 0-2 years old was comparable to that in older children, challenging current assumptions. Risk factor profiles varied by age group and setting, with inflammatory bowel disease being a prominent risk factor in children (28.9% vs. 14.8% in adults/older adults), particularly in adolescents (43.5%). Critically, nearly half of community-onset pediatric CDI cases had no prior antibiotic exposure.

Conclusion: This first large-scale study of pediatric CDI in Japan revealed that CDI can occur in children without prior antibiotic exposure, particularly in community settings. These findings support consideration of revisions to management strategies for pediatric CDI.

背景:儿童艰难梭菌感染(CDI)日益受到关注,但来自日本的全国数据很少。目前的指导方针通常不鼓励在婴儿中进行CDI检测,因为假定临床疾病的发病率较低。我们的目的是描述日本儿童CDI的流行病学和危险因素,重点关注特定年龄模式和社区发病病例。方法:我们使用日本医疗数据中心2013年至2022年索赔数据库进行回顾性分析。CDI病例的定义是在7天内进行诊断检测和抗CDI治疗。排除8周内复发的发作。根据CDC/NHSN标准对CDI发病环境进行分类。危险因素按年龄和发病环境进行评估。结果:4090例CDI病例中,284例为儿童。0-2岁儿童的发病率与年龄较大的儿童相当,挑战了目前的假设。危险因素概况因年龄组和环境而异,炎症性肠病是儿童的主要危险因素(28.9% vs.成人/老年人14.8%),特别是青少年(43.5%)。至关重要的是,近一半的社区发病儿童CDI病例之前没有抗生素暴露。结论:日本首次对儿童CDI进行的大规模研究表明,CDI可以发生在没有抗生素暴露的儿童中,特别是在社区环境中。这些发现支持修订儿科CDI管理策略的考虑。
{"title":"Epidemiology and Risk Factors of Pediatric Clostridioides difficile Infection: A Nationwide Claims-based Comparison With Adults in Japan.","authors":"Daisuke Yamasaki, Yoshiki Kusama, Shiho Ito, Masaki Tanabe","doi":"10.1097/INF.0000000000004992","DOIUrl":"10.1097/INF.0000000000004992","url":null,"abstract":"<p><strong>Background: </strong>Pediatric Clostridioides difficile infection (CDI) is a growing concern, yet nationwide data from Japan are scarce. Current guidelines often discourage CDI testing in infants due to a presumed low incidence of clinical disease. We aimed to characterize the epidemiology and risk factors of pediatric CDI in Japan, focusing on age-specific patterns and community-onset cases.</p><p><strong>Methods: </strong>We performed a retrospective analysis using the Japan Medical Data Center claims database from 2013 to 2022. CDI cases were defined by the presence of both diagnostic testing and anti-CDI treatment within 7 days. Episodes that relapsed within 8 weeks were excluded. CDI onset setting was classified according to CDC/NHSN criteria. Risk factors were evaluated by age and onset setting.</p><p><strong>Results: </strong>Of the 4090 CDI cases, 284 were pediatric. The incidence in children 0-2 years old was comparable to that in older children, challenging current assumptions. Risk factor profiles varied by age group and setting, with inflammatory bowel disease being a prominent risk factor in children (28.9% vs. 14.8% in adults/older adults), particularly in adolescents (43.5%). Critically, nearly half of community-onset pediatric CDI cases had no prior antibiotic exposure.</p><p><strong>Conclusion: </strong>This first large-scale study of pediatric CDI in Japan revealed that CDI can occur in children without prior antibiotic exposure, particularly in community settings. These findings support consideration of revisions to management strategies for pediatric CDI.</p>","PeriodicalId":19858,"journal":{"name":"Pediatric Infectious Disease Journal","volume":" ","pages":"126-131"},"PeriodicalIF":2.2,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12772002/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145086741","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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Pediatric Infectious Disease Journal
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