van Kempen Evelien B, Tulling Adam J, von Asmuth Erik G J, van der Aa Leontien B, Bijker Else M, Bijlsma Merijn, Borensztajn Dorine M, Brackel Caroline L H, de Gier Brechje, van Houten Marlies A, Jacobs Monique A M, Koenraads Marianne, Kooter Anjali I G, Lebon Ankie, van der Linden Jan W M, van Onzenoort-Bokken Lonneke, Oostenbrink Rianne, van Prehn Joffrey, van Sorge Nina M, Stol Kim, Tramper-Stranders Gerdien A, Verhage Aline R, van de Weijer Kirsten N G, Wildenbeest Joanne G, Boeddha Navin P, van Veen Mirjam, Buddingh Emilie P
Department of Pediatrics, Juliana Children's Hospital, Haga Hospital, the Hague, the Netherlands.
Department of Pediatrics, Erasmus Medical Center Sophia, Rotterdam, the Netherlands.
JAMA Netw Open. 2025 Aug 1;8(8):e2527717. doi: 10.1001/jamanetworkopen.2025.27717.
An increase in pediatric cases of invasive group A streptococcus (iGAS) disease was noted in the Netherlands starting in early 2022. GAS disease can range from mild to life-threatening invasive infections. Clinical and public health decisions rely on timely and detailed reporting of clinical data.
To determine risk factors associated with severe pediatric iGAS, defined as requiring admission to an intensive care unit and/or death, and to analyze pediatric iGAS incidence, presentations, and outcome between pre-COVID-19 pandemic (January 2015 to March 2020), COVID-19 pandemic (April 2020 to December 2021), and post-COVID-19 pandemic (January 2022 to June 2024) periods.
DESIGN, SETTING, AND PARTICIPANTS: This observational, retrospective and prospective cohort study in 20 hospitals (tertiary and nontertiary) in the Netherlands was conducted from January 2015 to June 2024, with real-time reporting of data on the study website since January 2022. Children aged 0 to 17 years with iGAS (positive culture or polymerase chain reaction test and/or clinical presentation) were included.
iGAS infection.
The primary outcome was risk factors for severe iGAS; secondary outcomes included iGAS incidence rate and clinical phenotypes prior, during, and after the COVID-19 pandemic. Risk factors for severity and mortality were analyzed using univariable and multivariable logistic regression analyses, and incidence rate ratios (IRRs) between pre-COVID-19 and postCOVID-19 pandemic periods were calculated using Poisson regression.
Of 617 children included, 351 (56.9%) were aged 0 to 4 years. For the 192 participants with detailed data collection, median (IQR) age was 4.2 (1.7-7.1) years and 91 (47.4%) were male. iGAS cases decreased during the COVID-19 pandemic and increased significantly in the post-COVID-19 period (IRR, 2.93; 95%, 2.46-3.49), as compared with the pre-COVID-19 pandemic period. By late 2023, the incidence of iGAS returned to pre-COVID-19 pandemic levels. Factors associated with increased risk of severe disease included a post-COVID-19 pandemic diagnosis (odds ratio [OR], 3.49; 95% CI, 2.31-6.26), pulmonary involvement (OR, 8.64; 95% CI, 5.50-13.55), streptococcal toxic shock syndrome (STSS; OR, 11.71; 95% CI, 4.39-31.18), and meningitis or encephalitis (OR, 4.38; 95% CI, 4.39-31.18). Clinical factors associated with increased risk of severe disease were reduced consciousness (OR, 7.61; 95% CI, 1.84-34.41), dyspnea (OR, 9.89; 95% CI, 3.04-32.14), abnormal auscultation (OR, 6.32; 95% CI, 2.18-18.32), and elevated C-reactive protein (OR, 6.32; 95% CI, 2.18-18.32), while estimated glomerular filtration rate was associated with a decreased risk (OR, 0.64; 95% CI, 0.49-0.84). Disease severity increased in post-COVID-19-pandemic cases, with higher mortality (13 of 294 cases [4.4%] vs 3 of 218 cases [1.4%]) and intensive care admission rates (113 of 294 cases [38.4%] vs 34 of 218 cases [15.6%]), as compared with pre-COVID-19 pandemic cases. Severity of pulmonary iGAS was similar in both periods. In the post-COVID-19 pandemic period, there was a significant increase in the incidence of pulmonary infections (IRR, 5.04; 95% CI, 3.27-7.97) , STSS (IRR, 10.30; 95% CI, 3.88-35.60), meningitis or encephalitis (IRR, 12.30; 95% CI, 4.14-52.70), and necrotizing fasciitis (IRR, 26.10; 95% CI, 5.14-475.00).
In this cohort study, risk factors for a complicated course of iGAS in children included pulmonary or central nervous system involvement, STSS, reduced consciousness or pulmonary clinical signs, elevated CRP, and decreased eGFR. Awareness of these risk factors is important to improve timely recognition of at-risk cases and improve clinical outcomes.
自2022年初起,荷兰侵袭性A组链球菌(iGAS)疾病的儿科病例有所增加。GAS疾病范围从轻度到危及生命的侵袭性感染。临床和公共卫生决策依赖于临床数据的及时和详细报告。
确定与严重儿科iGAS相关的危险因素,严重儿科iGAS定义为需要入住重症监护病房和/或死亡,并分析2019年新冠疫情大流行前(2015年1月至2020年3月)、新冠疫情大流行期间(2020年4月至2021年12月)和新冠疫情大流行后(2022年1月至2024年6月)期间儿科iGAS的发病率、临床表现和结局。
设计、设置和参与者:这项在荷兰20家医院(三级和非三级医院)开展的观察性、回顾性和前瞻性队列研究于2015年1月至2024年6月进行,自2022年1月起在研究网站上实时报告数据。纳入0至17岁患有iGAS的儿童(培养阳性或聚合酶链反应检测阳性和/或有临床表现)。
iGAS感染。
主要结局是严重iGAS的危险因素;次要结局包括新冠疫情大流行前、期间和之后的iGAS发病率及临床表型。使用单变量和多变量逻辑回归分析来分析严重程度和死亡率的危险因素,并使用泊松回归计算新冠疫情大流行前和后期间的发病率比(IRR)。
纳入的617名儿童中,351名(56.9%)年龄在0至4岁。对于192名进行详细数据收集的参与者,中位(IQR)年龄为4.2(1.7 - 7.1)岁,91名(47.4%)为男性。与新冠疫情大流行前相比,iGAS病例在新冠疫情大流行期间减少,在新冠疫情大流行后显著增加(IRR,2.93;95%,2.46 - 3.49)。到20