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在新冠疫情后时期,侵袭性A组链球菌感染作为并存或既往病毒感染的后果

Invasive group A streptococcal infections as a consequence of coexisting or previous viral infection in the post-COVID-19 pandemic period.

作者信息

Mania Anna, Mazur-Melewska Katarzyna, Witczak Cezary, Cwalińska Agnieszka, Małecki Paweł, Meissner Adam, Słopień Agnieszka, Figlerowicz Magdalena

机构信息

Department of Infectious Diseases and Child Neurology, Institute of Paediatrics, Poznan University of Medical Sciences, Poland.

Department of Infectious Diseases and Child Neurology, Institute of Paediatrics, Poznan University of Medical Sciences, Poland.

出版信息

J Infect Public Health. 2025 Jan;18(1):102622. doi: 10.1016/j.jiph.2024.102622. Epub 2024 Dec 16.

Abstract

BACKGROUND

Group A Streptococci (GAS) may cause infections of the pharynx and soft tissues and invasive infections in children (iGAS). A significant increase in severe iGAS infections has been reported in Europe since the fall of 2022.

OBJECTIVES

This retrospective study aims to analyse clinical data of children with invasive and non-invasive GAS infections in the post-COVID-19 pandemic era, searching for predisposing factors to developing invasive infections.

METHODS

History and clinical data of patients hospitalised due to or with coexisting GAS infections were analysed. iGAS and non-iGAS infections were compared.

RESULTS

The cohort comprised 45 children (median age 7 years). 31(69 %) children developed iGAS infections - sepsis with toxic shock syndrome (TSS) (4 children-13 %), deep soft tissue infections (3-10 %), meningitis (2-6 %), pneumonia (2-6 %) or respiratory tract infections - sinusitis or otitis (4-12 %). iGAS children developed complications more frequently (100 % vs 21 %, p < 0.0001) and required prolonged treatment (median 15 vs 10 days, p = 0.0001). Preceding or coexisting viral infections were more common in iGAS children (87 % vs 14 %; p < 0.0001). CRP and PCT were significantly higher in the iGAS group (median 17.95 vs 3.97 mg/dl, p = 0.0002; 6.8 vs 0.05 ng/ml, p = 0.0001, respectively). The multiple logistic regression revealed that preceding or coexisting viral infections and the rise in CRP level increased the risk of iGAS infections. The CRP cut-off > 14.94 mg/dl showed 68.2 % sensitivity (CI 45.13-86.14 %) and 100 % specificity (69.15-100 %).

CONCLUSION

Our study shows increased incidence and severity of GAS infections among hospitalised children. Previous or coexisting viral infections and CRP with cut-off > 14.94 mg/dl were significant risk factors.

摘要

背景

A 组链球菌(GAS)可导致儿童咽部和软组织感染以及侵袭性感染(iGAS)。自 2022 年秋季以来,欧洲报告的严重 iGAS 感染显著增加。

目的

这项回顾性研究旨在分析新冠大流行后时代侵袭性和非侵袭性 GAS 感染儿童的临床数据,寻找发生侵袭性感染的易感因素。

方法

分析因 GAS 感染或并存 GAS 感染而住院患者的病史和临床数据。比较 iGAS 和非 iGAS 感染情况。

结果

该队列包括 45 名儿童(中位年龄 7 岁)。31 名(69%)儿童发生 iGAS 感染——伴有中毒性休克综合征(TSS)的败血症(4 名儿童 - 13%)、深部软组织感染(3 - 10%)、脑膜炎(2 - 6%)、肺炎(2 - 6%)或呼吸道感染——鼻窦炎或中耳炎(4 - 12%)。iGAS 感染儿童更频繁地出现并发症(100% 对 21%,p < 0.0001),并且需要更长时间的治疗(中位 15 天对 10 天,p = 0.0001)。先前或并存的病毒感染在 iGAS 感染儿童中更常见(87% 对 14%;p < 0.0001)。iGAS 组的 CRP 和 PCT 显著更高(中位分别为 17.95 对 3.97mg/dl,p = 0.0002;6.8 对 0.05ng/ml,p = 0.0001)。多因素逻辑回归显示,先前或并存的病毒感染以及 CRP 水平升高增加了 iGAS 感染的风险。CRP 临界值 > 14.94mg/dl 的敏感性为 68.2%(CI 45.13 - 86.14%),特异性为 100%(69.15 - 100%)。

结论

我们的研究表明住院儿童中 GAS 感染的发病率和严重程度增加。先前或并存的病毒感染以及临界值 > 14.94mg/dl 的 CRP 是重要的危险因素。

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