Clinical phenotypes and household structure in pediatric invasive meningococcal disease: A retrospective cohort study.

IF 0.8 4区 医学 Q3 PEDIATRICS
Kubra Boydag Guvenc, Cansu Durak, Nihal Akcay, Ulkem Kocoglu Barlas, Guner Ozcelik, Hasan Serdar Kıhtır, Bahar Salihoğlu, Nevin Hatipoglu, Esra Sevketoğlu
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引用次数: 0

Abstract

Background: Invasive meningococcal disease is a rapidly progressive infection with heterogeneous clinical presentations. Phenotype-related severity differences in critically ill children remain incompletely defined. We evaluated the association between clinical phenotypes, early disease severity, and outcomes in a pediatric intensive care unit cohort.

Methods: This retrospective study included 42 children admitted to a tertiary pediatric intensive care unit with invasive meningococcal disease between 2006 and 2020. Patients were classified as meningococcal sepsis without meningitis or meningococcal meningitis. Disease severity was assessed using the Pediatric Risk of Mortality III score. Demographic, clinical, microbiological, and selected household characteristics were analyzed.

Results: Twenty-three patients (54.8%) had meningococcal sepsis without meningitis and 19 patients (45.2%) had meningococcal meningitis. The overall mortality was 21.4%. The sepsis phenotype was associated with higher Pediatric Risk of Mortality III scores (median 20 vs. 11, p=0.007), higher lactate, lower platelet counts, more organ support, and higher mortality (34.8% vs. 5.3%, p=0.023). Extended family living was more frequent in the meningitis group (26.3% vs. 4.3%, p=0.043). Serogroup data were available in 40.5% of cases, with serogroup B predominating.

Conclusions: In this pediatric intensive care unit cohort, meningococcal sepsis without meningitis was associated with greater early severity and higher mortality than meningococcal meningitis. Household-structure findings should be considered exploratory. Early phenotype-based risk assessment may support the management of critically ill children with invasive meningococcal disease.

儿童侵袭性脑膜炎球菌病的临床表型和家庭结构:一项回顾性队列研究
背景:侵袭性脑膜炎球菌病是一种具有异质性临床表现的快速进展性感染。危重儿童表型相关的严重程度差异仍未完全确定。我们评估了儿科重症监护病房队列中临床表型、早期疾病严重程度和结局之间的关系。方法:本回顾性研究纳入了2006年至2020年期间因侵袭性脑膜炎球菌病入住第三儿科重症监护病房的42名儿童。患者分为无脑膜炎的脑膜炎球菌败血症和脑膜炎球菌性脑膜炎。使用儿科死亡风险III评分评估疾病严重程度。分析了人口统计学、临床、微生物学和选定的家庭特征。结果:无脑膜炎的脑膜炎球菌败血症23例(54.8%),合并脑膜炎球菌性脑膜炎19例(45.2%)。总死亡率为21.4%。脓毒症表型与较高的儿科死亡风险III评分(中位数为20比11,p=0.007)、较高的乳酸水平、较低的血小板计数、更多的器官支持和较高的死亡率(34.8%比5.3%,p=0.023)相关。大家庭生活在脑膜炎组更常见(26.3%比4.3%,p=0.043)。40.5%的病例可获得血清组数据,以血清B组为主。结论:在这个儿科重症监护病房队列中,与脑膜炎球菌性脑膜炎相比,无脑膜炎的脑膜炎球菌性败血症具有更大的早期严重程度和更高的死亡率。家庭结构的调查结果应该被认为是探索性的。早期基于表型的风险评估可能支持侵袭性脑膜炎球菌病危重患儿的管理。
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来源期刊
Klinische Padiatrie
Klinische Padiatrie 医学-小儿科
CiteScore
1.10
自引率
0.00%
发文量
135
审稿时长
6-12 weeks
期刊介绍: Das Forum für wissenschaftliche Information in der Kinderheilkunde ausgewählte Originalarbeiten aus allen Bereichen der Pädiatrie Visite: Ihr Forum für interessante Krankengeschichten und außergewöhnliche Kasuistiken aktuelle Fortschritte in Diagnostik und Therapie jährliche Schwerpunkthefte: Ergebnisse der pädiatrischen Onkologie plus Medizin und Markt topaktuelle Informationen aus der Industrie
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