Alsina Laia, Basteiro Maria G, de Paz Hector D, Iñigo Melania, de Sevilla Mariona F, Triviño Miriam, Juan Manel, Muñoz-Almagro Carmen
Allergy and Clinical Immunology Department, Hospital Sant Joan de Déu, University of Barcelona, Barcelona, Spain; Functional Unit of Immunology, Hospital Sant Joan de Déu and Hospital Clinic. Barcelona, Spain.
Department of Pediatrics, Hospital Sant Joan de Déu, University of Barcelona, Barcelona, Spain.
PLoS One. 2015 Mar 4;10(3):e0118848. doi: 10.1371/journal.pone.0118848. eCollection 2015.
Clinical, immunological and microbiological characteristics of recurrent invasive pneumococcal disease (IPD) in children were evaluated, differentiating relapse from reinfection, in order to identify specific risk factors for both conditions.
All patients <18 years-old with recurrent IPD admitted to a tertiary-care pediatric center from January 2004 to December 2011 were evaluated. An episode of IPD was defined as the presence of clinical findings of infection together with isolation and/or pneumococcal DNA detection by Real-Time PCR in any sterile body fluid. Recurrent IPD was defined as 2 or more episodes in the same individual at least 1 month apart. Among recurrent IPD, we differentiated relapse (same pneumococcal isolate) from reinfection.
593 patients were diagnosed with IPD and 10 patients died. Among survivors, 23 episodes of recurrent IPD were identified in 10 patients (1.7%). Meningitis was the most frequent form of recurrent IPD (10 episodes/4 children) followed by recurrent empyema (8 episodes/4 children). Three patients with recurrent empyema caused by the same pneumococcal clone ST306 were considered relapses and showed high bacterial load in their first episode. In contrast, all other episodes of recurrent IPD were considered reinfections. Overall, the rate of relapse of IPD was 0.5% and the rate of reinfection 1.2%. Five out of 7 patients with reinfection had an underlying risk factor: cerebrospinal fluid leak (n = 3), chemotherapy treatment (n = 1) and a homozygous mutation in MyD88 gene (n = 1). No predisposing risk factors were found in the remainder.
recurrent IPD in children is a rare condition associated with an identifiable risk factor in case of reinfection in almost 80% of cases. In contrast, recurrent IPD with pleuropneumonia is usually a relapse of infection.
评估儿童复发性侵袭性肺炎球菌病(IPD)的临床、免疫和微生物学特征,区分复发与再感染,以确定这两种情况的特定危险因素。
对2004年1月至2011年12月入住三级儿科中心的所有18岁以下复发性IPD患者进行评估。IPD发作定义为在任何无菌体液中存在感染的临床发现以及通过实时PCR分离和/或检测肺炎球菌DNA。复发性IPD定义为同一个体至少间隔1个月发生2次或更多次发作。在复发性IPD中,我们区分了复发(相同肺炎球菌分离株)和再感染。
593例患者被诊断为IPD,10例死亡。在幸存者中,10例患者(1.7%)出现了23次复发性IPD发作。脑膜炎是复发性IPD最常见的形式(10次发作/4名儿童),其次是复发性脓胸(8次发作/4名儿童)。3例由相同肺炎球菌克隆ST306引起的复发性脓胸患者被认为是复发,且首次发作时细菌载量较高。相比之下,复发性IPD的所有其他发作均被认为是再感染。总体而言,IPD的复发率为0.5%,再感染率为1.2%。7例再感染患者中有5例有潜在危险因素:脑脊液漏(n = 3)、化疗(n = 1)和MyD88基因纯合突变(n = 1)。其余患者未发现易感危险因素。
儿童复发性IPD是一种罕见疾病,在近80%的再感染病例中与可识别的危险因素相关。相比之下,伴有胸膜肺炎的复发性IPD通常是感染复发。