Recurrent invasive pneumococcal disease in children: Underlying clinical conditions, and immunological and microbiological characteristics.

dc.contributor.authorAlsina Manrique de Lara, Laia
dc.contributor.authorBasteiro, Maria G.
dc.contributor.authorPaz, Hector D.de
dc.contributor.authorIñigo, Melania
dc.contributor.authorFernández de Sevilla Estrach, Mariona
dc.contributor.authorTriviño, Miriam
dc.contributor.authorJuan, Manel
dc.contributor.authorMuñoz-Almagro, Carmen
dc.date.accessioned2017-03-23T18:39:13Z
dc.date.available2017-03-23T18:39:13Z
dc.date.issued2015-03-04
dc.date.updated2017-03-23T18:39:13Z
dc.description.abstractPurpose Clinical, immunological and microbiological characteristics of recurrent invasive pneumo-coccal disease (IPD) in children were evaluated, differentiating relapse from reinfection, in order to identify specific risk factors for both conditions. Methods 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. Results 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 rein- fection 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. Conclusions 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.
dc.format.extent13 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec669509
dc.identifier.issn1932-6203
dc.identifier.pmid25738983
dc.identifier.urihttps://hdl.handle.net/2445/108858
dc.language.isoeng
dc.publisherPublic Library of Science (PLoS)
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.1371/journal.pone.0118848
dc.relation.ispartofPLoS One, 2015, vol. 10, num. 3, p. e0118848
dc.relation.urihttps://doi.org/10.1371/journal.pone.0118848
dc.rightscc-by (c) Alsina, Laia et al., 2015
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es
dc.sourceArticles publicats en revistes (Cirurgia i Especialitats Medicoquirúrgiques)
dc.subject.classificationInfeccions per pneumococs
dc.subject.classificationPneumococs
dc.subject.classificationPediatria
dc.subject.classificationInfants
dc.subject.classificationImmunologia
dc.subject.classificationPneumònia
dc.subject.otherPneumococcal Infections
dc.subject.otherStreptococcus pneumonia
dc.subject.otherPediatrics
dc.subject.otherChildren
dc.subject.otherImmunology
dc.subject.otherPneumonia
dc.titleRecurrent invasive pneumococcal disease in children: Underlying clinical conditions, and immunological and microbiological characteristics.
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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