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Clinical, biochemical and microbiological factors associated with the prognosis of pneumococcal meningitis in children.
Jordan, Iolanda; Calzada, Yolanda; Monfort, Laura; Vila-Pérez, David; Felipe, Aida; Ortiz, Jessica; Cambra, Francisco José; Muñoz-Almagro, Carmen.
Afiliação
  • Jordan I; Pediatric Intensive Care Unit Service, Hospital de Sant Joan de Déu, Barcelona, Spain. Electronic address: ijordan@hsjdbcn.org.
  • Calzada Y; Pediatric Intensive Care Unit Service, Hospital de Sant Joan de Déu, Barcelona, Spain.
  • Monfort L; Pediatric Service, Hospital de Sant Joan de Déu, Barcelona, Spain.
  • Vila-Pérez D; Pediatric Intensive Care Unit Service, Hospital de Sant Joan de Déu, Barcelona, Spain.
  • Felipe A; Pediatric Intensive Care Unit Service, Hospital de Sant Joan de Déu, Barcelona, Spain.
  • Ortiz J; Pediatric Service, Hospital de Sant Joan de Déu, Barcelona, Spain.
  • Cambra FJ; Pediatric Intensive Care Unit Service, Hospital de Sant Joan de Déu, Barcelona, Spain.
  • Muñoz-Almagro C; Molecular Microbiology Department, Hospital Sant Joan de Déu, Universitat de Barcelona, Barcelona, Spain.
Enferm Infecc Microbiol Clin ; 34(2): 101-7, 2016 Feb.
Article em En | MEDLINE | ID: mdl-25998267
ABSTRACT

BACKGROUND:

Pneumococcal meningitis (PM) has a high morbidity and mortality. The aim of the study was to evaluate what factors are related to a poor PM prognosis.

METHODS:

Prospective observational study conducted on patients admitted to the Pediatric Intensive Care Unit in a tertiary hospital with a diagnosis of PM (January 2000 to December 2013). Clinical, biochemical and microbiological data were recorded. Variable outcome was classified into good or poor (neurological handicap or death). A multivariate logistic regression was performed based on the univariate analysis of significant data.

RESULTS:

A total of 88 patients were included. Clinical variables statistically significant for a poor outcome were younger age (p=.008), lengthy fever (p=.016), sepsis (p=.010), lower Glasgow Score (p<.001), higher score on Pediatric Risk Mortality Score (p=0.010) and Sequential Organ Failure Assessment (SOFA) (p<.001), longer mechanical ventilation (p=.004), and inotropic support (p=.008) requirements. Statistically significant biochemical variables were higher level of C-reactive protein (p<.001) and procalcitonin (p=.014) at admission, low cerebrospinal (CSF) pleocytosis (p=.003), higher level of protein in CSF (p=.031), and severe hypoglycorrhachia (p=.002). In multivariate analysis, independent indicators of poor outcome were age less than 2 years (p=.011), high score on SOFA (p=.030), low Glasgow Score (p=.042), and severe hypoglycorrhachia (p=.009).

CONCLUSIONS:

Patients younger than 2 years of age, with depressed consciousness at admission, especially when longer mechanical ventilation is required, are at high risk of a poor outcome.
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 3_ND Base de dados: MEDLINE Assunto principal: Meningite Pneumocócica Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Revista: Enferm Infecc Microbiol Clin Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 3_ND Base de dados: MEDLINE Assunto principal: Meningite Pneumocócica Tipo de estudo: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Revista: Enferm Infecc Microbiol Clin Ano de publicação: 2016 Tipo de documento: Article