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    Por favor, use este identificador para citar o enlazar este ítem:http://uvadoc.uva.es/handle/10324/44931

    Título
    Superior accuracy of mid-regional proadrenomedullin for mortality prediction in sepsis with varying levels of illness severity
    Autor
    Andaluz Ojeda, DavidAutoridad UVA
    Nguyen, H. Bryant
    Meunier-Beillard, Nicolas
    Cicuéndez, Ramón
    Quenot, Jean-Pierre
    Calvo, Dolores
    Dargent, Auguste
    Zarca, Esther
    Andrés Iglesias, CristinaAutoridad UVA Orcid
    Nogales, Leonor
    Eiros Bouza, José MaríaAutoridad UVA Orcid
    Tamayo Gómez, EduardoAutoridad UVA
    Gandía Martínez, Francisco
    Bermejo Martín, Jesús FranciscoAutoridad UVA Orcid
    Charles, Pierre Emmanuel
    Año del Documento
    2017
    Editorial
    SpringerOpen
    Descripción
    Producción Científica
    Documento Fuente
    Annals of Intensive Care, 2017, vol.7, n. 1
    Resumen
    Background: The use of novel sepsis biomarkers has increased in recent years. However, their prognostic value with respect to illness severity has not been explored. In this work, we examined the ability of mid-regional proadrenomedullin (MR-proADM) in predicting mortality in sepsis patients with different degrees of organ failure, compared to that of procalcitonin, C-reactive protein and lactate. Methods: This was a two-centre prospective observational cohort, enrolling severe sepsis or septic shock patients admitted to the ICU. Plasma biomarkers were measured during the first 12 h of admission. The association between biomarkers and 28-day mortality was assessed by Cox regression analysis and Kaplan–Meier curves. Patients were divided into three groups as evaluated by the Sequential Organ Failure Assessment (SOFA) score. The accuracy of the biomarkers for mortality was determined by area under the receiver operating characteristic curve (AUROC) analysis. Results: A total of 326 patients with severe sepsis (21.7%) or septic shock (79.3%) were enrolled with a 28-day mortality rate of 31.0%. Only MR-proADM and lactate were associated with mortality in the multivariate analysis: hazard ratio 8.5 versus 3.4 (p < 0.001). MR-proADM showed the best AUROC for mortality prediction at 28 days in the analysis over the entire cohort (AUROC [95% CI] 0.79 [0.74–0.84]) (p < 0.001). When patients were stratified by the degree of organ failure, MR-proADM was the only biomarker to predict mortality in all severity groups (SOFA ≤ 6, SOFA = 7–12, and SOFA ≥ 13), AUROC [95% CI] of 0.75 [0.61–0.88], 0.74 [0.66–0.83] and 0.73 [0.59–0.86], respectively (p < 0.05). All patients with MR-proADM concentrations ≤0.88 nmol/L survived up to 28 days. In patients with SOFA ≤ 6, the addition of MR-proADM to the SOFA score increased the ability of SOFA to identify non-survivors, AUROC [95% CI] 0.70 [0.58–0.82] and 0.77 [0.66–0.88], respectively (p < 0.05 for both). Conclusions: The performance of prognostic biomarkers in sepsis is highly influenced by disease severity. MRproADM accuracy to predict mortality is not affected by the degree of organ failure. Thus, it is a good candidate in the early identification of sepsis patients with moderate disease severity but at risk of mortality.
    Materias Unesco
    32 Ciencias Médicas
    Palabras Clave
    Biomarcadores
    Sepsis
    ISSN
    2110-5820
    Revisión por pares
    SI
    DOI
    10.1186/s13613-017-0238-9
    Version del Editor
    https://annalsofintensivecare.springeropen.com/articles/10.1186/s13613-017-0238-9
    Propietario de los Derechos
    © SpringerOpen
    Idioma
    eng
    URI
    http://uvadoc.uva.es/handle/10324/44931
    Tipo de versión
    info:eu-repo/semantics/publishedVersion
    Derechos
    openAccess
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    • GIV - Artículos de Revista [46]
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