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<dc:title>Superior accuracy of mid-regional proadrenomedullin for mortality prediction in sepsis with varying levels of illness severity</dc:title>
<dc:creator>Andaluz Ojeda, David</dc:creator>
<dc:creator>Nguyen, H. Bryant</dc:creator>
<dc:creator>Meunier-Beillard, Nicolas</dc:creator>
<dc:creator>Cicuéndez, Ramón</dc:creator>
<dc:creator>Quenot, Jean-Pierre</dc:creator>
<dc:creator>Calvo, Dolores</dc:creator>
<dc:creator>Dargent, Auguste</dc:creator>
<dc:creator>Zarca, Esther</dc:creator>
<dc:creator>Andrés Iglesias, Cristina</dc:creator>
<dc:creator>Nogales, Leonor</dc:creator>
<dc:creator>Eiros Bouza, José María</dc:creator>
<dc:creator>Tamayo Gómez, Eduardo</dc:creator>
<dc:creator>Gandía Martínez, Francisco</dc:creator>
<dc:creator>Bermejo Martín, Jesús Francisco</dc:creator>
<dc:creator>Charles, Pierre Emmanuel</dc:creator>
<dc:description>Producción Científica</dc:description>
<dc:description>Background: The use of novel sepsis biomarkers has increased in recent years. However, their prognostic value&#xd;
with respect to illness severity has not been explored. In this work, we examined the ability of mid-regional proadrenomedullin&#xd;
(MR-proADM) in predicting mortality in sepsis patients with different degrees of organ failure, compared&#xd;
to that of procalcitonin, C-reactive protein and lactate.&#xd;
Methods: This was a two-centre prospective observational cohort, enrolling severe sepsis or septic shock patients&#xd;
admitted to the ICU. Plasma biomarkers were measured during the first 12 h of admission. The association between&#xd;
biomarkers and 28-day mortality was assessed by Cox regression analysis and Kaplan–Meier curves. Patients were&#xd;
divided into three groups as evaluated by the Sequential Organ Failure Assessment (SOFA) score. The accuracy of the&#xd;
biomarkers for mortality was determined by area under the receiver operating characteristic curve (AUROC) analysis.&#xd;
Results: A total of 326 patients with severe sepsis (21.7%) or septic shock (79.3%) were enrolled with a 28-day mortality&#xd;
rate of 31.0%. Only MR-proADM and lactate were associated with mortality in the multivariate analysis: hazard&#xd;
ratio 8.5 versus 3.4 (p &lt; 0.001). MR-proADM showed the best AUROC for mortality prediction at 28 days in the analysis&#xd;
over the entire cohort (AUROC [95% CI] 0.79 [0.74–0.84]) (p &lt; 0.001). When patients were stratified by the degree of&#xd;
organ failure, MR-proADM was the only biomarker to predict mortality in all severity groups (SOFA ≤ 6, SOFA = 7–12,&#xd;
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 &lt; 0.05). All&#xd;
patients with MR-proADM concentrations ≤0.88 nmol/L survived up to 28 days. In patients with SOFA ≤ 6, the addition&#xd;
of MR-proADM to the SOFA score increased the ability of SOFA to identify non-survivors, AUROC [95% CI] 0.70&#xd;
[0.58–0.82] and 0.77 [0.66–0.88], respectively (p &lt; 0.05 for both).&#xd;
Conclusions: The performance of prognostic biomarkers in sepsis is highly influenced by disease severity. MRproADM&#xd;
accuracy to predict mortality is not affected by the degree of organ failure. Thus, it is a good candidate in the&#xd;
early identification of sepsis patients with moderate disease severity but at risk of mortality.</dc:description>
<dc:date>2021-01-12T10:43:48Z</dc:date>
<dc:date>2021-01-12T10:43:48Z</dc:date>
<dc:date>2017</dc:date>
<dc:type>info:eu-repo/semantics/article</dc:type>
<dc:identifier>Annals of Intensive Care, 2017, vol.7, n. 1</dc:identifier>
<dc:identifier>2110-5820</dc:identifier>
<dc:identifier>http://uvadoc.uva.es/handle/10324/44931</dc:identifier>
<dc:identifier>10.1186/s13613-017-0238-9</dc:identifier>
<dc:identifier>1</dc:identifier>
<dc:identifier>Annals of Intensive Care</dc:identifier>
<dc:identifier>7</dc:identifier>
<dc:identifier>2110-5820</dc:identifier>
<dc:language>eng</dc:language>
<dc:relation>https://annalsofintensivecare.springeropen.com/articles/10.1186/s13613-017-0238-9</dc:relation>
<dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
<dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
<dc:rights>© SpringerOpen</dc:rights>
<dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 Internacional</dc:rights>
<dc:publisher>SpringerOpen</dc:publisher>
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