8 research outputs found

    Usefulness of midregional proadrenomedullin to predict poor outcome in patients with community acquired pneumonia.

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    midregional proadrenomedullin (MR-proADM) is a prognostic biomarker in patients with community-acquired pneumonia (CAP). We sought to confirm whether MR-proADM added to Pneumonia Severity Index (PSI) improves the potential prognostic value of PSI alone, and tested to what extent this combination could be useful in predicting poor outcome of patients with CAP in an Emergency Department (ED).Consecutive patients diagnosed with CAP were enrolled in this prospective, single-centre, observational study. We analyzed the ability of MR-proADM added to PSI to predict poor outcome using receiver operating characteristic (ROC) curves, logistic regression and risk reclassification and comparing it with the ability of PSI alone. The primary outcome was "poor outcome", defined as the incidence of an adverse event (ICU admission, hospital readmission, or mortality at 30 days after CAP diagnosis).226 patients were included; 33 patients (14.6%) reached primary outcome. To predict primary outcome the highest area under curve (AUC) was found for PSI (0.74 [0.64-0.85]), which was not significantly higher than for MR-proADM (AUC 0.72 [0.63-0.81, p > 0.05]). The combination of PSI and MR-proADM failed to improve the predictive potential of PSI alone (AUC 0.75 [0.65-0.85, p=0.56]). Ten patients were appropriately reclassified when the combined PSI and MR-proADM model was used as compared with the model of PSI alone. Net reclassification improvement (NRI) index was statistically significant (7.69%, p = 0.03) with an improvement percentage of 3.03% (p = 0.32) for adverse event, and 4.66% (P = 0.02) for no adverse event.MR-proADM in combination with PSI may be helpful in individual risk stratification for short-term poor outcome of CAP patients, allowing a better reclassification of patients compared with PSI alone

    MR-proADM and CAP severity.

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    <p>Fig 2a. Relationship between MR-proADM and severity as established by the PSI. Analysis performed with the Jonckheere-Terpstra trend test. Tau b: Kendall’s rank correlation. p: level of statistical significance. Fig 2b. MR-proADM levels according to hospital admission, bacteremia, ICU admission, hospital readmission and 30-day mortality.</p

    Baseline characteristics of the NACURG cohort.

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    <p>Differences between patients who died and those who survived were assessed by Cox regression survival analysis for independent continuous variables, and a Kaplan-Meyer survival curve with log-rank tests for independent categorical variables. Differences between patients with or without adverse event were assessed by the Student t test or the non-parametric Mann-Whitney U test for continuous variables and the [χ<sup>2</sup>] test or the Fisher exact test for dichotomous categorical variables.</p><p>*p: degree of statistical significance.</p><p>**Lactate levels only available for 122 patients (54%) and not therefore included in the multivariate analysis.</p><p>***The percentage of readmissions out of the total number of patients discharged (221; 4 patients died while in hospital and 1 was still inpatient at 30 days).</p><p>Relationship between different independent variables and adverse event and 90-day mortality after consulting the Emergency Department.</p

    Multivariate predictive models of adverse event and 90-day mortality.

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    <p>MaxM: Maximum Model: includes significant independent variables in the univariate analysis with AUC higher than 0.7.</p><p>OR: Odds Ratio and HR: Hazard Ratio.</p><p>CI 95%: confidence interval of 95%.</p><p>p: level of statistical significance.</p><p>AIC: Akaike Information Criterion (better fit of the model when AIC lower).</p><p>McFadden´s and Atkinson R2: proportion of uncertainty data explained by the model.</p><p>Calibration χ2 (p value): Hosmer and Lemeshow test.</p><p>Multivariate predictive models of adverse event and 90-day mortality.</p
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