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Volume 24, Number 6—June 2018
CME ACTIVITY - Research

Bioclinical Test to Predict Nephropathia Epidemica Severity at Hospital Admission

Maxime HentzienComments to Author , Stéphanie Mestrallet, Pascale Halin, Laure-Anne Pannet, Delphine Lebrun, Moustapha Dramé, Firouzé Bani-Sadr, Jean-Marc Galempoix, Christophe Strady, Jean-Marc Reynes, Christian Penalba, and Amélie Servettaz
Author affiliations: University of Reims Champagne-Ardenne, Reims, France (M. Hentzien, M. Dramé); Hôpital Universitaire Robert Debré, Reims (M. Hentzien, M. Dramé, F. Bani-Sadr, A. Servettaz); Manchester Hospital, Charleville-Mézières, France (S. Mestrallet, P. Halin, L.-A. Pannet, D. Lebrun, J.-M. Galempoix, C. Penalba); Groupe Courlancy, Reims (C. Strady); Institut Pasteur, Lyon, France (J.-M. Reynes)

Main Article

Table 4

Events observed in patients hospitalized with NE by risk group as determined by bioclinical test score, Ardennes Department, France, January 2000–December 2014*

Risk group Score No. NE patients Observed severe NE, no. (%)
Low 0–10 61 2 (3.3)
Intermediate 11–19 80 14 (17.5)
High 20–45 53 24 (45.3)

*Data were missing for 11 patients, who were excluded in this analysis. However, similar results for observed severe NE were obtained when assuming a score of zero for missing data: low (4.7%, 3/64), intermediate (20.1%, 18/87), and high (44.4%, 24/54). The leukocyte count and platelet count at admission were missing from the 1 additional patient with severe NE categorized as low risk in this analysis. NE, nephropathia epidemica.

Main Article

Page created: May 15, 2018
Page updated: May 15, 2018
Page reviewed: May 15, 2018
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