Laura F Alconcher1, Paula A Coccia2, Angela Del C Suarez3, Marta L Monteverde4, María Graciela Perez Y Gutiérrez5, Paula M Carlopio6, Mabel L Missoni7, Alejandro Balestracci8, Illiana Principi9, Flavia B Ramírez10, Patricia Estrella11, Susana Micelli12, Daniela C Leroy13, Nahir E Quijada14, Claudia Seminara15, Marta I Giordano16, Susana B Hidalgo Solís17, Mariana Saurit18, Alejandra Caminitti19, Andrea Arias20, Marta Rivas21, Paula Risso22, Miguel Liern23. 1. Pediatric Nephrology Unit, Pediatric Department, Hospital Dr. José Penna, Lainez 2401, (8000), Bahía Blanca, Argentina. laura.alconcher.la@gmail.com. 2. Department of Pediatrics Hospital Italiano Ciudad Autónoma de Buenos Aires (CABA), Pediatric Nephrology Division, Buenos Aires, Argentina. 3. Department of Nephrology Hospital de Niños Sor María Ludovica La Plata, Buenos Aires, Argentina. 4. Hospital Nacional de Pediatría JP Garrahan CABA, Buenos Aires, Argentina. 5. Department of Nephrology Hospital de Niños San Justo Buenos Aires, Buenos Aires, Argentina. 6. Department of Pediatrics Hospital Posadas Buenos Aires, Pediatric Nephrolgy Division, Buenos Aires, Argentina. 7. Department of Pediatrics Hospital Zonal Padre Pedro Tardivio Caleta Olivia Santa Cruz, Buenos Aires, Argentina. 8. Nephrology Unit Hospital General de Niños Pedro de Elizalde CABA, Buenos Aires, Argentina. 9. Department of Nephrology Hospital Pediátrico Humberto J Notti Mendoza, Mendoza, Argentina. 10. Pediatric Nephrolgy Division Department of Pediatrics Hospital Dr. Castro Rendon Neuquén, Neuquén, Argentina. 11. Dirección de Epidemiologia de La Pampa, Hospital Lucio Molas Santa Rosa La Pampa, Santa Rosa, Argentina. 12. Department of Nephrology Hospital del Niño Jesús Tucumán, San Miguel de Tucumán, Argentina. 13. Department of Pediatrics Hospital Interzonal de Agudos Abrahan Piñeyro Junín, Buenos Aires, Argentina. 14. Hospital Infantil Municipal Córdoba, Córdoba, Argentina. 15. Hospital Provincial de Córdoba, Córdoba, Spain. 16. Complejo Sanitario San Luis, San Luis, Argentina. 17. Department of Nephrology Hospital Juan Pablo II Corrientes, Corrientes, Argentina. 18. Hospital Público Materno Infantil de Salta, Salta, Argentina. 19. Department of Nephrology Hospital Provincial de Santa Fé, Santa Fé, Argentina. 20. Department of Nephrology Hospital Materno Infantil Dr. Héctor Quintana Jujuy, San Salvador de Jujuy, Argentina. 21. Instituto Nacional de Enfermedades Infecciosas-ANLIS "Dr. Carlos G. Malbrán", Buenos Aires, Argentina. 22. PhD student, PhD scholarship by Comisión de Investigaciones Científicas de la provincia de Buenos Aires, Teaching assistant in Classic and Bayesian Biostatistics Cathedra, Facultad de Cincias Veterinarias, Universidad Nacional de La Plata, Buenos Aires, Argentina. 23. Department of Nephrology Hospital Gutiérrez CABA, Buenos Aires, Argentina.
Abstract
OBJECTIVES: (1) Evaluate mortality rate in patients with Shiga toxin-producing Escherichia coli hemolytic uremic syndrome, (2) determine the leading causes of death, and (3) identify predictors of mortality at hospital admission. METHODS: We conducted a multicentric, observational, retrospective, cross-sectional study. It included patients under 18 years old with Shiga toxin-producing Escherichia coli hemolytic uremic syndrome hospitalized between January 2005 and June 2016. Clinical and laboratory data were obtained from the Argentine National Epidemiological Surveillance System of Hemolytic Uremic Syndrome. Clinical and laboratory variables were compared between deceased and non-deceased patients. Univariate and multivariate analyses were performed. ROC curves and area under the curve were obtained. RESULTS: Seventeen (3.65%) out of the 466 patients died, being central nervous system involvement the main cause of death. Predictors of death were central nervous system involvement, the number of days since the beginning of diarrhea to hospitalization, hyponatremia, high hemoglobin, high leukocyte counts, and low bicarbonate concentration on admission. In the multivariate analysis, central nervous system involvement, sodium concentration, and hemoglobin were independent predictors. The best cut off for sodium was ≤ 128 meq/l and for hemoglobin ≥ 10.8 g/dl. CONCLUSIONS: Mortality was low in children with Shiga toxin-producing Escherichia coli hemolytic uremic syndrome, being central nervous system involvement the main cause of death. The best mortality predictors found were central nervous system involvement, hemoglobin, and sodium concentration. Hyponatremia may be a new Shiga toxin-producing Escherichia coli hemolytic uremic syndrome mortality predictor.
OBJECTIVES: (1) Evaluate mortality rate in patients with Shiga toxin-producing Escherichia coli hemolytic uremic syndrome, (2) determine the leading causes of death, and (3) identify predictors of mortality at hospital admission. METHODS: We conducted a multicentric, observational, retrospective, cross-sectional study. It included patients under 18 years old with Shiga toxin-producing Escherichia coli hemolytic uremic syndrome hospitalized between January 2005 and June 2016. Clinical and laboratory data were obtained from the Argentine National Epidemiological Surveillance System of Hemolytic Uremic Syndrome. Clinical and laboratory variables were compared between deceased and non-deceased patients. Univariate and multivariate analyses were performed. ROC curves and area under the curve were obtained. RESULTS: Seventeen (3.65%) out of the 466 patients died, being central nervous system involvement the main cause of death. Predictors of death were central nervous system involvement, the number of days since the beginning of diarrhea to hospitalization, hyponatremia, high hemoglobin, high leukocyte counts, and low bicarbonate concentration on admission. In the multivariate analysis, central nervous system involvement, sodium concentration, and hemoglobin were independent predictors. The best cut off for sodium was ≤ 128 meq/l and for hemoglobin ≥ 10.8 g/dl. CONCLUSIONS: Mortality was low in children with Shiga toxin-producing Escherichia coli hemolytic uremic syndrome, being central nervous system involvement the main cause of death. The best mortality predictors found were central nervous system involvement, hemoglobin, and sodium concentration. Hyponatremia may be a new Shiga toxin-producing Escherichia coli hemolytic uremic syndrome mortality predictor.
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