Hyponatremia: a new predictor of mortality in patients with Shiga toxin-producing Escherichia coli hemolytic uremic syndrome

Autores
Alconcher, Laura F.; Coccia, Paula A.; Suarez, Angela del Carmen; Monteverde, Marta L.; Pérez Y Gutiérrez, María Graciela; Carlopio, Paula M.; Missoni, Mabel; Balestracci, Alejandro; Principi, Illiana; Ramírez, Flavia B.; Estrella, Patricia; Micelli, Susana; Leroy, Daniela C.; Quijada, Nahir E.; Seminara, Claudia; Giordano, Marta I.; Hidalgo Solís, Susana B.; Saurit, Mariana; Caminitti, Alejandra; Arias, Andrea; Rivas, Marta; Risso, Paula; Liern, Miguel
Año de publicación
2018
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
(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. 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. 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. 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.
Facultad de Ciencias Veterinarias
Materia
Ciencias Médicas
Thrombotic microangiopathy
Acute kidney injury
Outcome in typical uremic syndrome
Typical hemolytic uremic syndrome
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by-nc-sa/4.0/
Repositorio
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/134991

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oai_identifier_str oai:sedici.unlp.edu.ar:10915/134991
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repository_id_str 1329
network_name_str SEDICI (UNLP)
spelling Hyponatremia: a new predictor of mortality in patients with Shiga toxin-producing Escherichia coli hemolytic uremic syndromeAlconcher, Laura F.Coccia, Paula A.Suarez, Angela del CarmenMonteverde, Marta L.Pérez Y Gutiérrez, María GracielaCarlopio, Paula M.Missoni, MabelBalestracci, AlejandroPrincipi, IllianaRamírez, Flavia B.Estrella, PatriciaMicelli, SusanaLeroy, Daniela C.Quijada, Nahir E.Seminara, ClaudiaGiordano, Marta I.Hidalgo Solís, Susana B.Saurit, MarianaCaminitti, AlejandraArias, AndreaRivas, MartaRisso, PaulaLiern, MiguelCiencias MédicasThrombotic microangiopathyAcute kidney injuryOutcome in typical uremic syndromeTypical hemolytic uremic syndrome(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. 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. 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. 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.Facultad de Ciencias Veterinarias2018info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdf1791-1798http://sedici.unlp.edu.ar/handle/10915/134991enginfo:eu-repo/semantics/altIdentifier/issn/1432-198info:eu-repo/semantics/altIdentifier/issn/0931-041info:eu-repo/semantics/altIdentifier/doi/10.1007/s00467-018-3991-6info:eu-repo/semantics/altIdentifier/pmid/29961127info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-sa/4.0/Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-09-03T11:04:23Zoai:sedici.unlp.edu.ar:10915/134991Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-09-03 11:04:23.375SEDICI (UNLP) - Universidad Nacional de La Platafalse
dc.title.none.fl_str_mv Hyponatremia: a new predictor of mortality in patients with Shiga toxin-producing Escherichia coli hemolytic uremic syndrome
title Hyponatremia: a new predictor of mortality in patients with Shiga toxin-producing Escherichia coli hemolytic uremic syndrome
spellingShingle Hyponatremia: a new predictor of mortality in patients with Shiga toxin-producing Escherichia coli hemolytic uremic syndrome
Alconcher, Laura F.
Ciencias Médicas
Thrombotic microangiopathy
Acute kidney injury
Outcome in typical uremic syndrome
Typical hemolytic uremic syndrome
title_short Hyponatremia: a new predictor of mortality in patients with Shiga toxin-producing Escherichia coli hemolytic uremic syndrome
title_full Hyponatremia: a new predictor of mortality in patients with Shiga toxin-producing Escherichia coli hemolytic uremic syndrome
title_fullStr Hyponatremia: a new predictor of mortality in patients with Shiga toxin-producing Escherichia coli hemolytic uremic syndrome
title_full_unstemmed Hyponatremia: a new predictor of mortality in patients with Shiga toxin-producing Escherichia coli hemolytic uremic syndrome
title_sort Hyponatremia: a new predictor of mortality in patients with Shiga toxin-producing Escherichia coli hemolytic uremic syndrome
dc.creator.none.fl_str_mv Alconcher, Laura F.
Coccia, Paula A.
Suarez, Angela del Carmen
Monteverde, Marta L.
Pérez Y Gutiérrez, María Graciela
Carlopio, Paula M.
Missoni, Mabel
Balestracci, Alejandro
Principi, Illiana
Ramírez, Flavia B.
Estrella, Patricia
Micelli, Susana
Leroy, Daniela C.
Quijada, Nahir E.
Seminara, Claudia
Giordano, Marta I.
Hidalgo Solís, Susana B.
Saurit, Mariana
Caminitti, Alejandra
Arias, Andrea
Rivas, Marta
Risso, Paula
Liern, Miguel
author Alconcher, Laura F.
author_facet Alconcher, Laura F.
Coccia, Paula A.
Suarez, Angela del Carmen
Monteverde, Marta L.
Pérez Y Gutiérrez, María Graciela
Carlopio, Paula M.
Missoni, Mabel
Balestracci, Alejandro
Principi, Illiana
Ramírez, Flavia B.
Estrella, Patricia
Micelli, Susana
Leroy, Daniela C.
Quijada, Nahir E.
Seminara, Claudia
Giordano, Marta I.
Hidalgo Solís, Susana B.
Saurit, Mariana
Caminitti, Alejandra
Arias, Andrea
Rivas, Marta
Risso, Paula
Liern, Miguel
author_role author
author2 Coccia, Paula A.
Suarez, Angela del Carmen
Monteverde, Marta L.
Pérez Y Gutiérrez, María Graciela
Carlopio, Paula M.
Missoni, Mabel
Balestracci, Alejandro
Principi, Illiana
Ramírez, Flavia B.
Estrella, Patricia
Micelli, Susana
Leroy, Daniela C.
Quijada, Nahir E.
Seminara, Claudia
Giordano, Marta I.
Hidalgo Solís, Susana B.
Saurit, Mariana
Caminitti, Alejandra
Arias, Andrea
Rivas, Marta
Risso, Paula
Liern, Miguel
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv Ciencias Médicas
Thrombotic microangiopathy
Acute kidney injury
Outcome in typical uremic syndrome
Typical hemolytic uremic syndrome
topic Ciencias Médicas
Thrombotic microangiopathy
Acute kidney injury
Outcome in typical uremic syndrome
Typical hemolytic uremic syndrome
dc.description.none.fl_txt_mv (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. 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. 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. 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.
Facultad de Ciencias Veterinarias
description (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. 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. 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. 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.
publishDate 2018
dc.date.none.fl_str_mv 2018
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Articulo
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format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://sedici.unlp.edu.ar/handle/10915/134991
url http://sedici.unlp.edu.ar/handle/10915/134991
dc.language.none.fl_str_mv eng
language eng
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info:eu-repo/semantics/altIdentifier/issn/0931-041
info:eu-repo/semantics/altIdentifier/doi/10.1007/s00467-018-3991-6
info:eu-repo/semantics/altIdentifier/pmid/29961127
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
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Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
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repository.name.fl_str_mv SEDICI (UNLP) - Universidad Nacional de La Plata
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