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Volume expansion mitigates Shiga toxin-producing E. coli-hemolytic uremic syndrome in children.
Böckenhauer, Johannes; Schild, Raphael; Kemper, Markus J; Henne, Thomas; Stein, Marie V; Oh, Jun; Loos, Sebastian.
Afiliación
  • Böckenhauer J; University Medical Center Hamburg-Eppendorf, University Children's Hospital, Martinistrasse 52, 20246, Hamburg, Germany.
  • Schild R; University Medical Center Hamburg-Eppendorf, University Children's Hospital, Martinistrasse 52, 20246, Hamburg, Germany.
  • Kemper MJ; Department of Pediatrics, Asklepios Klink Nord, Hamburg, Germany.
  • Henne T; University Medical Center Hamburg-Eppendorf, University Children's Hospital, Martinistrasse 52, 20246, Hamburg, Germany.
  • Stein MV; University Medical Center Hamburg-Eppendorf, University Children's Hospital, Martinistrasse 52, 20246, Hamburg, Germany.
  • Oh J; University Medical Center Hamburg-Eppendorf, University Children's Hospital, Martinistrasse 52, 20246, Hamburg, Germany.
  • Loos S; University Medical Center Hamburg-Eppendorf, University Children's Hospital, Martinistrasse 52, 20246, Hamburg, Germany. s.loos@uke.de.
Pediatr Nephrol ; 39(6): 1901-1907, 2024 Jun.
Article en En | MEDLINE | ID: mdl-38240870
ABSTRACT

BACKGROUND:

Shiga toxin-producing E. coli-hemolytic uremic syndrome (STEC-HUS) is associated with high morbidity and relevant mortality. Previous small studies showed that volume expansion could improve the course and outcome of STEC-HUS. The aim of this single-center study was to evaluate the effect of volume expansion on the clinical course and outcome in STEC-HUS.

METHODS:

Data of pediatric patients with STEC-HUS were analyzed retrospectively. Course and outcome of patients treated with volume expansion (VE) from 2019 to 2022 (n = 38) were compared to historical controls (HC) from 2009 to 2018 (n = 111).

RESULTS:

Patients in the VE group had a significant relative median weight gain compared to HC (7.8% (3.4-11.3) vs. 1.2% (- 0.7-3.9), p < 0.0001) 48 h after admission. The need for dialysis was not reduced by VE (VE 21/38 (55.3%) vs. HC 64/111 (57.7%), p = 0.8). However, central nervous system involvement (impairment of consciousness, seizures, focal neurological deficits, and/or visual disturbances) was significantly reduced (VE 6/38 (15.8%) vs. HC 38/111 (34.2%), p = 0.039). None of the patients in the VE group died or developed chronic kidney disease (CKD) stage 5, whereas in the HC group, three patients died and three patients had CKD stage 5 at discharge.

CONCLUSIONS:

This study suggests that volume expansion may be associated with the mitigation of the acute course of STEC-HUS, especially severe neurological involvement and the development of CKD. Prospective trials should lead to standardized protocols for volume expansion in children with STEC-HUS.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Infecciones por Escherichia coli / Escherichia coli Shiga-Toxigénica / Síndrome Hemolítico-Urémico / Fallo Renal Crónico Tipo de estudio: Guideline Límite: Child / Humans Idioma: En Revista: Pediatr Nephrol Asunto de la revista: NEFROLOGIA / PEDIATRIA Año: 2024 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Infecciones por Escherichia coli / Escherichia coli Shiga-Toxigénica / Síndrome Hemolítico-Urémico / Fallo Renal Crónico Tipo de estudio: Guideline Límite: Child / Humans Idioma: En Revista: Pediatr Nephrol Asunto de la revista: NEFROLOGIA / PEDIATRIA Año: 2024 Tipo del documento: Article País de afiliación: Alemania