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Dexamethasone to prevent kidney scarring in acute pyelonephritis: a randomized clinical trial

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dc.contributor.author Rius-Gordillo, Neus
dc.contributor.author Ferre, Natalia
dc.contributor.author González-Rodríguez, Juan-David
dc.contributor.author Ibars, Zaira
dc.contributor.author Parada-Ricart, Ester
dc.contributor.author Fraga, María-Gloria
dc.contributor.author Chocrón, Sara
dc.contributor.author Samper, Manuel
dc.contributor.author Vicente, Carmen
dc.contributor.author Fuertes, Jordi
dc.contributor.author Escribano, Joaquín
dc.date.accessioned 2025-11-18T09:26:42Z
dc.date.available 2025-11-18T09:26:42Z
dc.date.issued 2022-09
dc.identifier.citation Rius-Gordillo N, Ferré N, González JD, Ibars Z, Parada-Ricart E, Fraga MG, et al. Dexamethasone to prevent kidney scarring in acute pyelonephritis: a randomized clinical trial. Pediatr Nephrol. septiembre de 2022;37(9):2109-18.
dc.identifier.issn 0931-041X
dc.identifier.uri https://sms.carm.es/ricsmur/handle/123456789/20729
dc.description.abstract BACKGROUND: Urinary tract infection (UTI) is one of the most common bacterial infections in childhood and is associated with long-term complications. We aimed to assess the effect of adjuvant dexamethasone treatment on reducing kidney scarring after acute pyelonephritis (APN) in children. METHODS: Multicenter, prospective, double-blind, placebo-controlled, randomized clinical trial (RCT) where children from 1 month to 14 years of age with proven APN were randomly assigned to receive a 3-day course of either an intravenous corticosteroid (dexamethasone 0.30 mg per kg/day) twice daily or placebo. The late technetium 99 m-dimercaptosuric acid scintigraphy (>-6 months after acute episode) was performed to assess kidney scar persistence. Kidney scarring risk factors (vesicoureteral reflux, kidney congenital anomalies, or urinary tract dilatation) were also assessed. RESULTS: Ninety-one participants completed the follow-up and were finally included (dexamethasone n-=-49 and placebo n-=-42). Both groups had similar baseline characteristics. Twenty participants showed persistent kidney scarring after->-6 months of follow-up without differences in incidence between groups (22% and 21% in the dexamethasone and placebo groups, p-=-0.907). Renal damage severity in the early DMSA (¿-=-0.648, p-=-0.023) and procalcitonin values (¿-=-0.065 p-=-0.027) significantly modulated scar development. Vesicoureteral reflux grade showed a trend towards significance (¿-=-0.545, p-=-0.054), but dexamethasone treatment showed no effect. CONCLUSION: Dexamethasone showed no effect on reducing the risk of scar formation in children with APN. Hence, there is no evidence for an adjuvant corticosteroid treatment recommendation in children with APN. However, the study was limited by not achieving the predicted sample size and the expected scar formation. TRIAL REGISTRATION: Clinicaltrials.gov, NCT02034851. Registered in January 14, 2014. "A higher resolution version of the Graphical abstract is available as Supplementary information."
dc.language.iso eng
dc.publisher Springer
dc.subject.mesh Acute Disease
dc.subject.mesh Child
dc.subject.mesh Cicatrix/epidemiology/etiology/prevention & control
dc.subject.mesh Dexamethasone/therapeutic use
dc.subject.mesh Glomerulonephritis/pathology
dc.subject.mesh Humans
dc.subject.mesh Infant
dc.subject.mesh Kidney/pathology
dc.subject.mesh Pyelonephritis/complications/drug therapy
dc.subject.mesh Technetium Tc 99m Dimercaptosuccinic Acid
dc.subject.mesh Urinary Tract Infections/complications/prevention & control
dc.subject.mesh Vesico-Ureteral Reflux/complications/drug therapy/pathology
dc.title Dexamethasone to prevent kidney scarring in acute pyelonephritis: a randomized clinical trial
dc.type info:eu-repo/semantics/article
dc.identifier.pmid 35041042
dc.relation.publisherversion https://link.springer.com/10.1007/s00467-021-05398-w
dc.identifier.doi 10.1007/s00467-021-05398-w
dc.journal.title Pediatric Nephrology
dc.identifier.essn 1432-198X


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