Evaluating the impact of pop-off mechanisms in boys with posterior urethral valves.

VURD bladder diverticula pop-off mechanism posterior urethral valves renal function urinoma

Journal

Frontiers in pediatrics
ISSN: 2296-2360
Titre abrégé: Front Pediatr
Pays: Switzerland
ID NLM: 101615492

Informations de publication

Date de publication:
2022
Historique:
received: 08 08 2022
accepted: 20 09 2022
entrez: 4 11 2022
pubmed: 5 11 2022
medline: 5 11 2022
Statut: epublish

Résumé

Posterior urethral valves are urethral leaflets that cause Lower Urinary Tract Obstruction (LUTO) in boys and are associated with congenital renal dysplasia and abnormal bladder function. They affect 1:4,000 to 1:25,000 births and can be responsible for End-Stage Renal Failure in childhood. There have been several studies on the effect of pop-off mechanisms in boys with posterior urethral valves, but results are contradictory. We aimed to assess and discuss the effect of pop-off mechanisms on renal function in a large cohort of patients. Boys with PUV with and without pop-off mechanisms (urinoma, VURD or giant bladder diverticula) were divided into three severity groups for renal function according to their nadir creatinine (low-risk NC < 35 μmol/L, intermediate-risk NC between 35 and 75 μmol/L, and high-risk NC > 75 μmol/L). We compared children with and children without pop-off mechanisms for mean renal function as well as patient distribution within each severity group. We included 137 boys of which 39 had a pop-off mechanism. Patients had complete data for at least 5 years follow-up. Though there was no significant statistical difference in mean renal function between the pop-off and non-pop-off group, patient distribution within each severity group varied according to whether patients had a pop-off mechanism or not. Though there was no significant difference in mean renal function between boys with and without pop-off mechanisms, it is possible that these are two different patient populations and direct comparison is not possible.

Identifiants

pubmed: 36330367
doi: 10.3389/fped.2022.1014422
pmc: PMC9622767
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1014422

Informations de copyright

© 2022 Delefortrie, Ferdynus, Paye-Jaouen, Michel, Dobremez, Peycelon, El Ghoneimi and Harper.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

T Delefortrie (T)

Department of Pediatric Surgery, Hôpital Robert Debré, Paris, France.
Department of Pediatric Surgery, CHU F Guyon, Saint-Denis de La Réunion, France.
Department of Pediatric Surgery, CHU Pellegrin-Enfants, Bordeaux, France.

C Ferdynus (C)

Unité de Soutien Méthodologique, CHU F Guyon, Saint-Denis de La Réunion, France.

A Paye-Jaouen (A)

Department of Pediatric Surgery, Hôpital Robert Debré, Paris, France.
Hôpital Robert Debré, Centre de Référence des Malformations Rares des Voies Urinaires (MARVU), Paris, France.

J L Michel (JL)

Department of Pediatric Surgery, CHU F Guyon, Saint-Denis de La Réunion, France.

E Dobremez (E)

Department of Pediatric Surgery, CHU Pellegrin-Enfants, Bordeaux, France.

M Peycelon (M)

Department of Pediatric Surgery, Hôpital Robert Debré, Paris, France.

A El Ghoneimi (A)

Department of Pediatric Surgery, Hôpital Robert Debré, Paris, France.
Hôpital Robert Debré, Centre de Référence des Malformations Rares des Voies Urinaires (MARVU), Paris, France.

L Harper (L)

Department of Pediatric Surgery, CHU F Guyon, Saint-Denis de La Réunion, France.
Department of Pediatric Surgery, CHU Pellegrin-Enfants, Bordeaux, France.

Classifications MeSH