Defecation disorders in Spina Bifida: Realistic goals and best therapeutic approaches.


Journal

Neurourology and urodynamics
ISSN: 1520-6777
Titre abrégé: Neurourol Urodyn
Pays: United States
ID NLM: 8303326

Informations de publication

Date de publication:
02 2019
Historique:
received: 27 07 2018
accepted: 23 09 2018
pubmed: 24 12 2018
medline: 15 2 2020
entrez: 22 12 2018
Statut: ppublish

Résumé

Spina Bifida (SB) is a rare congenital condition that frequently impairs the neurological control of both fecal continence and defecation. Several therapeutic strategies have been proposed but impact assessment is lacking. Our objectives were to quantify the symptomatic improvement and to determine the optimal strategy in this rare condition where randomized controlled trials are difficult to conduct. Data were extracted from a prospective database. The present analysis focused on patients having undergone at least two gastroenterological assessments. A standardized therapeutic approach was used from the first visit. Improvement was quantified by the variation of quantified symptomatic scores. The data of of 57 adults with SB (gender F/M: 30/27 [52.6/47.4%]; mean age: 33.8 [18.5] years) were extracted. After a mean follow-up of 46 months, 23/57 patients (40.4%) had at least improvement of one point of the Cleveland Clinic Incontinence score (CCIS); 13/57 (22.8%) reported a significant improvement of continence (delta score >50%). Five of the twelve patients (41.6%) with CCIS < 5 at baseline became incontinent over time. The neurological level was not associated with a worse continence outcome. Work on stool consistency and transanal irrigation were the most useful strategies in those with significant improvement of continence. Using conventional strategies, a benefit on fecal continence occurs in only one out of five patients suffering from Spina Bifida and continent patients at baseline can develop fecal incontinence over time. A strategy targeting improved control of defecation (transanal irrigation) and a standardization of follow-up protocol might be beneficial.

Identifiants

pubmed: 30575995
doi: 10.1002/nau.23904
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

719-725

Informations de copyright

© 2018 Wiley Periodicals, Inc.

Auteurs

Charlène Brochard (C)

CHU Rennes, Service d'Explorations Fonctionnelles Digestives, Université Rennes, Rennes, France.

Benoît Peyronnet (B)

CHU Rennes, Service d'Urologie, Université Rennes, Rennes, France.

Juliette Hascoet (J)

CHU Rennes, Service d'Urologie, Université Rennes, Rennes, France.

Raphael Olivier (R)

INSERM U1235, TENS, Université Nantes, Nantes, France.

Andréa Manunta (A)

CHU Rennes, Service d'Urologie, Centre Référence National Maladies Rares Spina Bifida-dysraphismes, Rennes, France.

Magali Jezequel (M)

CHU Rennes, Centre Référence National Maladies Rares Spina Bifida-dysraphismes, Rennes, France.

Quentin Alimi (Q)

CHU Rennes, Service d'Urologie, Centre Référence National Maladies Rares Spina Bifida-dysraphismes, Rennes, France.

Alain Ropert (A)

CHU Rennes, Service d'Explorations Fonctionnelles Digestives, Université Rennes, Rennes, France.

Michel Neunlist (M)

INSERM U1235, TENS, Université Nantes, Nantes, France.

Guillaume Bouguen (G)

CHU Rennes, Service des Maladies de l'Appareil Digestif, Université Rennes, INSERM, Institut NUMECAN (Nutrition Metabolisms and Cancer), Rennes, France.

Laurent Siproudhis (L)

CHU Rennes, Service des Maladies de l'Appareil Digestif, Université Rennes, INSERM, Institut NUMECAN (Nutrition Metabolisms and Cancer), Rennes, France.

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