[Bladder augmentation in the era of botulinum toxin: Indications and results].
L’entérocystoplastie d’agrandissement à l’ère de la toxine botulique : indications et résultats.
Augmentation cystoplasty
Autosondage propre intermittent
Botulinum toxins
Entérocystoplastie d’agrandissement
Intermittent urethral catheterization
Neurogenic
Toxine botulique
Type A
Urinary bladder
Vessie neurologique
Journal
Progres en urologie : journal de l'Association francaise d'urologie et de la Societe francaise d'urologie
ISSN: 1166-7087
Titre abrégé: Prog Urol
Pays: France
ID NLM: 9307844
Informations de publication
Date de publication:
Sep 2023
Sep 2023
Historique:
received:
28
04
2023
revised:
23
07
2023
accepted:
25
07
2023
medline:
25
9
2023
pubmed:
5
9
2023
entrez:
4
9
2023
Statut:
ppublish
Résumé
To determine the surgical indication and results of bladder augmentation (BA) during the last decade in a neurourology center in the era of intradetrusor botulinum toxin injection. We conducted a retrospective study that included patients with BA between January 1, 2012 and December 31, 2022 in our centre. We collected pre-operative demographic, clinical, and urodynamic data, BA indication, and associated procedures. We analyzed early and late complications as well as continence and postoperative voiding mode in patients with first BA in a neurological pathology context. We performed 77 BA over the study period. The main indication was neurogenic overactive bladder, which was secondarily resistant to botulinum toxin. The main associated procedure was continent cutaneous diversion (n=31, 57.4%). Among patients who had a first BA for neurogenic bladder, 34 patients had early complications (50%) including 12 patients with≥Clavien 3 complications (17.6%). After a median follow-up of 33 [14; 55] months, 23 patients had late complications (33.8%) and 59 patients had complete continence (86.8%). In the era of botulinum toxin, the main indication of BA is the secondary failure of botulinum toxin for overactive neurogenic bladder. The BA provided continence in 86.8% of patients. It remains however an intervention with a significant rate of severe complications whose indication must be discussed by a multidisciplinary team. Weak.
Identifiants
pubmed: 37666743
pii: S1166-7087(23)00150-1
doi: 10.1016/j.purol.2023.07.010
pii:
doi:
Substances chimiques
Botulinum Toxins
EC 3.4.24.69
Types de publication
English Abstract
Journal Article
Langues
fre
Sous-ensembles de citation
IM
Pagination
547-554Informations de copyright
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