Adjustable continence therapy balloons in ...
Document type :
Article dans une revue scientifique
PMID :
Permalink :
Title :
Adjustable continence therapy balloons in women: Evolution of efficacy within the 24 months following implantation.
Author(s) :
Guiffart, P [Auteur]
Reix, B [Auteur]
Centre Hospitalier Régional Universitaire [CHU Lille] [CHRU Lille]
Martin-Malburet, A [Auteur]
Marcelli, F [Auteur]
518922|||Gamétogenèse et Qualité du Gamète - ULR 4308 [GQG] (OLD)
Centre Hospitalier Régional Universitaire [CHU Lille] [CHRU Lille]
Biardeau, Xavier [Auteur]
Lille Neurosciences & Cognition - U 1172 [LilNCog]
Reix, B [Auteur]
Centre Hospitalier Régional Universitaire [CHU Lille] [CHRU Lille]
Martin-Malburet, A [Auteur]
Marcelli, F [Auteur]
518922|||Gamétogenèse et Qualité du Gamète - ULR 4308 [GQG] (OLD)
Centre Hospitalier Régional Universitaire [CHU Lille] [CHRU Lille]
Biardeau, Xavier [Auteur]

Lille Neurosciences & Cognition - U 1172 [LilNCog]
Journal title :
Progrès en Urologie
Abbreviated title :
Prog. Urol.
Volume number :
28
Pages :
927-934
Publication date :
2018-12
ISSN :
1166-7087
HAL domain(s) :
Sciences du Vivant [q-bio]
English abstract : [en]
PURPOSE: To analyze the functional outcomes over time of ACT balloon in women with stress urinary incontinence (SUI) secondary to intrinsic sphincter deficiency (ISD). METHOD: All patients with SUI secondary to ISD who ...
Show more >PURPOSE: To analyze the functional outcomes over time of ACT balloon in women with stress urinary incontinence (SUI) secondary to intrinsic sphincter deficiency (ISD). METHOD: All patients with SUI secondary to ISD who underwent bilateral ACT balloon implantation between September 2008 and November 2015 and regularly monitored for a period of at least 24 months were eligible. The results were studied at 6, 12 and 24 months. Efficacy was defined as: Success - maximum 1 safety pad per day and visual analogue scale (VAS) rating>/=9/10. Improvement - decrease in the number of pads used per day and VAS>/=5/10. Failure - increase or stability of the number of pads used per day and/or VAS<5/10. Failure was considered as primary when it occurred without any success or improvement. It was considered as secondary when it occurred after an initial period of success or improvement. RESULTS: 18 patients were monitored during 24 months. The success rate was respectively 17 %, 33 % and 33 % at 6, 12 and 24 months of follow-up. The improvement rate was respectively 61 %, 39 % and 17 % at 6, 12 and 24 months of follow-up. The primary failure rate was 22 %. The secondary failure rate was 6 % at 12 months and 33 % at 24 months of follow-up. CONCLUSION: ACT balloon efficacy tends to decrease with time requiring a long-term follow-up of implanted patients. LEVEL OF EVIDENCE: 4.Show less >
Show more >PURPOSE: To analyze the functional outcomes over time of ACT balloon in women with stress urinary incontinence (SUI) secondary to intrinsic sphincter deficiency (ISD). METHOD: All patients with SUI secondary to ISD who underwent bilateral ACT balloon implantation between September 2008 and November 2015 and regularly monitored for a period of at least 24 months were eligible. The results were studied at 6, 12 and 24 months. Efficacy was defined as: Success - maximum 1 safety pad per day and visual analogue scale (VAS) rating>/=9/10. Improvement - decrease in the number of pads used per day and VAS>/=5/10. Failure - increase or stability of the number of pads used per day and/or VAS<5/10. Failure was considered as primary when it occurred without any success or improvement. It was considered as secondary when it occurred after an initial period of success or improvement. RESULTS: 18 patients were monitored during 24 months. The success rate was respectively 17 %, 33 % and 33 % at 6, 12 and 24 months of follow-up. The improvement rate was respectively 61 %, 39 % and 17 % at 6, 12 and 24 months of follow-up. The primary failure rate was 22 %. The secondary failure rate was 6 % at 12 months and 33 % at 24 months of follow-up. CONCLUSION: ACT balloon efficacy tends to decrease with time requiring a long-term follow-up of implanted patients. LEVEL OF EVIDENCE: 4.Show less >
Language :
Anglais
Audience :
Internationale
Popular science :
Non
Administrative institution(s) :
Inserm
Université de Lille
CHU Lille
Université de Lille
CHU Lille
Collections :
Research team(s) :
Immunity, inflammation and fibrsis in auto and allo-reactivity
Submission date :
2019-03-01T14:07:55Z
2024-04-05T08:59:44Z
2024-04-05T08:59:44Z