A Novel Artificial Urinary Sphincter (VICTO®) for the Management of Postprostatectomy Urinary Incontinence: Description of the Surgical Technique and Preliminary Results from a Multicenter Series

被引:13
作者
Giammo, Alessandro [1 ]
Falcone, Marco [1 ,2 ]
Blecher, Gideon [3 ,4 ]
Ammirati, Enrico [1 ,2 ]
Geretto, Paolo [1 ,2 ]
Manassero, Alberto [1 ]
Bottero, Danilo [5 ]
Lorusso, Vito [5 ]
Signorello, Diego [6 ]
Gontero, Paolo [1 ,2 ]
Carone, Roberto [1 ]
机构
[1] AOU Citta Salute & Sci Torino, CTO Spinal Cord Unit, Dept Neurourol, Turin, Italy
[2] Univ Turin, Molinette Hosp, Dept Urol, AOU Citta Salute & Sci Torino, Turin, Italy
[3] Monash Univ, Monash Hlth, Sch Clin Sci, Dept Surg, Melbourne, Vic, Australia
[4] Alfred Hosp, Melbourne, Vic, Australia
[5] European Inst Oncol IEO, Dept Urol, Milan, Italy
[6] Bressanone Hosp, Dept Urol, Bressanone, Bolzano, Italy
关键词
Artificial urinary sphincter; Incontinence; Urinary incontinence; Postprostatectomy urinary incontinence; Stress urinary incontinence;
D O I
10.1159/000512722
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Aims: The objective of the study was to analyze short-term outcomes and safety profile of the newly designed artificial urinary sphincters (AUSs) VICTO (R) and VICTOplus (R). Methods: Data from the implant of VICTO (R) or VICTOplus (R) AUSs on a series of consecutive male patients with stress urinary incontinence (SUI) following radical prostatectomy (RP) were retrospectively collected in 3 tertiary referral centers between May 2017 and December 2019. Patients were affected by moderate-severe genuine SUI (200-400 or >400 g urine leakage in 24-h pad test) refractory to conservative treatment. Outcomes were evaluated through the 24-h pad test and the International Consultation on Incontinence Questionnaire-Urinary Incontinence Short Form (ICIQ-UI-SF). Follow-up was scheduled after 3, 6, and 12 months and then when clinically needed. Nonparametric tests were applied in subgroup analyses. Results: Seventeen patients were enrolled: 8 were implanted with the VICTO (R) device and 9 with VICTOplus (R). The median age at surgery was 69 (interquartile range (IQR) 60-75) years. The median follow-up was 15 (IQR 12-18) months. At 12 months, the dry rate was 76.4% and the social continence rate was 94%. The postoperative complication rate was 17.6%. All complications were classified as Clavien-Dindo I. No difference in terms of outcomes was observed between the VICTO (R) and the VICTOplus (R) subgroups. Conclusions: Preliminary outcomes of the VICTO (R) and VICTOplus (R) implantation are satisfactory. These devices may represent a safe and realistic solution for patients with moderate-severe SUI following RP.
引用
收藏
页码:414 / 420
页数:7
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