Artificial urinary sphincter or a second adjustable transobturator male system offer equivalent outcomes in patients whom required revision on the initial ATOMS device: An international multi-institutional experience

被引:15
作者
Angulo, Javier C. [1 ]
Schonburg, Sandra [2 ]
Giammo, Alessandro [3 ]
Queissert, Fabian [4 ]
Gonsior, Andreas [5 ]
Gonzalez-Enguita, Carmen [6 ]
Martins, Francisco E. [7 ]
Rourke, Keith [8 ]
Cruz, Francisco [9 ]
机构
[1] Univ Europea Madrid, Hosp Univ Getafe, Clin Dept, Madrid, Spain
[2] Martin Luther Univ Halle Wittenberg, Dept Urol & Kidney Transplantat, Halle, Saale, Germany
[3] AOU Citta Salute & Sci Torino, CTO Spinal Cord Unit, Dept Neuro Urol, Turin, Italy
[4] Univ Klinikum Munster, Dept Urol, Munster, Germany
[5] Univ Leipzig, Klin & Poliklin Urol, Leipzig, Germany
[6] Hosp Univ Fdn Jimenez Diaz, Dept Urol, Madrid, Spain
[7] Ctr Hosp Univ Lisboa Norte, Hosp Santa Maria, Lisbon, Portugal
[8] Alberta Univ, Dept Urol, Edmonton, AB, Canada
[9] Ctr Hosp Sao Joao, Dept Urol, Oporto, Portugal
关键词
adjustable transobturator male system; artificial urinary sphincter; male stress incontinence; second implant; surgical revision;
D O I
10.1002/nau.24646
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
Aim To evaluate treatment options after surgical revision of adjustable transobturator male system (ATOMS) and the results of further incontinence implantation. Materials and Methods A retrospective multicenter study evaluating patients with surgical revision of ATOMS in academic institutions. Causes and factors affecting revision-free interval were studied and also the frequency of device explant and placement of second ATOMS or artificial urinary sphincter (AUS) at surgeon discretion. Operative results, complications (Clavien-Dindo), and efficacy (postoperative pad-test, pad-count, patient satisfaction, and patient global impression of improvement [PGI-I scale]) of each treatment option were compared. Results Seventy-eight out of 902 patients (8.65%) with ATOMS underwent surgical revision at 4.1 +/- 2.4 years mean follow-up and 75 (8.3%) were explanted. The main causes for revision included persistence of incontinence (35.9%) and scrotal port erosion (34.6%). Independent risk factors of the shortened revision-free interval were previous anti-incontinence surgery (HR, 1.83; 95% CI, 1.06-3.16; p = 0.007) and port erosion (HR, 1.83; 95% CI, 1.06-3.16; p = 0.0027). Fifty-eight (6.4%) received a second implant: 31 repeated ATOMS and 27 AUS. Operative time was longer for AUS (p = .003). The visual analog scale of pain at hospital discharge (p = 0.837) and postoperative complications (p = 0.154) were equivalent. The predominant cuff size for AUS was 4.5 cm (59.3%). Mean follow-up after the second implant was 29.1 +/- 25.8 months. Postoperative efficacy of secondary treatment results favored ATOMS based on pad-test (p = 0.016), pad-count (p = 0.029), patient satisfaction (p = 0.04), and PGI-I (p = 0.025). Conclusions ATOMS surgical revision due to different reasons generally leads to device explant. Rescue treatment is possible with ATOMS or AUS. No difference in postoperative complications was detected between secondary devices, but efficacy favors repeating ATOMS implantation.
引用
收藏
页码:897 / 909
页数:13
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