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

dc.contributor.authorAngulo Cuesta, Javier
dc.contributor.authorSchönburg, Sandra
dc.contributor.authorGiammò, Alessandro
dc.contributor.authorQueissert, Fabian
dc.contributor.authorGonsior, Andreas
dc.contributor.authorGonzález Enguita, Carmen
dc.contributor.authorMartins, Francisco
dc.contributor.authorRourke, Keith
dc.contributor.authorCruz, Francisco
dc.date.accessioned2022-05-27T17:48:43Z
dc.date.available2022-05-27T17:48:43Z
dc.date.issued2021
dc.description.abstractAim: 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.spa
dc.description.filiationUEMspa
dc.description.impact2.367 JCR (2021) Q3, 63/90 Urology & Nephrologyspa
dc.description.impact1.288 SJR (2021) Q1, 73/378 Neurology (clinical)spa
dc.description.impactNo data IDR 2021spa
dc.description.sponsorshipSin financiaciónspa
dc.identifier.citationAngulo, J. C., Schönburg, S., Giammò, A., Queissert, F., Gonsior, A., González-Enguita, C., Martins, F. E., Rourke, K., & Cruz, F. (2021). 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. Neurourology and Urodynamics, 40(3), 897–909. https://doi.org/10.1002/nau.24646spa
dc.identifier.doi10.1002/nau.24646
dc.identifier.issn0733-2467
dc.identifier.issn1520-6777
dc.identifier.urihttp://hdl.handle.net/11268/11320
dc.language.isoengspa
dc.peerreviewedSispa
dc.relation.publisherversionhttp://ezproxy.universidadeuropea.es/login?url=http://dx.doi.org/10.1002/nau.24646spa
dc.rights.accessRightsrestricted accessspa
dc.subject.otherIncontinencia urinariaspa
dc.subject.unescoSistema endocrinospa
dc.subject.unescoTratamiento médicospa
dc.subject.unescoCirugíaspa
dc.titleArtificial 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 experiencespa
dc.typejournal articlespa
dspace.entity.typePublication
relation.isAuthorOfPublicationeaadbb3a-67c4-43f5-b477-5fb2318b809a
relation.isAuthorOfPublication.latestForDiscoveryeaadbb3a-67c4-43f5-b477-5fb2318b809a

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