Artigo Revisado por pares

Canadian Experience with the Adjustable Transobturator Male System for Post-Prostatectomy Incontinence: A Multicenter Study

2019; Lippincott Williams & Wilkins; Volume: 202; Issue: 5 Linguagem: Inglês

10.1097/ju.0000000000000420

ISSN

1527-3792

Autores

R. Christopher Doiron, Álvaro Saavedra, Trevor Haines, Geneviève Nadeau, Le-Mai Tu, Julie Morisset, Stephen Steele, Luc Valiquette, Dean Elterman, Conrad Maciejewski, Keith Rourke,

Tópico(s)

Reconstructive Surgery and Microvascular Techniques

Resumo

No AccessJournal of UrologyAdult Urology1 Nov 2019Canadian Experience with the Adjustable Transobturator Male System for Post-Prostatectomy Incontinence: A Multicenter StudyThis article is commented on by the following:Editorial CommentEditorial Comment R. Christopher Doiron, Alvaro Saavedra, Trevor Haines, Genevieve Nadeau, Le-Mai Tu, Julie Morisset, Stephen Steele, Luc Valiquette, Dean Elterman, Conrad Maciejewski, and Keith Rourke R. Christopher DoironR. Christopher Doiron Divisions of Urology, University of Alberta, Edmonton, Alberta, Canada More articles by this author , Alvaro SaavedraAlvaro Saavedra Divisions of Urology, University of Alberta, Edmonton, Alberta, Canada More articles by this author , Trevor HainesTrevor Haines Divisions of Urology, University of Alberta, Edmonton, Alberta, Canada More articles by this author , Genevieve NadeauGenevieve Nadeau Université Laval, Quebec City, Canada Financial interest and/or other relationship with Red Leaf Medical. More articles by this author , Le-Mai TuLe-Mai Tu University of Sherbrooke, Sherbrooke, Quebec, Canada More articles by this author , Julie MorissetJulie Morisset Université de Montréal en Mauricie, Trois-Rivières, Quebec, Canada More articles by this author , Stephen SteeleStephen Steele Department of Urology, Queen’s University, Kingston, Ontario, Canada More articles by this author , Luc ValiquetteLuc Valiquette Université de Montréal, Montréal, Quebec, Canada More articles by this author , Dean EltermanDean Elterman University of Toronto, Toronto, Canada More articles by this author , Conrad MaciejewskiConrad Maciejewski University of Ottawa, Ottawa, Canada More articles by this author , and Keith RourkeKeith Rourke Correspondence: Division of Urology, Department of Surgery, University of Alberta, 7th Floor, Kaye Edmonton Clinic, 11400 University Ave., Edmonton, Alberta T6G-1Z1, Canada telephone: 780-407-5800; FAX: 780-441-2597; E-mail Address: [email protected] Divisions of Urology, University of Alberta, Edmonton, Alberta, Canada Financial interest and/or other relationship with Red Leaf Medical. More articles by this author View All Author Informationhttps://doi.org/10.1097/JU.0000000000000420AboutFull TextPDF ToolsAdd to favoritesDownload CitationsTrack CitationsPermissionsReprints ShareFacebookLinked InTwitterEmail Abstract Purpose: We assessed the efficacy and safety profile of the ATOMS® (Adjustable Transobturator Male System) for post-prostatectomy incontinence in a multicenter North American setting. Materials and Methods: We reviewed outcomes from 8 centers in men who underwent treatment of post-prostatectomy incontinence with an ATOMS. Primary study outcomes were pad changes and continence, defined as requiring 1.0 or 0 pad postoperatively in patients who required 2.0 or more pads preoperatively and 0 pad in those who required more than 1.0 or 2.0 pads preoperatively. Secondary outcomes included improvement, 90-day complications and patient satisfaction. Results: A total of 160 patients were enrolled in study with a median followup of 9.0 months. Preoperative median pad use was 4 per day (IQR 3–5). Of the patients 36.3% reported severe preoperative incontinence, 31.3% received prior radiotherapy and 16.3% underwent previous incontinence surgery. Median postoperative pad use after adjustments was 0.5 per day (IQR 0–1, p <0.001). The overall continence rate was 80.0% with improvement in 87.8% of cases. Of the patients 70.1% underwent a mean ± SD of 2.4 ± 2.7 adjustments (IQR 0–16). The patient satisfaction rate was 86.3%, 22.3% experienced 90-day complications of any grade and 7 (4.4%) experienced Clavien III complications primarily related to the injection port. Patients with a history of radiotherapy were less likely to be continent (62.5% vs 87.9%, p=0.002), improved (77.1% vs 92.6%, p=0.02) or satisfied (69.8% vs 93.2%, p=0.001). Similarly patients with previous incontinence surgery had lower rates of continence, improvement and satisfaction (57.7%, 73.1% and 69.6%, respectively). Conclusions: In the short term the ATOMS is a safe and efficacious device to treat post-prostatectomy incontinence. Patients with concurrent radiotherapy and previous incontinence surgery respond to treatment but are less likely to be continent, improved or satisfied. References 1. : Health related quality of life significance of single pad urinary incontinence following radical prostatectomy. J Urol 2003; 170: 512. Link, Google Scholar 2. : Committee of the International Consultation on Incontinence: surgical treatment of stress incontinence in men. Neurourol Urodyn 2010; 29: 179. Google Scholar 3. : Population based study of long-term rates of surgery for urinary incontinence after radical prostatectomy for prostate cancer. J Urol 2012; 188: 502. Link, Google Scholar 4. : An artificial sphincter; a new device and operation for control of enuresis and urinary incontinence. J Urol 1947; 58: 250. 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Link, Google Scholar The corresponding author certifies that, when applicable, a statement(s) has been included in the manuscript documenting institutional review board, ethics committee or ethical review board study approval; principles of Helsinki Declaration were followed in lieu of formal ethics committee approval; institutional animal care and use committee approval; all human subjects provided written informed consent with guarantees of confidentiality; IRB approved protocol number; animal approved project number. The ATOMS® device manufacturer, Agency for Medical Innovations, Feldkirch, Austria, was not involved with trial funding, execution or analysis, or with manuscript preparation. No direct or indirect commercial, personal, academic, political, religious or ethical incentive is associated with publishing this article. © 2019 by American Urological Association Education and Research, Inc.FiguresReferencesRelatedDetailsRelated articlesJournal of Urology9 Oct 2019Editorial CommentJournal of Urology9 Oct 2019Editorial Comment Volume 202Issue 5November 2019Page: 1022-1028Supplementary Materials Advertisement Copyright & Permissions© 2019 by American Urological Association Education and Research, Inc.Keywordsstressprostheses and implantsmaleurethraprostatectomyurinary incontinenceAcknowledgmentThe AUS was introduced by American Medical System Holdings, Inc., Hopkins, Minnesota.MetricsAuthor Information R. Christopher Doiron Divisions of Urology, University of Alberta, Edmonton, Alberta, Canada More articles by this author Alvaro Saavedra Divisions of Urology, University of Alberta, Edmonton, Alberta, Canada More articles by this author Trevor Haines Divisions of Urology, University of Alberta, Edmonton, Alberta, Canada More articles by this author Genevieve Nadeau Université Laval, Quebec City, Canada Financial interest and/or other relationship with Red Leaf Medical. More articles by this author Le-Mai Tu University of Sherbrooke, Sherbrooke, Quebec, Canada More articles by this author Julie Morisset Université de Montréal en Mauricie, Trois-Rivières, Quebec, Canada More articles by this author Stephen Steele Department of Urology, Queen’s University, Kingston, Ontario, Canada More articles by this author Luc Valiquette Université de Montréal, Montréal, Quebec, Canada More articles by this author Dean Elterman University of Toronto, Toronto, Canada More articles by this author Conrad Maciejewski University of Ottawa, Ottawa, Canada More articles by this author Keith Rourke Divisions of Urology, University of Alberta, Edmonton, Alberta, Canada Correspondence: Division of Urology, Department of Surgery, University of Alberta, 7th Floor, Kaye Edmonton Clinic, 11400 University Ave., Edmonton, Alberta T6G-1Z1, Canada telephone: 780-407-5800; FAX: 780-441-2597; E-mail Address: [email protected] Financial interest and/or other relationship with Red Leaf Medical. More articles by this author Expand All The corresponding author certifies that, when applicable, a statement(s) has been included in the manuscript documenting institutional review board, ethics committee or ethical review board study approval; principles of Helsinki Declaration were followed in lieu of formal ethics committee approval; institutional animal care and use committee approval; all human subjects provided written informed consent with guarantees of confidentiality; IRB approved protocol number; animal approved project number. The ATOMS® device manufacturer, Agency for Medical Innovations, Feldkirch, Austria, was not involved with trial funding, execution or analysis, or with manuscript preparation. No direct or indirect commercial, personal, academic, political, religious or ethical incentive is associated with publishing this article. Advertisement PDF downloadLoading ...

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