A Minimally Invasive, Outpatient, Office Procedure for Severe Stress Urinary Incontinence in Women: Luksenburg Systems LSG3

Ariel Luksenburg, J. J. Barcia, J. Gaviria, Roberto Sergio, Santiago Palacios, M. Pelosi
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Abstract

The worldwide prevalence of female urinary incontinence (UI) is reported at 55%, and about 27% of UIs are severe. The complications in cases of severe UI treated surgically and the ineffective or incomplete results of prolonged treatments with thermal energies motivated us to develop an innovative treatment. Our hypothesis was based on correcting the descent and/or urethral hypermotility and repositioning the descended bladder urethral junction. We have designed a system for the development of a dense and resistant fibrosis that supports the urethra and can correct the alterations of severe UI, Luksenburg systems procedure, LSG3. A group of 652 women between the age of 46 and 74 years, post-menopausal, with more than 2 vaginal births and severe UI, documented by the clinical presentation and the International Consultation on Incontinence Questionnaire-Urinary Incontinence Short Form (ICIQ-UI SF) score index, were enrolled. Originally developed polycaprolactone threads were placed in suburethral space using specific designed tools (LSG3). Immediate results—24 hours (P < .05): 469 patients without clinical UI (72% efficacy), 122 patients with grade 1 UI (drops) (18% improvement), and 59 patients with grade 3 UI (unchanged 9%). Thirty-day results (P < .05): 560 patients without UI (86% efficacy), 58 patients with grade 1 UI (drops) (9% improvement), and 34 patients with grade 3 UI (unchanged 5%). Fifteen-month results (P < .05): 542 patients without UI (83%), 74 patients with grade 1 UI (drops) (11%), and 36 patients with grade 3 UI (6%). No complications or secondary effects were found after the procedure in the 15 months of follow-up. We have developed an innovative system called “suburethral spider web” to treat and cure severe (grade 3) UI in office, as outpatient, that is effective, safe, and cheap.
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一种微创、门诊、办公室手术治疗女性严重压力性尿失禁:Luksenburg Systems LSG3
据报道,全球女性尿失禁(UI)的患病率为55%,其中约27%的尿失禁是严重的。严重尿失血性手术治疗的并发症和长期热能治疗的无效或不完整的结果促使我们开发一种创新的治疗方法。我们的假设是基于纠正下降和/或尿道运动亢进和重新定位下降膀胱尿道交界处。我们设计了一个系统,用于发展致密和耐药纤维化,支持尿道,可以纠正严重UI的改变,Luksenburg系统程序,LSG3。纳入652名年龄在46 - 74岁,绝经后,阴道分娩2次以上,严重尿失禁的妇女,并通过临床表现和尿失禁国际咨询问卷-尿失禁简表(ICIQ-UI SF)评分指数进行记录。最初开发的聚己内酯螺纹使用特定设计的工具(LSG3)放置在椎管下空间。即时结果- 24小时(P < 0.05):无临床尿失禁患者469例(72%有效率),1级尿失禁患者122例(下降)(改善18%),3级尿失禁患者59例(不变9%)。30天的结果(P < 0.05):无尿失禁患者560例(有效率86%),1级尿失禁患者58例(下降)(改善9%),3级尿失禁患者34例(不变5%)。15个月的结果(P < 0.05):无UI患者542例(83%),1级UI 74例(下降)(11%),3级UI 36例(6%)。术后随访15个月,无并发症及其他不良反应。我们开发了一种创新的系统,称为“静脉下蜘蛛网”,在办公室治疗和治愈严重(3级)尿漏,作为门诊,有效,安全,廉价。
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