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前列腺尿道提升术治疗良性前列腺增生引起的前列腺增大相关下尿路症状:LIFT 研究。

The prostatic urethral lift for the treatment of lower urinary tract symptoms associated with prostate enlargement due to benign prostatic hyperplasia: the L.I.F.T. Study.

机构信息

University of Texas Southwestern Medical Center, Dallas, Texas; Scott and White Healthcare, Temple, Texas; Western Urological Clinic, Salt Lake City, Utah; Carolina Urological Research Center, Myrtle Beach, South Carolina; Cosmetic Surgery Hospital, Brampton, and Oakville Trafalgar Memorial Hospital, Oakville, Ontario, Canada; The Austin Hospital, Melbourne, Victoria, Australia, Urology Associates of Denver, Denver, Colorado; Atlantic Urological Associates, Daytona Beach, and Pinellas Urology, St. Petersburg, Florida; Northwestern University and Southern Illinois University, Springfield, Illinois; Weill Cornell Medical Center, New York, New York; Urology Associates of Silicon Valley, San Jose, and SD Uro-Research, San Diego, California; Port Macquarie Hospital, Port Macquarie, and Figtree Private Hospital, Figtree, New South Wales, Australia; Chesapeake Urology, Baltimore, Maryland; Freedman, MD, LTD, Las Vegas, Nevada; Geisinger Medical Center and Wake Forest University, Winston-Salem, North Carolina.

出版信息

J Urol. 2013 Dec;190(6):2161-7. doi: 10.1016/j.juro.2013.05.116. Epub 2013 Jun 11.

Abstract

PURPOSE

We report the first multicenter randomized blinded trial of the prostatic urethral lift for the treatment of lower urinary tract symptoms secondary to benign prostatic hyperplasia.

MATERIALS AND METHODS

Men at least 50 years old with AUASI (American Urological Association Symptom Index) 13 or greater, a maximum flow rate 12 ml per second or less and a prostate 30 to 80 cc were randomized 2:1 between prostatic urethral lift and sham. In the prostatic urethral lift group small permanent implants are placed within the prostate to retract encroaching lobes and open the prostatic urethra. Sham entailed rigid cystoscopy with sounds mimicking the prostatic urethral lift. The primary end point was comparison of AUASI reduction at 3 months. The prostatic urethral lift arm subjects were followed to 1 year and assessed for lower urinary tract symptoms, peak urinary flow rate, quality of life and sexual function.

RESULTS

A total of 206 men were randomized (prostatic urethral lift 140 vs sham 66). The prostatic urethral lift and sham AUASI was reduced by 11.1±7.67 and 5.9±7.66, respectively (p=0.003), thus meeting the primary end point. Prostatic urethral lift subjects experienced AUASI reduction from 22.1 baseline to 18.0, 11.0 and 11.1 at 2 weeks, 3 months and 12 months, respectively, p<0.001. Peak urinary flow rate increased 4.4 ml per second at 3 months and was sustained at 4.0 ml per second at 12 months, p<0.001. Adverse events were typically mild and transient. There was no occurrence of de novo ejaculatory or erectile dysfunction.

CONCLUSIONS

The prostatic urethral lift, reliably performed with the patient under local anesthesia, provides rapid and sustained improvement in symptoms and flow, while preserving sexual function.

摘要

目的

我们报告了首例多中心、随机、双盲前列腺尿道提升术治疗良性前列腺增生症下尿路症状的临床试验。

材料与方法

至少 50 岁的男性,国际前列腺症状评分(IPSS)为 13 或更高,最大尿流率为 12ml/秒或更低,前列腺体积为 30 至 80cc,按 2:1 的比例随机分为前列腺尿道提升术组和假手术组。在前列腺尿道提升术组中,将小的永久性植入物放置在前列腺内,以回缩侵入的叶并打开前列腺尿道。假手术组采用硬性膀胱镜检查,并使用声音模拟前列腺尿道提升术。主要终点是 3 个月时 IPSS 评分的降低。前列腺尿道提升术组的受试者随访至 1 年,并评估下尿路症状、最大尿流率、生活质量和性功能。

结果

共 206 名男性被随机分为前列腺尿道提升术组(140 例)和假手术组(66 例)。前列腺尿道提升术组和假手术组的 IPSS 评分分别降低了 11.1±7.67 和 5.9±7.66(p=0.003),达到了主要终点。前列腺尿道提升术组患者的 IPSS 评分从基线时的 22.1 降至 2 周时的 18.0、3 个月时的 11.0 和 12 个月时的 11.1,均显著降低(p<0.001)。最大尿流率在 3 个月时增加了 4.4ml/秒,并在 12 个月时持续增加到 4.0ml/秒(p<0.001)。不良事件通常为轻度和短暂的。没有新发的射精或勃起功能障碍。

结论

在局部麻醉下可靠地进行前列腺尿道提升术,可快速、持续地改善症状和尿流,并保留性功能。

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