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罗斯蒂吊带术:一种用于女性尿失禁手术治疗的新型、微创、无张力技术——首批217例患者

The Rosti sling: a new, minimally invasive, tension-free technique for the surgical treatment of female urinary incontinence-the first 217 patients.

作者信息

Laurikainen E, Rosti J, Pitkänen Y, Kiilholma P

机构信息

Department of Obstetrics and Gynecology, Turku University Hospital, Turku and Salo Local Hospital, Salo, Finland.

出版信息

J Urol. 2004 Apr;171(4):1576-80; discussion 1580. doi: 10.1097/01.ju.0000118050.97487.cd.

Abstract

PURPOSE

We evaluated the outcome of a new, innovative, inexpensive tension-free technique, the Rosti sling (RS), for female urinary incontinence.

MATERIALS AND METHODS

RS was performed in 217 patients under local (45%), spinal (52%) or general (3%) anesthesia. A 1.5 x 33 cm strip of polypropylene mesh was inserted under the mid urethra from above through small suprapubic stabs down and out through a 1.5 cm midline vaginal incision using the Stamey needle. Of the women 76% had stress urinary incontinence and 24% had mixed incontinence. Patient age was 24 to 90 years (mean 56) and parity was 0 to 6 (mean 2). The diagnosis of incontinence was based on history and physical examinations with a cough stress test. Mean followup was 23 months.

RESULTS

Mean operative time was 25 minutes (range 15 to 45) and mean hospital stay was 3 days (range 1 to 12). Perioperative complications were bladder and urethral perforations in 2 and 1 cases, respectively (1.4%), and hematoma in 3 (1.4%). There was postoperative retention with a variable duration in 49 patients (23%), of whom 41 underwent Hegar dilation. Altogether 186 of 215 patients (86.5%) were cured of incontinence. Two patients were lost to followup and 14 (16.3%) had de novo urge incontinence. The cure rates were 87% for stress urinary incontinence and 91% for mixed incontinence. The cure rate in patients treated under local and spinal anesthesia were 82% and 91%, respectively (p = 0.1084). The rates for RS with recurrent vs primary incontinence were 84% vs 87% (p = 0.5800) and for RS with vs without Hegar dilation 80% vs 88% (p = 0.2094).

CONCLUSIONS

The technique described is simple, safe and inexpensive. The cure rates are comparable to those of tension-free vaginal tape. However, because of the relatively high rate of postoperative voiding difficulties compared to tension-free vaginal tape, this technique can be criticized. To avoid these problems special attention should be focused on applying the mesh without tension and with precision.

摘要

目的

我们评估了一种新型、创新、低成本的无张力技术——罗斯蒂吊带(RS)治疗女性尿失禁的效果。

材料与方法

217例患者在局部麻醉(45%)、脊髓麻醉(52%)或全身麻醉(3%)下接受RS手术。使用斯塔梅针,将一条1.5×33厘米的聚丙烯网带从上方经耻骨上小切口插入尿道中段下方,再经1.5厘米的阴道中线切口穿出。其中76%的女性患有压力性尿失禁,24%患有混合性尿失禁。患者年龄为24至90岁(平均56岁),产次为0至6次(平均2次)。尿失禁的诊断基于病史、体格检查及咳嗽压力试验。平均随访时间为23个月。

结果

平均手术时间为25分钟(范围15至45分钟),平均住院时间为3天(范围1至12天)。围手术期并发症包括膀胱穿孔2例、尿道穿孔1例(1.4%)、血肿3例(1.4%)。49例患者(23%)术后出现不同持续时间的尿潴留,其中41例接受了黑加扩张术。215例患者中共有186例(86.5%)尿失禁治愈。2例患者失访,14例(16.3%)出现新发急迫性尿失禁。压力性尿失禁的治愈率为87%,混合性尿失禁的治愈率为91%。局部麻醉和脊髓麻醉下治疗的患者治愈率分别为82%和91%(p = 0.1084)。复发性尿失禁与原发性尿失禁患者接受RS手术的治愈率分别为84%和87%(p = 0.5800),接受黑加扩张术与未接受黑加扩张术的患者治愈率分别为80%和88%(p = 0.2094)。

结论

所描述的技术简单、安全且成本低。治愈率与无张力阴道吊带相当。然而,与无张力阴道吊带相比,术后排尿困难发生率相对较高,该技术可能受到批评。为避免这些问题,应特别注意无张力且精确地应用网带。

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