Laurikainen E, Rosti J, Pitkänen Y, Kiilholma P
Department of Obstetrics and Gynecology, Turku University Hospital, Turku and Salo Local Hospital, Salo, Finland.
J Urol. 2004 Apr;171(4):1576-80; discussion 1580. doi: 10.1097/01.ju.0000118050.97487.cd.
We evaluated the outcome of a new, innovative, inexpensive tension-free technique, the Rosti sling (RS), for female urinary incontinence.
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.
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).
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.
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。
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。
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)。
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。