Department of Urology, Mayo Clinic Graduate School of Medicine, Rochester, Minnesota 55905, USA.
Urology. 2010 Jun;75(6):1310-4. doi: 10.1016/j.urology.2009.12.061. Epub 2010 Mar 17.
To determine whether dextranomer/hyaluronic acid would be more efficacious or would produce fewer complications when using the material in a standard proximal-urethra cystoscopically-directed injection technique. Injectable periurethral bulking agents are an alternative to stress incontinence surgery. Dextranomer, a highly hydrophilic dextran polymer, solubilized in a base of nonanimal stabilized hyaluronic acid, has been approved as an injectable agent for the treatment of childhood vesicoureteric reflux (Deflux, Q-Med AB, Uppsala, Sweden), and in Europe for women with stress urinary incontinence (SUI) (Zuidex, Q-Med AB, Uppsala, Sweden). A previous multicenter trial demonstrated nonequivalence compared with bovine glutaraldehyde cross-linked collagen with a high complication rate. We sought to determine whether the failure of the treatment lay in the material itself or the use of a blind, midurethral injection technique.
A retrospective case series of 56 patients undergoing cystoscopically guided bladder neck injections of dextranomer/hyaluronic acid with follow-up in 42, included 35 women with intrinsic sphincter deficiency (ISD), 4 men with postprostatectomy incontinence, 2 men with sphincteric denervation secondary to spinal cord injury, and 1 woman with sphincteric failure after a neobladder. Outcome assessment used gender-appropriate International Consultation on Incontinence Questionnaire, clinical records, and/or urodynamic assessment.
Of 35 women with ISD, 4 developed pseudoabscess formation with outlet obstruction requiring multiple operative interventions. Patient-defined treatment failure occurred in all 4 carefully selected postprostatectomy incontinent men, and in 23 of 35 females with ISD.
Complications with cystoscopically injected dextranomer hyaluronic acid at the bladder neck occurred at a high rate, and using a validated questionnaire, the efficacy of dextranomer hyaluronic acid applied in this manner for ISD was poor.
确定在使用标准近端尿道膀胱镜引导注射技术时,葡聚糖/透明质酸是否更有效或产生更少的并发症。可注射尿道周围填充剂是治疗压力性尿失禁的一种替代手术方法。葡聚糖,一种高度亲水性葡聚糖聚合物,溶解在非动物稳定透明质酸的基础中,已被批准为治疗儿童膀胱输尿管反流(Deflux,Q-Med AB,Uppsala,瑞典)的注射剂,在欧洲用于治疗压力性尿失禁(SUI)的女性(Zuidex,Q-Med AB,Uppsala,瑞典)。先前的多中心试验表明,与牛戊二醛交联胶原相比,其等效性较低,且并发症发生率较高。我们试图确定治疗失败是由于材料本身还是使用盲目、中尿道注射技术。
对 56 例接受膀胱镜引导下葡聚糖/透明质酸膀胱颈注射治疗的患者进行回顾性病例系列研究,其中 42 例患者得到随访,包括 35 例固有括约肌缺陷(ISD)女性、4 例前列腺切除术后尿失禁男性、2 例脊髓损伤继发括约肌去神经男性和 1 例新膀胱后括约肌失败女性。结局评估采用性别适宜的国际尿失禁咨询问卷、临床记录和/或尿动力学评估。
在 35 例 ISD 女性中,有 4 例出现假性脓肿形成并伴有出口梗阻,需要多次手术干预。在 4 例精心选择的前列腺切除术后尿失禁男性和 35 例 ISD 女性中的 23 例中,均发生了患者定义的治疗失败。
膀胱镜下注射葡聚糖透明质酸在膀胱颈部的并发症发生率较高,并且使用经过验证的问卷,以这种方式应用于 ISD 的葡聚糖透明质酸的疗效较差。