Keshtgar A S, Rickwood A M
Department of Urology, Alder Hey Children's Hospital, Liverpool, UK.
Br J Urol. 1998 Aug;82(2):258-60. doi: 10.1046/j.1464-410x.1998.00721.x.
To determine the urological consequences of incomplete cord lesions in patients with myelomeningocele and a neuropathic bladder.
From a total of 407 patients with myelomeningocele and a neuropathic bladder, 31 (8%) were identified as having a combination of sacral sensory or motor sparing and positive conus reflexes. Their case-notes were reviewed with reference to spinal neurology, patterns of micturition, including the degree of spontaneous continence, findings on imaging and urodynamic studies, and forms and outcomes of any treatment given.
The anatomical distribution of the lesions was thoracic (two), thoracolumbar (three), lumbar (six), lumbosacral (four) and sacral (11). The mean age at presentation was 9.5 years (range 3.5-19.5) and the mean follow-up 4.5 years (range 0.5-10.5). At presentation, 14 patients had urinary incontinent episodes both day and night, 10 by day only, seven by night only, and the upper urinary tracts were dilated in eight (26%). Nineteen were ambulant unaided and 10 with aid of crutches or calipers, whilst two were wheelchair-bound. Only one patient had faecal incontinence. A urodynamic examination in 18 patients showed competent sphincteric mechanism and detrusor hyper-reflexia in all, and detrusor sphincter dyssynergia in 11. The methods of treatment included oxybutynin and/or clean intermittent catheterization alone or in combination. Thirty patients are currently reliably dry by day and 26 also by night. Five patients have undergone surgical treatment for vesico-ureteric reflux, three a Mitrofanoff procedure and two augmentation cystoplasty.
Although patients with congenital incomplete cord lesions and positive conus reflexes may gain some measure or urinary continence spontaneously, they are at serious risk of developing upper urinary tract complications. The treatment of urinary continence is simple and effective because there is a competent sphincter mechanism. These patients require life-long supervision even if they require no treatment for urinary incontinence.
确定脊髓脊膜膨出合并神经源性膀胱患者不完全性脊髓损伤的泌尿系统后果。
在总共407例脊髓脊膜膨出合并神经源性膀胱的患者中,31例(8%)被确定为存在骶部感觉或运动保留以及阳性圆锥反射。参照脊髓神经学、排尿模式(包括自主控尿程度)、影像学和尿动力学检查结果以及所给予的任何治疗的形式和结果,对他们的病历进行了回顾。
病变的解剖分布为胸段(2例)、胸腰段(3例)、腰段(6例)、腰骶段(4例)和骶段(11例)。就诊时的平均年龄为9.5岁(范围3.5 - 19.5岁),平均随访时间为4.5年(范围0.5 - 10.5年)。就诊时,14例患者日夜均有尿失禁发作,10例仅日间有尿失禁,7例仅夜间有尿失禁,8例(26%)上尿路扩张。19例患者无需辅助可独立行走,10例借助拐杖或支具行走,2例需坐轮椅。仅1例患者有大便失禁。18例患者的尿动力学检查显示,所有患者的括约肌功能正常且逼尿肌反射亢进,11例存在逼尿肌括约肌协同失调。治疗方法包括单独或联合使用奥昔布宁和/或清洁间歇性导尿。目前,30例患者日间可靠控尿,26例患者夜间也可靠控尿。5例患者因膀胱输尿管反流接受了手术治疗,3例行米氏术,2例行膀胱扩大术。
尽管先天性不完全性脊髓损伤且有阳性圆锥反射的患者可能会自发获得一定程度的尿失禁,但他们发生上尿路并发症的风险很高。由于括约肌功能正常,尿失禁的治疗简单有效。即使这些患者无需治疗尿失禁,也需要终身监护。