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原发性神经性大便失禁中的联合感觉和运动功能障碍

Combined sensory and motor deficit in primary neuropathic faecal incontinence.

作者信息

Rogers J, Henry M M, Misiewicz J J

机构信息

Department of Gastroenterology and Nutrition, Central Middlesex Hospital, London.

出版信息

Gut. 1988 Jan;29(1):5-9. doi: 10.1136/gut.29.1.5.

Abstract

Eleven patients with idiopathic faecal incontinence (IFI) and nine normal controls were studied with techniques of mucosal electrosensitivity and rectal distention for the quantitative assessment of anal and rectal sensation and with manometric and electromyographic tests for the assessment of anorectal motor function. The tests of motor function showed pelvic floor motor neuropathy in the patients with IFI, compared with controls, anal canal resting and voluntary contraction pressures were significantly (p less than 0.05, p less than 0.002) lower, pudendal nerve terminal motor latency and external anal sphincter fibre density were significantly (p less than 0.05, p less than 0.05) raised. The results of mucosal electrosensitivity (MES) disclosed a sensory deficit in the anal canal in patients with IFI, compared with controls, MES threshold was significantly (p less than 0.002) higher. Sensory thresholds to rectal distension were similar in the two groups. This study shows that sensory deficit of the anal canal occurs in combination with the motor neuropathy of the anal canal musculature in primary neuropathic faecal incontinence.

摘要

对11例特发性大便失禁(IFI)患者和9名正常对照者进行了研究,采用黏膜电敏感性和直肠扩张技术定量评估肛门和直肠感觉,采用测压和肌电图测试评估肛门直肠运动功能。运动功能测试显示,IFI患者存在盆底运动神经病变,与对照组相比,肛管静息压和随意收缩压显著降低(p<0.05,p<0.002),阴部神经终末运动潜伏期和肛门外括约肌纤维密度显著升高(p<0.05,p<0.05)。黏膜电敏感性(MES)结果显示,与对照组相比,IFI患者肛管存在感觉缺陷,MES阈值显著更高(p<0.002)。两组对直肠扩张的感觉阈值相似。本研究表明,在原发性神经性大便失禁中,肛管感觉缺陷与肛管肌肉组织的运动神经病变同时存在。

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