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使用葡聚糖凝胶透明质酸进行黏膜下注射治疗大便失禁的生活质量和功能结果

Quality of life and functional results of submucosal injection therapy using dextranomer hyaluronic acid for fecal incontinence.

作者信息

Schwandner Oliver, Brunner Marion, Dietl Otto

机构信息

Caritas-Krankenhaus St. Josef, Regensburg, Germany.

出版信息

Surg Innov. 2011 Jun;18(2):130-5. doi: 10.1177/1553350610392243. Epub 2011 Jan 18.

Abstract

BACKGROUND AND AIM

The aim of this prospective study was to analyze safety and functional outcome of transanal submucosal injection of dextranomer hyaluronic acid ("bulking agents therapy") in patients with passive fecal incontinence.

METHODS

All patients who underwent transanal injection therapy were prospectively enrolled in this study. Inclusion criteria included fecal incontinence (internal anal sphincter dysfunction) after failed conservative treatment. The procedure was performed in a standardized technique, including submucosal injection of 4 × 1 mL dextranomer hyaluronic acid 5 mm above the dentate line. The primary endpoint focused on symptom improvement provided as the change in incontinence status and quality of life using validated scores (Wexner incontinence score, symptom-specific Fecal Incontinence Quality of Life [FIQoL] scale, and generic EQ-5D-Visual Analogue Scale [EQ-5D-VAS]).

RESULTS

Within the observation period (July 2007 to May 2009), a total of 21 patients (17 women) with passive fecal incontinence were treated. Neither morbidity nor adverse events were documented. Three months postoperatively, 61.1% (11/18) showed significant improvement of symptoms (reduction of incontinence episodes and soiling), which was sustained after 20 months in 55.6% (10/18). Wexner incontinence score decreased from 16.8 to 12.3 (P > .05). Significant improvement was documented for FIQoL and EQ-5D-VAS (P < .05).

CONCLUSION

The current results indicate that injection therapy using hyaluronic acid is an innovative and minimally invasive procedure with no morbidity. Although Wexner incontinence score is not significantly influenced, a significant improvement in quality of life was observed in more than 50% of patients.

摘要

背景与目的

本前瞻性研究旨在分析经肛门黏膜下注射葡聚糖醛酸透明质酸(“填充剂疗法”)治疗被动性大便失禁患者的安全性和功能结局。

方法

所有接受经肛门注射治疗的患者均前瞻性纳入本研究。纳入标准包括保守治疗失败后的大便失禁(肛门内括约肌功能障碍)。该操作采用标准化技术进行,包括在齿状线以上5 mm处黏膜下注射4×1 mL葡聚糖醛酸透明质酸。主要终点集中在症状改善情况,通过使用经过验证的评分(韦克斯纳失禁评分、症状特异性大便失禁生活质量[FIQoL]量表和通用的EQ-5D视觉模拟量表[EQ-5D-VAS])来评估失禁状态和生活质量的变化。

结果

在观察期(2007年7月至2009年5月)内,共治疗了21例被动性大便失禁患者(17例女性)。未记录到发病率或不良事件。术后3个月,61.1%(11/18)的患者症状有显著改善(失禁发作次数和粪便污染减少),20个月后仍有55.6%(10/18)的患者维持改善。韦克斯纳失禁评分从16.8降至12.3(P>.05)。FIQoL和EQ-5D-VAS有显著改善(P<.05)。

结论

目前的结果表明,使用透明质酸的注射疗法是一种创新的微创方法,无发病率。虽然韦克斯纳失禁评分未受到显著影响,但超过50%的患者生活质量有显著改善。

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