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治疗粪便失禁的注射性填充剂 2 年后的疗效和生活质量。

Efficacy and quality of life 2 years after treatment for faecal incontinence with injectable bulking agents.

机构信息

Institution of Surgical Sciences, Uppsala University, Uppsala, Sweden.

出版信息

Tech Coloproctol. 2013 Aug;17(4):389-95. doi: 10.1007/s10151-012-0949-8. Epub 2012 Dec 7.

DOI:10.1007/s10151-012-0949-8
PMID:23224913
Abstract

BACKGROUND

Stabilized non-animal hyaluronic acid/dextranomer (NASHA Dx) gel as injectable bulking therapy has been shown to decrease symptoms of faecal incontinence, but the durability of treatment and effects and influence on quality of life (QoL) is not known. The aim of this study was to assess the effects on continence and QoL and to evaluate the relationship between QoL and efficacy up to 2 years after treatment.

METHODS

Thirty-four patients (5 males, mean age 61, range 34-80) were injected with 4 × 1 ml NASHA Dx in the submucosal layer. The patients were followed for 2 years with registration of incontinence episodes, bowel function and QoL questionnaires.

RESULTS

Twenty-six patients reported sustained improvement after 24 months. The median number of incontinence episodes before treatment was 22 and decreased to 10 at 12 months (P = 0.0004) and to 7 at 24 months (P = 0.0026). The corresponding Miller incontinence scores were 14, 11 (P = 0.0078) and 10.5 (P = 0.0003), respectively. There was a clear correlation between the decrease in the number of leak episodes and the increase in the SF-36 Physical Function score but only patients with more than 75 % improvement in the number of incontinence episodes had a significant improvement in QoL at 24 months.

CONCLUSIONS

Anorectal injection of NASHA Dx gel induces improvement of incontinence symptoms for at least 2 years. The treatment has a potential to improve QoL. A 75 % decrease in incontinence episodes may be a more accurate threshold to indicate a successful incontinence treatment than the more commonly used 50 %.

摘要

背景

稳定型非动物源透明质酸/葡聚糖(NASHA Dx)凝胶作为注射性填充疗法,已被证明可减轻粪便失禁的症状,但治疗的持久性、疗效以及对生活质量(QoL)的影响尚不清楚。本研究旨在评估对控便能力和 QoL 的影响,并评估治疗 2 年后 QoL 与疗效之间的关系。

方法

34 例患者(5 例男性,平均年龄 61 岁,范围 34-80 岁)接受了 4×1ml NASHA Dx 在黏膜下层的注射。患者接受了 2 年的随访,记录失禁发作次数、肠道功能和 QoL 问卷。

结果

26 例患者在 24 个月后报告了持续改善。治疗前失禁发作次数的中位数为 22 次,治疗 12 个月时降至 10 次(P=0.0004),24 个月时降至 7 次(P=0.0026)。相应的米勒失禁评分分别为 14、11(P=0.0078)和 10.5(P=0.0003)。失禁漏出次数的减少与 SF-36 生理功能评分的增加之间存在明显的相关性,但只有失禁发作次数减少超过 75%的患者在 24 个月时 QoL 才有显著改善。

结论

直肠内注射 NASHA Dx 凝胶可至少改善失禁症状 2 年。该治疗有改善 QoL 的潜力。失禁发作次数减少 75%可能比更常用的 50%更能准确地表明失禁治疗成功。

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