Department of Colorectal and Pelvic Surgery, Rome University, Rome, Italy.
Colorectal Dis. 2013 May;15(5):569-74. doi: 10.1111/codi.12155.
Randomized, controlled trials have demonstrated the efficacy and safety of injectable bulking agents for the treatment of faecal incontinence (FI), although the long-term outcome has not been assessed. NASHA/Dx gel, a biocompatible, nonallergenic bulking agent consisting of nonanimal stabilized hyaluronic acid and dextranomer microspheres, has demonstrated efficacy and safety for up to 12 months after treatment. The objective of this study was to evaluate the long-term efficacy and safety of NASHA/Dx, assessed 24 months after treatment.
This study was a 24-month follow-up assessment of patients treated with NASHA/Dx under open-label conditions. Data on FI episodes and quality of life measures were collected from diaries over the 28-day period immediately preceding the 24-month assessment. Adverse events were collected.
Eighty-three of 115 patients completed the 24-month follow-up assessment. At 24 months, 62.7% of patients were considered responders and experienced a ≥ 50% reduction in the total number of FI episodes. The median number of FI episodes declined by 68.8% (P < 0.001). Episodes of both solid and liquid stool incontinence decreased. The mean number of incontinence-free days increased from 14.6 at baseline to 21.7 at 24 months (P < 0.001). Incontinence scores and FI quality of life scores also showed significant improvements. The most common adverse events (AEs) were proctalgia (13.3%) and pyrexia (9.6%). The majority of AEs were mild to moderate, self-limited and resolved within 1 month of the injection.
NASHA/Dx is safe, effective and durable over a 24-month period with a majority of patients experiencing significant improvement in multiple symptoms associated with FI.
随机对照试验已经证明了注射性填充剂治疗粪便失禁(FI)的疗效和安全性,尽管尚未评估其长期效果。NASHA/Dx 凝胶是一种由非动物稳定透明质酸和葡聚糖微球组成的生物相容性、无致敏性填充剂,在治疗后长达 12 个月内显示出疗效和安全性。本研究的目的是评估 NASHA/Dx 的长期疗效和安全性,在治疗后 24 个月进行评估。
这是一项对接受 NASHA/Dx 开放性治疗的患者进行的 24 个月随访评估。在 24 个月评估前的 28 天内,通过日记收集 FI 发作和生活质量测量数据。收集不良事件。
115 例患者中有 83 例完成了 24 个月的随访评估。24 个月时,62.7%的患者被认为是应答者,FI 总发作次数减少≥50%。FI 发作次数中位数下降了 68.8%(P < 0.001)。固体和液体粪便失禁发作均减少。无失禁天数的平均值从基线时的 14.6 天增加到 24 个月时的 21.7 天(P < 0.001)。失禁评分和 FI 生活质量评分也显著改善。最常见的不良事件(AE)是直肠痛(13.3%)和发热(9.6%)。大多数 AE 为轻度至中度,自限性,且在注射后 1 个月内得到解决。
NASHA/Dx 在 24 个月的时间内是安全、有效且持久的,大多数患者的 FI 相关多种症状均有显著改善。