Department of Surgical Sciences, Uppsala University Hospital, 751 85, Uppsala, Sweden.
Department of Women's and Children's Health, Uppsala University Hospital, 751 85, Uppsala, Sweden.
Tech Coloproctol. 2022 Oct;26(10):813-820. doi: 10.1007/s10151-022-02645-6. Epub 2022 Jun 26.
The bulking agent NASHA Dx injected into the submucosal layer is effective in the treatment of fecal incontinence (FI) at short-and medium-term follow-up but efficacy after injection in the intersphincteric location is unknown. The aim of this study was to determine the short- and long-term efficacy and safety of NASHA Dx injected into the intersphincteric location for FI.
Patients were recruited from referrals to our Department for treatment of FI in November 2008-January 2010. Eligible patients were injected with 8 ml of NASHA Dx. Patients with a subtotal treatment effect were retreated after 2-4 weeks. The change in number of fecal incontinence episodes, the proportion of responders defined as at least 50% decrease in number of FI episodes and side effects were the main outcome measures.
Sixteen patients, 15 women and 1 man with a median age of 68, 5 (range 44-80) years and a median CCFIS of 15 (range 10-19) were included in the study. The median number of incontinence episodes decreased from 21.5 (range 8-61) at baseline to 10 (range 0-30) at 6 months (p = 0.003) and 6 (range 0-44) at 12 months (p = 0.05). The median number of incontinence episodes in the 11 patients completing the 10-year follow-up was 26.5 (range 0-68). The percentage of responders at 12 months and 10 years were 56% and 27%, respectively. Mild to moderate pain at the injection site was described by 69%. There was one case of mild infection, successfully treated with antibiotics and one implant had to be removed due to dislocation.
NASHA Dx as an intersphincteric implant improves incontinence symptoms in the short term with moderate side effects and can be used alone or as an adjunct to other treatment modalities. Long-term efficacy was observed in 27%.
NASHA Dx 填充剂注入黏膜下层在短期和中期随访中对治疗粪便失禁(FI)有效,但在注射到肛门括约肌间位置的疗效尚不清楚。本研究的目的是确定 NASHA Dx 注射到肛门括约肌间位置治疗 FI 的短期和长期疗效和安全性。
2008 年 11 月至 2010 年 1 月,我们从转介到我科治疗 FI 的患者中招募了患者。符合条件的患者接受了 8ml 的 NASHA Dx 注射。对于治疗效果不完全的患者,在 2-4 周后进行再次治疗。主要观察指标为粪便失禁发作次数的变化、定义为粪便失禁发作次数至少减少 50%的患者比例和不良反应。
本研究纳入了 16 名患者,其中 15 名女性和 1 名男性,年龄中位数为 68 岁(范围 44-80 岁),CCFIS 中位数为 15 分(范围 10-19 分)。失禁发作次数中位数从基线时的 21.5 次(范围 8-61 次)减少到 6 个月时的 10 次(范围 0-30 次)(p=0.003)和 12 个月时的 6 次(范围 0-44 次)(p=0.05)。11 名完成 10 年随访的患者的失禁发作次数中位数为 26.5 次(范围 0-68 次)。12 个月和 10 年时的应答率分别为 56%和 27%。69%的患者描述注射部位有轻到中度疼痛。有 1 例轻度感染,经抗生素治疗成功,1 例因脱位而取出植入物。
NASHA Dx 作为一种肛门括约肌间植入物可在短期内改善失禁症状,具有中度不良反应,可单独使用或作为其他治疗方式的辅助手段。在 27%的患者中观察到长期疗效。