Servicio de Cirugía General y Aparato Digestivo, Hospital Nuestra Señora del Prado. Talavera de La Reina, Toledo, Spain.
Servicio de Cirugía General y Aparato Digestivo, Hospital Universitario de Guadalajara, Guadalajara, Castilla-La Mancha, Spain.
BMC Gastroenterol. 2024 Sep 30;24(1):334. doi: 10.1186/s12876-024-03428-z.
Botulinum toxin type A is currently strongly recommended for the treatment of anal fissures (AFs). However, there is still no consensus on dosage or injection technique. This study provides further efficacy and safety evidence in a 2-year follow-up.
Prospective, open-label, single-arm, single-center study carried out in adult patients with AFs non-responsive to previous treatments. Patients were treated with incobotulinumtoxinA (incoBoNT/A) injected in both laterals and posterior intersphincteric groove. Healing rate at 2 years was the primary endpoint. Secondary endpoints included internal anal sphincter pressures, incontinence, and safety.
A total of 49 patients were treated with a mean incoBoNT/A dose of 40.5 U (spread across three locations). Healing rate at 2 years was 83.9% with a 24.5% of recurrence throughout the study. Only 7 patients (14.3%) reported adverse events (AEs) that were mild and temporary. Mean reduction in anal resting pressure was -9.1 mmHg at 3 months (p = 0.001). Mean reduction in voluntary squeeze pressure was -27.5 mmHg at 3 months (p < 0.001). Mean pain perception measured with a visual analog scale decreased by -6.5 points at 2 years (p < 0.001). There was an incontinence increase at 1 month of 1.3 points (p = 0.006), but baseline values were restored at 6 months.
We present results that support the use of incoBoNT/A as a second line for AFs that do not respond to ointment therapy. IncoBoNT/A injection is a less invasive treatment that should be considered before surgery due to its efficacy and its safety which includes no permanent impairment.
ISRCTN90354265; Registered on 16th February 2024. Retrospectively registered.
肉毒毒素 A 目前强烈推荐用于治疗肛裂(AFs)。然而,在剂量或注射技术方面仍未达成共识。本研究在 2 年的随访中提供了进一步的疗效和安全性证据。
前瞻性、开放标签、单臂、单中心研究,在对既往治疗无反应的 AFs 成年患者中进行。患者接受 incobotulinumtoxinA(incoBoNT/A)注射治疗,注射部位为两侧和后中间括约肌沟。2 年时的愈合率为主要终点。次要终点包括内括约肌压力、失禁和安全性。
共有 49 名患者接受了平均 40.5 U 的 incoBoNT/A 剂量(分布在三个部位)治疗。2 年时的愈合率为 83.9%,整个研究期间的复发率为 24.5%。只有 7 名患者(14.3%)报告了轻微且短暂的不良事件(AE)。3 个月时,肛门静息压力平均降低 9.1 mmHg(p = 0.001)。3 个月时,自愿收缩压力平均降低 27.5 mmHg(p<0.001)。2 年时,视觉模拟量表测量的疼痛感知平均降低 6.5 分(p<0.001)。1 个月时失禁增加了 1.3 分(p = 0.006),但在 6 个月时恢复到基线水平。
我们提供的结果支持将 incoBoNT/A 用作对软膏治疗无反应的 AFs 的二线治疗。与手术相比,incoBoNT/A 注射是一种侵入性较小的治疗方法,由于其疗效和安全性,包括无永久性损伤,应在手术前考虑。
ISRCTN90354265;于 2024 年 2 月 16 日注册。回顾性注册。