Efficacy and safety of a novel technique using endoscopic ultrasound—guided fine-needle injection of botulinum toxin and balloon dilation in achalasia

iGIE Pub Date : 2026-09-01 Epub Date: 2025-10-18 DOI:10.1016/j.igie.2025.10.014
Aqsa Khan MD, Harishankar Gopakumar MD, Ricardo J. Marrero Torres MD, Ahmad Abulawi MD, Talia Malik MD, Dushyant Singh Dahiya MD, Mariajose Rojas DeLeon MD, Amelia Roebuck PhD, Neil R. Sharma MD
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Abstract

Background and Aims

Achalasia is an esophageal motility disorder characterized by the inability of the lower esophageal sphincter to relax. Endoscopic methods are currently the mainstay treatment of achalasia and include local administration of botulinum toxin (Botox; Allergan Aesthetics, Westport, Ireland), pneumatic dilation, and peroral endoscopic myotomy. Botox injections traditionally have been performed by standard endoscopy, which lacks precision requiring frequent interventions. Our study introduces a novel technique using endoscopic ultrasound—guided fine-needle injection of Botox combined with controlled radial expansion balloon dilation (EUS-BTID) for treating achalasia. We hypothesize that this combined approach will enhance the efficacy and offer a favorable safety profile compared with standard endoscopic Botox injection.

Methods

We conducted a single-center retrospective study to evaluate the efficacy and safety of a novel technique using EUS-BTID to treat achalasia using electronic medical records.

Results

Our study included a total of 43 patients, with a mean age of 76 years (standard deviation 14 years). The most frequent achalasia subtype was type II (46%). Among 16 patients (37.2%) who underwent multiple sessions of EUS-BTID, the number of sessions ranged from 2 to 14, with the 14-session maximum occurring in a single patient. The average interval between repeat procedures across all patients was 273 days. The primary outcome of improved dysphagia scores, measured by the Eckardt score, was observed in 86.7% of patients, with 70.0% achieving scores indicative of complete remission. After EUS-BTID, the median Eckhardt score significantly improved from 6 (interquartile range, 4-7) to 2 (interquartile range, 1-4) (P < .0001). No serious adverse events were reported; only 2 patients (4.6%) experienced mild transient postprocedural symptoms, including chest discomfort and emesis.

Conclusion

The novel EUS-BTID technique appears to be an effective and safe treatment option for achalasia. The combination of endoscopic ultrasound—guided Botox injection and balloon dilation offers significant improvements in symptom relief with a favorable safety profile and durability and can be applied in high-risk patients or probably as a bridge to more definitive therapy. Although our study provides encouraging evidence supporting the use of EUS-BTID, further research is required to validate these findings.
超声引导下细针注射肉毒杆菌毒素和球囊扩张治疗贲门失弛缓症的疗效和安全性
背景和目的贲门失弛缓症是一种以食管下括约肌不能放松为特征的食道运动障碍。内窥镜方法是目前贲门失弛缓症的主要治疗方法,包括局部给药肉毒杆菌毒素(Botox; Allergan Aesthetics, Westport, Ireland)、气动扩张和经口内窥镜肌切开术。传统上,肉毒杆菌注射是通过标准的内窥镜检查进行的,缺乏精确性,需要经常干预。本研究介绍了超声引导下细针注射肉毒杆菌联合可控径向扩张球囊扩张(EUS-BTID)治疗贲门失弛弛症的新技术。我们假设,与标准的内窥镜注射肉毒杆菌相比,这种联合方法将提高疗效并提供良好的安全性。方法采用单中心回顾性研究,评价EUS-BTID电子病历治疗贲门失弛缓症的有效性和安全性。结果本研究共纳入43例患者,平均年龄76岁(标准差14岁)。最常见的失弛缓症亚型为II型(46%)。在16例(37.2%)接受多次EUS-BTID治疗的患者中,治疗次数从2到14次不等,单个患者最多发生14次。所有患者重复手术的平均间隔为273天。以Eckardt评分衡量的吞咽困难评分改善的主要结局在86.7%的患者中观察到,70.0%的患者达到完全缓解的评分。EUS-BTID后,Eckhardt评分中位数从6分(四分位范围4-7分)显著提高到2分(四分位范围1-4分)(P < .0001)。无严重不良事件报告;只有2例患者(4.6%)出现轻微的一过性术后症状,包括胸部不适和呕吐。结论新型EUS-BTID技术是治疗贲门失弛缓症的一种安全有效的方法。超声内镜引导下的肉毒杆菌注射和球囊扩张的结合在症状缓解方面有显著的改善,具有良好的安全性和持久性,可以应用于高风险患者或可能作为更明确治疗的桥梁。尽管我们的研究为EUS-BTID的使用提供了令人鼓舞的证据,但需要进一步的研究来验证这些发现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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