Gastroenterology and Hepatology, Veterans Affairs Medical Center, USA; Gastroenterology and Hepatology, University of Kansas Medical Center, USA.
Gastroenterology, Loyola University, USA.
United European Gastroenterol J. 2016 Apr;4(2):236-41. doi: 10.1177/2050640615594549. Epub 2015 Jul 3.
The safety and efficacy of radiofrequency ablation (RFA) in treatment of Barrett's esophagus (BE)-associated dysplasia has been well established. The effectiveness of focal and balloon RFA devices has not been compared. Therefore, the aim of our study was to assess the effectiveness of focal and balloon RFA devices in the treatment of BE by calculating absolute and percentage change in BE length with RFA therapy by comparing pre- and post-treatment BE length.
This is a retrospective cross-sectional study of patients who underwent at least one treatment with either focal and/or balloon RFA devices who were identified from two tertiary centers. Patients' demographics, hiatal hernia, pre- and post-treatment BE length, prior use of endoscopic therapies and number of sessions were recorded.
Sixty-one patients who had undergone 161 RFA treatment sessions met inclusion criteria. There was no significant difference in percentage change in BE length with greater number of RFA sessions. RFA with a focal device resulted in greater percentage reduction in BE length compared to the balloon system (73% vs. 39%, p < 0.01). After adjusting for initial BE length, pre-treatment BE length, hernia status, prior endoscopic mucosal resection (EMR), prior RFA, and prior EMR/RFA sessions, RFA with a focal device at each session remained an independent predictor for a significant reduction in BE extent as compared to the balloon system.
The focal RFA device alone was more effective in treatment of BE compared to the balloon system, with a greater reduction in extent of BE. The focal RFA device for endoscopic eradication therapy of BE should be considered the preferred technique.
射频消融(RFA)治疗 Barrett 食管(BE)相关异型增生的安全性和有效性已得到充分证实。目前尚未比较点状和球囊 RFA 设备的疗效。因此,我们的研究旨在通过比较治疗前后 BE 长度来评估点状和球囊 RFA 设备在 BE 治疗中的有效性,计算 RFA 治疗后 BE 长度的绝对和百分比变化。
这是一项回顾性的病例系列研究,纳入了从两个三级中心中筛选出的至少接受过一次点状和/或球囊 RFA 治疗的患者。记录了患者的人口统计学资料、食管裂孔疝、治疗前后 BE 长度、既往内镜治疗史和治疗次数。
61 例患者共接受了 161 次 RFA 治疗,符合纳入标准。RFA 治疗次数与 BE 长度的百分比变化无显著差异。与球囊系统相比,点状 RFA 设备可使 BE 长度的百分比减少更大(73%对 39%,p<0.01)。在校正初始 BE 长度、治疗前 BE 长度、疝状态、既往内镜黏膜切除术(EMR)、既往 RFA 和既往 EMR/RFA 治疗次数后,每次 RFA 治疗时使用点状设备仍然是 BE 范围显著减少的独立预测因素,与球囊系统相比。
与球囊系统相比,点状 RFA 设备单独治疗 BE 更有效,可更大程度地减少 BE 范围。点状 RFA 设备应被视为 BE 内镜根除治疗的首选技术。