首页> 中文期刊> 《世界核心医学期刊文摘:胃肠病学分册》 >可曲电子内镜下痔的胶圈套扎术:与传统直管直肠镜下该技术的前瞻性随机对照研究

可曲电子内镜下痔的胶圈套扎术:与传统直管直肠镜下该技术的前瞻性随机对照研究

         

摘要

cqvip:Background Elastic band ligation by means of a rigid proctoscope is the treatment of choice for patients with symptoms caused by internal hemorrhoids of grade 2 to 3. In contrast to the flexible videoendoscope, the rigid proctoscope has limited maneuverability, has a narrower field of view, and does not allow adequate documentation. Therefore, a randomized trial was conducted to compare the safety and the efficacy of conventional elastic band ligation with videoendoscopic elastic band ligation. Methods A total of 100 consecutive patients(mean age 47 12 years) with chronically bleeding grade 2 or 3 internal hemorrhoids were randomized to elastic band ligation or videoendoscopic elastic band ligation. For videoendoscopic elastic band ligation, a reusable multiband ligator was attached to the end of a therapeutic upper videoendoscope. From one to 3 bands were placed per session in both groups. Re-treatment was performed every 2 to 3 weeks in both groups until cessation of bleeding and eradication of the hemorrhoids (at least grade 2) were achieved. Thereafter, the patients were followed to assess complications and efficacy. Recurrent bleeding was considered a treatment failure. Results To achieve the desired therapeutic aims, a significantly lower number of treatment sessions was required in the videoendoscopic elastic band ligation group (1.8 0.8 vs. 2.4 0.9; p < 0.01) and the total number of bands applied was significantly less (2.8 1.1 vs. 3.7 1.4; p< 0.01). Pain was noted after ligation by 25% of patients in the elastic band ligation group compared with 27% of those who had videoendoscopic elastic band ligation. However, analgesic medications were required in only 7% after elastic band ligation and 9% after videoendoscopic elastic band ligation (NS). Postligation bleeding that had to be treated endoscopically occurred in 3.5% of the patients of the elastic band ligation group and 3.2% of those in the videoendoscopic elastic band ligation group(NS). Blood transfusion was not required. At a median followup of 12 months, there was no recurrence of bleeding in 40 patients (80% ) in the conventional elastic band ligation group vs. 43 (86% ) in the videoendoscopic elastic band ligation (NS).Conclusions The long-term efficacy and safety of conventional elastic band ligation and videoendoscopic elastic band ligation are highly comparable. However, when videoendoscopic elastic band ligation is performed, significantly fewer treatment sessions are required.

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