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首页> 外文期刊>Asian journal of surgery >Prospective randomized clinical trial on suction elastic band ligator versus forceps ligator in the treatment of haemorrhoids.
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Prospective randomized clinical trial on suction elastic band ligator versus forceps ligator in the treatment of haemorrhoids.

机译:抽吸弹性带结扎器与镊子结扎器治疗痔疮的前瞻性随机临床试验。

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摘要

OBJECTIVE: This prospective randomized clinical trial was undertaken to compare the use of a single-operator vacuum suction ligator and the traditional forceps ligator in terms of pain perception following the procedure, intra-procedure bleeding and other complications. METHODS: One hundred consecutive patients with second- and third-degree haemorrhoids presenting between July 2002 and September 2003 were randomized into suction and forceps groups for rubber band ligations. They were equally distributed in both groups, with a mean age of 48.7 years (range, 15-83 years). The immediate, 24-hour, 7-day and 14-day pain scores after the procedure were evaluated using a visual analogue scale. Intra-procedure bleeding and other complications at follow-up were evaluated. RESULTS: Pain perception was worse in the forceps group immediately after ligation, with a mean score of 6.08 compared with 3.08 in the suction group (p < 0.001). Pain score remained high among the forceps patients at 24 hours post-banding, with a mean score of 4.00 compared with 1.92 in the suction group (p < 0.001). There was no significant difference in terms of immediate and 24-hour pain perceptions whether two or three haemorrhoids were banded per session (p = 0.904 and p = 0.058). The amount of analgesia consumed after banding correlated well with the severity of pain reported, being higher among the forceps group with a mean of 4.48 tablets (p = 0.003). Intra-procedure bleeding occurred in 25 patients in the forceps group compared with five in the suction group (p < 0.001). There were no severe complications such as perianal sepsis, urinary retention, sphincter dysfunction or bleeding during the trial. CONCLUSION: Suction band ligation is superior to forceps ligation for the treatment of second- and third-degree haemorrhoids in terms of pain tolerance, amount of analgesia consumed and intra-procedure bleeding.
机译:目的:进行这项前瞻性随机临床试验,以比较单手术真空吸引结扎器和传统钳式结扎器在手术后的疼痛感,术中出血和其他并发症方面的使用。方法:将2002年7月至2003年9月之间连续出现的1-2度和3度痔疮患者随机分为吸管和镊子组,进行橡皮筋结扎。它们平均分布在两组中,平均年龄为48.7岁(范围15-83岁)。使用视觉模拟量表评估手术后的即刻,24小时,7天和14天疼痛评分。在随访中评估了术中出血和其他并发症。结果:结扎后镊子组疼痛感觉较差,平均得分为6.08,而抽吸组为3.08(p <0.001)。绑扎后24小时,钳子患者的疼痛评分仍然很高,平均评分为4.00,而抽吸组为1.92(p <0.001)。无论是每次使用两个或三个痔疮,在即刻和24小时止痛感方面均无显着差异(p = 0.904和p = 0.058)。绑扎后消耗的镇痛量与所报告的疼痛严重程度密切相关,在镊子组中较高,平均为4.48片(p = 0.003)。镊子组中有25例发生了术中出血,而抽吸组中有5例发生了术中出血(p <0.001)。试验期间没有严重并发症,如肛周脓毒症,尿retention留,括约肌功能障碍或出血。结论:在疼痛耐受性,消耗的止痛药量和术中出血方面,抽吸带结扎术优于镊子结扎术治疗二,三级痔疮。

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