内镜下套扎联合泡沫硬化剂注射治疗Ⅱ~Ⅲ度内痔的疗效及安全性分析

陈苏阳, 蒋燕, 焦胜, 黄震, 成宏伟

陈苏阳, 蒋燕, 焦胜, 黄震, 成宏伟. 内镜下套扎联合泡沫硬化剂注射治疗Ⅱ~Ⅲ度内痔的疗效及安全性分析[J]. 实用临床医药杂志, 2021, 25(22): 121-125. DOI: 10.7619/jcmp.20214123
引用本文: 陈苏阳, 蒋燕, 焦胜, 黄震, 成宏伟. 内镜下套扎联合泡沫硬化剂注射治疗Ⅱ~Ⅲ度内痔的疗效及安全性分析[J]. 实用临床医药杂志, 2021, 25(22): 121-125. DOI: 10.7619/jcmp.20214123
CHEN Suyang, JIANG Yan, JIAO Sheng, HUANG Zhen, CHENG Hongwei. Efficacy and safety of endoscopic ligation combined with foam sclerosing agent injection in treatment of patients with Ⅱ to Ⅲ degree internal hemorrhoids[J]. Journal of Clinical Medicine in Practice, 2021, 25(22): 121-125. DOI: 10.7619/jcmp.20214123
Citation: CHEN Suyang, JIANG Yan, JIAO Sheng, HUANG Zhen, CHENG Hongwei. Efficacy and safety of endoscopic ligation combined with foam sclerosing agent injection in treatment of patients with Ⅱ to Ⅲ degree internal hemorrhoids[J]. Journal of Clinical Medicine in Practice, 2021, 25(22): 121-125. DOI: 10.7619/jcmp.20214123

内镜下套扎联合泡沫硬化剂注射治疗Ⅱ~Ⅲ度内痔的疗效及安全性分析

详细信息
    通讯作者:

    成宏伟, E-mail: 22934141@qq.com

  • 中图分类号: R657.1;R574.8

Efficacy and safety of endoscopic ligation combined with foam sclerosing agent injection in treatment of patients with Ⅱ to Ⅲ degree internal hemorrhoids

  • 摘要:
      目的  探讨内镜下套扎联合泡沫硬化剂注射治疗Ⅱ~Ⅲ度内痔的临床疗效及安全性。
      方法  将56例Ⅱ~Ⅲ度内痔患者随机分为对照组和观察组,每组28例。对照组单纯应用内镜下套扎术治疗,观察组采用内镜下套扎术联合聚桂醇泡沫硬化剂注射治疗。比较2组手术情况(术中出血量、手术时间)、治疗总有效率、术后恢复情况(创面愈合时间、住院时间、术后疼痛评分、创面出血评分、肛门水肿评分)、术后并发症发生率及复发率。
      结果  2组术中出血量、手术时间比较,差异无统计学意义(P>0.05)。观察组治疗总有效率为96.43%,对照组为89.29%,差异无统计学意义(P>0.05)。观察组创面愈合时间、住院时间短于对照组,术后1周患者疼痛评分、创面出血评分、肛门水肿评分低于对照组,差异均有统计学意义(P < 0.05)。观察组术后尿潴留、肛门渗血、肛门肿痛的并发症发生率低于对照组,差异有统计学意义(P < 0.05)。观察组1年内痔疮复发率低于对照组,差异有统计学意义(P < 0.05)。
      结论  内镜下套扎联合泡沫硬化剂注射治疗Ⅱ~Ⅲ度内痔效果确切,能够快速改善症状,并具有并发症少、术后恢复快、复发率低、安全性良好等优点。
    Abstract:
      Objective  To explore the clinical efficacy and safety of endoscopic ligation combined with foam sclerosing agent injection in treatment of patients with Ⅱ to Ⅲ internal hemorrhoids.
      Methods  A total of 56 patients with Ⅱ to Ⅲ internal hemorrhoids were randomly divided into control group and observation group, with 28 cases in each group. The control group was treated with endoscopic ligation alone, and the observation group was treated with endoscopic ligation combined with lauromacrogol foam sclerosing agent injection. Surgery condition (intraoperative bleeding amount, operation time), total effective rate, postoperative recovery condition (wound healing time, hospitalization time, postoperative pain score, wound bleeding score and anal edema score), incidence of postoperative complication and recurrence rate were compared between two groups.
      Results  There were no significant differences in intraoperative bleeding volume and operation time between the two groups (P>0.05). Total effective rate was 96.43% in the observation group, which showed no significant difference when compared to 89.29% in the control group (P>0.05). In the observation group, the wound healing time and hospitalization time were significantly shorter than the control group, and the pain score, wound bleeding score and anal edema score at 1 week after surgery were also significantly lower than the control group (P < 0.05). The incidence of complications such as postoperative urinary retention, anal infiltration, anal swelling and pain was significantly lower than that in the control group (P < 0.05). The recurrence rate of hemorrhoids within a year in the observation group was significantly lower than that in the control group (P < 0.05).
      Conclusion  Endoscopic ligation combined with foam sclerosing agent injection is effective in the treatment of patients with Ⅱ to Ⅲ internal hemorrhoids, which can quickly improve symptoms and has the advantages of less complications, rapid postoperative recovery, low recurrence rate and good safety.
  • 表  1   2组术中出血量及手术时间比较(x±s)

    组别 n 术中出血量/mL 手术时间/min
    观察组 28 10.89±1.45 30.00±4.59
    对照组 28 11.07±1.61 27.07±7.89
    下载: 导出CSV

    表  2   2组临床疗效比较[n(%)]

    组别 n 痊愈 显效 有效 无效 总有效
    观察组 28 14(50.00) 11(39.29) 2(7.14) 1(3.57) 27(96.43)
    对照组 28 10(35.71) 10(35.71) 5(17.86) 3(10.71) 25(89.29)
    下载: 导出CSV

    表  3   2组术后恢复情况比较

    组别 n 创面愈合时间/d 住院时间/d 术后疼痛评分/分 创面出血评分/分 肛门水肿评分/分
    观察组 28 9.75±2.94* 5.43±1.50* 2.36±0.68* 0.36±0.49* 0.64±0.34*
    对照组 28 18.61±3.29 8.50±2.29 3.50±0.64 1.04±0.43 0.96±0.43
    与对照组比较, * P < 0.05。
    下载: 导出CSV

    表  4   2组术后并发症发生情况比较[n(%)]

    组别 n 尿潴留 肛门渗血 肛门肿痛 肛门狭窄 肛周感染
    观察组 28 0* 1(3.57)* 2(7.14)* 0 0
    对照组 28 4(14.29) 6(21.43) 10(35.71) 1(3.57) 1(3.57)
    与对照组比较, * P < 0.05。
    下载: 导出CSV
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出版历程
  • 收稿日期:  2021-10-20
  • 网络出版日期:  2021-11-23
  • 发布日期:  2021-11-27

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