[The effectiveness of flavonoids in the postoperative treatment of patients with hemorrhoids].

Q4 Medicine
M A Voinov
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引用次数: 0

Abstract

Objective: Evaluation of the effectiveness of flavonoids in the postoperative management of patients with hemorrhoids.

Material and methods: A single-center randomized controlled clinical trial was conducted. Patients with stage III and IV hemorrhoids aged over 18 years who patients who underwent hemorrhoidectomy were included.

The patients were divided into 2 groups - main and control. Patients in the main group were recommended to use a purified micronized flavonoid fraction - 65 patients. In the control group (70 patients), the use of this group of drugs was not expected.

The observation period was 60 days. After discharge from the hospital, 5 patient visits were scheduled: on the 3rd, 7th, 21st, 40th and 60th day after surgery. Patients independently assessed the intensity of symptoms - pain, tenesmus, itching and bleeding.

The randomization procedure was carried out using the method of simple randomization using envelopes.

Results: 135 patients were randomized. There were no patients who dropped out of the study. The number of participants whose data were included in the analysis was 65 patients in the main group and 70 patients in the control group.

Assessment of symptoms in the first 3 days of the postoperative period did not show a significant difference in the condition of the patients. Over time, we found significant changes in the dynamics of complaints between groups. After 7, 21, 40 and 60 days, a statistically significant lower severity of pain, bleeding and tenesmus was revealed among patients in the main group compared to the control group. This trend was not detected in the assessment of itching. There were no undesirable effects.

Conclusion: The use of purified micronized flavonoid fraction in the postoperative management of patients with hemorrhoids can significantly reduce the degree and duration of pain, bleeding and tenesmus.

[黄酮类化合物在痔疮患者术后治疗中的有效性]。
目的:评估黄酮类药物在痔疮患者术后治疗中的效果:评估黄酮类药物在痔疮患者术后治疗中的效果:进行了一项单中心随机对照临床试验。患者分为两组--主要组和对照组。主要组中的 65 名患者被建议使用纯化的微粉黄酮成分。在对照组(70 名患者)中,预计不会使用这类药物。观察期为 60 天。出院后,安排了5次患者回访:术后第3天、第7天、第21天、第40天和第60天。患者独立评估症状的强度--疼痛、胀痛、瘙痒和出血。随机程序采用信封简单随机法进行:结果:135 名患者被随机选中。没有患者退出研究。纳入分析数据的参与者人数为:主要组 65 名患者,对照组 70 名患者。随着时间的推移,我们发现各组之间的主诉动态发生了明显变化。在 7 天、21 天、40 天和 60 天后,与对照组相比,主要治疗组患者的疼痛、出血和排便严重程度明显降低。在瘙痒评估中未发现这一趋势。没有不良反应:结论:在痔疮患者的术后治疗中使用纯化的微粉化黄酮类成分可明显减轻疼痛、出血和肛门坠胀的程度并缩短其持续时间。
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来源期刊
Khirurgiya
Khirurgiya Medicine-Medicine (all)
CiteScore
0.70
自引率
0.00%
发文量
161
期刊介绍: Хирургия отдельных областей сердце, сосуды легкие пищевод молочная железа желудок и двенадцатиперстная кишка кишечник желчевыводящие пути печень
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