Rooh Ali Ghumro, Sughra Parveen, Dileep Kumar, Kanwal Hanif, Abdul Wheed, Jahangir Ali Soomro
{"title":"安慰剂与甲硝唑对痔疮切除术后疼痛缓解作用的比较研究","authors":"Rooh Ali Ghumro, Sughra Parveen, Dileep Kumar, Kanwal Hanif, Abdul Wheed, Jahangir Ali Soomro","doi":"10.48036/apims.v19i2.782","DOIUrl":null,"url":null,"abstract":"Objective: To assess the role of metronidazole versus placebo in terms of pain relief post hemorrhoidectomy.\nMethodology: This randomized control trial was done at the general surgery department of PUMHS from January 2022 to July 2022. The study included adult patients of both genders, aged 18-60, who underwent surgeries for grade III and grade IV hemorrhoids. The participants were divided into two groups: a control group and an intervention group that received oral metronidazole for seven days postoperatively. Both groups received a standardized post-operative analgesic treatment. Post-operative pain and its severity were assessed using the Visual Analog Scale (VAS). Data were collected using a study proforma, and statistical analysis was performed using SPSS version 26.\nResults: A total of 60 cases of hemorrhoids were comparatively studied; mean age of the case group was 39.36+10.43 years and the mean age of the control group was 35.33+9.35 years (p=0.120). The mean BMI and average disease duration was statistically insignificant according to both groups (p > 0.05). In the cases group, grade III hemorrhoids were 36.7% and grade IV hemorrhoids were 63.3%, while in the control group, grade III hemorrhoids were 46.7% and grade IV hemorrhoids were 53.3% (p=0121). The mean operative time was almost similar in both groups (p=0.515). Average VAS was significantly decreased in the case group after 2 hours, at 24 hours, at 36 hours, and at 48 hours (p=<0.05), while it was statistically insignificant according to both groups at the 7th post-operative day (p=0.091).\nConclusion: The use of oral or topical metronidazole in the post-operative period concludes to be more effective in terms of clinically significant early pain relief.","PeriodicalId":184398,"journal":{"name":"Annals of PIMS-Shaheed Zulfiqar Ali Bhutto Medical University","volume":"52 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-05-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Comparative Study of Placebo Versus Metronidazole as a Role of Pain Relief Post Hemorrhoidectomy\",\"authors\":\"Rooh Ali Ghumro, Sughra Parveen, Dileep Kumar, Kanwal Hanif, Abdul Wheed, Jahangir Ali Soomro\",\"doi\":\"10.48036/apims.v19i2.782\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Objective: To assess the role of metronidazole versus placebo in terms of pain relief post hemorrhoidectomy.\\nMethodology: This randomized control trial was done at the general surgery department of PUMHS from January 2022 to July 2022. The study included adult patients of both genders, aged 18-60, who underwent surgeries for grade III and grade IV hemorrhoids. The participants were divided into two groups: a control group and an intervention group that received oral metronidazole for seven days postoperatively. Both groups received a standardized post-operative analgesic treatment. Post-operative pain and its severity were assessed using the Visual Analog Scale (VAS). Data were collected using a study proforma, and statistical analysis was performed using SPSS version 26.\\nResults: A total of 60 cases of hemorrhoids were comparatively studied; mean age of the case group was 39.36+10.43 years and the mean age of the control group was 35.33+9.35 years (p=0.120). The mean BMI and average disease duration was statistically insignificant according to both groups (p > 0.05). In the cases group, grade III hemorrhoids were 36.7% and grade IV hemorrhoids were 63.3%, while in the control group, grade III hemorrhoids were 46.7% and grade IV hemorrhoids were 53.3% (p=0121). The mean operative time was almost similar in both groups (p=0.515). Average VAS was significantly decreased in the case group after 2 hours, at 24 hours, at 36 hours, and at 48 hours (p=<0.05), while it was statistically insignificant according to both groups at the 7th post-operative day (p=0.091).\\nConclusion: The use of oral or topical metronidazole in the post-operative period concludes to be more effective in terms of clinically significant early pain relief.\",\"PeriodicalId\":184398,\"journal\":{\"name\":\"Annals of PIMS-Shaheed Zulfiqar Ali Bhutto Medical University\",\"volume\":\"52 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-05-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Annals of PIMS-Shaheed Zulfiqar Ali Bhutto Medical University\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.48036/apims.v19i2.782\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Annals of PIMS-Shaheed Zulfiqar Ali Bhutto Medical University","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.48036/apims.v19i2.782","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
目的:评价甲硝唑与安慰剂在痔疮切除术后疼痛缓解方面的作用。方法:该随机对照试验于2022年1月至2022年7月在PUMHS普外科进行。该研究包括年龄在18-60岁之间,接受过III级和IV级痔疮手术的成年患者。参与者被分为两组:对照组和干预组,术后口服甲硝唑7天。两组术后均给予标准化的镇痛治疗。采用视觉模拟评分法(VAS)评估术后疼痛及其严重程度。数据收集采用研究形式表,统计分析采用SPSS version 26。结果:共对60例痔疮进行了比较研究;病例组平均年龄为39.36+10.43岁,对照组平均年龄为35.33+9.35岁(p=0.120)。两组患者的平均BMI和平均病程差异均无统计学意义(p > 0.05)。病例组中,III级占36.7%,IV级占63.3%,而对照组中,III级占46.7%,IV级占53.3% (p=0121)。两组患者平均手术时间差异无统计学意义(p=0.515)。病例组在术后2小时、24小时、36小时、48小时平均VAS均显著降低(p=<0.05),而两组在术后第7天差异无统计学意义(p=0.091)。结论:术后口服或外用甲硝唑能较好地缓解早期疼痛。
Comparative Study of Placebo Versus Metronidazole as a Role of Pain Relief Post Hemorrhoidectomy
Objective: To assess the role of metronidazole versus placebo in terms of pain relief post hemorrhoidectomy.
Methodology: This randomized control trial was done at the general surgery department of PUMHS from January 2022 to July 2022. The study included adult patients of both genders, aged 18-60, who underwent surgeries for grade III and grade IV hemorrhoids. The participants were divided into two groups: a control group and an intervention group that received oral metronidazole for seven days postoperatively. Both groups received a standardized post-operative analgesic treatment. Post-operative pain and its severity were assessed using the Visual Analog Scale (VAS). Data were collected using a study proforma, and statistical analysis was performed using SPSS version 26.
Results: A total of 60 cases of hemorrhoids were comparatively studied; mean age of the case group was 39.36+10.43 years and the mean age of the control group was 35.33+9.35 years (p=0.120). The mean BMI and average disease duration was statistically insignificant according to both groups (p > 0.05). In the cases group, grade III hemorrhoids were 36.7% and grade IV hemorrhoids were 63.3%, while in the control group, grade III hemorrhoids were 46.7% and grade IV hemorrhoids were 53.3% (p=0121). The mean operative time was almost similar in both groups (p=0.515). Average VAS was significantly decreased in the case group after 2 hours, at 24 hours, at 36 hours, and at 48 hours (p=<0.05), while it was statistically insignificant according to both groups at the 7th post-operative day (p=0.091).
Conclusion: The use of oral or topical metronidazole in the post-operative period concludes to be more effective in terms of clinically significant early pain relief.