普瑞巴林、法莫替丁与普瑞巴林、苯海拉明治疗术后腹痛的疗效比较

Pub Date : 2023-09-01 DOI:10.1016/j.ijso.2023.100674
Masoud Saadat Fakhr , Parnian Motamed Chaboki , Hemin Ashayeri , Pouria Sahranavard , Somayeh Mohammadipanah , Mahnaz Narimani Zamanabadi
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引用次数: 0

摘要

目的:西班牙是最重要的问题之一,其管理不善可导致血压升高、心肌缺血等并发症。控制术后疼痛的有效方法是在手术前结合药物进行先发制人的疼痛管理。本研究旨在比较普瑞巴林联合法莫替丁与普瑞巴林联合苯海拉明患者术后腹痛的程度。材料与方法本双盲临床试验从文献(XXX)中选取ASA身体状态分类为1或2的腹部手术(剖腹手术)患者34例,分为两组,每组17例,a组普瑞巴林联合法莫替丁,B组普瑞巴林联合苯海拉明。术前2小时给药。在完全意识恢复期及术后6、12、24 h采用视觉模拟评分法(VAS)测量患者的疼痛水平。此外,记录两组患者术后24小时内镇痛药的用量并进行比较。结果普瑞巴林联合苯海拉明组术后6 h平均疼痛强度评分为(6±0.2)分,普瑞巴林联合法莫替丁组术后6 h平均疼痛强度评分为(7.1±0.1)分(p = 0.002)。普瑞巴林联合法莫替丁组术后12 h平均疼痛强度评分为(6.1±0.3)分,普瑞巴林联合苯海拉明组术后12 h平均疼痛强度评分为(5.6±0.2)分(p = 0.021)。普瑞巴林联合法莫替丁组术后24 h平均疼痛强度评分为(5.2±0.2)分,普瑞巴林联合苯海拉明组术后24 h平均疼痛强度评分为(4.2±0.2)分(p = 0.014)。结果表明,疼痛强度评分在所有四个测量时间间隔内均下降(p <0.001),两组之间的这种减少有显著差异(p = 0.002),接受普瑞巴林和苯海拉明的组的最终平均疼痛评分低于另一组。结论应用苯海拉明、普瑞巴林等药物作为预防用药,可有效控制腹部手术患者术后腹痛,减少镇痛药的使用。
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Comparison of the effects of pregabalin and famotidine with pregabalin and diphenhydramine on postoperative abdominal pain

Objectives

Pain is one of the most significant problems, and its uncontrolled management can lead to complications such as increased blood pressure, myocardial ischemia, etc. An effective approach to control postoperative pain is preemptive pain management with a combination of drugs prior to surgery. The present study aims to compare the level of postoperative abdominal pain in patients receiving pregabalin and famotidine versus pregabalin and diphenhydramine.

Materials and methods

In this double-blind clinical trial, a total of 34 candidates for abdominal surgery (laparotomy) with ASA physical status classification of 1 or 2 were enrolled from the patients referring to (XXX). They were divided into two groups of 17 (Group A: pregabalin and famotidine, Group B: pregabalin and diphenhydramine). The drugs were administered to the patients 2 h before the surgery. The patients' pain levels were measured using the Visual Analog Scale (VAS) at the recovery stage after complete consciousness and at 6, 12, and 24 h postoperatively. Additionally, the amount of analgesic consumed within the first 24 h after the surgery was recorded and compared between the two groups.

Results

The average pain intensity score at 6 h postoperatively was (6 ± 0.2) in patients who received pregabalin and diphenhydramine, and (7.1 ± 0.1) in patients who received pregabalin and famotidine (p = 0.002). The average pain intensity score at 12 h postoperatively was (6.1 ± 0.3) in patients who received pregabalin and famotidine, and (5.6 ± 0.2) in patients who received pregabalin and diphenhydramine (p = 0.021). Furthermore, the average pain intensity score at 24 h postoperatively was (5.2 ± 0.2) in patients who received pregabalin and famotidine, and (4.2 ± 0.2) in patients who received pregabalin and diphenhydramine (p = 0.014). The results demonstrated that the pain intensity score decreased in all four measured time intervals in the overall patient population (p < 0.001), and this reduction was significantly different between the two groups (p = 0.002), with the final average pain score being lower in the group receiving pregabalin and diphenhydramine compared to the other group.

Conclusion

The results of this study indicate that the use of drugs such as diphenhydramine and pregabalin as preemptive medications can be effective in controlling postoperative abdominal pain and reducing the consumption of analgesics in patients after abdominal surgery.

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