Moghadam Manijeh Yousefi, Nemat-Shahi Mohammad, Soroosh Davood, Nemat-Shahi Mahbobeh, Asadi Atefeh
Department of Anesthesiology, Faculty of Medicine, Sabzevar University of Medical Sciences, Sabzevar, Iran.
Faculty of Medicine, Sabzevar University of Medical Sciences Sabzevar, Iran.
Biomedicine (Taipei). 2020 Mar 28;10(1):28-32. doi: 10.37796/2211-8039.1002. eCollection 2020.
Despite advances in surgical techniques and pharmacology, postoperative pain remains a common problem after appendectomy, and its management continues to be suboptimal. The aim of this study was to evaluate the effect of evening primrose oil on the reduction of postoperative pain after appendectomy.
In a double-blind, randomized, clinical trial, a total of 80 adults patients with acute appendicitis who were undergoing appendectomy at the Shahid Beheshti Emdad Hospital in Sabzevar, were included. Patients were randomly allocated into two equally sized groups (n = 40). In postoperative period and after recovering from the anesthesia, each of the intervention and control groups received one evening primrose (1000 mg) or placebo capsules every 30 min for 3 times, respectively. All patients in both groups were asked to rate the intensity of their pain on a 0-10 point Visual Analogue Scale (VAS) and also McGill pain questionnaire, before and 1 h after the last administration of the drug, postoperatively.
In patients who received evening primrose, both VAS and McGill pain intensity scores significantly decreased after intervention, when compared prior to initiation of the intervention (p < 0.0001). While in the control group, changes of pain intensity scores were not significantly different before and after the intervention (p > 0.05).
It seems that oral evening primrose can be used as a simple and safe potential adjunctive treatment for postoperative pain control after appendectomy.
尽管手术技术和药理学取得了进展,但阑尾切除术后疼痛仍是一个常见问题,其管理仍不尽人意。本研究的目的是评估月见草油对减轻阑尾切除术后疼痛的效果。
在一项双盲、随机临床试验中,纳入了在萨卜泽瓦尔的沙希德·贝赫什提·埃姆达德医院接受阑尾切除术的80例成年急性阑尾炎患者。患者被随机分为两组,每组40例。在术后麻醉恢复后,干预组和对照组分别每30分钟服用一粒月见草胶囊(1000毫克)或安慰剂胶囊,共服用3次。两组所有患者在术后最后一次给药前和给药后1小时,均被要求使用0至10分的视觉模拟量表(VAS)对疼痛强度进行评分,并填写麦吉尔疼痛问卷。
与干预开始前相比,接受月见草治疗的患者在干预后VAS和麦吉尔疼痛强度评分均显著降低(p < 0.0001)。而在对照组中,干预前后疼痛强度评分变化无显著差异(p > 0.05)。
口服月见草似乎可作为阑尾切除术后控制疼痛的一种简单、安全的潜在辅助治疗方法。