Diclofenac sodium vs. dexketoprofen trometamol: selecting NSAIDs for managing postoperative inflammatory complications after third molar surgery-a randomized clinical trial.

IF 2.4 2区 医学 Q2 DENTISTRY, ORAL SURGERY & MEDICINE
Mahmut Erkal, Cennet Neslihan Eroglu
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引用次数: 0

Abstract

Background: After surgical procedures involving bone and soft tissue, such as impacted tooth extraction, profen and diclofenac derivatives are commonly prescribed. Diclofenac sodium (DS) and dexketoprofen trometamol (DT), derivatives of diclofenac and profen, exhibit clinical differences from their parent compounds. Despite their widespread use, comparative studies of their effects on postoperative complications remain limited. This randomized controlled trial was performed to compare the analgesic and anti-inflammatory effects of DS and DT following impacted tooth extraction.

Methods: This split-mouth, randomized clinical study included healthy individuals aged 18 to 40 years with bilaterally impacted third molars. Left and right teeth were randomly assigned to either the DT or DS group. Participants took 25 mg of DS or 36.9 mg of DT twice daily for 7 days, beginning 1 h before extraction. Postoperative pain was assessed using a visual analogue scale at 4, 8, 12, and 24 h postoperatively, as well as on days 2 through 7. Trismus was evaluated by the interincisal distance, and edema was anatomically measured preoperatively and on postoperative days 2 and 7. The surgical duration and rescue analgesic use were also recorded.

Results: In total, 35 patients (28 women, 7 men) aged 18 to 31 years (mean, 21.31 ± 3.19 years) participated. The mean operation duration was 12.94 ± 2.26 min for the DT group and 13.26 ± 2.19 min for the DS group (p > 0.05). No statistically significant difference was observed between the groups regarding pain, edema, or trismus development (p > 0.05). However, from days 2 to 7, the DS group exhibited a greater reduction in edema than did the DT group (p < 0.05). Additionally, the DS group required 10% more frequent use of rescue analgesics than the DT group.

Conclusion: Following impacted tooth extraction, administering DT during the initial days-when pain is more intense and the inflammatory response is developing-followed by DS in the later recovery phase may enhance postoperative comfort.

Trial registration: This clinical trial was retrospectively registered on 03.10.2023 with the number TCTR20231003006.

双氯芬酸钠与dexketoprofen trometamol:选择非甾体抗炎药治疗第三磨牙手术后的术后炎症并发症-一项随机临床试验。
背景:在涉及骨和软组织的外科手术后,如阻生拔牙,通常会开洛芬和双氯芬酸衍生物。双氯芬酸钠(DS)和dexketoprofen trometamol (DT)是双氯芬酸和洛芬的衍生物,与它们的母体化合物表现出临床差异。尽管它们被广泛使用,但它们对术后并发症影响的比较研究仍然有限。这项随机对照试验是为了比较DS和DT在埋伏牙拔除后的镇痛和抗炎作用。方法:本研究纳入18 ~ 40岁双侧阻生第三磨牙的健康人群。左牙和右牙随机分为DT组和DS组。参与者在提取前1小时开始,每天两次服用25毫克DS或36.9毫克DT,持续7天。术后疼痛在术后4、8、12、24小时以及第2 ~ 7天采用视觉模拟评分法进行评估。术前及术后第2天、第7天解剖测量各组间的咬合程度。同时记录手术时间和抢救镇痛药的使用情况。结果:35例患者(女28例,男7例),年龄18 ~ 31岁(平均21.31±3.19岁)。DT组平均手术时间为12.94±2.26 min, DS组平均手术时间为13.26±2.19 min (p < 0.05)。在疼痛、水肿或牙关发育方面,两组间无统计学差异(p < 0.05)。然而,从第2天到第7天,DS组比DT组表现出更大的水肿减少(p结论:在阻生拔牙后的最初几天,疼痛更强烈,炎症反应正在发展,然后在后期恢复阶段进行DS,可以提高术后舒适度。试验注册:本临床试验于2023年10月3日回顾性注册,注册号为TCTR20231003006。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Head & Face Medicine
Head & Face Medicine DENTISTRY, ORAL SURGERY & MEDICINE-
CiteScore
4.70
自引率
3.30%
发文量
32
审稿时长
>12 weeks
期刊介绍: Head & Face Medicine is a multidisciplinary open access journal that publishes basic and clinical research concerning all aspects of cranial, facial and oral conditions. The journal covers all aspects of cranial, facial and oral diseases and their management. It has been designed as a multidisciplinary journal for clinicians and researchers involved in the diagnostic and therapeutic aspects of diseases which affect the human head and face. The journal is wide-ranging, covering the development, aetiology, epidemiology and therapy of head and face diseases to the basic science that underlies these diseases. Management of head and face diseases includes all aspects of surgical and non-surgical treatments including psychopharmacological therapies.
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