de Andrade Silva Silmara, Velozo Christianne, de Almeida Souto Montenegro Luiza, de Sousa Wesley Viana, da Cunha Isaltino Marina, de Fátima Formiga Melo Diniz Margareth, de Albuquerque Diana Santana
Department of Operative Dentistry and Endodontics, Dental College of Pernambuco, Recife, Pernambuco, Brazil.
Department of Operative Dentistry and Endodontics, Dental College of Pernambuco, Recife, Pernambuco, Brazil.
J Endod. 2024 Dec;50(12):1698-1704. doi: 10.1016/j.joen.2024.10.010. Epub 2024 Nov 4.
The aim of the present study was to evaluate the effectiveness of cannabidiol (CBD)-rich Cannabis extract in reducing anxiety and postoperative pain in patients submitted to endodontic treatment.
The study was carried out after approval by the Research Ethics Committee (Registration No. 5.075.961). The following groups were tested: CBD and placebo. Pain was measured using a visual analog scale before the start of treatment and 24, 48, and 72 hours and 7 days after the session. Anxiety was assessed using the Modified Dental Anxiety Scale and a visual analog scale, before and immediately after treatment. In addition, salivary cortisol was measured before drug administration and after anesthesia. Data were analyzed descriptively using absolute frequencies and percentages, with a 5% margin of error.
The mean anxiety scores were higher in the CBD group than in the placebo group in each assessment (pre: 5.06 vs 3.07, respectively; post: 4.61 vs 2.60). However, there was no significant difference in the reduction of dental anxiety at the beginning of the consultation and throughout the procedure. We did not find statistically significant differences in postoperative pain between the CBD and placebo groups at any of the time points.
There was no evidence of an exposure-response relationship between the intervention and control groups. However, more studies are needed to determine clinical outcomes.
本研究的目的是评估富含大麻二酚(CBD)的大麻提取物在减轻接受牙髓治疗患者的焦虑和术后疼痛方面的有效性。
本研究在获得研究伦理委员会批准后开展(注册号:5.075.961)。测试了以下几组:CBD组和安慰剂组。在治疗开始前以及治疗后24、48、72小时和7天使用视觉模拟量表测量疼痛。在治疗前和治疗后立即使用改良牙科焦虑量表和视觉模拟量表评估焦虑。此外,在给药前和麻醉后测量唾液皮质醇。使用绝对频率和百分比对数据进行描述性分析,误差幅度为5%。
在每次评估中,CBD组的平均焦虑评分均高于安慰剂组(治疗前:分别为5.06和3.07;治疗后:4.61和2.60)。然而,在咨询开始时和整个过程中,牙科焦虑的降低没有显著差异。在任何时间点,CBD组和安慰剂组之间的术后疼痛均未发现统计学上的显著差异。
没有证据表明干预组和对照组之间存在暴露-反应关系。然而,需要更多研究来确定临床结果。