Singla Mamta, Gugnani Megha, Grewal Mandeep S, Kumar Umesh, Aggarwal Vivek
Department of Conservative Dentistry & Endodontics, SGT Dental College, Gurgaon, Haryana, India.
Division of Conservative Dentistry and Endodontics, Post Graduate Institute of Medical Sciences, Chandigarh, India.
J Dent Anesth Pain Med. 2022 Feb;22(1):39-47. doi: 10.17245/jdapm.2022.22.1.39. Epub 2022 Jan 24.
This was a randomized controlled clinical trial that aimed to evaluate the anesthetic efficacy of 2% lidocaine combined with different concentrations of epinephrine (plain, 1:200,000 and 1:80,000) during endodontic treatment of maxillary molars with symptomatic irreversible pulpitis.
The trial included 144 adult patients who were randomly allocated to three treatment groups. All patients received buccal-plus-palatal infiltration. After 10 min, pulp sensibility testing was performed using an electric pulp test (EPT). If a tooth responded positively, anesthesia was considered to have failed. In the case of a negative EPT response, endodontic access was initiated under rubber dam isolation. The success of anesthesia was defined as having a pain score less than 55 on the Heft Parker visual analog scale (HP VAS), which was categorized as 'no pain' or 'faint/weak/mild' pain on the HP VAS. Baseline pre-injection and post-injection maximum heart rates were recorded. The Pearson chi-square test was used to analyze the anesthetic success rates at 5% significance.
Plain 2% lidocaine and 2% lidocaine with 1:200,000 epinephrine and 1:80,000 epinephrine had anesthetic success rates of 18.75%, 72.9%, and 82.3%, respectively. Statistical analysis indicated significant differences between the groups (P < 0.001, χ = 47.5, df = 2). The maximum heart rate increase was seen with 2% lidocaine solution with epinephrine.
Adding epinephrine to 2% lidocaine significantly improves its anesthetic success rates during the root canal treatment of maxillary molars with symptomatic irreversible pulpitis.
这是一项随机对照临床试验,旨在评估2%利多卡因联合不同浓度肾上腺素(普通、1:200,000和1:80,000)在上颌磨牙有症状不可逆性牙髓炎根管治疗期间的麻醉效果。
该试验纳入了144名成年患者,他们被随机分配到三个治疗组。所有患者均接受颊侧加腭侧浸润麻醉。10分钟后,使用牙髓电活力测试(EPT)进行牙髓敏感性测试。如果牙齿有阳性反应,则认为麻醉失败。如果EPT反应为阴性,则在橡皮障隔离下开始进行根管预备。麻醉成功的定义为在赫夫特-帕克视觉模拟量表(HP VAS)上疼痛评分低于55分,在HP VAS上被归类为“无疼痛”或“轻微/微弱/轻度”疼痛。记录注射前和注射后的基线最大心率。采用Pearson卡方检验分析5%显著性水平下的麻醉成功率。
普通2%利多卡因、含1:200,000肾上腺素的2%利多卡因和含1:80,000肾上腺素的2%利多卡因的麻醉成功率分别为18.75%、72.9%和82.3%。统计分析表明各组之间存在显著差异(P < 0.001,χ = 47.5,自由度 = 2)。含肾上腺素的2%利多卡因溶液使心率增加最多。
在2%利多卡因中添加肾上腺素可显著提高其在上颌磨牙有症状不可逆性牙髓炎根管治疗期间的麻醉成功率。