Paul Saurav, Nandamuri Sridevi, Raina Aakrati, Bansal Mukta
Department of Conservative Dentistry and Endodontics, Rama Dental College, Hospital and Research Centre, Kanpur, Uttar Pradesh, India.
Restor Dent Endod. 2021 Jan 26;46(1):e9. doi: 10.5395/rde.2021.46.e9. eCollection 2021 Feb.
This randomized clinical trial aimed to assess the effectiveness of buccal infiltration with piroxicam on the anesthetic efficacy of inferior alveolar nerve block (IANB) with buccal infiltration in irreversible pulpitis, with pain assessed using the Heft-Parker visual analogue scale (HP-VAS).
This study included 56 patients with irreversible pulpitis in mandibular molars, randomly distributed between 2 groups ( = 28). After evaluating the initial pain score with the HP-VAS, each patient received IANB followed by buccal infiltration of 2% lignocaine with adrenaline (1:80,000). Five minutes later, the patients in groups 1 and 2 were given buccal infiltration with 40 mg/2 mL of piroxicam or normal saline, respectively. An access opening procedure (AOP) was performed 15 minutes post-IANB once the individual showed signs of lip numbness as well as 2 negative responses to electric pulp testing. The HP-VAS was used to grade the patient's pain during caries removal (CR), AOP, and working length measurement (WLM). Successful anesthesia was identified either by the absence of pain or slight pain through CR, AOP, and WLM, with no requirement of a further anesthetic dose. A statistical analysis was done using the Shapiro-Wilk and Mann-Whitney tests.
The piroxicam group presented a significantly lower ( < 0.05) mean pain score than the saline group during AOP.
Buccal infiltration with piroxicam enhanced the efficacy of anesthesia with IANB and buccal infiltration with lignocaine in patients with irreversible pulpitis.
本随机临床试验旨在评估吡罗昔康颊部浸润对不可逆性牙髓炎患者下牙槽神经阻滞(IANB)联合颊部浸润麻醉效果的影响,采用赫夫特 - 帕克视觉模拟量表(HP - VAS)评估疼痛情况。
本研究纳入56例下颌磨牙不可逆性牙髓炎患者,随机分为2组(每组n = 28)。用HP - VAS评估初始疼痛评分后,每位患者先接受IANB,随后颊部浸润2%利多卡因加肾上腺素(1:80,000)。5分钟后,第1组和第2组患者分别接受40 mg/2 mL吡罗昔康或生理盐水的颊部浸润。在患者出现唇部麻木迹象以及对牙髓电测试有2次阴性反应后,于IANB后15分钟进行开髓操作(AOP)。采用HP - VAS对患者在去龋(CR)、AOP和工作长度测量(WLM)过程中的疼痛进行分级。若在CR、AOP和WLM过程中无疼痛或仅有轻微疼痛,且无需追加麻醉剂量,则判定麻醉成功。采用夏皮罗 - 威尔克检验和曼 - 惠特尼U检验进行统计学分析。
在AOP过程中,吡罗昔康组的平均疼痛评分显著低于生理盐水组(P < 0.05)。
对于不可逆性牙髓炎患者,吡罗昔康颊部浸润可增强IANB联合利多卡因颊部浸润的麻醉效果。