阿替卡因在下颌第一磨牙不可逆性牙髓炎的颊侧浸润麻醉:证据充分吗?
Articaine buccal infiltration for mandibular first molars with irreversible pulpitis: is the evidence enough?
作者信息
Majid Omer Waleed
机构信息
Professor, Department of Oral and Maxillofacial Surgery, College of Dentistry, Mosul University, Mosul, Iraq.
出版信息
Evid Based Dent. 2025 May 6. doi: 10.1038/s41432-025-01153-4.
A COMMENTARY ON
Saatchi M, Mohammadi G, Iranmanesh P et al. Articaine buccal infiltration for mandibular first molars with symptomatic irreversible pulpitis: is it as effective as inferior alveolar nerve block with lidocaine? A systematic review and meta-analysis. Clin Oral Investig 2025; 29: 146.
STUDY DESIGN
A systematic review and meta-analysis.
OBJECTIVE
To compare the anesthetic success rate of 4% articaine buccal infiltration (BI) with 2% lidocaine inferior alveolar nerve block (IANB) for lower first molars (LM1) presenting with symptomatic irreversible pulpitis.
PATIENTS AND METHODS
This systematic review, registered in PROSPERO and conducted per PRISMA guidelines, included randomized clinical trials (RCTs) on adults (≥18 years) with symptomatic irreversible pulpitis in LM1, using a single cartridge (1.7-1.8 ml) of either articaine BI or lidocaine IANB as the primary injection. Studies were excluded if they were non-RCTs, used other anesthetics or techniques, included supplemental injections, used articaine BI as a secondary method, or did not report results specific to LM1. Anesthetic success was defined as patient-reported pain <4 on a visual analog scale (VAS) during cavity access or canal instrumentation. A comprehensive English-language search was conducted across five databases and gray literature sources, with manual searches of key journals and textbooks. Two independent reviewers handled screening and data extraction. Risk of bias was assessed with the Cochrane RoB2 tool. A fixed-effect meta-analysis estimated pooled risk ratios, with tests for heterogeneity and publication bias. Trial Sequential Analysis (TSA) was utilized to evaluate the robustness of the evidence, and the GRADE approach assessed certainty.
RESULTS
From 780 initial records, five RCTs met the inclusion criteria after full screening. These trials included 405 patients aged 18-65, each comparing 4% articaine BI (1:100,000 epinephrine) against 2% lidocaine IANB (three with 1:100,000 and two with 1:200,000 epinephrine). No adverse effects were reported in three studies; the remaining two did not address safety. Risk of bias was low in three trials, with two showing some concerns due to unclear randomization and blinding. No publication bias was detected. Of the 405 first molars with irreversible pulpitis, 284 cases (70%) demonstrated successful pulpal anesthesia. The meta-analysis showed similar anesthetic success rates between articaine BI (72.2%) and lidocaine IANB (68.1%) [RR = 1.06, 95% CI: 0.93-1.20, I = 24.51%]. However, TSA indicated that current evidence is inconclusive due to insufficient sample size. According to GRADE, the overall certainty of evidence was rated as moderate, with concerns primarily related to imprecision.
CONCLUSION
Moderate evidence indicates that 4% articaine BI offers anesthetic efficacy comparable to 2% lidocaine IANB for LM1 with symptomatic irreversible pulpitis. Although additional high-quality clinical trials are needed to validate these results, articaine BI may present a promising alternative to the traditional IANB technique in dental practice.
对以下文献的评论
萨奇 M、穆罕默迪 G、伊朗马内什 P 等。4% 阿替卡因颊侧浸润用于下颌第一磨牙有症状的不可逆性牙髓炎:它与 2% 利多卡因下牙槽神经阻滞效果一样吗?一项系统评价和荟萃分析。《临床口腔研究》2025 年;29: 146。
研究设计
一项系统评价和荟萃分析。
目的
比较 4% 阿替卡因颊侧浸润(BI)与 2% 利多卡因下牙槽神经阻滞(IANB)用于患有症状性不可逆性牙髓炎的下颌第一磨牙(LM1)的麻醉成功率。
患者与方法
本系统评价在国际前瞻性系统评价注册库(PROSPERO)注册,并按照系统评价和荟萃分析优先报告项目(PRISMA)指南进行,纳入了关于 18 岁及以上患有 LM1 症状性不可逆性牙髓炎的成年人的随机临床试验(RCT),使用单支卡式瓶(1.7 - 1.8 毫升)的阿替卡因 BI 或利多卡因 IANB 作为主要注射方法。如果研究是非 RCT、使用其他麻醉剂或技术、包括补充注射、将阿替卡因 BI 用作次要方法或未报告特定于 LM1 的结果,则将其排除。麻醉成功定义为患者报告在开髓或根管预备期间视觉模拟量表(VAS)上的疼痛 <4。在五个数据库和灰色文献来源中进行了全面的英文文献检索,并对手动检索关键期刊和教科书。两名独立的审阅者负责筛选和数据提取。使用 Cochrane 偏倚风险 2 工具评估偏倚风险。固定效应荟萃分析估计合并风险比,并进行异质性检验和发表偏倚检验。采用累积 Meta 分析(TSA)评估证据的稳健性,并采用 GRADE 方法评估证据确定性。
结果
从 780 条初始记录中,经过全面筛选后有 5 项 RCT 符合纳入标准。这些试验纳入了 405 名年龄在 18 - 65 岁之间的患者,每项试验都将 4% 阿替卡因 BI(1:100,000 肾上腺素)与 2% 利多卡因 IANB(3 项使用 1:100,000,2 项使用 1:200,000 肾上腺素)进行比较。三项研究未报告不良反应;其余两项未涉及安全性。三项试验的偏倚风险较低,两项因随机化和盲法不明确而存在一些问题。未检测到发表偏倚。在 405 颗患有不可逆性牙髓炎的第一磨牙中,284 例(70%)显示牙髓麻醉成功。荟萃分析显示阿替卡因 BI(72.2%)和利多卡因 IANB(68.1%)之间的麻醉成功率相似 [风险比(RR)= 1.06,95% 置信区间(CI):0.93 - 1.20,I² = 24.51%]。然而,TSA 表明由于样本量不足,目前的证据尚无定论。根据 GRADE,证据的总体确定性被评为中等,主要担忧与不精确性有关。
结论
中等质量的证据表明对于患有症状性不可逆性牙髓炎的 LM1,4% 阿替卡因 BI 提供的麻醉效果与 2% 利多卡因 IANB相当。尽管需要更多高质量的临床试验来验证这些结果,但在牙科实践中,阿替卡因 BI 可能是传统 IANB 技术的一个有前景的替代方法。