Combined posterior superior alveolar and anterior middle superior alveolar nerve blocks with labial infiltration versus nerve blocks alone for pain management in minimally invasive non-surgical periodontal therapy: a split-mouth randomized controlled trial

一项关于微创非手术牙周治疗中疼痛管理的随机对照试验:采用唇侧浸润麻醉联合后上牙槽神经阻滞和前中上牙槽神经阻滞与单纯神经阻滞的比较

阅读:1

Abstract

BACKGROUND: To compare the efficacy of combining posterior superior alveolar (PSA) block, anterior middle superior alveolar (AMSA) block, and labial infiltration of the maxillary central incisor versus PSA + AMSA alone for pain control during minimally invasive nonsurgical periodontal therapy (MINST). METHODS: Twenty-four patients with stage II-III periodontitis were enrolled in the single-center, single-blind, split-mouth randomized controlled trial. The maxillary right and left quadrants were randomized to receive either PSA + AMSA blocks and labial infiltration (test group) or PSA + AMSA alone (control group) during subgingival instrumentation. Pain levels during injection and treatment were assessed using a 100 mm visual analog scale (VAS). Primary outcomes included intraoperative and injection-related pain scores, while secondary outcomes comprised treatment duration, injection time, patient satisfaction, and adverse events. Data were analyzed using GraphPad Prism 9. RESULTS: Twenty-one subjects completed the study. No significant difference in injection pain was observed between groups (test: 22.74 ± 14.10 mm vs. control: 20.21 ± 12.27 mm; P = 0.248). However, the test group exhibited a statistically significant reduction in intraoperative pain (test: 11.07 ± 10.36 mm vs. control: 16.43 ± 11.55 mm; P = 0.021). Patient satisfaction was significantly higher in the test group [test: 90 (IQR 90-100) vs. control: 90 (80-90); P = 0.004]. No clinically meaningful differences were detected in treatment duration or adverse event rates (P > 0.05). CONCLUSIONS: The combined PSA + AMSA blocks and labial infiltration protocol reduced intraoperative pain and improved satisfaction versus PSA + AMSA blocks, without prolonging treatment. Despite clinical promise, the small sample size limits generalizability, necessitating multicenter trials to validate efficacy and broader applicability. TRIAL REGISTRATION: The trial protocol was retrospectively registered in the Chinese Clinical Trial Registry (ChiCTR2400086566) on 05-07-2024.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。