超声引导对无复位椎间盘移位的妇女进行关节置换术能缩短手术时间并改善结果吗?一项随机临床试验。

IF 1.8
Moataz Bahaa, Abdelrahman Mohamed Fahmy Abdelhameed Azab, Hisham Mohamed Mahmoud Ali El Sheikh, Bassam A Abulnoor, Amr Amin Ghanem, Sherif Shafik El Bahnasy, Karim Mohamed AbdelMohsen
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引用次数: 0

摘要

使用超声引导(USG)关节穿刺的目的是减少针的插入次数,这被假设为减少手术时间,术后疼痛,从而减少活动范围的限制。目的:比较USG单穿刺关节穿刺(SPA) 2型与无超声引导的SPA 2型关节穿刺治疗颞下颌关节(TMJ)内脱位(ID)的疗效和手术效果。椎间盘无复位位移(DDWOR)。材料与方法:于2022年12月至2023年12月在艾因沙姆斯大学医院进行双盲前瞻性随机临床试验(RCT)。研究对象为平均年龄27.00±3.70岁、保守治疗失败的DDWOR女性,排除有错颌合、功能不良习惯、全身性疾病、心理障碍或需要特殊需要的女性。本研究将40例女性DDWOR患者随机分为对照组(SPA 2型关节穿刺)和干预组(USG SPA 2型关节穿刺)。评估患者的针插入尝试作为主要结局。同时评估手术时间、视觉模拟评分法(VAS)测量疼痛、最大开口(MMO)。随访时间为4周、8周和12周。排除年龄和性别差异、错颌、功能习惯、全身性疾病或心理障碍的患者。结果:干预组的插针次数更少(1.6次对2.9次),手术时间更短(11.75次对16分钟),p结论:USG SPA 2型关节穿刺术的手术效率更高,插针次数更少,手术时间更短。然而,在治疗结果上没有统计学上的显著差异,包括疼痛减轻或最大开口(MMO)。进一步的研究是必要的,以确定超声引导是否提供额外的临床效益,除了技术上的便利。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Does ultrasound guidance during arthrocentesis in women with disc displacement without reduction reduce procedure time and improve outcomes? A randomized clinical trial.

Introduction: The goal of using ultrasound-guided (USG) arthrocentesis is to reduce number of needle insertion attempts, which is hypothesized to reduce procedure time, postoperative pain, and consequently, limitation in range of motion.

Purpose: The objective of this study was to compare the therapeutic and operative efficiency of USG Single-Puncture Arthrocentesis (SPA) Type 2 and SPA Type 2 arthrocentesis without ultrasound guidance in the treatment of temporomandibular joint (TMJ) internal derangement (ID) "disc displacement without reduction (DDWOR)."

Materials and methods: A double-blinded prospective randomized clinical trial (RCT) was conducted from December 2022 to December 2023 at Ain Shams University Hospital. It enrolled females with a mean age of 27.00 ± 3.70 years with DDWOR and failed conservative treatment, excluding those with malocclusion, parafunctional habits, systemic diseases, psychological disorders or requiring special needs. In the study, 40 female patients with DDWOR were randomly divided into a control group (SPA Type 2 arthrocentesis) and an intervention group (USG SPA Type 2 arthrocentesis). Patients were assessed for needle insertion attempts as the primary outcome. procedure time, pain measured using visual analogue scale (VAS), and maximum mouth opening (MMO) were also assessed. Follow-up was conducted at 4, 8, and 12 weeks. Patients with differences in age and gender, malocclusion, parafunctional habits, systemic diseases, or psychological disorders were excluded.

Results: The intervention group had fewer needle insertion attempts (1.6 vs. 2.9) and shorter procedure time (11.75 vs. 16 min, p < 0.001). Pain scores (p = 0.846) and maximum mouth opening (p = 0.341) showed no statistically significant differences after 12 weeks. Data were summarized as mean, SD, median, and IQR, with normality assessed by examining the distribution and using the Shapiro-Wilk test. Non-parametric variables were compared using the Mann-Whitney U test. Linear mixed models were assessed via residual plots, Q-Q plots, Shapiro-Wilk, Breusch-Pagan, and VIF tests. Fixed effects were analyzed with ANOVA or Wald Chi-Square tests, followed by Tukey's post-hoc comparisons. Analyses were conducted using R 4.5.0.

Conclusions: USG SPA Type 2 arthrocentesis demonstrated improved procedural efficiency, evidenced by fewer needle insertion attempts and shorter procedure duration. However, it did not result in statistically significant differences in therapeutic outcomes, including pain reduction or maximum mouth opening (MMO). Further research is warranted to determine whether ultrasound guidance provides additional clinical benefits beyond technical facilitation.

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