School of Medicine and Health Sciences, Campus de Bellvitge. University of Barcelona C/ Feixa Llarga, s/n; Pavelló Govern, 2ª planta, Despatx 2.9 08907, L'Hospitalet de Llobregat; Barcelona, Spain
Med Oral Patol Oral Cir Bucal. 2020 Mar 1;25(2):e217-e223. doi: 10.4317/medoral.23315.
A single-blinded randomized controlled trial among patients requiring an upper third molar extraction was performed to evaluate the anxiety degree after receiving information or not about the functioning of The Wand system. Secondarily, perceived pain and the need of re-anesthesia were assessed.
Patients were randomly assigned to the experimental group (detailed explanation about The Wand) or control group (no specific information). Local anesthesia with The Wand consisted in a supraperiosteal infiltrative technique injection 1.6 mL at the buccal and 0.2 mL at the palatal side. Distinct questionnaires for assessing dental anxiety and 100-mm visual analog scales to assess pain were delivered. Demographic data, radiological parameters, operative time and type of intervention were also registered. A descriptive bivariate analysis by non-parametric tests to detect differences in anxiety, pain and re-anesthesia was performed by SPSS 22.0 (SPPS Inc. Chicago, USA).
A total of 85 patients were assessed for eligibility but 17 participants were lost due to the cancellation of the visit for the surgical intervention. Finally, sixty-eight patients were included (34 participants in each group), 47 women (69.1%) and 21 men (30.9%), with an average age of 28.8 (± 9.3) years.
Patients that received a detailed explanation of The Wand did not have a significant reduction of the anxiety degree and perceived pain during the anesthetic act compared to patients that received no information. The need of re-anesthesia was not related to the anxiety level but was significantly related to increasing operative time.
一项针对需要拔除上颌第三磨牙的患者的单盲随机对照试验,旨在评估在接受或不接受 Wand 系统功能信息后患者的焦虑程度。其次,评估了感知疼痛和再次麻醉的需求。
患者被随机分配到实验组(详细解释 Wand 系统)或对照组(无特定信息)。Wand 局部麻醉采用骨膜下浸润技术,在颊侧注射 1.6 mL,在腭侧注射 0.2 mL。使用专门的问卷调查表评估牙科焦虑程度和 100 毫米视觉模拟量表评估疼痛。记录人口统计学数据、影像学参数、手术时间和干预类型。使用 SPSS 22.0(SPPS Inc. Chicago,USA)进行非参数检验的描述性双变量分析,以检测焦虑、疼痛和再次麻醉的差异。
共有 85 名患者符合入选标准,但有 17 名患者因取消手术预约而失访。最终,68 名患者入选(每组 34 名患者),其中 47 名女性(69.1%)和 21 名男性(30.9%),平均年龄为 28.8(±9.3)岁。
与未接受信息的患者相比,接受 Wand 系统详细解释的患者在麻醉过程中并未显著降低焦虑程度和感知疼痛。再次麻醉的需求与焦虑程度无关,但与手术时间的延长显著相关。