虚拟现实催眠对局部麻醉下端口植入术围手术期疼痛和焦虑的影响:随机对照试验(VIP 试验)。

IF 2 3区 医学 Q2 ANESTHESIOLOGY Perioperative Medicine Pub Date : 2024-10-10 DOI:10.1186/s13741-024-00454-z
Kira C Steinkraus, Hannah Feldmann, Lisa S Hunold, Sandra Graf, Colette Dörr-Harim, Nadir Nasir, Christoph W Michalski, Felix J Hüttner
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引用次数: 0

摘要

背景:这项单中心随机对照试验调查了虚拟现实(VR)催眠对局部麻醉下端口植入术的围术期焦虑、疼痛、患者满意度和药物使用的影响:共招募了 120 名在 2022 年 1 月至 2023 年 8 月期间接受选择性端口植入术的患者,并按 1:1 的比例随机分配到 VR 催眠组或对照组。VR 组使用市售的 VR 头显和 HypnoVR 应用程序,提供各种环境、音乐背景和指导语音,而对照组则在没有 VR 的情况下进行手术。排除了 ASA > 3、慢性疼痛、认知问题和有 VR 使用禁忌症的患者。测量的主要结果是围手术期疼痛和焦虑评分,次要结果包括围手术期药物使用情况。由于干预措施的性质,对患者和医生进行盲法是不可行的。统计分析主要是描述性和探索性的,重点是估计未来试验的效应大小:研究发现,无 VR 组和 VR 组的术后即刻疼痛评分(1.43 ± 1.63 vs. 1.6 ± 2.05,p = 0.62)或焦虑评分(30.65 ± 9.13 vs. 31.78 ± 13.34,p = 0.60)无明显差异。此外,VR 组与无 VR 组相比,某些药物的使用量呈减少趋势,尤其是瑞芬太尼(平均剂量为 200 毫克对 100 毫克(p = 0.12))和诺伐明磺(平均剂量为 1250 毫克对 900 毫克(p = 0.26))。然而,这些差异在统计学上并不显著,因此无法根据这些数据就药物使用情况得出明确结论:虽然在这项试点试验中,VR 催眠并没有显著减轻围手术期的疼痛或焦虑,但观察到的用药量减少趋势表明,VR 催眠具有潜在的益处。这些发现值得在更大规模的确证试验中进一步研究,以更好地了解 VR 在提高患者舒适度方面的作用,并减少手术过程中对药物干预的依赖:试验注册:德国临床试验注册中心:试验注册:德国临床试验注册:DRKS00028508;注册日期:2022年3月15日;通用试验编号:U1111-1275-4995:U1111-1275-4995.
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Impact of virtual reality hypnosedation on perioperative pain and anxiety in port implantation under local anesthesia: a randomized controlled pilot trial (VIP Trial).

Background: This monocentric randomized controlled pilot trial investigates the impact of virtual reality (VR) hypnosedation on perioperative anxiety, pain, patient satisfaction, and medication usage during port implantation under local anesthesia.

Methods: A total of 120 patients undergoing elective port implantation between January 2022 and August 2023 were enrolled and randomized in a 1:1 ratio to either a VR hypnosedation group or a control group. The VR group used a commercially available VR headset with the HypnoVR application, providing various environments, musical backgrounds, and a guiding voice, while the control group underwent the procedure without VR. Patients with ASA > 3, chronic pain, cognitive issues, and contraindications against VR use were excluded. The main outcomes measured were perioperative pain and anxiety scores, with secondary outcomes including perioperative medication usage. Due to the nature of the interventions, blinding of patients and physicians was not feasible. Statistical analysis was primarily descriptive and exploratory, focusing on estimating effect sizes for future trials.

Results: The study found no significant differences in immediate postoperative pain with 1.43 ± 1.63 vs. 1.6 ± 2.05 (p = 0.62) or anxiety scores 30.65 ± 9.13 vs. 31.78 ± 13.34 (p = 0.60) between the no VR and VR group, respectively. Additionally, there was a trend to less usage of certain medications, particularly remifentanil (mean dose of 200 mg vs. 100 mg (p = 0.12)) and novaminsulfon (mean dose of 1250 mg vs. 900 mg (p = 0.26)) in the VR group vs. no VR group, respectively. However, these differences were not statistically significant and therefore no definitive conclusions can be drawn regarding medication usage based on this data.

Conclusion: While VR hypnosedation did not significantly reduce perioperative pain or anxiety in this pilot trial, the observed trends in reduced medication usage suggest potential benefits. These findings warrant further investigation in larger, confirmatory trials to better understand the role of VR in enhancing patient comfort and potentially reducing reliance on pharmacological interventions during surgical procedures.

Trial registration: German Clinical Trials Register: DRKS00028508; registration date 15 March 2022; Universal Trial Number: U1111-1275-4995.

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