Measuring Stress Reduction in Patients Receiving Multimedia Entertainment During Vascular Surgery Under Regional Anesthesia: Protocol for a Randomized Controlled Study.

IF 1.4 Q3 HEALTH CARE SCIENCES & SERVICES
Hagen Kerndl, Thomas Peter Millian, Karlheinz Gürtler, Alexander Hyhlik-Duerr
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引用次数: 0

Abstract

Background: This study explores the treatment of internal carotid artery stenosis in patients with a high risk for cardiovascular events. The use of regional anesthesia permits ongoing neurological monitoring and enhances patient safety during the procedure. However, the operation can be stressful and lengthy, highlighting the need for strategies to alleviate patient discomfort. This study evaluates audiovisual distractions such as video goggles to potentially improve patient experiences during carotid surgeries, a topic that has not yet been comprehensively researched.

Objective: We aimed to (1) determine whether there is a benefit for patients regarding stress reduction when using video goggles during vascular surgery of the carotid artery and (2) determine whether any parameters can effectively measure such a potential benefit.

Methods: This prospective, randomized study at the University Hospital Augsburg is evaluating the use of HappyMed video goggles by patients undergoing carotid endarterectomy under regional anesthesia. Participants are randomized into either the intervention group, which receives the video goggles, or the control group, which does not. The surgical and anesthetic procedures remain consistent across both groups. Patients are eligible if they meet the surgical criteria, are able to lie supine, and are cooperative. Patients are excluded if they are receiving corticosteroids, have dementia, or have a language barrier. The study uses questionnaires and vital/laboratory parameters, including cortisol levels and heart rate, to assess stress and anxiety. To monitor potential motion sickness, the occurrence of nausea or vomiting is documented. Both patients and surgical staff will evaluate the experience postoperatively to determine the goggles' impact on patient experience and stress management during surgery.

Results: The study has been approved by the local ethics committee and is registered at ClinicalTrials.gov. Patient inclusion started in September 2022 and should be completed within 3 to 4 years. This paper presents a study protocol that was finalized and approved by the local ethics committee in September 2022. At the time of this protocol's final submission for publication, approximately 90% of the recruitment had been completed. Following completion of recruitment and data acquisition, the results are intended to be published within one year.

Conclusions: This study aims to improve patient comfort and perioperative care during vascular surgery. Therefore, our study aims to investigate if the use of video goggles during surgery is feasible and if there are parameters that indicate a benefit for patients. This study is being conducted as a pilot trial to provide a foundation for future research aimed at improving patient comfort during carotid artery surgery under local anesthesia.

Trial registration: ClinicalTrials.gov NCT06704230; https://clinicaltrials.gov/study/NCT06704230.

International registered report identifier (irrid): DERR1-10.2196/70597.

测量在区域麻醉下血管手术中接受多媒体娱乐的患者的应激减轻:一项随机对照研究的方案。
背景:本研究探讨了心血管事件高危患者颈内动脉狭窄的治疗方法。区域麻醉的使用允许持续的神经监测,并在手术过程中提高患者的安全性。然而,手术可能是紧张和漫长的,强调需要策略来减轻患者的不适。这项研究评估了视听干扰,如视频护目镜,以潜在地改善颈动脉手术期间的患者体验,这一主题尚未得到全面研究。目的:我们的目的是(1)确定在颈动脉血管手术中使用视频护目镜对患者是否有减轻压力的好处,(2)确定是否有任何参数可以有效地衡量这种潜在的好处。方法:这项前瞻性、随机研究在奥格斯堡大学医院进行,旨在评估在区域麻醉下接受颈动脉内膜切除术的患者使用HappyMed视频护目镜的情况。参与者被随机分为干预组和对照组,前者接受视频护目镜,后者不接受视频护目镜。手术和麻醉过程在两组中保持一致。如果患者符合手术标准,能够仰卧,并且愿意合作,则符合条件。如果患者正在接受皮质类固醇,患有痴呆症或有语言障碍,则排除在外。这项研究使用问卷调查和重要的/实验室参数,包括皮质醇水平和心率,来评估压力和焦虑。为了监测潜在的晕动病,记录恶心或呕吐的发生情况。患者和手术人员将对术后体验进行评估,以确定护目镜对患者体验和手术期间压力管理的影响。结果:该研究已获得当地伦理委员会的批准,并已在ClinicalTrials.gov上注册。患者纳入于2022年9月开始,应在3至4年内完成。本文介绍了一项研究方案,该方案于2022年9月由当地伦理委员会最终确定并批准。在本议定书最后提交出版时,大约90%的征聘工作已经完成。在完成招募和数据采集后,结果将在一年内公布。结论:本研究旨在改善血管手术患者的舒适度和围手术期护理。因此,我们的研究旨在调查在手术中使用视频护目镜是否可行,是否有参数表明对患者有益。本研究是一项试点试验,旨在为未来旨在改善局部麻醉下颈动脉手术患者舒适度的研究奠定基础。试验注册:ClinicalTrials.gov NCT06704230;https://clinicaltrials.gov/study/NCT06704230.International注册报告标识符(irrid): DERR1-10.2196/70597。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.40
自引率
5.90%
发文量
414
审稿时长
12 weeks
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