虚拟现实环境对术后疼痛管理的效果

Srinidhi Thippabathuni, Venkata Anil Chandra Dronamraju, Himavathy Kodandarao Gara, Dharma Rao Vanamali
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引用次数: 0

摘要

术后的当务之急是有效控制疼痛。虚拟现实(VR)可以从心理上分散疼痛刺激,从而减轻疼痛。这项研究旨在确定 VR 分散注意力对术后疼痛的影响,以及患者对 VR 体验的感受。这项以医院为基础的干预研究为期两个月,目的是估计 VR 体验后术后疼痛强度的变化,并分析与 VR 干预相关的体验。研究对象包括接受手术并住院 1-3 天的男女患者,他们被随机分为两组(年龄和性别匹配)。对照组接受标准的术后疼痛治疗。干预组在接受标准护理治疗的同时,还接受了 VR 体验。术后两天内进行两次数字评定量表(NRS)评分。对照组和干预组各有 25 人参加分析。对照组和干预组各有 25 名参与者进行分析。两组中的大多数人都使用布比卡因进行麻醉,并在术后联合使用扑热息痛和双氯芬酸进行镇痛。两组患者术后在未接受 VR 干预的标准疗法中获得的 NRS 评分没有显示出任何显著差异。然而,VR 会话后的 NRS 评分显示,与会话前相比,干预组参与者的 NRS 评分明显下降。通过 IPQ 获得的回答显示,受试者接受 VR 干预过程中的真实感、参与感和临场感。由于 VR 模拟转移了人们对疼痛的大量注意力,因此 VR 课程有助于显著降低疼痛感。大多数人对在病人综合护理中使用 VR 表示了积极的倾向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effectiveness of Virtual Reality Environment for Post-Operative Pain Management
The imperative need of post-operative period is effective pain management. Virtual reality (VR) causes psychological distraction from pain stimuli, and thus may cause pain alleviation. The study was undertaken to determine the effectiveness of VR distraction on post-operative pain and experience of VR sessions among the patients. A hospital-based interventional study was conducted for a period of two months with the objectives to estimate changes in post-operative pain intensity after VR session as well as to analyze experience related to VR interventions. It comprised patients of either gender undergoing surgery and with 1–3 days of hospitalization, who were randomized into two groups (age and gender matched). The control group was kept on standard post-operative pain management. The interventional group was subjected to VR exposure in addition to standard care therapy. The Numerical Rating Scale (NRS) scores were obtained twice post-operatively in subsequent days. I-group presence questionnaire (IPQ) responses were obtained after the VR session. Both control and interventional groups had 25 participants each for analysis. In both the groups, majority were given bupivacaine for anesthesia and combination of paracetamol and diclofenac for post-operative analgesia. The NRS scores of both groups obtained post-operatively on standard therapy without VR intervention did not show any significant difference. However, the post-VR-sessions’ NRS scores showed significant reduction as compared to pre-session scores among the participants of the interventional group. The responses obtained via IPQ revealed acceptance for the features of realism, engagement, and presence during VR intervention. Majority confirmed their willingness to undergo VR sessions in future. VR session helped in significant reduction of pain perception as VR simulation diverted considerable attention away from the pain. Majority expressed positive inclination for utilization of VR in comprehensive patient care.
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