Department of Electrical Engineering and Computer Science, University of California, Irvine, California, USA.
Sue & Bill Gross School of Nursing, University of California, Irvine, California, USA.
Paediatr Anaesth. 2024 Dec;34(12):1231-1239. doi: 10.1111/pan.14998. Epub 2024 Sep 18.
Pediatric surgery is associated with high levels of anxiety for both children and parents/caregivers. To mitigate anxiety, auricular acupuncture has shown its potential in the perioperative setting. Accordingly, our team developed a wearable prototype auricular laser acupuncture system, AcuHealth V1.0, as a portable acupuncture device and conducted a proof-of-concept evaluation with parents of children undergoing surgery.
The primary aim of this study was to conduct feasibility testing of the AcuHealth V1.0 system in delivering auricular laser acupuncture.
Parents of children who were scheduled to undergo outpatient surgery were randomly assigned to one of three groups: authentic acupuncture (laser beams at known anxiolytic acupoints, n = 13), sham acupuncture (non-anxiolytic acupoints, n = 14), or a placebo control group (inactive laser, n = 14). Parent self-reported anxiety (0-10 numerical rating scale) was assessed at baseline, pre-intervention (once child was taken to the OR), post-intervention, and at 30 min after the intervention. Usability and acceptability data regarding the device were assessed after the intervention.
Baseline data revealed no significant difference in anxiety between the three groups. Parent-reported anxiety level at 30-min post-intervention as compared to baseline in the authentic group was significantly decreased (delta mean ± std = -3.58 ± 2.07) compared to both the sham acupuncture (-1.35 ± 2.65) and placebo control group (0.54 ± 1.13). Evaluation of changes in parent-reported anxiety between groups over time using two-way repeated-measures analysis of variance (ANOVA) revealed a significant difference between the three groups (p = 0.001). Post hoc analysis with Scheffe test pairwise comparisons showed that at 30-min post-intervention compared to baseline, the authentic intervention group was significantly less anxious compared with both the sham group (p = 0.033) and the placebo control group (p = 0.001). Additionally, feedback regarding the usage of the device supported the acceptability and usability of the device with no adverse events.
This pilot study administering laser auricular acupuncture via the AcuHealth V1.0 system decreased parental anxiety after 30 min in parents who received treatment immediately after their children were taken to the operating room with no adverse effect.
小儿外科手术会引起儿童及其父母/看护者高度焦虑。为了减轻焦虑,耳针在围手术期显示出了潜力。因此,我们的团队开发了一种可穿戴式耳穴激光针灸系统,即 AcuHealth V1.0,作为一种便携式针灸设备,并对接受手术的儿童的父母进行了概念验证评估。
本研究的主要目的是对 AcuHealth V1.0 系统进行可行性测试,以实施耳穴激光针灸。
随机将计划接受门诊手术的儿童的父母分为三组:真针灸(激光束作用于已知的安神穴位,n=13)、假针灸(非安神穴位,n=14)或安慰剂对照组(无激光,n=14)。在基线、术前(一旦患儿被带到手术室)、术后和干预后 30 分钟,父母用 0-10 数字评分量表(numerical rating scale)报告焦虑程度。干预后评估了对设备的可用性和可接受性的数据。
基线数据显示,三组之间的焦虑程度无显著差异。与假针灸组(-1.35±2.65)和安慰剂对照组(0.54±1.13)相比,真针灸组在干预后 30 分钟时的父母报告焦虑程度较基线显著降低(差值均值±标准差=-3.58±2.07)。采用双向重复测量方差分析(ANOVA)对组间父母报告焦虑程度随时间变化的评估显示,三组之间存在显著差异(p=0.001)。Scheffe 事后检验两两比较显示,与基线相比,干预后 30 分钟时,真针灸组与假针灸组(p=0.033)和安慰剂对照组(p=0.001)相比,焦虑程度显著降低。此外,对设备使用的反馈表明该设备具有可接受性和易用性,且无不良事件发生。
本研究通过 AcuHealth V1.0 系统给予耳穴激光针灸,在将患儿带到手术室后立即接受治疗的父母中,在 30 分钟后降低了父母的焦虑,且无不良影响。