Department of Emergency Medicine, Icahn School of Medicine at Mount Sinai, 1 Gustave L. Levy Place, New York, NY 10029, United States.
Department of Rehabilitation Medicine, Icahn School of Medicine at Mount Sinai, 1 Gustave L. Levy Place, New York, NY 10029, United States.
Am J Emerg Med. 2018 Jun;36(6):1045-1048. doi: 10.1016/j.ajem.2018.02.038. Epub 2018 Feb 27.
Battlefield acupuncture (BFA) is an ear acupuncture protocol used by the military for immediate pain relief. This is a pilot feasibility study of BFA as a treatment for acute low back pain (LBP) in the emergency department (ED).
Thirty acute LBP patients that presented to ED were randomized to standard care plus BFA or standard care alone. In the BFA group, outcomes were assessed at the time of randomization, 5 min after intervention, and again within 1 h after intervention. In the standard care group outcomes were assessed at the time of randomization and again an hour later. Primary outcomes included post-intervention LBP on a 10-point numeric pain rating scale (NRS) and the timed get-up-and-go test (GUGT). t-Test and chi squared tests were used to compare differences between groups demographics to evaluate randomization, and Analysis of Covariance (ANCOVA) was used to assess differences in primary/secondary outcomes.
We randomized 15 patients to BFA plus standard care, and 15 patients to standard care alone. Demographics were similar between groups. Post-intervention LBP NRS was significantly lower in the BFA group compared with the standard care group (5.2 vs. 6.9, ANCOVA p = 0.04). GUGT was similar between groups (21.3 s vs. 19.0 s, ANCOVA p = 0.327). No adverse events from acupuncture were reported.
This pilot study demonstrates that BFA is feasible as a therapy for LBP in the ED. Furthermore, our data suggest that BFA may be efficacious to improve LBP symptoms, and thus further efficacy studies are warranted. (Clinicaltrials.gov registration number NCT02399969).
战场针灸(BFA)是一种耳部针灸方案,被军方用于即时缓解疼痛。这是一项关于 BFA 治疗急诊急性腰痛(LBP)的初步可行性研究。
30 名急性 LBP 患者被随机分为标准治疗加 BFA 组或单纯标准治疗组。在 BFA 组中,在随机分组时、干预后 5 分钟和干预后 1 小时评估结局。在标准治疗组中,在随机分组时和 1 小时后再次评估结局。主要结局指标包括干预后 10 点数字疼痛评分(NRS)和计时起身行走测试(GUGT)。使用 t 检验和卡方检验比较组间人口统计学差异以评估随机分组情况,使用协方差分析(ANCOVA)评估主要/次要结局的差异。
我们将 15 名患者随机分配至 BFA 加标准治疗组,15 名患者分配至单纯标准治疗组。组间人口统计学特征相似。BFA 组干预后的 LBP NRS 明显低于标准治疗组(5.2 比 6.9,ANCOVA p=0.04)。GUGT 两组间相似(21.3 秒比 19.0 秒,ANCOVA p=0.327)。没有报告与针灸相关的不良事件。
这项初步研究表明,BFA 作为 ED 中 LBP 的治疗方法是可行的。此外,我们的数据表明 BFA 可能有效改善 LBP 症状,因此需要进一步的疗效研究。(临床试验注册号:NCT02399969)。