Department of Diagnostics, College of Korean Medicine, Wonkwang University, Iksan 54538, Republic of Korea.
7Days Inc., Seoul 06247, Republic of Korea.
J Integr Med. 2024 Sep;22(5):579-587. doi: 10.1016/j.joim.2024.08.003. Epub 2024 Aug 13.
Acupotomy, a more invasive procedure than acupuncture, involves the use of a thicker needle with an integrated knife at the tip, necessitating safety research. We aimed to define relevant adverse events (AEs) and create a standardized form of the ACUPOtomy-related AEs CHECKlist (ACUPOCHECK).
Before conducting the Delphi process, a systematic review and pilot prospective study were conducted to gather information on previously reported AEs. Using these data, pilot versions of the ACUPOCHECK and Delphi questionnaires were developed. The Delphi questionnaire involved selecting types of AE for inclusion, establishing separate criteria for acupotomy-related AEs, and achieving a consensus on AE assessment. Thirteen Korean doctors with experience in acupotomy or AE research were recruited to participate in each Delphi round. Consensus was considered to have been reached if the critical value for the content validity ratio met or exceeded 0.538.
The final ACUPOCHECK was developed using four rounds of the Delphi method and one face-to-face consensus meeting. It included 12 local AEs (pain, hemorrhage, bruise, hematoma, edema, pruritus, rash, infection, nerve damage, dysesthesia, movement impairment, and pneumothorax) and 14 systemic AEs (disease aggravation, needle fatigue, sleepiness, procedural nausea, procedural vomiting, procedural headache, procedural dizziness, sweating, procedural shock, syncope, dyspnea, procedural pain, sleep disorder, and postprocedural infection). Separate criteria were established for pain, hemorrhage and bruising: pain was defined as pain that occurrs during daily activities and persists for longer than 72 h, hemorrhage as bleeding that continues for ≥ 3 min despite pressure application, and bruising as having a bruise with a diameter of ≥ 3 cm. Open-ended descriptions were allowed for AEs not covered by the checklist, and severity and causality were assessed using the Common Terminology Criteria for Adverse Events and modified World Health Organization-Uppsala Monitoring Center criteria.
ACUPOCHECK provides a standardization framework that can help research on traditional practices as well as new tools and techniques that are more invasive and may cause more severe AEs. Subsequent studies will use ACUPOCHECK to develop rational safety guidelines for acupotomy techniques. Please cite this article as: Jun H, Lee H, Yoon SH, Kwon CY, Jeon D, Lee JH, Leem J. Delphi study for developing a checklist of adverse events associated with acupotomy. J Integr Med. 2024; 22(5): 579-587.
针刀疗法比针灸更具侵入性,它使用的是带有一体式刀的更粗的针,因此需要进行安全性研究。我们旨在定义相关的不良事件(AE),并创建针刀相关不良事件检查表(ACUPOCHECK)的标准化形式。
在进行 Delphi 流程之前,我们进行了系统评价和前瞻性试点研究,以收集先前报告的 AE 信息。使用这些数据,开发了 ACUPOCHECK 和 Delphi 问卷的试点版本。Delphi 问卷涉及选择纳入的 AE 类型、为针刀相关 AE 建立单独的标准,并就 AE 评估达成共识。我们招募了 13 名具有针刀或 AE 研究经验的韩国医生参与每一轮 Delphi 研究。如果内容有效性比率的临界值满足或超过 0.538,则认为达成了共识。
最终的 ACUPOCHECK 使用四轮 Delphi 方法和一次面对面共识会议开发而成。它包括 12 种局部 AE(疼痛、出血、瘀伤、血肿、水肿、瘙痒、皮疹、感染、神经损伤、感觉异常、运动障碍和气胸)和 14 种全身 AE(病情加重、针疲劳、嗜睡、程序恶心、程序呕吐、程序头痛、程序头晕、出汗、程序休克、晕厥、呼吸困难、程序疼痛、睡眠障碍和程序后感染)。为疼痛、出血和瘀伤制定了单独的标准:疼痛定义为在日常活动中发生且持续超过 72 小时的疼痛;出血定义为按压后持续出血≥3 分钟;瘀伤定义为直径≥3 厘米的瘀伤。允许检查表未涵盖的 AE 使用开放式描述,并使用不良事件通用术语标准和世界卫生组织-乌普萨拉监测中心修订标准评估严重程度和因果关系。
ACUPOCHECK 提供了一个标准化框架,可帮助研究传统实践以及更具侵入性且可能引起更严重 AE 的新工具和技术。后续研究将使用 ACUPOCHECK 为针刀技术制定合理的安全指南。请引用本文:Jun H, Lee H, Yoon SH, Kwon CY, Jeon D, Lee JH, Leem J. Delphi 研究制定针刀相关不良事件检查表。综合医学杂志。2024;22(5):579-587.