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药物穴位注射疗法治疗腰椎管狭窄症的附加效应和安全性。

Add-on Effect and Safety of Pharmacopuncture Therapy in the Treatment of Patients with Lumbar Spinal Stenosis.

机构信息

Department of Acupuncture and Moxibustion Medicine, Pusan National University Korean Medicine Hospital, Yangsan, Korea.

KM Science Research Division, Korea Institute of Oriental Medicine, Daejeon, Korea.

出版信息

J Acupunct Meridian Stud. 2023 Feb 28;16(1):40-48. doi: 10.51507/j.jams.2023.16.1.40.

Abstract

BACKGROUND

Recently, Korean Medicine treatment with pharmacopuncture therapy (PPT) has been increasingly used in clinical practice to improve symptoms in patients with lumbar spinal stenosis (LSS). The aim of this study is to evaluate the effectiveness and safety of PPT in addition to conventional Korean Medicine treatment (CKMT) for the treatment of patients with LSS, compared with CKMT alone.

METHODS

This study is designed as a pragmatic, randomized, two-armed, parallel, stratified (by sex), controlled pilot trial. Forty patients diagnosed with LSS will be randomly allocated to the PPT + CKMT group or the CKMT group. Patients in the two groups will receive treatment two times weekly for 5 weeks. The primary outcome will be the mean change in the 100-mm visual analog scale score from the baseline to the end of treatment (week 5). The secondary outcomes will include the clinically important difference, Zurich Claudication Questionnaire score, self-reported walking capacity, Modified-Modified Schober test, EuroQol 5-dimension 5-level questionnaire, and Patients' Global Impression of Change. Adverse events will be assessed at each visit.

DISCUSSION

The results of this study will provide meaningful data to evaluate the add-on effect and safety of PPT in the medical care of patients with LSS.

摘要

背景

最近,在临床实践中,越来越多地使用韩医学治疗中的药物穴位注射疗法(PPT)来改善腰椎管狭窄症(LSS)患者的症状。本研究的目的是评估与单独使用韩医学常规治疗(CKMT)相比,PPT 联合 CKMT 治疗 LSS 患者的疗效和安全性。

方法

本研究设计为一项实用的、随机的、双臂的、平行的、分层(按性别)、对照的试点试验。将 40 名诊断为 LSS 的患者随机分配到 PPT+CKMT 组或 CKMT 组。两组患者每周接受两次治疗,共 5 周。主要结局将是从基线到治疗结束(第 5 周)时 100mm 视觉模拟评分的平均变化。次要结局包括临床重要差异、苏黎世间歇性跛行问卷评分、自我报告的步行能力、改良改良 Schober 试验、EuroQol 5 维度 5 级问卷和患者整体变化印象。将在每次就诊时评估不良事件。

讨论

该研究的结果将提供有意义的数据,以评估 PPT 在 LSS 患者医疗中的附加效应和安全性。

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