Shi Yun-Zhou, Yu Shu-Guang, Zheng Hui, Zheng Qian-Hua, Zhou Si-Yuan, Huang Ying, Zhang Lei-Xiao, Xiao Xian-Jun, Cao Wei, Li Ying
Department of Acupuncture and Moxibustion, Chengdu University of Traditional Chinese Medicine, Chengdu, 610075, China.
Dermatology Department of Affiliated Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, 610075, China.
Chin J Integr Med. 2023 Oct;29(10):924-931. doi: 10.1007/s11655-023-3741-x. Epub 2023 Aug 10.
To determine the feasibility of conducting a full-scale randomized controlled trial (RCT) and investigate the basic information and safety of acupuncture for patients with chronic spontaneous urticaria (CSU).
A total of 80 participants with CSU from July 2018 to July 2019 were randomly assigned to receive active acupuncture (n=41) on a fixed prescription of acupoints or sham acupuncture (n=39) with superficial acupuncture on non-acupuncture points through the completely randomized design. Patients in both groups received 5 sessions per week for 2 weeks, and participants were followed for a further 2 weeks. Feasibility was assessed by recruitment and randomization rates, retention of participants, treatment protocol adherence, and the incidence of adverse events (AEs). The clinical primary outcome was the changes from baseline weekly urticaria activity scores (UAS7) after treatment at 2 weeks. Secondary outcomes included the Visual Analogue Scale (VAS) score of itching intensity, Dermatology Life Quality Index (DLQI), Hamilton Depression Scale (HAMD), and Hamilton Anxiety Scale (HAMA).
A total of 80 participants were enrolled. The recruitment rate of 24.02%, randomization rate of 100%, a loss rate of 6.25%, and no obvious AEs were observed in either group. The decrease from baseline in the mean UAS7 total score at week 2 in the active acupuncture group was -8.63 (95%CI, -11.78 to -5.49) and -6.21 (95%CI, -9.43 to -2.98) in the sham acupuncture group for a between-group difference of -2.42 (95% CI, -6.93 to 2.07). The change in the DLQI, VAS of itching intensity, HAMA, and HAMD were a slightly better improvement trend in the active acupuncture group than the sham acupuncture group, but the between-group difference was not significant.
Active acupuncture had a better improvement trend in alleviating symptoms, improving quality of life and regulating the mood of anxiety and depression in patients with CSU than sham acupuncture. (Registration Nos. AMCTR-ICR-18000190 and ChiCTR2100054776).
确定开展一项全面随机对照试验(RCT)的可行性,并调查针刺治疗慢性自发性荨麻疹(CSU)患者的基本信息和安全性。
采用完全随机设计,将2018年7月至2019年7月共80例CSU患者随机分为两组,分别接受按固定穴位处方的真针刺治疗(n = 41)或在非穴位进行浅刺的假针刺治疗(n = 39)。两组患者均每周接受5次治疗,共2周,之后对参与者进行为期2周的随访。通过招募率、随机化率、参与者保留率、治疗方案依从性以及不良事件(AE)发生率评估可行性。临床主要结局指标为治疗2周后每周荨麻疹活动评分(UAS7)相对于基线的变化。次要结局指标包括瘙痒强度视觉模拟量表(VAS)评分、皮肤病生活质量指数(DLQI)、汉密尔顿抑郁量表(HAMD)和汉密尔顿焦虑量表(HAMA)。
共纳入80例参与者。招募率为24.02%,随机化率为100%,失访率为6.25%,两组均未观察到明显的AE。真针刺组第2周时UAS7总分相对于基线的下降值为-8.63(95%CI,-11.78至-5.49),假针刺组为-6.21(95%CI,-9.43至-2.98),组间差异为-2.42(95%CI,-6.93至2.07)。真针刺组在DLQI、瘙痒强度VAS、HAMA和HAMD方面的改善趋势略优于假针刺组,但组间差异无统计学意义。
与假针刺相比,真针刺在缓解CSU患者症状、改善生活质量以及调节焦虑和抑郁情绪方面具有更好的改善趋势。(注册号:AMCTR-ICR-18000190和ChiCTR2100054776)