Department of Physical Medicine and Rehabilitation, Tri-Service General Hospital, School of Medicine, National Defense Medical Center, Neihu, Taipei, Taiwan, Republic of China.
Integrated Pain Management Center, Tri-Service General Hospital, School of Medicine, National Defense Medical Center, Neihu, Taipei, Taiwan, Republic of China.
Pain Med. 2021 Nov 26;22(11):2676-2685. doi: 10.1093/pm/pnab109.
To investigate the effect of hyaluronic acid (HA) in patients diagnosed with mild or moderate carpal tunnel syndrome (CTS).
A prospective randomized, double-blinded control study with 6 months of follow-up.
Rehabilitation outpatient clinic of one single medical center.
Thirty-five participants with mild or moderate CTS.
Participants were enrolled and randomly assigned to HA or control groups. The HA group received one ultrasound-guided perineural injection of 2.5 mL HA while the control group received 2.5 mL normal saline injection through in-plane, long-axis approach to separate the median nerve from the flexor retinaculum via nerve hydrodissection. Boston Carpal Tunnel Syndrome Questionnaire (BCTQ) scores were the primary outcome, while secondary outcomes included the numeric rating scale (NRS), electrophysiological domains, and the cross-sectional area of the median nerve. The assessment was conducted prior to injection and during the second week and 1-, 3-, and 6-months post-injection.
Thirty-two patients (17 wrists in HA group and 15 wrists in control group) completed the study. Compared with the control group, the HA group did not show significantly superior outcomes, except in BCTQ and NRS at the second week post-injection (all P < .0125).
A single ultrasound guided perineural HA injection may have short-term therapeutic efficacy for mild or moderate CTS; however, the 2-weeks superior efficacy was not beneficial for chronic neuropathy. Further studies with larger sample sizes are required to verify its therapeutic efficacy.
研究透明质酸(HA)对轻度或中度腕管综合征(CTS)患者的疗效。
前瞻性随机、双盲对照研究,随访 6 个月。
一家医疗中心的康复门诊。
35 名轻度或中度 CTS 患者。
将患者纳入并随机分为 HA 组或对照组。HA 组接受一次超声引导下的神经周围 2.5 mL HA 注射,而对照组通过平面内长轴方法从屈肌支持带与正中神经之间进行神经水分离,向神经内注射 2.5 mL 生理盐水。Boston 腕管综合征问卷(BCTQ)评分是主要结局,次要结局包括数字评分量表(NRS)、电生理域和正中神经横截面积。评估在注射前、注射后第 2 周、第 1、3 和 6 个月进行。
32 名患者(HA 组 17 腕,对照组 15 腕)完成了研究。与对照组相比,HA 组除了在注射后第 2 周的 BCTQ 和 NRS 评分外(均 P < .0125),其他结果均无明显优势。
单次超声引导下的神经周围 HA 注射可能对轻度或中度 CTS 具有短期疗效,但 2 周的优势疗效对慢性神经病变并无益处。需要更大样本量的进一步研究来验证其疗效。