单次关节内注射甘露醇修饰的交联透明质酸(HANOX-M-XL)治疗第一跖趾骨关节炎(拇僵硬)的开放标签试点研究:REPAR试验

IF 1.9 Q2 ORTHOPEDICS
L. Galois, J. Coillard, J. Porterie, S. Melac-Ducamp, T. Conrozier
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引用次数: 1

摘要

目的:本研究的目的是获得单次关节内注射甘露醇修饰交联透明质酸(HANOX-M-XL)治疗疼痛性第一跖趾关节骨关节炎(1stMTPJ-OA)患者的安全性和短期疗效信息。方法:本研究采用观察性、单臂、前瞻性多中心试验,随访3个月。纳入标准是有症状的第1 MTPJ-OA患者,未通过止痛药和/或非甾体抗炎药和/或足部矫形器缓解。所有患者均在第一MTPJ接受单次影像学引导下关节内注射1ml HANOX-M-XL。主要观察结果是注射之日至第3个月期间疼痛的变化。次要结局是患者对疗效的评价、止痛药使用的减少以及x线评分对临床疗效的影响。结果:65名受试者(72.3%为女性,平均年龄60岁)被纳入试验。28例患者的Coughlin-Shurnas放射分级为1级,29例为2级,6例为3级。在基线和第3个月,平均疼痛(0-10)分别为6.5±1.8和2.8±2.3。疼痛评分变化极显著(−3.1±2.9;p < 0.0001)。在基线时,放射学分期之间疼痛无统计学差异(P = 0.69)。终点时,x线1期平均疼痛评分为2.0±1.9分,2期为3.1±2.3分,3期为3.3±2.4分(P = 0.001)。轻至中度不良反应15例。所有病例均为短暂性拇痛加重,在注射后立即和6小时内发生,并在1至7天内消退。结论:本初步研究提示单次IA注射HANOX-M-XL是安全的,且主要受益于轻中度1期MTPJ-OA患者。需要进一步的随机对照试验来证实这些初步的令人鼓舞的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Open-Label Pilot Study of a Single Intra-Articular Injection of Mannitol-Modified Cross-Linked Hyaluronic Acid (HANOX-M-XL) for the Treatment of the First Metatarsophalangeal Osteoarthritis (Hallux Rigidus): The REPAR Trial
Purpose: The purpose of this study was to obtain information on safety and short-term efficiency of a single intra-articular injection of mannitol-modified cross-linked hyaluronic acid (HANOX-M-XL) in patients with painful first metatarsophalangeal joint osteoarthritis (1stMTPJ-OA). Methods: The study involved an observational, single-arm, prospective multicentre trial, with a 3-month follow-up. Inclusion criteria were patients with symptomatic 1st MTPJ-OA not relieved by analgesics and / or non-steroidal-anti-inflammatory drugs and / or foot orthotic. All patients received a single, imaging-guided intra-articular (IA) injection of 1 mL of HANOX-M-XL in the 1st MTPJ. The primary outcome was the change in pain between the date of injection and month 3. The secondary outcomes were the patient assessment of effectiveness, the decrease in painkiller use and the influence of the radiographic score on the clinical efficacy. Results: Sixty-five participants (72.3% women, mean age = 60) were included in the trial. Coughlin-Shurnas radiological grade was 1 in 28 patients, 2 in 29, and 3 in 6. At baseline and month 3, the average pain (0-10) was 6.5 ± 1.8 and 2.8 ± 2.3, respectively. The change in pain score was highly significant (−3.1 ± 2.9; P < .0001). At baseline there was no statistically difference in pain between the radiological stages (P = .69). At endpoint, the average pain score was 2.0 ± 1.9 in x-ray stage 1, 3.1 ± 2.3 in stage 2 and 3.3 ± 2.4 in stage 3 (P = .001). Mild to moderate adverse reactions were reported by 15 patients. All were a transient increase of the hallux pain that occurred immediately and up to 6 hours after injection and resolved in 1 to 7 days. Conclusion: This pilot study suggests that a single IA injection of HANOX-M-XL is safe and mainly benefits patients with mild moderate 1st MTPJ-OA. Further randomized controlled trials are necessary to confirm these preliminary encouraging results.
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来源期刊
CiteScore
4.40
自引率
0.00%
发文量
14
审稿时长
8 weeks
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