Galois Laurent, Coillard Jean-Yves, Porterie Jérôme, Melac-Ducamp Sylvie, Conrozier Thierry
Service de chirurgie orthopédique, Centre hospitalier Universitaire de Nancy, Nancy, France.
Service de chirurgie du pied et de la cheville, Clinique Orthopédique du Parc, Lyon, France.
Clin Med Insights Arthritis Musculoskelet Disord. 2022 Mar 10;15:11795441211055882. doi: 10.1177/11795441211055882. eCollection 2022.
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).
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.
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; < .0001). At baseline there was no statistically difference in pain between the radiological stages ( = .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 ( = .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.
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.
本研究旨在获取有关单次关节腔内注射甘露醇修饰的交联透明质酸(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的信息。
该研究为一项观察性、单臂、前瞻性多中心试验,随访3个月。纳入标准为症状性1st MTPJ-OA患者,其疼痛不能通过镇痛药和/或非甾体抗炎药和/或足部矫形器缓解。所有患者在第一跖趾关节接受1mL HANOX-M-XL的单次影像引导下关节腔内(IA)注射。主要结局是注射日期至第3个月之间疼痛的变化。次要结局包括患者对疗效的评估、止痛药使用的减少以及影像学评分对临床疗效的影响。
65名参与者(72.3%为女性,平均年龄 = 60岁)纳入试验。Coughlin-Shurnas放射学分级为1级的患者有28例,2级的有29例,3级的有6例。在基线和第3个月时,平均疼痛评分(0-10分)分别为6.5±1.8和2.8±2.3。疼痛评分变化具有高度显著性(-3.1±2.9;<0.0001)。基线时,放射学分期之间的疼痛无统计学差异(P = 0.69)。在终点时,X线1期的平均疼痛评分为2.0±1.9,2期为3.1±2.3,3期为3.3±2.4(P = 0.001)。15名患者报告了轻度至中度不良反应。所有不良反应均为拇趾疼痛短暂加重,在注射后立即出现并持续至6小时,1至7天内缓解。
这项初步研究表明,单次关节腔内注射HANOX-M-XL是安全的,主要对轻度至中度1st MTPJ-OA患者有益。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。