Petrella Robert J, Petrella Michael J, Cogliano Anthony
Faculties of Medicine and Health Sciences University of Western Ontario London, Canada.
Clin J Sport Med. 2007 Jul;17(4):251-7. doi: 10.1097/JSM.0b013e3180f6169f.
To determine the efficacy and safety of periarticular hyaluronic acid injections in acute lateral ankle sprain during 9 months at a sports injuries center.
Randomized controlled prospective trial.
Primary sport medicine and emergency practice.
One hundred fifty-eight consecutive competitive athletes who suffered acute grade 1 or 2 lateral ankle sprains were randomized within 48 hours of injury.
Patients were randomized at baseline to periarticular injection with hyaluronic acid (HA) + standard of care [rest, ice, compression, and elevation (RICE)] or placebo injection (PL) + standard of care (RICE) treatment at baseline assessment and on day 4 after injury.
Assessments at baseline and days 4, 8, 30, and 90 included Visual Analogue Scale (VAS; 0-10 cm) pain on weight bearing and walking 20 m, patient global assessment of ankle injury (five-point categorical scale), patient satisfaction with treatment (five-point categorical scale), time to return to pain-free and disability-free sport, and adverse events. Differences between groups were determined using an intent-to-treat analysis of variance.
About 30% of the ankle sprains were "first" events, and no differences in clinical assessments with those presenting but not volunteering for the study (n = 341) were observed. Time to intervention was 39 +/- 4 hours, with no difference between groups. No serious adverse events were recorded during the 8-day treatment period. No difference in concomitant treatment or physical therapy was observed between groups. A significant reduction in VAS pain on both weight bearing and walking was observed at day 8 for HA compared with PL (P < 0.05). Significantly greater patient satisfaction was observed for HA versus PL at days 4 (P < 0.05), 8 (P < 0.001), 30 (P < 0.001), and 90 (P < 0.05). Patient global assessment of ankle injury was significantly better compared with baseline in the HA group at day 8, but this was not different between groups. Time to pain-free and disability-free return to sport was 11 (+/-8) versus 17 (+/-8) days for HA and PL, respectively (P < 0.05).
HA treatment for acute ankle sprain was highly satisfactory in the short term and the long term versus PL. This was associated with reduced pain and more rapid return to sport, with few associated adverse events.
在一家运动损伤中心确定关节周围注射透明质酸治疗急性外侧踝关节扭伤9个月的疗效和安全性。
随机对照前瞻性试验。
初级运动医学和急诊实践机构。
158名连续的竞技运动员,他们在受伤48小时内被随机分组,这些运动员均遭受了急性1级或2级外侧踝关节扭伤。
在基线评估时以及受伤后第4天,患者被随机分为关节周围注射透明质酸(HA)+标准护理[休息、冰敷、加压包扎和抬高患肢(RICE)]组或安慰剂注射(PL)+标准护理(RICE)组。
在基线以及第4、8、30和90天进行评估,包括视觉模拟评分法(VAS;0 - 10厘米)评估负重和行走20米时的疼痛、患者对踝关节损伤的整体评估(五点分类量表)、患者对治疗的满意度(五点分类量表)、恢复无痛和无功能障碍运动的时间以及不良事件。使用意向性分析方差法确定组间差异。
约30%的踝关节扭伤为“首次”发作,与那些未参与本研究的患者(n = 341)相比,临床评估无差异。干预时间为39±4小时,组间无差异。在8天的治疗期内未记录到严重不良事件。组间在联合治疗或物理治疗方面未观察到差异。与PL相比,HA组在第8天负重和行走时的VAS疼痛显著降低(P < 0.05)。在第4天(P < 0.05)、第8天(P < 0.001)、第30天(P < 0.001)和第90天(P < 0.05),HA组患者的满意度显著高于PL组。在第8天,HA组患者对踝关节损伤的整体评估与基线相比显著改善,但组间无差异。HA组和PL组恢复无痛和无功能障碍运动的时间分别为11(±8)天和17(±8)天(P < 0.05)。
与PL相比,HA治疗急性踝关节扭伤在短期和长期均非常令人满意。这与疼痛减轻和更快恢复运动相关,且不良事件较少。