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Periarticular hyaluronic acid in acute ankle sprain.

机译:急性踝关节扭伤的关节周围透明质酸。

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摘要

OBJECTIVES: To determine the efficacy and safety of periarticular hyaluronic acid injections in acute lateral ankle sprain during 9 months at a sports injuries center. DESIGN: Randomized controlled prospective trial. SETTING: Primary sport medicine and emergency practice. PATIENTS: One hundred fifty-eight consecutive competitive athletes who suffered acute grade 1 or 2 lateral ankle sprains were randomized within 48 hours of injury. INTERVENTIONS: 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. OUTCOMES MEASURES: 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. RESULTS: 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). CONCLUSION: 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.
机译:目的:确定在运动损伤中心进行的9个月内急性侧踝扭伤的关节周围透明质酸注射液的疗效和安全性。设计:随机对照的前瞻性试验。地点:初级运动医学和急诊科。患者:158名连续1或2级急性侧踝扭伤的连续运动员在受伤48小时内随机分组。干预措施:在基线评估时,患者在基线时随机接受透明质酸(HA)+护理标准[休息,冰,压迫和抬高(RICE)]或安慰剂注射(PL)+护理标准(RICE)治疗的关节周围注射受伤后第4天。结果指标:基线,第4、8、30和90天的评估包括视觉模拟量表(VAS; 0-10 cm)负重和步行20 m疼痛,患者踝关节整体损伤评估(五点分类量表) ,患者对治疗的满意度(五点分类量表),恢复无痛和无残障运动的时间以及不良事件。组间差异使用意向性治疗方差分析确定。结果:约30%的踝关节扭伤是“第一”事件,与观察到但未自愿参加研究的患者(n = 341)在临床评估中没有差异。干预时间为39 +/- 4小时,两组之间无差异。在为期8天的治疗期间,未记录到严重的不良事件。两组之间在伴随治疗或物理治疗方面均未见差异。与PL相比,HA的第8天观察到负重和行走时VAS疼痛明显减轻(P <0.05)。在第4天(P <0.05),第8天(P <0.001),第30天(P <0.001)和90天(P <0.05),观察到HA与PL的患者满意度显着提高。第8天,HA组的患者对踝关节损伤的整体评估明显优于基线,但这在两组之间没有差异。 HA和PL的无痛和无残障恢复时间分别为11(+/- 8)天和17(+/- 8)天(P <0.05)。结论:与PL相比,HA治疗急性和踝关节扭伤的短期和长期效果令人满意。这与减轻疼痛和更快地恢复运动有关,几乎没有相关的不良事件。

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