Abstract
Background:
Acute lateral ankle sprains are among the most common musculoskeletal injuries, accounting for up to 20% of all sports-related injuries and a leading cause of time lost from athletic participation. Although most cases respond to conservative care, 20% to 40% of athletes develop persistent pain, recurrent sprains, or chronic instability. Biologic therapies such as platelet-rich plasma (PRP) have gained interest for their potential to accelerate ligament healing, but evidence in acute athletic ankle sprains remains limited.
Methods:
This study was designed as a nonmasked randomized controlled trial of consecutively recruited patients presenting with acute lateral ankle sprain. This prospective comparative study enrolled 40 athletic patients (mean age 33.1 years; 50% male) who sustained an acute lateral ankle sprain and presented within 2 weeks of injury. All patients engaged in ≥3 sports sessions weekly, including 8 professional athletes. Participants were randomized to conventional treatment with rest, ice, compression, elevation (RICE) and physiotherapy (n = 20) or the same regimen plus 3 leukocyte-poor PRP injections administered at weekly intervals (n = 20). Primary outcomes were functional and pain assessment using Patient-Reported Outcomes Measurement Information System (PROMIS) Physical Function (PF) and Pain Interference (PI) computer adaptive tests at baseline, 6, and 12 months. The secondary outcome was time to return to unrestricted sport.
Results:
Baseline PROMIS scores were similar between groups. PROMIS PF improved from 42.6 to 69.8 in the control group and from 43.0 to 71.4 in the PRP group by 12 months, whereas PROMIS PI decreased from 61.2 to 38.4 and 60.8 to 37.4, respectively. Both groups exceeded established minimal clinically important differences by 6 months, with no significant between-group differences at 6 or 12 months (PF,
Conclusion:
Leukocyte-poor PRP did not improve PROMIS Pain Interference, PROMIS Physical Function, or overall return to sport rates compared with conventional care. Although a statistically significant and clinically meaningful acceleration in time to return to sport with a moderate effect size was observed, this outcome was exploratory and underpowered, and larger prospective trials are required for confirmation.
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