Issue: November 2018
October 23, 2018
2 min read
Save

No benefits seen with PRP injection in patients with acute Achilles tendon ruptures

Issue: November 2018
You've successfully added to your alerts. You will receive an email when new content is published.

Click Here to Manage Email Alerts

We were unable to process your request. Please try again later. If you continue to have this issue please contact customerservice@slackinc.com.

ORLANDO, Fla. — Results of a double-blind, multicenter, randomized, placebo-controlled trial presented at the Orthopaedic Trauma Annual Meeting suggest platelet-rich plasma injection offered no patient benefits in the management of acute Achilles tendon ruptures.

Joseph Alsousou OTA headshot
Joseph Alsousou

“So, I suggest that the use of [platelet-rich plasma] PRP in soft tissue injuries and possibly chronic injuries is not supported, unless we have more studies similar to this trial with [a] positive effect to justify using PRP in these patients,” Joseph Alsousou, PhD, said during his presentation.

Alsousou and colleagues randomized 230 patients with Achilles ruptures who started non-surgical management within 12 days of surgery and were treated at 19 trauma units. There were 114 patients assigned to receive PRP injection. Overall, 103 patients received PRP injection and 116 patients received placebo. At 4, 7, 13 and 24 weeks, blinded outcome assessments were performed. The primary outcome was muscle-tendon friction assessed at 24 weeks by heel-rise endurance test and limb symmetry index. Other outcomes included the Achilles tendon rupture score, quality of life measured with SF-12, and pain and goal attainment. Whole blood and PRP samples were assessed at a central laboratory.

Results showed that at 24 weeks, 201 of the 230 patients completed the heel-rise endurance test and 214 patients had patient-reported outcomes. At 24 weeks, no difference was seen between patients treated with PRP and those treated with placebo with regard to limb symmetry index, SF-12 and pain or goal attainment. Also, at 4, 7 and 13 weeks, there was no difference between the treatment groups with regard to patient-reported outcomes. Complications were similar between treatment groups. – by Monica Jaramillo

 

Reference:

Keene D, et al. Paper 142. Presented at: Orthopaedic Trauma Association Annual Meeting; Oct. 18-20, 2018; Orlando, Florida.

 

Disclosure: Alsousou reports no relevant financial disclosures.