• Br J Sports Med · Apr 2011

    Randomized Controlled Trial

    No effects of PRP on ultrasonographic tendon structure and neovascularisation in chronic midportion Achilles tendinopathy.

    • R J de Vos, A Weir, J L Tol, J A N Verhaar, H Weinans, and H T M van Schie.
    • Department of Orthopaedic Surgery, Erasmus Medical Centre, Rotterdam, The Netherlands. r.devos@erasmusmc.nl
    • Br J Sports Med. 2011 Apr 1; 45 (5): 387-92.

    ObjectiveTo assess whether a platelet-rich plasma (PRP) injection leads to an enhanced tendon structure and neovascularisation, measured with ultrasonographic techniques, in chronic midportion Achilles tendinopathy.DesignDouble-blind, randomised, placebo-controlled clinical trial.SettingSports medical department of The Hague medical centre.Patients54 patients with chronic midportion Achilles tendinopathy were included.InterventionsPatients were randomised to eccentric exercise therapy with either a PRP injection (PRP group) or a saline injection (placebo group).Main Outcome MeasurementsTendon structure was evaluated by ultrasonographic tissue characterisation, a novel technique which quantifies tendon structure into four echo-types: echo-types I+II represent organised tendon bundles, whereas echo-types III+IV represent a disorganised tendon structure. Colour Doppler ultrasonography was used to measure the degree of neovascularisation. Follow-up was at 6, 12 and 24 weeks.ResultsA significant improvement in echo-types I+II was found after 24 weeks within both the PRP group (n=27) and the placebo group (n=27), but there was no significant between-group difference (95% CI -1.6 to 7.8, p=0.169). After 6 weeks, the neovascularisation score increased within the PRP group (p=0.001) and the placebo group (p=0.002), but there was no significant between-group difference in change in neovascularisation score at any point in time.ConclusionInjecting PRP for the treatment of chronic midportion Achilles tendinopathy does not contribute to an increased tendon structure or alter the degree of neovascularisation, compared with placebo.FundingBiomet Biologics LLC, Warsaw, Indiana.

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