Efficacy of Platelet-Rich Plasma for the Treatment of Interstitial Supraspinatus Tears: A Double-Blinded, Randomized Controlled Trial.

Details

Serval ID
serval:BIB_3821C0329399
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Efficacy of Platelet-Rich Plasma for the Treatment of Interstitial Supraspinatus Tears: A Double-Blinded, Randomized Controlled Trial.
Journal
The American journal of sports medicine
Author(s)
Schwitzguebel A.J., Kolo F.C., Tirefort J., Kourhani A., Nowak A., Gremeaux V., Saffarini M., Lädermann A.
ISSN
1552-3365 (Electronic)
ISSN-L
0363-5465
Publication state
Published
Issued date
07/2019
Peer-reviewed
Oui
Volume
47
Number
8
Pages
1885-1892
Language
english
Notes
Publication types: Journal Article ; Randomized Controlled Trial
Publication Status: ppublish
Abstract
The benefits of platelet-rich plasma (PRP) for the treatment of rotator cuff tears remain inconclusive, as it is administered either as an adjuvant to surgical repair or as a primary infiltration without targeting the index lesion, which could dilute its effect.
To determine whether PRP infiltrations are superior to saline solution infiltrations (placebo) at improving healing, pain, and function when injected under ultrasound guidance within isolated interstitial supraspinatus tears.
Randomized controlled trial; Level of evidence, 1.
In this single-center, double-blinded, randomized controlled trial, 80 adults with symptomatic isolated interstitial tears of the supraspinatus, confirmed by magnetic resonance arthrography, were randomized to PRP or saline injections. Each patient received 2 injections with a 1-month interval. The primary outcome was the change in lesion volume, calculated on magnetic resonance arthrography, at 7 months. The secondary outcomes were improvements in shoulder pain and the Single Assessment Numerical Evaluation (SANE) score at >12 months.
Preoperative patient characteristics did not differ between the 2 groups. At 7 months, there were no significant differences between the PRP and control groups in terms of a decrease in lesion size (-0.3 ± 23.6 mm <sup>3</sup> vs -8.1 ± 84.7 mm <sup>3</sup> , respectively; P = .175); reduction of pain on a visual analog scale (VAS) (-2.3 ± 3.0 vs -2.0 ± 3.0, respectively; P = .586); and improvement in SANE (16.7 ± 20.0 vs 14.9 ± 29.0, respectively; P = .650), Constant (8.6 ± 13.0 vs 10.7 ± 19.0, respectively; P = .596), and American Shoulder and Elbow Surgeons (19.5 ± 20.0 vs 21.9 ± 28.0, respectively; P = .665) scores. At >12 months, there were no significant differences between the PRP and control groups in terms of a reduction of pain on a VAS (-3.3 ± 2.6 vs -2.3 ± 3.2, respectively; P = .087) or improvement in the SANE score (24.4 ± 27.5 vs 23.4 ± 24.9, respectively; P = .846). At 19.5 ± 5.3 months, the incidence of adverse effects (pain >48 hours, frozen shoulder, extension of lesion) was significantly higher in the PRP group than the control group (54% vs 26%, respectively; P = .020).
PRP injections within interstitial supraspinatus tears did not improve tendon healing or clinical scores compared with saline injections and were associated with more adverse events.
NCT02672085 (ClinicalTrials.gov identifier).
Keywords
Adolescent, Adult, Aged, Arthrography, Double-Blind Method, Female, Humans, Injections, Magnetic Resonance Imaging, Male, Middle Aged, Platelet-Rich Plasma, Rotator Cuff Injuries/therapy, Shoulder Pain/therapy, Treatment Outcome, Visual Analog Scale, Young Adult, inflammation, tendinitis, treatment, ultrasonography
Pubmed
Web of science
Create date
17/06/2019 17:25
Last modification date
20/06/2020 6:18
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