Background:
Platelet-rich plasma (PRP) is expected to have a biological augmentation
potential in the healing of various diseases and
injuries, including rotator cuff tears. However,
few evaluations have been performed specifically for large to massive
tears.
Purpose: To assess the efficacy of PRP augmentation in patients undergoing arthroscopic repair for large to massive rotator cuff tears.
Study Design: Randomized controlled trial; Level of evidence, 1.
Methods: A total of 48
patients scheduled for arthroscopic repair of large to massive rotator
cuff tears were randomly assigned to
receive either PRP-augmented (PRP group) or
conventional treatment (conventional group). In the PRP group, 3 PRP
gels (3 ×
3 mL) were applied to each patient between the
torn end and the greater tuberosity. The primary outcome measure was the
retear
rate assessed by magnetic resonance imaging
(MRI) or computed tomographic arthrography (CTA) at a minimum of 9
months after
surgery. Secondary outcome measures included
pain, range of motion, muscle strength, overall satisfaction, functional
scores,
and the change in cross-sectional area (CSA) of
the supraspinatus.
Results: The retear rate of the PRP group (20.0%) was significantly lower than that of the conventional group (55.6%) (P = .023). Clinical outcomes showed no statistical difference between the 2 groups (all P > .05) except for the overall function (P = .043). The change in 1-year postoperative and immediately postoperative CSA was significantly different between the 2 groups:
–15.54 ± 94.34 mm2 in the PRP group versus −85.62 ± 103.57 mm2 in the conventional group (P = .047).
Conclusion: The
application of PRP for large to massive rotator cuff repairs
significantly improved structural outcomes, as evidenced
by a decreased retear rate and increased CSA of
the supraspinatus compared with repairs without PRP augmentation. While
there
was no significant difference in clinical
outcomes except the overall shoulder function after 1-year follow-up,
better structural
outcomes in the PRP group might suggest improved
clinical outcomes at longer term follow-up.
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