The Effect of Delayed Injection of Leukocyte-Rich Platelet-Rich Plasma Following Rotator Cuff Repair on Patient Function: A Randomized Double-Blind Controlled Trial

医学 肩袖 磁共振成像 富血小板血浆 外科 肘部 随机对照试验 生理盐水 超声波 肩袖损伤 袖口 运动范围 分级(工程) 麻醉 血小板 放射科 内科学 土木工程 工程类
作者
Martyn Snow,Faisal Nazeer Hussain,Joseph Pagkalos,Tomasz Kowalski,Marcus Green,Samir N. Massoud,Steven James
出处
期刊:Arthroscopy [Elsevier]
卷期号:36 (3): 648-657 被引量:42
标识
DOI:10.1016/j.arthro.2019.09.026
摘要

Purpose To investigate the effect of delayed application of leukocyte-rich platelet-rich plasma (PRP) on rotator cuff repair results as assessed by outcome scores and imaging at one year. Methods Patients with a symptomatic rotator cuff tear awaiting arthroscopic repair were approached to take part in the study. Final eligibility for the study was confirmed at the time of surgery. A total of 97 patients were randomized to an ultrasound guided injection of leukocyte-rich PRP or normal saline between 10 and 14 days postsurgery. A total of 87 patients completed clinical evaluation and underwent magnetic resonance imaging imaging at 1 year. Outcome scores included the American Shoulder and Elbow Score, Constant score, Western Ontario Rotator Cuff Index, and the Disabilities of the Arm, Shoulder and Hand Score. Structural integrity of the repair was assessed according to the Sugaya grading. Muscle fatty infiltration was assessed on magnetic resonance imaging using the Goutallier classification. Results At 1 year postsurgery, there was no significant difference between the treatment groups on any of the patient-reported outcome measures or Constant score. On postoperative imaging analysis, there was no difference in the retear rates (Sugaya 4 and 5) between the groups (21% in control group vs 15.3% in PRP group). Fatty infiltration on postoperative imaging was found to be significantly higher in the normal saline group compared with the PRP group (Kendall’s tau-b P = .032). Conclusions The delayed application of PRP postrotator cuff repair did not improve function as measured by patient-reported outcome measures and Constant score at 1 year postoperatively. Level of Evidence Level II, prospective randomized therapeutic trial.
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