Outcomes After Ultrasound-Guided Platelet-Rich Plasma Injections for Chronic Tendinopathy: A Multicenter, Retrospective Review

被引:92
|
作者
Mautner, Kenneth [1 ]
Colberg, Ricardo E. [2 ]
Malanga, Gerard [3 ]
Borg-Stein, Joanne P. [4 ]
Harmon, Kimberly G. [5 ]
Dharamsi, Aisha S. [4 ]
Chu, Samuel [3 ]
Homer, Paul [5 ]
机构
[1] Emory Orthoped & Spine Ctr, Atlanta, GA 30329 USA
[2] Emory Univ, Dept Rehabil Med, Atlanta, GA 30322 USA
[3] Univ Med & Dent New Jersey, Dept Phys Med & Rehabil, Newark, NJ 07103 USA
[4] Harvard Univ, Sch Med, Dept Phys Med & Rehabil, Boston, MA USA
[5] Univ Washington, Dept Orthopaed & Sports Med, Seattle, WA 98195 USA
关键词
RANDOMIZED CONTROLLED-TRIAL; LATERAL EPICONDYLITIS; ACHILLES TENDINOPATHY; FOLLOW-UP; CORTICOSTEROID INJECTIONS; JUMPERS KNEE; TENDON; ELBOW; TENDINOSIS; REPAIR;
D O I
10.1016/j.pmrj.2012.12.010
中图分类号
R49 [康复医学];
学科分类号
100215 ;
摘要
Objective:. To determine whether ultrasound-guided platelet-rich plasma (PR?) injections are an effective treatment for chronic tendinopathies. Design: A retrospective, cross-sectional survey. Setting: Four academic sports medicine centers from across the United States. Patients: A total of 180 men and women between the ages of 18 and 75 years who received ultrasound-guided PRP injections for tendinopathy refractory to conventional treatments. Interventions: Survey on satisfaction and functional outcome. Main Outcome Measurements: Perceived improvement in symptoms at least 6 months after treatment, perceived change in visual analog scale score, assessment of functional pain, and overall satisfaction. Results: On average, patients were 48 years old, had symptoms for a median of 18 months before treatment, and answered the survey on average 15 months after treatment. Overall, 82% of patients indicated moderate to complete improvement in symptoms. The most common injection sites were the lateral epicondyle, Achilles, and patellar tendons. Other sites treated included the rotator cuff, hamstring, gluteus medius, and medial epicondyle, among others. Furthermore, 60% of patients received only 1 injection, 30% received 2 injections, and 10% received 3 or more injections. Patients' perceived decrease in visual analog scale score was 75%, from 7.0 +/- 1.8 to 1.8 +/- 2.0 (-5.2, SD 2.7, 95% confidence interval -5.65 to -4.86, P <.0001). In addition, at follow-up, 95% of patients reported having no pain at rest that disrupted their activities of daily living and 68% reported no pain during activities. A total of 85% of patients were satisfied with the procedure. Conclusions: In this retrospective study, in which we evaluated administration of PRP for chronic tendinopathy, we found that the majority of patients reported a moderate (>50%) improvement in pain symptoms. PM R 2013;5:169-175
引用
收藏
页码:169 / 175
页数:7
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