Platelet-Rich Plasma Injection for Chronic Achilles Tendinopathy A Randomized Controlled Trial

被引:555
作者
de Vos, Robert J. [1 ]
Weir, Adam [3 ]
van Schie, Hans T. M. [1 ,4 ]
Bierma-Zeinstra, Sita M. A. [2 ]
Verhaar, Jan A. N. [1 ]
Weinans, Harrie [1 ]
Tol, Johannes L. [3 ]
机构
[1] Erasmus Univ, Med Ctr, Dept Orthoped, NL-3000 CA Rotterdam, Netherlands
[2] Erasmus Univ, Med Ctr, Dept Gen Practice, NL-3000 CA Rotterdam, Netherlands
[3] Hague Med Ctr Antoniushove, Dept Sports Med, Leidschendam, Netherlands
[4] Univ Utrecht, Dept Equine Sci, Utrecht, Netherlands
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 2010年 / 303卷 / 02期
关键词
TENDINOSIS; OSTEOARTHRITIS; MANAGEMENT; SURGERY; TENDON; PAIN;
D O I
10.1001/jama.2009.1986
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context Tendon disorders comprise 30% to 50% of all activity-related injuries; chronic degenerative tendon disorders (tendinopathy) occur frequently and are difficult to treat. Tendon regeneration might be improved by injecting platelet-rich plasma (PRP), an increasingly used treatment for releasing growth factors into the degenerative tendon. Objective To examine whether a PRP injection would improve outcome in chronic midportion Achilles tendinopathy. Design, Setting, and Patients A stratified, block-randomized, double-blind, placebo-controlled trial at a single center ( The Hague Medical Center, Leidschendam, the Netherlands) of 54 randomized patients aged 18 to 70 years with chronic tendinopathy 2 to 7 cm above the Achilles tendon insertion. The trial was conducted between August 28, 2008, and January 29, 2009, with follow-up until July 16, 2009. Intervention Eccentric exercises ( usual care) with either a PRP injection ( PRP group) or saline injection ( placebo group). Randomization was stratified by activity level. Main Outcome Measures The validated Victorian Institute of Sports Assessment-Achilles (VISA-A) questionnaire, which evaluated pain score and activity level, was completed at baseline and 6, 12, and 24 weeks. The VISA-A score ranged from 0 to 100, with higher scores corresponding with less pain and increased activity. Treatment group effects were evaluated using general linear models on the basis of intention-to-treat. Results After randomization into the PRP group (n=27) or placebo group (n=27), there was complete follow-up of all patients. The mean VISA-A score improved significantly after 24 weeks in the PRP group by 21.7 points (95% confidence interval [CI], 13.0-30.5) and in the placebo group by 20.5 points ( 95% CI, 11.6-29.4). The increase was not significantly different between both groups ( adjusted between-group difference from baseline to 24 weeks, -0.9; 95% CI, -12.4 to 10.6). This CI did not include the predefined relevant difference of 12 points in favor of PRP treatment. Conclusion Among patients with chronic Achilles tendinopathy who were treated with eccentric exercises, a PRP injection compared with a saline injection did not result in greater improvement in pain and activity. Trial Registration clinicaltrials. gov Identifier: NCT00761423 JAMA. 2010;303(2):144-149 www.jama.com
引用
收藏
页码:144 / 149
页数:6
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