Effectiveness of platelet-rich plasma in partial-thickness rotator cuff tears: a systematic review

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Abstract

Importance

Partial-thickness rotator cuff tears (PTRCTs) commonly affect overhead athletes, leading to a decline in sports performance. Platelet-rich plasma (PRP) is being explored as an alternative treatment modality for individuals with PTRCTs to reduce discomfort and enhance functional recovery. We conducted a systematic review study of randomized controlled clinical trials to determine the effectiveness of PRP in treating PTRCTs.

Aim

To determine the effectiveness of PRP in treating PTRCTs.

Evidence review

We conducted a comprehensive literature search for randomized controlled trials (RCTs) that compared the effectiveness of PRP with eccentric exercise and placebo injections as treatments for PTRCTs. We searched databases such as the Cochrane Library, Web of Science, PubMed, and EMBASE. The visual analog scale (VAS) score, American Shoulder and Elbow Surgeon (ASES) score, and Constant–Murley Score (CMS) was utilized as an outcome measure. Statistical analysis was performed using RevMan 5.3 software.

Findings

Our meta-analysis included 12 studies involving 762 patients. At six weeks post-treatment, the PRP group had significantly higher VAS scores compared to the control group, indicating improvement (standard mean difference (SMD): −2.04 [95% confidence interval (CI): −4.00 to −0.08], I2 ​= ​97%, P-value ​= ​0.04). Patients who received PRP showed statistically significant improvements in VAS scores at 3 months and 6 months follow-up (SMD, −1.78 [95% CI: −3.03 to −0.52], I2 ​= ​96%, P-value ​= ​0.005) (SMD: −2.26 [95% CI: −3.77 to −0.76], I2 ​= ​97%, P-value ​= ​0.003). A statistically significant difference was also observed in VAS scores at the long-term 1-year follow-up (SMD: −2.27 [95% CI: −4.07 to −0.47]; I2 ​= ​98%; P-value ​= ​0.031). There were statistically significant differences in ASES scores and CMS scores in the short-term (SMD: 1.21 [95% CI: 0.19 to 2.24], I2 ​= ​96%, P-value ​= ​0.02) (SMD, 2.01 [95% CI: 0.14 to 3.88], I2 ​= ​97%, P-value ​= ​0.04). However, in the long-term ASES and CMS scores did not show any statistical significance (SMD: 2.06 [95% CI: −0.54 to 4.65], I2 ​= ​99%, P-value ​= ​0.12) (SMD: 4.36 [95% CI: −5.48 to 14.21], I2 ​= ​99%, P-value ​= ​0.39).

Conclusions and relevance

Our findings suggest that PRP treatment is effective in reducing pain for individuals with PTRCTs, providing benefits in the short and long term. However, its impact on functional recovery appears somewhat constrained and doesn't endure over time. Additionally, significant heterogeneity exists among studies, encompassing variations in PRP composition and control group treatments. Consequently, we conclude that compelling evidence for symptom improvement in PTRCT patients following PRP treatment remains elusive.

Level of evidence

Level I.

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富血小板血浆对部分厚度肩袖撕裂的疗效:一项荟萃分析。
重要性:肩袖部分厚度撕裂(PTRCT)通常会影响高空运动员,导致运动成绩下降。富血小板血浆(PRP)作为一种替代治疗方法,正在为患有肩袖部分撕裂症的患者进行探索,以减轻不适感并促进功能恢复。我们对随机对照临床试验进行了系统回顾研究,以确定 PRP 治疗 PTRCTs 的有效性:我们对随机对照试验(RCT)进行了全面的文献检索,这些试验比较了 PRP 与偏心运动和安慰剂注射治疗 PTRCTs 的有效性。我们检索了 Cochrane Library、Web of Science、PubMed 和 EMBASE 等数据库。采用视觉模拟量表(VAS)评分、美国肩肘外科医生(ASES)评分和康斯坦茨-默里评分(CMS)作为结果测量指标。统计分析使用 RevMan 5.3 软件进行:我们的荟萃分析包括 12 项研究,涉及 762 名患者。在治疗后六周,PRP 组的 VAS 评分明显高于对照组,表明病情有所改善(标准平均差(SMD),-2.04 [95% 置信区间(CI),-4.00 至 -0.08],I2 =97%,P 值 =0.04)。接受PRP治疗的患者在3个月和6个月随访时的VAS评分有显著统计学改善(SMD,-1.78 [95% CI,-3.03至-0.52],I2 =96%,P值 =0.005)(SMD,-2.26 [95% CI,-3.77至-0.76],I2 =97%,P值 =0.003)。在 1 年的长期随访中,VAS 评分也出现了统计学意义上的显著差异(SMD,-2.27 [95% CI,-4.07 至 -0.47];I2 =98%;P 值 =0.031)。ASES 评分和 CMS 评分的短期差异有统计学意义(SMD,1.21 [95% CI,0.19 至 2.24],I2 =96%,P 值 =0.02)(SMD,2.01 [95% CI,0.14 至 3.88],I2 =97%,P 值 =0.04)。然而,长期的ASES和CMS评分没有显示出任何统计学意义(SMD,2.06 [95% CI,-0.54至4.65],I2 =99%,P值=0.12)(SMD,4.36 [95% CI,-5.48至14.21],I2 =99%,P值=0.39):我们的研究结果表明,PRP 治疗能有效减轻 PTRCT 患者的疼痛,并带来短期和长期的益处。然而,它对功能恢复的影响似乎受到了一定的限制,并且不会随着时间的推移而持续。此外,不同研究之间存在明显的异质性,包括 PRP 成分和对照组治疗方法的差异。因此,我们得出结论,PTRCT 患者在接受 PRP 治疗后症状得到改善的有力证据仍然难以捉摸:证据等级:一级。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.90
自引率
6.20%
发文量
61
审稿时长
108 days
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