Return to play after treating acute muscle injuries in elite football players with radial extracorporeal shock wave therapy
- PMID: 34876172
- PMCID: PMC8650394
- DOI: 10.1186/s13018-021-02853-0
Return to play after treating acute muscle injuries in elite football players with radial extracorporeal shock wave therapy
Abstract
Background: To compare lay-off times achieved by treating acute muscle injuries in elite football players with a multimodal therapy approach that includes a specific protocol of almost daily radial extracorporeal shock wave therapy (rESWT) with corresponding data reported in the literature.
Methods: We performed a retrospective analysis of treatments and recovery times of muscle injuries suffered by the players of an elite football team competing in the first/second German Bundesliga during one of the previous seasons.
Results: A total of 20 acute muscle injuries were diagnosed and treated in the aforementioned season, of which eight (40%) were diagnosed as Type 1a/muscular tightness injuries, five (25%) as Type 2b/muscle strain injuries, four (20%) as Type 3a/partial muscle tear injuries and three (15%) as contusions. All injuries were treated with the previously mentioned multimodal therapy approach. Compared with data reported by Ekstrand et al. (Br J Sports Med 47:769-774, 2013), lay-off times (median/mean) were shortened by 54% and 58%, respectively, in the case of Type 1a injuries, by 50% and 55%, respectively, in the case of Type 2b injuries as well as by 8% and 21%, respectively, in the case of Type 3a injuries. No adverse reactions were observed.
Conclusions: Overall, the multimodal therapy approach investigated in this study is a safe and effective treatment approach for treating Type 1a and 2b acute muscle injuries amongst elite football players and may help to prevent more severe, structural muscle injuries.
Keywords: Acute muscle injury; Athletes; Extracorporeal shock wave therapy; Rehabilitation; Return-to-play.
© 2021. The Author(s).
Conflict of interest statement
CS has received research funding from Electro Medical Systems (Nyon, Switzerland) (the inventor, manufacturer and distributor of the Swiss DolorClast rESWT device as well as the distributor of the Swiss PiezoClast fESWT device) for his preclinical research at LMU Munich (unrestricted grant) and consulted (until December 31, 2017) for Electro Medical Systems. Furthermore, Electro Medical Systems provided the rESWT and fESWT devices used in this study. However, Electro Medical Systems had no role in study design, data collection and analysis, interpretation of the data, and no role in the decision to publish and write this manuscript. No other potential competing interest relevant to this article were reported.
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References
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