Clinical evaluation of the efficacy and safety of focused extracorporeal shock-wave therapy in patients with cervical spondylosis

Author:

Li Shuangyue1,Liu Jie1,Wang Yan1,Zhu Chan1,Tang Yahong1,Gu Minghong1

Affiliation:

1. Jiangwan Hospital of Shanghai Hongkou District

Abstract

Abstract

Background Extracorporeal shock wave therapy (ESWT) has emerged as a contemporary modality in physiotherapy, demonstrating efficacy in addressing musculoskeletal disorders. Despite its potential, the clinical efficacy of ESWT in the context of cervical spondylosis remains understudied, with a dearth of robust empirical evidence. To bridge this gap, the present study was designed to evaluate the therapeutic impact of focused extracorporeal shock wave therapy (fESWT) on pain alleviation and functional improvement in individuals afflicted with cervical spondylosis. Method A multicenter, randomized controlled clinical study was conducted, collecting data from five clinical studies on the treatment of cervical spondylosis with fESWT from June 2021 to March 2024. The inclusion criteria were patients diagnosed with cervical spondylosis, aged 20–70, without severe underlying diseases such as heart disease, hypertension, diabetes, etc. The exclusion criteria included pregnant women, nursing women, patients with bleeding tendencies, or those with cardiac pacemakers. The control group received conventional physical therapy, while the experimental group received fESWT in addition to conventional physical therapy. The main observation indicators included the Visual Analogue Scale (VAS) for pain scoring, Neck Disability Index (NDI) scoring, cervical range of motion (ROM) scoring, and the Short Form-36 (SF-36) quality of life survey scoring. Results A total of 320 subjects were included in the study, with 160 in the experimental group and 160 in the control group. Post-treatment, the VAS and NDI scores in the experimental group were significantly lower than those in the control group (P < 0.05), while the cervical range of motion (ROM) and SF-36 scores were significantly higher than in the control group (P < 0.05). The overall treatment efficacy rate in the experimental group exceeded 90%, markedly higher than the approximately 70% rate in the control group (P < 0.05). There was no significant difference in the incidence of adverse reactions between the two groups. Conclusion As a non-invasive treatment method, fESWT has shown promising therapeutic effects in the treatment of cervical spondylosis. It effectively reduces patient pain, improves cervical function, and enhances the quality of life, with a high safety profile and minimal adverse reactions, making it worthy of clinical promotion and application.

Publisher

Springer Science and Business Media LLC

Reference16 articles.

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