Abstract
Background:
The best nonsurgical treatment for frozen shoulder is still unclear. Extracorporeal shockwave therapy (ESWT) is an innovative adjunctive treatment for frozen shoulder, but its effect is still unclear.
Purpose:
To evaluate the published literature regarding the potential of ESWT as an adjunctive therapy for frozen shoulder.
Study Design:
Systematic review; Level of evidence, 1.
Methods:
Searches were conducted in the PubMed, EMBASE, Cochrane Library, China National Knowledge Infrastructure (CNKI), and VIP Information databases for relevant studies between inception and November 2020. Included were randomized controlled trials (RCTs) for frozen shoulder that compared ESWT with routine treatments to controls. There were no restrictions on the treatment period, type of ESWT, or severity of symptoms. At least 1 of the following outcome indices was assessed: visual analog scale (VAS) for pain, Constant-Murley score (CMS) for shoulder function assessment, or external rotation range of movement (ER ROM). RevMan 5.3 software was used to evaluate the bias and quality of the included studies. For continuous variables, the mean difference (MD) or standardized MD (SMD) with the 95% CI was extracted. For dichotomous data, event ratios and sample sizes were extracted.
Results:
Overall, 20 studies were included. The ESWT used as an adjunct to other interventions had better outcomes compared with control groups regarding immediate and short-term analgesic effects (immediate: MD, –1.10 [95% CI, –1.27 to –0.92], P < .00001; short-term: MD, –0.72 [95% CI, –0.94 to –0.50], P < .00001) as well as immediate function (SMD, 1.54 [95% CI, 1.19 to 1.89], P < .00001], I 2 = 0%). There was significant heterogeneity between studies for long-term analgesia (MD, –0.90 [95% CI, –1.40 to –0.41], P < .00001, I 2 = 89%) and ER ROM (MD, 10.31 [95% CI, 3.46 to 17.17], P < .003, I 2 = 93%).
Conclusion:
ESWT seems to be beneficial to patients with frozen shoulder by alleviating pain and improving function. ESWT could be used as an adjunct therapy to routine treatments, although the quality of the included RCTs was hampered by significant heterogeneity regarding long-term analgesia and joint ROM.
Keywords: extracorporeal shockwave therapy, frozen shoulder, pain, motor function, meta-analysis
Frozen shoulder is a common musculoskeletal disorder characterized by pain, limited joint mobility, and dysfunction, 18 with prevalence rates ranging from <1% to 2%. 19 Frozen shoulder is clinically divided into 3 overlapping phases. The painful freezing phase has a duration of 10 to 36 weeks and is characterized by pain and stiffness around the shoulder, which may worsen at night. The adhesive phase is characterized by restricted range of movement (ROM) with a gradual relief of pain, which occurs at 4 to 12 months. The resolution phase with spontaneous improvement in the ROM takes 12 to 42 months. 7 Frozen shoulder is a self-limited condition, but the recovery may be slow and incomplete, which reduces patients’ activities of daily living and increases their medical burden. 18,26
Because of the uncertainty of the efficacy and risk of surgical treatment, nonsurgical treatments are more likely chosen by patients. 2,17 Among them, intra-articular steroid injection and physical therapy are commonly used nonsurgical treatments and have shown some benefits. 27,40 However, because the 3 stages of frozen shoulder often overlap and the clinical symptoms of patients are complex, adjuvant therapy is often needed throughout the course of treatment. Zhang et al 40 and Dias et al 7 identified that the benefits of steroid injection were specific to the painful freezing phase and not to the adhesive phase of frozen shoulder. Physical therapy provides more obvious benefits in the adhesive phase than in the painful freezing phase. 40
In recent years, extracorporeal shockwave therapy (ESWT) has been increasingly used as an adjunct to other interventions in some randomized controlled trials (RCTs) and has shown satisfactory improvement in multiple aspects. 3,13,30 To date, there is no specialized meta-analysis or systematic review evaluating the effectiveness of ESWT as an adjunctive therapy in treating frozen shoulder. Therefore, the purpose of this study was to perform a meta-analysis to evaluate the effectiveness of ESWT as adjunctive therapy for frozen shoulder. We hypothesized that ESWT would be a positive adjunctive therapy in the treatment of frozen shoulder.
Methods
Search Strategy
A comprehensive search utilizing Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines was performed via PubMed, EMBASE, Cochrane Library, China National Knowledge Infrastructure (CNKI), and VIP Information databases between inception and November 2020. The medical subject headings/keywords were “extracorporeal shockwave therapy,” “frozen shoulder,” “randomized controlled trial,” and “meta-analysis.” Variations of different terms were used to make a systematic search. The complete search strategy used in PubMed is shown in Appendix Table A1. The reference lists of relevant reviews and registered trials were also reviewed to ensure completeness of the search.
Inclusion Criteria
The inclusion criteria were as follows: (1) RCTs; (2) patients who were diagnosed with frozen shoulder and were experiencing pain and restricted joint movement; (3) the experimental groups were treated with ESWT plus routine treatments, the control groups were treated with routine treatments, and the routine treatments were the same in both groups; (4) there were no restrictions on the treatment period, type of ESWT, or severity of symptoms, and the energy intensity was dependent on the tolerance of the patient; (5) the languages were limited to Chinese and English; (6) whether or not to adopt a blinded method was unlimited; and (7) the authors used at least 1 of the following outcome indices: visual analog scale (VAS), Constant-Murley score (CMS), and external rotation ROM (ER ROM).
Exclusion Criteria
The exclusion criteria were as follows: (1) patients experiencing the following comorbidities: rotator cuff disease, fractures, calcifying tendinitis, glenohumeral arthrosis, myofascial pain syndrome, or other diseases that can cause shoulder pain and dysfunction; (2) the original data were not suitable for a meta-analysis, and it was impossible to obtain usable data by contacting the authors; and (3) different types of ESWT were compared with each other.
Data Extraction
Two reviewers (N.Z., J.G.) independently screened the titles and abstracts according to the inclusion and exclusion criteria and thoroughly read the full texts of relevant literature. Studies that met the predefined criteria were included. In the case of a disagreement, a third reviewer (Z.W.) was consulted to assist in the assessment.
Another 2 reviewers (R.L., Y.H.) independently extracted the following data: first author, publication year, sample size, intervention details, follow-up (where available), measurement time, and outcome indices.
Pain intensity was assessed via the VAS (the lower the score, the better the effectiveness). Shoulder function was assessed via CMS (the higher the score, the better the function). The joint ROM was assessed via ER ROM (the higher the degree, the better the curative effect).
The period of assessment was artificially defined as follows: immediate, short-term (<3 months), and long-term (≥3 months). The results at multiple follow-up times from the same study were included in the subgroup analyses by time point. When 2 studies used the same group of participants, the 2 studies were included only when different outcome measures were used.
Bias Assessment and Quality Classification
We evaluated the quality of the included studies using the Cochrane Collaboration’s tool for assessing risk of bias in randomized trials, 11 using RevMan version 5.3 (Nordic Cochrane Centre, The Cochrane Collaboration).
Statistical Processing and Assessment of Heterogeneity
For continuous variables, the mean difference (MD) or standardized MD (SMD) with the 95% CI was extracted. For dichotomous data, event ratios and sample sizes were extracted. Throughout the analyses, a 2-sided test was used, and P values ≤.05 were considered to be statistically significant.
Heterogeneity was evaluated by using the I 2 statistic and the Cochran Q statistic with P values. 26 The data were pooled using the random-effects model if significant heterogeneity was present (I 2 > 50% or PQ < .1); otherwise, a fixed-effects model was used. In the case of significant heterogeneity, subgroup analyses were further conducted to investigate the potential source of heterogeneity on the treatment effect size. 11 The statistical software used was RevMan 5.3 software. A descriptive analysis was performed if data could not be combined.
Results
Study Selection
Initially, 200 records were identified via the electronic database search. Of these, we evaluated 121 full texts for eligibility. Ultimately, 20 RCTs § were included in this review. The flow diagram of the selection process is shown in Figure 1.
Study Characteristics
The characteristics of the included studies are listed in Appendix Table A2. Patients in the adhesive phase were identified in 18 studies, ∥ and patients in the remaining 2 studies 8,34 were in the overlap of the painful freezing phase and adhesive phase. Two 1,8 of the included studies were 3-arm studies, and appropriate data were selected for the statistical analysis based on the inclusion and exclusion criteria.
Methodological Quality and the Risk of Bias Within Studies
The risk of bias graph and the risk of bias summary are shown in Figure 2. Of the included studies, 18 ¶ utilized a suitable method to minimize bias and were considered to have a low risk of selection bias, performance bias, detection bias, attrition bias, reporting bias, and other biases. One 24 of the included studies had a high risk of bias in the randomization scheme, and one 36 of the included studies had a high risk of other biases.
Pain Intensity
Overall, 18 studies # assessed the postintervention effectiveness of ESWT plus routine treatments compared with routine treatments in terms of alleviating pain intensity (MD, –0.97 [95% CI, –1.13 to –0.82], P < .00001, I 2 = 69%). A subgroup analysis was performed based on the assessment time. Compared with routine treatments, both immediate efficacy and short-term efficacy were better. The results were significant and had low heterogeneity (immediate: MD, –1.10 [95% CI, –1.27 to –0.92], P < .00001, I 2 = 40%; short-term: MD, –0.72 [95% CI, –0.94 to –0.50], P < .00001, I 2 = 39%). However, in terms of long-term efficacy, although ESWT plus routine treatments was favored in terms of pain intensity compared with routine treatments, obvious heterogeneity was found, so reliable conclusions could not be drawn (MD, –0.90 [95% CI, –1.40 to –0.41], P < .00001, I 2 = 89%) (Figure 3).
Shoulder Function
Compared with routine treatments, the effectiveness of ESWT plus routine treatments on shoulder function after intervention was assessed in terms of CMS in 4 trials 12,24,29,36 (SMD, 1.13 [95% CI, 0.76-1.49], P < .00001, I 2 = 57%). Strong evidence was detected that ESWT plus routine treatments was more effective for improving shoulder function in terms of immediate efficacy, with no heterogeneity (SMD, 1.54 [95% CI, 1.19–1.89], P < .00001, I 2 = 0%) (Figure 4). However, we could not draw reliable conclusions about short- and long-term efficacy.
Joint Range of Motion
ER ROM was used to reflect the ROM, which was assessed in 4 RCTs. 5,6,9,38 Because of the limited number of studies, ER ROM was measured immediately after treatment in all included studies. The pooled result of the included studies showed that the heterogeneity was high and unacceptable (MD, 10.31 [95% CI, 3.46–17.17], P < .003, I 2 = 93%) (Figure 5).
Discussion
This is the first meta-analysis comparing the effectiveness of ESWT plus routine treatments and routine treatments in frozen shoulder. We preliminarily found that analgesic effects (immediate and short-term) and function (immediate) were better in the groups where ESWT was used as an adjunct to other interventions (immediate analgesic effects: MD, –1.10 [95% CI, –1.27 to –0.92], P < .00001; short-term analgesic effects: MD, –0.72 [95% CI, –0.94 to –0.50], P < .00001; immediate function: SMD, 1.54 [95% CI, 1.19 to 1.89], P < .00001, I 2 = 0%). However, for the improvement of long-term analgesia (MD, –0.90 [95% CI, –1.40 to –0.41], P < .00001, I 2 = 89%) and external rotation of the shoulder joint (MD, 10.31 [95% CI, 3.46 to 17.17], P < .003, I 2 = 93%), although there was evidence pointing to the effectiveness of ESWT plus routine treatments compared with routine treatments, the data were heterogeneous, and the conclusions were not reliable. In addition, because of the limited number of studies and the fact that data reflecting short-term and long-term improvement in shoulder function relied on the same RCT, 29 we could not prove that ESWT as an adjuvant therapy better promotes the improvement of shoulder function.
The pathophysiology of frozen shoulder remains unclear. Although disagreements exist, cytokine-mediated synovial inflammation with fibroblastic proliferation is the most recognized explanation. 22 Increased expression levels of growth factors, cytokines, and matrix metalloproteinases are found in the patient’s capsular biopsy specimens, suggesting that these substances are involved in the inflammatory and fibrotic cascade of frozen shoulder. 7
ESWT refers to a series of acoustic pulses with a certain energy density transmitted to a specific target area via an appropriate generator, thus achieving therapeutic effect. 28 First, the energy emitted via shockwaves can reach the affected area via body fluid and tissue, improve the distribution of local blood flow, promote the activation of molecular and immunological reactions, stimulate angiogenesis, promote microcirculation, increase cell oxygen carrying, produce anti-inflammatory effects, and alleviate pain. 10,14,15 Second, ESWT can upregulate nitric oxide levels, promote the ingrowth of endothelial nitric oxide synthase activity, and downregulate nuclear factor kappa B expression. 21 Third, shockwave therapy can produce a cavitation effect between tissues, cause intertissue release, promote the separation of adhesion, and release the adhesive tissue. 23 Fourth, this method can change the acceptance frequency of nociceptors to pain, change the composition of chemical mediators around nociceptors, cause changes in free radicals around cells, release substances that inhibit pain, and inhibit the transmission of pain information. 10 Fifth, local high-intensity shockwaves can produce superstimulation to nerve endings, reduce nerve sensitivity, hinder nerve conduction function, and relieve pain. 35 Finally, intensification of tissue regeneration, decrease in tissue apoptosis, and effective recruitment of fibroblasts have been observed in some basic studies. 16
Study Limitations
There are some potential limitations that should be addressed in this study. First, because of the time overlap, the clinical stages of disease were not completely uniform. The vast majority were in the adhesive phase, and a small number were in the overlap of the painful freezing phase and adhesive phase. Second, because of the limited number of studies included, we were not able to perform further subgroup analysis on the results with high heterogeneity, or the studies included in subgroup analysis were insufficient, resulting in incomplete conclusions. Third, the characteristics of each included population were inevitably different, which more or less reduced the reliability and clinical applicability of the results to some extent. Clinical trials should be standardized in the future so that meta-analyses will better elaborate subgroups, including stages of frozen shoulder, main symptoms, comorbidity, and sex.
Conclusion
Although the quality level of the included RCTs was limited, based on this meta-analysis, we can conclude that ESWT seems to be beneficial to patients with frozen shoulder by alleviating pain and improving function. ESWT could be used as an adjunct therapeutic method to routine treatments. Considering methodological imperfections, future multicenter, prospective clinical trials with large sample sizes, placebo control, successful blinding, and effective follow-up are needed.
APPENDIX
Table A1.
#1 | Search “Frozen shoulder”[MeSH] |
---|---|
#2 | Search: (((((((((((((((((((((frozen shoulder[Title/Abstract]) OR (Bursitides[Title/Abstract])) OR (Bursitis[Title/Abstract])) OR (Frozen Shoulders[Title/Abstract])) OR (Shoulder, Frozen[Title/Abstract])) OR (Adhesive Capsulitis of the Shoulder[Title/Abstract])) OR (Shoulder Adhesive Capsulitis[Title/Abstract])) OR (Adhesive Capsulitides, Shoulder[Title/Abstract])) OR (Adhesive Capsulitis, Shoulder[Title/Abstract])) OR (Capsulitides, Shoulder Adhesive[Title/Abstract])) OR (Capsulitis, Shoulder Adhesive[Title/Abstract])) OR (Shoulder Adhesive Capsulitides[Title/Abstract])) OR (Capsulitis[Title/Abstract])) OR (Capsulitides[Title/Abstract])) OR (Pes Anserine Bursitis[Title/Abstract])) OR (Bursitides, Pes Anserine[Title/Abstract])) OR (Bursitis, Pes Anserine[Title/Abstract])) OR (Pes Anserine Bursitides[Title/Abstract])) OR (Adhesive Capsulitis[Title/Abstract])) OR (Adhesive Capsulitides[Title/Abstract])) OR (Capsulitides, Adhesive[Title/Abstract])) OR (Capsulitis, Adhesive[Title/Abstract]) |
#3 | Search “Extracorporeal Shockwave Therapy”[MeSH] |
#4 | Search: ((((((((((((((Extracorporeal Shockwave Therapies[Title/Abstract]) OR (Shockwave Therapies, Extracorporeal[Title/Abstract])) OR (Shockwave Therapy, Extracorporeal[Title/Abstract])) OR (Therapy, Extracorporeal Shockwave[Title/Abstract])) OR (Shock Wave Therapy[Title/Abstract])) OR (Shock Wave Therapies[Title/Abstract])) OR (Therapy, Shock Wave[Title/Abstract])) OR (Extracorporeal Shock Wave Therapy[Title/Abstract])) OR (Extracorporeal High-Intensity Focused Ultrasound Therapy[Title/Abstract])) OR (Extracorporeal High Intensity Focused Ultrasound Therapy[Title/Abstract])) OR (HIFU Therapy[Title/Abstract])) OR (HIFU Therapies[Title/Abstract])) OR (Therapy, HIFU[Title/Abstract])) OR (High-Intensity Focused Ultrasound Therapy[Title/Abstract])) OR (High Intensity Focused Ultrasound Therapy[Title/Abstract]) |
#5 | Search (randomized controlled trial[Publication Type]OR randomized[Title/Abstract] OR placebo[Title/Abstract]) |
#6 | #1 OR #2 |
#7 | #3 OR #4 |
#8 | #5 AND #6 AND #7 |
Table A2.
Lead Author (Year) | Sample Size (ESWT/Control) | ESWT Group | Control Group | Intervention Time | Follow-up | Measurement Time | Outcomes |
---|---|---|---|---|---|---|---|
Cai (2019) 1 | 40/40 | ESWT + pain point injection + intra-articular injection b + manual therapy | Pain point injection + intra-articular injection b + manual therapy | 2 wk | 3 mo | Before treatment and 3 mo after treatment | VAS |
Chen (2014) 4 | 35/35 | ESWT (1500 shockwaves, 10 Hz, 1.5 bar) + manual therapy | Manual therapy | Once every 6 d for 20 d | NR | Before and after treatment | VAS |
Choi (2017) 5 | 11/10 | ESWT (800 impulses, 5 Hz, 0.129 mJ/mm2) + kinesio taping | Kinesio taping | Twice a wk for 4 wk | NR | Before and after treatment | ER ROM |
Deng (2019) 6 | 31/31 | ESWT (2000 waves, 8 Hz, 1.0 bar) + ultra-short-wave therapy + joint loosening | Ultra-short-wave therapy + joint loosening | Once every 6 d for 30 d | NR | Before and after treatment | VAS, ER ROM |
Ding (2013) 8 | 65/63 | ESWT (2000 shockwaves, 4.5 J) + massage | Massage | 3×/wk (10× total) | NR | Before and after treatment | VAS |
Gao (2013) 9 | 30/29 | ESWT (600-2000 shocks, 12-15 Hz, 1.6-2.5 bar) + routine rehabilitation therapy | Routine rehabilitation therapy | Once a wk for 3 wk | NR | Before and after treatment | VAS, ER ROM |
Huang (2014) 12 | 24/24 | ESWT (1000 impulses, 0.18-0.25 mJ/mm2) + routine rehabilitation therapy | Routine rehabilitation therapy | Once a wk for 3 wk | NR | Before and after treatment | VAS, CMS |
Li (2018) 20 | 42/42 | ESWT (1500 shockwaves, 10 Hz, 5 bar) + manual therapy | Manual therapy | Once every 6 d (2× total) | NR | Before and after treatment | VAS |
Mo (2017) 24 | 16/20 | ESWT (2500-3500 waves, 10-15 Hz, 1.5-2.8 bar) + warming | Warming acupuncture | Once every 5 d for 25 d | NR | Before and after treatment | CMS |
Qin (2013) 25 | 23/23 | ESWT (1500-2000 shocks, 6.5-11.0 kV) + routine rehabilitation therapy | Routine rehabilitation therapy | Once every 6-7 d for 1 mo | NR | Before and after treatment | VAS |
Shao (2020) 29 | 27/26 | ESWT (1200 shocks, 0.25 mJ/mm2) + oral corticosteroid + transcutaneous electrical nerve stimulation | Oral corticosteroid + transcutaneous electrical nerve stimulation | Once a wk for 6 wk | NR | Before treatment and 2, 6, and 12 wk after treatment | VAS, CMS |
Wang (2017) 32 | 63/63 | ESWT (2000 waves, 0.16 mJ/mm2) + intra-articular injection c + manual therapy | Intra-articular injection c + manual therapy | Once every 2 wk for 8 wk | NR | Before and after treatment | VAS |
Wang (2018) 31 | 36/36 | ESWT (2000-2500 waves, 1.8-2.6 bar, 8-12 Hz) + acupuncture | Acupuncture | 3×/wk for 2 wk | NR | Before and after treatment | VAS |
Wu (2017) 33 | 53/53 | ESWT (2000 shocks, 0.16-2 mJ/mm2) + intra-articular injection | Intra-articular injection | Once a wk for 3 wk | 6 wk | Before treatment and 6 wk after treatment | VAS |
Xie (2019) 34 | 43/44 | ESWT (2000 shockwaves, 8 Hz) + manual therapy | Manual therapy | Once every 5 d for 20 d | NR | Before and after treatment | VAS |
Xu (2016) 36 | 40/40 | ESWT (1000 shockwaves, 10 Hz, 0.18-0.25 mJ/mm2) + manual therapy | Manual therapy | Once a wk (20 d total) | NR | Before and after treatment | VAS, CMS |
Yang (2017) 37 | 26/26 | ESWT (1000-1500 shocks, 50-60 Hz) + routine rehabilitation therapy | Routine rehabilitation therapy | Once every 5 d (3× total) | NR | Before and after treatment | VAS |
Yang (2020) 38 | 25/25 | ESWT (1500-2000 shockwaves, 2.5-3.5 bar, 6 Hz) + massage | Massage | Once every 5-7 d (2-3× total | NR | Before and after treatment | VAS, ER ROM |
Yang (2019) 39 | 20/20 | ESWT (2000 waves, 1.5 bar, 5 Hz) + traditional Chinese medicine (fumigation) | Traditional Chinese medicine fumigation | Once every 6 d for 4 wk | NR | Before and after treatment | VAS |
Zhang (2016) 41 | 30/30 | ESWT (200-300 waves, 2.5 bar) + pain point injection | Pain point injection | For 4 wk | 6 mo | Before treatment and 1 and 6 mo after treatment | VAS |
a CMS, Constant-Murley shoulder function assessment score; ER ROM, external rotation range of movement; ESWT, extracorporeal shockwave therapy; NR, not reported; VAS, visual analog scale.
b Compound betamethasone injection + mecobalamin + lidocaine + normal saline.
c Sodium hyaluronate + triamcinolone acetonide.
Footnotes
Final revision submitted August 3, 2021; accepted September 3, 2021.
One or more of the authors has declared the following potential conflict of interest or source of funding: This study was supported by funds from the National Natural Science Foundation of China (NSFC No. 81674066); the Natural Science Foundation of Chongqing Province (No. cstc2017jcyjAX0397); the TCM Foundation of Chongqing Health Committee of China (No. zy201602119); and the Science Foundation, Yongchuan Hospital of Chongqing Medical University (No. YJYJ201603). AOSSM checks author disclosures against the Open Payments Database (OPD). AOSSM has not conducted an independent investigation on the OPD and disclaims any liability or responsibility relating thereto.
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