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. 2020 Nov 13;99(46):e23201. doi: 10.1097/MD.0000000000023201

Effects of dextrose prolotherapy on tendinopathy, fasciopathy, and ligament injuries, fact or myth?

A systematic review and meta-analysis

Meng-Wu Chung a, Chih-Yang Hsu b, Wen-Kuei Chung b, Yen-Nung Lin b,c,
Editor: Atul Dwivedi
PMCID: PMC7668443  PMID: 33181700

Supplemental Digital Content is available in the text

Keywords: connective tissue, injections, musculoskeletal diseases, proliferation therapy

Abstract

Objectives:

Prolotherapy or proliferative therapy is a treatment option for damaged connective tissues involving the injection of a solution (proliferant) which theoretically causes an initial cell injury and a subsequent “proliferant” process of wound healing via modulation of the inflammatory process. Nonetheless, the benefits of dextrose prolotherapy have not been adequately evaluated. Therefore, the present study assesses the effectiveness and superiority of prolotherapy separately in treating dense fibrous connective tissue injuries.

Methods:

PubMed, Scopus, and Embase were searched from the earliest record to February 18, 2019. This study included randomized controlled trials which

  • 1.

    involved adult patients with tendinopathy, fasciopathy, and ligament injuries;

  • 2.

    compared dextrose prolotherapy to placebo or no treatment or corticosteroid injection;

  • 3.

    provided quantitative measurements of pain and activity before and after intervention.

Both analysis at individual studies level and pooled meta-analysis were performed.

Results:

Ten trials involving 358 participants were included for review. At study level, the majority of comparisons did not reveal significant differences between dextrose prolotherapy and no treatment (or placebo) regarding pain control. The meta-analysis showed dextrose prolotherapy was effective in improving activity only at immediate follow-up (i.e., 0–1 month) (standardized mean difference [SMD]: 0.98; 95% confidence interval [CI]: 0.40–1.50; I2 = 0%); and superior to corticosteroid injections only in pain reduction at short-term follow-up (i.e., 1–3 month) (SMD: 0.70; 95% CI: 0.14–1.27; I2 = 51%). No other significant SMDs were found in this analysis.

Conclusions:

There is insufficient evidence to support the clinical benefits of dextrose prolotherapy in managing dense fibrous tissue injuries. More high-quality randomized controlled trials are warranted to establish the benefits of dextrose prolotherapy.

Review registration:

PROSPERO (CRD42019129044).

1. Introduction

Dense fibrous connective tissues, or dense regular connective tissues, are predominantly collagenous tissues with dense and regular orientation of the fibers with respect to each other.[1] They are found in highly fibrous tissues such as ligaments, tendons, fascia, and aponeuroses and are known for their high tensile strength.[2] Unlike skeletal muscle and bone, which are to some degree capable of regeneration, dense fibrous connective tissues heal by the formation of collagen and scar tissue after being injured. The healing process is characterized by angiofibroblastic hyperplasia, including hypercellularity, neovascularization, increased protein synthesis, and matrix disorganization.[35] In general, this process is slow,[6] and the resulting fibroblastic scars often possess inferior mechanical and biochemical properties compared to native tissues.[7,8] These factors can contribute to chronic pain and disabilities observed in patients with tendinopathies, fasciopathies, and ligament injuries. So far, experts have not agreed upon an effective treatment that optimizes the healing process.

Several injective medications have been tried to facilitate the healing process after fibrotic tissue injuries. Corticosteroid injection therapies have been used in managing these injuries; however, the lack of inflammation in the healing process, along with poor long-term outcomes[9,10] and adverse effects,[1113] have led investigators to question the use of corticosteroid injections. Prolotherapy with hypertonic dextrose (PrT) is an available option in clinical practice. Advocates have suggested that such injectates may induce an inflammatory process, initiate the body's wound-healing cascade, and lead to cellular proliferation, collagen deposition, and eventually tissue repair,[1416] thereby leading to pain reduction and functional improvement. Recently, PrT has become increasingly popular in the United States and internationally in managing various soft tissue problems.[17]

Several reviews have investigated the effectiveness of PrT for individual pathologies such as temporomandibular joint hypermobility[18] and Achilles tendinopathy,[19] and some network meta-analyses have compared all of the injection therapies, including PrT and corticosteroid injections for rotator cuff tendinopathy[20] and lateral epicondylopathy.[21,22] However, no definite conclusion was drawn due to insufficient high-quality randomized controlled trials (RCTs). Though the above-mentioned structures are not histologically identical, they are all made up of dense fibrous connective tissue and share some similarities. For instance, they are composed of abundant parallel-ordered collagen fibers; they rely on the hierarchical structure to resist tension and stretch; and they all have a slow healing process. Pooling studies involving these structures were hence reviewed to provide insights into the effects of PrT on this histologic entity.

Therefore, a systematic review with meta-analysis was conducted to explore both the effectiveness (prolotherapy vs placebo or no treatment) and superiority (prolotherapy vs corticosteroid injection) of PrT regarding pain control and activity improvements in patients with dense fibrous connective tissue injuries.

2. Methods

This review study was reported in accordance with the PRISMA guidelines and registered with PROSPERO (CRD42019129044).

2.1. Eligibility criteria

This study included RCTs published in peer-review journals, and focused on studies which included adult participants diagnosed with dense fibrous connective tissue injuries, including injuries to tendons, ligaments, or fascia, for which they received injection therapy. As prolotherapy may refer to injections of various proliferent agents, this review will limit the scope to hypertonic-dextrose injection. Studies were eligible if they compared the treatment effects of PrT with placebo, no PrT, or corticosteroids, and evaluated either pain or the activity level at follow-up. Co-interventions (e.g., physical therapy) were allowed if they were arranged in the same condition for comparing groups. Injections to irrelevant tissues (e.g., intra-articular, intramuscular, subcutaneous, or perineural) were not considered.

2.2. Study Identification

Relevant articles were searched in the PubMed, Scopus, and Embase databases from the earliest record to February 18, 2019. Main search terms were “(prolotherapy) OR [(dextrose OR glucose) AND (tendin∗ OR tendon∗ OR ligament OR fasci∗ OR joint∗ OR arthr∗ OR epicondyl∗)].” (See Supplemental Table I, Supplemental file, which displays our search plan). The Cochrane Library and Google Scholar were scrutinized for additional references. Three authors (MWC, CYH, and WKC) searched and evaluated the literature for inclusion of studies based on their titles and abstracts. After pooling studies obtained from different sources and removing duplicates, the full texts of potentially relevant articles were retrieved, and each article was independently evaluated by MWC, CYH, and WKC for eligibility. The involved articles were exported to EndNote 5.4 (Clarivate Analytics) for review.

2.3. Quality assessment

This study assessed the quality of included studies using the Physiotherapy Evidence Database (PEDro) scale. The methodological quality was assessed by ten items regarding random allocation, blinding procedures, and the dropout rate and statistical reporting. Aggregate scores ranged 0 to 10 points with a higher score indicating better quality. Quality was classified as high (6–10), fair (4 or 5), and poor (≤3). Using the Cochrane risk of bias tool, this study assessed seven domains of bias and stratified the risk of bias into low, high and unclear risk. Discrepancies between reviewers at any stage were resolved through discussion and consensus.

2.4. Outcomes

This study investigated the treatment effects on pain reduction and activity improvement. Pain reduction was assessed by the subjective perception of pain severity or satisfaction with the pain condition, including using a visual analogue scale, Likert scale, or any other continuous pain scale. Activity improvement was measured by questionnaires about activities of daily living or disabilities (e.g., Shoulder Pain and Disability Index, Patient-Rated Tennis Elbow Evaluation).

2.5. Data extraction

This study extracted relevant data from each study with a standard data recording form. Data of three time points was collected to evaluate the immediate (i.e., 0–1 month after the first injection), short-term (i.e., 1–3 months after the first injection), and long-term (i.e., 6–12 months after the first injection) effects of the interventions. If a study included multiple measures within the above-mentioned intervals, the measurements closest to 0, 3, and 12 months after the first injection were selected as the immediate, short-term and long-term follow-up data, respectively. The means, mean changes, and corresponding standard deviations (SDs) of outcomes in the three follow-up periods were extracted. One study can be used only once in one comparison. If a study used PrT in more than one experimental group,[23,24] an estimated mean SD would be calculated by merging means and SDs from the experimental groups. If a study contained a placebo and no-PrT groups as the control groups, the results from the placebo group was used to assess the effectiveness.

2.6. Data analysis

The analyses were performed using Review Manager Software 5.4. Studies comparing PrT to placebo or no PrT were re-analyzed and interpreted individually to understand the effectiveness of PrT on pain control in the short- and long-term at individual studies level. A meta-analysis which pertained to the comparison “PrT vs placebo or no PrT” and “PrT vs corticosteroids” was then conducted separately for the three time points of interest.[25] The meta-analysis aimed to evaluate the overall effectiveness and superiority (compared to corticosteroids) of PrT in respect of pain and activity improvements. Standardized mean differences (SMDs) were obtained to assess the effect size. A random-effects model was used, and a point estimate with a 95% confidence interval (CI) was presented. Heterogeneity across studies was tested using the I2 test. An I2 score of >50% indicated significant heterogeneity.

3. Results

Five hundred seventy non-duplicated records were yielded. After exclusion based on the title, abstract, full-text review, and the same study sample, seven effectiveness[23,24,2630] and three superiority[3133] (compared to corticosteroids) studies were included for review. Figure 1 displays the flow diagram of study development. In total, 10 studies regarding rotator cuff tendinopathy (n = 3), lateral epicondylitis (n = 3), temporomandibular joint hypermobility (n = 2), Achilles tendinopathy (n = 1), and plantar fasciitis (n = 1) involving 358 participants were reviewed and analyzed.

Figure 1.

Figure 1

The graph shows the flow of the study selection.

Table 1 displays the main characteristics of the included studies. Of the seven effectiveness studies, five were placebo-controlled studies,[23,2629] and co-interventions of physical therapy were performed in two studies.[26,30] The number of total injections ranged from one to 12, while the interval ranged from once every week to once every month. In one trial,[30] the number of total injections differed from patient to patient and ranged from four to 12. The follow-up period ranged from 6 weeks to 3 years.

Table 1.

Summary of included studies.

Injection
Study Diagnosis Study type Participants Treatment arms and participants (n) at enrollment Contents Dose Frequency Total Follow-up period Outcomes PEDro score
Yelland et al. (2011, Australia)[30] Achilles tendinopathy Effectiveness Pain ≥6 weeks≥18 y/oVISA-A < 80 (sport), or < 70 (no sport) PrT (n = 14) 20% glucose/0.1% lignocaine/ 0.1% ropivacaine 0.5–1 mL at each tender pointMax. 5 mL Everyweek 4–12 12 months VISA-A scorePain level (7-point Likert scale)PGIC scaleCosts and cost-effectiveness 7
PrT + PT (n = 14)
PT (n = 15)
Lin et al. (2018, Taiwan)[28] Rotator cuff tendinopathy Effectiveness Pain > 6 monthsConfirmed with US > 20 y/o PrT (n = 16) 50% dextrose 4 mL 1 6 weeks Pain level (VAS)SPADIAROMUltrasonography 10
NS 1 mL
Placebo (n = 15) NS 5 mL
Bertrand et al. (2015, Canada)[26] Rotator cuff tendinopathy Effectiveness Pain > 3 monthsConfirmed with PE and US19–75 y/o PrT + PT (n = 27) 25% dextrose/0.1% lidocaine/NS 1 mL at each primary injection site0.5 mL at other tender areasMax. 3 mL Every month 3 9 months Pain level (VAS)Satisfaction measurementUltrasonography (USPRS) 8
Placebo +PT (n = 20) 0.1% lidocaine/NS
Placebo-superficial+ PT (n = 26) 0.1% lidocaine/NS
Scarpone et al. (2008, USA)[29] Lateral epicondylitis Effectiveness Pain, ≥6 months18–65 y/o PrT (n = 12) 10.7% dextrose/14.7% sodium motthuate 0.5 mL/tendon insertionsMax. 1.5 mL Every4 weeks 3 52 weeks Pain level (Likert scale)Grip strengthIsometric resistance strengthpain questionnaires 7
Placebo (n = 12) NS
Rabago et al. (2013, USA)[24] Lateral epicondylitis Effectiveness Pain, ≥3 monthsVAS ≥418–65 y/o PrT (n = 8) 50% dextrose 4 mL Every4 weeks 3 32 weeks PRTEEPain-free grip strengthMRI severity score 7
NS 4 mL
1% lidocaine 2 mL
PrT-DM (n = 9) 5% morrhuate sodium 1 mL
50% dextrose 1.5 mL
NS 2.5 mL
1% lidocaine 2 mL
No PrT (n = 10) 16 weeks
Mustafa et al. (2018, Turkey)[23] Tmporo-mandibular hypermobility Effectiveness 18–44 y/o PrT-10% (n = 10) 10% dextrose 1.5 mL Every month 4 4 months Maximum mouth openingPain level (VAS)TMJ soundsFrequency of locking episodes 6
2% lidocaine 1.5 mL
PrT-20% (n = 9) 20% dextrose 1.5 mL
2% lidocaine 1.5 mL
PrT-30% (n = 9) 30% dextrose 1.5 mL
2% lidocaine 1.5 mL
Placebo (n = 9) NS 1.5 mL
2% lidocaine 1.5 mL
Comert Kilic et al. (2016, Turkey)[27] Temporo-mandibular hypermobility Effectiveness Confirmed with CBCT > 16 y/o PrT (n = 15) 30% dextrose 2 mL Every month 3 12 months Pain level (VAS)Maximum mouth openingLateral and protrusive mandibular motions 6
NS 2 mL
2% articiane or mepivacaine 1 mL
Placebo (n = 15) NS 4 mL
2% articiane or mepivacaine 1 mL
Uğurlar et al. (2018, Turkey) Plantar fasciitis Superiority Pain ≥6 months≥18 y/oVAS > 5BMI < 30 ESWT (n = 39) 36 months Pain level (VAS)FFI-R 5
PrT (n = 40) 5 mg/ml bupivacaine 1 mL Every week 3
5% dextrose 3 mL
NS 6 mL
PRP (n = 39)
CS (n = 40) 5 mg/mL bupivacaine 2 mL
40 mg/mL betamethasone 1 mL
Cole et al. (2018, Australia) Rotator cuff tendinopathy Superiority Pain ≥3 months > 18 y/oX-ray and US performed PrT (n = 17) 50% dextrose 1 mL 1 6 months Level and frequency of general pain, night pain, and pain at activityOverall shoulder satisfactionROMImpingement testShoulder strength 8
1% lignocaine 1 mL
CS (n = 19) 40 mg/mL methylprednisolone 1 mL
1% lignocaine 1 mL
Carayannopoulos et al. (2011, USA) Lateral epicondylitis Superiority Pain: 3 months-2 years18–75 y/o PrT (n = 8) 1.2% phenol/12.5% glycerine/12.5% dextrose 0.9 ml Every month 2 6 months Pain level (VAS)QVASDASH 6
Sodium morrhuate 0.1 mL
Procaine 1 mL
CS (n = 9) 40 mg/mL methylprednisolone 1 mL
Procaine 1 mL

PEDro scores ranged from 5 to 10, with medians of 7.3 for effectiveness studies and 6.3 for superiority studies (compared to corticosteroids). (See Table 1 and Supplemental Table ii, Supplementary file, which displays the PEDro scale of each study.) Only three trials[2830] reported a suitable method for allocation concealment. Three studies[24,30,33] had high risks of bias in the blinding of participants and personnel. Only three[26,28,31] studies presented a successful method of outcome assessor blinding. Most studies reported an adequate description for incomplete results, generating unclear risk in presenting reporting bias. In general, most of the included studies had low-to-moderate risks of bias. (See Supplemental Figure a, Supplementary file, which displays the risks of bias of each study.)

The results of study-level evaluation are summarized in the supplementary file (see Supplemental Table iii, Supplementary file, which displays the study-level evaluations of each study). Across comparisons in various disorders, all the study results demonstrated non-significant mean differences between the groups. Two comparisons from one Achilles tendon[30] and one rotator cuff[26] study found significant mean change difference indicating that PrT might be effective in improving pain in the long-term.

Figure 2 outlines the effectiveness and superiority (compared to corticosteroids) of PrT at different time points. No significant SMD was found regarding its effectiveness on pain control at any time point (i.e., immediate, short-term, long-term) (Fig. 2A). PrT was only superior to corticosteroids in the short-term (SMD: 0.70; 95% CI: 0.14–1.27; I2 = 51%) but inferior in the immediate-term, and not superior in the long-term (Fig. 2B). PrT was effective in improving activity only in the immediate-term (SMD: 0.98; 95% CI: 0.40∼1.55; I2 = 0%) (Fig. 2C), but not superior to corticosteroids at any time point (Fig. 2D). (See Supplemental Figure b to m, Supplementary file, which displays the forest plots of pairwise meta-analysis.)

Figure 2.

Figure 2

(A–D) The graph summarized the results of this meta-analysis, for (A) effectiveness of prolotherapy (prolotherapy vs placebo or no injection) regarding pain reduction; (B) superiority of prolotherapy (prolotherapy vs corticosteroids) regarding pain reduction; (C) effectiveness of prolotherapy (prolotherapy vs placebo or no injection) regarding activity improvement; and (D) superiority of prolotherapy (prolotherapy vs corticosteroids) regarding activity improvement. Immediate, short-term, and long-term outcomes are shown within each figure (A–D), referring to 0–1, 1–3, and 6–12 months after the first injection, respectively. The forest plots can be reached out in the supplementary file.

Considering that histological features of peri-temporomandibular joint soft tissues (i.e., synovial capsule) can differ from the other soft tissues of interest (i.e., ligament, tendon, and fascia), a subgroup analysis was performed after removing two studies[23,27] involving the temporomandibular joint. No change of significance of original SMDs in any outcome categories was found. Sensitivity analyses after removing 2 studies[24,30] without placebo control also did not result in significance changes of original SMDs.

4. Discussion

This review investigated the effects of PrT on various fibrous connective tissue injuries. The majority of included studies were of moderate-to-high quality and possessed minor-to-moderate risks of bias. The results of the analysis at individual study level and the meta-analysis were inconsistent. In general, the majority of the comparisons of did not yield positive results. Consequently, this study suggests that there is insufficient evidence to support the clinical benefits of PrT in managing fibrous tissue injuries.

Prolotherapy or proliferative therapy is a treatment option for damaged connective tissues involving the injection of a solution (proliferant) which theoretically causes an initial cell injury and a subsequent “proliferant” process of wound healing via modulation of the inflammatory process.[34] Several in vitro studies have shown that cells exposed to hypertonic glucose have an initially decreased viability in terms of decreased cell counts, DNA synthesis, and cellular metabolic activities,[14,16,35] as well as an inflammatory reaction.[15] However, it is unclear whether the subsequent “proliferant” process can lead to better outcomes.

Freeman et al administered various dosages of P2G (namely phenol, glycerin, and glucose) to mouse preosteoblast cells and patellar tendon fibroblasts in vitro. In their best result, only the group treated with 25 μL/mL P2G was associated with a higher cellular viability of preosteoblasts compared to the control group, which was noted only at weeks 2 to 3 during the 6-week observation period. Also, such superiority was not seen in fibroblast viability or collagen production.[16] Martins et al assessed the histology of collagen fibers after administering prolotherapy with 12.5% dextrose into rat Achilles tendons, and found no changes in neovascularization or fibroblasts numbers.[36]

Perhaps the strongest support of prolotherapy came from a Korean language journal.[17] Kim et al reported that chondrocytic tissue filling of 2-mm punch lesions in adult rabbit femoral cartilage was present 6 weeks after injection of 10% dextrose but not after injection of controls.[37] Ahn et al and Kim et al reported that significantly more fibroblasts were recruited after a dextrose injection into injured and non-injured rat Achilles tendons.[38,39] Whether these findings are reproducible and applicable to the human body remains to be seen.

Three of the included trials in this review used imaging methods to assess recovery following prolotherapy. In a trial conducted on patients with lateral epicondylitis, Rabago et al reported no within- or between-group changes in magnetic resonance imaging scores of common extensor tendons despite the better clinical outcomes associated with prolotherapy.[24] Similarly, a trial conducted by Bertrand et al reported no between-group differences in an Ultrasound Shoulder Pathology Rating Scale, while reporting positive effects of prolotherapy on clinical outcomes in patients with rotator cuff tendinopathy.[26] Lin et al also reported no between-group differences in histograms or sonographic morphology in a study involving supraspinatus tendinopathy.[28] In general, histologic and imaging evidence supporting prolotherapy-induced cell proliferation are still lacking, and further studies are required to establish the effects and mechanisms of PrT.

A number of reviews have previously evaluated the effects of prolotherapy on various body parts. A meta-analysis of three temporomandibular joint studies suggested that PrT might lead to significant reductions in mouth opening and associated pain.[18] A network meta-analysis study of rotator cuff tendinopathy including only one prolotherapy trial reported that prolotherapy was effective over 24 weeks.[20] Two network meta-analyses for lateral epicondylitis which respectively included only one and two RCTs suggested that prolotherapy resulted in better outcomes than placebo.[21,22] A meta-analysis study of Achilles tendinopathy including only one RCT stated that eccentric loading exercise combined with prolotherapy provided more-rapid symptomatic improvements than exercise alone in the short term.[19] Given that most of these reviews were based on a limited number of RCTs, they provide very weak evidence as to the effects of prolotherapy.

The present study updated the current knowledge and considered all dense fibrous connective tissue injuries as a whole. However, still only a limited number of high-quality studies explored the beneficial effects of PrT. Considering that prolotherapy is a cheap and convenient treatment option for managing soft-tissue disorders with less probable side effects, more clinical and basic studies are warranted to fully explore its potential benefits.

4.1. Limitations

Several limitations should be addressed. The involved study population differed in diagnosis, durations of symptoms, mechanisms, severity of injuries, and methods of injection, which potentially contributed to the evident heterogeneity. Although the tendons, ligaments, and fascia shared many common features, the surrounding environment, vasculature, and tensile loads within these structures vary. Finally, only three databases were searched, and only a limited number of trials and participants were available for this analysis.

5. Conclusions

There is insufficient evidence to support the clinical benefits of dextrose prolotherapy in managing fibrous tissue injuries, either in aspect of pain management or activity improvement. More high-quality randomized controlled trials are warranted to establish the benefits of prolotherapy.

Acknowledgments

Acknowledgments for Dr Dean Reeves and Prof Michael Yelland who provided detailed data of their studies.

Author contributions

The authors’ responsibilities were as follows—YNL and MWC conceived of and designed the experiments; MWC, CYH, and WKC searched for relevant studies, conducted quality assessment, and extracted the data; MWC and YNL analyzed the data; MWC and YNL wrote the manuscript; and all authors reviewed and approved the final manuscript.

Conceptualization: Meng-Wu Chung, Yen-Nung Lin.

Data curation: Meng-Wu Chung.

Formal analysis: Meng-Wu Chung, Chih-Yang Hsu.

Funding acquisition: Yen-Nung Lin.

Investigation: Meng-Wu Chung.

Methodology: Yen-Nung Lin.

Software: Meng-Wu Chung, Wen-Kuei Chung, Yen-Nung Lin.

Supervision: Wen-Kuei Chung, Yen-Nung Lin.

Validation: Chih-Yang Hsu, Wen-Kuei Chung, Yen-Nung Lin.

Visualization: Chih-Yang Hsu, Yen-Nung Lin.

Writing – original draft: Meng-Wu Chung.

Writing – review & editing: Meng-Wu Chung, Chih-Yang Hsu, Wen-Kuei Chung, Yen-Nung Lin.

Supplementary Material

Supplemental Digital Content

Footnotes

Abbreviations: CI = confidence interval, P2G = phenol, glycerin, and glucose, PrT = prolotherapy with hypertonic dextrose, RCT = randomized controlled trial, SD = standard deviations, SMD = standardized mean difference.

How to cite this article: Chung MW, Hsu CY, Chung WK, Lin YN. Effects of dextrose prolotherapy on tendinopathy, fasciopathy, and ligament injuries, fact or myth? A systematic review and meta-analysis. Medicine. 2020;99:46(e23201).

Ethical Statement: All the included studies were conducted in accordance with the Declaration of Helsinki and had ethical approval.

Funded by Ministry of Science and Technology, Taiwan (Grand: MOST 108-2745-8-038-005); Wan-Fung Hospital, Taipei Medical University (109-wf-eva-37).

Each author certifies that he or she has no commercial associations.

The authors have no conflicts of interest to disclose.

The datasets generated during and/or analyzed during the present study are available from the corresponding author on reasonable request.

AROM = active range of motion, BMI = body mass index, CBCT = cone-beam computed tomography, DASH = Disabilities of the Arm, Shoulder and Hand questionnaire, ESWT = extracorporeal shock wave therapy, FFI-R = Foot Function Index-Revised, MRI = magnetic resonance imaging, NPPS = Nirschl Pain Phase Scale, NS = normal saline, PE = physical examination, PF = plantar fasciopathy, PGIC = Patient Global Impression of Change, PrT = prolotherapy, PRTEE = Patient-rated Tennis Elbow Evaluation, PT = physical therapy, QVAS = quadruple visual analog scale, SPADI = Shoulder Pain and Disability Index, USPRS = Ultrasound Shoulder Pathology Rating Scale, VAS = Visual Analogue Scale, VISA-A = Victorian Institute of Sports Assessment—Achilles.

References

  • [1].Ross MH, Pawlina W. Histology. Philadelphia: Lippincott Williams & Wilkins; 2006. [Google Scholar]
  • [2].Ombregt L. A System of Orthopaedic Medicine-E-Book. Edinburgh: Elsevier Health Sciences; 2013. [Google Scholar]
  • [3].Khan KM, Cook JL, Kannus P, et al. Time to abandon the “tendinitis” myth. BMJ 2002;324:626–7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [4].Maffulli N, Testa V, Capasso G, et al. Similar histopathological picture in males with Achilles and patellar tendinopathy. Med Sci Sports Exerc 2004;36:1470–5. [DOI] [PubMed] [Google Scholar]
  • [5].Rees JD, Maffulli N, Cook J. Management of tendinopathy. Am J Sports Med 2009;37:1855–67. [DOI] [PubMed] [Google Scholar]
  • [6].Tozer S, Duprez D. Tendon and ligament: development, repair and disease. Birth Defects Res C Embryo Today 2005;75:226–36. [DOI] [PubMed] [Google Scholar]
  • [7].Liu C-F, Aschbacher-Smith L, Barthelery NJ, et al. What we should know before using tissue engineering techniques to repair injured tendons: a developmental biology perspective. Tissue Eng Part B Rev 2011;17:165–76. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [8].Yang G, Rothrauff BB, Tuan RS. Tendon and ligament regeneration and repair: clinical relevance and developmental paradigm. Birth Defects Res C Embryo Today 2013;99:203–22. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [9].Bisset L, Beller E, Jull G, et al. Mobilisation with movement and exercise, corticosteroid injection, or wait and see for tennis elbow: randomised trial. BMJ 2006;333:939. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [10].Coombes BK, Bisset L, Vicenzino B. Efficacy and safety of corticosteroid injections and other injections for management of tendinopathy: a systematic review of randomised controlled trials. Lancet 2010;376:1751–67. [DOI] [PubMed] [Google Scholar]
  • [11].Mahler F, Fritschy D. Partial and complete ruptures of the Achilles tendon and local corticosteroid injections. Br J Sports Med 1992;26:7–14. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [12].Shrier I, Matheson GO, Kohl HW., 3rd Achilles tendonitis: are corticosteroid injections useful or harmful? Clin J Sport Med 1996;6:245–50. [PubMed] [Google Scholar]
  • [13].Wei AS, Callaci JJ, Juknelis D, et al. The effect of corticosteroid on collagen expression in injured rotator cuff tendon. J Bone Joint Surg Am 2006;88:1331–8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [14].Ekwueme EC, Mohiuddin M, Yarborough JA, et al. Prolotherapy induces an inflammatory response in human tenocytes in vitro. Clin Orthop Relat Res 2017;475:2117–27. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [15].Jensen KT, Rabago DP, Best TM, et al. Early inflammatory response of knee ligaments to prolotherapy in a rat model. J Orthop Res 2008;26:816–23. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [16].Freeman JW, Empson YM, Ekwueme EC, et al. Effect of prolotherapy on cellular proliferation and collagen deposition in MC3T3-E1 and patellar tendon fibroblast populations. Transl Res 2011;158:132–9. [DOI] [PubMed] [Google Scholar]
  • [17].Reeves KD, Sit RW, Rabago DP. Dextrose prolotherapy: a narrative review of basic science, clinical research, and best treatment recommendations. Phys Med Rehabil Clin N Am 2016;27:783–823. [DOI] [PubMed] [Google Scholar]
  • [18].Nagori SA, Jose A, Gopalakrishnan V, et al. The efficacy of dextrose prolotherapy over placebo for temporomandibular joint hypermobility: a systematic review and meta-analysis. J Oral Rehabil 2018;45:998–1006. [DOI] [PubMed] [Google Scholar]
  • [19].Morath O, Kubosch EJ, Taeymans J, et al. The effect of sclerotherapy and prolotherapy on chronic painful Achilles tendinopathy—a systematic review including meta-analysis. Scand J Med Sci Sports 2018;28:4–15. [DOI] [PubMed] [Google Scholar]
  • [20].Lin MT, Chiang CF, Wu CH, et al. Comparative effectiveness of injection therapies in rotator cuff tendinopathy: a systematic review, pairwise and network meta-analysis of randomized controlled trials. Arch Phys Med Rehabil 2019;100:336–49. [DOI] [PubMed] [Google Scholar]
  • [21].Dong W, Goost H, Lin XB, et al. Injection therapies for lateral epicondylalgia: a systematic review and Bayesian network meta-analysis. Br J Sports Med 2016;50:900–8. [DOI] [PubMed] [Google Scholar]
  • [22].Krogh TP, Bartels EM, Ellingsen T, et al. Comparative effectiveness of injection therapies in lateral epicondylitis: a systematic review and network meta-analysis of randomized controlled trials. Am J Sports Med 2013;41:1435–46. [DOI] [PubMed] [Google Scholar]
  • [23].Mustafa R, Gungormus M, Mollaoglu N. Evaluation of the efficacy of different concentrations of dextrose prolotherapy in temporomandibular joint hypermobility treatment. J Craniofac Surg 2018;29:e461–5. [DOI] [PubMed] [Google Scholar]
  • [24].Rabago D, Lee KS, Ryan M, et al. Hypertonic dextrose and morrhuate sodium injections (prolotherapy) for lateral epicondylosis (tennis elbow): results of a single-blind, pilot-level, randomized controlled trial. Am J Phys Med Rehabil 2013;92:587–96. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [25].Hsu CY, Lin YN. Meta-analyzability concerns in meta-analyses. Arch Phys Med Rehabil 2019;100:1574–7. [DOI] [PubMed] [Google Scholar]
  • [26].Bertrand H, Reeves KD, Bennett CJ, et al. Dextrose prolotherapy versus control injections in painful rotator cuff tendinopathy. Arch Phys Med Rehabil 2016;97:17–25. [DOI] [PubMed] [Google Scholar]
  • [27].Comert Kilic S, Gungormus M. Is dextrose prolotherapy superior to placebo for the treatment of temporomandibular joint hypermobility? A randomized clinical trial. Int J Oral Maxillofac Surg 2016;45:813–9. [DOI] [PubMed] [Google Scholar]
  • [28].Lin CL, Huang CC, Huang SW. Effects of hypertonic dextrose injection on chronic supraspinatus tendinopathy of the shoulder: randomized placebo-controlled trial. Eur J Phys Rehabil Med 2019;55:480–7. [DOI] [PubMed] [Google Scholar]
  • [29].Scarpone M, Rabago DP, Zgierska A, et al. The efficacy of prolotherapy for lateral epicondylosis: a pilot study. Clin J Sport Med 2008;18:248–54. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [30].Yelland MJ, Sweeting KR, Lyftogt JA, et al. Prolotherapy injections and eccentric loading exercises for painful Achilles tendinosis: a randomised trial. Br J Sports Med 2011;45:421–8. [DOI] [PubMed] [Google Scholar]
  • [31].Carayannopoulos A, Borg-Stein J, Sokolof J, et al. Prolotherapy versus corticosteroid injections for the treatment of lateral epicondylosis: a randomized controlled trial. PM&R 2011;3:706–15. [DOI] [PubMed] [Google Scholar]
  • [32].Cole B, Lam P, Hackett L, et al. Ultrasound-guided injections for supraspinatus tendinopathy: corticosteroid versus glucose prolotherapy—a randomized controlled clinical trial. Shoulder Elbow 2018;10:170–8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • [33].Ugurlar M, Sonmez MM, Ugurlar OY, et al. Effectiveness of four different treatment modalities in the treatment of chronic plantar fasciitis during a 36-month follow-up period: a randomized controlled trial. J Foot Ankle Surg 2018;57:913–8. [DOI] [PubMed] [Google Scholar]
  • [34].Banks AR. A rationale for prolotherapy. J Orthop Med 1991;13:54–9. [Google Scholar]
  • [35].Di Paolo S, Gesualdo L, Ranieri E, et al. High glucose concentration induces the overexpression of transforming growth factor-beta through the activation of a platelet-derived growth factor loop in human mesangial cells. Am J Pathol 1996;149:2095–106. [PMC free article] [PubMed] [Google Scholar]
  • [36].Martins CA, Bertuzzi RT, Tisot RA, et al. Dextrose prolotherapy and corticosteroid injection into rat Achilles tendon. Knee Surg Sports Traumatol Arthrosc 2012;20:1895–900. [DOI] [PubMed] [Google Scholar]
  • [37].Kim SA, Kim EH, Kim SY, et al. The effects of hyperosmolar dextrose and autologous serum injection in the experimental articular defect of rabbit. J Korean Acad Rehabil Med 2006;30:173–8. [Google Scholar]
  • [38].Ahn KH, Kim HS, Lee WK, et al. The effect of the prolotherapy on the injured Achilles tendon in a rat model. J Korean Acad Rehabil Med 2002;26:332–6. [Google Scholar]
  • [39].Kim HJ, Jeong TS, Kim WS, et al. Comparison of histological changes in accordance with the level of dextrose-concentration in experimental prolotherapy model. J Korean Acad Rehabil Med 2003;27:935–40. [Google Scholar]

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