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The effects of regenerative injection therapy compared to corticosteroids for the treatment of lateral Epicondylitis: a systematic review and meta-analysis

Archives of Physiotherapy volume 9, Article number: 12 (2019) Cite this article

A Correction to this article was published on 27 January 2020

This article has been updated

Abstract

Background

The lateral epicondyle is a common site for chronic tendinosis (i.e. lateral epicondylitis), a condition characterized by overuse and degeneration of a tendon due to repeated microtrauma. This leads to pain and functional limitations. There is a growing interest in non-surgical forms of treatment for this condition including provision of corticosteroid injections and regenerative injection therapy (provision of autologous blood and platelet rich plasma injections).

Objective

We compared the effectiveness of corticosteroids with regenerative injection therapy for the treatment of lateral epicondylitis.

Methods

We systematically reviewed randomized controlled trials published in English language from 2008 to 2018. Databases used included PEDro, Scopus, PubMed, and CINAHL. Nine articles met our selection criteria. The PEDRo scale scores helped assess study quality. Cochrane risk of bias criteria helped assess bias. We analyzed results focusing on pain and function using meta-analyses.

Results

Six out of 9 studies had low risk of bias. There were no short-term (1 and 2 month) differences in pain scores between the corticosteroid and regenerative injection groups. Participants receiving regenerative injections demonstrated greater long-term improvements lasting for a period of ≈2 years.

Conclusion

Regenerative injections provision results in greater long–term pain relief and improved function for people with lateral epicondylitis.

Introduction

Lateral epicondylitis or tennis elbow is a relatively common condition for which people seek treatment. It is a disorder, which severely affects an individual’s function and mobility and results in multiple visits to orthopedic clinicians each year. This condition has an estimated incidence of 15.1 cases per 10,000 patients seen [1]. This condition is caused by repetitive microtrauma resulting in tendon degeneration [2]. Overexertion of the extremity with repetitive movements of wrist extension and alternating forearm pronation/supination are the main contributing factors to the repetitive microtrauma [3]. Traditionally, the condition is managed conservatively [4], with only a small proportion of individuals seeking surgery to alleviate pain [5]. Conservative treatment options including rest, bracing, prescription of non-steroidal anti-inflammatory drugs [6], provision of physiotherapy [7] and extracorporeal shock wave therapy [8]. Other conservative management options include the use of corticosteroid injections and regenerative injections. The injections are utilized as a means to postpone and/or prevent surgical intervention.

Corticosteroid injections

One common conservative non-surgical option for the management of lateral epicondylitis involves the use of corticosteroid injections [9]. Corticosteroid injections work by down-regulation of immune function and reduction of inflammatory cells and mediators, such as lymphocytes, macrophages and mast cells [10]. Essentially, corticosteroid injections reduce pain caused by inflammation and are delivered using intra-articular or extra-articular injections. While intra-articular injections are used for conditions such as osteoarthritis, extra-articular (soft tissue) injections are used to target areas outside the joint and can be useful for tendinosis when they are injected directly into or in the area around the tendon [11]. However, corticosteroid injections increase protein catabolism, decrease type I collagen and glycosaminoglycan syntheses, and therefore slow the healing process [10]. Taking into consideration the lack of inflammation in cases of tendinosis and inhibition of collagen repair by corticosteroids, the utility of these injections for long-term symptom resolution in chronic tendinosis has been questioned at locations such as the Achilles tendon [12].

Regenerative injections

The use of regenerative injections has been emerging as a conservative treatment method to not only treat musculoskeletal injuries, but also facilitate tissue regeneration and healing [13]. Common forms of regenerative injections include autologous blood injections or autologous conditioned plasma, platelet rich plasma, and prolotherapy. This treatment is based on the theory of introducing blood and platelet products to initiate maturation and proliferation within the tendon [14]. The regenerative injections stimulate cellular activity to initiate a healing response by increasing growth factors by increasing platelets or aseptic inflammation to trigger the reparative process of tendons [15]. It is possible to deliver the injections using ultrasound guidance to target either the most affected portion of the tendon or the point of tenderness. Each injection is prepared differently and is discussed below briefly.

Autologous blood injections

Autologous blood injections involve performing a peripheral blood draw to extract blood from a distal site and injecting it directly into the affected tendon. A prospective observational cohort study by Edwards and Candruccio [15] evaluated the effects of autologous blood injections in the treatment of refractory lateral epicondylitis. The authors concluded autologous blood is an alternative minimally invasive treatment that is beneficial for patients with lateral epicondylitis with other failed conservative options.

Platelet rich plasma injections

Platelet rich plasma is a biological blood product derived from centrifuged whole blood to extract concentrated platelets. The platelets stimulate the release of many growth factors imperative for tissue recovery and regeneration. They are injected directly into the site of injury to promote tissue healing [16]. Platelet rich plasma consists of concentrated platelets 5-10x the baseline amount in normal blood, which allows for increased tendon repair at the localized site of injection. Compared to surgical interventions that cost around $16,000 [4], the cost of platelet rich plasma injections range from $800–1200 per injection with 1–2 injections providing significant relief of pain and improvement in physiologic tissue recovery [17]. However, there is limited evidence currently available regarding standardized protocols and efficacy of platelet rich plasma with specific injuries [18]. However, platelet rich plasma may be a beneficial conservative treatment option for those seeking to postpone or prevent a surgical procedure.

Surgery

About 10% of lateral epicondylitis patients will require some sort of surgical management because of inadequate relief from non-surgical measures [19]. Surgery is an option that many patients choose to delay in favor of conservative treatment. This decision can minimize personal financial hardship, decrease fear, and prevent adverse effects. Surgery involves removal of unhealthy tissue and promotes tendon healing [20]. Common procedures include open surgical debridement as well as arthroscopic tendon repairs. Reviews of surgical procedures for lateral epicondylitis have reported mixed evidence on the benefit of surgical interventions for lateral epicondylitis [19, 21]. The primary reason for the mixed evidence was the lack of well-controlled studies using direct comparisons between surgical procedures.

Given that a large proportion of individuals with lateral epicondylitis do not require surgical management, the purpose of this systematic review and meta-analysis is to investigate the effectiveness of two commonly used non-surgical options, regenerative injections and corticosteroid injections in the management of lateral epicondylitis. The question guiding our review in the Participant, Intervention, Comparison and Outcome (PICO) format [22] was “In participants with lateral epicondylitis, does using regenerative injections result in lower pain and better functional outcomes compared to corticosteroid injections?” Preliminary results have appeared in the abstract form [23].

Materials and methods

A comprehensive literature review was conducted using the databases PubMed, PEDro, Scopus, and Ovid with time parameters from June 2008 to May 2018. The following search terms were utilized in varying combinations: ‘chronic tendinopathy’, ‘regenerative injection therapy’, corticosteroid injection’, ‘platelet rich plasma’, and ‘autologous blood injections’. The search was limited to availability of full text, human subjects, and English language. Inclusion criteria were: i) study design of randomized control trials (RCTs), ii) the comparison of regenerative injections with corticosteroid injections for lateral epicondylitis, and iii) the outcomes of pain and function. We excluded articles focusing on use of corticosteroids and/or regenerative injections for other joint conditions (e.g. knee OA). We reviewed all abstracts to select relevant articles and assessed the bibliography of each study to find any other relevant articles.

Each article was read independently by two of three (MNB, JLK and HNS) authors to determine if all inclusion criteria were met. In case of any discrepancy, a third author helped make the decision. We performed data extraction to obtain study design, population, intervention, outcome measure, results, and limitations. The quality of the published studies was evaluated using PEDro scale [24]. The scoring was completed by two of three authors, as mentioned before and discrepancies, if any, resolved by JBB and SKS. We interpreted the quality of the RCTs based upon the assessment of Foley et al. [25], where scores to 9–10, 6–8, 4–5 and ≤ 3/10 reflected ‘excellent’, ‘good’, ‘fair’ and ‘poor’ study quality respectively. Although utilized primarily in trials reporting neurorehabilitation interventions, use of the quality ratings based on PEDro scores is slowly increasing in the musculoskeletal rehabilitation literature [26,27,28]. We also performed a risk of bias assessment of included studies using the Cochrane Risk of Bias criteria for Effective Practice and Organization of Care reviews [29, 30]. Domains assessed included sequence generation, allocation concealment, blinding of participants, personnel and outcome assessors, incomplete outcome data, selective outcome reporting, and other sources of bias. For each domain, we assigned a judgment: Yes - indicating low risk of bias, No - indicating a high risk of bias, and Unclear - indicating unclear or unknown risk of bias where reported details were insufficient to reach a conclusion.

We calculated descriptive statistics of the study populations in terms of age, sex and time since diagnosis. All studies used outcomes at two International Classification of Functioning (ICF) levels [31] including impairment and limitations in activity performance. The underlying measurement construct for all outcomes was continuous. Meta-analyses (RevMan 5.3, Review Manager, Cochrane Collaboration, London, UK) examined the change in clinical outcomes after the provision of corticosteroids and regenerative injections. Outcomes included in the meta-analyses comprised of those used to measure change in two or more studies (the minimum number to be included in a meta-analysis) [32]. In studies using multiple outcomes, we conducted separate meta-analyses for each of the outcomes. Standardized mean differences (using Hedges g) and 95% confidence intervals helped quantify the pooled effects of the interventions. We calculated effect sizes to help quantify intervention effectiveness [33]. We assessed heterogeneity using tau-squared values (within study variance) and I2 (the ratio of true heterogeneity to total observed variation) values [34]. Studies were deemed heterogeneous if I2 values exceeded 50% [35]. Given the use of both autologous blood and protein rich plasma injections; we used the random effects model.

Results

The Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) flow diagram provides details of the search process and the selection results (Fig. 1). After initial screening, we selected seventeen articles. Eight articles were excluded, as they did not meet the inclusion criteria. The remaining nine articles were suitable for the study. The reference lists of these nine articles did not yield any additional citations. All nine of these studies were included in both the meta-analysis and qualitative (systematic review part) of the study.

Fig. 1
figure 1

PRISMA Flow Diagram

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Main study characteristics

Five hundred and seventy-seven individuals with lateral epicondylitis participated in the nine studies included in the analysis. All studies included participants diagnosed with lateral epicondylitis at a mean of ≥ 2 months. The participants were predominantly female (60%) and the age range was from 36 to 54 years.

Study quality, evidence levels and risk of Bias assessment

The study quality was excellent (one study; PEDro score = 9) [36], good (six studies; PEDRo score = 6 for five studies and 8 for one study), [37,38,39,40,41,42] or fair (two studies; PEDro = 5) [43, 44] according to PEDro scale scores. There is evidence that provision of regenerative injections in the form of both autologous blood (three good quality studies; PEDro score 6/10) [37,38,39] and platelet rich plasma (one excellent study; PEDro score 9/10 [36]; and one good study; PEDro score 6/10 [41] decreases pain and improves function). Study details in terms of the numbers of participants, ages, the interventions (including type of injections received and site), outcomes, results and conclusions are available in Tables 1 and 2. Table 1 lists studies comparing autologous blood compared to corticosteroid injections and Table 2 list the studies comparing platelet rich plasma to corticosteroid injections. Figure 2 represents the summary information on the risk of bias assessment. All studies had a low risk for attrition bias and reporting bias and all but one for other bias. In terms of selection bias, information on random sequence allocation was missing in three studies, [41, 43, 44]. In addition, information on allocation concealment was unclear in two studies [39, 43], which potentially gives rise to a risk of high selection bias, particularly for the study by Arik and colleagues [43]. Information on performance bias in terms of blinding of personnel was unclear in five studies [36,37,38,39, 43]. Similarly, information on detection bias (blinding of outcome assessment) was missing in five studies [38, 39, 42,43,44]. This can also be a matter of concern, as not having blinded assessors can tend to influence the eventual results of the study. In terms of other bias, information on age and sex distribution was missing in one study [41].

Table 1 Details of studies comparing autologous blood and corticosteroid injections
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Table 2 Details of studies comparing PRP and corticosteroid injections
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Fig. 2
figure 2

Risk of bias summary for included RCTs

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Most commonly used outcomes across all studies included the Visual Analog Scale (VAS) for assessing pain and the Disabilities of the Arm, Shoulder and Hand (DASH) and quick DASH outcomes assessing self-perceived upper limb use in daily life activities. As these were the most-commonly reported outcomes, we performed our meta-analyses using these two outcomes.

Effects of the provision of regenerative injections on pain levels

The VAS was used to assess pain levels after the provision of corticosteroid or regenerative injections at four different time points: 1 month [36,37,38, 42, 44], 2 months [37, 40, 41], 3 months [38, 41, 42, 44] and 6 months post-injection [36, 38, 40, 41, 43]. There were no differences in the amount of pain reported after 1 month (Hedges g: 0.35, 95% CI: − 0.27 to 0.96, small effect size; p = 0.27; Fig. 3a) and at 2 months (Hedges g: -0.25, 95% CI: − 1.27 to 0.76, small effect size; p = 0.62; Fig. 3b). A significant reduction in pain levels with provision of regenerative injections was noted at three (Hedges g: -0.36, 95% CI: − 0.59 to − 0.12, small effect size; p = 0.003; Fig. 3c) and 6 months (Hedges g: -0.73, 95% CI: − 1.14 to − 0.33, moderate effect size; p < 0.001; Fig. 3d).

Fig. 3
figure 3

Results of meta-analyses examining the effectiveness of the corticosteroid injections compared to regenerative injections on pain using the VAS scale at 1 month (a), 2 months (b), 3 months (c) and 6 months (d) post-injection. Larger squares indicate bigger study effect sizes. The diamonds represent pooled effects of results of individual studies. The location of the diamond indicates the estimated effect size and precision of the estimate is indicated by the width of the diamond

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Effects of the provision of regenerative injections on self-perceived upper limb use in daily life activities

The DASH was used to assess self-perceived upper limb use after the provision of corticosteroid or regenerative injections at three different time points: 3 months [36, 39, 40] and 6 months [36, 39,40,41] and at one-year post-injection [36, 39]. Individuals receiving regenerative injections reported a significant improvement (with small effect sizes) in upper limb use at 3 months (Hedges g: -0.36, 95% CI: − 0.69 to − 0.04, p = 0.03; Fig. 4a). Individuals continued to improve at 6 months (Hedges g: -0.32, 95% CI: − 0.58 to − 0.06, p = 0.02, Fig. 4b) and at 1 year (Hedges g: -0.45, 95% CI: − 0.73 to − 0.17, p = 0.002; Fig. 4c).

Fig. 4
figure 4

Results of meta-analyses examining the effectiveness of the corticosteroid injections compared to regenerative injections on self reported upper limb use in daily life activities using the DASH scale at 3 months (a), 6 months (b) and one-year (c) post-injection. Larger squares indicate bigger study effect sizes. The diamonds represent pooled effects of results of individual studies. The location of the diamond indicates the estimated effect size and precision of the estimate is indicated by the width of the diamond

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Discussion

We found evidence supporting the provision of regenerative injection therapy as a conservation treatment in individuals with lateral epicondylitis. Individuals receiving these injections had long- term pain relief and increased self-perceived upper limb use. The results also suggest that injections of whole autologous blood as well as platelet rich plasma are useful to decrease pain and increase self-rated upper limb use in individuals with lateral epicondylitis. An additionally important consideration is that the regenerative injections were useful in the acute as well as chronic stages of lateral epicondylitis.

Use of subjective assessments

The outcomes used in this study assessed the body structure and body function as well as activities of daily living domains of the ICF. When analyzing the literature regarding chronic elbow tendinopathies, we found that treatment effectiveness was quantified using a variety of outcomes. There was a preponderance of the use of subjective outcome measures that included the VAS, Patient Rated Tennis Elbow Evaluation (PRTEE), Oxford Elbow Score and Nirschl score for pain and DASH and quick DASH for arm function. Only one study assessed pain in grip formation and pain pressure threshold, a more objective assessment of pain. Thus, it is currently unclear as to which assessment is most appropriate or whether it is better to use more than one outcome. It might be a better idea to use an objective as well as subjective assessment of pain, as the use of a single outcome may not present the entire picture and the use of more than one measure is sometimes warranted [45].

Use of objective assessments

Objective assessments of body function included the grip strength assessments employed in four studies and ultrasound guided (USG) assessments in two studies. Specifically, these two studies assessed the effects of platelet rich plasma injections. Provision of platelet rich plasma injections resulted in better tendon thickness outcomes compared to corticosteroid at 3 months and 6 months after the injection (Table 2). While the first study [41] did not present specific values in terms of tendon thickness, only one out of 15 participants had reduced thickness of the common extensor tendon. These participants in addition had greater functional improvements. The mean reduction in tendon thickness in the second study ranged from 0.5 to 0.8 mm [42], which is identical to the range of smallest detectable change in healthy individuals [46]. USG findings are reliable for measurement of tendon thickness at the elbow in individuals with lateral epicondylitis [47]. It is currently unknown whether the range of smallest detectable change is similar in individuals with lateral epicondlylitis.

In addition, no study included in the current review evaluated the effects of the provision of autologous blood injections results on changes in tendon morphology as measured by USG and color Doppler outcomes. However, other studies have reported a reduction in tendon thickness and hyperechoic changes on USG, with the use of autologous blood injections [48]. Thus, the use of USG to measure tendon thickness may be encouraged as a more objective measurement to understand the effects of regenerative injections on body structures, in addition to body function and activity levels of the ICF. In addition, the findings support the use of grip strength as an objective functional outcome in this population.

Follow-up assessments

The period for which the treatment provides symptom relief accompanied by functional improvement is an important factor to consider when determining a specific treatment’s efficacy. Four fair to good quality studies included in this review investigated short-term effects of corticosteroid and regenerative injections for lateral epicondylitis with follow-up assessments until 2–3 months post-injection. Individually, in the systematic review, results of three articles [37, 43, 44] reported significant short-term improvements at 1 month for all outcomes in the corticosteroid group (Tables 1 and 2). The relatively higher risk of bias (Fig. 2) in these three studies do limit the generalizability of their findings. In addition, when included in the meta-analysis, no differences between groups were present in terms of pain, as measured using the VAS (using the random effects model due to high heterogeneity, Fig. 3a). Besides, in these three studies, at the 3 months follow-up assessment, the improvements due to corticosteroid had declined and the group receiving regenerative injections continued to improve with respect to pain and self-perceived upper limb use (Figs. 3c and 4a).

Five studies evaluated the effects of injections on pain at a six-month follow up and four studies examined the effects of the injections on self-perceived arm use (Figs. 3d and 4b). In these studies, the patients in the platelet rich plasma group continued to improve and had significantly better results concerning decreased level of pain, improvement of function, and evidence of tendon healing at the six-month follow up. Results of one article [40] comparing corticosteroid, autologous blood, and saline injections demonstrated no significant differences between groups with all participants improving significantly at the six-month follow up. Lack of details regarding exact time from initial diagnosis and the type of corticosteroid injected confound the interpretation of these results and probable reasons to explain the lack of between group changes. However, the results of our meta-analysis demonstrate significant improvement in pain and function at 6 months post-injection in the group receiving regenerative injections.

Lastly, two studies evaluated the effects at one-year post-injection and one study had an assessment at 2 years. At the one-year follow-up assessments, greater improvements in pain relief and functional performance were present in the groups receiving RIT injections. In the study by Gosens et al. [36], at the two-year post-injection assessment, the corticosteroid group had returned to their baseline DASH scores and had mild improvements of pain while the autologous blood group had sustained the level of recovery with significant improvements in the VAS and DASH scores.

When considering the variable of time with respect to the efficacy of corticosteroid compared to regenerative injections, it is evident that in the short-term (one to 2 months), our results indicate that use of corticosteroid injections is not superior to regenerative injections. These findings are similar to results obtained by Sirico and colleagues, who found no short-term benefit for corticosteroid presentation [9]. Our results also agree with those found from other metanalyses in this area of study [49,50,51] in terms of lack of efficacy of corticosteroids injections in the longer term. However, ours is the only study that considered the effects of provision of both autologous blood as well as platelet rich plasma compared to corticosteroid injections. Additionally, we looked at both pain and function, something that was not a primary focus in the other meta-analyses. Provision of regenerative injections seem to result in long-term improvements lasting until one to 2 years.

Platelet rich plasma versus autologous blood injections

Amongst the trials included in this study, five and four articles investigated the effects of provision of autologous blood and platelet rich plasma injection provision respectively to corticosteroid injections. As mentioned previously, platelet rich plasma injections are a variation of the autologous blood injection technique, where there is a greater amount of whole blood removed from the patient and centrifuged to produce a higher concentration of platelets for healing [12, 15]. For both platelet rich plasma and autologous blood injection studies, seven of the studies found significant, beneficial effects of the regenerative injections while two found the injections were not significantly superior to placebo saline injections. A systematic review by Thøger Persson et al. [52] found similar results comparing many types of injections for effectiveness in lateral epicondylitis, including two trials for platelet rich plasma and three for autologous blood. A recent network meta-analysis [53] found no difference between autologous blood and platelet rich plasma injections. Thus, it seems that regenerative injections are useful for the long-term resolution of symptoms and the kind of injection does not matter.

PEDro scale and risk of bias

As stated earlier, the quality of the studies based on PEDro scales ranges from excellent (one study), good (six studies) to fair (two studies). None of the studies were rated as being of poor quality. The two studies ranked as fair [43, 44] also had a high risk of selection bias (on random allocation) in addition to unclear risk on detection bias (Fig. 2). While the items on the PEDro scale talk about randomization and concealed allocation, they do not need specific information on how the process of randomization and allocation were carried out. There are a few guidelines available like the non-acceptability of coin-toss methods. However, this information may be insufficient.

The unclear risk of detection bias in other studies was due to the inadequate information on whether blinded assessors were employed and some of them used objective outcomes including grip force measurement using dynamometry. Inadequate information on blinded assessors can lead to a risk of assigning scores to the intervention group indicative of better recovery. One study [41] had a high risk of other bias in terms on non-provision of information regarding average age and sex distribution of participants. This study was of good quality, scoring 6/10 in the PEDro scale. The PEDro scale, however, does not account for sample size and age and sex distribution. This study did not have information on random allocation and scored lower in that regard on the PEDro. Future studies must ensure inclusion of all relevant details to avoid the risk of bias and help ensure correct reporting standards by using both the PEDro scale and Risk of Bias tool to help better interpret their results.

Heterogeneity in results of the metanalyses

The results of our metanalyses for pain and self-perceived function revealed considerable heterogeneity. Factors that could have contributed to the heterogeneity include a wide range of sample sizes across all studies (ranging from 18 to 100 participants) and choice of the outcome measures. Only four [36, 37, 40, 42] had explicit sample size analyses mentioned in the paper. In addition, as mentioned above, the PEDro scale does not take sample size into account. Future studies must include an explicit sample size analysis to understand the rationale behind the numbers of participants in the study. In terms of outcome measures, data was available for the VAS and DASH (subjective outcomes) as a measure of pain and functional performance respectively. It remains to be seen if the use of more objective outcomes (without the risk of detection bias) helps reduce heterogeneity amongst studies.

Limitations and future directions

It is important to acknowledge the limitations and gaps in the literature presented in this review. Out search was limited to papers published in English between June 2008 and May 2018. Although we found no RCTs directly comparing corticosteroids to either autologous blood and/or platelet rich plasma injections published in English prior to 2008 in our literature search, we may have missed some articles published in other languages. This issue may have introduced a possible selection bias. A lack of standardization for the preparation of regenerative injections was present amongst the different studies. There was also no control regarding prior use of either injection or receiving multiple injections during the study [36, 42]. There was a high risk of selection bias in three studies and unclear risk of performance and detection bias in other studies that could have influenced the results. The use of a meta-analytic approach helps safeguard against some of these risks, as it pools all the data together. However, these results need to be interpreted with due consideration to the different types of bias. In addition, only three out of the nine studies [36, 40, 42] provided details regarding prescription of exercises after the provision of RIT or corticosteroid injections. Future studies should investigate the effects of: i) a single corticosteroid or regenerative injection when compared to multiple injections for the treatment of lateral epicondylitis; ii) a standardized exercise protocol provided after the injections on levels of pain and self-rated disability between groups; iii) autologous blood injections on tendon thickness assesses using USG and color Doppler outcomes; and iv) development of a standardized protocol for preparation of regenerative injections.

Conclusion

Lateral epicondylitis can be a chronic condition that tends to influence the quality of life of people afflicted by the condition severely. For this reason, individuals with lateral epicondylitis are constantly searching for alternative therapies to expedite healing time. While corticosteroid injections are a common option, the use of regenerative injections has been successful in clinical trials with long-term follow-ups and signs of tendon repair. While both types of injections aim to provide relief, the mechanism of action varies. This in turn leads to differing effects on the tendon and healing process. Our results suggest that regenerative injections are useful in the long-term with no short-term differences in pain-reduction between corticosteroid and regenerative injections.

Availability of data and materials

Data sharing not applicable to this article as no datasets were generated or analyzed during the current study.

Change history

  • 27 January 2020

    In the original version of this article [1] the legends of Figs. 2 and 3 were inadvertently interchanged.

References

  1. Degen RM, Conti MS, Camp CL, Altchek DW, Dines JS, Werner BC. Epidemiology and disease burden of lateral Epicondylitis in the USA: analysis of 85,318 patients. HSS J. 2018;14:9–14.

    Article  Google Scholar 

  2. Degen RM, Cancienne JM, Camp CL, Altchek DW, Dines JS, Werner BC. Three or more preoperative injections is the most significant risk factor for revision surgery after operative treatment of lateral epicondylitis: an analysis of 3863 patients. J Shoulder Elb Surg. 2017;26:704–9.

    Article  Google Scholar 

  3. Goldie I. Epicondylitis lateralis humeri (epicondylalgia or tennis elbow). A pathogenetical study. Acta Chir Scand Suppl. 1964;57:331–9.

    Google Scholar 

  4. Sanders TL, Maradit Kremers H, Bryan AJ, Ransom JE, Morrey BF. Health care utilization and direct medical costs of tennis elbow: a population-based study. Sports Health. 2016;8(4):355–8.

    Article  PubMed  PubMed Central  Google Scholar 

  5. Calfee RP, Patel A, DaSilva MF, Akelman E. Management of lateral epicondylitis: current concepts. J Am Acad Orthop Surg. 2008;16(1):19–29.

    Article  Google Scholar 

  6. Jeon JY, Lee MH, Jeon I-H, Chung HW, Lee SH, Shin MJ. Lateral epicondylitis: associations of MR imaging and clinical assessments with treatment options in patients receiving conservative and arthroscopic managements. Eur Radiol. 2018;28(3):972–81.

    Article  Google Scholar 

  7. Stasinopoulos D, Stasinopoulos I. Comparison of effects of eccentric training, eccentric-concentric training, and eccentric-concentric training combined with isometric contraction in the treatment of lateral elbow tendinopathy. J Hand Ther. 2017;30:13–9.

    Article  Google Scholar 

  8. Altun RD, Incel NA, Cimen OB, Sahin G. Efficacy of ESWT for lateral Epicondylitis treatment: comparison with physical therapy modalities. J Musculoskelet Res. 2018;21:1850001. https://doi.org/10.1142/S021895771850001X.

    Article  Google Scholar 

  9. Sirico F, Ricca F, Nurzynska D, Castaldo C, Spera R, Montagnani S. Local corticosteroid versus autologous blood injections in lateral epicondylitis: meta-analysis of randomized controlled trials. Eur J Phys Rehabil Med. 2017;53:483–91.

    PubMed  Google Scholar 

  10. MacMahon PJ, Eustace SJ, Kavanagh EC. Injectable corticosteroid and local anesthetic preparations: a review for radiologists. Radiology. 2009;252:647–61.

    Article  Google Scholar 

  11. Cole BJ, Schumacher RH Jr. Injectable corticosteroids in modern practice. JAAOS-J Am Acad Orthop Surg. 2005;13:37–46.

    Article  Google Scholar 

  12. Fredberg U, Bolvig L, Pfeiffer-Jensen M, Clemmensen D, Jakobsen B, Stengaard-Pedersen K. Ultrasonography as a tool for diagnosis, guidance of local steroid injection and, together with pressure algometry, monitoring of the treatment of athletes with chronic jumper's knee and Achilles tendinitis: a randomized, double-blind, placebo-controlled study. Scand J Rheumatol. 2004;33:94–101.

    Article  CAS  Google Scholar 

  13. Reeves KD, Fullerton BD, Topol G. Evidence-based regenerative injection therapy (prolotherapy) in sports medicine. In: The sports medicine resource manual. Philadelphia: Saunders (Elsevier); 2008. p. 611–9.

  14. Moraes VY, Lenza M, Tamaoki MJ, Faloppa F, Belloti JC. Platelet-rich therapies for musculoskeletal soft tissue injuries. Cochrane Database Syst Rev. 2014;:CD010071. https://doi.org/10.1002/14651858.CD010071.pub3.

  15. Edwards SG, Calandruccio JH. Autologous blood injections for refractory lateral epicondylitis. J Hand Surg. 2003;28:272–8.

    Article  Google Scholar 

  16. Saucedo JM, Yaffe MA, Berschback JC, Hsu WK, Kalainov DM. Platelet-rich plasma. J Hand Surg. 2012;37:587–9.

    Article  Google Scholar 

  17. Mlynarek R, Kuhn A, Bedi A. Platelet-rich plasma (PRP) in orthopedic sports medicine. Am J Orthop. 2016;45:290–326.

    PubMed  Google Scholar 

  18. Foster TE, Puskas BL, Mandelbaum BR, Gerhardt MB, Rodeo SA. Platelet-rich plasma: from basic science to clinical applications. Am J Sports Med. 2009;37:2259–72.

    Article  Google Scholar 

  19. Gregory BP, Wysocki RW, Cohen MS. Controversies in surgical Management of Recalcitrant Enthesopathy of the extensor carpi Radialis Brevis. J Hand Surg. 2016;41:856–9.

    Article  Google Scholar 

  20. Gill TJ IV, Carroll KM, Hariri S. Open patellar tendon debridement for treatment of recalcitrant patellar tendinopathy: indications, technique, and clinical outcomes after a 2-year minimum follow-up. Sports Health. 2013;5:276–80.

    Article  PubMed  PubMed Central  Google Scholar 

  21. Lo MY, Safran MR. Surgical treatment of lateral epicondylitis: a systematic review. Clin Orthop Relat Res. 2007;463:98–106.

    PubMed  Google Scholar 

  22. Richardson WS, Wilson MC, Nishikawa J, Hayward RS. The well-built clinical question: a key to evidence-based decisions. ACP J Club. 1995;123:A12.

    CAS  PubMed  Google Scholar 

  23. Barnett JB, Bernacki MN, Kainer JL, Smith HN, Zaharoff AM, Subramanian SK. The effects of regenerative injection therapy compared to corticosteroids for the treatment of lateral epicondylitis. Med Sci Sports Exerc. 2019;49:S653.

    Google Scholar 

  24. Maher CG, Sherrington C, Herbert RD, Moseley AM, Elkins M. Reliability of the PEDro scale for rating quality of randomized controlled trials. Phys Ther. 2003;83:713–21.

    Article  PubMed  PubMed Central  Google Scholar 

  25. Foley NC, Teasell RW, Bhogal SK, Speechley MR. Stroke rehabilitation evidence-based review: methodology. Top Stroke Rehabil. 2003;10:1–7.

    PubMed  Google Scholar 

  26. Gill SD, McBurney H. Does exercise reduce pain and improve physical function before hip or knee replacement surgery? A systematic review and meta-analysis of randomized controlled trials. Arch Phys Med Rehabil. 2013;94:164–76.

    Article  Google Scholar 

  27. Hauser RA, Lackner JB, Steilen-Matias D, Harris DK. A systematic review of dextrose prolotherapy for chronic musculoskeletal pain. Clin Med Insights Arthritis Musculoskelet Disord. 2016;9:139–59.

    Article  PubMed  PubMed Central  Google Scholar 

  28. Gonzalez GZ, Moseley AM, Maher CG, Nascimento DP. Costa LdCM, Costa LO: Methodologic quality and statistical reporting of physical therapy randomized controlled trials relevant to musculoskeletal conditions. Arch Phys Med Rehabil. 2018;99:129–36.

    Article  Google Scholar 

  29. JPT H, Altman DG, editors. Assessing risk of bias in included studies. In: In the Cochrane Handbook for Systematic Reviews of Interventions. Version 5.0. 1. London: The Cochrane Collaboration Wiley; 2008.

  30. Higgins JP, Altman DG, Gotzsche PC, Juni P, Moher D, Oxman AD, Savovic J, Schulz KF, Weeks L, Sterne JA, et al. The Cochrane Collaboration's tool for assessing risk of bias in randomised trials. BMJ. 2011;343:d5928. https://doi.org/10.1136/bmj.d5928.

    Article  PubMed  PubMed Central  Google Scholar 

  31. World Health Organization. International Classification of Functioning, Disability and Health: ICF. Geneva: World Health Organization; 2001. Available at: http://www.who.int/classifications/icf/en/. Accessed 01 Nov 2018. Updated March 2, 2018.

  32. Valentine JC, Pigott TD, Rothstein HR. How many studies do you need? A primer on statistical power for meta-analysis. J Educ Behav Stat. 2010;35:215–47.

    Article  Google Scholar 

  33. Cohen J. A power primer. Psychol Bull. 1992;112:155–9.

    Article  CAS  Google Scholar 

  34. Borenstein M, Hedges LV, Higgins J, Rothstein HR. A basic introduction to fixed-effect and random-effects models for meta-analysis. Res Synth Methods. 2010;1:97–111.

    Article  Google Scholar 

  35. Higgins JP, Green S. Cochrane handbook for systematic reviews of interventions vol. 5. Chichester: Wiley; 2005.

    Google Scholar 

  36. Gosens T, Peerbooms JC, van Laar W, den Oudsten BL. Ongoing positive effect of platelet-rich plasma versus corticosteroid injection in lateral epicondylitis: a double-blind randomized controlled trial with 2-year follow-up. Am J Sports Med. 2011;39:1200–8.

    Article  PubMed  PubMed Central  Google Scholar 

  37. Kazemi M, Azma K, Tavana B, Moghaddam FR, Panahi A. Autologous blood versus corticosteroid local injection in the short-term treatment of lateral elbow tendinopathy: a randomized clinical trial of efficacy. Am J Phys Med Rehabil. 2010;89:660–7.

    Article  PubMed  PubMed Central  Google Scholar 

  38. Dojode C. A randomised control trial to evaluate the efficacy of autologous blood injection versus local corticosteroid injection for treatment of lateral epicondylitis. Bone Joint Res. 2012;1:192–7.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  39. Lebiedziński R, Synder M, Buchcic P, Polguj M, Grzegorzewski A, Sibiński M. A randomized study of autologous conditioned plasma and steroid injections in the treatment of lateral epicondylitis. Int Orthop. 2015;39:2199–203.

    Article  PubMed  PubMed Central  Google Scholar 

  40. Wolf JM, Ozer K, Scott F, Gordon MJ, Williams AE. Comparison of autologous blood, corticosteroid, and saline injection in the treatment of lateral epicondylitis: a prospective, randomized, controlled multicenter study. J Hand Surg. 2011;36:1269–72.

    Article  Google Scholar 

  41. Gautam V, Verma S, Batra S, Bhatnagar N, Arora S. Platelet-rich plasma versus corticosteroid injection for recalcitrant lateral epicondylitis: clinical and ultrasonographic evaluation. J Orthop Surg (Hong Kong). 2015;23:1–5.

    Article  CAS  Google Scholar 

  42. Krogh TP, Fredberg U, Stengaard-Pedersen K, Christensen R, Jensen P, Ellingsen T. Treatment of lateral epicondylitis with platelet-rich plasma, glucocorticoid, or saline: a randomized, double-blind, placebo-controlled trial. Am J Sports Med. 2013;41:625–35.

    Article  Google Scholar 

  43. Arik HO, Kose O, Guler F, Deniz G, Egerci OF, Ucar M. Injection of autologous blood versus corticosteroid for lateral epicondylitis: a randomised controlled study. J Orthop Surg (Hong Kong). 2014;22:333–7.

    Article  Google Scholar 

  44. Yadav R, Kothari S, Borah D. Comparison of local injection of platelet rich plasma and corticosteroids in the treatment of lateral epicondylitis of humerus. J Clin Diagn Res. 2015;9:RC05–7.

    CAS  PubMed  PubMed Central  Google Scholar 

  45. Bagiella E. Clinical trials in rehabilitation: single or multiple outcomes? Arch Phys Med Rehabil. 2009;90:S17–21.

    Article  Google Scholar 

  46. Teggeler M, Schmitz M, Fink A, Jansen JACG, Pisters MF. Reliability and agreement of ultrasonographic thickness measurements of the common lateral extensors of the elbow. Ultrasound Med Biol. 2015;41:1592–8.

    Article  Google Scholar 

  47. Poltawski L, Ali S, Jayaram V, Watson T. Reliability of sonographic assessment of tendinopathy in tennis elbow. Skelet Radiol. 2012;41:83–9.

    Article  Google Scholar 

  48. Connell DA, Ali KE, Ahmad M, Lambert S, Corbett S, Curtis M. Ultrasound-guided autologous blood injection for tennis elbow. Skelet Radiol. 2006;35:371–7.

    Article  Google Scholar 

  49. 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.

    Article  CAS  Google Scholar 

  50. Qian X, Lin Q, Wei K, Hu B, Jing P, Wang J. Efficacy and safety of autologous blood products compared with corticosteroid injections in the treatment of lateral epicondylitis: a meta-analysis of randomized controlled trials. PM&R. 2016;8:780–91.

    Article  Google Scholar 

  51. Tsikopoulos K, Tsikopoulos A, Natsis K. Autologous whole blood or corticosteroid injections for the treatment of epicondylopathy and plantar fasciopathy? A systematic review and meta-analysis of randomized controlled trials. Phys Ther Sport. 2016;22:114–22.

    Article  Google Scholar 

  52. Thøger Persson K, Else Marie B, Torkell E, Kristian S-P, Rachelle B, Ulrich F, Henning B, Robin C. Comparative effectiveness of injection therapies in lateral Epicondylitis: a systematic review and network meta-analysis of randomized controlled trials. Am J Sports Med. 2012;41(6):1435–46.

    Google Scholar 

  53. Arirachakaran A, Sukthuayat A, Sisayanarane T, Laoratanavoraphong S, Kanchanatawan W, Kongtharvonskul J. Platelet-rich plasma versus autologous blood versus steroid injection in lateral epicondylitis: systematic review and network meta-analysis. J Orthop Traumatol. 2016;17:101–12.

    Article  Google Scholar 

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Acknowledgements

The authors would like to acknowledge the UT Health San Antonio Briscoe library for access to numerous databases.

Funding

The authors did not receive any funding to carry out this review.

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  1. Department of Physical Therapy, School of Health Professions, UT Health San Antonio, 7703 Floyd Curl Drive, MSC 6247, San Antonio, TX, 78229, USA

    Julie Barnett, Madison N. Bernacki, Jessica L. Kainer, Hannah N. Smith & Sandeep K. Subramanian

  2. The Non-Surgical Center of Texas, San Antonio, USA

    Julie Barnett & Annette M. Zaharoff

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  1. Julie Barnett
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Contributions

MNB, JLK, HNS and JB conceived the research idea. MNB, JLK and HNS searched the literature and analyzed the papers, under supervision of JB. SKS was responsible for the meta-analysis. JB, SKS and AMZ supervised the drafting and editing of the manuscript. All authors shared equal responsibilities in the final preparation of the manuscript. All authors read and approved the final manuscript.

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Correspondence to Julie Barnett.

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Barnett, J., Bernacki, M.N., Kainer, J.L. et al. The effects of regenerative injection therapy compared to corticosteroids for the treatment of lateral Epicondylitis: a systematic review and meta-analysis. Arch Physiother 9, 12 (2019). https://doi.org/10.1186/s40945-019-0063-6

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Keywords

  • Platelet rich plasma
  • Autologous blood injection
  • Elbow
  • Tendinosis
  • Enthesopathy

Archives of Physiotherapy

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