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Platelet-Rich Plasma versus Corticosteroid Injection for Recalcitrant Lateral Epicondylitis: Clinical and Ultrasonographic Evaluation

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To evaluate the clinical and ultrasonographic changes in the morphology and vascularity of the common extensor tendon after injecting platelet-rich plasma (PRP) or corticosteroid (CS) for recalcitrant lateral epicondylitis (LE). 30 patients aged 18 to 60 years with recalcitrant (>6 months) LE not responsive to oral medication or non-invasive treatment were randomised to receive PRP (n=15) or CS (n=15) injection. Patients were assessed using the visual analogue scale (VAS) for pain, Disabilities of the Arm, Shoulder and Hand Scale (DASH) score, Oxford Elbow Score, modified Mayo Clinic performance index for the elbow (modified Mayo score), and hand grip strength. Ultrasonography was performed by a musculoskeletal ultrasonologist to evaluate for tear at the common extensor origin, oedema at the common extensor origin, cortical erosion, probe-induced tenderness, and thickness of the tendon. The VAS for pain, DASH score, Oxford Elbow Score, modified Mayo score, and hand grip strength all improved significantly from pre-injection to the 6-month follow-up in the PRP and CS groups. However, in the CS group, the scores generally peaked at 3 months and then deteriorated slightly at 6 months indicating recurrence of symptoms, which involved 46.7% of the CS patients. At 6 months, the number of patients positive for various ulrasonographic findings generally decreased. However, in the CS group, the number of patients with reduced thickness of the common extensor tendon increased from 2 to 12, and the number of patients with cortical erosion at the lateral epicondyle increased from 9 to 11. PRP appeared to enable biological healing of the lesion, whereas CS appeared to provide short-term, symptomatic relief but resulted in tendon degeneration.
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ABSTRACT
Purpose. To evaluate the clinical and ultrasonographic
changes in the morphology and vascularity of the
common extensor tendon after injecting platelet-rich
plasma (PRP) or corticosteroid (CS) for recalcitrant
lateral epicondylitis (LE).
Methods. 30 patients aged 18 to 60 years with
recalcitrant (>6 months) LE not responsive to
oral medication or non-invasive treatment were
randomised to receive PRP (n=15) or CS (n=15)
injection. Patients were assessed using the visual
analogue scale (VAS) for pain, Disabilities of the Arm,
Shoulder and Hand Scale (DASH) score, Oxford
Elbow Score, modied Mayo Clinic performance
index for the elbow (modied Mayo score), and hand
grip strength. Ultrasonography was performed by a
musculoskeletal ultrasonologist to evaluate for tear at
the common extensor origin, oedema at the common
extensor origin, cortical erosion, probe-induced
tenderness, and thickness of the tendon.
Results. The VAS for pain, DASH score, Oxford
Elbow Score, modied Mayo score, and hand grip
Platelet-rich plasma versus corticosteroid
injection for recalcitrant lateral epicondylitis:
clinical and ultrasonographic evaluation
VK Gautam,1 Saurabh Verma,1 Sahil Batra,1 Nidhi Bhatnagar,2 Sumit Arora1
1 Department of Orthopaedic Surgery, Maulana Azad Medical College and associated Lok Nayak Hospital, New Delhi,
India
2 Department of Radiology, Sanjeevan Hospital, Delhi, India
Address correspondence and reprint requests to: Sumit Arora, c/o Mr Sham Khanna, 2/2, Vijay Nagar, Delhi, 110009, India. Email:
mamc_309@yahoo.co.in
Journal of Orthopaedic Surgery 2015;23(1):1-5
strength all improved signicantly from pre-injection
to the 6-month follow-up in the PRP and CS groups.
However, in the CS group, the scores generally peaked
at 3 months and then deteriorated slightly at 6 months
indicating recurrence of symptoms, which involved
46.7% of the CS patients. At 6 months, the number
of patients positive for various ulrasonographic
ndings generally decreased. However, in the CS
group, the number of patients with reduced thickness
of the common extensor tendon increased from 2 to
12, and the number of patients with cortical erosion at
the lateral epicondyle increased from 9 to 11.
Conclusion. PRP appeared to enable biological
healing of the lesion, whereas CS appeared to provide
short-term, symptomatic relief but resulted in tendon
degeneration.
Key words: platelet-rich plasma; tennis elbow;
ultrasonography
introduction
Lateral epicondylitis (LE) is caused by mechanical
overloading and abnormal microvascular response
2 VK Gautam et al. Journal of Orthopaedic Surgery
and affects approximately 1% to 3% of the
population.1–3 Treatment options include rest, non-
steroidal anti-inammatory medication, physical
therapy, extracorporeal shock wave therapy,
ultrasound therapy, botulinum injection, and
corticosteroid (CS) injection. Recalcitrant cases
necessitate surgical release.4 Injection of biological
agents achieves a favourable long-term clinical
outcome.5–8 Histological analysis of chronic LE reveals
angiobroblastic and mucoid degeneration secondary
to a failure of natural tendon repair mechanism rather
than acute inammation. Platelet-rich plasma (PRP)
enhances healing by delivering high concentrations
of alpha-granules containing biologically active
moieties (such as vascular endothelial growth
factor and transforming growth factor-β) to the
areas of soft-tissue damage.9,10 In PRP, platelet count
increases 2- to 8-fold, and different growth factors
increase 1- to 25-fold.11 PRP injection for LE reduces
pain and induces healing of the common extensor
tendon injury and vascularisation of the diseased
tendon.12,13 Ultrasonography enables visualisation
of the tendon structures around the elbow.14,15 This
randomised, prospective study evaluated the clinical
and ultrasonographic changes in the morphology
and vascularity of the common extensor tendon after
injecting PRP or CS for recalcitrant LE.
Materials and Methods
Between May 2011 and October 2012, 30 patients
aged 18 to 60 years with recalcitrant (>6 months) LE
not responsive to oral medication or non-invasive
treatment were randomised to receive PRP (n=15)
or CS (n=15) injection. No patient had bilateral
involvement. Pregnant patients or patients with
symptoms of carpal tunnel syndrome or cervical
radiculopathy or systemic disorders (diabetes,
rheumatoid arthritis, or hepatitis) were excluded, as
were those who had undergone surgery or local CS
injection in the past 6 months.
20 ml of blood was collected in an acid citrate
dextrose vacutainer and centrifuged at 1500 rpm for
15 minutes to separate the blood into layers of red
blood cells, buffy-coat of leucocytes, and plasma.
The platelet counts for PRP and unprocessed blood
were calculated. 2 ml of PRP or methylprednisolone
(40 mg/ml) was injected at the most tender point
over the lateral epicondyle of the humerus using the
peppering technique.
After injection, patients rested for 30 minutes and
were advised against massage or hot fomentation. Ice
packs or paracetamol were advised for discomfort
rather than non-steroidal anti-inammatory drugs,
as the latter may interfere with platelet function.
Patients were assessed using the visual analogue
scale (VAS) for pain, Disabilities of the Arm, Shoulder
and Hand Scale (DASH) score, Oxford Elbow Score,
modied Mayo Clinic performance index for the
elbow (modied Mayo score), and hand grip strength
before and after treatment at 2 weeks, 6 weeks, 3
months, and 6 months. Ultrasonography (HD 11,
linear array transducer MF L12-4 MHz, Philips
Healthcare, MA) was performed before and after
treatment at 3 and 6 months by a musculoskeletal
ultrasonologist blind to the treatments to evaluate
for tear at the common extensor origin, oedema at
Table 1
The visual analogue scale (VAS) for pain, Disabilities of the Arm, Shoulder and Hand Scale (DASH) score, Oxford Elbow
Score, modified Mayo score, and hand grip strength of the platelet-rich plasma (PRP) and corticosteroid (CS) groups
Assessment VAS for pain DASH score Oxford Elbow Score Modified Mayo score Hand grip strength
PRP CS p Value PRP CS p Value PRP CS p Value PRP CS p Value PRP CS p Value
Pre-injection 7.1±0.8 7.0±0.8 0.650 69.7±6.1 67.5±6.9 0.378 27.4±3.9 31.2±4.1 0.015 56.1±6.9 56.8±5.4 0.770 18.5±5.1 19.2±4.6 0.683
Post-injection
2 weeks 4.5±1.1 2.1±0.7 0.000 51.6±6.8 39.7±6.7 0.000 34.7±4.3 39.7±3.4 0.001 61.3±3.1 68.5±3.9 0.000 22.5±6.6 25.5±4.9 0.159
6 weeks 2.7±0.8 1.4±0.5 0.000 38.6±5.7 32.7±4.1 0.003 39.3±3.1 41.5±2.5 0.045 67.7±2.6 70.4±3.2 0.017 25.5±6.3 25.5±6.0 0.976
3 months 1.8±0.6 1.7±0.5 0.493 33.6±5.1 34.3±3.3 0.675 39.3±3.3 41.7±2.4 0.029 70.2±2.2 69.6±3.5 0.578 25.5±5.6 25.8±6.7 0.884
6 months 1.6±0.5 2.9±1.2 0.001 32.0±4.5 39.6±1.0 0.012 41.2±2.7 36.3±5.9 0.007 70.7±3.0 61.5±5.8 0.000 25.9±6.2 23.3±6.5 0.258
p Value
Pre-injection vs. 2 weeks <0.001 <0.001 - <0.001 <0.001 - <0.001 <0.001 - 0.047 <0.001 - 0.087 0.001 -
2 weeks vs. 6 weeks <0.001 0.016 - <0.001 0.01 - <0.001 0.072 - <0.001 0.159 - <0.001 1.00 -
6 weeks vs. 3 months 0.001 0.104 - 0.007 0.316 - 1.00 0.788 - 0.013 0.387 - 1.00 0.907 -
3 months vs. 6 months 0.384 0.002 - 0.451 0.066 - 0.136 <0.001 - 0.546 <0.001 - 0.844 0.221 -
Pre-injection vs. 6 months <0.001 <0.001 - 0.001 <0.001 - <0.001 0.022 - 0.001 0.072 - 0.005 0.012 -
Vol. 23 No. 1, April 2015 Platelet-rich plasma versus corticosteroid injection for recalcitrant lateral epicondylitis 3
the common extensor origin, cortical erosion, probe-
induced tenderness, and thickness of the tendon.
The paired t-test (or paired Wilcoxon signed
rank test) was used for detection of improvement
over time. The resulting 2-tailed p value of <0.05 was
considered statistically signicant.
results
The VAS for pain, DASH score, Oxford Elbow Score,
modied Mayo score, and hand grip strength all
improved signicantly from pre-injection to the
6-month follow-up in the PRP and CS groups.
However, in the CS group, the scores generally
peaked at 3 months and then deteriorated slightly at
6 months indicating recurrence of symptoms, which
involved 46.7% of the CS patients (Table 1).
At 6 months, the number of patients positive
for various ulrasonographic ndings generally
decreased. However, in the CS group, the number
of patients with reduced thickness of the common
extensor tendon increased from 2 to 12, and the
number of patients with cortical erosion at the lateral
epicondyle increased from 9 to 11 (Table 2).
discussion
CS injection used to be the treatment of choice for LE.
CS suppresses the immune system by suppressing the
pro-inammatory proteins. Its potential side effects
include lipodystrophy, skin pigmentation changes,
and tendon atrophy/ruptures. PRP is an increasingly
popular treatment for LE. It increases expression
of the collagen gene and production of vascular
endothelial growth factor and hepatocyte growth
factor in human tenocytes,16,17 and type-I collagen.18
Assessment VAS for pain DASH score Oxford Elbow Score Modified Mayo score Hand grip strength
PRP CS p Value PRP CS p Value PRP CS p Value PRP CS p Value PRP CS p Value
Pre-injection 7.1±0.8 7.0±0.8 0.650 69.7±6.1 67.5±6.9 0.378 27.4±3.9 31.2±4.1 0.015 56.1±6.9 56.8±5.4 0.770 18.5±5.1 19.2±4.6 0.683
Post-injection
2 weeks 4.5±1.1 2.1±0.7 0.000 51.6±6.8 39.7±6.7 0.000 34.7±4.3 39.7±3.4 0.001 61.3±3.1 68.5±3.9 0.000 22.5±6.6 25.5±4.9 0.159
6 weeks 2.7±0.8 1.4±0.5 0.000 38.6±5.7 32.7±4.1 0.003 39.3±3.1 41.5±2.5 0.045 67.7±2.6 70.4±3.2 0.017 25.5±6.3 25.5±6.0 0.976
3 months 1.8±0.6 1.7±0.5 0.493 33.6±5.1 34.3±3.3 0.675 39.3±3.3 41.7±2.4 0.029 70.2±2.2 69.6±3.5 0.578 25.5±5.6 25.8±6.7 0.884
6 months 1.6±0.5 2.9±1.2 0.001 32.0±4.5 39.6±1.0 0.012 41.2±2.7 36.3±5.9 0.007 70.7±3.0 61.5±5.8 0.000 25.9±6.2 23.3±6.5 0.258
p Value
Pre-injection vs. 2 weeks <0.001 <0.001 - <0.001 <0.001 - <0.001 <0.001 - 0.047 <0.001 - 0.087 0.001 -
2 weeks vs. 6 weeks <0.001 0.016 - <0.001 0.01 - <0.001 0.072 - <0.001 0.159 - <0.001 1.00 -
6 weeks vs. 3 months 0.001 0.104 - 0.007 0.316 - 1.00 0.788 - 0.013 0.387 - 1.00 0.907 -
3 months vs. 6 months 0.384 0.002 - 0.451 0.066 - 0.136 <0.001 - 0.546 <0.001 - 0.844 0.221 -
Pre-injection vs. 6 months <0.001 <0.001 - 0.001 <0.001 - <0.001 0.022 - 0.001 0.072 - 0.005 0.012 -
Table 2
Ultrasonographic evaluation of the platelet-rich plasma (PRP) and corticosteroid (CS) groups
Assessment No. (%) of patients with positive ultrasonographic finding
Tear of the common
extensor tendon
Oedema of the
common extensor
tendon
Reduced thickness
of the common
extensor tendon
Probe-induced
tenderness
Cortical erosion
at the lateral
epicondyle
PRP
(n=15)
CS
(n=15)
PRP
(n=15)
CS
(n=15)
PRP
(n=15)
CS
(n=15)
PRP
(n=15)
CS
(n=15)
PRP
(n=15)
CS
(n=15)
Pre-injection 10 (67) 5 (33) 7 (47) 7 (47) 3 (20) 2 (13) 15 (100) 15 (100) 14 (93) 9 (60)
Post-injection
3 months 8 (53) 4 (27) 6 (40) 3 (20) 2 (13) 4 (27) 10 (67) 9 (60) 14 (93) 11 (73)
6 months 4 (27) 5 (33) 1 (7) 2 (13) 1 (7) 12 (80) 6 (40) 10 (67) 14 (93) 11 (73)
4 VK Gautam et al. Journal of Orthopaedic Surgery
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Table 3
Studies of platelet-rich plasma (PRP) versus corticosteroid (CS) injection for lateral epicondylitis
PRP initially inhibits the inammatory process and
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production within the rst 72 hours.21,22 PRP injection
is superior to CS injection for chronic LE (Table 3).22
The recurrence rate and need for repeated injection
or surgery are higher in the CS than PRP group.23,24
Ultrasonography revealed a decrease in thickness
of the tendon after CS injection and an increase in
thickness after PRP injection.25 Increase in tendon
vascularity following PRP injection is associated with
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formations and anechoic foci, tendon thickness, and
neovascularity.27
conclusion
PRP appeared to enable biological healing of the
lesion, whereas CS appeared to provide short-
term, symptomatic relief but resulted in tendon
degeneration. PRP injection may be appropriate for
other forms of tendinopathies, such as plantar fasciitis
and medial epicondylitis.
disclosure
No conicts of interest were declared by the authors.
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... Kortikosteroide (wie Glukokortikoide, Kortison und Derivate) wirken entzündungshemmend und immunmodulierend durch Unterdrückung des Immunsystems und Hemmung proinflammatorischer Proteine [6].DiekataboleWirkungderSteroideführt jedoch zu einer Veränderung der Zellaktivität der Knorpelzellen mit Verminderung des Knorpelvolumens, was eine Apoptoseinduktion zur Folge hat [7]. Aufgrund der schmerzlindernden Wirkung werden intraartikuläre Kortikosteroid-Injektionen seit vielen Jahren bei der symptomatischen Gonarthrose eingesetzt und sind in die Empfehlungen der wichtigsten internationalen Gesellschaften aufgenommen worden [8]. ...
... Thrombozyten enthal-ten α-Granula, die durch biologisch aktive Wachstumsfaktoren, wie z. B. der vaskuläre endotheliale Wachstumsfaktor und der Transforming Growth Factor β (TGFβ) die Proliferation stromaler und mesenchymaler Stammzellen fördern und die Bildung von fibrösem Narbengewebe vermindern [6]. Katabole Reaktionen werden durch PRP gehemmt und der chondrale Umbau gefördert [20]. ...
... Katabole Reaktionen werden durch PRP gehemmt und der chondrale Umbau gefördert [20]. Zusätzlich hat PRP antientzündliche Eigenschaften durch Unterdrückung der Makrophagenproliferation und Interleukin(IL)-1-Produktion [6]. Dennoch gibt es noch viele Kon ...
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... In our study, the mean pre-injection VAS score among the PRP and steroid group was 6.77 ± 0.971 and 6.97 ± 0.964, respectively. Almost similar baseline VAS score was seen in a study done by Gawtham et al. [14]. The result in their study showed that the baseline VAS score was 7.1 and 7.0 in PRP and steroid group, respectively. ...
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... The mean VAS score was 1.6 and 2.8 in the PRP and steroid group, respectively, in the later study. This is in contrast with the study done by Gawtham et al. [14], they showed that the mean VAS score was 1.8 and 1.7 in PRP and steroid group, respectively. The mean VAS score in our study at 6 months was 0.90 and 1.501 in the PRP and steroid group, respectively. ...
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Introduction Lateral epicondylitis, or tennis elbow, affects 1%–3% of adults aged 35–50, causing pain and weakness in the dominant elbow due to chronic inflammation of the extensor tendon. While corticosteroid injections (CSI) are commonly used for treatment, they offer only short-term relief. Platelet-rich plasma (PRP) is a promising alternative with potential for long-term benefits. This study compares the efficacy of PRP and CSI in treating lateral epicondylitis. Materials & Methods A randomized controlled trial was conducted at Chettinad Hospital and Research Institute from February 2020 to March 2021, involving patients with lateral epicondylitis unresponsive to non-invasive treatments. Patients were randomly assigned to receive either PRP or CSI, with pre- and post-treatment pain and function assessed using VAS, PSFS, and PRTEE scores. Results PRP showed better long-term pain reduction and functional improvement than CSI. At 6 months, PRP-treated patients had significantly lower VAS and PRTEE scores, indicating superior outcomes. Discussion Although CSI provided quicker initial relief, PRP demonstrated sustained benefits at 3 and 6 months. PRP’s effectiveness in promoting tissue healing may explain its long-term success. Conclusion PRP is more effective than CSI for long-term management of lateral epicondylitis, offering superior pain relief and functional improvement.
... There were 450 males (47.2%) and 504 females (52.8%). Nineteen studies were LOE I [11,[25][26][27][28][29][30][31][32][33][34][35][36][37][38][39][40][41][42], six studies were LOE II [43][44][45][46][47][48], and one study was LOE III [49]. According to the ROBINS-I criteria, there were 21 studies (81%) with low risk of bias, four studies (15%) with moderate risk of bias, and one study (4%) with serious risk of bias. ...
Article
Background: Lateral epicondylitis (LE), commonly known as tennis elbow, is a condition involving inflammation of the extensor carpi radialis brevis tendon at its attachment to the lateral epicondyle of the humerus. In recent years, platelet-rich plasma (PRP) therapy, an ortho-biologic treatment, has emerged as a promising option for the treatment of LE. Despite promising results in clinical trials, variability in PRP preparation and administration is a barrier to consistent outcomes. To address this, the Minimum Information for Studies Evaluating Biologics in Orthopedics (MIBO) guidelines were created in 2017 to establish a standardized approach for reporting findings in PRP-based studies. The objective of this study was to analyze and compare the rate of adherence of the MIBO guidelines in the use of PRP in treating LE. Methods: This systematic review evaluates the adherence of studies on PRP for LE to MIBO guidelines using Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. Adherence was determined by calculating the total percentage of checklist items that each study adequately and clearly reported from the 46-point checklist.Results: A total of ¬¬¬26 studies (954 patients) were included. Overall, only 52.2% of the 46-point MIBO checklist was reported per article on average with 0 articles displaying adherence rates of 100%. There was no significant difference in the mean adherence rates between studies prior to publication of the MIBO guidelines (45.2%) and after (53.7%). Conclusions: This review demonstrated that studies evaluating the outcomes and procedures of the use of PRP in the setting of LE have poor adherence to MIBO guidelines. There was no difference in the adherence rates in studies published before and after the creation of MIBO guidelines in 2017. Level of evidence: II.
... 1 PRP in particular has become an attractive option for treating the tendinopathic processes of LE, as early randomized controlled trials (RCTs) demonstrated improved efficacy over alternative therapies. 2,12,13,15,18,28,29,33 However, more recent RCTs have been unable to replicate these initial benefits, 14,20 leading to a high degree of heterogeneity in previous meta-analyses 8,11,25 and the inability to draw meaningful conclusions as to whether PRP is a reliable and effective management option for LE. ...
Article
Background Randomized controlled trials (RCTs) evaluating the efficacy of platelet-rich plasma (PRP) for the management of lateral epicondylitis (LE) have been characterized by substantial variability in reported outcomes. The source of this heterogeneity is uncertain. Purpose To determine the effect of estimated platelet concentration on the efficacy of PRP for the management of LE. Study Design Systematic review and meta-analysis; Level of evidence, 2. Methods All RCTs evaluating the efficacy of PRP in managing LE were identified. RCTs were classified according to whether the study documented a platelet concentration factor of PRP representing a greater than 3-fold increase over whole blood or a supraphysiological platelet dose (high-dose vs low-dose PRP). The primary outcome was the mean difference (MD) in the visual analog scale (VAS) score at latest follow-up. Random-effects and mixed-effects meta-analyses were performed, and meta-regression was used to evaluate whether differences in outcomes after treatment with PRP could be explained by differences in the concentration of PRP used. Results Overall, 13 RCTs with a total of 791 patients were included in this analysis, with 5 that utilized low-dose PRP and 8 that used high-dose PRP. Meta-analysis of VAS scores reported by studies that used high-dose PRP resulted in an MD of −1.31 (95% CI, −1.87 to −0.75) in favor of PRP over all alternative treatment strategies ( P < .001). Meta-analysis of VAS scores reported by studies that used low-dose PRP resulted in an MD of 0.08 (95% CI, −0.51 to 0.68), suggesting no difference in the effect between PRP and all alternative treatment strategies ( P = .79). The platelet concentration factor of PRP used in each RCT was found to be strongly predictive of the VAS score at final follow-up in meta-regression ( P < .001), with 58.5% of the heterogeneity in the outcomes of PRP between studies explained by the platelet concentration factor alone. Conclusion The platelet concentration of PRP may play a significant role in the outcomes of patients with LE. A direct linear relationship was observed between the platelet concentration factor of PRP used and the magnitude of patient-reported symptom relief after the management of LE with PRP. Clinicians should ensure a supraphysiological platelet concentration when preparing PRP for the management of LE.
... With nearly half reporting VAS scores ≤3 and 21.05% (4/19) of patients experiencing complete pain resolution (VAS=0), PRP therapy was linked to significant pain reduction [13]. The overall mean DASH scores also demonstrated a notable improvement, falling from 87.5% prior to therapy to 18.5% following it, indicating improved functionality and the capacity to carry out everyday tasks [14]. These results are consistent with other research, including that conducted by Gosens et al., which showed that PRP, as opposed to corticosteroid injections, produced long-term benefits in pain and function. ...
Article
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Objective: This study aimed to evaluate the efficacy of platelet-rich plasma (PRP) injections in managing lateral epicondylitis (LE), focusing on pain relief, functional improvement, side effects, and patient satisfaction. Methods: A retrospective analysis of 19 patients treated with PRP injections at a tertiary care center was conducted. Data included demographic characteristics, Visual Analog Scale (VAS) pain scores, Disabilities of the Arm, Shoulder, and Hand (DASH) scores, and patient satisfaction. Statistical analyses utilized paired t-tests and one-sample proportion tests. Statistical significance was set at p<0.05. Results: PRP injections significantly reduced VAS pain scores, with 21.05% (4/19) of patients achieving complete pain relief (VAS=0) and 47.37% (9/19) reducing scores to ≤3 (p=0.027). DASH scores improved substantially, with mean scores decreasing from 87.5% (19/19) (95% CI: 82.3-92.7%) pre-treatment to 18.5% (19/19) (95% CI: 12.7-24.3%) post-treatment (p<0.001). Prior corticosteroid use was associated with poorer outcomes (p=0.012). Patient satisfaction was high, with 89.5% (16/19) of patients reporting being "very satisfied" or "satisfied" (p=0.001). Conclusion: PRP injections offer significant pain relief and functional improvement for patients with LE. This minimally invasive treatment is particularly valuable for high-demand populations, such as professional athletes, due to faster recovery times and reduced need for surgery. However, high patient satisfaction rates underscore its clinical utility. Prospective studies with larger cohorts are needed to further validate these findings and refine PRP protocols.
Article
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Introduction Lateral epicondylitis, also termed as “tennis elbow”, is the most common reason for elbow pain and dysfunction. This study aimed to assess the research activity on lateral epicondylitis worldwide. Methods Publications on lateral epicondylitis from Web of Science database were recorded and analyzed in June 2024. For each article, citations, authors, title, organization, country, journal, year, keywords, topic, and H-index were extracted. VOSviewer and Excel 2020 were used to operate the bibliometric and visualized study. Results A total of 913 publications between 1950 and 2023 were included. The total number of citations was 27,866 with the average citation per publication of 31 times. “Orthopedics” became the dominant topic ( n = 365, 40.0%). The United States contributed the most publications ( n = 201, 22.0%). The latest keywords “platelet rich plasma”, “autologous conditioned plasma”, and “extracorporeal shockwave therapy” mainly appeared since 2018. Conclusion This bibliometric study indicates that there is a growing trend in the number of publications on lateral epicondylitis. The United States dominated studies of lateral epicondylitis and the Journal of Shoulder and Elbow Surgery was the most productive journal. “Platelet rich plasma”, “autologous conditioned plasma”, and “extracorporeal shockwave therapy” may become new interests in lateral epicondylitis research.
Article
Background and Objectives: Lateral epicondylitis, commonly known as tennis elbow, is a prevalent condition characterized by pain and tenderness over the lateral epicondyle. Various treatment options, including corticosteroids, platelet-rich plasma (PRP), and saline injections, are utilized, yet their comparative efficacy remains unclear. Hypothesis: This study hypothesizes that PRP injections result in superior functional and clinical outcomes compared to corticosteroid and saline treatments, as assessed by clinical scoring systems and radiological findings. Materials and Methods: The study enrolled patients aged 18 years and older with pain and tenderness over the lateral epicondyle persisting for at least three months and no prior treatment. Patients with comorbidities affecting the upper extremity were excluded. Fifty-five elbows from 50 patients were randomized into three groups (glucocorticoid, PRP, and saline). Functional outcomes were assessed using the Visual Analog Scale (VAS), Patient-Rated Tennis Elbow Evaluation (PRTEE), and Disabilities of the Arm, Shoulder, and Hand (DASH) questionnaire. Radiological evaluations included vascularity and superb microvascular imaging (SMI) indices via ultrasonography before injection and three months post-injection. Results: Fourteen patients were lost to follow-up, leaving 36 patients (36 elbows, 16 males and 20 females; mean age 42.4 ± 6.15 years) for analysis. The glucocorticoid group included 13 elbows, PRP group 14 elbows, and saline group 14 elbows. Baseline functional and radiological scores were similar across groups. At three months, PRP and glucocorticoid groups showed no significant differences in VAS scores (p = 0.7), but PRP outperformed both of the other groups in DASH and PRTEE scores, with the saline group performing the worst (p < 0.001). PRP consistently achieved the best outcomes at both three and six months. Radiological assessments revealed no significant group differences in vascularity or SMI indices (p = 0.3 and p = 0.2, respectively). Conclusions: PRP treatment demonstrated superior functional outcomes in early and mid-term evaluations compared to glucocorticoid and saline. However, ultrasonographic measures of vascularity and SMI did not correlate with functional outcomes. Clinical Relevance: PRP offers a promising treatment option for lateral epicondylitis, with superior functional improvements over other commonly used injections. Radiological assessments of vascularity and SMI may not reliably predict clinical outcomes.
Article
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Background: Lateral epicondylitis, colloquially known as tennis elbow, is a common cause of elbow pain and daily task disability. Caused by repetitive movement, it is typically a degenerative rather than inflammatory event and affects mostly middle-aged patients. Despite its good prognostic nature, its economic burden on the healthcare system encourages research on the efficacity of non-operative injection treatments. This article aims to compare the clinical effectiveness of platelet-rich plasma (PRP) and corticosteroid (CS) injections in managing lateral epicondylitis. Methods: PubMed, Cochrane, and Google Scholar (pages 1-20) were searched up to March 2024. Only randomized controlled trials were included. The clinical outcomes evaluated were the visual analog scale (VAS) and Disabilities of the Arm, Shoulder, and Hand (DASH) score. Results: Twenty-six randomized controlled trials with 1.877 patients were included in this meta-analysis. In terms of VAS scores, short-term results (<2 months) favored CS over PRP (P=0.03; mean difference [MD], 0.67; 95% CI, 0.05 to 1.28), whereas long-term results (>6 months) favored PRP (P<0.001; MD,-1.60; 95% CI,-2.01 to-1.20]). Intermediate-term results (2-6 months) showed no significant difference between injection treatments. In terms of DASH scores, short-and intermediate-term results showed no significant difference, whereas long-term results favored PRP (P<0.001; MD,-4.87; 95% CI,-7.69 to-2.06). Conclusions: CS provides significantly better short-term pain relief, while PRP provides better long-term functional improvement and clinical long-term pain relief. However, future studies should focus on other injection protocols or addition of other non-invasive modalities.
Article
Introduction Lateral epicondylitis, commonly known as tennis elbow, is one of the most common chronic disabling painful conditions that affect the forearm’s common extensor tendons. This study aimed to compare the effectiveness of platelet-rich plasma (PRP) versus corticosteroid injection in the treatment of lateral epicondylitis. Aims The purpose of this study is to compare the efficacy of PRP versus corticosteroid injection in the treatment of lateral epicondylitis, focusing on the early response. Settings and Design This was a prospective randomised controlled study. Materials and Methods This study was a prospective randomised control trial of 100 patients, clinically diagnosed with lateral epicondylitis in Karnataka Institute of Medical Sciences Hospital, Hubli. Patients were randomly allocated (1:1) using computer-generated random numbers to two groups. Group A received corticosteroid injection. Group B received PRP injection. Outcome assessment was done using the Oxford Elbow Score (OES), Visual Analogue Scale (VAS), Patient-rated Tennis Elbow Evaluation (PRTEE) and Disabilities of Arm, Shoulder and Hand Score (DASH). All patients were followed up at regular intervals of 2 weeks, 4 weeks, 3 months and 6 months post-injection. Statistical Analysis Used Using SPSS Statistics version 25 software, statistical analysis was done. Results Pre–injection, the mean OES, VAS, PRTEE and DASH scores were similar in both the groups with insignificant P value. The mean pre-injection OES, VAS, PRTEE and DASH scores in the corticosteroid group were 11.22, 7.88, 75.950 and 69.364, whereas in the PRP group, it was 10.66, 7.96, 76.170 and 69.466, with P = 0.165, 0.322, 0.834 and 0.869, respectively. At the end of 6 months in the corticosteroid group, the mean score of OES increased from 11.22 ± 1.71 to 38.94 ± 5.17, VAS decreased from 7.88 ± 0.385 to 1.74 ± 1.24, PRTEE decreased from 75.95 ± 4.86 to 24.3 ± 12 and DASH decreased from 69.36 ± 2.90 to 23.31 ± 11.5, with a significant P < 0.005. At the end of 6 months in the PRP group, the mean scores of OES increased from 10.66 ± 2.07 to 45.38 ± 1.41, VAS decreased from 7.96 ± 0.45 to 0.06 ± 0.31, PRTEE decreased from 76.1 ± 5.04 to 7.47 ± 3.16 and DASH decreased from 69.47 ± 3.44 to 7.78 ± 2.65, with a significant P < 0.005. Conclusion We concluded that patients treated with PRP had significantly reduced pain, increased functional activity, less recurrence and without requirement of any further intervention, outperforming corticosteroid injection effect at the end of 6 months follow up.
Article
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To compare the compressive strength of cannulated versus non-cannulated cancellous screws for undisplaced femoral neck fractures in synthetic bones. 18 synthetic proximal femurs simulating an AO B1 valgus impacted femoral neck fracture in osteoporotic bone were used. The fracture angles were between 55º and 63º (Pauwels grade 2). Fixation was made using 6.5-mm non-cannulated screws (n=6), 6.5-mm cannulated screws (n=6), or 7.3-mm cannulated screws (n=6). A custom-built jig was designed to guide the insertion of the screws in an identical triangular configuration. Screws were tightened by a single operator using a torquemeasuring screwdriver. The femoral head was subjected to progressive axial loading at 5 mm/min. The load to failure and displacement were recorded. The 3 groups did not differ significantly except that the load to failure was higher in the construct with 6.5-mm non-cannulated screws than that with 6.5-mm cannulated screws (1222 N vs 1008 N, p=0.003). The compressive strength of a synthetic bone hip fracture model fixed with non-cannulated screws was higher than that of cannulated screws of the same diameter.
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Objective: To investigate the efficacy of using contrast-enhanced ultrasound to assess the relationship of altered vascularity and tendon morphology following injection of platelet-rich plasma (PRP) for lateral epicondylitis. Materials and methods: This study prospectively evaluated six patients who had a baseline ultrasound confirming tendinosis of the common extensor tendon. Patients received a single 3-ml PRP injection under ultrasound guidance. Grayscale images of the injected elbow were obtained at baseline and were repeated at 1 and 6 months after injection. DEFINITY® contrast was also injected after by 2 sets of wrist-extension exercises in order to obtain contrast-enhanced images of the elbow. Qualitative and quantitative analyses of the level of enhancement to the regions of interest were performed using off-line quantitative analysis software. Results: All patients had either moderate or severe common extensor tendinosis as determined on clinical examination and baseline imaging. Five patients demonstrated improved tendon morphology using ultrasound imaging 6 months after PRP injection (one patient was lost to follow-up). At baseline, there was evidence of increased vascularity at the myotendinous junction (MT) of the common extensor tendon when compared to its footprint (FP). There was a trend towards no change in FP vascularity between baseline and 6 months (p = 0.062) and between 1 and 6 months (p = 0.288). There was a trend for increased vascularity to the MT region from baseline to 6 months (p = 0.433) and from 1 to 6 months (p = 0.783). Conclusions: Contrast-enhanced ultrasound provides a sensitive method the display alterations in vascularity in the common extensor tendon of the elbow. PRP therapy for lateral epicondylitis can improve extensor tendon morphology. Corresponding increased extensor tendon FP vascularity, however, was not seen. There is a trend for increased vascularity at the MT up to 6 months following PRP injection, based on limited pilot data.
Article
Eighteen patients (20 elbows) who underwent percutaneous tenotomy of the common extensor origin for lateral epicondylitis were evaluated. There were 11 female and 7 male patients. Two patients were operated on both the elbows. The symptoms were present for an average of 10 months before surgery. All these patients failed to respond to treatment by conservative methods i.e. activity modification, analgesics, splints, physiotherapy, and steroid injections. The mean follow-up period was 17 months. The forearm common extensor origin was released per-cutaneously under local anesthesia. The clinical results were evaluated in terms of pain relief, return to pre-pain activity level, grip strength, and patient satisfaction. Pain relief was obtained on average of 4 weeks after the surgical procedure. The results were excellent in 16 elbows and good in 4 elbows. The percutaneous tenotomy is a simple and quick procedure for lateral epicondylitis resistant to conservative mode of treatment.
Article
Platelet-rich plasma (PRP) is an emerging biological treatment option in sports medicine. Its value is best established for elbow-related disorders, such as lateral epicondylar tendinopathy. This common condition typically resolves with simple treatment modalities, such as rest, icing, anti-inflammatory medications, and physical therapy. In cases that are not resolved by these measures, other options such as cortisone injections and surgery are considered. Level one data now support the use of PRP in patients who have chronic tennis elbow. It is important to note that the formulation of PRP contains both concentrated platelets and white blood cells. The specific technical steps on how to prepare PRP and treat a patient with chronic lateral epicondylitis are outlined in this article. Using PRP to treat medial epicondylar tendinopathy, triceps tendinopathy, distal biceps tendinopathy, and partial elbow ligament injuries is under investigation.
Article
Background: Lateral epicondylitis (LE) is a common musculoskeletal disorder for which an effective treatment strategy remains unknown. Purpose: To examine whether a single injection of platelet-rich plasma (PRP) is more effective than placebo (saline) or glucocorticoid in reducing pain in adults with LE after 3 months. Study design: Randomized controlled trial; Level of evidence, 1. Methods: A total of 60 patients with chronic LE were randomized (1:1:1) to receive either a blinded injection of PRP, saline, or glucocorticoid. The primary end point was a change in pain using the Patient-Rated Tennis Elbow Evaluation (PRTEE) questionnaire at 3 months. Secondary outcomes were ultrasonographic changes in tendon thickness and color Doppler activity. Results: Pain reduction at 3 months (primary end point) was observed in all 3 groups, with no statistically significant difference between the groups; mean differences were the following: glucocorticoid versus saline: -3.8 (95% CI, -9.9 to 2.4); PRP versus saline: -2.7 (95% CI, -8.8 to 3.5); and glucocorticoid versus PRP: -1.1 (95% CI, -7.2 to 5.0). At 1 month, however, glucocorticoid reduced pain more effectively than did both saline and PRP; mean differences were the following: glucocorticoid versus saline: -8.1 (95% CI, -14.3 to -1.9); and glucocorticoid versus PRP: -9.3 (95% CI, -15.4 to -3.2). Among the secondary outcomes, at 3 months, glucocorticoid was more effective than PRP and saline in reducing color Doppler activity and tendon thickness. For color Doppler activity, mean differences were the following: glucocorticoid versus PRP: -2.6 (95% CI, -3.1 to -2.2); and glucocorticoid versus saline: -2.0 (95% CI, -2.5 to -1.6). For tendon thickness, mean differences were the following: glucocorticoid versus PRP: -0.5 (95% CI, -0.8 to -0.2); and glucocorticoid versus saline: -0.8 (95% CI, -1.2 to -0.5). Conclusion: Neither injection of PRP nor glucocorticoid was superior to saline with regard to pain reduction in LE at the primary end point at 3 months. However, injection of glucocorticoid had a short-term pain-reducing effect at 1 month in contrast to the other therapies. Injection of glucocorticoid in LE reduces both color Doppler activity and tendon thickness compared with PRP and saline.
Article
We designed a prospective, randomized study to evaluate the effects of iontophoresis delivery of dexamethasone versus corticosteroid injection therapy on patient outcomes. We randomized 82 patients to 10 mg dexamethasone via iontophoresis using a self-contained patch with a 24-hour battery; 10 mg dexamethasone injection; or 10 mg triamcinolone injection. All patients received the same hand therapy protocol. Primary outcomes tracked were change in grip strength (flexion vs extension), pain, and function scores on a validated questionnaire. The secondary outcome was return-to-work status. Patients were evaluated at baseline, completion of physical therapy, and 6-month follow-up. The iontophoresis patients had statistically significant improvement in grip strength at the conclusion of hand therapy compared with baseline. They were also more likely to get back to work without restriction. By 6-month follow-up, all groups had equivalent results for all measured outcomes. Dexamethasone via iontophoresis produced short-term benefits because for this group grip strength and unrestricted return to work were significantly better. This study suggests that this iontophoresis technique for delivery of corticosteroid may be considered a treatment option for patients with lateral epicondylitis. Therapeutic II.
Article
We compared saline, corticosteroid, and autologous blood injections for lateral epicondylitis in a prospective, blinded, randomized, controlled trial. The null hypothesis was that patient-rated outcomes after autologous blood injection would not be superior to corticosteroid and saline injections. Patients with clinically diagnosed lateral epicondylitis of less than 6 months' duration were randomized into 1 of 3 groups to receive a 3-mL injection of saline and lidocaine, corticosteroid and lidocaine, or autologous blood and lidocaine. Of 34 subjects who enrolled, 28 completed follow-up. A total of 10 were randomized to the saline group, 9 to the autologous blood group, and 9 to the steroid group. Every participant had 3 mL blood drawn, and the injection syringe was foil-covered to prevent the subject from knowing the contents. The primary outcome measure was the Disabilities of the Arm, Shoulder, and Hand (DASH) score. Patients completed a pain visual analog scale, DASH, and the Patient-Rated Forearm Evaluation before injection and at 2 weeks, 2 months, and 6 months after injection. We performed statistical analysis using repeated measures of analyses of variance. There were no significant differences in DASH scores among the 3 groups at 2- and 6-month follow-up points, with the mean scores for saline at 20 and 10, respectively, compared with 28 and 20 for autologous blood and 28 and 13 for steroid injections. Secondary measures showed similar findings, with outcomes scores showing improvement in all 3 groups. In this prospective, randomized, controlled trial, autologous blood, corticosteroid, and saline injection provide no advantage over placebo saline injections in the treatment of lateral epicondylitis. Patients within each injection group demonstrated improved outcome scores over a 6-month period.