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To investigate the outcome of ultrasound (US)-guided intratissue percutaneous electrolysis (EPI(®)) and eccentric exercise in the treatment of patellar tendinopathy during a long-term follow-up. Forty patients with patellar tendinopathy were prospectively evaluated over a 10-year follow-up period. Pain and function were evaluated before treatment, at 3 months and at 2, 5 and 10 years using the Victorian Institute of Sport Assessment-Patella (VISA-P) score, the Tegner score and Blazina's classification. According to VISA-P score at baseline, patients were also dichotomized into Group 1 (<50 points) and Group 2 (≥50 points). There were 21 patients in Group 1 and 19 in Group 2. Patient satisfaction was measured according to the Roles and Maudsley score. The VISA-P score improved globally by 41.2 points (p < 0.01) after a mean 4.1 procedures. In Group 1, VISA-P score improved from 33.1 ± 13 to 78.9 ± 14.4 at 3-month and to 88.8 ± 10.1 at 10-year follow-up (p < 0.001). In Group 2, VISA-P score improved from 69.3 ± 10.5 to 84.9 ± 9 at 3-month and to 96.0 ± 4.3 at 10-year follow-up (p < 0.001). After 10 years, 91.2 % of the patients had a VISA-P score >80 points. The same level (80 % of patients) or the Tegner score at no more than one level lower (20 % of patients) was restored, and 97.5 % of the patients were satisfied with the procedure. Treatment with the US-guided EPI(®) technique and eccentric exercises in patellar tendinopathy resulted in a great improvement in knee function and a rapid return to the previous level of activity after few sessions. The procedure has proved to be safe with no recurrences on a long-term basis. Therapeutic study, Level IV.
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KNEE
Clinical results after ultrasound-guided intratissue percutaneous
electrolysis (EPI
Ò
) and eccentric exercise in the treatment
of patellar tendinopathy
F. Abat P. E. Gelber F. Polidori
J. C. Monllau J. M. Sanchez-Iban
˜ez
Received: 15 September 2013 / Accepted: 12 January 2014
ÓSpringer-Verlag Berlin Heidelberg 2014
Abstract
Purpose To investigate the outcome of ultrasound (US)-
guided intratissue percutaneous electrolysis (EPI
Ò
) and
eccentric exercise in the treatment of patellar tendinopathy
during a long-term follow-up.
Methods Forty patients with patellar tendinopathy were
prospectively evaluated over a 10-year follow-up period.
Pain and function were evaluated before treatment, at
3 months and at 2, 5 and 10 years using the Victorian
Institute of Sport Assessment–Patella (VISA-P) score, the
Tegner score and Blazina’s classification. According to
VISA-P score at baseline, patients were also dichotomized
into Group 1 (\50 points) and Group 2 (C50 points). There
were 21 patients in Group 1 and 19 in Group 2. Patient
satisfaction was measured according to the Roles and
Maudsley score.
Results The VISA-P score improved globally by 41.2
points (p\0.01) after a mean 4.1 procedures. In Group 1,
VISA-P score improved from 33.1 ±13 to 78.9 ±14.4 at
3-month and to 88.8 ±10.1 at 10-year follow-up
(p\0.001). In Group 2, VISA-P score improved from
69.3 ±10.5 to 84.9 ±9 at 3-month and to 96.0 ±4.3 at
10-year follow-up (p\0.001). After 10 years, 91.2 % of
the patients had a VISA-P score[80 points. The same level
(80 % of patients) or the Tegner score at no more than one
level lower (20 % of patients) was restored, and 97.5 % of
the patients were satisfied with the procedure.
Conclusion Treatment with the US-guided EPI
Ò
tech-
nique and eccentric exercises in patellar tendinopathy
resulted in a great improvement in knee function and a
rapid return to the previous level of activity after few
sessions. The procedure has proved to be safe with no
recurrences on a long-term basis.
Level of evidence Therapeutic study, Level IV.
Keywords Intratissue percutaneous electrolysis EPI
Eccentric exercises
Introduction
Patellar tendinopathy or jumper’s knee is a frequent con-
dition that most commonly affects the tendon’s origin on
the inferior pole of the patella [2,4,10]. Once considered
an inflammatory condition, it is currently considered a
degenerative process due to the presence of myxoid
degeneration, the disruption of the collagen fibres and signs
of hypoxia in tenocytes and resident macrophages [6,17].
The overall prevalence of patellar tendinopathy is
around 14 % in the sports population [3,16], but may be as
high as 40 % in highly demanding athletes [8]. The ten-
don’s overuse in sports that involve running, jumping or
rapid change in direction is considered the main risk factor
for developing the said condition [16].
Current treatment options include eccentric training [15,
18,29], open or arthroscopic surgery, extracorporeal
shockwave therapy [25], ultrasound (US)-guided sclerosis
[12], non-steroidal anti-inflammatory drugs, platelet-rich
F. Abat (&)F. Polidori J. M. Sanchez-Iban
˜ez
CEREDE-Sports Medicine, Dr. Roux 8-10, 08017 Barcelona,
Spain
e-mail: FERRANABAT@GMAIL.COM; drabat@cerede.es
P. E. Gelber J. C. Monllau
Department of Orthopedic Surgery, Hospital de la Santa Creu i
Sant Pau, Universitat Auto
`noma de Barcelona, Barcelona, Spain
P. E. Gelber J. C. Monllau
ICATME-Hospital Universitari Quiro
´n Dexeus, Universitat
Auto
`noma de Barcelona, Barcelona, Spain
123
Knee Surg Sports Traumatol Arthrosc
DOI 10.1007/s00167-014-2855-2
plasma injection [30] and aprotinin [1]. These studies have
also suggested that, in general, patients with a worse
functional status before treatment obtain inferior final
outcomes. However, due to the limited evidence-based
therapies, there are still several controversies regarding the
real efficacy of these treatment modalities [1].
Intratissue percutaneous electrolysis (EPI
Ò
) treatment is
a pioneering US-guided technique developed by one of the
authors. It leads to a non-thermal electrochemical ablation
through a cathodic flow directly at the clinical focus of
degeneration. EPI
Ò
causes an organic reaction leading to a
highly localized inflammation, exclusively at the region of
treatment that conduces to a rapid regeneration of the
injured tendon [26].
The present study provides the first analysis of the
results of EPI
Ò
in the treatment of patellar tendinopathy at
10 years follow-up. This study could be clinically relevant
given the lack of effective techniques in the treatment of
patellar tendinopathy.
The aim of this study was to investigate the outcome of
the US-guided EPI
Ò
technique in terms of pain, function
and the return to the previous level of activity in patients
with patellar tendinopathy. The mean follow-up of
10 years provides information on safety and the rate of
recurrence. The main hypothesis was that the US-guided
EPI
Ò
technique would quickly improve the outcome in
patients with patellar tendinopathy and that this improve-
ment would be maintained over a long period of time. The
second hypothesis was that good outcomes would be
obtained regardless of the initial degree of functional
impairment. It was also hypothesized that the patients
would be restored to their pre-injury activity level.
Materials and methods
From January 2002 to October 2002, 41 patients with
patellar tendinopathy were included in the investigation.
Demographic data and patient information (age, gender,
affected and dominant side, kind of sport or activity level)
were recorded.
The inclusion criteria were a history of patellar tendon
pain, tenderness upon palpation, functional limitation
directly related to the studied tendon and sonographic
confirmation of tendon degeneration. A tendon injury
located at the inferior pole of the patella was considered a
requisite. Other inclusion criteria were more than 4 weeks
of symptoms and an age of \60 years old. Patients were
classified according to Blazina’s scale [22]. Exclusion
criteria were pain at the proximal pole of the patella (fre-
quently included in jumper’s knee), chronic articular dis-
ease, a concomitant knee pathology, contraindications to
the EPI
Ò
technique and the concomitant administration of
certain drugs (at least 2 weeks before receiving treatment).
The inclusion and exclusion criteria are summarized in
Table 1.
Ultrasound examination
All the patients went through an exhaustive US examina-
tion of the tendon and adjacent structures using a high-
resolution greyscale US (Fig. 1) with Doppler power and
linear multi-frequency probe (6–15 MHz). The injured and
the contralateral knees were studied in all patient. The US
efficacy for the proper diagnosis of patellar tendinopathy
was previously reported [11,36,37].
Intratissue percutaneous electrolysis (EPI
Ò
) protocol
The EPI
Ò
technique was applied using a specifically
developed medically certified (Directive 93/42/EEC)
device (EPI Advanced Medicine, Barcelona, Spain), which
produces modulated galvanic electricity through the neg-
ative electrode cathodic flow. This is applied using a
modified electrosurgical scalpel that uses acupuncture
needles (0.3 mm in diameter) with different lengths. The
intensity can be adjusted by changing the duration or the
milliamps of the device. Conversely, the polarity of the
machine is fixed (i.e. only the cathodic flow is usable).
During the procedure, performed by the same experienced
operator, the patients are supine so as to minimize any
potential vagal reaction.
Isopropyl alcohol was used to prepare the skin despite
the bacteriostatic action of the EPI
Ò
system. Polyvidone
iodine was avoided to prevent a tattoo effect of the
Table 1 Inclusion and exclusion criteria
Inclusion criteria Exclusion criteria
\60 years old Chronic articular disease
History of patellar tendon pain
[4 weeks
Concomitant knee pathology (e.g.
cruciate ligament injury of
meniscal tear)
Tenderness to palpation Contraindications of EPI
Ò
technique
(i.e. pregnancy, knee prosthesis,
osteosynthesis, cardiac disease,
malign tumour or coagulopathy)
Functional limitation directly
related to the tendon injury
Concomitant administration of drug
(i.e. fluoroquinolones,
anticoagulants, corticosteroids or
non-steroidal anti-inflammatory
Sonographic confirmation of
tendon degeneration
Injury located at the inferior
pole of the patella
Blazina’s
classification Cgrade I
Knee Surg Sports Traumatol Arthrosc
123
cathodic flow. Finally, three US-guided precise punctures
at 3 mA (Fig. 2) were performed until a complete
debridement of the treated area was obtained. The
debridement was assessed with the sonographic images.
After the first EPI
Ò
treatment, the patients underwent
consecutive sessions of EPI
Ò
every 2 weeks and 2 weekly
sessions of an eccentric exercise training using the resis-
tance isoinertial leg-press machine (YoYo
TM
Technology
AB, Stockholm, Sweden). Eccentric exercises were per-
formed in three sets of ten repetitions twice a week in order
to obtain maturation of collagen fibres [24,31]. Each
repetition was performed with the concentric phase with
both extremities, whereas the eccentric phase was only
performed with the affected limb at a maximum of 60°of
knee flexion.
Patients received US-guided EPI
Ò
treatment up to a
maximum of ten sessions. The treatment finished either
when the patients were symptom free or if there was no
improvement in terms of pain or function after those ten
sessions.
Treatment evaluation
All the patients were evaluated before treatment and pro-
spectively when their treatments were finished (at the third
month), at 2-year, at 5-year and at 10-year follow-up.
The primary outcome measure was knee function using
the Victorian Institute of Sport Assessment–Patella (VISA-P)
score, a specific validated questionnaire to quantify pain
and knee function and ability to play sport in patients with
patellar tendinopathy [9,34]. The VISA-P score ranged
from a maximum of 100 in asymptomatic patients to the
theoretical minimum of 0. The authors of the score sug-
gested that a score between 80 and 100 points might be
considered as the optimal outcome category. Functional
evaluation was further assessed with Blazina’s classifica-
tion [22]. This classification categorizes the symptomatic
patients as in phase I (pain only after activity), phase II
(discomfort during activity), phase III (pain during activity
that interferes with participation) and phase IV (complete
tendon disruption). The Tegner score was also used to
assess the influence of the treatment in terms of restoring
the previous sports activity level. All the written ques-
tionnaires were personally filled out by all patient before
treatment, at the end of the treatment (at 3-month) and at
the 2-year follow-up. The questionnaires corresponding to
the 5- and 10-year follow-up evaluations were all filled out
through a telephone interview. Patient satisfaction was
Fig. 1 High-resolution colour
Doppler ultrasound of patellar
tendinopathy. aLongitudinal
and btransversal views of the
involved tendon showing a high
degree of neovascularization
before the EPI
Ò
treatment. The
same patient 3 months after
initiation of the EPI
Ò
procedures had a remarkable
decrease in the vascularization
of the patellar tendon clearly
seen in these longitudinal
(c) and transversal (d) views
Fig. 2 Intratissue percutaneous electrolysis (EPI
Ò
) procedure. The
0.3-mm needle (Asterisks) is being guided by high-resolution
greyscale ultrasound to puncture the injured region of the tendon
Knee Surg Sports Traumatol Arthrosc
123
measured according to the Roles and Maudsley score [23].
In this score, patients are classified as Excellent (no pain,
full movement and full activity), Good (occasional dis-
comfort, full movement and full activity), Fair (some
discomfort after prolonged activity) or Poor (pain limiting
activities).
All those patients that scored\50 points with the VISA-
P questionnaire at baseline were denominated Group 1,
whereas the remaining patients scoring equal to or higher
than 50 points were denominated Group 2. This classifi-
cation allows to display the results in different degrees of
injury of the patellar tendon: more (VISA-P \50 points)
or less affected (VISA-P [50 points).
The Clinical Research Ethics Committee of ICATME-
Institut Universitari Dexeus, University of Barcelona,
approved the study (09/06/0049). All the patients signed
informed consent to participate in the study as well as for
the evaluation and publication of their results.
Statistical analysis
Categorical variables are presented as number of cases and
percentages. Continuous variables are presented as
mean ±SD (range). The relationships between categorical
variables were described using contingency tables, and
inference was studied using the chi-square test or Fisher’s
exact test. The relation between the VISA-P score and
dichotomous variables was assessed using the Mann–
Whitney test, showing the median value. Analysis of var-
iance (ANOVA) was used to compare the evolution
between groups. Statistical significance was set at 0.05
two-sided. Statistical analysis was performed using SPSS
19 (SPSS Inc., Chicago, IL, USA).
Results
One patient was lost during the first 3 months of follow-up.
The remaining 40 patients were available at the 3-month
and at the 2-year evaluations. At the 5-year evaluation,
another three patients were lost (37 patients available,
90.2 % of the cases) and another three patients at the
10-year assessment (34 patients available, 82.9 % of the
cases).
Patient description
Twenty-one patients (52.5 %) were included in Group 1
and the remaining 19 (47.5 %) in Group 2. Both groups
were comparable in terms of age, gender, side and func-
tional scores at baseline (Table 2). Sports involvement is
summarized in Table 3. No relation (n.s.) between the
injured tendon and the dominant extremity, the type of
sport, the age of the patient and gender, and the VISA-P
values obtained after the treatments was observed.
The mean duration of symptoms prior to the treatment was
69.4 ±65.6 weeks (range 4–288 weeks). The athletes were
off sports activities due to their patellar tendinopathy for a
mean time of 40.6 ±50.9 weeks (range 0–192 weeks).
Treatment duration averaged 7.5 ±2.6 weeks (range
1–10 weeks), and the patients required a mean of 4.1 ±2.6
EPI
Ò
procedures (range 1–10). According to Blazina’s
classification, one patient (2.5 %) was of stage I at baseline,
seven patients (17.5 %) stage II and the remaining 32
patients (80 %) stage III. At the 3-month evaluation, once all
the treatments were finished, five patients (12.5 %) were
classified as of stage I and six patients (15 %) stage II. All the
remaining 30 cases (72.5 %) were considered completely
cured (less than Blazina’s stage I). At the 2-year follow-up
evaluation, 31 cases (77.5 %) were asymptomatic (less than
Blazina’s stage I) and nine (22.5 %) were in stage I. Analysis
Table 2 Patient characteristics at baseline
Group 1 n=21
(52.5 %)
Group 2 n=19
(47.5 %)
pvalue
Age (years)
Mean ±SD 26.0 ±8.49 25.7 ±8.12 n.s.
Gender % (n)
Male 81.0 (17) 94.7 (18) n.s.
Female 19.0 (4) 5.3 (1)
Dominant extremity % (n)
Right 81.0 (17) 89.5 (17) n.s.
Left 19.0 (4) 10.5 (2)
Injured knee % (n)
Right 38.1 (8) 15.8 (3) n.s.
Left 47.6 (10) 68.4 (13)
Bilateral 14.3 (3) 15.8 (3)
Baseline VISA-P
Mean ±SD 32.5 ±12 69.5 ±10.05 \0.001
Values expressed as mean ±SD or frequencies and percentages
Table 3 Patient sports involvement at baseline
Series n=40
Blazina’s stage
Median (range) 3 (2–3)
Sports type % (n)
Soccer 60 (24)
Other 40 (16)
Sports level % (n)
Professional (first division) 12.5 (5)
Semi-professional (second division or similar) 67.5 (27)
Recreational 20 (8)
Values expressed as mean ±SD or frequencies and percentages
Knee Surg Sports Traumatol Arthrosc
123
of the patients using the Blazina’s classification remained
unchanged throughout the remaining follow-up evaluations
of the period studied (n.s.).
Clinical outcomes over time
The VISA-P (Fig. 3) and Tegner scores before treatment, at
3 months and at 2, 5 and 10 years of follow-up are sum-
marized in Table 4. Group 1 improved by 45.8 points
(p\0.001) at 3 months to obtain a mean VISA-P score of
78.9 ±14.4. In Group 2, the mean improvement in VISA-
P score at 3 months was 15.6 points at 3 months
(p\0.001). The Tegner level did not drop over the
10 years of the study period, and no differences between
the intermediate evaluations (n.s.) were observed either.
According to the Roles and Maudsley score, patient
satisfaction at 3 months of follow-up was considered
Excellent in 32 cases (80 %), Good in seven cases (17.5 %)
and Fair in one case (2.5 %). These values persisted
without significant differences throughout the period
studied. No recurrences, adverse episodes or any additional
modality of treatments were reported after the 10 years of
follow-up.
At the 3-month follow-up evaluation, 32 (80 %) patients
restored their previous activity level according to Tegner
scale (n.s.). In eight patients (20 %), there was a decrease
in only one single level on the same scale. These values
were maintained over the remaining period studied (n.s.).
Discussion
Treatment with EPI
Ò
in combination with eccentric exer-
cises has been shown to effectively improve the symptoms
of patellar tendinopathy quickly and steadily for at least
10 years. It confirmed the first hypothesis. This improve-
ment in patients that had different severities of VISA-P
scores at baseline was equally obtained in terms of symp-
tomatology, knee function and return to sports activity,
which is also in concordance with the second hypothesis.
The results observed in the first study reporting on the
clinical use of EPI
Ò
are encouraging [26]. Its effects are
based on a local and non-thermal electrochemical therapy
that induces a localized short inflammatory response
through an electrolytic reaction produced by a cathodic
flow. Consequently, this causes an organic reaction leading
to the regeneration of the injured tendon [26].
Conservative treatment was traditionally considered the
first option of treatment of tendinopathies. Many different
techniques were used [1,8], such as modification of
activity, eccentric physical training, patellar straps, cold
and heat compression transfriction massage and stretching
for quadriceps, hamstrings and patellar tendons. Despite
some good results reported with eccentric programmes [18,
28], it is still unclear as to the more effective exercise
protocol, its frequency, load and dosage. While Zwerver
et al. [37], in a recent randomized clinical trial, concluded
that no benefit came of extracorporeal high-energy shock-
wave therapy during competition, Rompe et al. [25]
reported, at 4-month follow-up, that eccentric loading
Fig. 3 Linear diagram of the mean Victorian Institute of Sport
Assessment–Patella (VISA-P) scores for Group 1, Group 2 and all the
patients (Global) at baseline (Initial), at 3 months and at 2, 5 and
10 years
Table 4 Victorian Institute of Sport Assessment–Patella (VISA-P) values during follow-up
Time VISA-P score Tegner score
Group 1 Group 2 Global Group 1 Group 2 Global
Baseline (n=40) 33.1 (±13) 69.3 (±10.5) 51.2 (±21.7) 8.1 (6–10) 7.8 (4–9) 7.9 (4–10)
3 months (n=40) 78.9* (±14.4) 84.9* (±9) 81.9* (±12.2) 7.7 (4–10) 7.6 (3–9) 7.7 (3–10)
2 years (n=40) 83.2 (±13.6) 88.6 (±7.4) 85.9 (±11.1) 8.1 (5–10) 7.7 (4–9) 7.8 (4–10)
5 years (n=37) 85.2 (±12.2) 91.9 (±5.6) 88.6 (±10) 7.9 (5–10) 7.6 (4–9) 7.8 (4–10)
10 years (n=34) 88.8 (±10.1) 96.0 (±4.3) 92.4 (±8.5) 7.7 (5–10) 7.3 (4–9) 7.5 (4–10)
Victorian Institute of Sport Assessment–Patella (VISA-P) values expressed as mean (±SD). Tegner values are expressed as median (range)
*p\0.001. No statistically significant differences were observed in the results between any intermediate outcome measurements other than
from baseline
Knee Surg Sports Traumatol Arthrosc
123
alone was less effective when compared with a combina-
tion of eccentric loading and repetitive low-energy shock-
wave treatment. Similarly, low-intensity US is not
currently considered a reliable method for the treatment of
patellar tendinopathy [14,15,35].
Different injection treatments for patellar tendinopathy
have been proposed. While some studies on the effect of
dry needling, autologous blood and high volume have been
put forward as providing functional improvements, steroid
treatment has shown a relapse of symptoms after few
months, not to mention the deleterious effect on the tendon
histology [32]. Recent investigations have observed
slightly better outcomes after treatment with platelet-rich
plasma injections in association with an eccentric training
programme than an eccentric training programme alone in
short-term studies [7,30,32]. Some authors had initially
reported pain relief after sclerosing injections of polidoc-
anol [10], but recent studies have shown contradictory
results [33]. Hoksrud et al. reported their results with US-
guided sclerosis of neovessels in 29 patients with
44 months of follow-up [12] and in 101 patients with
24 months of follow-up [13]. The patients needed several
injections over 8 months of treatment, and only a moderate
improvement in knee function was observed. One-third of
their patients obtained a VISA-P score \50 points, and
only few patients were completely cured. Conversely, in
the present investigation with short- and long-term reported
outcomes, even the patients with lowest VISA-P score
(\50 points) at baseline significantly improved to around
80 points at 3 months and to around 90 points at 10 years.
These final outcomes were comparable with those obtained
by the patients with better VISA-P scores before treatment.
This is of considerable relevance because the professional
sports patients included in this series started from lower
VISA-P values and they still obtained excellent scores.
Overall, 80 % (n=32) of the treated patients returned to
the same level of sports activity at 3 months, and the
remaining eight patients only decreased a single level in
the Tegner score.
Regarding surgical treatment of patellar tendinopathy,
some open [5,21] and arthroscopic [5,20,27] techniques
have also been recommended when conservative treatment
fails. However, surgery usually provides unpredictable and
inconsistent results [4,15], which is often no more effective
than an isolated eccentric exercise programme [2], and it
does not allow the athletes to resume their previous sports at
the same level, at least within the first year of treatment [19].
The main strengths of the current study are that, as far as
we know, it is the first investigation reporting on any
treatment modality for patellar tendinopathy over the
course of 10 years. Few patients were lost during this long
follow-up period. In addition, it is also the first study
reporting on the clinical outcome using the EPI
Ò
technique
in the treatment of tendinopathy at long term follow-up.
The promising results obtained with the EPI
Ò
procedure
showed excellent functional results assessed with the
VISA-P score as well as with the Blazina’s classification in
around 80 % of the patients at 3 months and over 90 % at
10 years. It also allowed a full recovery to the previous
activity level in most patients. This outcome’s improve-
ment with the use of EPI
Ò
in the treatment of patellar
tendinopathy was achieved after a short period of time
(mean 7.5 weeks) and with a few number of treatment
sessions (mean 4.1 EPI
Ò
treatments).
Besides the low sample size, one of the most relevant
limitations of the current study is the lack of a control
group. Comparison with a placebo-treated group of
patients would have made for much stronger conclusions.
However, most of our patients were professional or semi-
professional athletes referred by other physicians after
failure of conservative therapy. It seems highly unlikely
that this sort of patients would be willing to accept pla-
cebo treatment for a long enough period. Another weak-
ness might be that the combination of treatment with
eccentric exercises might have positively affected the
results attributed to the EPI
Ò
technique. Although this
could more logically affect the results during the first
months of follow-up, it does not seem that it should have
had any influence in the long-term results. Regardless of
the aforementioned limitations, this study provides the
first analysis of the EPI
Ò
technique on the treatment of
patellar tendinopathy, with promising results after a long
follow-up period.
The clinical relevance of the reported results was that
EPI
Ò
technique brought about a major improvement in pain
and function in comparison with the so far known techniques
and offers a good treatment option in patellar tendinopathy.
Conclusion
Treatment with the US-guided EPI
Ò
technique and eccentric
exercises in patellar tendinopathy resulted in a great
improvement in knee function and a rapid return to the pre-
vious level of activity after few sessions. The procedure has
proved to be safe with no recurrences on a long-term basis.
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... Of the 14 articles, four applied percutaneous electrolysis to the knee, [21][22][23][24] three to the shoulder, [25][26][27] three to the elbow, [28][29][30] two to the hip 31,32 and two to the ankle and foot. 33,34 The methodological characteristics of the investigations are shown in Table 2 and a summary of the findings of each can be found in Supplementary Table 1. ...
... Regarding the experimental designs of the investigations analyzed, six studies were randomized controlled trials 21,[24][25][26]29,31 and the remaining studies were quasi-experimental studies: five with a single experimental group, 22,23,28,30,32 two with two experimental groups 27,34 and one with three experimental groups 33 (only two of them with random assignment of participants 27,33 ). ...
... The methodological quality of the studies was four or five points on the JADAD scale in 71.4% 21,24,26,27,29 of the randomized controlled trials. At the same time, as can be seen in Table 3, 85.7% 22,23,28,30,33,34 of the non-randomized trials scored at most three points. ...
Article
Objective To evaluate the efficacy of percutaneous electrolysis for the treatment of patients with tendinopathies. Data sources A systematic search of publications was conducted in Pubmed, Cinahl, Medline, Scopus and Web of Science. Methods The Oxford 2011 Levels of Evidence and the Jadad scale were used to assess the quality of studies. The mean and standard deviation were obtained for each study group and used to calculate the effect size. The DerSimonian and Laird method was used to develop a random-effects model. Results Of the 14 articles, four applied percutaneous electrolysis to the knee, three to the shoulder, three to the elbow, two to the hip and two to the ankle and foot. A meta-analysis on intensity of pain (evaluated with algometer and the Visual Analogue Scale) was performed on studies comparing percutaneous electrolysis with a control group, indicating that the groups treated with percutaneous electrolysis had better results ( p = 0.01). Although percutaneous electrolysis did not overcome the analgesic effect achieved by corticosteroid injections. Conclusions The percutaneous electrolysis is effective for the treatment of tendinopathies. The combination of this technique with eccentric training has proven to be one of the most effective treatments to date for improving pain. PROSPERO Registration: CRD42021230005.
... PID is a minimally invasive ultrasoundguided technique that consists of the application of a high-intensity galvanic current through an acupuncture needle that stimulates a local inflammatory process in soft tissues, enabling phagocytosis and repair of the affected tissue [15]. Echo-guided punctures of three milliamps are performed with the ultrasound device to obtain a controlled debridement of the injured tendon, in addition, it is combined with two weekly sessions of eccentric exercise using isoinertial resistance machines consisting of 3 sets of 10 repetitions; each repetition was performed with the concentric phase with both limbs while the eccentric phase was only performed with the affected limb at a maximum of a 60° angle of knee flexion [3]. ...
... HA is a key molecule in several cellular activities and is normally present in the extracellular matrix of tendons and ligaments. Among its properties, HA injections can reduce pain and determine the diseasemodifying effects [15]. In vitro models suggest that HA may increase tenocyte viability and collagen I production and deposition, w ith a positive collagen I/collagen III ratio in a dose-dependent manner. ...
Article
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Patellar tendinopathy is a very common, yet very difficult pathology to treat. Its’ frequency in elite athletes, especially in jumping sports, can go as high as 14%. Recently it has been suggested that chronic tendinopathy may be an active process of ongoing tendon degeneration bearing close relation with inflammation-mediated responses, the intensity of pain in patellar tendinopathy appears to have a stronger relation with the number of newly formed blood vessels observed on Doppler ultrasound. This article is a descriptive review of the available information which was obtained during a 1-month period (September 2021) and the following search keywords were used: interventional ultrasonography; patellar ligament; tendinopathy. Based on the information obtained, a total of 787 articles were revied, mainly published in the last 10 years in Pubmed, Medline, and SciELO databases; out of these, a total of 15 articles were used as citations. Even though conservative treatment is preferred as a first-line treatment, if, during a 6-month period it fails, then surgical treatment is proposed; however, recovery time is a crucial issue for elite athletes. Treatment by ultrasound-guided interventionism is presented as an effective alternative and allows athletes to return to their regular activities in less time, with optimal results. In the literature there are not many articles that describe the various techniques of ultrasound-guided interventionism for the treatment of patellar tendinopathy, thus, we have carried out this bibliographic review. Keywords: Interventional ultrasonography, Patellar ligament, Tendinopathy.
... Dentro de las terapias percutáneas invasivas destaca la electrólisis ecoguiada, conocida como ultrasound guided galvanic electrolysis technique (USGET), que es una técnica mínimamente invasiva que consiste en la aplicación en el tejido dañado de una corriente galvánica bajo unos parámetros específicos. Produce una reacción electroquímica no termal que desencadena un proceso inflamatorio y posteriormente regenerativo en el tejido dañado (5,(33)(34)(35) . El proceso proinflamatorio y regenerativo producido por la USGET debe ser complementado con ejercicio excéntrico para estimular la fase proliferativa y de remodelación que conducirá en muchos casos a la curación de la lesión tendinosa (5) . ...
... El proceso proinflamatorio y regenerativo producido por la USGET debe ser complementado con ejercicio excéntrico para estimular la fase proliferativa y de remodelación que conducirá en muchos casos a la curación de la lesión tendinosa (5) . Los resultados de la electrólisis ecoguiada o USGET han sido descritos en la literatura tanto a largo plazo de seguimiento para verificar así su seguridad (34) , como en ensayos clínicos controlados (35) . ...
... PNET has gained significant popularity as a treatment for chronic soft-tissue overuse injuries, especially within the realm of sports medicine. Numerous studies have reported the effectiveness of this technique in non-acute conditions [4]. The therapy typically involves the application of the direct current for several minutes, followed by a period of rest. ...
Article
Full-text available
Percutaneous Needle Electrolysis Therapy (PNET) is a relatively recent technique introduced by Sánchez-Ibáñez in Spain during the early 2000s. It has gained rapid popularity and adoption in Western Europe. The procedure involves applying a short galvanic current to a specifi c musculoskeletal target area by inserting percutaneous acupuncture-like needles.
... However, these treatments have continued to develop, leading to the emergence of percutaneous electrolysis (PE). PE involves passing a low-intensity galvanic current through a needle to generate a controlled local inflammatory response in the target tissue and thus promote a process of phagocytosis and subsequent regeneration of the damaged tissue [11,12]. ...
Article
Full-text available
Deep dry needling (DDN) and percutaneous electrolysis (PE) provide the benefit of the mechanical effect of the needle, and PE adds the potential advantages of the galvanic current it incorporates in myofascial trigger points (MTrPs) therapy. The aim of this study was to compare the short-term efficacy between PE and DDN on active MTrPs of the levator scapulae by considering pain intensity. A simple-blind randomized controlled trial was carried out, recruiting patients suffering from non-specific neck pain lasting more than 3 months and with active MTrPs in the levator scapulae muscle (n = 52). Patients were divided into intervention (PE; n = 26) and control (DDN; n = 26) groups and received one treatment session on the active MTrPs of the levator scapulae. Patients were assessed for pain intensity, pressure pain threshold (PPT), cervical range of motion (CROM), neck disability and post-needling soreness, immediately after treatment, at 72 h and at 14 days. In addition, pain during treatment was recorded after the procedure. There were no significant differences for pain intensity, post-needling soreness and PPT. We found significant differences in CROM, immediately after treatment (p = 0.043), and at 72 h (p = 0.045), in favor of the PE group. Significant differences were found for neck disability (p < 0.047), immediately post-treatment, in favor of the DDN group. Moreover, there were significant differences for pain during the intervention (p < 0.002), in favor of the DDN group (4.54 ± 2.21) versus the PE group (6.54 ± 2.27). PE and DDN appear to have similar short-term effects. PE proved to be a more painful treatment than DDN. Clinical trial registry: NCT04157426.
... PE is an invasive physiotherapy technique that consists of the application of a galvanic current through a puncture needle implanted by means of ultrasound support around the lesion, with the proposed objective of generating an analgesic and local inflammatory effect repairing the affected soft tissue (11)(12)(13). ...
Article
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ObjectiveA meta-analysis of randomized controlled trials (RCTs) was conducted to determine the effect of ultrasound-guided percutaneous electrolysis (PE) alone or as an adjunct to other interventions on pain intensity generated by musculoskeletal disorders, depending on the intensity of the technique.Data sourcesPUBMED, EMBASE, Cochrane Library, Web of Science, SCOPUS, Health Medical Collection, and CINALH from inception to September 2022 were searched to identify documents.Study selectionPublications investigating the effect of ultrasound-guided PE in musculoskeletal pain.Data extractionData were extracted into predesigned data extraction and tables. Risk of bias was evaluated with the Cochrane Risk of Bias Tool (Rob 2.0). Thirteen articles met inclusion criteria.Data analysisRandom-effects meta-analysis models were used to quantify the difference in pain between the PE and control groups.Data synthesisA significant reduction in pain was found in favor of low- (−1.89; 95% CI: −2.69; −1.10; p < 0.001) and high-intensity PE (−0.74; 95% CI: −1.36; −0.11; p: 0.02) compared to control group. Low-intensity PE showed significant reduction in pain in the short (−1.73; 95% CI: −3.13; −0.34; p < 0.02) and long term (−2.10; 95% CI: −2.93; −1.28; p = 0.005), with large effect sizes compared to control group. High-intensity PE only showed significant lower pain than control group in the long term (−0.92; 95% CI: −1.78; −0.07; p < 0.03), with a small effect size, but not in the short term.Conclusion We found small evidence suggesting that low-intensity PE could be more effective for musculoskeletal pain reduction than high-intensity PE. Nevertheless, scientific evidence on this subject is still scarce and studies comparing the two modalities are warranted.Systematic review registrationwww.crd.york.ac.uk/prospero, identifier CRD42022366935.
... This procedure generates a controlled inflammatory response in a specific targeted tissue, allowing phagocytosis of degenerated tissue, permitting a specific posterior repair [4]. The clinical effects of PNE have been evaluated when applied to different tissues such as tendons [7,8], muscles [9], or nerves [3,4]. In fact, a recent meta-analysis has found moderate-quality evidence supporting a positive effect of ultrasound-guided PNE for decreasing pain and related disability in musculoskeletal pain conditions [10]. ...
Article
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Percutaneous needle electrolysis (PNE) consists of the ultrasound-guided application of a galvanic electrical current through a solid filament needle. One proposed therapeutic mechanism for this intervention is a potential thermal effect. The aim of this study was to investigate if the application of PNE induces changes in temperature in different cadaveric musculoskeletal tissues. A repeated measure experimental cadaveric study was designed with 10 cryopreserved knees (5 men, 5 women). Sterile stainless-steel needles of 40 mm length and 0.30 mm caliber were used in this study. An ultrasound-guided needling puncture was performed in the targeted tissue (patellar tendon, infra-patellar fat, and vastus medialis muscle). Additionally, the tip of the needle was placed next to the thermometer sensor at the minimum possible distance without direct contact with it. The temperature differences before and after different applications were measured. The applications were: three applications for 3 s of 3 mA of intensity (3:3:3) when the tendon was the targeted tissue, three applications for 3 s of 1.5 mA of intensity (1.5:3:3) when the fat or muscle was the targeted tissue, and 24 s of 1 mA of intensity (1:24:1) in all tissues. No statistically significant Group*Time interactions were found in any tissue (tendon: F = 0.571, p = 0.459, ŋ2 = 0.03; fat pad: F = 0.093; p = 0.764, ŋ2 = 0.01; muscle: F = 0.681; p = 0.420, ŋ2 = 0.04). Overall, no changes in temperature were observed between both applications in the tendon (3:3:3 vs. 1:24:1) and fat/muscle (1.5:3:3 vs. 1:24:1) tissues. The application of two different percutaneous needle electrolysis protocols did not produce appreciable thermal changes in the tendon, fat, and muscle tissues of human cadavers. The results from the current cadaver study support that a thermal effect should not be considered as a mechanism of clinical action regardless of the targeted human tissue when applying percutaneous needle electrolysis since no changes in temperature after its application were observed.
Article
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Background Tendinopathy is a common, painful and functionally limiting condition, primarily managed conservatively using exercise therapy. Review questions (i) What exercise interventions have been reported in the literature for which tendinopathies? (ii) What outcomes have been reported in studies investigating exercise interventions for tendinopathy? (iii) Which exercise interventions are most effective across all tendinopathies? (iv) Does type/location of tendinopathy or other specific covariates affect which are the most effective exercise therapies? (v) How feasible and acceptable are exercise interventions for tendinopathies? Methods A scoping review mapped exercise interventions for tendinopathies and outcomes reported to date (questions i and ii). Thereafter, two contingent systematic review workstreams were conducted. The first investigated a large number of studies and was split into three efficacy reviews that quantified and compared efficacy across different interventions (question iii), and investigated the influence of a range of potential moderators (question iv). The second was a convergent segregated mixed-method review (question v). Searches for studies published from 1998 were conducted in library databases ( n = 9), trial registries ( n = 6), grey literature databases ( n = 5) and Google Scholar. Scoping review searches were completed on 28 April 2020 with efficacy and mixed-method search updates conducted on 19 January 2021 and 29 March 2021. Results Scoping review – 555 included studies identified a range of exercise interventions and outcomes across a range of tendinopathies, most commonly Achilles, patellar, lateral elbow and rotator cuff-related shoulder pain. Strengthening exercise was most common, with flexibility exercise used primarily in the upper limb. Disability was the most common outcome measured in Achilles, patellar and rotator cuff-related shoulder pain; physical function capacity was most common in lateral elbow tendinopathy. Efficacy reviews – 204 studies provided evidence that exercise therapy is safe and beneficial, and that patients are generally satisfied with treatment outcome and perceive the improvement to be substantial. In the context of generally low and very low-quality evidence, results identified that: (1) the shoulder may benefit more from flexibility (effect size Resistance:Flexibility = 0.18 [95% CrI 0.07 to 0.29]) and proprioception (effect size Resistance:Proprioception = 0.16 [95% CrI −1.8 to 0.32]); (2) when performing strengthening exercise it may be most beneficial to combine concentric and eccentric modes (effect size EccentricOnly:Concentric+Eccentric = 0.48 [95% CrI −0.13 to 1.1]; and (3) exercise may be most beneficial when combined with another conservative modality (e.g. injection or electro-therapy increasing effect size by ≈0.1 to 0.3). Mixed-method review – 94 studies (11 qualitative) provided evidence that exercise interventions for tendinopathy can largely be considered feasible and acceptable, and that several important factors should be considered when prescribing exercise for tendinopathy, including an awareness of potential barriers to and facilitators of engaging with exercise, patients’ and providers’ prior experience and beliefs, and the importance of patient education, self-management and the patient-healthcare professional relationship. Limitations Despite a large body of literature on exercise for tendinopathy, there are methodological and reporting limitations that influenced the recommendations that could be made. Conclusion The findings provide some support for the use of exercise combined with another conservative modality; flexibility and proprioception exercise for the shoulder; and a combination of eccentric and concentric strengthening exercise across tendinopathies. However, the findings must be interpreted within the context of the quality of the available evidence. Future work There is an urgent need for high-quality efficacy, effectiveness, cost-effectiveness and qualitative research that is adequately reported, using common terminology, definitions and outcomes. Study registration This project is registered as DOI: 10.11124/JBIES-20-00175 (scoping review); PROSPERO CRD 42020168187 (efficacy reviews); https://osf.io/preprints/sportrxiv/y7sk6/ (efficacy review 1); https://osf.io/preprints/sportrxiv/eyxgk/ (efficacy review 2); https://osf.io/preprints/sportrxiv/mx5pv/ (efficacy review 3); PROSPERO CRD42020164641 (mixed-method review). Funding This project was funded by the National Institute for Health and Care Research (NIHR) HTA programme and will be published in full in HTA Journal; Vol. 27, No. 24. See the NIHR Journals Library website for further project information.
Chapter
Percutaneous electrolysis (EPI®) is an ultrasound-guided minimally invasive new technology consisting of the application of a galvanic electrolytic current through an acupuncture. The objective of this therapy is to generate a local inflammatory response and start regeneration mechanisms. Different studies report promising clinical results with the EPI® technique in the treatment of musculoskeletal pathologies, mainly tendinopathies, such as the patellar tendinopathy. This study provides an analysis of patellar tendinopathy treated with the combination of EPI and eccentric exercises. The working hypothesis is that intratissue percutaneous electrolysis obtains a significant improvement in terms of pain and function in the patellar tendinopathies. A prospective study was performed involving 23 soccer players diagnosed with patellar tendinopathy. All patients underwent EPI® technique that was applied with an intensity of 3 mA during a period of 10 s. In all cases, the EPI® procedure was performed guided by high-resolution Doppler ultrasound. All patients received a weekly session of EPI combined with two weekly sessions of eccentric exercise consisting of three sets of ten repetitions at low velocity and without pain. Functional improvement was assessed in 91.7% of the total sample (n = 22), measured by the Victorian Institute of Sport Assessment-Patellar Tendon (VISA-P) questionnaire. The present study has shown promising results obtained with EPI® combined with eccentric exercise in the treatment of proximal patellar enthesopathy in a population of soccer players.
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We report the results of nonoperative and operative management of patellar tendinopathy in 42 athletes with Blazina stage 2 (26 patients) or stage 3 (16 patients) patellar tendinopathy. All patients were initially managed nonoperatively with nonsteroidal antiinflammatory drugs, physical therapy, and a progressive rehabilitation program based on isometric exercises, stretching, and eccentric exercises. After 6 months, 33 patients showed symptomatic improvement and were able to resume their sports. In nine patients with Blazina stage 3 tendinopathy, nonoperative measures failed, and surgery was performed. Operative treatment consisted of removal of the degenerated areas of the tendon, multiple longitudinal tenotomies, and drilling of the lower pole of the patella at the site of tendon attachment. Histologic examination of the excised tendon tissue showed areas of necrosis and mucoid degeneration, and alterations of the bone-tendon junction. After a mean follow-up of 4.8 years, clinical results were excellent or good in all patients. In the group treated nonoperatively, results were better in the patients who had stage 2 tendinopathy than in those with stage 3.
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Introduction Achilles and patellar tendinopathy are overuse injuries that are common among athletes. Isolated eccentric muscle training has become the dominant conservative management strategy for Achilles and patellar tendinopathy but, in some cases, up to 45 % of patients may not respond. Eccentric-concentric progressing to eccentric (Silbernagel combined) and eccentric-concentric isotonic (heavy-slow resistance; HSR) loading have also been investigated. In order for clinicians to make informed decisions, they need to be aware of the loading options and comparative evidence. The mechanisms of loading also need to be elucidated in order to focus treatment to patient deficits and refine loading programmes in future studies. Objectives The objectives of this review are to evaluate the evidence in studies that compare two or more loading programmes in Achilles and patellar tendinopathy, and to review the non-clinical outcomes (potential mechanisms), such as improved imaging outcomes, associated with clinical outcomes. Methods Comprehensive searching (MEDLINE, EMBASE, CINAHL, Current Contents and SPORTDiscus™) identified 403 studies. Two authors independently reviewed studies for inclusion and quality. The final yield included 32 studies; ten compared loading programmes and 28 investigated at least one potential mechanism (six studies compared loading programmes and investigated potential mechanisms). Results This review has identified limited (Achilles) and conflicting (patellar) evidence that clinical outcomes are superior with eccentric loading compared with other loading programmes, questioning the currently entrenched clinical approach to these injuries. There is equivalent evidence for Silbernagel combined (Achilles) and greater evidence for HSR loading (patellar). The only potential mechanism that was consistently associated with improved clinical outcomes in both Achilles and patellar tendon rehabilitation was improved neuromuscular performance (e.g. torque, work, endurance), and Silbernagel-combined (Achilles) HSR loading (patellar) had an equivalent or higher level of evidence than isolated eccentric loading. In the Achilles tendon, a majority of studies did not find an association between improved imaging (e.g. reduced anteroposterior diameter, proportion of tendons with Doppler signal) and clinical outcomes, including all high-quality studies. In contrast, HSR loading in the patellar tendon was associated with reduced Doppler area and anteroposterior diameter, as well as greater evidence of collagen turnover, and this was not seen following eccentric loading. HSR seems more likely to lead to tendon adaptation and warrants further investigation. Improved jump performance was associated with Achilles but not patellar tendon clinical outcomes. The mechanisms associated with clinical benefit may vary between loading interventions and tendons. Conclusion There is little clinical or mechanistic evidence for isolating the eccentric component, although it should be made clear that there is a paucity of good quality evidence and several potential mechanisms have not been investigated, such as neural adaptation and central nervous system changes (e.g. cortical reorganization). Clinicians should consider eccentric-concentric loading alongside or instead of eccentric loading in Achilles and patellar tendinopathy. Good-quality studies comparing loading programmes and evaluating clinical and mechanistic outcomes are needed in both Achilles and patellar tendinopathy rehabilitation.
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Objectives To assess if continuous topical glyceryl trinitrate (GTN) treatment improves outcome in patients with chronic patellar tendinopathy when compared with eccentric training alone. Methods Randomised double-blind, placebo-controlled clinical trial comparing a 12-week programme of using a GTN or placebo patch in combination with eccentric squats on a decline board. Measurements were performed at baseline, 6, 12 and 24 weeks. Primary outcome measure was the Victorian Institute of Sports Assessment-Patella (VISA-P) questionnaire. Secondary outcome measures were patient satisfaction and pain scores during sports. Generalised estimated equation was used to analyse the treatment, time and treatment×time effect. Analyses were performed following the intention-to-treat principle. Results VISA-P scores for both groups improved over the study period to 75.0±16.2 and 80.7±22.1 at 24 weeks. Results showed a significant effect for time (p<0.01) but no effect for treatment×time (p=0.80). Mean Visual Analogue Scores pain scores during sports for both groups increased over the study period to 6.6±3 and 7.8±3.1. Results showed a significant effect for time (p<0.01) but no effect for treatment×time (p=0.38). Patient satisfaction showed no difference between GTN and placebo groups (p=0.25) after 24 weeks, but did show a significant difference over time (p=0.01). Three patients in the GTN group reported some rash. Conclusion It seems that continuous topical GTN treatment in addition to an eccentric exercise programme does not improve clinical outcome compared to placebo patches and an eccentric exercise programme in patients with chronic patellar tendinopathy.
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A randomized controlled study has shown promising clinical results after treatment with sclerosing injections in a group of patients with patellar tendinopathy, but no study has investigated medium- or long-term outcome in a large and unselected group of patients. To investigate if sclerosing treatment would affect the level of patellar tendon pain and knee function after 24 months in a large group of patients with patellar tendinopathy. Case series; Level of evidence, 4. This prospective study recruited patients with a clinical diagnosis of jumper's knee and visible neovascularization corresponding to the painful area on power Doppler ultrasound. They received up to a maximum of 5 ultrasound-guided sclerosing injections using polidocanol at 4- to 6-week intervals. Knee pain and function were recorded using the Victorian Institute of Sport Assessment-Patella (VISA-P) score before treatment and 6, 12, and 24 months after the first injection. In total, 101 patients (15 women and 86 men) with 120 tendons were included and given from 1 to 5 sclerosing injections (mean [SD], 2.5 [0.9]). The patients reported a significantly improved VISA-P score from baseline (mean, 39; 95% confidence interval [CI], 36-42) to the 24-month follow-up (mean, 65; 95% CI, 60-70) (range, 21-100; P < .001, paired t test). However, a VISA-P score of >95 points was reported in only 22 cases (20%), whereas 37 cases (36%) reported a VISA-P score of <50 at 24 months. Sclerosing treatment with polidocanol resulted in a moderate improvement in knee function and reduced pain in a heterogeneous group of patients with patellar tendinopathy. Nevertheless, few of the patients were cured, and the majority still had reduced function and substantial pain after 24 months of follow-up.
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Patellar tendinopathy is a common, painful, overuse disorder. Although many different treatment methods have been described, there is no consensus regarding the optimal treatment for this condition. The purpose of this study was to systematically review, summarize, and compare treatments for patellar tendinopathy from published randomized controlled trials. Database searches were performed for randomized prospective controlled trials comparing treatment methods for patellar tendinopathy. The thirteen articles considered relevant were scrutinized according to quality assessment guidelines and levels of evidence. Strong evidence was found for the use of eccentric training to treat patellar tendinopathy. Moderate evidence was found for conservative treatment (heavy slow resistance training) as an alternative to eccentric training. Moderate evidence suggests that low-intensity pulsed ultrasound treatment did not influence treatment outcomes. Limited evidence was found for surgery, sclerosing injections, and shockwave therapy. Physical training, and particularly eccentric training, appears to be the treatment of choice for patients suffering from patellar tendinopathy. However, type of exercise, frequency, load, and dosage must also be analyzed. Other treatment methods, such as surgical treatment, sclerosing injections, and shockwave therapy, must be investigated further before recommendations can be made regarding their use. Ultrasound can likely be excluded as a treatment for patellar tendinopathy. There is a persistent lack of well-designed studies with sufficiently long-term follow-up and number of patients to draw strong conclusions regarding therapy. II.
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Chronic patellar tendinopathy often requires surgical treatment. We compared the outcomes in 25 subjects (29 tendons) who had had open patellar tenotomy and 23 subjects (25 tendons) who had had arthroscopic patellar tenotomy at a mean follow-up of 3.8 and 4.3 years, respectively. At follow-up, outcomes in the open and arthroscopic groups were as follows: 1) symptomatic benefit was seen in 81% of open and 96% of arthroscopic tenotomy patients, 2) sporting success was seen in 54% of open and 46% of arthroscopic tenotomy patients, 3) median time to return to preinjury level of activity was 10 months for open and 6 months for arthroscopic tenotomy patients, and 4) median Victorian Institute of Sport Assessment score at follow-up was 88 for open and 77 for arthroscopic tenotomy patients. There were no significant differences between groups for all outcomes. The appearance of the tendon on sonography remained abnormal in over 70% of subjects at follow-up, and sonographic appearance did not correlate with clinical outcome. Thus, arthroscopic patellar tenotomy was as successful as the traditional open procedure. Both procedures provided virtually all subjects with symptomatic benefit, but only about half the subjects who underwent either open or arthroscopic patellar tenotomy were competing at their former sporting level at follow-up.
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Symptoms of jumper's knee (patellar tendinosis) are not easily quantified and this may explain why there are no evidence-based guidelines for managing the condition. A simple, practical questionnaire-based index of severity would facilitate jumper's knee research and subsequently, clinical management. Thus we devised and tested the Victorian Institute of Sport Assessment (VISA) questionnaire. The brief questionnaire assesses (i) symptoms, (ii) simple tests of function and (iii) ability to play sport. Six of the eight questions are scored on a visual analogue scale from 0–10 with 10 representing optimal health. The maximal VISA score for an asymptomatic, fully performing individual is 100 points and the theoretical minimum is 0 points. We found the VISA scale to have excellent short-term test-retest, and inter-tester reliability (both, r>0.95) as well as good short-term (one week) stability (r=0.87). Mean (SD) of the VISA scores ranged from 95 (8) points in asymptomatic control subjects to 55 (12) points in patients who presented to a sports medicine clinic with jumper's knee and 22 (17) points in patients before surgery for chronic jumper's knee. Six- and twelve-months after surgery VISA scores returned to 49 (15) and 75 (17) points respectively, mirroring clinical recovery. We conclude that the VISA score is a reliable index of the severity of jumper's knee that has potential to aid clinicians and researchers.
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From previous research on tendinopathy of the Achilles tendon, wrist extensors and the supraspinatus, it is known that topical glyceryl trinitrate (GTN) has a healing effect. To our knowledge, no studies have been published on the application of GTN in patients with PT. The aim of this study was to assess if continuous topical GTN treatment improved outcome in patients with chronic PT compared to placebo patches, both combined with heavy load eccentric training. A randomised double blind, placebo-controlled clinical trial was done, comparing a 12 week programme of using a GTN patch or placebo patch in combination with eccentric squats on a decline board. Measurements were performed at baseline, 6, 12 and 24 weeks. Primary outcome measure was the VISA-P questionnaire. Secondary outcome measures were patient satisfaction and pain scores during sports. Generalised Estimated Equation was used to analyse the treatment, time and treatment x time effect. Analyses were performed following the intention-to-treat principle. VISA-P scores for both groups improved over the study period to 75.0±16.2 and 80.7±22.1 at 24 weeks. Results showed a significant effect for time (p<0.01) but no effect for treatment x time (p=0.80). Mean VAS pain scores during sports for both groups increased over the study period to 6.6±3.0 and 7.8±3.1. Results showed a significant effect for time (p<0.01) but no effect for treatment x time (p=0.38). Patient satisfaction showed no difference between the GTN and the placebo group (p=0.25) after 24 weeks, but did show a significant difference over time (p=0.01). Three patients in the GTN group reported some rash. Continuous topical GTN treatment in addition to an eccentric exercise programme does not improve clinical outcome compared to placebo patches and an eccentric exercise programme in patients with chronic patellar tendinopathy.
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Patellar tendinopathy is often treated surgically after failure of conservative treatment but clinical experience suggests that results are not uniformly excellent. The aim of this review was to (i) identify the different surgical techniques that have been reported and compare their success rates, and (ii) critically assess the methodology of studies that have reported surgical outcomes. Twenty-three papers and two abstracts were included in the review. Surgical procedures were categorized and outcomes summarized. Using ten criteria, an overall methodology score was derived for each paper. Criteria for which scores were generally low (indicating methodological deficiency) concerned the type of study, subject selection process and outcome measures. We found a negative correlation between papers’ reported success rates and overall methodology scores (r=−0.57, P<0.01). There was a positive correlation between year of publication and overall methodology score (r=0.68, P<0.001). We conclude that study methodology may influence reported surgical outcome. We suggest practical guidelines for improving study design in this area of clinical research, as improved study design would provide clinicians with a more rigorous evidence-base for treating patients who have recalcitrant patellar tendinopathy.
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A randomized controlled study has shown good clinical results after treatment with sclerosing injections into the area with neovessels in patients with patellar tendinopathy, but no study has investigated medium- or long-term outcomes. This study investigates the effect of sclerosing treatment 44 months (range, 42-47 months) after start of treatment. Case series; Level of evidence, 4. Patients with a diagnosis of jumper's knee and neovascularization corresponding to the painful area were recruited and treated with ultrasound-guided sclerosing injections using polidocanol. Primary outcome was Victorian Institute of Sport Assessment (VISA) score, which was recorded before the start of treatment, after 12 months, and 44 months after the start of the study period. Twelve of the 29 patients (14 tendons) who were followed up at 44 months had undergone arthroscopic surgery after sclerosing treatment, either to the patellar tendon (n = 6) or for other intra-articular lesions (n = 8). For patients who did not receive additional treatment after the sclerosing injections (n = 23 tendons), VISA score was 55 (range, 28-71) at baseline and 81 (range, 39-100) at 12-month follow-up (P < .001 vs baseline).Their VISA score at 44 months' follow-up was 89 (range, 73-100; P = .047 vs 12 months). For patients who went through arthroscopic tendon surgery, VISA score was 53 (range, 39-71) at baseline and 71 before surgery (range, 48-98; P = .14 vs baseline). Their VISA score at 44 months was 91 (range, 76-100; P = .0.16 vs 12 months; P = .005 vs baseline). For patients who went through non-tendon surgery, VISA score was 45 (range, 15-69) at baseline and 57 (range, 32-95) before surgery (P = .29 vs baseline). Their VISA score at 44 months was 92 (range, 72-100; P = .006 vs before surgery; P < .001 vs baseline). Sclerosing treatment with polidocanol was effective for the majority of the patients. Nevertheless, one-third elected to seek additional treatment through arthroscopic surgery during the 44-month follow-up period.