achilles and patellar tendinopathy loading programmes · conclusion there is little clinical or...
TRANSCRIPT
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SYSTEMATIC REVIEW
Achilles and Patellar Tendinopathy Loading Programmes
A Systematic Review Comparing Clinical Outcomes and Identifying PotentialMechanisms for Effectiveness
Peter Malliaras • Christian J. Barton •
Neil D. Reeves • Henning Langberg
! Springer International Publishing Switzerland 2013
AbstractIntroduction Achilles and patellar tendinopathy areoveruse injuries that are common among athletes. Isolated
eccentric muscle training has become the dominant con-servative management strategy for Achilles and patellar
tendinopathy but, in some cases, up to 45 % of patients
may not respond. Eccentric-concentric progressing toeccentric (Silbernagel combined) and eccentric-concentric
isotonic (heavy-slow resistance; HSR) loading have also
been investigated. In order for clinicians to make informeddecisions, 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 patientdeficits and refine loading programmes in future studies.
Objectives The objectives of this review are to evaluatethe evidence in studies that compare two or more loadingprogrammes in Achilles and patellar tendinopathy, and to
review the non-clinical outcomes (potential mechanisms),
such as improved imaging outcomes, associated withclinical outcomes.
Methods Comprehensive searching (MEDLINE, EM-BASE, CINAHL, Current Contents and SPORTDiscus
TM
)
identified 403 studies. Two authors independently
reviewed studies for inclusion and quality. The final yieldincluded 32 studies; ten compared loading programmes and
28 investigated at least one potential mechanism (six
studies compared loading programmes and investigatedpotential mechanisms).
Results This review has identified limited (Achilles) andconflicting (patellar) evidence that clinical outcomes aresuperior with eccentric loading compared with other
loading programmes, questioning the currently entrenched
clinical approach to these injuries. There is equivalentevidence for Silbernagel combined (Achilles) and greater
evidence for HSR loading (patellar). The only potential
mechanism that was consistently associated with improvedclinical 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. Inthe Achilles tendon, a majority of studies did not find an
association between improved imaging (e.g. reduced
anteroposterior diameter, proportion of tendons withDoppler signal) and clinical outcomes, including all high-
quality studies. In contrast, HSR loading in the patellar
tendon was associated with reduced Doppler area andanteroposterior diameter, as well as greater evidence of
collagen turnover, and this was not seen following eccen-
tric loading. HSR seems more likely to lead to tendonadaptation and warrants further investigation. Improved
jump performance was associated with Achilles but not
patellar tendon clinical outcomes. The mechanisms asso-ciated with clinical benefit may vary between loading
interventions and tendons.
Electronic supplementary material The online version of thisarticle (doi:10.1007/s40279-013-0019-z) contains supplementarymaterial, which is available to authorized users.
P. Malliaras (&) ! C. J. BartonCentre for Sports and Exercise Medicine, Mile End Hospital,Queen Mary, University of London, London, UKe-mail: [email protected]
N. D. ReevesInstitute for Biomedical Research into Human Movementand Health, Manchester Metropolitan University,Manchester, UK
H. LangbergInstitute of Sports Medicine, Bispebjerg Hospital,Copenhagen, Denmark
Sports Med
DOI 10.1007/s40279-013-0019-z
http://dx.doi.org/10.1007/s40279-013-0019-z
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Conclusion There is little clinical or mechanistic evi-dence for isolating the eccentric component, although it
should be made clear that there is a paucity of good qualityevidence and several potential mechanisms have not been
investigated, such as neural adaptation and central nervous
system changes (e.g. cortical reorganization). Cliniciansshould consider eccentric-concentric loading alongside or
instead of eccentric loading in Achilles and patellar ten-
dinopathy. Good-quality studies comparing loading pro-grammes and evaluating clinical and mechanistic outcomes
are needed in both Achilles and patellar tendinopathy
rehabilitation.
1 Introduction
Achilles and patellar tendinopathy are overuse injuries
characterized by localized tendon pain with loading and
dysfunction. Both are common among athletes and Achil-les tendinopathy may also affect sedentary people. Achilles
and patellar tendinopathy is the focus of this review
because these are the two major locomotor tendons affec-ted by tendinopathy. Injury to these tendons can severely
impact upon recreational and everyday activities. Patho-
logical features include altered cellularity (increased ordecreased), break down in the extracellular matrix (ground
substance accumulation, disorganized collagen, neurovas-
cular ingrowth) [1, 2]. Endocrine tenocytes and nerveendings release biochemicals that are thought to have a role
in tendon pain (e.g. substance P) [3, 4]. Both extrinsic (e.g.
overuse) and intrinsic factors (e.g. lipid levels, genes) maypredispose to injury, but pathoaetiology is poorly under-
stood [5].
Eccentric muscle loading has become the dominantconservative intervention strategy for Achilles and patellar
tendinopathy over the last decade. Eccentric loading
involves isolated, slow-lengthening muscle contractions.Other contraction types have been investigated, including
eccentric-concentric and isolated concentric, and, in some
studies, they have been compared with eccentric loading.Previous systematic reviews have evaluated the evidence
for eccentric muscle loading in Achilles [6–10] and patellar
[11, 12] tendinopathy, concluding that outcomes arepromising but high-quality evidence is lacking. The first
aim of this review is to synthesis evidence from studies
comparing two or more loading programmes in Achillesand patellar tendinopathy. The findings of this review will
guide clinical decisions and identify areas for further
research.It is clear from the eccentric loading evidence that not
all patients respond to this intervention. In one study, 45 %of patients were considered to have failed treatment (a less
than 10-point improvement in the Achilles version of the
Victorian Institute of Sports Assessment [VISA-A] score)
[13]. This clearly indicates eccentric loading may not beeffective for all patients with tendinopathy. Understanding
the mechanisms of loading interventions in tendinopathy,
and which mechanisms are associated with improvedclinical outcomes, may improve rehabilitation outcomes.
Loading programmes can then be targeted to patient defi-
cits (e.g. neuromuscular deficits) and mechanisms associ-ated with clinical outcomes can be maximized (e.g. load
intensity to maximize muscle and tendon adaptation),potentially improving clinical outcomes. The second aim is
to investigate the non-clinical outcomes (potential mecha-
nisms), such as improved strength and imaging pathology,associated with improved clinical outcomes following
Achilles and patellar tendinopathy rehabilitation.
2 Methods
A systematic review was undertaken following the protocol
guidelines outlined in the PRISMA statement [14].
2.1 Search Criteria
A search of MEDLINE, EMBASE, CINAHL, CurrentContents and SPORTDiscus
TM
electronic databases was
undertaken from inception to June 2012. Search terms
relating to exercise (‘eccentric’, ‘rehabilitation’, ‘resistancetraining’, ‘exercise therapy’), pathology (‘tendinopathy’,
‘tendinitis’, etc.) and the site (‘Achilles’, ‘patellar’) were
combined in the final search (Table 1 shows the MEDLINEexample). Each search term was mapped to specific MeSH
subject headings within each database. The reference lists
of eccentric loading systematic reviews and the studies inthe final yield were manually checked to identify other
studies.
2.2 Selection Criteria
Studies investigating clinical outcomes of loading pro-grammes in Achilles and patellar tendinopathy were
included. This comprised any type of muscle-tendon unit
loading, including eccentric, concentric, combined eccen-tric-concentric, isometric and stretch-shortening cycle
(SSC), loading involving a fast muscle tendon unit
eccentric-concentric turnaround (e.g. jumping, hopping).Human studies with a minimum follow-up period of
4 weeks and single cohort studies and trials comparing two
or more groups were included. From this, broad yieldstudies that compared two or more loading programmes in
Achilles and patellar tendinopathy formed a subgroup. This
included randomized controlled trials (RCTs) and con-trolled clinical trials (CCTs) that were not randomized.
P. Malliaras et al.
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Stretching alone was not considered a loading programme,but studies that compared loading with and without con-
tinued sport were included. Single cohort studies and trials
that investigated one or more non-clinical or mechanisticoutcome (e.g. imaging and muscle performance measures
such as peak torque) were included in another subgroup.
Studies that did not include any participants with ten-dinopathy were excluded, as were studies if they investi-
gated loading following another primary intervention, such
as injections or surgery. Other exclusion criteria includednon-English studies, abstracts, non-peer-reviewed studies,
case reports and reviews.
2.3 Review Process
Two reviewers (PM, CB) independently reviewed the titleand abstract of all retrieved studies and those satisfying the
inclusion and exclusion criteria were included in the finalyield. If there was insufficient information in the title and
abstract, the full text was obtained for adequate evaluation.
Disagreement between the two authors was resolved byconsensus.
2.4 Quality Assessment
A modified version [15] of a scale developed to assess the
quality of intervention studies in patellofemoral joint painsyndrome [16] was used to evaluate study quality. Four
quality components were evaluated (participants, inter-
ventions, outcome measures, and data presentation andanalysis), each scored a maximum of 10 points (40 points
in total) and contained three to four items. The item
relating to the control and placebo group was modified torelate to the control group only because placebo is not
practical with exercise interventions. The item was scored
out of 4, with 2 points for comparison to another exerciseintervention and 4 points for adequate control (i.e. a wait-
and-see group or equivalent comparison group minus the
exercise intervention). The adequate numbers item wasscored out of 2 rather than 4 and the group homogeneity
item was scored out of 4 rather than 2 and modified to
pertain to adequate description and homogeneity of keygroup characteristics (age, gender, activity, severity). Case
series studies could score a maximum of 34 points (the
control group and randomization items were excluded).Two reviewers independently assessed the quality of
included studies and disagreement was resolved by con-
sensus. Studies scoring greater than 70 % on the qualityassessment were considered high quality.
2.5 Data Extraction and Analysis
Key data relating to sample demographics, interventions
and outcomes were extracted from each study. Thisincluded study design (e.g. an RCT), groups/description of
loading and sample sizes, participant demographics (age,
gender, activity level) and clinical and mechanistic out-comes. Only data from loading interventions were extrac-
ted. Given the heterogeneity in interventions and outcomemeasures a qualitative data synthesis was performed.
Definitions for ‘levels of evidence’ were guided by rec-
ommendations made by van Tulder et al. [17] and areshown in Table 2.
3 Results
Figure 1 shows the process of identifying studies. Therewere 403 studies in the initial yield after removing dupli-
cates. Ninety-two studies were assessed in full text, and a
further 60 studies were excluded, leaving a yield of 33studies either comparing two loading programmes or eval-
uating at least one non-clinical outcome (potential mecha-
nism). In the final yield there were ten studies comparingloading programmes and 29 studies investigating at least one
potential mechanism (six studies compared loading pro-
grammes and investigated potential mechanisms).The quality assessment of all studies in this systematic
review is shown in the table in the Online Resource [Online
Resource 1]. The mean quality score was 54 % and therange was from 26 % to 83 %. Only seven (21 %) studies
achieved a high-quality rating [11, 18–23]. Five (15 %)
Table 1 Search terms in MEDLINE database
Search term
1 ‘eccentric’, ‘concentric’, ‘isometric’, ‘training’, ‘exercise’ (title & abstract) ‘Exercise Therapy’, ‘Exercise’, ‘Rehabilitation’, ‘Resistancetraining’ (MeSH)
AND
2 ‘achilles tendon’, ‘achilles’, ‘tendoachilles’, ‘tendo-achilles’, ‘triceps-surae’, ‘patellar tendon’, ‘patellar ligament’ (title & abstract) ‘AchillesTendon’, ‘Patellar Ligament’ (MeSH)
AND
3 ‘tendinopathy’, ‘tendinitis’, ‘tendinosis’, ‘partial rupture’, ‘paratenonitis’, ‘peritendinitis’, ‘Achillodynia’ (title & abstract) ‘Tendinopathy’,‘Tendon Injuries’ (MeSH)
Loading of Achilles and Patellar Tendinopathy
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studies had a quality score below 40 % [24–28] and find-
ings from these studies were not included in the recom-
mended levels of evidence. Eleven (55 %) trials wereadequately randomized [11, 18, 19, 21–23, 29–33]. Three
studies did not randomize participants into groups [27, 34,
35], and the remaining studies did not adequately describethe randomization process [26, 28, 36–39]. Only seven
studies (21 %) reported adequate blinding of outcomeassessors [19–23, 29, 38], so experimenter bias may have
influenced the findings in a majority of studies. Only two
studies (6 %) adequately reported inclusion and exclusioncriteria [18, 36]. In many studies, tendon pain with loading
was not clear as an inclusion criterion and previous surgery
or other injuries were not explicitly excluded. Forty-twopercent (14 of 33) used adequate outcome measures [11,
19–23, 30, 31, 36, 39–43]. This was usually a pain outcome
that was not validated, such as a visual analogue scale(VAS) or an absence of functional outcomes. Only 12
(36 %) studies used the VISA-A or patellar tendon version
of the VISA questionnaire, which is a disease-specific andvalidated pain and functional outcome measure (0–100
points, 100 = no pain and full function). Most studies
described the loading interventions partially, with the meanscore for that item being 2.8 of 4 (63 %). Few studies
described the speed of each contraction [28, 44] and
maximum load [11, 19, 29, 45]. A key issue with thisliterature is that the severity and irritability of tendons is
generally not reported, so tendons may be at very different
places along the reactive-degenerative symptomatic spec-trum, and this will influence the response to load [46].
3.1 Description of Clinical Loading Programmes
Twenty-three Achilles [21–25, 28, 30, 32–35, 37–42, 44,
45, 47–49, 51] and 11 patellar tendon studies [11, 18–20,26, 27, 29, 31, 36, 43, 47] were included in this review (one
study included both Achilles and patellar tendon cohorts
[47]). A majority of studies in the Achilles (16 of 23, 70 %)and patellar tendon (6 of 10, 60 %) investigated the iso-
lated eccentric loading programme popularized by Al-
fredson [35] in at least one group. One Achilles [37] (4 %)
and two patellar tendon studies [29, 31] (20 %) used theeccentric-concentric Stanish and Curwin model [50]. Some
studies have described this programme as ‘eccentric’ when
it actually involves both concentric and eccentric contrac-tion [37, 50]. In the Achilles studies, four [23, 30, 40, 41]
(17 %) investigated the combined Silbernagel programme
[30] involving progression from eccentric-concentric toeccentric load and, finally, faster eccentric-concentric and
plyometric loading. Two patellar tendon studies [19, 20]
(20 %) investigated heavy-slow resistance (HSR) loadingthat involves slow double leg isotonic eccentric-concentric
contractions. Table 3 shows the characteristics of the four
main loading programmes used in Achilles and patellartendinopathy rehabilitation. Few studies included groups
undertaking isotonic loading [29, 37], isokinetic loading
[26, 47], concentric [32, 36] and flywheel loading [43].
3.2 Comparison of Loading Programmes in Achilles
and Patellar Tendinopathy
Ten studies compared loading programmes in either
Achilles [23, 30, 32, 37] or patellar tendinopathy [11, 19,27, 29, 31, 36]. This included nine RCTs and one CCT. The
mean quality score of studies comparing loading pro-
grammes was 57 % (range 34–83 %). Only two studies[19, 23] (20 %) had a high-quality score ([70 %) and one
Table 2 Grading the recommendations for comparing loadingprogrammes
Evidencegrade
Recommendation
Strong Consistent findings among n C2 high-quality studies
Moderate Consistent findings amongst multiple low-qualitystudies, or one high-quality study
Limited Findings from one low-quality study.
Conflicting Inconsistent findings among multiple studies
None No studies found
398 papers identified after
removing duplicates
403 papers identified
92 retrieved in full text
32 studies compared two loading programmes or investigated at least one
potential mechanism
311 excluded based on abstract16 animal studies7 cruciate ligament repair83 opinion pieces, abstracts, case studies, reviews113 post-surgery, rupture, other treatment79 no-exercise intervention3
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other study scored just below the cut off for a high-quality
rating (68 %) [31].
Data extracted from each study comparing loadingprogrammes and investigating mechanisms are shown in
Table 4. There were 139 participants with a mean age of
44 years in the four studies comparing loading programmesin Achilles tendinopathy, with slightly more men than
women (61 %), and the proportion participating in sport
ranged from 57 % to 100 %.There is limited evidence from three low-quality studies,
which showed that (i) a greater proportion of patients are
satisfied and return to a preinjury level of activity followingeccentric, compared with concentric, loading [32]; (ii)
VAS pain outcomes and patient satisfaction are greater
following Silbernagel-combined loading compared withcalf raises and stretching [30]; and (iii) VAS pain and
return-to-sport outcomes were greater following Stanish
and Curwin, compared with isotonic loading [37]. In onehigh-quality study there was moderate evidence, which
showed that VISA-A improvement following Silbernagel-
combined loading is similar whether sport is continued ornot [23].
There were six patellar tendon studies including 112
participants with a mean age of 27 years. All participantswere active in sports and greater than three-quarters were
men (77 %). There is moderate evidence from two high-
quality studies, which showed that (i) VISA improvementis comparable but patient satisfaction is greater following
HSR versus eccentric loading [19]; (ii) there is no differ-
ence in change in VISA scores during a volleyball seasonwith and without the addition of eccentric loading [11].
There is limited evidence from three low-quality studies,
which showed that (i) clinical outcomes are superior fol-lowing eccentric, compared with Stanish and Curwin
loading [31] and concentric loading [36]; (ii) VAS pain and
return-to-sport outcomes are superior following Stanishand Curwin, compared with isotonic loading [29]. In one
very low-quality study, clinical outcomes were superior
following eccentric compared with eccentric loading
without a decline board [27].
3.3 Potential Mechanisms of Achilles and Patellar
Tendinopathy Loading Programmes
Twenty-nine studies investigated non-clinical potential
mechanisms of loading programmes in Achilles [21–25, 28,
30, 33–35, 37–42, 44, 45, 48, 49, 51] and patellar tendin-opathy [11, 18–20, 26, 29, 43, 47]. This included 14 RCTs,
two CCT’s and 13 single cohort studies. Studies investi-
gating mechanisms had a mean quality score of 54 % (range26–79 %) and seven studies (25 %) had a high-quality
rating [11, 18–22, 42]. There were 293 participants with
Achilles tendinopathy in 21 studies. They had a mean age of47 years, 79 % were active in sport and 59 % were men.
One-hundred and sixty-three participants with patellar
tendinopathy were investigated in eight studies. They had amean age of 28 years, the majority were men (81 %) and
almost all were active in sport (98 %).
3.3.1 Achilles
3.3.1.1 Neuromuscular and Jump Performance Outcomes
3.3.1.1.1 Eccentric Loading. There is limited evidence
from one low-quality study that improved clinical out-
comes are associated with increased ankle planterflexiontorque [35]. There is moderate evidence from three low-
quality studies, which show that (i) improved clinical
outcomes are associated with increased calf work [35, 38](ii) resolution in side-to-side ankle planterflexor work and
torque deficits [34, 35].
3.3.1.1.2 Silbernagel-Combined Loading. There is lim-ited evidence from one low-quality study, which showed
that (i) improved clinical outcomes are associated with
increased planterflexor endurance [30], (ii) improvement in
Table 3 Characteristics of Alfredson, Stanish and Curwin, Silbernagel and HSR programmes
Programmes Type of exercise Sets, reps Frequency Progression Pain
Alfredson Eccentric 3, 15 Twice daily Load Enough load to achieve upto moderate pain
Stanish and Curwin Eccentric-concentric, power 3, 10–20 Daily Speed then load Enough load to be painfulin third set
Silbernagel Eccentric-concentric, eccentric, fastereccentric-concentric, balanceexercise [30, 41], plyometric [23]
Various Daily Volume, type ofexercise
Acceptable if withindefined limitsa
HSR Eccentric-concentric 4, 15–6 39/week 15–6 RM Acceptable if was not worseafter
reps repetitions, RM repetition maximuma Moderate (less than 5 of 10 on a visual analogue scale, 10 = worst pain imaginable); subsided by the following day
Loading of Achilles and Patellar Tendinopathy
-
Tab
le4
Gro
up
char
acte
rist
ics,
inte
rven
tio
ns
and
ou
tco
mes
for
each
stu
dy
Stu
dy
(yea
r)D
esig
nG
rou
ps,
inte
rven
tio
ns
Par
tici
pan
tch
arac
teri
stic
saC
lin
ical
ou
tco
me
Mec
han
isti
co
utc
om
es
Alf
red
son
etal
.[3
5]
(19
98
)C
CT
,A
T1
.E
L=
15
pat
ien
ts,
ecce
ntr
icca
lfd
rop
ov
era
step
Mea
nag
e4
4y
ears
,8
0%
men
,al
lm
idp
ort
ion
,u
nil
ater
alan
dru
nn
ers
12
wee
ks;
94
%;
inV
AS
pai
n(p
\0
.00
1),
10
0%
retu
rnto
run
nin
g
12
wee
ks;:
con
cen
tric
wo
rk1
4%
(p\
0.0
5),
no
chan
ge
inec
cen
tric
wo
rk,:
con
cen
tric
torq
ue
11
–1
5%
(p\
0.0
5),
:ec
cen
tric
torq
ue
18
%(p
\0
.01
),to
rqu
ean
dw
ork
defi
cits
reso
lved
2.
Su
rger
y=
15
pat
ien
ts
Alf
red
son
etal
.[3
4]
(19
99
)C
CT
,A
T1
.E
L=
14
pat
ien
tsM
ean
age
44
yea
rs,
86
%m
en,
all
mid
po
rtio
n,
un
ilat
eral
and
run
ner
s
12
wee
ks:
[9
5%
;in
VA
Sp
ain
(p\
0.0
1)
12
wee
ks:
con
cen
tric
and
ecce
ntr
icto
rqu
ed
efici
tsre
solv
ed2
.S
urg
ery
=1
0p
atie
nts
Alf
red
son
[51
](2
00
3)
SC
,A
TE
L=
6p
atie
nts
Mea
nag
e4
8y
ears
,m
idp
ort
ion
12
wee
ks:
75
%;
inV
AS
pai
n1
2w
eek
s;n
och
ang
ein
glu
tam
ate
con
cen
trat
ion
(p[
0.0
5)
Bah
ret
al.
[18]
(20
06
)R
CT
,P
T1
.E
L=
20
ten
do
ns,
ecce
ntr
icsq
uat
on
ad
ecli
ne
bo
ard
Mea
nag
e3
1y
ears
,9
0%
men
and
all
acti
ve,
14
%b
ilat
eral
3,
6,
12
mo
nth
s:7
3–
13
0%
imp
rov
emen
tin
VIS
A(p
\0
.00
1)
6,
12
mo
nth
s::
leg
pre
ss1
RM
(kg
)1
7–
30
%(p
\0
.05
),n
och
ang
ein
SJ,
CM
Jin
bo
thg
rou
ps
2.
Su
rger
y=
20
ten
do
ns
Can
nel
let
al.
[29
](2
00
1)
RC
T,
PT
1.
Sta
nis
han
dC
urw
in=
10
pat
ien
ts,
all
pat
ella
r=
fast
dro
psq
uat
un
til
thig
hs
alm
ost
par
alle
l
Mea
nag
e2
6y
ears
,6
8%
men
,al
lac
tiv
e,1
7%
bil
ater
al
12
wee
ks:
VA
Sp
ain;
inb
oth
gro
up
s(5
5%
ver
sus
31
%,
p\
0.0
1)
wit
hn
od
iffe
ren
ceb
etw
een
the
gro
up
s.M
ore
retu
rned
tosp
ort
ind
rop
squ
atg
rou
pb
ut
no
tsi
gn
ifica
nt
(90
%v
ersu
s6
7%
;p[
0.0
5)
12
wee
ks:
qu
adri
cep
sco
nce
ntr
icto
rqu
ed
idn
ot
incr
ease
inei
ther
gro
up
s,h
amst
rin
gco
nce
ntr
icto
rqu
e:
inb
oth
gro
up
s1
4–
18
%(p
\0
.00
1),
no
dif
fere
nce
bet
wee
ng
rou
ps
2.
Iso
ton
ic=
9p
atie
nts
,ec
cen
tric
-co
nce
ntr
icle
gex
ten
sio
ns
and
curl
s
Cro
isie
ret
al.
[47
](2
00
1)
SC
,A
Tan
dP
TA
T=
9p
atie
nts
,iso
late
dec
cen
tric
iso
kin
etic
calf
;P
T=
10
pat
ien
ts,
iso
late
dec
cen
tric
iso
kin
etic
qu
adri
cep
s
Mea
nag
e2
8y
ears
,6
3%
men
,8
4%
acti
ve,
all
un
ilat
eral
10
wee
ks:
73
%;
inV
AS
pai
nin
AT
(p\
0.0
01
);7
1%
;in
VA
Sin
PT
(p\
0.0
01
)
10
wee
ks:
con
cen
tric
and
ecce
ntr
icto
rqu
e,n
od
efici
tb
etw
een
sid
esfo
rb
oth
AT
and
PT
,4
1%
had
no
rmal
ized
US
stru
ctu
re
de
Jon
ge
[22]
(20
10
)R
CT
,A
T1
.E
L=
34
ten
do
ns
Mea
nag
e4
5y
ears
,5
9%
men
,al
lm
idp
ort
ion
and
acti
ve,
21
%b
ilat
eral
12
mo
nth
s:5
1%
imp
rov
emen
tin
VIS
A-A
(p\
0.0
1)
12
mo
nth
s:n
och
ang
ein
Do
pp
ler
pre
val
ence
(65
%at
bas
elin
e,7
1%
atfo
llo
w-u
p).
Bas
elin
eD
op
ple
rn
ot
asso
ciat
edw
ith
VIS
A-A
chan
ge
2.
EL
?n
igh
tsp
lin
t=
36
ten
do
ns
Gar
din
etal
.[4
8](2
01
0)
SC
,A
TE
L=
20
pat
ien
ts;
foll
ow
-up
of
Sh
alab
i2
00
4st
ud
yco
ho
rtM
ean
age
49
yea
rs,
67
%m
en,
38
%ac
tiv
e,3
8%
bil
ater
al
50
mo
nth
s:9
5%
rep
ort
edn
oo
rim
pro
ved
sym
pto
ms—
imp
rov
emen
tw
assi
gn
ifica
ntl
yb
ette
rth
anb
asel
ine
(p\
0.0
01
)an
dp
ost
-ecc
entr
ics
(p\
0.0
1)
50
mo
nth
s:p
rese
nce
of
intr
aten
din
ou
ssi
gn
al;
fro
m6
0%
atb
asel
ine
to1
0%
atfo
llo
w-u
p(p
\0
.05
).3
.50
mo
nth
s:n
och
ang
ein
ten
do
nC
SA
P. Malliaras et al.
-
Tab
le4
con
tin
ued
Stu
dy
(yea
r)D
esig
nG
rou
ps,
inte
rven
tio
ns
Par
tici
pan
tch
arac
teri
stic
saC
lin
ical
ou
tco
me
Mec
han
isti
co
utc
om
es
Jen
sen
and
Di
Fab
io[2
6](1
98
9)
RC
T,
PT
1.
Ho
me
exer
cise
=7
pat
ien
ts,
qu
adri
cep
san
dh
amst
rin
gst
retc
hes
Mea
nag
e2
4y
ears
,5
2%
men
(mo
rew
om
enin
gro
up
2),
all
acti
ve
Ch
ang
ein
pai
nn
ot
rep
ort
ed8
wee
ks:
affe
cted
:u
naf
fect
edec
cen
tric
wo
rkra
tio:
fro
m7
8%
atb
asel
ine
to1
06
%at
foll
ow
-u
p.
Ho
me
exer
cise
gro
up:
fro
m8
2%
atb
asel
ine
to9
4%
.N
on
-te
nd
ino
pat
hy
gro
up
per
form
ing
EL:
fro
m1
08
%to
14
0%
(no
pv
alu
esg
iven
).A
t8
wee
ks
foll
ow
-up
:p
ain
freq
uen
cy(p
=0
.80
)an
din
ten
sity
(p=
0.7
8)
neg
ativ
ely
corr
elat
edw
ith
affe
cted
:u
naf
fect
edec
cen
tric
wo
rkra
tio
2.
Ho
me
exer
cise
and
qu
adri
cep
sIE
L=
8p
atie
nts
(ran
do
miz
edan
oth
erg
rou
pw
ith
ou
tp
atel
lar
ten
din
op
ath
yin
toth
esa
me
2g
rou
ps)
Jon
sso
nan
dA
lfre
dso
n[3
6](2
00
5)
RC
T,
PT
1.
EL
=1
0p
atie
nts
Mea
nag
e2
5y
ears
,8
7%
men
,al
lac
tiv
e,2
7%
bil
ater
al
12
wee
ks:
29
imp
rov
emen
t(p
\0
.00
1)
inV
ISA
inE
Lg
rou
pv
ersu
sn
och
ang
ein
CL
gro
up
.M
ore
retu
rned
tosp
ort
/sat
isfi
edin
EL
gro
up
(70
%v
ersu
s2
2%
,p\
0.0
5)
NA
2.
CL
=9
pat
ien
ts,
iden
tica
lto
EL
bu
tis
ola
ted
con
cen
tric
com
po
nen
t
Kn
ob
loch
etal
.[2
8]
(20
07
)R
CT
,A
T1
.E
L=
15
pat
ien
tsM
ean
age
33
yea
rs,
55
%m
en,
40
%m
idp
ort
ion
12
wee
ks:
48
%;
inV
AS
pai
n(p
\0
.05
)1
2w
eek
s:;
po
st-c
apil
lary
fill
ing
pre
ssu
reat
2o
f1
6si
tes
mea
sure
d9
–2
7%
(p\
0.0
5),;
cap
illa
ryfl
ow
at2
of
16
site
s3
1–
45
%(p
\0
.05
),o
xy
gen
satu
rati
on
no
chan
ge
2.
Co
ntr
ol
=5
pat
ien
ts
Kn
ob
loch
[44]
(20
07
)S
C,
AT
EL
=5
9p
atie
nts
Mea
nag
e4
9y
ears
,6
1%
men
,8
3%
mid
po
rtio
n1
2w
eek
s:3
5%
;in
VA
Sp
ain
12
wee
ks:
;p
ost
cap
illa
ryfi
llin
gp
ress
ure
at2
of
16
site
s1
9–
24
%(p
\0
.01
),;
cap
illa
ryfl
ow
at2
of
16
site
s(2
3–
35
%)
p\
0.0
1),
ox
yg
ensa
tura
tio
nn
och
ang
e
Ko
ng
sgaa
rdet
al.
[19
](2
00
9)
RC
T,
PT
1.
EL
=1
2p
atie
nts
Mea
nag
e3
2y
ears
,al
lm
enan
dac
tiv
e,3
2%
bil
ater
al1
2,
26
wee
ks:
39
-65
%:
inV
ISA
inea
chg
rou
p(p
\0
.01
),n
od
iffe
ren
ceb
etw
een
gro
up
s,E
Lg
rou
pm
ore
sati
sfied
than
HS
Rg
rou
p(7
0–
73
%v
ersu
s2
2–
42
%;
p\
0.0
5)
12
wee
ks:
12
–1
3%
;in
ten
do
nA
Pd
iam
eter
HS
Rg
rou
p(p
\0
.01
),4
5%
;U
Sco
lou
rar
eain
HS
R(p
\0
.01
),n
och
ang
ein
EL
gro
up
for
eith
er.
17
%:
pat
ella
rte
nd
on
CS
Ain
ecce
ntr
icg
rou
po
nly
(p\
0.0
5),
no
chan
ge
ino
ther
gro
up
s.7
%:
qu
adri
cep
sm
usc
leC
SA
bo
thg
rou
ps
(p\
0.0
1),
no
dif
fere
nce
bet
wee
ng
rou
ps.
No
chan
ge
inco
llag
enco
nte
nt,
HP
,L
Pco
nce
ntr
atio
nin
any
gro
up
.:
HP
:L
Pra
tio
(19
%)
and;
pen
tosi
din
e(2
3%
)in
HS
Rg
rou
p,
no
chan
ge
ino
ther
gro
up
s.8
–1
1%
:M
VC
inb
oth
exer
cise
gro
up
s(p
\0
.05
).N
och
ang
ein
stif
fnes
san
dm
od
ulu
sin
eith
erex
erci
seg
rou
p
2.
HS
R=
13
pat
ien
ts,
leg
pre
ss,
hac
ksq
uat
,sq
uat
—al
ld
ou
ble
leg
3.
CS
I=
12
pat
ien
ts,
1–
2in
ject
ion
s
Loading of Achilles and Patellar Tendinopathy
-
Tab
le4
con
tin
ued
Stu
dy
(yea
r)D
esig
nG
rou
ps,
inte
rven
tio
ns
Par
tici
pan
tch
arac
teri
stic
saC
lin
ical
ou
tco
me
Mec
han
isti
co
utc
om
es
Ko
ng
sgaa
rdet
al.
[20
](2
01
0)
SC
,P
TH
SR
=8
pat
ien
ts(c
om
par
edw
ith
ag
rou
pw
ith
ou
tte
nd
ino
pat
hy
wh
od
idn
ot
per
form
the
exer
cise
)
Mea
nag
e3
3y
ears
,al
lm
enan
dac
tiv
e1
2w
eek
s:2
7%
imp
rov
emen
tin
VIS
A(p
=0
.02
)1
2w
eek
s:q
uad
rice
ps
CS
A:
7%
,p
eak
kn
eeex
ten
sio
nm
om
ent:
10
%,
ten
do
nst
iffn
ess;
9%
inH
SR
gro
up
(p\
0.0
5).
Mo
du
lus
ten
ded
tod
ecre
ase
(p=
0.1
5)
bu
tn
och
ang
ein
pat
ella
rte
nd
on
CS
A,
stra
inan
dst
ress
.F
ibri
ld
ensi
ty:
70
%(p
=0
.08
),fi
bri
lm
ean
area
;2
6%
(p=
0.0
4)
inH
SR
gro
up
,fi
bri
lv
olu
me
frac
tio
nn
och
ang
e.N
och
ang
ein
no
n-t
end
ino
pat
hy
gro
up
for
any
ou
tco
me
Lan
gb
erg
etal
.[4
9]
(20
07
)S
C,
AT
EL
=6
pat
ien
ts(c
om
par
edw
ith
ag
rou
pw
ith
ou
tte
nd
ino
pat
hy
wh
op
erfo
rmed
the
sam
eex
erci
se)
Mea
nag
e2
6y
ears
,al
lac
tiv
em
enw
ith
mid
po
rtio
nsy
mp
tom
s,al
lu
nil
ater
al
12
wee
ks:
71
%;
inV
AS
pai
n(p
\0
.05
)1
2w
eek
s:4
9:
coll
agen
syn
thes
is(p
\0
.05
).N
osi
gn
ifica
nt
chan
ge
inn
on
-te
nd
ino
pat
hy
gro
up
.N
och
ang
ein
eith
erg
rou
pin
coll
agen
deg
rad
atio
n
Mafi
etal
.[3
2]
(20
01
)R
CT
,A
T1
.E
L=
22
pat
ien
tsM
ean
age
48
yea
rs,
55
%m
en,a
llm
idp
ort
ion
,57
%ac
tiv
e
12
wee
ks:
mo
resa
tisfi
ed/r
etu
rned
top
re-i
nju
ryac
tiv
ity
inE
Lg
rou
p(8
2%
ver
sus
36
%;
p=
0.0
02
)
NA
2.
Mafi
com
bin
ed=
22
pat
ien
ts,
ecce
ntr
ic-c
on
cen
tric
ther
aban
dP
Fan
dh
eel
rais
es,
step
-up
s,sk
ipp
ing
,h
op
pin
g
Nie
sen
-V
erto
mm
enet
al.
[37
](1
99
2)
RC
T,
AT
1.
Sta
nis
han
dC
urw
in=
8p
atie
nts
,fa
stec
cen
tric
calf
dro
p,
slo
wco
nce
ntr
icco
mp
on
ent
Mea
nag
e3
8y
ears
men
;3
0y
ears
wo
men
,5
9%
men
(mo
rew
om
enin
Sta
nis
hg
rou
p),
all
mid
po
rtio
nan
dac
tiv
e
12
wee
ks:
VA
Sp
ain;
inb
oth
gro
up
s(5
0–
72
%;
p\
0.0
5),
gre
ater
dec
reas
ein
Sta
nis
hg
rou
p(p
\0
.01
).M
ore
retu
rned
tosp
ort
/im
pro
ved
acti
vit
yin
Sta
nis
han
dC
urw
ing
rou
pb
ut
no
tsi
gn
ifica
nt
(75
%v
ersu
s3
3%
;p
=0
.15
)
12
wee
ks:
app
rox
imat
ely
29
:co
nce
ntr
ican
dec
cen
tric
torq
ue
inb
oth
gro
up
s(p
\0
.00
1),
no
dif
fere
nce
bet
wee
nth
eg
rou
ps
2.
Iso
ton
ic=
9p
atie
nts
,ec
cen
tric
-co
nce
ntr
icp
lan
terfl
exio
nan
dd
ors
iflex
ion
No
rreg
aard
etal
.[3
3]
(20
07
)R
CT
,A
T1
.E
L=
21
ten
do
ns,
pro
gre
ssed
tofa
ster
calf
dro
paf
ter
3w
eek
sM
ean
age
42
yea
rs,
51
%m
en,
3–
4p
atie
nts
per
gro
up
had
inse
rtio
nal
,4
9%
bil
ater
al
3,
6,
12
,2
4,
52
wee
ks:
imp
rov
emen
tsin
sym
pto
ms
and
pai
n(1
8–
76
%;
p\
0.0
1–
0.0
5)
inb
oth
gro
up
s,n
od
iffe
ren
ceb
etw
een
the
gro
up
s
12
(no
t3
)m
on
ths:
AP;
9–
17
%(p
\0
.05
)in
bo
thg
rou
ps,
no
dif
fere
nce
bet
wee
nth
eg
rou
ps.
12
mo
nth
s:g
reat
erA
Pd
iam
eter
init
iall
yas
soci
ated
wit
hle
ssp
ain
inte
nsi
tyan
db
ette
rq
ual
ity
of
life
at1
2m
on
ths
(p\
0.0
1),
bu
tch
ang
ein
sym
pto
ms
no
tco
rrel
ated
toch
ang
ein
AP
2.
Str
etch
ing
=2
4te
nd
on
s,so
leu
san
dg
astr
ocn
emiu
sst
retc
hes
P. Malliaras et al.
-
Tab
le4
con
tin
ued
Stu
dy
(yea
r)D
esig
nG
rou
ps,
inte
rven
tio
ns
Par
tici
pan
tch
arac
teri
stic
saC
lin
ical
ou
tco
me
Mec
han
isti
co
utc
om
es
Oh
ber
gan
dA
lfre
dso
n[2
4](2
00
4)
SC
,A
TE
L=
34
pat
ien
tsM
ean
age
48
yea
rs,
76
%m
en,
62
%ac
tiv
e,al
lh
adm
idp
ort
ion
sym
pto
ms,
37
%b
ilat
eral
Mea
n2
8m
on
ths:
88
%h
adn
op
ain
du
rin
gac
tiv
ity
Mea
n2
8m
on
ths:
‘mo
ren
orm
al’
gre
y-s
cale
US
app
eara
nce
in9
0%
,D
op
ple
rsi
gn
alre
solv
edin
78
%.
Mo
reli
kel
yto
hav
ere
mai
nin
gD
op
ple
rif
stil
lp
ain
ful
(p\
0.0
01
).T
ren
dto
war
ds
US
abn
orm
alit
yre
mai
nin
gin
ten
do
ns
that
wer
est
ill
pai
nfu
l(p
=0
.07
)
Oh
ber
get
al.
[25
](2
00
4)
SC
,A
TE
L=
25
pat
ien
ts,
foll
ow
-up
of
Oh
ber
g2
00
4st
ud
yco
ho
rtM
ean
age
50
yea
rs,
76
%m
en,
72
%ac
tiv
e,4
%b
ilat
eral
Mea
n3
.8y
ears
:8
8%
retu
rned
top
re-i
nju
ryac
tiv
ity
/sat
isfi
edM
ean
3.8
yea
rs:
AP
dia
met
er;
14
%(p
\0
.00
5),
mo
reli
kel
ysa
tisfi
edif
stru
ctu
rere
solv
ed(8
6%
ver
sus
5%
;p\
0.0
01
)
Pao
lin
iet
al.
[38]
(20
04
)R
CT
,A
T1
.E
L?
pla
ceb
o=
33
pat
ien
tsM
ean
age
49
yea
rs,
62
%m
en,a
llm
idp
ort
ion
,29
%b
ilat
eral
2,
6,
12
,2
4w
eek
s:p
ain
(sca
lefr
om
0to
4)
wit
hac
tiv
ity;
21
–6
1%
,V
AS
pai
nw
ith
ho
pp
ing;
29
–5
4%
(wit
hin
gro
up
sig
nifi
can
cen
ot
rep
ort
ed)
2,
6,
12
,2
4w
eek
s:2
.4–
2.8
9:
inan
kle
pla
nte
rflex
or
mea
nto
tal
wo
rk(s
ign
ifica
nce
no
tg
iven
)2
.E
L?
GT
N=
31
pat
ien
ts
Pet
erso
net
al.
[39
](2
00
7)
RC
T,
AT
1.
EL
=3
7p
atie
nts
Mea
nag
e4
3y
ears
,6
0%
men
,9
2%
acti
ve,
all
had
mid
po
rtio
nsy
mp
tom
s,b
ilat
eral
=1
1%
6,
12
,5
4w
eek
s:1
0–
16
%im
pro
vem
ent
inA
mer
ican
Ort
ho
pae
dic
Fo
ot
and
An
kle
Ass
essm
ent
sco
re,
20
–6
0%
;in
VA
Sp
ain
wit
hac
tiv
ity
(p\
0.0
01
)
12
wee
ks:
no
sig
nifi
can
tch
ang
ein
ten
do
nA
Pd
iam
eter
2.
Air
hee
lb
race
35
pat
ien
ts
3.
EL
and
Air
hee
lb
race
=2
8p
atie
nts
Pu
rdam
etal
[27]
(20
04
)C
CT
,P
T1
.E
L=
8p
atie
nts
Mea
nag
e2
5y
ears
,7
5%
men
,al
lac
tiv
e(d
ecli
ne
squ
atg
rou
po
lder
,m
ore
fem
ales
and
mo
reb
ilat
eral
inju
ries
bu
tn
ot
sig
nifi
can
t)
12
wee
ks:
VA
Sp
ain;
sig
nifi
can
tly
inth
eE
Lg
rou
po
nly
(62
%;
p\
0.0
5).
Mo
rere
turn
edto
pre
-in
jury
acti
vit
yin
EL
gro
up
(75
%v
ersu
s1
1%
;p
=0
.04
)
NA
2.
EL
wit
ho
ut
dec
lin
eb
oar
d=
9p
atie
nts
Ro
mer
o-
Ro
dri
gu
ezet
al.
[43
](2
01
1)
SC
,P
TF
lyw
hee
l=
10
pat
ien
ts,
iner
tial
load
ing
usi
ng
fly
wh
eel
dev
ice
Mea
nag
e2
5y
ears
,al
lac
tiv
em
en,5
0%
bil
ater
al6
,12
wee
ks:
86
%im
pro
vem
ent
inV
ISA
(p\
0.0
1),
60
%;
inV
AS
pai
n(p
\0
.01
)
6w
eek
s:ec
cen
tric
forc
e:
90
%(p
=0
.03
),co
nce
ntr
icre
ctu
sfe
mo
ris
EM
G:
73
%(p
=0
.03
),n
och
ang
ein
con
cen
tric
forc
e,ec
cen
tric
rect
us
fem
ori
sE
MG
and
bil
ater
alC
MJ
hei
gh
t
Ro
mp
eet
al.
[21]
(20
07
)R
CT
,A
T1
.E
L=
25
pat
ien
tsM
ean
age
=4
9y
ears
,4
0%
men
,3
2%
acti
ve,
all
mid
po
rtio
n,
all
un
ilat
eral
16
wee
ks:
57
%im
pro
vem
ent
inV
ISA
-A(p
\0
.01
).N
oim
pro
vem
ent
inth
ew
ait-
and
-see
gro
up
.M
ore
pat
ien
tsco
mp
lete
lyre
cov
ered
or
mu
chb
ette
rin
the
EL
(60
%)
ver
sus
wai
tan
dse
eg
rou
p(2
4%
)[p
\0
.01
]
16
wee
ks:
no
chan
ge
inA
Pd
iam
eter
2.
ES
WT
=2
5p
atie
nts
3.
Wai
t-an
d-s
ee=
25
pat
ien
ts
Sh
alab
iet
al.
[45
](2
00
4)
SC
,A
TE
L=
25
pat
ien
tsM
ean
age
51
yea
rs,
64
%m
en,
40
%ac
tiv
e,al
lh
adm
idp
ort
ion
sym
pto
ms,
32
%b
ilat
eral
12
wee
ks:
40
%im
pro
vem
ent
in5
-po
int
pai
nsc
ale
(p\
0.0
1)
12
wee
ks:
ten
do
nC
SA
;1
4%
(p\
0.0
5),
intr
aten
din
ou
ssi
gn
alin
ten
sity
;2
3%
(p\
0.0
5),
pai
nsc
ore
po
stco
rrel
ated
wit
hch
ang
ein
sig
nal
/no
tv
olu
me
Loading of Achilles and Patellar Tendinopathy
-
Tab
le4
con
tin
ued
Stu
dy
(yea
r)D
esig
nG
rou
ps,
inte
rven
tio
ns
Par
tici
pan
tch
arac
teri
stic
saC
lin
ical
ou
tco
me
Mec
han
isti
co
utc
om
es
Sil
ber
nag
elet
al.
[30
](2
00
1)
RC
T,
AT
1.
Co
mb
ined
=2
2p
atie
nts
,ca
lfra
ises
,b
alan
ce,
then
ecce
ntr
iclo
adin
g,
then
add
edsp
eed
Mea
nag
e4
4y
ears
,7
7%
men
,al
lm
idp
ort
ion
and
acti
ve
(ex
cep
t1
pat
ien
tin
gro
up
2),
41
%b
ilat
eral
12
,2
6w
eek
s:V
AS
wal
kin
g(4
0%
)an
dp
ain
wit
hp
alp
atio
n(2
9–
57
%);
inco
mb
ined
gro
up
on
ly(p
\0
.05
)
26
wee
ks:
VA
Sac
tiv
ity;
inb
oth
gro
up
s(5
7–
80
%),
also
;in
com
bin
edg
rou
pat
6w
eek
s(4
4%
)[p
\0
.05
].1
2m
on
ths:
com
bin
edg
rou
pm
ore
lik
ely
sati
sfied
(78
%v
ersu
s3
8%
;p\
0.0
5)
and
con
sid
ered
them
selv
esre
cov
ered
(60
%v
ersu
s3
8%
,p\
0.0
5),
no
sig
nifi
can
td
iffe
ren
cein
retu
rnto
pre
-in
jury
acti
vit
y(5
5%
com
bin
ed,
35
%ca
lfra
ise/
stre
tch
ing
)
6,
12
,2
6w
eek
s:ca
lfen
du
ran
ce:
14
–3
0%
bo
thg
rou
ps,
no
gro
up
dif
fere
nce
s.1
2,
26
wee
ks:
:C
MJ
hei
gh
t7
–3
0%
bo
thg
rou
ps,
calf
rais
e/st
retc
hin
gg
rou
pal
so:
at6
wee
ks,
no
gro
up
dif
fere
nce
s.2
6w
eek
s:P
FR
OM
:4
%co
mb
ined
gro
up
on
ly.
No
chan
ge
inD
Fat
any
tim
e
2.
Cal
fra
ises
and
stre
tch
ing
=1
8p
atie
nts
Sil
ber
nag
elet
al.
[23
](2
00
7)
RC
T,
AT
1.
Co
mb
ined
=1
9p
atie
nts
,id
enti
cal
toS
ilb
ern
agel
20
01
bu
tad
ded
ho
pp
ing
Mea
nag
e4
6y
ears
,5
3%
men
(mo
rew
om
eng
rou
p2
),al
lm
idp
ort
ion
and
acti
ve,
34
%b
ilat
eral
6,
12
,2
4,
52
wee
ks:
VIS
A-A
imp
rov
emen
tin
bo
thg
rou
ps
(p\
0.0
1,
up
to6
0%
com
bin
ed,
up
to4
9%
com
bin
ed?
spo
rt),
no
dif
fere
nce
bet
wee
nth
eg
rou
ps
6,
12
,2
6,
52
wee
ks:
:ec
cen
tric
-co
nce
ntr
icw
ork
20
–2
9%
(p\
0.0
5)
[no:
at1
2w
eek
sin
gro
up
1].
12
,2
6,
52
wee
ks:
:ec
cen
tric
-co
nce
ntr
icto
e-ra
ise
po
wer
17
–2
6%
gro
up
2o
nly
(p\
0.0
5)
[on
ly:
at6
wee
ks
ing
rou
p1
],n
och
ang
ein
con
cen
tric
toe-
rais
ep
ow
erin
eith
erg
rou
p.
26
wee
ks:
:d
rop
CM
Jh
eig
ht
11
%,:
ho
pq
uo
tien
t2
7%
,g
rou
p2
on
ly(p
\0
.05
).N
och
ang
ein
CM
Jh
eig
ht
inei
ther
gro
up
.6
,2
6w
eek
s:;
DF
RO
M5
–6
%,
gro
up
2o
nly
(p\
0.0
5)
2.
Co
mb
ined
?co
nti
nu
edsp
ort
=1
9p
atie
nts
Sil
ber
nag
elet
al.
[41
](2
00
7)
SC
,A
TC
om
bin
ed=
37
pat
ien
tsM
ean
age
46
yea
rs,
54
%m
en,
all
had
mid
po
rtio
nsy
mp
tom
s
12
mo
nth
s:5
9%
imp
rov
emen
tin
VIS
A-A
on
sym
pto
mat
icsi
de
(p\
0.0
5),
67
%cl
assi
fied
asfu
lly
reco
ver
ed(V
ISA
-AC
90
)
12
mo
nth
s:lo
wco
rrel
atio
nb
etw
een
VIS
A-A
sco
res
and
test
bat
tery
(r=
0.1
8;
p=
0.4
1)
(cal
fra
ise
end
ura
nce
,d
rop
CM
Jh
eig
ht,
ho
pp
ing
ply
om
etri
cq
uo
tien
t,co
nce
ntr
icto
e-ra
ise
po
wer
,ec
cen
tric
toe-
rais
ep
ow
er).
On
lyd
rop
CM
Jh
eig
ht
was
sig
nifi
can
tly
corr
elat
edw
ith
VIS
A-A
sco
res
(r=
0.1
78
;p
=0
.61
,p\
0.0
1).
Am
on
gth
e‘f
ull
yre
cov
ered
’p
atie
nts
,2
5%
had
C9
0%
of
un
affe
cted
sid
eo
nfu
nct
ion
alte
stb
atte
ry
P. Malliaras et al.
-
Tab
le4
con
tin
ued
Stu
dy
(yea
r)D
esig
nG
rou
ps,
inte
rven
tio
ns
Par
tici
pan
tch
arac
teri
stic
saC
lin
ical
ou
tco
me
Mec
han
isti
co
utc
om
es
Sil
ber
nag
elet
al.
[40
](2
01
1)
SC
,A
TC
om
bin
ed=
34
pat
ien
ts,
foll
ow
-u
po
fS
ilb
ern
agel
20
07
stu
dy
coh
ort
Mea
nag
e5
1y
ears
,5
3%
men
,al
lac
tiv
ean
dh
adm
idp
ort
ion
sym
pto
ms
5y
ears
:fu
nct
ion
alev
alu
atio
nam
on
g1
3p
atie
nts
wh
ow
ere
asy
mp
tom
atic
,5
pat
ien
tsw
ho
had
con
tin
ued
sym
pto
ms
5y
ears
:d
efici
tb
etw
een
affe
cted
and
un
affe
cted
sid
e—as
ym
pto
mat
ics:
9%
for
ecce
ntr
ic-c
on
cen
tric
wo
rk(p
=0
.09
),1
4%
for
con
cen
tric
po
wer
(p=
0.0
4).
No
defi
cit
for
ecce
ntr
ic-c
on
cen
tric
po
wer
,d
rop
CM
Jh
eig
ht,
ho
pq
uo
tien
t.C
on
tin
ued
sym
pto
mat
ics
had
an1
8%
defi
cit
for
con
cen
tric
po
wer
(p=
0.0
3)
Van
der
Pla
set
al.
[42
](2
01
2)
SC
,A
TE
L=
46
pat
ien
ts,
foll
ow
-up
of
de
Jon
ge
20
10
stu
dy
coh
ort
Mea
nag
e5
1y
ears
,9
1%
acti
ve,
all
had
mid
po
rtio
nsy
mp
tom
s,2
6%
bil
ater
al
5y
ears
:7
0%
imp
rov
emen
tin
VIS
A-A
fro
mb
asel
ine
(p\
0.0
01
),1
2%
imp
rov
emen
tin
VIS
A-A
fro
m1
yea
r(p
=0
.00
6)
5y
ears
:A
P;
7%
(p=
0.0
51
),D
op
ple
rp
rese
nt
59
%b
asel
ine
and
47
%at
foll
ow
-up
(p[
0.0
5).
VIS
A-A
chan
ge
and
at5
yea
rsw
asn
ot
asso
ciat
edw
ith
bas
elin
eD
op
ple
r.P
ain
pre
sen
cean
dV
ISA
-Aat
5y
ears
no
tco
rrel
ated
wit
hb
asel
ine
AP
dia
met
er
Vis
nes
etal
.[1
1](2
00
5)
RC
T,
PT
1.
EL
=1
3ac
tiv
eat
hle
tes
Mea
nag
e2
7y
ears
,6
5%
men
,v
oll
eyb
all
pla
yer
s,4
2%
bil
ater
al
12
,1
8w
eek
s:n
osi
gn
ifica
nt
chan
ge
inV
ISA
sco
res,
no
sig
nifi
can
td
iffe
ren
ceto
con
tro
lg
rou
p
12
wee
ks:
:b
ilat
eral
CM
Jh
eig
ht
(1.2
cm,
p=
0.0
46
)in
ET
gro
up
.S
Jh
eig
ht
(un
i-,
bil
ater
al),
CM
Jh
eig
ht
(un
ilat
eral
)n
och
ang
eei
ther
gro
up
2.
Co
ntr
ol
=1
6ac
tiv
eat
hle
tes
Yo
un
get
al.
[31]
(20
05
)R
CT
,P
T1
.E
L=
9ac
tiv
eat
hle
tes
Mea
nag
e2
7y
ears
,7
7%
men
,v
oll
eyb
all
pla
yer
s1
2m
on
ths:
mo
reli
kel
ycl
inic
ally
sig
nifi
can
tV
ISA
chan
ge
inE
Lg
rou
p(9
4%
ver
sus
41
%)
NA
2.
Sta
nis
han
dC
urw
in=
8ac
tiv
eat
hle
tes
AP
ante
rop
ost
erio
r,A
TA
chil
les
ten
do
n,
CC
Tco
ntr
oll
edtr
ial,
CL
con
cen
tric
load
ing
,C
MJ
cou
nte
rmo
vem
ent
jum
p,
CSA
cro
ss-s
ecti
on
alar
ea,
do
rsifl
exio
n,
EL
ecce
ntr
iclo
adin
g,
ESW
TE
xtr
aco
rpo
real
sho
ckw
ave
ther
apy
,E
MG
elec
tro
my
og
rap
hic
acti
vit
y,
GT
Ng
lyce
rol
tri-
nit
rate
,H
SRh
eav
ysl
ow
resi
stan
ce,
HP
hy
dro
xy
lysy
lp
irid
ino
lin
e,IE
Lis
ok
inet
icec
cen
tric
load
ing
,L
Ply
syl
py
rid
ino
lin
e,M
RI
mag
net
icre
son
ance
imag
ing
,M
VC
max
imal
vo
lun
tary
con
trac
tio
n,
NA
no
tap
pli
cab
le,
PF
pla
nte
rflex
ion
,P
Tp
atel
lar
ten
do
n,
RC
Tra
nd
om
ized
con
tro
lled
tria
l,R
OM
ran
ge
of
mo
tio
n,
RM
rep
etit
ion
max
imu
m,
SCsi
ng
leco
ho
rt,
SJsq
uat
jum
p,
US
ult
raso
un
dim
agin
g,
VA
Sv
isu
alan
alo
gu
esc
ore
,V
ISA
Vic
tori
anIn
stit
ute
of
Sp
ort
Ass
essm
ent,
VIS
A-A
VIS
A-
Ach
ille
sv
ersi
on
:,in
dic
ates
incr
ease
;;,
ind
icat
esd
ecre
ase
aM
ean
age,
gen
der
,u
ni-
ver
sus
bil
ater
al,
mid
po
rtio
nv
ersu
sin
sert
ion
(fo
rA
To
nly
)an
dac
tiv
ity
.A
llim
agin
gst
ud
ies
use
ult
raso
un
dex
cep
tfo
rS
hal
abi
etal
.[1
01]
and
Gar
din
etal
.[4
8]
(MR
I)
Loading of Achilles and Patellar Tendinopathy
-
calf endurance and jump performance is greater with Sil-
bernagel-combined loading versus calf raises/stretching[30]. There is moderate evidence from one high-quality and
three-low quality studies, showing that (i) improved clinical
outcomes are associated with improved jump performance[23, 30] (ii) improved clinical outcomes are associated with
increased calf power [23] (iii) calf power and jump perfor-
mance is greater with Silbernagel-combined loading whensport is continued [23] (iv) improvement in clinical
outcomes is not associated with resolution in side-to-sidedeficits in various functional measures (planterflexor
endurance, torque, power and work, jump and hop tests) [40,
41]. There is conflicting clinical evidence from one high-quality and one low-quality study that improved clinical
outcomes are associated with increased planterflexion and
decreased dorsiflexion range of motion [23, 30].
3.3.1.1.3 Other Loading. There is limited evidence from
one low-quality study that improved clinical outcomes are
associated with increased planterflexor torque followingStanish and Curwin loading but not isotonic loading [37],
and increased planterflexor torque following isokinetic
loading [47].
3.3.1.2 Imaging Measures
3.3.1.2.1 Eccentric Loading. There is conflicting evi-
dence from seven low-quality studies, which show thatimproved clinical outcomes are associated with
(i) decreased anteroposterior diameter [21, 25, 33, 39, 42];
(ii) a decrease in the proportion of tendons containingDoppler signal [22, 24, 42] (one study is high quality and
shows no change in the proportion of tendons containing
Doppler signal) [22]. There is conflicting evidence from twolow-quality studies that investigate the same cohort at dif-
ferent times and found that improved clinical outcomes are
associated with decreased cross-sectional area (CSA) [45,48]. There was only one high-quality study that showed no
change in tendon dimensions in association with reduced
symptoms (anteroposterior diameter) [21]. There is mod-erate evidence from one high-quality and four low-quality
studies, which show that (i) imaging (Doppler presence and
anteroposterior diameter at baseline, change in anteropos-terior diameter) does not predict a change in symptoms
[22, 33, 42] (ii) improved clinical outcomes following
isokinetic loading are associated with decreased intraten-dinous signal intensity [45, 48].
3.3.1.2.2 Other Loading. There is limited evidence from
one low-quality study that improved clinical outcomesfollowing isokinetic loading are associated with a decrease
in the proportion of abnormal tendons on greyscale ultra-
sound [47].
3.3.1.3 Biochemical and Blood Flow
3.3.1.3.1 Eccentric Loading. There is limited evidence
from two low-quality studies, showing that improvedclinical outcomes are associated with (i) an increase in type
I collagen synthesis [49], but not associated with reduced
glutamate concentration [51]; (ii) reduced Achilles tendoncapillary blood flow and post-capillary filling pressure [44].
3.3.2 Patellar
3.3.2.1 Neuromuscular and Jump Performance Outcomes
3.3.2.1.1 Eccentric Loading. There is moderate evidencefrom two high-quality studies, which showed that improved
clinical outcomes are associated with (i) increased knee
extensor torque [19]; (ii)increased leg press 1-repetitionmaximum (1RM) [18]; (iii) increased quadriceps muscle
CSA [19]. There is conflicting evidence from two high-
quality studies that improved clinical outcomes are notassociated with improved jump performance [11, 18].
3.3.2.1.2 Heavy-Slow Resistance (HSR) Loading. There
is strong evidence from two high-quality studies thatimproved clinical outcomes are associated with increased
knee extensor torque [19, 20]. There is moderate evidence
from one high-quality study that improved clinical out-comes are associated with increased quadriceps muscle
CSA [19].
3.3.2.1.3 Stanish and Curwin Loading. There is limitedevidence from one low-quality study that improved clinical
outcomes are associated with increased knee flexor but not
extensor torque [29]. There is limited evidence from onelow-quality study that there is no group difference in
change in knee flexor and extensor torque between Stanish
and Curwin and isotonic loading [29].
3.3.2.1.4 Other Loading. There is limited evidence from
two low-quality studies, which showed that; (i) torque
deficits resolve following isokinetic loading [47] (ii)improved clinical outcomes are associated with increased
eccentric force on a flywheel device (but not concentric
force), but no change in jump performance following fly-wheel loading [43].
3.3.2.2 Imaging, Structural and Mechanical PropertyOutcomes
3.3.2.2.1 Eccentric Loading. There is moderate evidence
from one high-quality study, which showed that
(i) improved clinical outcomes are not associated withreduced Doppler area and anteroposterior diameter [19];(ii)
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increase in CSA is greater following eccentric, compared
with HSR loading [19];(iii) improved clinical outcomes arenot associated with change in tendon stiffness and modulus
[19].
3.3.2.2.2 HSR. There is moderate evidence from twohigh-quality studies, which showed that improved clinical
outcomes are associated with (i) reduced Doppler area and
anteroposterior diameter [19]; (ii) increased fibril density,decreased fibril mean area and no change in fibril volume
fraction [20]. There is conflicting evidence from two high-quality studies that improved clinical outcomes are asso-
ciated with a decrease in tendon stiffness and modulus
[19, 20].
3.3.2.3 Biochemical Outcomes
3.3.2.3.1 Eccentric Loading. There is moderate evidence
from one high-quality study that improved clinical out-comes are not associated with change in collagen content,
hydroxylysyl pyridinoline (HP) and lysyl pyridinoline (LP)
concentration, HP/LP ratio, and pentosidine concentration[19].
3.3.2.3.2 HSR Loading. There is moderate evidence
from one high-quality study that collagen content, HP andLP concentration do not change but HP/LP ratio increases
and pentosidine concentration decreases alongside
improved clinical outcomes [19].
4 Discussion
4.1 Comparison of Loading Programmes
Ten studies were identified that compared loading pro-
grammes in Achilles and patellar tendinopathy. Only two
studies, both investigating patellar tendinopathy, were highquality [11, 19]. Although the Alfredson eccentric loading
model is a popular clinical intervention, there is limited
evidence in the Achilles tendon to support its use whencompared with other loading programmes. There was
limited evidence from one study that patient satisfaction/
return to preinjury activity is greater following eccentriccompared with concentric loading in the Achilles tendon
[32]. This evidence should be interpreted with caution, as
the concentric group performed different exercises that arelikely to have involved a much lower load (i.e. non- or
partial weightbearing initially). The Silbernagel-combined
loading programme incorporates eccentric-concentric,eccentric and then faster loading and has been investigated
in four Achilles tendon studies. There is limited evidence
that this programme offers superior clinical outcomes to
eccentric-concentric calf raises and stretching alone [30]. It
is important for clinicians to appreciate that there is asmuch evidence for the Silbernagel-combined programme
as there is for the Alfredson eccentric programme when
comparing them to other loading programmes in Achillestendinopathy. The gradual progression from eccentric-
concentric to eccentric followed by faster loading may
benefit patients who are unable to start with an Alfredsoneccentric programme due to pain or calf weakness.
In the patellar tendon, there is conflicting evidence thateccentric loading is superior to other loading programmes.
There is limited evidence that VISA improvement is
greater following eccentric loading compared with con-centric loading [36], and Stanish and Curwin loading [31]
in patellar tendinopathy. However, there is moderate evi-
dence that eccentric loading is equivalent on VISA out-comes and inferior on patient subjective satisfaction to
HSR loading [19]. HSR loading is performed three times
per week rather than twice daily, and this may explain thegreater patient satisfaction. Good-quality evidence is
lacking for both Achilles and patellar tendinopathy, but
there is clearly benefit from loading programmes thatinvolve eccentric-concentric muscle actions.
Some studies investigated tendon loading prior or during
a competition phase. Young et al. [31] found that sloweccentric decline squats preseason, led to superior post-
volleyball season patellar tendon VISA outcomes than that
of the Stanish and Curwin loading. Visnes et al. [11] foundeccentric decline squatting did not improve patellar tendon
VISA outcomes when performed during a volleyball sea-
son. Silbernagel et al. [23] found continued sport activitydid not compromise clinical outcomes at 12 months, as
long as sport was gradually introduced to ensure minimal
pain during and after loading. Continuing sport withrehabilitation may be more successful in Achilles tenden-
opathy, as sport load may be lower than typical patellar
tendon loads in some sports (e.g. volleyball).
4.2 Mechanisms of Achilles and Patellar Tendon
Loading Programmes
4.2.1 Neuromuscular Performance and Muscle Size
Loading was shown to be associated with improved neu-
romuscular outcomes (e.g. 1RM torque) in most studies.
The highest level of evidence supported eccentric andSilbernagel-combined loading in the Achilles (moderate
evidence) [23, 30, 34, 35] and HSR loading in the patellar
tendon (strong evidence) [19, 20]. There is limited evi-dence for Stanish and Curwin and isokinetic loading in the
Achilles [37, 47] and evidence for eccentric (moderate) and
flywheel (limited) in the patellar tendon [19, 43]. There isalso limited evidence that quadriceps size increase is
Loading of Achilles and Patellar Tendinopathy
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similar following HSR and eccentric loading in the patellar
tendon [19]. Overall, Silbernagel and eccentric loading inthe Achilles and HSR loading in the patellar have the
highest level of evidence for improving neuromuscular
function in Achilles and patellar tendinopathy.Although eccentric loading is often linked with greater
muscle-tendon unit load and adaptation, this systematic
review did not identify any evidence of this among ten-dinopathy patients. Among normal participants, eccentric
loading results in greater muscle strength gains andhypertrophy (especially type II fibres) than concentric
loading [52], but not when the load is equalized [52],
suggesting load intensity rather than contraction type is thestimulus. There is an unfounded perception among many
clinicians that eccentric muscle action always leads to
greater muscle-tendon unit load than concentric and iso-metric contractions. During eccentric muscle action, there
are less active motor units than concentric contraction
when external load and speed are constant, with lessresultant muscle EMG activity [53, 54] and oxygen con-
sumption [55, 56]. This increases the force potential with
eccentric contraction, but this potential can only be realizedvia the following two mechanisms:(i) if the external load is
greater than the maximal concentric and isometric load
capability; and (ii) by increasing the speed of eccentriccontraction under load, as predicted by the force-velocity
curve [55, 57] (Fig. 2). For example, when a sprinter
increases running speed the hamstring muscle-tendonduring limb deceleration will increase. Therefore, clinical
eccentric loading among tendinopathy patients may not
lead to a greater change in neuromuscular outcomesbecause load intensity is often not maximized [11, 19, 45].
Clinically, the load potential of eccentric contractions may
be limited by symptom irritability.
4.2.2 Power and Jump Performance
There is moderate evidence, which shows that calf power
and jump performance improves alongside symptoms fol-
lowing Silbernagel-combined loading but only at 6 months[23, 30], and there is moderate evidence, which shows that
improvement in both outcomes is greater if sport is con-tinued [23]. Continued sport, as long as symptoms are
stable, seems to have a specific effect on these power
outcomes, which is not gained even with the Silbernagel-combined programme that includes faster calf loading and
stretch-shorten cycle rehabilitation. In contrast, there is
moderate evidence that jump performance is not associatedwith clinical improvement in patellar tendinopathy fol-
lowing eccentric [11, 18], and limited evidence following
flywheel loading [43], even though sport was continued inthese studies based on pain monitoring. A recent systematic
review found some evidence for increased vertical jump
performance in patellar tendon patients compared withasymptomatic cohorts, which may partly explain this
finding [58].
4.2.3 Do Side-to-Side Neuromuscular and JumpPerformance Deficits Resolve?
Side-to-side deficits (e.g. torque, work, endurance) were
only evaluated in the Achilles tendon. There is moderate
[34, 35, 47] evidence that deficits resolve in the short term(10–12 weeks), but also that they are present at longer-term
follow up (12 months to 5 years) [40, 41]. It is possible that
deficits recur when rehabilitation ceases, indicating thatperformance may need to be maintained with ongoing
loading.
4.2.4 Imaging, Structure and Biochemicals
The only evidence for change in imaging measures in theAchilles tendon is decreased intratendinous signal inten-
sity on magnetic resonance imaging (MRI) following
eccentric loading (moderate evidence) [45, 48]. Thisreview did not identify any evidence that tendon dimen-
sions (anteroposterior diameter, CSA) and the proportion
of tendons with Doppler signal change following Achilleseccentric loading, despite limited evidence for increased
collagen type 1 production. In the patellar tendon,
improved clinical outcomes were not associated withreduced Doppler area and anteroposterior diameter in
eccentric loading, but they were following HSR (moderate
evidence) [19]. There is also moderate evidence, that HSR
Fig. 2 Force velocity curve. LO isometric length, PO maximumisometric tension, Vmax maximum velocity (reproduced from Leiber[57], with permission from Lippincott, Williams and Wilkins)
P. Malliaras et al.
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is less likely to lead to increased patellar tendon CSA, and
more likely to lead to increased pentosidine concentrationand HP/LP ratio, indicative of collagen turnover [19]. This
suggests that HSR has