Professional Documents
Culture Documents
dislocation (Review)
This is a reprint of a Cochrane review, prepared and maintained by The Cochrane Collaboration and published in The Cochrane Library
2011, Issue 11
http://www.thecochranelibrary.com
1 Department of Trauma & Orthopaedic Surgery, Watford General Hospital, Watford, UK. 2 School of Allied Health Professions,
University of East Anglia, Norwich, UK. 3 School of Medicine, Health Policy and Practice, University of East Anglia, Norwich, UK
Contact address: Caroline B Hing, Department of Trauma & Orthopaedic Surgery, Watford General Hospital, Vicarage Road, Watford,
WD18 0HB, UK. CaroH2712@aol.com.
Citation: Hing CB, Smith TO, Donell S, Song F. Surgical versus non-surgical interventions for treating patellar dislocation. Cochrane
Database of Systematic Reviews 2011, Issue 11. Art. No.: CD008106. DOI: 10.1002/14651858.CD008106.pub2.
Copyright © 2012 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
ABSTRACT
Background
Patellar dislocation occurs when the patella disengages completely from the trochlear (femoral) groove. Following reduction of the
dislocation, conservative rehabilitation with physiotherapy may be used. Since recurrence of dislocation is common, some surgeons
have advocated surgical intervention in addition to rehabilitation.
Objectives
The purpose of this review was to assess the clinical and radiological outcomes of surgical, compared with non-surgical, interventions
for treating people with primary or recurrent patellar dislocation.
Search methods
We searched the Cochrane Bone, Joint and Muscle Trauma Group’s Specialised Register, the Cochrane Central Register of Controlled
Trials (The Cochrane Library), MEDLINE, EMBASE, AMED, CINAHL, ZETOC, Physiotherapy Evidence Database (PEDro), and
a variety of other literature databases and trial registries. Corresponding authors were contacted to identify additional studies. Date
searched: August 2010.
Selection criteria
Eligible for inclusion were randomised and quasi-randomised controlled clinical trials evaluating surgical versus non-surgical interven-
tions for treating lateral patellar dislocation.
Two reviewers independently examined titles and abstracts of each identified study to assess study eligibility, extract data and assess risk
of bias. Primary outcomes assessed were the frequency of recurrent dislocation, and validated patient-rated knee or physical function
scores. When appropriate, data were pooled. Risk ratios were calculated for dichotomous outcomes, and mean differences for continuous
outcomes.
Surgical versus non-surgical interventions for treating patellar dislocation (Review) 1
Copyright © 2012 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
Main results
Five studies (339 participants) were included. All studies had methodological shortcomings, especially the two quasi-randomised trials
that presented a high risk for selection bias. Follow-up was a minimum of two years in two studies and between five and seven years
in three studies. There was no significant difference between surgical and non-surgical management of primary (first-time) patellar
dislocation in the risk of recurrent dislocation (47/182 versus 53/157; risk ratio 0.81, 95% confidence interval 0.56 to 1.17; 5 trials),
Kujala patellofemoral disorder scores (mean difference 3.13, 95% confidence interval -7.34 to 13.59; 5 trials) nor the requirement
for subsequent surgery (risk ratio 1.09, 95% CI 0.72 to 1.65; 3 trials). Adverse events were reported by one trial, citing four major
complications that occurred in the surgical group. No randomised controlled trials have assessed populations with recurrent patellar
dislocation.
Authors’ conclusions
There is insufficient high quality evidence to confirm any significant difference in outcome between surgical or non-surgical initial
management of people following primary patellar dislocation, and none examining this comparison in people with recurrent patellar
dislocation. Adequately powered randomised, multi-centre controlled trials, conducted and reported to contemporary standards are
recommended.
The patella or knee cap is a lens shaped bone situated at the front of the knee. It is incorporated into the tendon of the quadriceps
muscles of the thigh and moves within a groove at the lower end of the thigh bone (femur). Patellar dislocation occurs when the patella
completely moves out of this groove. It commonly occurs in young and physically active people, often during sporting activities.
When the patella dislocates, injury to the soft tissues of the knee joint occurs, which requires a period of rehabilitation. This may
include treatments such as immobilisation and bracing to limit knee movement, exercises, manual therapy, taping and electrotherapeutic
modalities. Some surgeons have suggested that people may have a better outcome if surgical procedures repairing or reconstructing the
injured soft tissues, or carrying out other procedures to restrain the knee cap from dislocating again.
This Cochrane review included five studies (339 participants) which have looked at the results of surgery compared with non-surgical
treatment alone for people who have sustained a knee cap dislocation. All the trial participants were being treated for a primary (first-
time) dislocation. These studies were small and had some weaknesses in their design and conduct.
Based on pooled data from all five studies, the review found no significant differences between surgical and non-surgical management
for risk of recurrent dislocation or in the scores of a condition-related knee outcome measure. The pooled data from three studies
indicated no difference between the treatment groups for the need for subsequent operations. The only study reporting complications
reported that all four treatment complications occurred in the surgical management group.
The review concluded that there was insufficient evidence to confirm a significant difference in outcome between surgical or non-
surgical initial management of people who have sustained a patellar dislocation. Further research is recommended.
Assessment of heterogeneity
Data extraction and management
We appraised the clinical diversity in terms of participants, inter-
Two authors (TS and CH) independently extracted data from trial
ventions and outcomes for the included studies. Statistical hetero-
reports. We contacted corresponding authors when key informa-
geneity was assessed by visual inspection of the forest plot and by
tion was missing. In cases of disagreement, a consensus was sought
using the I² and Chi² statistical tests.
through discussion or adjudication by a third author (SD). Once
completed, these data were synthesised to form a comprehensive
and agreed data extraction table. This presented all key trial data Assessment of reporting biases
and participant information from the included articles.
Outcome reporting bias was assessed by considering the effects
of missing data on measured outcomes. Had sufficient data been
available (from at least 10 trials), we planned to assess publication
Assessment of risk of bias in included studies bias using funnel plots.
Two authors (TS and CH) independently assessed the risk of bias
of the included studies using The Cochrane Collaboration’s ’Risk
Data synthesis
of bias’ tool (Higgins 2011). Risk of bias was categorised as low,
uncertain or high for each of the included studies. If differences The main characteristics and results of included studies were de-
between the ratings of the two assessors could not be resolved scriptively summarised. When judged appropriate, results from
through discussion, a third author (SD) was asked to adjudicate. individual studies was quantitatively pooled in meta-analyses us-
ing fixed- or random-effects models (depending on the results of
heterogeneity tests) and 95% confidence intervals (CI).
Figure 1. Risk of bias graph: review authors’ judgements about each risk of bias item presented as
percentages across all included studies.
Effects of interventions
Blinding
None of the studies reviewed blinded their assessors to treatment
Primary outcomes
allocation. Due to the design of these studies, and the topic under
investigation, it would have been very difficult, if not impossible, to
Recurrent dislocation
blind treating clinicians to treatment allocation, or participants to
their allocation intervention. All were assessed as carrying ’unclear’ All five studies reported the findings of the frequency of recur-
risk of bias, with the exception of Christiansen 2008 which was rent dislocation after surgery compared with non-surgical inter-
assessed at high risk of bias, as the study report clearly states that ventions.
the control group ’received no further treatment or brace usage’. Pooling of data from all five trials showed no significant difference
between surgical and non surgical management (47/182 versus
53/157; RR 0.81, 95% CI 0.56 to 1.17; Analysis 1.1; Figure 3).
Incomplete outcome data There was no significant difference in the risk ratio between the
Small losses to follow-up, assessed as carrying ’unclear risk of bias’ minimum two year and five to seven year follow-up periods (test
were reported in all but one study (Camanho 2009) which was for subgroup differences: Chi² = 0.32, df = 1 (P = 0.57), I² = 0%).
Figure 3. Forest plot of comparison 1. Surgical versus non-surgical management. Outcome: 1.1 Number of
participants sustaining recurrent patellar dislocation.
Figure 4. Forest plot of comparison 2. Surgical versus non-surgical management. Patient reported
outcomes. Outcome: 2.1 Kujala patellofemoral disorder score (2 years or more follow-up).
Secondary outcomes
Hughston VAS patellofemoral score
The Hughston VAS patellofemoral score was evaluated in two
studies (Nikku 1997; Palmu 2008). The pooled data (Analysis 2.2) Other knee function and activity scores
demonstrated a difference between the treatment groups (MD - Nikku 1997 conducted performance tests consisting of timed ’fig-
4.07, 95% CI -7.85 to -0.29). ure-of-eight’ running, one leg hop distance, maximum number of
squat downs in one minute, reporting a significantly better squat
result (P = 0.03) and superior timed ’figure-of-eight’ run perfor-
Other validated patient-rated knee and physical function
mance (P = 0.004) in the adults in the non-surgical group com-
scores
pared with the surgery group. There was, however, no statistically
Three trials reported the Tegner activity score. Pooled data from significant difference in one-leg hop quotient between the inter-
Nikku 1997, Palmu 2008 and Sillanpaa 2009 showed no statisti- ventions (P = 0.8). Patient reported outcomes of activity level were
cally significant difference between groups (MD = -0.46, 95% CI evaluated in Sillanpaa 2009. They reported that there was no sta-
-0.96 to 0.05; P = 0.08; Analysis 2.3). tistically significant difference in the subjective assessment of pain
The Knee Injury and Osteoarthritis Outcome Score (KOOS) was and functional knee limitations for stairs, running and squatting
assessed by Christiansen 2008, who found small non-significant (P > 0.05).
differences between surgical and non-surgical intervention groups
at two years in respect to the KOOS symptoms, pain, ADL, sports
and recreation or quality of life subsections (P > 0.05). The results Return to pre-injury activities
from this analysis are presented in Analysis 2.4. Sillanpaa 2009 reported no statistically significant difference be-
Finally, the Lysholm knee score was reported by Nikku 1997, who tween their surgical and non-surgical groups in respect to the fre-
found no statistically significant difference between the two groups quency of participants who regained the same activity level as be-
(MD 1.00, 95% CI -4.63 to 2.63; P = 0.6) at two year follow-up fore their dislocation (13/17 versus 15/21; RR 1.07 95% CI 0.73
(see Analysis 2.5). to 1.56; P = 0.73; analysis not shown).
Surgical versus non-surgical interventions for treating patellar dislocation (Review) 10
Copyright © 2012 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
Knee pain The proportion of participants in each group reporting an episode
Two studies assessed knee pain using a visual analogue scale (VAS), or episodes of patellar subluxation during follow up was reported
one at two year follow-up (Nikku 1997) and the other at medium in three studies (Camanho 2009; Nikku 1997; Sillanpaa 2009).
of seven years (Sillanpaa 2009). Overall, pooled data (Analysis There was no significant difference between groups (RR 0.67, 95%
2.6) showed a statistically difference between treatment groups CI 0.23 to 1.94; Analysis 1.2).
with significantly lower pain scores for the non-surgical group The number of participants in each group suffering episodes of
(MD 0.51, 95% CI 0.10 to 0.93). However, this pooled analysis instability (dislocation, subluxation, or both) was reported in three
exhibited substantial heterogeneity (Chi² = 5.50, df = 1 (P = 0.02), studies (Camanho 2009; Nikku 1997; Sillanpaa 2009). Pooled
I² = 82%). data showed that surgical treatment was associated with a statis-
tically significant reduction in episodes of instability during par-
ticipant follow-up (RR 0.70, 95% CI 0.54 to 0.90; Analysis 1.3).
However, this significant difference was lost (RR 0.80, 95% CI
Complications / adverse events of interventions
0.62 to 1.03) on removal of Camanho 2009, a study judged at
Only one study (Nikku 1997) reported on adverse effects. All four high risk of bias on account of incomplete outcome data.
’major’ complications occurred in the surgical group. Paresis of the
sciatic nerve, possibly due to tourniquet compression and resulting
in severe permanent disability, was reported in one participant in Patient satisfaction
the surgical group. A deep wound infection and bacterial arthritis, Patient satisfaction was assessed in two studies (Nikku 1997;
which resolved with revision surgery and antibiotic therapy, oc- Palmu 2008). Overall, pooled data (Analysis 2.7) showed a sta-
curred in one operated participant. A superficial wound infection tistically difference between treatment groups with a significantly
and a burn injury on the insensible anterior aspect of the knee greater frequency of good to excellent patient satisfaction out-
occurred in one participant. comes in the non-surgical treatment group (RR 0.61, 95% CI
0.44 to 0.84). However, this pooled analysis exhibited substantial
heterogeneity (Chi² = 2.39, df = 1 (P = 0.12), I² = 58%).
Range of knee motion
Range of knee motion was assessed in one study (Sillanpaa 2009).
Subsequent requirement for surgery
There was no statistically significant difference in total knee range
of motion of the affected knee between surgical (median 138 de- Three studies (Nikku 1997; Palmu 2008; Sillanpaa 2009) reported
grees) and non-surgical (median 140 degrees) interventions at the the number of participants in each group who had undergone
seven year follow-up (P > 0.05). subsequent surgical intervention by five to seven year follow-up.
There was no statistically significant difference between groups
(36/123 versus 27/106; RR 1.09, 95% CI 0.72 to 1.65; Analysis
1.4; Figure 5). Several participants in both Nikku 1997 and Palmu
Patient-reported instability symptoms
2008 had more than one operation.
Figure 5. Forest plot of comparison: 1 Surgical versus non-surgical management. Recurrent instability
episodes, outcome: 1.4 Number of participants who underwent subsequent surgery (five to seven year follow-
up).
REFERENCES
Camanho 2009
Participants Trial performed in Brazil. The period in which the study was undertaken was not stated
N = 33; Primary patellar dislocation with a convincing history of traumatic dislocation,
requirement for reduction and absence of osteochondral fracture and no previous knee
surgery
Interventions Surgery (n = 17; mean age 24.6; 11 females/6 males) - arthroscopic MPFL repair followed
by three weeks in a removable immobiliser and physiotherapy
Non-surgery (n = 16; mean age 26.8; 9 females/7 males) - immobilised in a cylinder
cast for three weeks, followed by a physiotherapy programme consisting of strengthening
exercises particularly VMO. Hamstring and retinacular stretching begun after one month
post-dislocation
Outcomes Participants reviewed at least once every six months during a maximum of 60 months
(mean 40.4 months). Outcome measurements collected included: recurrent patellar dis-
location, positive apprehension test, recurrent instability symptoms, Smillie test results,
and the Kujala patellofemoral disorders score
Notes Not concealed allocation; location and person who randomised not stated. No details
provided on rehabilitation programme used. Sample size was not based on a power
calculation. Number of surgeons not stated
Additional standard deviation values were obtained from the authors. The authors kindly
reviewed the search strategy results
Risk of bias
Random sequence generation (selection Unclear risk Quote “Patients were randomly divided
bias) into 2 groups by means of a drawing, by
blindly selecting a slip of paper that as-
signed them to either the surgical treatment
group or the conservative treatment group”
No report of how sequence was generated.
Allocation concealment (selection bias) Unclear risk Quote “Patients were randomly divided
into 2 groups by means of a drawing, by
blindly selecting a slip of paper that as-
signed them to either the surgical treatment
Blinding of participants and personnel Unclear risk Blinding of participants and personnel not
(performance bias) reported, but extremely unlikely
All outcomes
Blinding of outcome assessment (detection Unclear risk Blinding of outcome assessors not reported,
bias) and unlikely. Participants completing ques-
All outcomes tionnaires for the Kujala and Tegner scores
were clearly unblinded
Incomplete outcome data (attrition bias) High risk The title indicates that it is a study on the
management of acute patellar dislocation,
and the text (page 621 right hand col-
umn) states “All were operated on less than
1 month after the trauma causing the lesion
had occurred.”
However, in the inclusion criteria we find
“a minimum follow-up time of 25 months
after the dislocation episode”, and in the ex-
clusion criteria we find “follow-up after the
first dislocation shorter than 24 months.”
This appears to mean that randomised par-
ticipants from both groups were excluded
from the analysis, but there is no report of
losses
Selective reporting (reporting bias) Unclear risk Planned outcomes defined in the methods
section were reported, but did not include
adverse effects of surgery
Christiansen 2008
Interventions Surgery (n = 42; 18 females/24 males; mean age 20.0; mean BMI 22.6) repair of the
MPFL performed on average 50 days post-dislocation
Non-surgical (n = 35; 17 females/18 males; mean age 19.9; mean BMI 22.2) brace from
zero to two weeks immobilised 0 to 20 knee range of motion degrees
Outcomes Outcomes recorded at two weeks, six weeks, one year and two years post-injury. Out-
comes measured included the incidence of re-dislocation at 2 years, Kujala patellofemoral
disorders score, and the Knee Injury and Osteoarthritis Outcome Score (KOOS)
Notes Power calculation used. Requiring 39 in each group. Intention-to-treat analysis principles
were not adopted
The authors kindly reviewed the search strategy results.
Risk of bias
Allocation concealment (selection bias) Unclear risk Sealed envelope system. Quote: “Random-
ization between surgery and conservative
treatment was performed by random draw-
ing of 100 envelopes” but no report of
whether these were securely sealed and al-
located sequentially
Blinding of participants and personnel High risk Blinding is not mentioned in the study re-
(performance bias) port. Treatment staff and participants un-
All outcomes likely to be blinded, as randomisation was
conducted at arthroscopy. After care clearly
not identical in both groups (Quote: “Pa-
tients randomised to conservative treat-
ment received no further treatment or brace
usage.”)
Blinding of outcome assessment (detection Unclear risk Blinding of outcome assessors not reported,
bias) and unlikely. Participants completing ques-
All outcomes tionnaires for the Kujala and KOOS scores
were clearly unblinded
Incomplete outcome data (attrition bias) Unclear risk Three lost to follow-up post-randomisation
and data not included
Selective reporting (reporting bias) Unclear risk Planned outcomes defined in the methods
section were reported, but did not include
adverse effects of surgery.
Participants Trial performed in Finland with participants recruited from January 1991 to December
1992
N = 125. Primary lateral patellar dislocation where injury was less than 14 days; no
previous knee injury or surgery, no fractures or tibiofemoral injury
Interventions Surgery (n = 70; 52 females; 18 males; mean age 19.5 SD 9; mean BMI 21.8 SD 4)
medial reefing (18), repair or medial retinaculum (39) or augmentation of MPFL (6) or
lateral release (54). Post-op: Thigh muscle exercises and FWB. If patellar dislocatable on
EUA, immobilised on splint/cast for three weeks. Mobilisation started with orthosis for
three weeks and used during sporting activities for the first six months post-dislocation
Non-surgery (n = 55; 30 females/25 males; mean age 19.1 SD 7.5; mean BMI 22.2 SD
3.9) identical rehabilitation programme to surgical group
Outcomes Outcomes were collected at the final evaluation, a mean of 25 months (range 20 to 45
months) post-randomisation. Outcomes collected included: patient satisfaction to out-
come, Lysholm knee score, Hughston VAS knee score, Tegner activity score, recurrent
dislocation rates, recurrent subluxation rates; subsequent surgical intervention, perfor-
mance tests consisting of timed figure of eight running, one leg hop distance, maximum
number of squat downs in one minute, and subsequent pain on VAS, thigh circumference
knee range of motion, patellofemoral crepitus, apprehension test, prepatellar sensibility,
and scar sensibility
Notes Two orthopaedic consultants and two registrars did 88% of operations. Assessment
clinically performed by two surgeons. Intention-to-treat analysis principles were not
adopted. Sample size was not based on a power calculation
The authors kindly reviewed the search strategy results.
Risk of bias
Random sequence generation (selection High risk Quote: “randomization was based on the
bias) year of birth (even/odd)
Allocation concealment (selection bias) High risk Quote: ”randomization was based on the
year of birth (even/odd)
Blinding of participants and personnel Unclear risk Quote: “After-care was identical in both
(performance bias) groups”.
All outcomes
Blinding of outcome assessment (detection Unclear risk Quote: “Recurrences were asked about
bias) twice: by a mailed questionnaire and by the
All outcomes examiner at the final evaluation”. Quote:
“The clinical examination was performed
Incomplete outcome data (attrition bias) Low risk Quote: “123/125 patients attended the
performance test and clinical examination.
2 patients returned only the questionnaires.
”
Selective reporting (reporting bias) Low risk Planned outcomes defined in the methods
section were reported. Adverse effects of
surgery were reported
Palmu 2008
Participants Trial performed in Finland with participants recruited from 1991 to 1992
Children under 16 years of age
N = 74 knees (71 patients) satisfied at least one of three diagnostic criteria of acute patellar
dislocation: lateral dislocation necessitating reduction (30 knees), ability to dislocate the
patella on EUA (55 knees), presence of findings typical of acute patellar dislocation in-
cluding synovial tear medial to patella on diagnostic arthroscopy (74 knees). Dislocation
had occurred within two weeks of randomisation, no previous knee surgery or substan-
tial knee injury, no concomitant tibiofemoral ligament injury, no large osteochondral
fracture
Interventions Surgery (n = 36; 27 females; 9 males; mean age 13 SD 2) repair of the MPFL (36) in
addition to lateral release (32). Post-operatively, those with patella dislocatable under
anaesthesia immobilised in removable knee brace for three weeks followed by orthosis,
those who were not dislocatable immediately managed in an orthosis and used during
rehabilitation and sporting activities during the first six months. Thigh muscle exercises
and FWB started as tolerated
Non-surgery (n = 28; 19 females/9 males; mean age 13 SD 2) rehabilitation programme
as operative group
Outcomes Outcome measures were collected clinically at two years, and then by telephone interview
at an mean of six years (range five to eight years) and 14 years (range 11 to 15 years)
. Outcomes recorded included: participant reported satisfaction, frequency of recurrent
patellar dislocation, frequency of recurrent patellar subluxation, frequency of subsequent
surgical interventions, Tegner activity score, Hughston VAS knee score, and the Kujala
patellofemoral disorders score
Notes Independent observer but not clear if this person was blinded. Intention-to-treat analysis
principles were not adopted
Risk of bias
Random sequence generation (selection High risk Quote: “randomization was performed ac-
bias) cording to the year of birth, with pa-
tients who had been born in odd years
being randomised to non-operative treat-
ment (twenty eight knees) and those who
had been born in even years being ran-
domized to operative treatment (thirty-six
knees). Randomization was performed by
the treating surgeon (Y.N.) at the time of
admission.”
Allocation concealment (selection bias) High risk Quote: “randomization was performed ac-
cording to the year of birth, with pa-
tients who had been born in odd years
being randomised to non-operative treat-
ment (twenty eight knees) and those who
had been born in even years being ran-
domised to operative treatment (thirty-six
knees). Randomization was performed by
the treating surgeon (Y.N.) at the time of
admission.”
Blinding of participants and personnel Unclear risk Blinding is not mentioned in the study re-
(performance bias) port. Treatment staff and participants un-
All outcomes likely to be blinded
Blinding of outcome assessment (detection Unclear risk Blinding of outcome assessors not reported,
bias) and unlikely. Participants completing ques-
All outcomes tionnaires for Kujala, Tegner and Hughston
visual analogue scale scores were clearly un-
blinded
Incomplete outcome data (attrition bias) Unclear risk Four participants lost to follow-up in the
surgical group; none in the control group
Selective reporting (reporting bias) Unclear risk Data for a planned outcome defined in
the methods section.were incompletely re-
ported for the two treatment groups. All
episodes of instability was reported only
as “Patellofemoral instability, including re-
current patellar dislocation and subjective
sensations of subluxation occurred in 91%
Sillanpaa 2009
Participants Trial performed in Finland with participants recruited from 1998 to 2000
N = 40. Primary acute traumatic patellar dislocation individuals with no previous sub-
luxation or pre-existing ipsilateral or contralateral knee pathology or previous ligament
or fracture injury to the involved knee, or large osteochondral fracture
Interventions Surgery (n = 18; females 1/males 17; mean age 20.0) medial reefing and repair of MPFL
(14); Roux-Goldthwaite procedure (4) arthroscopic repair of osteochondral fracture (6)
Non-surgical intervention (n = 22; females 2/males 21; mean age 20.0) knee orthosis,
guided isometric quadriceps exercises. First three weeks immobilised 0 to 30 degrees knee
flexion, three to six weeks immobilised form 0 to 90 degrees and free range of motion
from six weeks onwards. (All participants of this group received knee aspiration to relieve
pain and four underwent arthroscopic removal of an osteochrondral fragment.)
Outcomes Outcome measures were collected at a mean of seven years (range 6 to 9 years). Outcomes
recorded included: recurrent dislocation rates, frequency of subluxation rates, Kujala
patellofemoral disorder score, VAS pain, knee range of motion, Tegner score, Quadri-
ceps girth, MRI presence of patellar and femoral chondral lesions, participant reported
outcomes of activity level, frequency of reoperation rate, severity of patellofemoral joint
osteoarthritis, subjective assessment of pain and functional knee limitations for stairs,
running, squatting, and pain, radiological findings for sulcus angle, lateral patellofemoral
angle, lateral patellar displacement, Blackburne-Peel ratio
Notes Not clear whether the assessors were blinded. Sample size was based on power calculation
Additional standard deviation values were obtained from the authors. The authors kindly
reviewed the search strategy results
Risk of bias
Random sequence generation (selection Unclear risk No report of how sequence was generated.
bias)
Allocation concealment (selection bias) Unclear risk Quote: “Written informed consent was
obtained from each patient. With use of
a sealed-envelope method, forty patients
Blinding of participants and personnel Unclear risk Quote: “The post-injury or postoperative
(performance bias) rehabilitation protocols were identical for
All outcomes the two groups”. However, quote: “Four
patients in the nonoperatively treated
group underwent arthroscopic removal of
an osteochondral fragment, but no addi-
tional procedures were performed. Since
primary traumatic patellar dislocations
are frequently associated with osteochon-
dral fractures, we believe that perform-
ing arthroscopy initially in some patients
may be unavoidable, even in a randomized
study. Ten patients (four treated nonoper-
atively and six treated with surgical stabi-
lization) had removable fragments, and the
osteochondral fractures were treated iden-
tically (i.e. with arthroscopic removal of the
fragments) in the two treatment groups.”
Blinding of outcome assessment (detection Unclear risk Blinding of outcomes assessment not de-
bias) scribed. Participants completing question-
All outcomes naires for the Kujala and Tegner scores were
clearly unblinded
Incomplete outcome data (attrition bias) Unclear risk One participant lost from each group (flow
chart)
Selective reporting (reporting bias) Unclear risk Planned outcomes defined in the methods
section were reported, but adverse events
were not reported
Sillanpaa 2008a Not a randomised controlled trial. All received some operative procedure
No. of No. of
Outcome or subgroup title studies participants Statistical method Effect size
1 Number of participants 5 339 Risk Ratio (M-H, Random, 95% CI) 0.81 [0.56, 1.17]
sustaining recurrent patellar
dislocation
1.1 Two years minimum 2 110 Risk Ratio (M-H, Random, 95% CI) 0.55 [0.12, 2.57]
follow-up
1.2 Five to seven years 3 229 Risk Ratio (M-H, Random, 95% CI) 0.82 [0.53, 1.29]
follow-up
2 Number of participants 3 198 Risk Ratio (M-H, Random, 95% CI) 0.67 [0.23, 1.94]
sustaining recurrent patellar
subluxation
2.1 Two years minimum 1 33 Risk Ratio (M-H, Random, 95% CI) 0.09 [0.01, 1.44]
follow-up
2.2 Five to seven years 2 165 Risk Ratio (M-H, Random, 95% CI) 0.99 [0.61, 1.61]
follow-up
3 Number of participants 3 198 Risk Ratio (M-H, Fixed, 95% CI) 0.70 [0.54, 0.90]
sustaining any episode of
instability
3.1 Two years minimum 1 33 Risk Ratio (M-H, Fixed, 95% CI) 0.06 [0.00, 0.89]
follow-up
3.2 Five to seven years 2 165 Risk Ratio (M-H, Fixed, 95% CI) 0.80 [0.62, 1.03]
follow-up
4 Number of participants who 3 229 Risk Ratio (M-H, Fixed, 95% CI) 1.09 [0.72, 1.65]
underwent subsequent surgery
(five to seven year follow-up)
No. of No. of
Outcome or subgroup title studies participants Statistical method Effect size
1 Kujala patellofemoral disorder 5 341 Mean Difference (IV, Random, 95% CI) 3.13 [-7.34, 13.59]
score (0: worst outcome to 100:
best outcome)
1.1 Two years minimum 2 110 Mean Difference (IV, Random, 95% CI) 14.36 [1.00, 29.72]
follow-up
1.2 Five to seven years 3 231 Mean Difference (IV, Random, 95% CI) -4.51 [-9.29, 0.26]
follow-up
2 Hughston VAS patellofemoral 2 189 Mean Difference (IV, Random, 95% CI) -4.07 [-7.85, -0.29]
score (28 to 100: best outcome)
2.1 Two years follow-up 1 125 Mean Difference (IV, Random, 95% CI) -2.80 [-6.70, 1.10]
Surgical versus non-surgical interventions for treating patellar dislocation (Review) 26
Copyright © 2012 The Cochrane Collaboration. Published by John Wiley & Sons, Ltd.
2.2 Six years follow-up 1 64 Mean Difference (IV, Random, 95% CI) -5.00 [-13.48, -0.52]
3 Tegner activity score (over 2 year 3 229 Mean Difference (IV, Random, 95% CI) -0.46 [-0.96, 0.05]
follow-up)
3.1 Two year minimum 1 125 Mean Difference (IV, Random, 95% CI) -0.60 [-1.28, 0.08]
follow-up
3.2 Six to nine years follow-up 2 104 Mean Difference (IV, Random, 95% CI) -0.28 [-1.04, 0.48]
4 KOOS at two year follow-up 1 Mean Difference (IV, Fixed, 95% CI) Totals not selected
4.1 Symptoms 1 Mean Difference (IV, Fixed, 95% CI) 0.0 [0.0, 0.0]
4.2 Pain 1 Mean Difference (IV, Fixed, 95% CI) 0.0 [0.0, 0.0]
4.3 Activities of Daily Living 1 Mean Difference (IV, Fixed, 95% CI) 0.0 [0.0, 0.0]
4.4 Sports and recreation 1 Mean Difference (IV, Fixed, 95% CI) 0.0 [0.0, 0.0]
4.5 Quality of life 1 Mean Difference (IV, Fixed, 95% CI) 0.0 [0.0, 0.0]
5 Lysholm score (0 to 100: best 1 Mean Difference (IV, Fixed, 95% CI) Totals not selected
score) at two year follow-up
6 Knee pain 2 163 Mean Difference (IV, Fixed, 95% CI) 0.51 [0.10, 0.93]
6.1 Two year follow-up 1 125 Mean Difference (IV, Fixed, 95% CI) 0.20 [-0.29, 0.69]
6.2 Six to nine year follow-up 1 38 Mean Difference (IV, Fixed, 95% CI) 1.30 [0.52, 2.08]
7 Patient satisfaction (reported 2 133 Risk Ratio (M-H, Fixed, 95% CI) 0.61 [0.44, 0.84]
good or excellent)
7.1 Two year follow-up 1 69 Risk Ratio (M-H, Fixed, 95% CI) 0.38 [0.17, 0.83]
7.2 Six year follow-up 1 64 Risk Ratio (M-H, Fixed, 95% CI) 0.74 [0.53, 1.04]
Non-surgical
Study or subgroup Surgical intervention intervention Risk Ratio Weight Risk Ratio
M- M-
H,Random,95% H,Random,95%
n/N n/N CI CI
1 Two years minimum follow-up
Camanho 2009 0/17 3/16 1.6 % 0.13 [ 0.01, 2.42 ]
Non-surgical
Study or subgroup Surgical intervention intervention Risk Ratio Weight Risk Ratio
M- M-
H,Random,95% H,Random,95%
n/N n/N CI CI
(1) Reported data were for dislocations, and all episodes of instability. Event data entered are all episodes minus dislocations
Non-surgical
Study or subgroup Surgical intervention intervention Risk Ratio Weight Risk Ratio
n/N n/N M-H,Fixed,95% CI M-H,Fixed,95% CI
(1) Data are one episode of dislocation in the surgery group, and all reported episodes of recurrence in the control group, of which 3 apppear to have been dislocations
and 5
(3) The reported data are the sum of redislocations and painful subluxations.
Outcome: 4 Number of participants who underwent subsequent surgery (five to seven year follow-up)
Non-surgical
Study or subgroup Surgical intervention intervention Risk Ratio Weight Risk Ratio
n/N n/N M-H,Fixed,95% CI M-H,Fixed,95% CI
Nikku 1997 20/70 13/57 48.0 % 1.25 [ 0.68, 2.29 ]
Outcome: 1 Kujala patellofemoral disorder score (0: worst outcome to 100: best outcome)
Christiansen 2008 42 84.6 (17.5) 35 78.1 (15.9) 19.7 % 6.50 [ -0.97, 13.97 ]
-20 -10 0 10 20
Favours non-surgical Favours surgical
(1) Standard deviation values obtained directly from authors (Bitar A, Personal communication, 2010)
(2) Standard deviation values obtained directly from authors (Sillanpaa P, personal communication, 2010).
-20 -10 0 10 20
Favours non-surgical Favours surgical
-2 -1 0 1 2
Favours non-surgical Favours surgical
(1) Standard deviation values obtained directly from authors (Sillanpaa P, personal communication, 2010).
1 Symptoms
Christiansen 2008 42 80.9 (17.4) 35 80.2 (15.9) 0.70 [ -6.75, 8.15 ]
2 Pain
Christiansen 2008 42 95.5 (6.9) 35 92.3 (7.9) 3.20 [ -0.15, 6.55 ]
5 Quality of life
Christiansen 2008 42 90.4 (8.9) 35 87.7 (9.7) 2.70 [ -1.49, 6.89 ]
-10 -5 0 5 10
Favours non-surgical Favours surgical
-4 -2 0 2 4
Favours non-surgical Favours surgical
-2 -1 0 1 2
Favours surgical Favours non-surgical
Non-surgical
Study or subgroup Surgical intervention intervention Risk Ratio Weight Risk Ratio
n/N n/N M-H,Fixed,95% CI M-H,Fixed,95% CI
0.2 0.5 1 2 5
Favours non-surgical Favours surgical
OpenSIGLE
1 Patellar dislocation/ (415)
FEEDBACK
Summary
We have used this new review for teaching purposes in our post-graduate programme and realized that Figure 3 is wrong and does not
match with Analysis 1.1:
1. It does not contain all the graphical elements for sections 1.1.1 and 1.1.2.
2. The point estimates and diamonds shown are on the wrong side (i.e. favouring non-surgical interventions).
3. In Analysis 1.3, the label of the x-axis (exp/control) differs from the other forest plots.
We hope these errors can be corrected.
Reply
We thank Dr von Elm for contacting us and are glad with his use of our review. His observations are all correct. Regarding the mismatch
between Analysis 1.1 and Figure 1, errors of reproduction appear to have occurred at some point in the processing of the review,
including in the generation of the pdf files for publication. We have revised the scale of Analysis 1.1 and checked that Figure 1 accurately
reflects this in RevMan before resubmission for publication. The Managing Editor of the Bone, Joint and Muscle Trauma Group has
notified the RevMan support team and Wiley of this problem.
The inconsistent labelling of Analysis 1.3 has now been changed to read “surgical” : “non-surgical” for consistency.
Contributors
Comment from: Dr Erik von Elm
Reply from: Professor William Gillespie and Dr Helen Handoll (Cochrane, Bone, Joint and Muscle Trauma Group), 22 November
2011
WHAT’S NEW
Last assessed as up-to-date: 16 August 2010.
22 November 2011 Feedback has been incorporated Feedback incorporated and minor changes made.
HISTORY
Protocol first published: Issue 4, 2009
Review first published: Issue 11, 2011
CONTRIBUTIONS OF AUTHORS
Caroline Hing and Toby Smith co-ordinated and conceived the protocol, and with assistance of Lesley Gillespie from the Cochrane
Bone, Joint and Muscle Trauma Group, designed the search strategy. Fujian Song provided a methodological and statistical analysis
perspective during the development of the protocol. Caroline Hing, Toby Smith and Simon Donell provided a clinical perspective
during the protocol development and review preparation. Caroline Hing, Toby Smith, Fujian Song and Simon Donell designed and
wrote the protocol.
Caroline Hing and Toby Smith performed the search strategy, identified the studies, extracted the data and prepared the data extraction
table for analysis. Toby Smith and Fujian Song analysed the data. Caroline Hing, Toby Smith and Simon Donell provided a clinical
perspective during the full review development and preparation. Caroline Hing, Toby Smith, Fujian Song and Simon Donell all revised
and agreed the full review.
Caroline Hing is the guarantor of the protocol and full review.
DECLARATIONS OF INTEREST
Simon Donell was an investigator of a trial on this topic. This trial was assessed independently by other review authors.
SOURCES OF SUPPORT
Internal sources
• West Hertfordshire Hospitals NHS Trust, Watford, UK.
• Norfolk and Norwich University Foundation Hospital NHS Trust, Norwich, UK.
• University of East Anglia, Norwich, UK.
INDEX TERMS