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Long-term outcome after operative treatment of traumatic patellar dislocation in adolescents.
[trochlear dysplasia]
Retrospective
evaluation
of
the
long
-term
outcomes
after
surgical
treatment
of
traumatic
patellar
dislocations
in
adolescents
and
identification
of
possible
predictive
factors
of
poor
outcomes
.
Retrospective
clinical
study
.
University
Clinic
,
Level
I
Trauma
Center
.
All
33
adolescents
,
with
a
mean
age
of
14
.
8
years
,
who
were
treated
surgically
after
traumatic
patellar
dislocation
between
1994
and
2006
,
were
involved
in
this
study
.
Mini-
open
medial
reefing
and
arthroscopic
lateral
release
.
The
clinical
outcome
was
evaluated
with
the
visual
analogue
scale
,
the
Lysholm
score
,
the
Kujala
score
,
and
the
Tegner
activity
level
scale
.
On
preoperative
radiographs
and
magnetic
resonance
imaging
scans
,
trochlear
dysplasia
and
patella
alta
were
assessed
.
The
variables
analyzed
were
sex
,
associated
osteochondral
injuries
,
the
number
of
redislocations
before
surgery
,
and
the
number
of
redislocations
after
surgery
.
At
the
mean
follow-up
of
9
.
8
years
,
the
mean
Lysholm
score
was
82
.
6
,
the
mean
Kujala
score
was
84
.
4
,
the
mean
Tegner
activity
level
was
4
.
8
,
and
the
mean
visual
analogue
scale
was
0
.
2
.
We
found
no
significant
differences
in
the
subgroups
regarding
functional
outcomes
.
Fifteen
patients
with
patella
alta
and
4
patients
with
trochlear
dysplasia
were
assessed
radiologically
.
Redislocations
after
surgery
were
observed
in
4
patients
,
2
of
them
were
female
patients
who
exhibited
quadriceps
angles
requiring
tibial
tubercle
osteotomy
to
be
performed
after
maturation
.
The
techniques
of
mini-
open
medial
reefing
and
lateral
release
demonstrate
a
good
functional
long
-term
outcome
and
effectively
prevent
recurrent
instability
.
The
major
predictive
factor
for
poor
outcomes
and
redislocations
is
an
inadequately
addressed
pathology
.
Therapeutic
Level
IV
.
See
Instructions
for
Authors
for
a
complete
description
of
levels
of
evidence
.
Diseases
Validation
Diseases presenting
"female patients"
symptom
adrenomyeloneuropathy
aromatase deficiency
benign recurrent intrahepatic cholestasis
carcinoma of the gallbladder
classical phenylketonuria
congenital adrenal hyperplasia
cushing syndrome
erdheim-chester disease
esophageal adenocarcinoma
esophageal carcinoma
esophageal squamous cell carcinoma
fabry disease
familial hypocalciuric hypercalcemia
familial mediterranean fever
heparin-induced thrombocytopenia
lymphangioleiomyomatosis
oligodontia
papillon-lefèvre syndrome
phenylketonuria
pyruvate dehydrogenase deficiency
sneddon syndrome
trochlear dysplasia
von hippel-lindau disease
wolf-hirschhorn syndrome
x-linked adrenoleukodystrophy
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