A triple innominate osteotomy can be considered for the older child or adolescent in whom the triradiate cartilage remains open.. Salter stated that the potential for remod-Residual Untr
Trang 1Although the true incidence of
per-sistent acetabular dysplasia in
adults is unknown, its role as a
sig-nificant cause of premature hip
osteoarthritis is well established.1-4
It is estimated that between 20%
and 50% of cases of degenerative
disease of the hip are secondary to
subluxation or acetabular
dyspla-sia.3 In a classic study of 130
pa-tients with degenerative arthritis of
the hip, Stulberg and Harris2found
that 63 patients (48%) had
underly-ing acetabular dysplasia
Ideally, patients with acetabular
dysplasia and subluxation are
identified and treated in infancy
Failing this, treatment instituted as
early as possible in childhood,
preferably before age 4, will take
maximum advantage of the
inher-ent remodeling capabilities of the
hip joint.5 In the older child or young adult, recognition of persis-tent acetabular dysplasia may at least allow treatment before the onset of irreversible cartilage in-jury and thereby favorably influ-ence an otherwise worrisome nat-ural history
The goal of treatment of patients with persistent acetabular dysplasia
is to forestall or prevent the devel-opment of osteoarthritis and to obviate the need for arthroplasty at
a relatively young age Pelvic oste-otomies can play a central role in this strategy by reorienting the architecture of the pelvis so as to normalize the forces of weight bear-ing To enhance understanding of this important tool in the preven-tion of hip osteoarthritis, we will outline the general categories of
pelvic osteotomies, discuss the indi-cations for their use, and provide a brief technical description of those that are most commonly utilized in current practice
Etiology and Biomechanics of Acetabular Dysplasia
The abnormally steep acetabular roof and the shallow joint surface
Dr Gillingham is Director, Division of Pediatric Orthopedics, Departments of Ortho-pedics and Clinical Investigation, Naval Medical Center, San Diego, Calif; and Assistant Professor of Surgery, Uniformed Services University, Bethesda, Md Dr Sanchez is Head, Department of Orthopedics, Naval Hospital, Twenty-nine Palms, Calif Dr Wenger is Director of Pediatric Orthopedics, Children’s Hospital, San Diego; and Clinical Professor of Orthopedic Surgery, University of California, San Diego.
Reprint requests: Dr Gillingham, Department
of Clinical Investigation, Naval Medical Center San Diego, Suite 5, 34800 Bob Wilson Drive, San Diego, CA 92134-1005.
The Chief, Bureau of Medicine and Surgery, Navy Department, Washington, DC, Clinical Investigation Program, sponsored this report S93-094 as required by NSHSBETHINST 6000.41A The views expressed in this article are those of the authors and do not reflect the official policy or position of the Department of the Navy, the Department of Defense, or the United States Government.
Abstract
Persistent acetabular dysplasia is a well-known cause of premature hip
osteoarthritis In the dysplastic hip, point loading occurs at the edge of the
steep, shallow acetabulum Pelvic osteotomies reduce this load by increasing the
contact area, relaxing the capsule and muscles about the hip, improving the
moment arm of the hip, and normalizing the forces of weight bearing The
orthopaedic surgeon can choose from among a variety of pelvic osteotomies (e.g.,
redirectional, reshaping, and salvage) for the purpose of restoring normal
anato-my and biomechanical forces across the hip joint Treatment of residual
dyspla-sia is based on the patient's age and the presence or absence of congruent hip
reduction A Salter or Pemberton procedure is generally appropriate for a child
between the ages of 2 and 10 A triple innominate osteotomy can be considered
for the older child or adolescent in whom the triradiate cartilage remains open.
After triradiate closure, the Ganz periacetabular osteotomy can be considered in
addition to the triple innominate osteotomy.
J Am Acad Orthop Surg 1999;7:325-337
Dysplasia in Children and Young Adults
CDR Bruce L Gillingham, MC, USN; LCDR Anthony A Sanchez, MC, USNR; and
Dennis R Wenger, MD
Trang 2that characterize acetabular
dyspla-sia can be due to several causes
Although acetabular dysplasia is
most commonly seen as a
compo-nent of developmental dysplasia of
the hip (DDH), it can also be a
residual of Legg-Perthes disease
and is frequently seen in patients
with neuromuscular diseases, such
as cerebral palsy and
myelomenin-gocele
The importance of a concentric
hip reduction during development
of both components of the hip joint
is well known.5,6 The development
of appropriate acetabular depth
depends in large part on the
stimu-lus of the femoral head pushing into
the triradiate cartilage Conversely,
if the femoral head is to achieve its
normal spherical shape in
adult-hood, it must be well seated within
the acetabulum during infancy and
early childhood Any condition that
interferes with this interdependent
relationship can lead to acetabular
dysplasia Left untreated, a
mean-ingful reduction in the longevity of
the hip joint can result.2
When evaluating an infant or
child with acetabular dysplasia, it is
important to ascertain whether
there is associated hip subluxation
Disruption of ShentonÕs line on a
standing anteroposterior (AP)
radio-graph of the pelvis indicates that
the femoral head is proximally and
laterally subluxated (ShentonÕs
line is created by drawing a line
along the proximal medial femoral
metaphysis and extending onto the
superior border of the obturator
foramen In a normal hip, the line
is an arc of continuous contour.) If
the condition is not treated,
prema-ture joint degeneration and clinical
disability predictably follow The
age at onset of symptoms correlates
well with the severity of the
sublux-ation.2,4,7 The patients with the
most serious disease begin to
expe-rience pain in the second decade;
those with the least serious disease
may reach the fifth decade before
noting symptoms.7 However, even
in moderate cases, functionally dis-abling symptoms can occur during the most vigorous and productive years of life
Less predictable is the effect of acetabular dysplasia without sub-luxation Patients without subluxa-tion are frequently asymptomatic, and osteoarthritis tends to develop much later and less commonly than in patients with subluxation.1 Cooper-man et al1concluded that the usual radiographic indices by which acetabular morphology is character-ized are not predictive of the rate at which osteoarthritis develops in patients with acetabular dysplasia alone In a more recent study of the contralateral hip in patients who had undergone a total hip replace-ment for osteoarthritis secondary to dysplasia, Murphy et al8 noted a
significant (P<0.0001) difference in
standard radiographic indices be-tween patients in whom osteoarthri-tis developed in the opposite hip before age 65 and those in whom it did not Adolescent patients with acetabular dysplasia without associ-ated subluxation should be carefully evaluated for clinical findings, as they (particularly females) are at greater risk than the general popu-lation for the development of clini-cal signs and symptoms of degener-ative hip disease.2
Acetabular dysplasia eventually results in degenerative joint disease due to alterations in load In a study of patients followed up for an average of 29 years after reduction
of a congenitally dislocated hip, Hadley et al9 concluded that over the long term, articular cartilage can tolerate mean contact pressures
of 2 MPa, with an inverse relation-ship between higher pressures and the time needed to develop degen-erative changes In a normal hip, peak acetabular contact pressures may be as high as 10 MPa, depend-ing on activity, but are distributed throughout the entire acetabulum,
with the dome being subjected to the highest pressure and the rim to essentially none.10
In the dysplastic hip, point load-ing occurs at the edge of the steep, shallow acetabulum Pelvic oste-otomies reduce this load by in-creasing contact area, relaxing the capsule and muscles about the hip, and improving the moment arm of the hip.10
Clinical Evaluation History and Physical Examination
The initial evaluation focuses on
a characterization of the patientÕs symptoms, activity level, functional limitations, and expectations The patient with residual dysplasia may
be asymptomatic or may experience only vague discomfort with strenu-ous weight-bearing activities The presence of more extensive com-plaints may suggest that degenera-tive arthritis is already established Most children and teenagers with radiographic evidence of severe subluxation that requires treatment will have no symptoms
Physical examination includes inspection of the extremity for muscle wasting of the quadriceps and gluteus, longitudinal malalign-ment of the limb, and limb-length discrepancy Analysis of the pa-tientÕs gait may reveal a limp or an abductor lurch Palpation of the posterior iliac crest is performed with the patient standing, in order
to detect pelvic obliquity The Trendelenburg test, performed both immediately and after a 20-second delay, allows assessment of the competence and resistance to fatigue of the hip abductors The range of hip motion is carefully documented, with particular atten-tion paid to hip rotaatten-tion and the presence of contractures Pain with active or passive motion sug-gests synovitis or impingement
Trang 3Pain elicited by internal rotation
of the flexed and adducted hip
may signify the presence of a
de-tached limbus Termed
Òacetabu-lar rim syndromeÓ by Klaue et al,11
this condition is considered to be a
precursor of osteoarthritis of the
hip in patients with acetabular
dysplasia Most children and
ado-lescents, even those with severe
dysplasia, have few, if any,
physi-cal findings
Radiologic Evaluation
A comprehensive radiographic
evaluation is essential to clarify the
degree of deformity before
per-forming a hip osteotomy The
ini-tial plain films should include
weight-bearing (standing) AP,
frog-leg lateral, and abductionÐinternal
rotation views of the pelvis and
hips, as well as a faux profil (French
for Òfalse profileÓ) view of the
affected hip
Analysis of the AP view should
include a qualitative assessment of
ShentonÕs line and the acetabular
sourcil (a term derived from the
French word for ÒeyebrowÓ) As
mentioned previously, a break in
the normal smooth arc of ShentonÕs
line is suggestive of hip subluxation
The appearance of the acetabular
sourcil is a sensitive radiographic
indicator of asymmetric loading of
the hip joint.12 Ordinarily, this
dense subchondral bone appears as
a smooth curve of uniform
thick-ness In the dysplastic hip, lateral
sourcil thickening occurs, which
represents increased focal loading
due to underlying malalignment
(Fig 1) Careful analysis of the
sourcil, especially if there is
side-to-side asymmetry, is an important
tool for the hip surgeon
Measurements of the
center-edge angle of Wiberg,4the adult
acetabular angle of Sharp,13and the
acetabular depth are useful means
of quantitating the severity of the
dysplasia Prior to ossification of
the femoral head, the acetabular
index is generally used to assess acetabular configuration, with nor-mal mean values decreasing to less than 20 degrees by age 24 months (Table 1).14
The abductionÐinternal rotation view neutralizes femoral
antever-sion and allows accurate assess-ment of the true femoral neck-shaft angle In addition, this view simu-lates the coverage possible with a proximal femoral varus osteotomy
A single innominate osteotomy can
be simulated by taking a
radio-Fig 1 Anteroposterior radiograph of the pelvis of an 18-year-old girl with left hip dyspla-sia The right acetabular sourcil appears as a smooth curve of uniform thickness In con-trast, the left sourcil is wider laterally, indicating focal loading.
Table 1 Radiographic Assessment of the Hip *
Children Acetabular index at 3 months, degrees
Acetabular index at 24 months, degrees
Adults Acetabular angle, degrees 25-41 ³43 Acetabular depth, mm 15-27 <15 mm in men,
<14 mm in women Acetabular roof, degrees >0 ²0
Center-edge angle, degrees 24-46 ²20
Normal values represent mean ± 2 SD.
Trang 4graph with the hip held in 25
de-grees of flexion, 10 dede-grees of
ab-duction, and neutral rotation, with
the x-ray beam directed posteriorly
and caudally 25 degrees.15
The faux profil view, first
de-scribed by Lequesne and de S•ze16
in 1961, is a true lateral view of
the acetabulum made with the
patient standing with the pelvis
rotated 25 degrees toward the
x-ray beam The result is a
center-edge angle-type assessment of
an-terior coverage
Fluoroscopic examination of the
hip in various positions can be a
useful means of gauging the effect
of a proposed osteotomy
Arthrog-raphy is of particular value when
assessing the incompletely ossified
femoral head of a child
The recent advances in
three-dimensional reconstruction of
computed tomographic (CT)
stud-ies have greatly expanded our
understanding of the underlying
pathoanatomy in patients with
residual acetabular dysplasia
This modality is emerging as a valuable preoperative tool for sur-gical decision making and plan-ning.17,18 The three-dimensional display provides superior infor-mation about the fit of the femoral head in the acetabulum, as well as the size, shape, and orientation of the acetabulum This increased detail has clearly demonstrated that acetabular dysplasia is more complex than previously thought
More than just malrotation or maldirection, acetabular dysplasia
is a combination of acetabular maldirection, margin erosion, tor-sion, hypoplasia (localized or global), abnormal shape, and decreased acetabular surface area.19 With this greater under-standing has come an improved ability to match the osteotomy to the type of acetabular deficiency
In addition, comparison of the ini-tial study with one performed postoperatively is a valuable tool
in assessing the success of the osteotomy in reproducing normal
hip architecture and will further refine the surgeonÕs ability to choose the appropriate osteotomy
Treatment Overview
The goal of treatment of the patient with acetabular dysplasia is to establish normal biomechanical forces about the hip joint The means by which this can be accom-plished vary greatly depending on the patientÕs age, the severity of dysplasia, and the morphology of the hip joint (Fig 2)
In the infant and young child, the initial assessment and treat-ment are directed toward ensuring that a concentric hip reduction is present Restoration of hip-joint concentricity may set the stage for profound remodeling The amount
of remodeling that can be relied on
to produce a normal acetabulum and the relationship of remodeling and age have been debated Salter stated that the potential for
remod-Residual
Untreated
Developmental dysplasia of the hip
Patient aged 8 years or older Patient aged
2-8 years
Innominate or Pemberton osteotomy
± proximal femoral osteotomy
Triple innominate osteotomy ± proximal femoral osteotomy
Triple innominate
or periacetabular osteotomy ± proximal femoral osteotomy
Patient aged
18 months
to 3 years
Patient aged
3 years or older
Patient aged
2 to 10 years
Patient aged
10 to 14 years (open triradiate)
Patient aged
14 years or older (closed triradiate)
Consider innominate osteotomy
Shelf procedure, Chiari osteotomy,
or hip fusion
± Femoral
derotational
osteotomy
Femoral derotational
and shortening
osteotomy
Open reduction and
capsulorrhaphy
Innominate osteotomy
Fig 2 Algorithm for treatment of developmental dysplasia of the hip.
Trang 5eling was greatest at birth and
gradually decreased until age 18
months, when it would no longer be
ensured.20 Harris5concluded, on
the basis of a prospective radiologic
study of 79 dislocated hips, that the
critical point beyond which
restora-tion of hip congruence would not
necessarily result in a normal
ace-tabulum was age 4; the risk of
pro-ducing a moderately or severely
dysplastic acetabulum more than
doubled if hip reduction occurred
beyond this age Thus, in the
18-month-old to 3-year-old child with
acetabular dysplasia due to hip
dis-location, the need for an acetabular
procedure at the time of open
re-duction and capsulorrhaphy is
con-troversial One approach is to
delay a secondary procedure so
that the adequacy of the acetabular
remodeling response can be
as-sessed.21 Most North American
centers, however, are moving
toward following SalterÕs advice to
include the acetabular procedure at
the time of primary treatment in
order to maximize the likelihood
that a normal acetabulum will
ulti-mately develop.20,22
DelBello et al22compared the
re-sults of open reduction alone, open
reduction followed by delayed
innominate osteotomy, and open
reduction plus immediate
innomi-nate osteotomy in a group of older
children with DDH Only the
im-mediate osteotomy group achieved
acetabular indices comparable to
those in normal control subjects
In addition, the hips of 95% of the
patients in the immediate
innomi-nate osteotomy group were
classi-fied as group I or II on the Severin
hip dysplasia scale, compared with
61% in the group of patients who
underwent open reduction alone
and 60% in the delayed innominate
osteotomy group No differences
were found in the rate of
osteo-necrosis of the femoral head, the
estimated surgical blood loss, and
the operative time On the basis of
these findings, the authors recom-mended routine innominate oste-otomy at the time of open reduc-tion for all patients over the age of
18 months
In the child aged 3 years or older, innominate osteotomy is per-formed routinely because of the unpredictable remodeling potential beyond this age.23 In the patient older than age 8, the treatment plan
is based on the symptoms and the severity of the residual dysplasia
In terms of clinical characteristics, patients with DDH vary greatly, ranging from the asymptomatic patient in whom the dysplasia is an incidental finding to the severely incapacitated individual who is in constant pain
Nonoperative therapy is directed toward minimizing excessive point loading across the joint by avoiding unnecessary impact-loading activi-ties, achieving ideal body weight, and maintaining overall physical fitness and muscle tone This can
be supplemented by judicious use
of nonsteroidal anti-inflammatory agents in patients for whom they are not contraindicated While this can be an effective means of treat-ing the symptoms, this strategy does not address the underlying malalignment that is the ultimate cause of osteoarthritis It is impor-tant that parents and older patients understand this, particularly when there are few, if any, symptoms
Paradoxically, these are the pa-tients who may have the most to gain from surgery
The goal and type of surgery chosen depend on the severity of the patientÕs condition In general, there are two groups of patients with residual dysplasia.24 The group amenable to Òreconstruc-tiveÓ procedures are minimally symptomatic and have normal joint congruence and no irreversible car-tilage injury The goal of surgery
in this setting is realignment of the joint surfaces to produce more
nor-mal loading and to forestall the development of osteoarthritis Reconstructive osteotomies include Salter, Pemberton, triple innomi-nate, and periacetabular proce-dures.20,25-27 These procedures have
a relatively predictable outcome
In contrast, the ÒsalvageÓ group demonstrate evidence of irreversible cartilage injury In this setting, the goal of surgery is to relieve pain, delay the inevitable arthroplasty, and improve function in the mean-time The procedures used have a less certain outcome Examples in-clude Chiari28and shelf procedures, often performed on an incongruent, already distorted hip joint
Primary Treatment of Complete Hip Dislocation
If closed treatment has not been effective in a child less than 18 months of age, establishment of normal hip alignment can gener-ally be achieved by open reduc-tion and capsulorrhaphy alone
In patients between 18 months and 3 years of age, immediate in-nominate osteotomy at the time of open reduction maximizes the remodeling potential of the hip
In the presence of excessive fe-moral anteversion or valgus of the femoral neck, a varus derota-tional osteotomy can be included (Fig 3)
We do not advocate the Pember-ton or Dega procedure as part of the treatment for primary dislocation of the hip because both either decrease acetabular volume or change ace-tabular shape The Salter procedure allows redirection but avoids shape
or volume changes
For the child over age 3 years with untreated DDH, the approach
is similar The only difference is the addition of a derotational femoral shortening osteotomy to decrease the compressive forces on the fe-moral head after reduction
Trang 6Treatment of Residual
Dysplasia
Treatment of residual dysplasia is
based on the patientÕs age and the
presence or absence of congruent
hip reduction In the child between
the ages of 2 and 10 with a
well-reduced hip with anterolateral
acetabular deficiency of a moderate
degree, either a Salter or a
Pember-ton procedure can be performed
Theoretically, with the Pemberton
procedure, the relative relationship
of the cuts in the inner and outer
tables of the ilium can be adjusted
to change the location of the
de-sired augmentation As a
configu-ration-changing osteotomy, the
Pemberton is particularly helpful in
the case of a shallow, capacious, or
ÒwanderingÓ acetabulum
Although many cogent
argu-ments have been made regarding
the relative usefulness of the Salter
and Pemberton procedures, there is
little objective basis for choosing
one over the other The Pemberton
procedure has the advantage that
because the osteotomy is so secure,
fixation pins are not required, and a
second operation to remove pins is
unnecessary If severe coxa valga
or anteversion is present, a femoral osteotomy may have to be added to achieve an anatomically correct radiographic appearance
In the older child or adolescent
in whom the triradiate cartilage remains open (usually over age 10), the triple innominate
osteoto-my26 is our procedure of choice
Although a more extensive dissec-tion is required, this procedure offers the advantage of increased acetabular fragment mobility and thus a wider range of coverage options
After triradiate cartilage closure, the periacetabular osteotomy pop-ularized by Ganz et al27can be con-sidered in addition to a triple oste-otomy The Ganz procedure is technically challenging, but it af-fords nearly unlimited acetabular mobility
In the patient between 2 and 8 years of age with an incongruent joint, a Salter or Pemberton inno-minate osteotomy can be consid-ered provided sufficient remodel-ing potential is present However, the outcome is less predictable than
in the child less than age 4 with
concentric reduction In such cir-cumstances, a femoral osteotomy is commonly added to decompress the joint Beyond age 8, when no remodeling will occur, a salvage osteotomy, such as a Chiari or shelf procedure, is necessary.28,29
Redirectional (Complete) Osteotomies
As their name implies, redirectional osteotomies improve the coverage
of the femoral head by shifting the position of the acetabulum The acetabulum itself remains un-changed Because these procedures involve complete cuts through the innominate bone, fixation is re-quired to maintain the new align-ment until the osteotomy heals In general, there is a direct relation-ship between the technical com-plexity of a redirectional osteotomy and the amount and range of cover-age possible
Single Innominate Osteotomy (Salter)
First described by Salter in 1961,20 the single innominate osteotomy
Fig 3 Bilateral DDH in a 2-year-old girl A, Preoperative AP radiograph of the pelvis B, AP radiograph obtained after staged bilateral
open reductions, proximal femoral varus osteotomies, and innominate osteotomies Ideal graft position is present on the left; undesirable slightly posterior displacement of the osteotomy is present on the right.
Trang 7remains in widespread use (Fig 4).
Salter conceptualized that
acetabu-lar maldirection was responsible
for the deficiency of femoral head
coverage and designed an osteotomy
to redirect the acetabulum and
thereby provide a stable hip
reduc-tion in the funcreduc-tional weight-bearing
position The amount of acetabular
fragment mobility obtained with
the single innominate osteotomy
depends on rotation and hinging
through the pliable fulcrum of the
pubic symphysis
The primary indication for a
Salter osteotomy is a deficiency of
anterolateral femoral head coverage
in an otherwise concentrically
re-duced hip A shallow acetabulum
is a relative contraindication
Im-provement in the center-edge angle
of 20 to 22 degrees and a 10-degree
improvement in the acetabular
index can be expected.30,31
Skillful exposure and clearing of
the sciatic notch is critical The
Gigli saw cut begins low in the
sci-atic notch and exits just above the
anterior inferior iliac spine The
inferior fragment is pulled distally
and anteriorly with a towel clamp
to provide increased anterolateral
coverage Care should be taken to
prevent displacing the proximal fragment, as this will lead to open-ing of the osteotomy posteriorly at the sciatic notch, resulting primarily
in leg lengthening Mobility of the fragment is enhanced by placing the ipsilateral leg into the figure-of-four position of hip flexion, abduction, and external rotation A triangular wedge of anterior iliac crest is fixed into place at the osteotomy site with two threaded pins directed posteromedially These are subse-quently removed at 6 to 8 weeks in young children and at 3 to 4 months
in older children, who are at a greater risk for graft collapse An iliopsoas tenotomy at the pelvic brim is considered an essential com-ponent of the procedure to both de-crease compression on the femoral head and allow distal fragment mo-bility
In a review of the 15-year data
on 140 patients treated primarily for hip dislocation and subluxation, Salter and Dubos32 reported 93.6%
excellent or good results in patients aged 18 months to 4 years, with no failures In the 4- to 10-year-old age group, however, only 56.7%
had good or excellent results, and the failure rate was 6.6% Initial operative complications included superficial wound infections (inci-dence of 1.5%), femoral head osteo-necrosis (5.7%), loss of osteotomy position prior to the use of two pins (2.8%), redislocation (5.6%), resubluxation (14.3%), and supra-condylar femur fracture (6.4%)
There were no deep infections
Therefore, because less satisfactory results generally occur in older children, triple innominate osteot-omy is preferable for children over age 10
Triple Innominate Osteotomy
The triple osteotomy described
by Steel26in 1965 consists of oste-otomies of the ischium and pubis
in addition to a Salter innominate osteotomy (Fig 5) Tšnnis et al33
have described a modification of the triple osteotomy that is also widely used The triple osteotomy
is generally indicated for older children and adolescents, in whom symphyseal rotation is more limited than in younger children due to skeletal maturity and decreased ligamentous laxity (Fig 6) As is the case with the single innomi-nate osteotomy, concentric hip re-duction is a prerequisite Because
it is a circumacetabular osteotomy, significant mobility of the acetabu-lar fragment is possible In addi-tion, if the ischial osteotomy is directed obliquely from lateral to medial, the acetabular fragment can be displaced medially, moving the hip center to a more physio-logic position and improving gait mechanics
The triple osteotomy requires two incisions Steel26originally ad-vised a horizontal incision made over the ischial tuberosity for the ischial osteotomy and an anterior incision (as in the single innominate procedure) for the pubic and in-nominate osteotomies We now prefer to make the Salter cut only through the anterolateral incision and to make the superior pubic
Fig 4 Salter single innominate osteotomy.
Fig 5 Triple innominate osteotomy.
Trang 8ramus and ischial cuts through a
single transverse groin incision
Placement of bone graft and
fixa-tion are performed as for the Salter
osteotomy Care must be taken to
avoid excessive external rotation of
the free distal fragment Also,
mus-cle should not intervene in the
pubic and ischial cuts, as
pseudar-throsis can occur Use of a
tempo-rary Schanz screw to guide the
ace-tabular segment allows appropriate
acetabular redirection, avoiding
excessive external rotation
In SteelÕs original series,26 the
results were considered to be
satis-factory in 19 of the 23 hips with
congenital dysplasia followed up
between 2 and 10 years
postopera-tively Five complications were
reported: two cases of
postopera-tive ileus, one ischial wound
infec-tion (Escherichia coli), and two
instances of pressure necrosis of
the skin over the anterior inferior
spine of the displaced acetabular
fragment
In a review of 44 patients (56
hips) an average of 7 years after
triple osteotomy, Faciszewski et
al34reported improvement in both
pain and function in 94% of pa-tients The center-edge angle in-creased by a mean of 33 degrees, and the acetabular angle decreased
by a mean of 15 degrees Two com-plications occurred: one pulmo-nary embolism and one superficial wound infection
Periacetabular Osteotomy
Introduced in 1988 by Ganz et
al,27 the periacetabular osteotomy allows extensive acetabular reori-entation, including medial and lat-eral displacement Osteotomies are performed in the pubis, ilium, and ischium A vertical posterior-column osteotomy connects the posterior extremes of the iliac and ischial osteotomies approximately
1 cm anterior to the sciatic notch (Fig 7) This osteotomy must be done after skeletal maturity, be-cause it crosses the triradiate carti-lage; therefore, it is indicated only for older adolescent and adult pa-tients with dysplastic hips that re-quire improvement of congruency and containment (Fig 8)
Because no complete cut is made into the sciatic notch (the posterior
column is split vertically), the Ganz procedure is very stable, and no postoperative cast is required Im-mediate crutch weight bearing is advised Additional advantages include preservation of the blood supply to the acetabular fragment, use of a single surgical approach, and preservation of the shape of the pelvis, which permits normal vaginal delivery A disadvantage
Fig 6 Images of a female patient with left acetabular dysplasia (same patient as in Fig 1) A, At age 18, AP radiograph of the abducted, internally rotated left hip shows joint congruence B, AP view obtained at age 19, 11 Ú 2 years after left proximal femoral varus osteotomy.
C,Three-dimensional reconstruction of a CT study of the hip obtained at age 21 demonstrates persistent left acetabular dysplasia with
deficient anterolateral coverage D, AP radiograph obtained after triple innominate osteotomy on the left shows improved coverage.
Fig 7 Ganz periacetabular osteotomy.
Trang 9is that the procedure is difficult to
learn
In 1995, Trousdale et al35reported
the results of use of the Ganz
peri-acetabular osteotomy, with or
without intertrochanteric
osteot-omy, on 42 patients with
dysplas-tic, osteoarthritic hips The
aver-age follow-up interval was 4 years
They found that the Harris hip
score improved from an average
of 62 points preoperatively to 86
points postoperatively (P<0.0001).
The average anterior-edge angle
was 1 degree preoperatively and
27 degrees postoperatively
Com-plications included deep venous
thrombosis in 2 patients, pubic
nonunion in 2, and heterotopic
bone formation in 14 There were
no major neurovascular
complica-tions in this series, although nerve
and/or vessel injury is possible
with this rather complex
oste-otomy
Reshaping (Incomplete)
Osteotomies
The object of reshaping
osteoto-mies is restoration of acetabular
morphology by changing the shape
of the acetabulum They are
pri-marily indicated for the patient
with a capacious or wandering
acetabulum, as is commonly seen
in both childhood DDH and
cere-bral palsy Depending on the os-teotomy, additional lateral and/or posterior coverage can be obtained
They should be used only in the skeletally immature, as the osteot-omy hinges through the triradiate cartilage Because the osteotomy is incomplete, there is inherent stabil-ity after graft placement, and inter-nal fixation is not required
Pemberton Osteotomy
In 1965, Pemberton25 described
an incomplete osteotomy that hinges through the triradiate carti-lage (Fig 9) A Smith-Peterson approach is used to expose the in-ner and outer tables of the ilium
The outer ilium is osteotomized beginning immediately superior to the anterior inferior iliac spine
The osteotomy extends posteriorly 0.25 inch above and parallel to the joint capsule and is carried to the ilioischial limb of the triradiate car-tilage The inner ilium is osteoto-mized separately to match the outer cut (if anterior coverage is primarily desired); alternatively, the posterior limb may be shifted anteriorly to provide additional lat-eral coverage Care must be taken
to remain halfway between the anterior edge of the sciatic notch and the posterior rim of the acetab-ulum
The osteotomy is opened enough
to create an acetabular angle of
approximately 0 degrees A groove
is created to hold the graft in posi-tion, and a triangular wedge of bone from the anterior ilium is placed and impacted No internal fixation is required A spica cast is used for 8 weeks This osteotomy is appropriate for patients between the age of 18 months and skeletal maturity (Fig 10)
In PembertonÕs original series of
91 patients (115 hips), all 46 chil-dren less than 4 years of age had a good result.25 There were 20 good and 4 fair results in children aged 4
to 7 years, and 12 good, 6 fair, and
3 poor results in children between the ages of 7 and 12 years
Fig 8 Images of a 15-year-old girl with left acetabular dysplasia A, Preoperative AP radiograph of the pelvis B, Three-dimensional CT reconstruction shows significant uncovering of the left hip C, AP radiograph obtained after a Ganz periacetabular osteotomy.
Fig 9 Pemberton osteotomy.
Trang 10plications included 5
redisloca-tions, 12 cases of osteonecrosis (all
eventually healed), and 2 sciatic
nerve palsies (in cases of high
dis-location)
Faciszewski et al36 reported the
results in 52 hips with acetabular
dysplasia treated with the
Pember-ton osteotomy The average age of
the 42 patients was 4 years at the
time of surgery The mean
follow-up interval was 10 years At the
time of follow-up, 42 hips (81%)
were radiographically normal No
patient had pain, three patients had
decreased range of motion, and one
patient had a positive
Trendelen-burg test There were no
complica-tions
Dega Osteotomy
The Dega osteotomy is an
tabuloplasty that also changes
ace-tabular configuration and shape
It provides increased
posterolater-al coverage by means of an osteot-omy of the lateral cortex of the ilium only, hinging through the open triradiate cartilage.37 The primary indication for this osteot-omy is the presence of a capacious acetabulum with posterolateral deficiency, as is often found in children with cerebral palsy
Some authors also use it for persis-tent acetabular dysplasia in DDH
The technique has been well de-scribed by Mubarak et al.37
Salvage/Augmentation Procedures
A salvage osteotomy may be indi-cated when a congruent reduction between the femoral head and the
acetabulum cannot be obtained Such an osteotomy may also be appropriate for an adolescent or adult with a painful subluxated hip
or for a patient with prior surgical failures Selection of one of the var-ious salvage/augmentation proce-dures presupposes that the remain-ing hyaline cartilage is inadequate
or cannot be redirected to provide coverage of the femoral head These procedures act to increase the weight-bearing surface and rely on capsular metaplasia to provide an articulating surface Commonly, an associated valgus or varus
osteoto-my will help to realign the joint and decompress the joint
Chiari Osteotomy
The primary indication for use of the Chiari osteotomy is a painful, subluxated hip without the
Fig 10 Images of a girl with bilateral acetabular dysplasia A, At 3 years of age, AP radiograph of the pelvis showed bilateral dysplasia.
B,At 7 1 Ú 2years of age, three-dimensional reconstruction of a CT study of the pelvis showed persistent dysplasia C, Radiograph of the right hip obtained during a Pemberton osteotomy D, Anteroposterior radiograph of the pelvis obtained 2 months after bilateral
Pemberton osteotomies shows graft incorporation and improved coverage.