8th
CONGRESS OF THE FEDERATION OF EUROPEAN IRISH WOLFHOUND
CLUBS (EIWC)
LE TOUQUET, 2 SEPTEMBER 2006
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ELBOW
DYSPLASIA
Jean-Pierre GENEVOIS, DVM, PhD, Professor of Small Animal
Surgery
Head of Small Animal Department
Ecole Nationale Vétérinaire de Lyon
1 Avenue Bourgelat 69280 MARCY L’ETOILE (France)
Elbow dysplasia (ED) is a general term which was proposed
by the IEWG (International Elbow Working Group) in 1989.
It depicts a developmental problem of the elbow joint. ED
is an inherited polygenic disease, made up by 4 specific
abnormalities, called primary lesions, which may occur independently
or in conjunction with one another. They affect the articular
surface of the joint, or its congruence – or congruity
(i.e. the perfect adaptation of the shape of the three bones
constituting the elbow joint. As a consequence, a secondary
degenerative joint disease (DJD) will develop.
The
4 primary lesions are :
Ununited Anconeal Process (UAP)
Fragmented (medial) Coronoid Process (FCP) of the ulna
Osteochondritis Dissecans (OCD) of the medial humeral condyle
Elbow Incongruities (EI)
Dogs
with ED are young dogs of large breeds, 50% of which bilateraly
affected. An undetermined portion of affected dogs remain
clinically silent. Lame dogs show a non-specific unilateral
or bilateral frontleg lameness, which generally appears
between 4 and 8 months of age. Due to the secondary development
of DJD, more later lameness is also encountered.
I/
UNUNITED ANCONEAL PROCESS
UAP results from a lack of fusion of the anconeal process
to the ulna. The condition is seen in large breeds, with
a separate center of ossification within the anconeal process.
Normal fusion should occur at about 5 months of age. The
origin of the problem is due to either an abnormal shape
of the trochlear notch, or a dyssymetric growth of the ulna
and the radius with a relatively short ulna. This puts abnormal
pressure on the anconeal process (distractio cubiti), preventing
it from fusing with the ulna. Diagnosis of UAP is easy and
relies on radiograph, with lateral projection of the elbow
in a flexed position.
II/
FRAGMENTED CORONOID PROCESS
The medial coronoid process (MCP) is the cranio-medial part
of the ulno-humeral joint and lies medially to the elbow
joint. MCP can be partially or totally fragmented (FCP)
or insufficiently ossified (chondromalcia). FCP is the most
frequent cause of frontleg lameness linked to Elbow Dysplasia.
Unhappily, it is also the most difficult of the 4 primary
lesions to diagnose accurately. Oblique radiographic views
may show the separated piece of bone, or related osteophytes,
but in many cases diagnosis is made with arthroscopic examination,
CT scan or MRI (when avalaible). Sometimes, the displaced
coronoid can cause an erosion on the opposite site (medial
humeral condyle), wich is referred as a « kissing
lesion » and mimics an OCD of the medial humeral condyle.
The origin of FCP is generaly attributed to a slowing of
radial growth compared to ulnar growth. This puts abnormal
pressure on the medial coronoid process, leading to fragmentation.
III/
OSTEOCHONDRITIS DISSECANS (OCD) OF THE MEDIAL HUMERAL
CONDYLE
OCD on this site, as other epiphyseal OCD, results of abnormal
thickening of the joint cartilage, which acts as a growing
cartilage. This is due to lack of transformation of this
cartilage into bone tissue. Then a fissure line develops
in the thickened cartilage and leads to a cartilage flap.
The release of several debris from the broken cartilage
initiates a synovial inflammation, and may induce development
of a secondary degenerative joint disease.
Radiographic diagnosis of OCD of the medial humeral condyle
is easy. On cranio-caudal projection, or oblique views of
the elbow joint in extended position, a defect in the sub-chondral
bone is clearly visible. Sometimes the « flap »
is also visible when it is partially mineralised.
Several publications (Guthrie & al, Grondalen &
al, Swenson & al, Audell & al, Lavelle and Studert,
Studert & al) have emphasised the heritable aspect of
OCD of the medial humeral condyle as a multifactorial polygenic
threshold trait. Excess food intake, high calcium and phosphorus
intake, increase the severity and frequency of OCD in growing
puppies.
IV/
INCONGRUITIES (EI)
Most of EI are related to malalignment between the radius
and ulnar surface, due to dyssymetric growth of the two
bones. Several types of EI may be seen :
- a relatively short radius, which may coincide with FCP
- a relatively short ulna, wich may coincide with UAP
- a modified shape of the ulnar notch, which may coincide
either with UAP or FCP, or
both pathologies.
Even if EI doesn’t lead to FCP or UAP, due to abnormal
pressure on cartilaginous joint surface, osteoarthrosis
will develop.
Diagnosis relies on strict medio-lateral radiographs of
the extended joint. EI is shown as a « step »
between the ulnar and radial proximal surfaces, or a descreased
joint space between the ulnar notch and the humeral trochlea.
Very small steps may be controversial as it has been shown
that radiographic positioning of the elbow play a role on
interpretation of cubital congruity (Murphy & al, Mason
& al)
ED
THERAPY
Conservative treatment (weight control, adapted exercice,
analgesics or long terme NSAID treatment) must be considered
when severe DJD is already present as in such cases, the
benefit of surgical treatment is not always certain.
In early presented cases, surgical treatment is indicated.
For UAP (provided that the anconeal process is not too displaced
and keeps an anatomic » shape), proximal ulnar osteotomy
with or without lag-screw fixation may lead to anconeal
fusion. In other cases, excision of UAP is an alternative
option. For OCD, conventional or mini invasive approach
allows to cut free the cartilage flap and trim the abnormal
cartilage around the lesion. A forcefull lavage of the joint
helps to flush out any remaining debris. FCP needs excision
of the fragmented bone fragment, in conjonction with surgical
correction of any elbow incongruity. EI is corrected via
ulnar osteotomy (too short ulna) or ulnar ostectomy (too
short radius).
ED
RADIOGRAPHIC SCREENING PROGRAM :
Several
studies have proven that ED is an inheritable condition,
and that exclusion of affected dogs from the breeding program
will decrease the breed prevalence of the condition. As
affected dogs may or may not be lame, using lameness to
determine the presence of ED or the breed value of an animal
is not reliable. Therefore, the only feasible screening
is based on radiographs.
Minimal age is 12 months for official screening (check breed-club
for specific requirements). Both elbow must be radiographed.
Radiographs must be fully and permanently identified. The
veterinarian must state that he has personally checked the
dog’s identity (tatoo number or electronic identification).
The limb is placed directly on the cassette.
In France, we use 3 projections for each elbow joint : medio-lateral
projection on hyper flexed (45°) joint, medio-lateral
projection on extended elbow, oblique cranio-caudal latero-medial
projection.
Radiographic interpretation and scoring (ED 0, Sub-normal
elbow joint, ED 1, ED2, ED3) of the dog is based on presence
of arthrosis and/or primary lesions.