Congenital Dislocation of the Hips CDH

 


Definition
Congenital Dislocation of the Hip, the terminology has been replaced by: DDH: generic term encompassing the many variations of congenital hip dysplasia, subluxation, and dislocation
 
Radiographic Appearance
Xrays taken before four months old - before the head of the thigh bone (femur) starts to convert from invisible-on-xray cartilage to visible bone (ossification) - are unreliable to rule out hip dysplasia. They must be repeated after ossification has begun to be trusted.
 On plain radiographs, after the femoral head has started to ossify features to note are, delayed appearance of the ossifying nucleus, a shallow acetabulum with displacement of the femoral head upwards and laterally from its normal position. (Image 1)

Ultrasonography serves as an excellent method for diagnostic imaging of the immature hip. Sonography affords direct visualization of the cartilaginous components of the hip joint. The value of ultrasonography diminishes as development of the ossification center occurs. Between six months and a year of age, radiography becomes more reliable. Usually by one year of age the center is sufficiently developed to prevent good visualization of the acetabulum with ultrasound. he ultrasound test of the hip is the best under four months.
 

Pathology
Developmental dysplasia of the hip (DDH) was formerly referred to as congenital dislocation of hip. Now that the condition is better understood, the former term is preferred to reflect the facts that

DDH is a developmental (ongoing) process, variable in manifestation and not always detectable at birth
DDH involves a dysplasia, or abnormal formation of the hip joint occurring between fetal life and maturity as a result of instability
The hips are not dislocated at birth, but if a dislocation occurs, then the complications of the dislocation - malformation of the hip socket, twisting of the thigh bone (femoral anteversion), and hip muscle shortening (contractures) will develop.
Hips that are found to be normal at birth (and even in the first few months of life) can subsequently be found to be abnormal later. This cannot be overemphasized! The best orthopedist in the world can be fooled by the initial hip exam. We cannot be complacent about your child's hip stability and development.

The cause of DDH is both physiologic - having to do with the child's basic makeup as well as the child's response to the maternal hormones
mechanical - a result of positional influences in utero
The majority of children with DDH have ligamentous laxity - looseness of the fibrous bands connecting bones together in joints. This predisposes to hip instability; instability allows the hip to slip out of position; and certain mechanical factors such as breech presentation can aggravate the problem. Maternal hormones associated with pelvic relaxation around the time of birth also aggravate the instability of the newborn hip joint by allowing softening and stretching of the baby's hip ligaments.

It has been estimated that only 1 in 100 newborn infants have clinically unstable hips (subluxatable - the ball of the hip is able to be moved around loosely in the hip joint - or dislocatable - the ball of the hip is able to be actually slid in and out of joint with a "clunk" that can be felt), whereas only one in 800 to 1,000 of newborn infants eventually experience a true dislocation whereby the ball of the hip lies outside the socket.

There is a 9:1 female predominance; apparently the baby's own female hormones must aggravate the abnormal looseness of the hip ligaments.
Of children with DDH, approximately 60% are firstborn
30-50% develop in the breech position; 2% to 3% of all babies are breech presentations, but about 20% of DDH patients are born breech.
The breech position tends to force the ball of the hip out of the socket, predisposing to dislocation after birth. Highest risk is the frank breech position with the hips flexed and the knees extended - basically feet up by the shoulders. There is also an association of congenital muscular torticollis ("wry neck"), metatarsus adductus (toes bent inward) or talipes equinovarus (club foot) with DDH. A child with any condition caused by intrauterine cramping deserves very careful attention to rule out DDH.

If an abnormal hip remains untreated, the child will develop the long-term complications, including:
osteoarthritis
pain
abnormal gait
unequal leg length
decreased agility

Diagnosis
The Barlow test is the most important manoeuvre in examining the newborn hip. The examiner attempts to push the ball of the hip rearward out of the socket.
The Ortolani test is a manoeuvre to reduce a recently dislocated hip. If positive, the examiner feels a "clunk" as it pops back into place. It is most likely to be positive in infants who are 1-2 month old because adequate time must have passed for the true dislocation to have occurred. After 2 mo of age, this test is no longer useful because of the development of soft tissue contractures which prevent the hip from being relocated.
The thigh creases should be symmetrical from side to side; if they are not, possible hip dislocation has to be considered carefully.
Leg length inequality is another tip-off to dislocation, as is uneven knee position from side to side.
 
Treatment:
If an unstable hip is recognized at birth, treatment consists of maintaining the position of the hip in flexion (knee up towards the head) and abduction (knee away from the centreline) for about 1-2 months. The Pavlik harness is the most widely used device, but the Frejka splint and some other devices are also used. The device chosen for treatment maintains proper position of the femoral head and allows for "tightening up" of the ligamentous structures as well as for stimulation of normal formation of the hip socket. The treatment must be continued until the hip is stable and xrays or ultrasound examinations are normal.

From 1-6 months, true dislocations may develop. As a consequence, treatment is directed toward reduction of the femoral head into the socket (acetabulum), usually with the Pavlik harness or similar device. The harness pushes the femoral head toward the socket, and usually, relocation of the femoral head will occur within 3-4 wk. The Pavlik harness is approximately 95% successful in dysplastic or subluxated hips and 80% successful in true dislocations. Triple diapering is frowned upon now because it promotes hip extension, which is not a good position for normal hip development. If a spontaneous reduction does not occur by splinting, then a surgical closed reduction (manipulation under anaesthesia) is done.

In the older infant from 6-18 Mo, surgical closed reduction (manipulation under general anaesthesia) is the major method of treatment.

After 18 months of age, the progressive deformities become so severe that major open surgical intervention is necessary to realign the hip.
 
Image 1

 

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