Development Dysplasia of Hip

Development Dysplasia of Hip

| Development Dysplasi
what is Development Dysplasia of Hip ?

DDH, formely known as congenital dislocation of hip, is a congenital or developmental deformation or misalignment of the hip joint.

Hip dysplasia can range fro

m barely detectable to severely malformed or dislocated.

  The condition can be bilateral or unilateral.

  • Although DDH is most often present at birth, it may also develop during a child's first year of life. Recent research shows that babies whose legs are swaddled (wrap) tightly with the hips and knees straight are at a notably higher risk for developing DDH after birth. As swaddling becomes increasingly popular, it is important for parents to learn how to swaddle their infants safely, and to understand that when done improperly, swaddling may lead to problems like DDH.
  • In all cases of DDH, the socket (acetabulum) is shallow, meaning that the ball of the thighbone (femur) cannot firmly fit into the socket. Sometimes, the ligaments that help to hold the joint in place are stretched. The degree of hip looseness, or instability, varies among children with DDH.
  • Dislocated. In the most severe cases of DDH, the head of the femur is completely out of the socket.
  • Dislocatable. In these cases, the head of the femur lies within the acetabulum, but can easily be pushed out of the socket during a physical examination.
  • Subluxatable. In mild cases of DDH, the head of the femur  simply loose in the socket. During a physical examination, the bone can be moved within the socket, but it will not dislocate.


Who Gets Developmental Dysplasia of the Hip?

Any baby can have DDH. But there's a higher chance of being born with it in babies who:

  • are girls
  • are first-born
  • were breech babies (in the womb buttocks-down instead of head-down), especially during the third trimester of pregnancy
  • have a family member with the condition, such as parent or sibling
SIGN AND SYMPTOMS
  • The baby's hips make a popping or clicking that is heard or felt.
  • The baby's legs are not the same length.
  • One hip or leg doesn't move the same as the other side.
  • The skin folds under the buttocks or on the thighs don't line up.
  • The child has a limp when starting to walk.
Investigations
  • An ultrasounduses sound waves to make pictures of the baby's hip joint. This works best with babies under 6 months of age. That's because most of a baby's hip joint is still soft cartilage, which won't show up on an X-ray.
  • An X-rayworks best in babies older than 4–6 months. At that age, their bones have formed enough to see them on an X-ray.
TREATMENT

When DDH is detected at birth, it can usually be corrected with the use of a harness or brace. If the hip is not dislocated at birth, the condition may not be noticed until the child begins walking. At this time, treatment is more complicated, with less predictable results.

 Nonsurgical Treatment

Treatment methods depend on a child's age.

Newborns. The baby is placed in a soft positioning device, called a Pavlik harness, for 1 to 2 months to keep the thighbone in the socket. This special brace is designed to hold the hip in the proper position while allowing free movement of the legs and easy diaper care. The Pavlik harness helps tighten the ligaments around the hip joint and promotes normal hip socket formation.

Newborns are placed in a Pavlik harness for 1 to 2 months to treat DDH.

Parents play an essential role in ensuring the harness is effective. Your doctor and healthcare team will teach you how to safely perform daily care tasks, such as diapering, bathing, feeding, and dressing.

 

1 month to 6 months. Similar to newborn treatment, a baby's thighbone is repositioned in the socket using a harness or similar device. This method is usually successful, even with hips that are initially dislocated.

How long the baby will require the harness varies. It is usually worn full-time for at least 6 weeks, and then part-time for an additional 6 weeks.

If the hip will not stay in position using a harness, your doctor may try an abduction brace made of firmer material that will keep your baby's legs in position.

In some cases, a closed reduction procedure is required. Your doctor will gently move your baby's thighbone into proper position, and then apply a body cast (spica cast) to hold the bones in place. This procedure is done while the baby is under anesthesia.

Caring for a baby in a spica cast requires specific instruction. Your doctor and healthcare team will teach you how to perform daily activities, maintain the cast, and identify any problems.

6 months to 2 years. Older babies are also treated with closed reduction and spica casting. In most cases, skin traction may be used for a few weeks prior to repositioning the thighbone. Skin traction prepares the soft tissues around the hip for the change in bone positioning. It may be done at home or in the hospital.

Surgical Treatment

6 months to 2 years. If a closed reduction procedure is not successful in putting the thighbone is proper position, open surgery is necessary. In this procedure, an incision is made at the baby's hip that allows the surgeon to clearly see the bones and soft tissues.

In some cases, the thighbone will be shortened in order to properly fit the bone into the socket. X-rays are taken during the operation to confirm that the bones are in position. Afterwards, the child is placed in a spica cast to maintain the proper hip position.

Older than 2 years. In some children, the looseness worsens as the child grows and becomes more active. Open surgery is typically necessary to realign the hip. A spica cast is usually applied to maintain the hip in the socket.

 

Recovery

In many children with DDH, a body cast and/or brace is required to keep the hip bone in the joint during healing. The cast may be needed for 2 to 3 months. Your doctor may change the cast during this time period.X-rays and other regular follow-up monitoring are needed after DDH treatment until the child's growth is complete.

PHYSICAL THERAPY

A treatment that isn’t often used is traction. Traction exists of the application of a force to stretch certain parts of the body in a certain direction. This will soften the tissue around the caput femoris and will allow the caput femoris to move back in the acetabulum.

Traction consists of pulleys, strings, weights, and a metal frame attached over or on the bed. Traction is most often used for approximately 10 to 14 days. The application of ice on the painful regions helps to numb pain and reduces the inflammation.

Regular, low- or non-impact exercise such as swimming, aquatic therapy or cycling train strength and range of motion. Strong muscles will act like shock absorbers and provide greater support for the hip. Weight loss for those overweight can significantly reduce the stress on the hip and reduce pain. Physical therapy can be used to increase strength and flexibility around the joint which will decrease pain. Physical therapy can also be used to teach the body to better align itself which will lead to a decrease of stress on the joint. 

Complications

Children treated with spica casting may have a delay in walking. However, when the cast is removed, walking development proceeds normally.

The Pavlik harness and other positioning devices may cause skin irritation around the straps, and a difference in leg length may remain. Growth disturbances of the upper thighbone are rare, but may occur due to a disturbance in the blood supply to the growth area in the thighbone.

Even after proper treatment, a shallow hip socket may still persist, and surgery may be necessary in early childhood to restore the normal anatomy of the hip joint.

Outcomes

If diagnosed early and treated successfully, children are able to develop a normal hip joint and should have no limitation in function. Left untreated, DDH can lead to pain and osteoarthritis by early adulthood. It may produce a difference in leg length or decreased agility.

Even with appropriate treatment, hip deformity and osteoarthritis may develop later in life. This is especially true when treatment begins after the age of 2 years.

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