Recognizing Developmental Dysplasia of the Hip in Your Baby

Recognizing Developmental Dysplasia of the Hip in Your Baby

Developmental dysplasia of the hip (DDH) occurs when a baby’s hip joint doesn’t form properly. In most cases, the problem is present at birth, but DDH can also develop as a child grows. It’s essential for parents to know the signs of DDH. The earlier a specialist treats the condition, the better a child’s chances of appropriate development and living without hip problems later in life. DDH occurs in about one in 100 infants.

Defining DDH

The hip is a ball-and-socket joint. The ball, called the femoral head, sits at the upper end of the thighbone and fits snugly into a socket in the large pelvis bone. This ball moves around but always stays inside the hip socket, allowing the hip to move backward, forward and side-to-side while supporting body weight.

When a child has DDH, the ball is not fully covered in the socket or the socket is shallow, which can easily lead to a dislocated hip. Or the hip may already be dislocated or completely or partially out of the socket. Without treatment, the hip joint will not grow properly. As a child gets older, he or she might have pain when walking or develop arthritis at a young age.

Babies at Higher Risk of DDH

While any baby can have DDH, the risk is higher in babies who:

  • Are female
  • Are the first-born child
  • Have a family history of DDH
  • Were born in the breech position (buttocks first instead of head first)

In rare cases, babies can develop DDH after birth. For example, swaddling a baby with the legs straight and tight together can increase the risk of DDH. To help prevent this, talk to your provider about how to use sleep sacks and how to swaddle your infant correctly.

“There’s a lot of importance in how we take care of our babies’ hips after they’re born,” said hip specialist and pediatric orthopedic surgeon William Z. Morris, M.D. “Swaddling the legs in a forced extension can cause the hips to develop incorrectly. The ball and the socket are almost like moldable pieces of clay when you are young, so letting the hips and legs move into a flexed and separated position helps keep the ball tucked up in the socket and makes the socket deeper and the ball rounder.”

When swaddling your baby, focus on wrapping the arms and upper torso only, allowing the hips and legs to move without constriction.

Know the Signs

Babies with DDH do not have pain from the condition. However, parents may notice:

  • A clicking or popping in the hip that you can hear or feel
  • Differences in leg length (one leg being shorter than the other)
  • One leg or hip is not moving the same as the other
  • Skin folds under the buttocks do not line up
  • A limp when the child starts to walk

If you notice your baby has any of these symptoms, immediately make an appointment with your pediatrician.

Doctors usually find signs of DDH during a child’s annual checkup. If symptoms are present or the child has risk factors, the doctor will likely order tests to confirm a diagnosis. These might include:

  • Ultrasound: This imaging test uses sound waves to create pictures of the hip joint. Ultrasound works best with babies younger than 6 months old because the hip joint is mostly cartilage at this age and doesn’t show up on an X-ray.
  • X-ray: In babies older than 6 months, bones have formed well enough to appear on X-ray images.

If your child has DDH, your pediatrician will refer you to a pediatric orthopedic surgeon. The surgeon will choose the best treatment to hold the hip in place and help the ball stay in the socket so the hip joint will grow normally and not cause problems as your child gets older. Early intervention with DDH is important.

“Parents should know that DDH caught early is treated very successfully,” Morris said. “And the vast majority of the time we can do so without surgery.”

Treatment options for developmental dysplasia of the hip include:

  • Bracing: This is the most common treatment for babies younger than 6 months old. The soft fabric brace, called a Pavlik harness, is a shoulder harness with attached foot stirrups. The brace puts the baby’s legs in a “frog-like” position that allows the ball of the hip joint to fit into the socket properly. This treatment usually lasts about six to 12 weeks. Many babies don’t need additional treatment. Even severe cases, where the hip is fully dislocated, are treatable with a harness or brace more than 80% of the time.
  • Closed reduction and spica casting: If bracing does not correct the problem or the child is older than 6 months at the time of diagnosis, the surgeon might do a closed reduction procedure. The surgeon will inject contrast dye into the hip joint to see the cartilage and gently move the thighbone, guiding the ball of the joint into the socket. The baby will then wear a special cast, called a hip spica cast, for two to four months. The cast will hold the hip joint in place.
  • Open reduction: This is a type of surgery done if a closed reduction is unsuccessful or when the child is older than 18 months at the start of treatment. During the surgery, the surgeon moves muscles to see the hip joint and puts the ball properly in place. An open reduction also requires a hip spica cast to hold the hip joint in place.

When doctors find DDH early, your child will likely benefit more from nonsurgical treatment and may not need surgery. If you have any concerns about your child’s hips, talk to your pediatrician about a referral to a pediatric orthopedic specialist.

Is your baby showing signs of developmental dysplasia of the hip? Schedule an appointment with a specialist at the Scottish Rite for Children.

Share Your Story: Andi’s Life Changing Journey

Share Your Story: Andi’s Life Changing Journey

Meet Andi, a patient who is treated by our spine and hip experts. Learn more about her journey below.

Blog written by Andi’s mom, Tera, of McComb, Mississippi. 

Andi’s life changing journey started the moment she was born. At birth, we were told something was severely wrong with her hips and we would need to double diaper her to keep her hips spread apart. Nobody actually went into details with us until later at our post-delivery follow-up when Andi was three days old. At that time, our pediatrician told us he had never heard or felt a clunk in hips the way Andi’s hips were reacting to the hip check. Our pediatrician told us he thought she had hip dysplasia and we would need to meet with an orthopedic doctor.

We were initially referred to Children’s Hospital of New Orleans and Andi was just 1 week old when we had our first appointment with the orthopedic doctor. She was officially diagnosed with bilateral hip dysplasia and was put into a Pavlik harness, which was to be worn 24/7 for three months. We did harness adjustments every couple of weeks and after three months, the X-rays showed that the left hip responded to treatment, but the right hip did not. Our doctor, at the time, decided to try the Rhino abduction brace. It was then that we noticed that Andi was in a lot of pain. Hip dysplasia is generally not painful, but for her it was very painful.

When you touched her right leg or made any hip movement, her entire spine curved like a ‘C’ and she screamed in pain. She had X-rays done on her spine, but this did not give us any answers. We were told her spinal curvature (32 degrees) was not severe enough to be true scoliosis.
 
My husband and I began to research our options and that is when we found Texas Scottish Rite Hospital for Children. We live eight hours away and did not even hesitate about travelling to Dallas for a second opinion. The appointment process was quick, easy and we were able to get something scheduled right away.

Our first appointment was wonderful. 

Andi had Dr. Ramo and the staff scratching their heads, but they never gave up on her. They saw how much pain she was in and were able to pick up on developmental delays that nobody else had mentioned before. X-rays showed her right hip was still out of socket, her spinal curvature was now 42 degrees and the pain she was experiencing was being caused by inflammation.

Dr. Ramo suggested we allow Andi to continue to grow and develop and the plan was to repeat her scans in a couple of months. Time passed and we made another trip to Dallas. Her scans showed that her spinal curvature had since progressed to 54 degrees and Dr.Ramo decided to focus on her spine before we continued with further hip treatment. She was then placed in a Mehta cast – this process was rather simple, and the hospital staff made it easy.
 

From the moment we walked in the doors of the hospital to when we were discharged, our family felt comfortable, safe, loved and we knew our daughter was receiving the best care possible.

 
Fast forward a year later and Andi’s last Mehta cast was removed. Her spinal curvature had improved to 28 degrees and we were over joyed. She continues with nighttime bracing for a few months and then decided it was time to fix her hip.

Andi underwent a pelvic Osteomoy of the right hip and was placed in a unique spica/Mehta combination cast. She was in the combo cast for 13 weeks and at the end of this treatment, her hip looked wonderful! She did lose a little correction in her spine, but Dr. Ramo knew this would improve once she was able to wear a brace. She wore a rhino abduction brace for a month and then we continued with nighttime bracing.
 
Andi has been such a trooper throughout this entire process. For her, this is her normal nighttime routine – take a bath and then put on her brace. We had a follow-up appointment in December 2018 and her spinal curvature is now just 16 degrees. We will continue with her nighttime brace until our follow-up this summer and hopefully then, she will become an observation patient.

Everyone at Scottish Rite Hospital – from the registration staff, to the volunteers, nurse Marviel, Dr. Ramo and the cafeteria staff – they are all amazing. So kind, helpful, caring and welcoming! All of the hospital volunteers are always so giving and constantly put smiles on people’s faces.

This hospital made our struggles bearable.

Additional information on Developmental Dysplasia of the Hip

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Share Your Story: Too Hip for Dysplasia

Share Your Story: Too Hip for Dysplasia

Meet Sadie, a patient who is treated by our experts in our Center for Excellence in Hip. Learn more about her journey below.

Blog written by Sadie’s mom, Sarah Beth, of Longview. 

Sadie on her bed, smiling.

Sadie was diagnosed with Developmental Hip Dysplasia (DDH) at the age of 2 months old, when our pediatrician noticed a clicking in her right hip. We lived in Houston at the time and initially saw a pediatric orthopedic surgeon there. She wore a pavlik harness until she was 6 months old, with little to no improvement, and then switched to a Rhino brace. Both the Pavlik and the Rhino were worn for 23 hours a day, only giving her one hour of “freedom” each day. While she was hitting her development milestones, she was making little improvement on the angle of her hip. As we approached her second birthday, surgery became more and more of an option.
During this time, we moved to the Dallas area and made the switch to Texas Scottish Rite Hospital for Children.

We immediately felt a sense of calmness when we met with Dr. Herring and his staff for the first time.

His knowledge on her condition and his willingness to wait to let her body continue to grow was exactly what we were hoping for. For the first time in Sadie’s hip journey, I felt peace with her condition.

As time passed, we continued with her checkups and eventually decided that a pelvic osteotomy would be necessary for Sadie to gain adequate coverage of her hip socket.  The hospital staff did a great job answering all of our questions and helped us through this journey. Sadie likes to explain the surgery by telling people that her hip was shaped like an “L” and they had to shape it more like a “C.”
Deciding to have a major surgery did not come without some hesitation, but the doctors and nurses were incredibly patient with my lists of questions.

Dr. Herring with Saddie

The child life specialists were able to provide a sense of calm for Sadie in situations where my husband and I did not know how to keep her calm. 

They walked her through the surgery beforehand, helped keep her entertained throughout her inpatient stay, distracted her when different lines were removed and eventually told her that it was okay to giggle when the cast came off because it may tickle. That team was an absolute life-saver!

Sadie
Sadie spent six weeks in a Spica cast and during that time, learned to army crawl, maneuver herself and function with absolutely no problems. Her attitude and determination during this time was amazing.

Since having her cast removed, she has had two X-rays and they each show good coverage of her right hip socket. She quickly returned to normal activity and seeing her now, you would never know that there had ever been anything wrong with her hip or that she was in a cast for six weeks.

I completely trust the doctors, nurses, child life specialists and staff of the hospital. Their knowledge and welcoming atmosphere have made many potentially stressful situations a lot easier for our family.

From Sadie’s point of view – “My favorite part of staying in the hospital was getting to go the playroom and meeting the Texas Rangers. I love getting popcorn after each checkup and playing on the playground.”

Additional information on Developmental Dysplasia of the Hip

 

DO YOU HAVE A STORY? WE WANT TO HEAR IT! SHARE YOUR STORY WITH US.