Dallas Morning News: Building true connections: Dallas Mavericks Mavs Academy keeps kids on the move with virtual camps this summer

Dallas Morning News: Building true connections: Dallas Mavericks Mavs Academy keeps kids on the move with virtual camps this summer

In partnership with the Dallas Mavericks, Scottish Rite for Children helps to reach youth and keep them active and healthy. The Mavs Academy promotes safety and wellness and our experts teach participants how to “Warm up the RITE way.”

In an ideal summer, the Mavs Academy would be serving more than 3,000 young student-athletes through camps at 25-plus locations across D-FW. But when the COVID-19 pandemic slowed normal life to a standstill earlier this year, Mavs Academy moved quickly to adjust to a new normal.

Read more about the virtual camps.

In-toeing, Out-toeing and Crooked Legs: Treatment Options and When to be Concerned

In-toeing, Out-toeing and Crooked Legs: Treatment Options and When to be Concerned

The following is a summary of a presentation on rotational and angular alignment conditions in the lower extremity. Corey S. Gill, M.D., pediatric orthopedic surgeon addresses when to be concerned and when to make a referral. The lecture was given as part of the Coffee, Kids and Sports Medicine series and is available in our on-demand learning offerings.

Watch the full lecture I Print the PDF

Physical Exam

Tips for Infant and Toddler Exam

  • Set up the environment for a relaxed exam: evaluate on the caregiver’s lap, dim the lights and play music.
  • Screening for other conditions is important.
    • Measure height, weight, and head circumference.
    • Evaluate the hip to rule out developmental hip dysplasia.
  • Toddlers are more likely to walk away from you than toward you.

Tips for School Age Children Exam

  • Must be able to see the legs. Provide or ask the child to wear shorts.
  • Leave the exam room to observe walking and running if space allows.
  • Talk to the child directly to help him or her relax.

Rotational Deformities

Structural abnormalities that cause rotational alignment issues can be measured with these tests:

  • Foot progression angle
  • Hip internal and external rotation in prone position
  • Thigh-foot angle
  • Forefoot alignment

Watch the full lecture to learn these tests.

In-toeing

This is likely the most common condition referred to pediatric orthopedics. In a study at Scottish Rite, only one percent of referrals had a diagnosis other than “benign in-toeing.” It is important to educate families that there is wide range of normal in all of these measures and it changes over time. Parents may feel that this condition will lead to long-term problems without surgery or bracing, which is inaccurate.

Common misperceptions include:

  • “My toddler falls all of the time because of in-toeing.”
  • “My child’s feet will be stuck this way forever without treatment.”
  • “The in-toeing is going to cause my child to have arthritis and joint problems.”
  • “In-toeing will prevent my child from being a high-level athlete.”

Metatarsus adductus
Most commonly identified in infants, congenital adductus of the forefoot on the midfoot may be related to intrauterine positioning. Check the contralateral foot (bilateral metatarsus adductus), hips (developmental hip dysplasia) and neck (torticollis). Studies suggest 4% of children with metatarsus adductus have hip dysplasia. Treatment is focused on observation. Stretching may help and gives the parent something to offer the child. Casting may be used if the condition persists for 6-12 months. Surgery is extremely rare. The condition commonly resolves within the first one to three years of life.

Internal Tibial Torsion
Most commonly identified in toddlers, internal tibial torsion does not require treatment, often resolving on its own. Historically, bracing was commonly used, but this is not recommended for this condition. In cases with significant torsion that causes functional problems, surgery may be discussed after the age of ten. This condition is often associated with infantile Blount disease or genu varum which is more likely to cause functional problems than the torsion.

Femoral Anteversion
Most femoral anteversion decreases and resolves around age 8-9 years (elementary school age). These children may prefer to “w” sit because it is comfortable, but there is no clear data supporting “w” sitting causing worsening femoral anteversion. This condition is typically not related to long-term problems like arthritis or other functional disability. In cases of severe functional or cosmetic deformity, surgery can be successful, but can have significant risks. Our multidisciplinary team for these complex cases includes a psychological evaluation.

Out-toeing

Though slightly more functionally limiting than typical in-toeing, out-toeing rarely causes long-term problems or requires surgical intervention.

Femoral Retroversion
This condition rarely causes long-term problems, however, in some, it may predispose to slipped capital femoral epiphysis (SCFE). Osteotomy to correct the alignment is rarely needed.

External Tibial Torsion
Much like internal tibial torsion, this condition improves in most children before or around the age of 10. In patients with suspected external tibial torsion, checking the foot for tarsal coalition or a rigid flatfoot is important. The foot may turn out causing a stance and gait that mimics external tibial torsion. In cases where the deformity causes functional limitations, typically with excessive torsion greater than 40 degrees, surgical corrective osteotomy may be indicated.

Slipped Capital Femoral Epiphysis (SCFE)
With increased obesity in growing adolescents, the nation continues to see a dramatic rise in the incidence of SCFE. If a child presents to a health care provider with hip or knee pain, especially if he or she is an overweight adolescent with an out-toeing gait, ruling out SCFE is essential. These patients present with hip and sometimes knee pain and in about 25% the condition occurs bilaterally. Referral for unstable SCFE’s needs to be made immediately (talk to an orthopedic doctor on the phone or send patient to the ER). Treatment is to surgically stabilize and prevent worsening position and avascular necrosis in the hip.

Gill emphasizes that the factors that make this population at high risk of SCFE also makes them at high risk of poor long-term outcomes. Counseling these patients to manage weight and co-morbidities is a multidisciplinary concern. He encourages the audience to “not miss” this diagnosis so it can be treated early.

Angular Deformities
Babies have a natural progression of genu varum (bow-legged) as an early walker to genu valgum (knock-kneed) in the first few years of life. Counseling parents regarding typical development can provide reassurance. However, there are some conditions that may need to be referred.

Genu Varum – “Bow-Legs”
Pre-existing conditions such as infection, trauma, metabolic bone diseases and skeletal dysplasia’s that cause growth plate disruptions, may cause genu varum. These are typically already known conditions and are not the focus of this discussion.

Physiologic Genu Varum (PGV)
This is a condition that will get better on its own without treatment. The varus may be dramatic, but will resolve without treatment. It is important to distinguish between PGV and Blount’s disease.

Blount’s Disease
Unlike PGV, this will not improve on its own. By age 2, varum should resolve. If it doesn’t, radiologic evaluation may reveal proximal tibia growth deformity. Historically, bracing or osteotomy were provided to improve the alignment. Currently, growth modulation, a less involved procedure, is offered if bracing is not effective by the age of three. In some, the condition does not develop until a later age and may be bilateral. Referral for pain, swelling or unilateral genu varum is appropriate.

Genu Valgum – “Knock-Knees”
Other systemic conditions like rickets, trauma or osteochondromatosis may cause this positioning and need to be addressed directly. Treatment for the genu valgum may be necessary, however, these causes are not the focus of this discussion.

Genu valgum is most noticeable around age 3 in normal children, and then gradually improves until the age of 8 or 9. The structural condition may be minor and cause a cosmetic concern or a many contribute to significant orthopedic problems such as patellar instability and osteochondritis dissecans.

Treatment, when indicated, is surgical. In children who have open growth plates, growth modulation by temporarily tethering the growth plate with a plate and screws is effective. In older children, an osteotomy to remove or add a wedge of the bone realigns the lower extremity.

Get to Know our Staff: Courtney Warren, Physical Therapy

Get to Know our Staff: Courtney Warren, Physical Therapy

What is your role at Scottish Rite for Children? 
I am an outpatient physical therapist in the Orthopedic department at the Frisco campus. I evaluate and treat children and adolescents with musculoskeletal, neurologic and rheumatologic conditions through specialized exercises, activities and other techniques. I work with many specific populations including patients with scoliosis, amputations, birth defects and acquired injuries. My goal is to figure out physical barriers that may keep a child from their goals and then design treatment to improve or adapt those barriers in order to achieve their highest level of function.   
 
What do you enjoy most about Scottish Rite?
I enjoy working with the large variety of patients that Scottish Rite treats. This includes a wide spectrum of age, level of function and even nationalities. People come from all over to be treated here. 
 
I also really enjoy the fact that the staff are here to do what is best for the patients and everyone works hard to make sure finances or other barriers do not restrict treatment. 
 
What was your first job? What path did you take to get here?
My first official job was working at a grocery store when I was a teenager. I had odd jobs all throughout high school and college. My path to becoming an employee at Scottish Rite is kind of interesting. My mother began working as a surgical nurse in Dallas when I was just 3 years old, so I grew up attending holiday parties and staff picnics. I eventually became a junior volunteer, a shadow student and then completed my final clinical rotation for physical therapy school – all at Scottish Rite. It was my first job out of school, and I have been here six years now. 
 
I can actually remember the exact day and specific patient I was observing at Scottish Rite when I decided I wanted to be a physical therapist. I was 14 years old and I never changed my mind! 
What’s the coolest or most interesting thing you’re working on right now?
I completed my first level certification in the BSPTS Schroth based method for the treatment of adolescent idiopathic scoliosis in 2018 and I was planning to attend/test for the second level certification this summer. That was put on hold with the current events, but I’m hoping to complete it soon. 
 

What are you currently watching on Netflix/Hulu/TV/etc.? 
In our home, Daniel Tiger or Sesame Street is usually playing (I have a 2-year-old), but I recently started watching The Amazing Race series and have enjoyed seeing the world travels, even just by TV screen. 
 
What would be the most amazing adventure to go on?
When I was younger, I always wanted to run a race on every continent. So far, I have done two – North America and Europe. I would love to check off more! 
 
What are some small things that make your day better?
At work, I really enjoying watching a child reach a goal or come back for a social visit when they have been discharged for a while. Seeing/hearing children doing what they love is the best!
 
At home, there is nothing better than my son running up to hug me and tell me about his day when I get home. 
 
What is special about the place you grew up?
I grew up in Wylie, Texas. We have a bit of an unusual motto, “AHMO”, that originated from a Dean Martin comedy roast. It means a lot of different things to different people and can be found literally all over the town. 
 
What is your favorite thing to do when you’re not working? 
I can be found doing lots of things to stay active. Running, playing soccer and keeping up with my son are just a few of my favorite things!

The Limping Child

The Limping Child

Article originally published in an issue of the Pediatric Society of Greater Dallas newsletter. Written by Assistant Chief of Staff Emeritus Charles E. Johnston, M.D. 

Print the PDF

It may seem obvious to say, but a limp is never a normal finding, and in fact can be an ominous symptom in any child. The differential diagnosis can be fairly extensive, but by far the most important feature is whether or not the limp is associated with pain, known as an antalgic limp, because such a limp can be the presenting symptom of a serious infection, malignancy, or repetitive injury that requires timely and appropriate management.

Diagnosis – Gait and Physical Exam
The history and physical examination are probably the most important aspects of the evaluation of a limping child. Is there really a limp? It is not always obvious that a child, especially a toddler who cannot communicate, is, in fact, limping, especially when the limp is painless. The default position is that the mother is always right until proven otherwise, and of course parents will not hesitate to bring the limp to the physician’s attention.
One must remember that all toddlers fall, they probably fall every day, and most falls are not witnessed nor are related to an underlying sinister process. Recent medical history may be totally negative or clouded with uncertainty, unless there is an important birth history or recent febrile illness.

Physical examination of a child with a limp complaint where the gait disturbance isn’t that obvious requires that he/she be observed in a quiet area with a minimum of the upper half of the buttocks exposed. Placing an ink mark on each sacral dimple, and observing the undiapered gait from behind, will provide the best opportunity to confirm “waddling”, or pelvic rise and fall during stance phase by watching the sacral dots and the shoulders shifting concomitantly. Toe-walking, however subtle, may be another sign confirming a painless limp.

In an antalgic limp, the stance phase is shortened n the affected side, as the child avoids weight-bearing due to pain by getting off the affected extremity as quickly as possible. Refusal to bear weight on one or both lower extremities raises the additional possibility of axial (spinal) involvement, or a systemic illness. An antalgic limp demands a more urgent evaluation, especially if the child has evidence of illness (fever, malaise, poor appetite, failure to thrive) or a suggestive recent medical history.

The next step is pain localization, especially if the child is calm enough for palpation. With the child seated on a parent’s lap, or an equivalent relaxed position on an examination table, one should begin a systematic palpation of both extremities, beginning with the non-affected side‘s toes and foot, and then gradually working up the leg to gently move the ankle through its range of motion, moderately compress/ squeeze the tibia and fibula every 3-5 cm along the diaphysis, gently move the knee through its range of motion, squeeze the thigh, and then move the hip through its range of motion. By starting with the non-affected side (if that can be determined) and placing the child (and parent) at ease, the likelihood of eliciting an interpretable response when the affected area is approached is enhanced. Additionally, one should never pass up the chance to examine a sleeping child, proceeding as just described but with the affected side, trying to localize the problem before the child abruptly awakes when the painful region is reached. Obviously, identification of the painful area is critical to guide the ordering of subsequent imaging studies, which will be diagnostic.

Refusal to walk, or in the older child that refuses to bend over to pick up an object on the floor, may identify a rigid, guarded back as the presentation of discitis/vertebral osteomyelitis or tumor.

Painless limping suggests either a developmental abnormality of the hip, such as dislocation or an early case of synovitis (e.g. transient, Legg-Perthes); a congenital leg abnormality such as a discoid meniscus, patella mechanism problem, or limb reduction deformity (short femur, coxa vara); a neuromuscular diagnosis, determined best by noting apparent weakness, abnormal tone (hypo- or hypertonic) or poor balance; or a fairly obvious limb length discrepancy. The classic “waddle” of a congenital hip dislocation is identified by the drop of the unaffected hemi-pelvis (unilateral involvement) during single limb stance on the affected side, coupled with a trunk lean or shoulder shift toward the affected side, a compensation for maintaining the body center over the unstable hip joint. Static physical examination should confirm a restriction of motion or, in the case of developmental dysplasia of the hip (DDH), a possible “clunk” if the hip can actually be reduced with abduction and flexion (the “Ortolani” maneuver). Generally, in the walking aged child, the latter cannot be demonstrated because the dislocation has become more “fixed” and thus the main physical finding will be restricted abduction in flexion of the hip in question.

Keep in mind that hip pathology pain can be referred to the lower thigh or knee. Both Legg-Perthes and slipped capital femoral epiphysis (SCFE) can present with “knee pain” as chief complaint. The clinician will note on gait inspection that the foot is externally rotated in SCFE, while the patient walks with a stiff, non-moving hip due to synovitis in Perthes.

Muscle weakness or decreased tone, especially of more proximal muscle groups (e.g. hip girdle muscles) may be confirmed by the Gower sign, where a child will “climb” up their legs when asked to stand up from a sitting or lying position on the floor. Toe walking, especially unilateral, or a child with spasticity or seeming rigidity from increased tone, may be the first recognized sign of cerebral palsy.

Imaging Studies
Plain radiographs in the acute setting are usually indicated to survey the area of concern, the key is to pinpoint that area in the physical exam. In acute infections (< 1 week), bone changes (periosteal reaction, lytic lesions), may not yet be visible, but deep soft tissue swelling may be visible to confirm the likelihood of an inflammatory fluid collection purulence.

For a non-acute condition (painless limp), plain radiographs may provide the exact diagnosis of a dislocated hip, Perthes or a SCFE. Remember to order a lateral view of the hip when considering either the latte 2 diagnoses, as a single AP view may not be diagnostic.

Ultrasound of the painful suspected septic hip is a standard imaging modality looking for an effusion. Actually, ultrasound can be useful for any joint suspected of septic effusion and can also confirm the soft tissue fluid collection of pyomyosistis or abscess, and thus direct a needle aspiration for culture.

MRI is the best and most precise modality, but should NOT be the first-line imaging to be considered in the majority of cases. Because of the need for anesthesia, MRI should NOT be used as a screening test, but is best used to determine the need for surgery, as well as the extent of the surgery to adequately drain a fluid collection or treat a bony lesion, or to direct a needle biopsy of a suspected bone or soft tissue neoplasm in the non-acute setting. A common scenario for suspected infection would be to review the focused MRI imaging immediately and then proceed to the operating room under the same anesthetic.

Similarly, bone scan is rarely indicated as a screening test, due to the amount of radiation and the greater degree of information obtained by MRI. CT scan is valuable for surgical planning, and may play an important diagnostic role in certain axial (spine, pelvis) lesions of bone that are not well visualized by MRI. Again, CT is NOT a screening modality.

Lab Tests
Any child suspected of an infection of musculoskeletal origin should have a CBC with differential, sedimentation rate (ESR) and C reactive protein (CRP) determinations. WBC count and differential may help to differentiate a bacterial from a viral synovitis by virtue of both absolute count (e.g. < 10000 = non-bacterial) as well as percent of neutrophils vs. lymphocytes. With a ESR > 40 and WBC > 12000, combined with a painful joint or refusal to bear weight, the chance of a septic arthritis exceeds 70 %. Add a fever and the incidence  exceeds 90%. Minimally elevated ESR and CRP provide evidence of a non-inflammatory acute process. Don’t overlook an unusually high or low WBC count, and/or elevated platelet count, as these may be an early indication of leukemia which can present with the clinical picture of bone pain/limp/refusal to walk in a child with malaise and systemic symptoms of illness.

Final Thought
The key to diagnosis and treatment for the limping child is a well-performed physical exam after obtaining key points of history. Localizing the “lesion” in the acute setting is critical to the timely diagnosis and management of what may be a life- or limb-threatening condition.

O.I. Coordinated Care Center: A Multidisciplinary Approach to Care

O.I. Coordinated Care Center: A Multidisciplinary Approach to Care

At Scottish Rite for Children, our experts care for the common to the complex of pediatric orthopedic conditions. Depending on the severity, a child might require treatment from various disciplines – needing specialists who can provide care for the different aspects of the disease. In order to do this, we have developed specialty clinics – like the Osteogenesis Imperfecta (O.I.) Coordinated Care Clinic.

Osteogenesis Imperfecta (O.I.), also known as brittle bone disease, is a group of genetic disorders that predominantly impacts the bones. Children born with O.I. have bones that break and/or fracture very easily from a minor injury or even from no apparent cause. Other common characteristics of the disease include:

  • Skeletal Deformity
  • Short stature
  • Severity of the disease determines the type: Type I, II, III, IV

As an institution who is dedicated to caring for the whole child, the purpose of the O.I. Coordinated Care Clinic is to provide comprehensive treatment for every aspect of the disease – making it easy for families to receive expert care for their child from different specialists in one location. Led by Chief Medical Officer B. Stephens “Steve” Richards, M.D., medical director of Abulatory Care Brandon A. Ramo, M.D., and pediatric nephrologist Mouin Seikaly, M.D., the clinic includes experts from the following disciplines:

  • Orthopedic surgery
  • Bone metabolism
  • Occupational and Physical Therapy
  • Psychology
  • Nutrition
  • Child Life
  • Therapeutic Recreation
  • Dentistry
  • Family Services
  • Developmental pediatrics

Our team understands that this can be an overwhelming diagnosis. We are here to help guide our families and provide support wherever it is needed.

WFAA: Healthcare Heroes

WFAA: Healthcare Heroes

Scottish Rite for Children joined other North Texans to visibly express solidarity with local health care workers who are on the frontlines of fighting the coronavirus. As a show of support, white ribbons can be seen across the grounds. 

Watch the full story on YouTube.