At the Forefront of Innovation: Spinal Surgery at Scottish Rite for Children

At the Forefront of Innovation: Spinal Surgery at Scottish Rite for Children

Hearing that your child needs spinal surgery for scoliosis brings a flood of questions and a lot of uncertainty. Using the newest technology and innovative methods, the experts at Scottish Rite for Children are some of the best pediatric orthopedic surgeons in the world. Our leaders support your child throughout treatment, making their spinal surgery a success from start to finish.

We provide a multidisciplinary, patient-centered approach to scoliosis treatment. Spinal maturity; the degree, extent and location of the curve; and the potential for progression are all considered when determining treatment.

Types of Scoliosis

  •  Adolescent idiopathic scoliosis (AIS) –  the most common form of scoliosis that occurs in children ages 10 to 18
  • Congenital scoliosis –  scoliosis that is present at birth and is due the intra-uterine formation of abnormally shaped/formed vertebrae
  • Early-onset scoliosis – scoliosis that occurs before the age of 9
  • Neuromuscular scoliosis –  secondary scoliosis that develops because of an underlying medical condition that adversely affects the brain, nerves, or muscles
  • Syndromic Scoliosis: An underlying genetic syndrome that causes the scoliosis

Additionally, scoliosis can be categorized by the following:

  • Thoracic scoliosis –  curve in the middle, or thoracic, part of the spine
  • Lumbar scoliosis – curve in the lower, or lumbar, part of the spine
  • Thoracolumbar scoliosis – curve in both the spine’s lower thoracic and upper lumbar parts

When Surgery is Needed for Scoliosis

Depending on the child and the severity of their curve, surgery may be the best treatment option. While not all cases of scoliosis require surgery, the following factors are an indication that surgery is needed:

  • Your curve is greater than 50 degrees, and/or
  • You have significant growth remaining
  • Your curve progressed to 50 degrees despite compliance with brace wear
  • You have a underlying neuromuscular or syndromic condition.

The most common type of surgery performed for scoliosis is a spinal fusion. In a spinal fusion, the curved vertebrae are fused together to create a single, solid bone. This stops the growth in the abnormal part of the spine and prevents the curve from worsening. Metal rods attached by screws, hooks or wires are used to hold the spine in place until the bone heals. In all spinal fusions, a bone graft is used to help promote the fusion and the bones grow together to create one solid bone.

Having Spinal Surgery at Scottish Rite

Led by Daniel J. Sucato, M.D., M.S., our Center for Excellence in Spine employs six pediatric orthopedic surgeons who specialize in spinal surgery for scoliosis. Our diverse team of surgeons works together to create individualized treatment plans for each patient and ensure that the child and the family know what to expect each step of the way. Multiple departments work together to provide a multidisciplinary approach to care and treatment. Orthopedics, Psychology, Physical Therapy and more will address all your child and their needs to ensure they are prepared for surgery. Our psychologists help our patients cope with having surgery and address their feelings about their procedure, giving children the opportunity to express their emotions. Following surgery, our team works with your child to make recovery as easy as possible.

Tackling the Most Complex Cases

New and innovative techniques allow our experts to tackle the most difficult cases.  This includes Magnetic Expanded Growth Rods (MCGR), Halo Gravity Traction (HGT), Vertebral Body Tethering (VBT), and Posterior Spinal Fusion (PSF). Our experts have experience treating complex cases, such as treating patients with a curve of over 100 degrees.

Road to Recovery

Following surgery, our team begins the recovery process with the patient. Using different pain management techniques. Our physicians are dedicated to seeing each patient through their recovery.

After a spinal fusion, it is common to need to minimize bending or heavy lifting. Our surgeons will go over limitations and discuss the importance of proper aftercare. Our team works with each patient to determine readiness to return to activities and coaches them through the recovery process.

How to Learn More and Become a Patient

Learn more about our Center for Excellence in Spine and scoliosis treatment.

Learn how to and how to make an appointment with one of our world-renowned experts.

Scottish Rite for Children Awarded Department of Defense Research Grant

Scottish Rite for Children Awarded Department of Defense Research Grant

Researchers at Scottish Rite for Children were awarded a $100,000 grant from the Department of Defense’s Neurofibromatosis Research Program. This grant will fund efforts to investigate new treatments for bone fractures in children with Neurofibromatosis Type 1 (NF1).
 
NF1 is an uncommon genetic disorder associated with pediatric and adult tumors. Some children with NF1 develop orthopedic conditions requiring treatment, such as scoliosis and persistent bone fractures. For many years, Scottish Rite has been recognized as an international leader in the care of children with NF1. Recently researchers at Scottish Rite, led by former Assistant Chief of Staff B. Stephens Richards, M.D., co-led a clinical trial testing the INFUSE graft to treat persistent fractures in children with NF1. Surgery is currently the best option for children with NF1, but a team of Scottish Rite researchers is dedicated to developing new, less invasive treatment methods.
 
“Our team has dedicated years of research to understand why these persistent fractures occur in children with NF1,” says Jonathan Rios, Ph.D., assistant director of Molecular Genetics and lead investigator of the study. While several drugs are either approved by the FDA or currently in clinical trials to treat tumor manifestations of NF1, no such treatments exist for orthopedic conditions associated with NF1. “All of our team’s efforts have led to this moment, where we can now test new therapies in the lab. And by evaluating therapies already in clinical trials for other aspects of NF1, we hope to rapidly translate the most promising of these therapies to treat fractures in children with NF1,” Rios says.
 
“Dr. Rios’ research will allow us to advance how we care for children with NF1 suffering from persistent fractures and will improve the lives of children with NF1 at Scottish Rite and around the world,” Chief of Staff for Scottish Rite for Children Daniel J. Sucato, M.D., M.S., says. “Dr. Rios’ research exemplifies Scottish Rite’s reputation as an international leader in translational research that will bring new treatments to children for years to come,” Director of Basic Research Carol Wise says.
 
search about our leading-edge research.
 
Jonathan J. Rios, Ph.D., is the assistant director of Molecular Genetics at Scottish Rite, as well as an associate professor in the McDermott Center for Human Growth and Development and the Departments of Orthopaedic Surgery and Pediatrics and is a member of the Simmons Comprehensive Cancer Center at the University of Texas Southwestern Medical Center (UTSW). Carol Wise, Ph.D., is the Director of Basic Research at Scottish Rite and is a professor in the McDermott Center for Human Growth and Development and the Departments of Orthopaedic Surgery and Pediatrics at UTSW. Dr. Sucato is the Chief of Staff at Scottish Rite and is a Professor in the Department of Orthopaedic Surgery at UTSW.
World-Renowned Hip Care

World-Renowned Hip Care

Scottish Rite for Children’s Center for Excellence in Hip has a long tradition of providing the highest-quality medical care to thousands of children, from newborns to adolescents and young adults. Led by director and pediatric orthopedic surgeon Harry Kim, M.D., M.S., the team provides a coordinated and comprehensive approach to care that brings together hip specialists from orthopedics, radiology, physical therapy, psychology and more. This multidisciplinary team approach allows us to offer a broad spectrum of operative and nonoperative care options to preserve, improve and repair the native hip joint. At the Forefront of Innovation  Our experts are committed to advancing clinically important research to provide the best care to our patients. Several of the center’s research projects have led to revolutionary, life-changing results. Patients who had evaluation and treatment at our center have the opportunity to participate in large patient registries to allow for evaluation of treatment outcomes for a variety of conditions. These studies lead to new insight and significant improvement as our team modifies treatment algorithms based on these results. In addition, doctors and researchers are involved in multicenter hip research groups with peers at top-tier institutions around the country. They regularly collaborate to discuss the latest innovations and treatment techniques regarding patients diagnosed with pediatric hip conditions and injuries. Movement Science Laboratory The accredited movement science laboratory is an integral part of the treatment of our patients. The multidisciplinary team of engineers and kinesiologists use leading-edge technology to evaluate and identify joint motion, net joint forces, muscle activity, strength, foot plantar pressures and oxygen consumption. These analyses guide the development of individualized treatment plans for our patients and support research. The clinical research team partners with movement science to study the changes experienced with surgical intervention to ensure each patient continues to maintain improved hip functions. Multidisciplinary Complex Hip Clinic This clinic brings all of our hip experts together in one clinic to review and evaluate each patient in person together. The history, physical examination and images are evaluated, and various options are discussed for treatment. The multidisciplinary approach also includes experts in the fields of physical therapy, psychology, pain management and nursing. A comprehensive diagnostic (if necessary) and treatment plan is then developed specifically for each patient. If surgical treatment is necessary, the full range of procedures are available with the experts in the field to include hip preservation surgery (both open and arthroscopic options) as well as the potential for utilizing total hip arthroplasty (replacement) when appropriate. This clinic occurs every month and only those patients requiring this multidisciplinary approach are included. Patients may request to be seen in this clinic. Hip Team All of our pediatric orthopedic surgeons are board certified in orthopedic surgery and also completed a fellowship in pediatric orthopedics. Several of our medical staff have a particular interest in treating and studying pediatric and adolescent hip conditions. Harry Kim, M.D., M.S. 
  • Special interest in treating patients with Perthes disease, adolescent and young adult avascular necrosis, and developmental dysplasia of the hip (a member of International Hip Dysplasia Institute).
  • Leader and chair of the International Perthes Study Group – multicenter research study focused on advancing the care of children diagnosed with Perthes disease.
  • Extensive basic and clinical research on Perthes disease and avascular necrosis.
Daniel J. Sucato, M.D., M.S. 
  • Special interest in treating adolescent patients with various hip conditions including hip dysplasia, adolescents and young adults with Perthes disease, slipped capital femoral epiphysis and femoroacetabular impingement.
  • A member of the Academic Network of Conservational Hip Outcomes Research (ANCHOR) study. A multi-center project that analyzes hip function and pain, quality of life and other factors on patients who undergo hip preservation surgeries.
Henry B. Ellis, M.D. 
  • Special interest in treating femoral acetabular impingement, labral tears and other sport-related injuries and conditions in the hip.
  • Involved in multi-center research projects with a special interest in hip arthroscopy.
  • A member of the Academic Network of Conservational Hip Outcomes Research (ANCHOR) study.
David A. Podeszwa, M.D. 
  • Special interest in treating patients with hip dysplasia, slipped capital femoral epiphysis and femoroacetabular impingement.
  • A member of the Academic Network of Conservational Hip Outcomes Research (ANCHOR) study.
William Z. Morris, M.D. 
  • Special interest in treating patients with hip dysplasia, slipped capital femoral epiphysis and femoroacetabular impingement.
  • Extensive clinical research in the pediatric and adolescent developing hip with expertise in the pathogenesis of slipped capital femoral epiphysis and femoroacetabular impingement.
Corey S. Gill, M.D. 
  • Special interest in treating infants with hip dysplasia and patients with cerebral palsy with various hip disorders/dysplasia.
  • Other common hip conditions seen include slipped capital femoral epiphysis, Perthes disease, transient synovitis of the hip, osteoid osteoma and proximal femur cysts.
Learn more about the Center for Excellence in Hip.
Share Your Story: A Family Affair

Share Your Story: A Family Affair

Meet Anna and Ellen, patients seen by our multidisciplinary team of experts. Learn more about their journey below.

Blog written by Anna and Ellen’s mom, Keeley.  

When our daughter Anna was 5 years old, she started telling us that her left arm felt funny and not right, so we took her to be seen at our local hospital in Oxfordshire, England. She had X-rays taken, and we were told all was well, so we continued on with our life. Our family was in the middle of packing and preparing for a move, a less-stressful life on the Isle of Man just off the U.K. mainland.

After being in our new home about four weeks, one day Anna came home from school really upset, saying that her arm was in a lot of pain. I immediately took her to another doctor to have it re-examined. I could tell this doctor was concerned, and he instantly referred us to see another specialist the very next day. At that appointment, our lives were changed forever.

We learned the devastating news that Anna’s X-rays actually showed a very large tumor, from her left shoulder down to her elbow. He advised us to move straight back to Oxfordshire, so she could be under the care of an oncology team. After a whirlwind couple of weeks, we were back in Oxfordshire, and Anna started her very long journey of chemotherapy and other treatments for her Osteosarcoma bone cancer.

patient sitting on a chair

In May 2017, on her 6th birthday, she had a surgery to remove the tumor. The cancerous humerus bone was taken out and replaced with the fibula from her right leg. Many months of rehabilitation followed, but by May 2018, Anna was in remission. Unfortunately, this was short lived, and by December, she once again had that “funny” feeling in her left shoulder. Investigative scans confirmed a recurrence.

Further surgery and many more months of chemo followed. It was devastating telling her she had to go through it all again, and lose her beautiful new hair. But Anna is a real fighter and a true inspiration to all. She persevered through treatment to make it back into remission for the second time.

Her father and I researched every possible option to try and keep this beast at bay. In August 2019, she was accepted onto a clinical trial at Memorial Sloan Kettering Cancer Center in New York. Our wonderful friends and small community of Chipping Norton in England rallied together. A Team Anna fundraising campaign took off, and many celebrities, pop stars and kind-hearted generous people joined in to help raise the huge amount of funding needed to get Anna to New York. By January 2020, we had made it, and Anna was able to start the treatment.

Just as we were about to leave for New York, life threw us another challenge. Our 13-year-old daughter Ellen was diagnosed with scoliosis and needed spinal fusion surgery. It was very difficult to come to terms with another one of our children having medical problems. The NHS doctors in the U.K. were unable to treat it within the necessary timescales. Even if we could somehow have managed to have the surgery done privately in the U.K., our family would have been separated for many months while my husband and I both took care of the girls, in different countries.

mirror selfie
Having Ellen’s spinal surgery done in New York wasn’t an option due to the huge costs involved. We were at a complete loss about what to do.

Once we arrived in New York, we serendipitously crossed paths with a wonderful woman, who just so happened to be a nurse at Scottish Rite for Children. We began talking, and before we knew it, Ellen had an appointment with Dr. Sucato. Our family was taking a road trip to Texas.

Ellen had a consultation with Dr. Sucato, and we scheduled her spinal fusion surgery. His entire team was wonderful, and we couldn’t actually believe all of this was happening! She underwent successful surgery in July 2020, and with the support of Dr. Sucato and his fabulous team, she is doing great.

Just as we were due to return home to England, we had another unbelievable turn of events. Anna had a fall at a swimming pool and broke right through the new bone in her arm. Another terrifying ordeal, but yet again, Scottish Rite came to our rescue. Anna was able to be seen by Dr. Oishi. She underwent surgery, where metal plates and brackets were inserted into her arm, and the blood supply was stimulated. Anna was also able to talk through things with Dr. Herge in psychology. Both Dr. Oishi and Dr. Herge are incredible members of Scottish Rite’s formidable team, and we are incredibly thankful for them!

 

At every turn, our entire family felt like we were being taken care of. Each and every person we interacted with at Scottish Rite genuinely cares and only wants what is best for the patient.

Following a period of rehab and checkups, our family was able to return home to England with two very healthy, strong and happy daughters. It was amazing to be back under one roof with our oldest daughter, who had stayed in England this entire time. Words cannot express how eternally grateful, thankful and overwhelmed we are with the care, kindness and support we have received. Thank you Scottish Rite. You’re the best!

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

Luke’s Journey: Not Missing a Beat Through Scoliosis Treatment

Luke’s Journey: Not Missing a Beat Through Scoliosis Treatment

Cover story previously published in Rite Up, 2021 – Issue 1.

by Hayley Hair

The rhythm, the tempo, and the heartbeat — all fitting descriptors for the function of a band’s percussion section, but using an even more compelling name like the backbone depicts their role more succinctly. Just like a spine, all those sharp pops of the quad drums, the satisfying crashes of the cymbals, and the low, palpable rumbles of the bass drums provide stability, support, flexibility, and movement to the ensemble. No one knows this juxtaposition more personally than Luke, the McKinney North High School bass drum percussionist and Scottish Rite for Children patient cared for by our scoliosis experts.

Plenty can be learned about adolescent idiopathic scoliosis (AIS) by following Luke’s journey. AIS, or scoliosis with an unknown cause starting after age 10, makes the spine curve or twist into a “C” or “S” shape. Luke’s personal experience covers the broad spectrum of how the progressive condition is diagnosed, observed, and expertly managed with an individualized treatment plan.

“Luke’s pediatrician identified the minor curvature of his spine and uneven shoulders at his 9-year-old well visit,” Luke’s mom, Christy, says about the outset. “The pediatrician immediately referred us to Scottish Rite, and the initial plan was to monitor Luke every six months to identify any changes that may occur.”

Scoliosis Observation and Expertise 
Luke and Christy’s first visit at Scottish Rite for Children was with Amy L. McIntosh, M.D., medical director of clinical safety and a pediatric orthopedic surgeon. “I think that’s one of the greatest things about Scottish Rite — we have so many treatment options for scoliosis,” McIntosh says about the expertise and exceptional care the institution offers.

Clinical observation might not seem like much of an active plan at first, but consistent monitoring of the child’s growth is key. Catching any progression in spine curvature is crucial for effectively managing scoliosis. Christy, a registered nurse, is the coordinator of health services for McKinney Independent School District, which serves more than 23,000 students in North Texas. She has experience with AIS through her work with state-mandated scoliosis screenings in school as well as training other health professionals about the condition, so McIntosh and Christy are on the same page about early detection. “Scoliosis screening is very important.” McIntosh says. “Catching a curve early, when it is small, is the most important factor when it relates to brace treatment success.”

A Brace Just for Luke 
As Luke continued to grow, unfortunately, so did his curve. McIntosh first prescribed a Providence brace, or a nighttime brace made for smaller curves, for Luke to wear while he slept that would help to slow his curve progression. “I thought it would just go away like a sickness, like braces for your teeth,” Luke says.

His new brace, along with all of Scottish Rite patients’ braces, is custom-made for his curve. “The coolest thing about our bracing program is that the orthotists work at Scottish Rite, and they make all the braces in-house,” McIntosh says. “If you are going to wear a brace, it might as well work really well for you.”

And during each patient’s clinic visit, the multidisciplinary care team specific to the child’s condition is nearby. “We have the orthotists with us, the nursing team, physicians, the physical and occupational therapists — everybody’s ready on hand in the clinic to provide the best comprehensive care for each patient,” Chief of Staff Daniel J. Sucato, M.D., M.S., says. As director of the Sarah M. and Charles E. Seay/Martha and Pat Beard Center for Excellence in Spine Research, Sucato leads an institution-wide team that focuses on researching the cause and behavior of scoliosis in children and adolescents and controlling and correcting curve progression with innovative treatments.

More Hours in the Brace
As Luke kept growing, again, so did his curve. McIntosh had more in her arsenal and upped his support to a custom thoracolumbosacral orthosis (TLSO) brace. Made for wear under clothing day and night, the TLSO brace wraps around the upper body from under the arms to the pelvic bone. Luke’s curve affected both the upper, or thoracic, and the lower, or lumbar, regions, creating a twisted “S” shape.

Patients, like Luke, wear their braces for 18 to 24 months for many hours a day. That timing is determined by the age at presentation, the curve magnitude, and how much growth remains. “Currently, the brace is the only treatment that has been scientifically proven to prevent the progression of scoliosis to a surgical magnitude,” McIntosh says.

Correcting Scoliosis with Surgery
“He wore his brace until the ninth grade, and he was so compliant,” Christy says. “He even tried to wear the brace while he was in marching band while carrying  the bass drum, but he couldn’t. It was too much, so  he started taking it off for band.”

Luke literally and metaphorically carries the beat on his back while he zigs and zags across the football field holding his enormous bass drum. Fastened to a frame that hooks over both shoulders, the drum weighs more than 20 pounds and juts out far enough to move when the wind blows. Luke loves to be a part of the drumline, and when asked if he plans to continue studying music in college, he replies, “100 percent.” Some of his best friends are in the band. “It’s a great way to meet people, and I’ve made close friends that will probably last quite  a while,” Luke says.

Luke wore his brace up to 22 hours a day, but his curve kept progressing. When his curve grew to more than 50 degrees, surgical correction was recommended. Luke experienced some discomfort and breathing difficulty as well. “When it was really bad, like after band practice, after marching out there with my drum for a while, it just hurt,” Luke says. “I tried to get Luke’s spine through it as best as I could, X-ray before surgery but sometimes I’d have to sit out and do stretches. It wasn’t bad to the point where I couldn’t do anything, but it was just constant.”

Getting ready for surgery, Luke looked to McIntosh to explain the next steps. “She gave me a 3-D model of what the surgery would look like on my back,” Luke says. “I got to play with it and bend it to see the difference between a normal back and a back with spinal fusion. It made me feel better.”

Luke had a posterior spinal fusion with instrumentation and bone grafting, the most common scoliosis surgical procedure. By attaching rods to the spinal column and then grafting bone to the affected area, the spinal curve is corrected and encouraged to fuse to prevent further curve progression. Following surgery, the fused section is no longer flexible.

Recovery takes several months for patients to get back to their desired activities, and it takes up to a year for the spinal fusion to fully heal. During Luke’s recovery, the drumline and their teacher, Michael Reed, brought a huge card signed by everyone with well wishes during a visit to his house.

After years of wearing a brace and surgery, Luke has advice for others going through bracing and surgery for scoliosis. “If they are going through bracing, I’d tell them to wear their brace as much as possible to try to avoid the surgery,” Luke says. “If they are about to get into the surgery, don’t worry about it too much. They are professionals, and they know what they are doing.”

Luke gained a few inches in height and has no more pain following surgical correction. “It is a lot easier to do stuff with my back like this,” Luke says. Even though there are reminders each day about his spinal fusion, he says he wouldn’t change a thing about his treatment at Scottish Rite for Children. “You are in the best hands,” he says. “They know exactly what to do.”

Read the full issue.