Dr. McConnell First in Lehigh Valley to Perform Spine Surgery Using activL® Artificial Disc

New Procedure Gives Young, Active Lehigh Valley Patient with Degenerative Disc Disease Hope for an End to Chronic Pain.

Dr. Jeffrey McConnell is the first spine surgeon in the Lehigh Valley to successfully implant an innovative artificial spinal disc replacement device to address chronic low back pain caused by degenerative disc disease. The  activL® Artificial Disc from Aesculap Implant Systems is designed to closely mirror the natural movement of a healthy human spine, preserving more motion in the spine than traditional fusion surgery.

With traditional fusion surgery, some patients with degenerative disc disease have reported pain at levels adjacent to their initial fusion several years after surgery. In clinical studies, patients who received a lumbar artificial disc were three times less likely to experience pain at adjacent levels 5 years after their procedure than patients who received a fusion.

activL artificial disc

activL® Artificial Disc

“I have been an early adopter of motion-preserving procedures because I have seen the value in both my own patients as well as in the academic literature,” said Dr. McConnell. “I believe that the activL Artificial Disc represents the next generation of spinal disc replacement technology, especially for younger, more active patients.”

McConnell performed the first surgery using activL Artificial Disc at St. Luke’s Allentown campus in May. “Two weeks following my patient’s initial surgery she is already reporting a significant reduction in the pain she experienced before the procedure, and she is up and walking around,” said McConnell. “I am confident as she continues to heal that she will greatly benefit from receiving this artificial disc.”

Aesculap’s activL Artificial Disc was approved by the FDA in June 2015, making it the first new lumbar disc on the market in nine years.

total disc replacement

Cervical Artificial Disc Replacement: 10 Years and Going Strong

This video tells the story of Stephen Miller, one of the first patients Dr. McConnell treated with the Prestige-LP Cervical Total Disc Replacement.

When Stephen was 24, he dove into a swimming pool and was temporarily paralyzed. Fortunately, his girlfriend was present and she saved his life by dragging him off the bottom of the pool.

Stephen had persistent symptoms – enormous pain and stiffness in his arms and legs – and showed signs of cervical myelopathy associated with herniated discs at C5-6 and C6-7. He was an excellent candidate for a clinical trial starting at the time for the Prestige-LP Cervical Total Disc Replacement. Stephen was one of the first patients treated by Dr. McConnell with this groundbreaking cervical artificial disc replacement.

Stephen checked in this week with Dr. McConnell for his 10-year follow-up and we’re happy to say that Stephen is doing extraordinarily well. In the video he describes his symptoms prior to receiving the procedure, and how the Prestige-LP Cervical Total Disc Replacement procedure changed his life.

The Prestige LP Cervical Disc System is an option for patients suffering from degenerative disc disease at one or two contiguous levels in the cervical spine from C3 to C7.

Symptoms of Cervical Myelopathy

Cervical myelopathy produces two types of symptoms: the ones you may feel in the neck, and the ones appearing elsewhere in the body at or below the compressed area of the spinal cord.

Neck symptoms may include:

  • Neck pain
  • Stiffness
  • Reduced range of motion

As the disease progresses, one may experience shooting pain that originates in the neck and travels down the spine. Other cervical myelopathy symptoms may include:

  • Weakness in the arms and hands
  • Numbness or tingling in the arms and hands
  • Clumsiness and poor coordination of the hands
  • Difficulty handling small objects, like pens or coins
  • Balance issues
Johns Hopkins Medicine

One and Two Level Artificial Disc Replacement are Effective in Treating Disc Problems in the Neck

Monday, April 24, 2017 | Los Angeles, California

During the recent American Association of Neurological Surgeons meeting in Los Angeles,  Dr Jeffrey McConnell  presented a paper which explored the results of one of the longest follow-up studies on cervical total disc replacement to date.

Comparison of the Long Term Results of One-Level vs Two-level Cervical Total Disc Replacement and Anterior Cervical Discectomy and Fusion”, compared patients who received fusion surgery vs patients who received artificial disc replacement surgery at one or two discs in the neck.

The highlights:

  • After 7 years, patients who received the Prestige-LP two level artificial disc replacement had superior overall clinical results when compared to the fusion patients.
  • One and 2-level artificial disc replacement appear to be equally safe and effective in the treatment of cervical disc disease at 7 years
  • Patients receiving two artificial disc replacements did equally as well as patients receiving one level disc replacement.
  • Patients who received cervical fusion had higher reoperation rates at the index and adjacent disc levels.

These long-term clinical results demonstrate the effectiveness of total disc replacement at 2 contiguous levels in the cervical spine and the importance of maintaining motion in the cervical spine.

Cervical artificial disc replacement is a type of joint replacement procedure. An artificial disc, such as the Prestige LPTM cervical disc made by Medtronic, is placed between two adjacent cervical vertebrae to replace a diseased cervical disc. It is designed to maintain the distance between two adjacent cervical vertebrae.

The Prestige-LP two level artificial disc replacement.

Cervical total disc replacement has been demonstrated to be a very effective alternative to the traditional surgery of fusion for painful herniated discs in the neck.  Total disc replacement in the neck is more successful because it maintains normal motion in the neck while fusion eliminates motion.  This preservation of motion is key to minimizing the degeneration of adjacent cervical discs.

Learn more about cervical disc replacement.

Published: Two Level Cervical Disc Replacement Better Than Fusion After 7 years

Dr. Jeff McConnell was co-author of the recently published article in the Journal of Neurosurgery Spine, Long-term clinical and radiographic outcomes of the Prestige LP artificial cervical disc replacement at 2 levels: results from a prospective randomized controlled clinical trial. ( 2017 Apr 7:1-13. doi: 10.3171/2016.11.SPINE16746. [Epub ahead of print])

This landmark study was the culmination of an FDA Investigational Device Exemption clinical trial comparing artificial disc replacement at two consecutive levels in the neck versus the traditional surgical treatment of fusion.

Fusion for painful herniated discs in the neck is effective, however this type of surgery permanently stops movement of the vertebra that are fused together. It is now well established that fusing vertebrae in the neck can cause detrimental effects on the remaining normal discs in the neck. It has been shown that patients who have had fusion in their neck can develop accelerated degeneration of the discs above and below the fused levels. These degenerative changes can then cause additional problems and may require additional surgery for treatment.

In the article published in the Journal of Neurosurgery, patients requiring surgery for two herniated discs in the neck were randomized to undergo either total disc replacement using the Prestige-LP device or the traditional fusion surgery. After 7-years, overall success and Neck Disability Index scores were superior for total disc replacement when compared to fusion. The authors concluded that total disc replacement with the Prestige-LP device at two contiguous levels is safe and effective and is a very good alternative to the traditional fusion surgery treatment. This is a longer term follow-up study on the same group of patients that Dr McConnell and his co-authors published previously.

Prestige-LP artificial cervical disc.

X-ray showing two level artificial disc replacement using the Prestige-LP performed by Dr. McConnell.

X-ray of traditional 2-level anterior fusion with spinal plate and screws.

Cervical Artificial Discs Minimize Future Surgery Risk

Wednesday, April 12, 2017 | Boca Raton, Florida

International Society for the Advancement of Spinal Surgery, ISASS

Dr McConnell recently reported the long term beneficial effects of total disc replacement in the neck at the International Society for the Advancement of Spinal Surgery (ISASS) in Boca Raton, Florida.

The presentation, Motion Preservation and the Incidence of Subsequent Surgical Intervention after Treatment with the Selectively Constrained SECURE®-C Cervical Artificial Disc, concluded that artificial total disc replacement surgery for painful herniated discs in the neck is a sound alternative to the traditional treatment of discectomy and fusion.

While fusion surgery is generally successful for treating herniated discs in the neck, it comes at the expense of lost motion between two vertebra.  Lack of movement at one disc will increase stress and strain at the adjacent discs.  As a result, the disc adjacent to a fusion can degenerate faster and may become painful and require additional surgical intervention.

SECURE®-C Cervical Artificial Disc

SECURE®-C Cervical Artificial Disc

The study followed 380 patients for 7 years. Each patient suffered with herniated discs and were treated with either total disc replacement (Secure-C artificial disc) or fusion surgery. The study attempted to determine the effects on the discs adjacent to the site of each surgery.

Of the patients who received fusion in their neck, 17.4% eventually required additional surgery at an adjacent disc, while only 4.2% of patients treated with Secure-C required adjacent disc surgery. After 7 years, patients treated with fusion surgery in the neck for a herniated disc were 4 times more likely to require surgery at any adjacent disc level than patients treated with an artificial disc.

These study results were significant and highlight the benefits of total disc replacement in helping to prevent accelerated degeneration of adjacent discs, as well as the importance of maintaining normal motion in the neck.

Read more about cervical total disc replacement.

Published: Artificial Disc Replacement at Two Levels in the Neck is Superior to Fusion

Dr Jeff McConnell was co-author of the recently published article in the Journal of Neurosurgery Spine (2017 March 17:1-15) titled: Cervical Disc Arthroplasty with the Prestige LP Disc Versus Anterior Cervical Discectomy and Fusion, at 2 Levels: Results of a Prospective, Multicenter Randomized Controlled Clinical Trial at 24 Months.

This landmark study was the culmination of an FDA Investigational Device Exemption clinical trial comparing artificial disc replacement at two consecutive levels in the neck versus the traditional surgical treatment of fusion. Fusion for painful herniated discs in the neck is effective, however this type of surgery permanently stops movement of the vertebra that are fused together. It is now well established that fusing vertebrae in the neck can cause detrimental effects on the remaining normal discs in the neck. It has been shown that patients who have had fusion in their neck can develop accelerated degeneration of the discs above and below the fused levels. These degenerative changes can then cause additional problems and may require additional surgery for treatment.

In the article published in the Journal of Neurosurgery, patients requiring surgery for two herniated discs in the neck were randomized to undergo either total disc replacement using the Prestige-LP device or the traditional fusion surgery. Overall success and Neck Disability Index scores were superior for total disc replacement when compared to fusion. The authors concluded that total disc replacement with the Prestige-LP device at two contiguous levels is safe and effective and is a very good alternative to the traditional fusion surgery treatment.

Prestige-LP artificial cervical disc.

X-ray showing two level artificial disc replacement using the Prestige-LP performed by Dr. McConnell.

X-ray of traditional 2-level anterior fusion with spinal plate and screws.

Case Study: Congenital Scoliosis in an 18 Month-old Boy

baby scoliosis surgery

18-month old Arannya Adhakary with congenital scoliosis waiting for his surgery

Operation Straight Spine (OSS) is an annual mission trip to Kolkata, India, where doctors, nurses and spinal monitoring technicians from the US, England and India treat patients with spinal disorders. During the 2017 trip, Dr. Jeffrey McConnell and the OSS team treated an 18-month old boy with congenital scoliosis.

Arannya Adhakary, 18 months old, was the youngest patient treated during OSS 2017.  He was diagnosed with congenital scoliosis when he was just 3 months of age.

 Congenital scoliosis can be caused by a number of different defects in the development of the spine during the first trimester of fetal growth. Abnormalities occur when part of a vertebra fails to form or several vertebra fail to separate during the very earliest stages of fetal development when the spine and other major organs are starting to form. Patients can have a single abnormality or multiple defects throughout the spine. 

Arannya’s congenital spine defect was known as a hemivertebra, which occurs when the vertebra is triangular in shape instead of the normal rectangular shape.   This type of congenital defect has a very high propensity to cause a severe and progressive deformity of the spine, usually a kyphosis or scoliosis,  as the child grows.

Arannya’s hemivertebra was located at the 11th thoracic vertebra, approximately in the middle of his spine. Hemivertebra are best treated at an early age by removing the abnormal vertebra, correcting the deformity and fusing the growth plates above and below the hemivertebra so the deformity does not recur. Arannya’s surgery consisted of removal of the T11 hemivertebra, correction of the local kyphosis and scoliosis, and limited fusion from T10 to T12.  To stabilize the spine and help fuse where the hemivertebra was removed, two small screws and a single 3.5mm diameter rod was placed from T10 to T12 on the right side.

Arannya did amazingly well after surgery, a testament to his young age, and by the 4th postoperative day was going on walks in the courtyard, smiling, carried in his mother’s arms.

scoliosis deformity xray

Pre-operative MRI of the thoracic spine showing the T11 hemivertebra and acutely angled scoliosis deformity.

scoliosis postop xray

Post-operative X-ray after removal of the T11 hemivertebra and placement of spinal screws and rod.

india scoliosis

Four days after surgery on walk with his mother.

Case Study: Severe Scoliosis in an 11-Year Old Girl with Rare Syndrome

Shruti Sharma during her pre-operative evaluation with the OSS 2017 team.

Kolkata, India,  January 25, 2017

During their annual mission trip to Kolkata, India, Dr McConnell and the other members of the Operation Straight Spine (OSS) team were faced with a very challenging case of severe scoliosis in an 11 year-old girl.

Shruti Sharma was diagnosed with Prader-Willi syndrome (PWS) at a young age.  PWS is a complex genetic disorder affecting approximately one in 15,000-30,000 individuals. The disorder results in short stature, disorders of metabolism, cognitive disabilities and behavioral problems. One of the hallmarks of the disorder is insatiable appetite and obesity which often leads to childhood diabetes mellitus (Type 2 diabetes).  Due to low muscle tone, patients will often develop spinal deformities such as scoliosis. Shruti was certainly the most challenging case the OSS team faced this year, not only from a medical management standpoint, but also by the severity of her spinal deformity.

Shruti originally presented to the OSS team in 2016 for consideration of corrective surgery for her thoracic scoliosis, however her diabetes was newly diagnosed and poorly controlled. The team thought it best to delay her surgery until their return trip in 2017 so that her diabetes could be brought under better control. By 2017 her left thoracic scoliosis curvature had progressed to 92 degrees.

Pre-operative X-ray showing severe, 92 degree thoracic scoliosis

Shruti’s scoliosis surgery

After Shruti was placed under anaesthesia, blood started collecting in her right lung for unknown reasons. This delayed her surgery for several hours. The bleeding eventually stopped and she was stable enough to complete the procedure, which lasted about 6 hours. It consisted of a posterior correction of the scoliosis and the placement of spinal rods and fusion from the 2nd thoracic vertebra to the 3rd lumbar vertebra. Due to her relatively small size, small 4.5mm rods and implants were used. Then, special bands resembling zip ties, known as  “Jazz Bands”, were attached to several vertebra. By slowly tightening the Jazz Bands the severe curvature of Shruti’s spine was gradually straightened and anchored to the spinal rods.

Shruti’s postop and recovery

Shruti’s postoperative course was somewhat stormy.  She remained intubated in the ICU for the first 24 hours. as her blood pressure was unstable and she ran a high temperature. On post-op day #1 the breathing tube was removed, but her right lung had filled with fluid and she required aggressive manual pulmonary therapy to help clear the lung. Ultimately, Shruti did very well and by the 4th post-op day she was smiling, walking, and coloring pictures.

About 3-4 weeks after her scoliosis surgery, Shruti had a slight setback when part of her spinal incision came open and developed an infection.  Luckily, Dr Ujjwal Debnath, based in India, was able to re-operate on Shruti’s back, wash out the wound and clear the infection. She required additional hospitalization and antibiotic therapy but ultimately recovered.

Post-operative X-ray showing excellent correction of the scoliosis deformity.

Shruti walking on 4th post-op day with OSS team member Bethan Salmon, RN

cervical replacement surgery

Two Level Cervical Artificial Disc Replacement Superior To Fusion

 

eurospine conference

During the recent Eurospine meeting in Berlin, Germany,  a paper co-authored by Dr Jeffrey McConnell was presented, which explored the results of one of the longest follow-up studies on cervical total disc replacement to date.

Long Term Clinical and Radiographic Results of Two-level Cervical Total Disc Replacement from a Level 1 Prospective, Randomized, Clinical Trial”, compared patients who received fusion surgery vs patients who received artificial disc replacement surgery. The highlights:

  • After 7 years, patients who received the Prestige-LP two level artificial disc replacement had superior overall clinical results when compared to the fusion patients.
  • Subsequent surgeries were required 3 times less often in patients who received the two-level artificial disc replacement.
  • Patients who had cervical fusion required surgery at adjacent disc levels twice as often as the patients who had disc replacement.

These long term clinical results demonstrate the effectiveness of total disc replacement at 2 contiguous levels in the cervical spine and the importance of maintaining motion in the cervical spine.

 

The Prestige-LP two level artificial disc replacement.

Cervical artificial disc replacement is a type of joint replacement procedure. An artificial disc, such as the Prestige LPTM cervical disc made by Medtronic, is placed between two adjacent cervical vertebrae to replace a diseased cervical disc. It is designed to maintain the distance between two adjacent cervical vertebrae.

Cervical total disc replacement has been demonstrated to be a very effective alternative to the traditional surgery of fusion for painful herniated discs in the neck.  Total disc replacement in the neck is more successful because it maintains normal motion in the neck while fusion eliminates motion.  This preservation of motion is key to minimizing the degeneration of adjacent cervical discs.

Learn more about cervical disc replacement.

Laser Spine Surgery: Trick or Treat?

laser-back-medical1Contrary to popular belief, laser spine surgery is not better than currently accepted surgical techniques when it comes to treating common conditions affecting your spine.

Lasers have been used in medicine since the 1960’s and have proven to be very effective in treating many conditions – for example, LASIK surgery to correct common vision problems or treating certain skin conditions. But due to insufficient evidence,  lasers in spine surgery are not endorsed by most large health authorities like the Mayo Clinic and the National Institutes of Health (NIH). Lasers are more often used as a marketing tool by some clinics that promote “laser spine surgery” as being minimally invasive or noninvasive and risk-free.

There are no well-controlled clinical studies documenting the benefits of laser spine surgery. In fact, in one study comparing percutaneous lumbar laser discectomy (PLLD) with more traditional forms of discectomy (surgical removal of the whole or a part of an intervertebral disc), the results of PLLD were inferior.

The most accepted method to remove a herniated disc in the lumbar spine is to make a small incision, open the spinal canal (a laminotomy), visualize and protect the compressed nerve root and remove the herniated disc material with small mechanical instruments.  Lasers are also ineffective in treating spinal stenosis because lasers cannot cut bone to open the spinal canal or remove bone spurs compressing the nerves.

The key to success in any spinal surgical procedure is an accurate diagnosis and the application of clinically proven procedures performed by qualified, experienced, board certified surgeons.

Learn more about lumbar discectomy surgery.

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