Age at time of treatment: 18 – 25
Injury Level: C5
Treatment Received: Epidural Stimulation
Location of Treatment: Thailand
Time between injury and treatment: 2 – 5 years
Date of Surgery: 25/06/2018
Date of Discharge: 21/07/2018
Patient sustained a C5 level spinal cord injury on November 12th, 2015, during a hockey game. Initial diagnosis of ASIA A score was changed to ASIA B within a few weeks of the trauma. Patient has no hand or leg function. Triceps and core strength were initially very weak, but have improved with time. Patient has neurogenic bowel and bladder function but is otherwise a healthy individual with no secondary injuries or diagnoses present.
Patient had not received any surgery since his injury besides broken vertebrae repair. Patient received mesenchymal stem cells and allogenic stem cells, in the form of IV infusion and lumbar punctures, as well as physical rehabilitation. This resulted in minor improvements in his functions.
Patient sustained a C5 level spinal cord injury on November 12th, 2015, during a hockey game. Initial diagnosis of ASIA A score was changed to ASIA B within a few weeks of the trauma. Patient has no hand or leg function. Triceps and core strength were initially very weak, but have improved with time. Patient has neurogenic bowel and bladder function but is otherwise a healthy individual with no secondary injuries or diagnoses present.
After a spinal MRI scan, an EMG, and comprehensive blood work, patient underwent laminectomy and epidural spinal cord stimulator implantation on June 25th, 2018. The device is the ‘Medtronic Restore Advance 16-electrode MRI Compatible Device’. The surgery was completed without issue and no serious complications were reported during the postoperative hospital stay. Surgical wounds healed normally and no spinal cord or superficial wound infection was reported.
After 35 days, patient was discharged to continue his physiotherapy back home.
Improvements are monitored in 15 targeted areas: 11 Motor areas and 4 Sensory areas. However, the number of targeted areas may vary depending on patient’s condition prior to admission. If patient does not experience symptoms in certain Motor/Sensory functions, or is not impaired in a specific targeted area prior to surgery, it is excluded from the report (Not Applicable). If there is progress in any given area — either mild, moderate, or significant — it is measured and reported as positive (“Yes”). No improvement, the existence of pain or spasms, or an inability to perform a measured function is reported as “No”.
In this patient, neuropathic pain was not present, therefore 14 areas instead of 15 were reviewed. The primary treatment focus was to regain motor functions, which improved in 10 out of 11 targeted areas when the epidural stimulation device was switched on. Patient did not receive any stem cell injections therefore no improvements were visible in the 3 sensory function areas.
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All medical treatments have varied outcomes. Results from the treatments will vary from patient to patient. All examples of what has been achieved by others should not be taken as typical or in any way a guarantee or projection of what any individual can expect from treatment.