Percutaneous spinal endoscopic surgery for thoracic ossification of the posterior longitudinal ligament: a noval bilateral crossover decompression technique

OBJECTIVE: To investigate the feasibility and clinical efficacy of bilateral crossover decompression technique under percutaneous spinal endoscopic surgery for thoracic ossification of the posterior longitudinal ligament (T-OPLL). METHODS: (2 cases). Total operative time, intraoperative blood loss, length of hospital stay, and complications were recorded. Neurological function was evaluated using the modified Japanese Orthopaedic Association (mJOA) score and the Oswestry Disability Index (ODI) preoperatively, at 3 days and 6 months postoperatively, and at the final follow-up. Clinical efficacy at the last follow-up was assessed using the modified MacNab criteria, and the excellent-to-good rate was calculated. Sagittal canal diameter and canal area were measured to evaluate spinal cord decompression. RESULTS: The mean total operative time was 102.39 min (range: 90-130 min), intraoperative blood loss was 40.61 ml (range: 30-55 ml), and mean hospital stay was 10.22 days (range: 8-14 days). All patients were followed up for a mean duration of 16.78 months (range: 12-24 months). Compared with the preoperative period, mJOA scores significantly improved at 3 days, 6 months, and at the final follow-up (p < 0.05), with further improvement observed at the final follow-up compared with 3 days and 6 months postoperatively (p < 0.05). Similarly, ODI scores were significantly reduced at 3 days, 6 months, and at the final follow-up compared with preoperative scores (p < 0.05). According to the modified MacNab criteria at the final follow-up, 9 cases were rated as excellent, 7 as good, and 2 as fair, yielding an excellent-to-good rate of 88.89%. Compared with preoperative measurements, both the sagittal canal diameter and canal area were significantly increased at 3 days, 6 months, and at the final follow-up (p < 0.05). Complications included intercostal neuralgia in 2 patients, dural tear in 2 patients, and transient postoperative muscle weakness in 1 patient; no cases of epidural hematoma, neck pain, or iatrogenic neurological injury were observed. CONCLUSION: Bilateral crossover decompression percutaneous spinal endoscopic surgery is a safe and effective minimally invasive technique for the treatment of T-OPLL, with satisfactory short-term clinical outcomes.

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Journal
Journal of Orthopaedic Surgery and Research
Published
2026-04-25
DOI
https://doi.org/10.1186/s13018-026-06870-9
Primary Topic
Cervical and Thoracic Myelopathy
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article
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article

Percutaneous spinal endoscopic surgery for thoracic ossification of the posterior longitudinal ligament: a noval bilateral crossover decompression technique

Haiyang Wu, Yiping Zheng, Xizhong Zhu, Y K Xu et al.
Journal of Orthopaedic Surgery and Research
Cervical and Thoracic Myelopathy
article

Percutaneous spinal endoscopic surgery for thoracic ossification of the posterior longitudinal ligament: a noval bilateral crossover decompression technique

Haiyang Wu, Yiping Zheng, Xizhong Zhu, Y K Xu, Luyang Wang, Xingchen Li
article en

Abstract

OBJECTIVE: To investigate the feasibility and clinical efficacy of bilateral crossover decompression technique under percutaneous spinal endoscopic surgery for thoracic ossification of the posterior longitudinal ligament (T-OPLL). METHODS: (2 cases). Total operative time, intraoperative blood loss, length of hospital stay, and complications were recorded. Neurological function was evaluated using the modified Japanese Orthopaedic Association (mJOA) score and the Oswestry Disability Index (ODI) preoperatively, at 3 days and 6 months postoperatively, and at the final follow-up. Clinical efficacy at the last follow-up was assessed using the modified MacNab criteria, and the excellent-to-good rate was calculated. Sagittal canal diameter and canal area were measured to evaluate spinal cord decompression. RESULTS: The mean total operative time was 102.39 min (range: 90-130 min), intraoperative blood loss was 40.61 ml (range: 30-55 ml), and mean hospital stay was 10.22 days (range: 8-14 days). All patients were followed up for a mean duration of 16.78 months (range: 12-24 months). Compared with the preoperative period, mJOA scores significantly improved at 3 days, 6 months, and at the final follow-up (p < 0.05), with further improvement observed at the final follow-up compared with 3 days and 6 months postoperatively (p < 0.05). Similarly, ODI scores were significantly reduced at 3 days, 6 months, and at the final follow-up compared with preoperative scores (p < 0.05). According to the modified MacNab criteria at the final follow-up, 9 cases were rated as excellent, 7 as good, and 2 as fair, yielding an excellent-to-good rate of 88.89%. Compared with preoperative measurements, both the sagittal canal diameter and canal area were significantly increased at 3 days, 6 months, and at the final follow-up (p < 0.05). Complications included intercostal neuralgia in 2 patients, dural tear in 2 patients, and transient postoperative muscle weakness in 1 patient; no cases of epidural hematoma, neck pain, or iatrogenic neurological injury were observed. CONCLUSION: Bilateral crossover decompression percutaneous spinal endoscopic surgery is a safe and effective minimally invasive technique for the treatment of T-OPLL, with satisfactory short-term clinical outcomes.

Journal of Orthopaedic Surgery and Research
First Affiliated Hospital of Zhengzhou University (CN)
Good health and well-being
Openalex Percentile: Top 6%
Cervical and Thoracic Myelopathy
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