4.2 Article

Percutaneous Full-Endoscopic versus Biportal Endoscopic Posterior Cervical Foraminotomy for Unilateral Cervical Foraminal Disc Disease

Journal

CLINICS IN ORTHOPEDIC SURGERY
Volume 14, Issue 4, Pages 539-547

Publisher

KOREAN ORTHOPAEDIC ASSOC
DOI: 10.4055/cios22050

Keywords

Cervical radiculopathy; Unilateral cervical foraminal disc disease; Posterior cervical foraminotomy; Percutaneous full-endoscopy; Biportal endoscopy

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This study compares the short-term clinical outcomes of biportal endoscopic technique (BE) posterior cervical foraminotomy (PCF) with percutaneous full-endoscopic technique (PE) PCF. The results demonstrate that the 1-year postoperative clinical outcomes of both techniques for cervical pain and disability caused by unilateral cervical foraminal disc disease (UCFD) are good and comparable. PE-PCF resulted in significantly less immediate postoperative neck pain, but BE-PCF required shorter total operation time.
Background: The biportal endoscopic technique (BE) is a fast-growing surgical modality that can be applied to posterior cervical foraminotomy (PCF), as well as lumbar discectomy and decompressive laminectomy. It has several technical differences from the percutaneous full-endoscopic technique (PE), which has been standardized as the representative endoscopic spinal surgery tech-nique. The purpose of this study was to compare the short-term clinical outcomes between BE-PCF and PE-PCF.Methods: A retrospective review was conducted on 66 patients who had single-level unilateral cervical foraminal disc disease (UCFD). All patients underwent PE-or BE-PCF. Clinical outcomes including visual analog scale (VAS)-arm, VAS-neck, and Neck Dis-ability Index (NDI) were evaluated. Perioperative data including operation time, length of hospital stay (LOS), amount of surgical drain, postoperative complications, and reoperation were collected. Serum creatine phosphokinase (CPK) and C-reactive protein (CRP) levels were recorded.Results: A total of 65 patients were included in the final analysis: 32 with PE-PCF and 33 with BE-PCF. There was no statistically significant difference in demographic and preoperative data between the two groups. All patients had significant improvement in VAS-arm, VAS-neck, and NDI compared to the baseline value. The improvement of all parameters was comparable between the two groups at each point for 1 year after surgery (p > 0.05), except for the significantly lower VAS-neck at postoperative 2 days in PE-PCF (p = 0.005). The total operation time was significantly shorter in BE-PCF (p = 0.036). There were no statistically significant differences between the two groups in regard to LOS, amount of surgical drain, and serum CPK and CRP levels (p > 0.05). Reopera-tion and complications between the two groups were comparable (p > 0.05).Conclusions: The 1-year postoperative clinical outcomes of PE-PCF and BE-PCF for cervical pain and disability caused by UCFD were good and comparable. PE-PCF resulted in significantly less immediate postoperative neck pain, but BE-PCF required shorter total operation time.

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