Here, we present a protocol to describe the technical key points of applying the ultrasonic osteotome in posterior endoscopic cervical discectomy.
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Method Article
* These authors contributed equally
Here, we present a protocol to describe the technical key points of applying the ultrasonic osteotome in posterior endoscopic cervical discectomy.
The ultrasonic osteotome, as a novel osteotomy system, demonstrates unique advantages in posterior endoscopic cervical discectomy (PECD), though its technical implementation remains challenging. Accumulated evidence has validated the safety profile of this device in spinal surgery. Meta-analysis has revealed its superior efficacy in enhancing decompression efficiency, reducing intraoperative blood loss, and shortening operative duration compared to conventional high-speed burrs. Notably, no significant differences were observed in symptom improvement rates, hospital stay duration, or postoperative complication incidence between the two techniques. This study provides a video-documented technical protocol for ultrasonic osteotome utilization in PECD, demonstrating successful clinical implementation in a patient with cervical radiculopathy. We enrolled a 62-year-old female patient who presented with a 10-year history of left-sided cervical and upper back pain. She was admitted for surgery following a recent exacerbation that was accompanied by numbness and pain in her left upper limb. The duration of the surgical procedure was 109 minutes. The patient was mobilized with the help of a standard cervical brace on postoperative day 1. The patient demonstrated significant resolution of left-sided neck pain (preoperative visual analog scale [VAS] score 6, decreasing to 1) and left upper limb radiculopathy. Postoperative magnetic resonance imaging (MRI) confirmed adequate nerve root decompression, with significant symptom resolution and absence of device-related complications such as dural tears or neurological deficits. These findings substantiate the technical feasibility and procedural reliability of the ultrasonic osteotome in endoscopic cervical spine surgery.
Cervical radiculopathy, a prevalent spinal disorder, affects approximately 3.3 cases per 1,000 individuals in the general population1. Anterior cervical discectomy and fusion (ACDF) has long been recognized as one of the standard surgical treatments for cervical radiculopathy2. However, hardware-related complications following ACDF, including hardware failure, pseudarthrosis, adjacent segment degeneration, and graft subsidence, present significant management challenges3,4,5,6,7,8. In recent years, percutaneous endoscopic spine surgery has rapidly advanced due to its minimally invasive nature, rapid recovery, and favorable outcomes9,10,11,12. Percutaneous posterior endoscopic technique may serve as a potential alternative to ACDF in the management of cervical radiculopathy, with recent studies showing comparable therapeutic outcomes that warrant further clinical investigation9,13,14,15,16.
The anatomical location of cervical disc herniation is closely associated with surgical difficulty17,18. Based on the anatomical position of the herniated material, it can be classified into three subtypes (Figure 1): Type A, Type B, and Type C. Among these, Type C (where the herniation is completely located within the intervertebral foramen) presents greater challenges for surgical decompression, with higher risks of nerve root injury and vertebral artery laceration. Compared to ACDF, posterior endoscopic cervical discectomy (PECD) offers superior decompression of the stenotic nerve root canal17,19,20. This is particularly evident in cases where foraminal stenosis is caused by osseous compression, such as hypertrophy of the Luschka joint, osteophyte formation, or calcified intervertebral discs21.
The key to the PECD technique lies in achieving adequate decompression of the compressed structures while avoiding injury to critical anatomical elements such as nerve roots and vertebral arteries during the decompression process. However, when using standard surgical instruments (high-speed burr) for bone removal, capillary bleeding often obscures the endoscopic visual field in the irrigation fluid22,23. This phenomenon not only increases surgical risks but also prolongs operative time due to the necessity of additional hemostatic procedures24,25. The ultrasonic osteotome, as an alternative osteotomy instrument, has been recognized as an efficient and safe option and is being increasingly adopted in various spinal surgical procedures24,25,26.
The ultrasonic osteotome generates high-frequency ultrasonic vibrations to cut bone tissue through micro-oscillations27,28. Consequently, compared to the layer-by-layer grinding of high-speed burs, the osteotomy mode of the ultrasonic osteotome demonstrates higher efficiency when cutting large bone segments25. Due to the distinct physical properties (e.g., elasticity, hardness) of soft and bone tissues, the ultrasonic osteotome exerts a relatively weaker effect on soft tissues24,25. Thus, for specific procedural steps, the ultrasonic osteotome offers superior safety over high-speed burs. Furthermore, the ultrasonic bone scalpel offers an added advantage over the high-speed burr. During the bone removal process, the cavitation effect induced by the ultrasonic vibrations promotes the coagulation and denaturation of hemoglobin within the cutting area, thereby achieving hemostasis23,28,29,30. Currently, research on the application of the ultrasonic bone scalpel in PECD is extremely limited. Therefore, this study aims to establish a systematic operational scheme for this technique.
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The protocol follows the guidelines of the ethics committee of the local hospital. The ethics committee approved the protocol. The patient provided written informed consent.
NOTE: A 62-year-old female patient was included in the study, admitted for treatment due to a 10-year history of left-sided cervical and back pain, which had worsened over the past 10 days and was accompanied by numbness and pain in the left upper limb. Physical examination findings were as follows: (1) restricted left lateral flexion and extension of the cervical spine; (2) positive left brachial plexus stretch test and Spurling's test; (3) muscle strength of the left triceps graded as 4/5; (4) numbness and pain in the left upper limb, primarily radiating to the middle finger of the left hand; and (5) a visual analog scale (VAS) score of 6. The MRI imaging indicates compression of the left C7 nerve root (Figure 2A) and stenosis of the left C7 intervertebral foramen (Figure 2B). The patient had previously undergone conservative outpatient treatment for 3 months with recurrent symptoms and opted for surgical intervention. The surgical instruments and equipment used in the study are listed in the materials table.
1. Pre-endoscopic decompression procedures
2. Ultrasonic osteotome osteotomy
3. Postoperative management
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The left C7 nerve root of the patient was successfully and adequately decompressed. Under endoscopic visualization, the ventral herniation compressing the nerve root was effectively removed, and partial laminectomy, facetectomy, and spur removal were achieved on the dorsal aspect of the nerve root. Ultimately, it was confirmed that the compressed nerve root had achieved sufficient space for movement. Postoperative MRI imaging demonstrated sufficient foraminal decompression at the left C7 level, in contrast to the preoper...
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Compared with ACDF, PECD achieves more effective decompression in stenotic nerve root canals, making it a viable minimally invasive alternative17,20,32,33. The ultrasonic osteotome, as a novel osteotomy power system, serves as a reliable tool for bone removal during PECD17,23,24. Numerous studies have ...
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The authors in this study declare that no conflict of interest exists.
This work is funded by the Science, Technology, and Innovation Commission of Shenzhen Municipality (Grant No. JCYJ20230807115918039) from Zhouyang Hu; the Nanshan District Health Science and Technology Major Project (Grant No. NSZD2023026; NSZD2023023) from Zhouyang Hu and Guoxin Fan; Nanshan District Health Science and Technology Project (Grant No. NS2023002; NS2023044) from Xiang Liao and Guoxin Fan; the Medical Scientific Research Foundation of Guangdong Province of China (Grant No. A2023195) from Guoxin Fan.
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| Name | Company | Catalog Number | Comments |
|---|---|---|---|
| 0.5% lidocaine | Beijing Tide Pharmaceutical Co., Ltd | H37022768 | Local Anesthesia |
| Dilatation cannula | Beijing Tianqi Medical technology Co., Ltd., Beijing | ZJ289019 | Cannulation |
| Flurbiprofen axetil | Shandong Hualu Pharmaceutical Co., Ltd. | H20041508 | For postoperative pain |
| Irrigation sleeves | Beijing Sumai Medical Technology Co., Ltd | OS1SPT19 | Restricted operating range of the ultrasonic osteotome |
| Joimax Endoscopy System | Joimax | FS7347171O | TESSYS |
| Puncture needle | Beijing Tianqi Medical technology Co., Ltd., Beijing | ZJ289033 | Puncture |
| Ultrasonic osteotome | Beijing Sumai Medical Technology Co., Ltd | OT1SPT19 | Bone Cutting |
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This corrects the article 10.3791/68461