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Percutaneous full-endoscopic anterior transcorporeal cervical discectomy and channel repair: a technique note report

BMC Musculoskeletal Disorders201920:280

https://doi.org/10.1186/s12891-019-2659-0

  • Received: 12 October 2018
  • Accepted: 29 May 2019
  • Published:
Open Peer Review reports

Abstract

Background

Compared to anterior cervical discectomy and fusion (ACDF), cervical motion segment and disc was retained through anterior transcorporeal herniotomy (ATH). But surgical field and manipulation in traditional ATH was restricted by the narrow channel. Percutaneous full-endoscopic transdiscal cervical discectomy is a minimally invasive and functional spine surgery. However, significant loss of intervertebral disc height was inevitable. This study was done to illustrate the feasibility, safety, and efficacy and present our surgical experience of percutaneous full-endoscopic anterior transcorporeal cervical discectomy (PEATCD) and channel repair (CR) for the treatment of cervical disc herniation (CDH).

Methods

Four patients with CDH were chosen to undergo PEATCD and CR with a follow-up care for at least 22 months. The visual analogue score (VAS), Japanese Orthopedic Association (JOA), and modified Macnab criteria were recorded during the postoperative periods. CT images were obtained to observe the healing of the channel at 1 week and 3 months after the operation.

Results

The average operating time was 83.75 min. Drainage tubes were unnecessary. No procedure-related complications occurred. The postoperative VAS and JOA scores were improved compared to those of the preoperative assessment. The clinical efficacy was excellent in 3 patients and good in 1 patient at final follow up stage according to the modified Macnab criteria. The hernia was removed completely in all patients according to postoperative MRI. Migration of the repair implementation and collapse of the drilled vertebrae were not observed during the postoperative periods. The bony channel was nearly absent on CT images obtained at 3 months postoperative.

Conclusion

This is the first time that the anterior transcorporeal cervical discectomy and CR have been performed simultaneously under endoscopy. Less damage to disc and the retained cervical motion segment were achieved through this method. This is a feasible, safe, and minimally invasive procedure.

Trial registration

Numbers: ChiCTR1800016383. Registered 29 may 2018. Retrospectively registered. Trial registry: Chinese Clinical Trial Registry.

Keywords

  • Endoscopy
  • Cervical disc herniation
  • Transcorporeal
  • Minimally invasive surgery
  • Discectomy
  • Channel repair

Background

Cervical disc herniation (CDH) is a degenerative disease of the cervical spine in which the lesion induces a series of symptoms due to an oppressed spinal cord. Anterior cervical discectomy and fusion (ACDF) has become the standard surgical procedure for single- and multiple-levels degenerative cervical spine diseases due to its excellent clinical results and good fusion rates since it was introduced by Smith and Robinson and then Cloward in the 1950s [1, 2]. However, intervertebral fusion decreases the cervical motion segment and accelerates the degeneration of the adjacent segments [3, 4]. Many other complications are also associated with ACDF [58]. Various modifications and procedures have been reported to minimize the surgical disturbance of the biomechanics of the cervical spine [915].

With the rapid development of the percutaneous full-endoscopic technique, the endoscopic anterior transdiscal method has become an accepted procedure for CDH [15]. However, significant loss of intervertebral disc height (IDH) in the operated segment has been confirmed in long-term follow-up studies due to the perforating damage to the disc and excessive removal of the nucleus pulposu [1518]. Anterior transcorporeal discectomy (ATH) was first reported by George in a study that treated lesions in the cervical spinal canal [19], and was derived from a reformation of the technique of Verbiest and Hakuba et al. [2024]. The transcorporeal technique retains the cervical motion segment, protects the disc from surgical damage and has been modified by several surgeons since its introduction [2530]. In the 1990s, Nakai sand Sakai improved this procedure by locating the channel close to the center of vertebrae to avoid damage to the longus colli muscle and cervical sympathetic nerve [31, 32]. An operating microscope was used in their procedure to improve surgical vision, cause less damage to soft tissues and increase the safety of the manipulation.

Conventional ATH was performed with a dilator or open approach. The details in the bottom of the channel observed by the naked eye are obscure, even with a microendoscopy, especially if active bleeding is present. Subsequently, the manipulation is difficult for surgeons. Before this study, we conducted percutaneous full-endoscopic anterior transcorporeal cervical discectomy (PEATCD) for patients with central CDH and acquired excellent follow-up outcomes [33]. Due to the merits of the endoscopic system, we greatly reduced the injury to soft tissues and obtained improved vision for the operation. Based on our previous study [33], we performed PEATCD and channel repair (CR) under endoscopy for patients with CDH in order to accelerate the healing process of the bony channel, which has not been reported previously. In this study, a relatively larger bony channel was used compared to our earlier study, which was more beneficial for manipulations and providing sufficient decompression for patients with a large or broad-based hernia. We share our experiences of PEATCD and CR and report the clinical and radiological outcomes during the follow-up periods.

Materials and methods

Patient characteristics

This study was approved by local institutional review board (IRB) and the informed consent was acquired from all the patients. In our study, PEATCD with CR was performed for 4 consecutive patients, including 1 female and 3 males with an age range of 41 to 46 years old, with soft CDH from Jul. 2016 to Sep. 2016. The duration of neck pain ranged from 14 to 26 weeks. The demographic characteristics, clinical data, and treatment level are shown in Table 1. The visual analog score (VAS) was used to record the neck pain scores during the postoperative periods. The clinical outcomes were evaluated using the Japanese Orthopedic Association (JOA) scores and modified Macnab criteria (Table 2).
Table 1

Summary of demographic characteristics, clinical date, and treatment level

Case

Age (years)

Gender

Level

Duration (weeks)

Postoperative hospital stay (days)

Follow up period (months)

1

43

M

C5–6

14

1

24

2

46

M

C4–5

26

1

24

3

41

M

C4–5

18

1

23

4

46

F

C4–5

17

1

22

Average

44

18.75

1

23.25

Table 2

Modified Macnab Criteria

Grading

Definition

Excellent

Complete resolution of symptoms, recovery of original work activity level and quality of life

good

Mild symptoms, slight activity limitation that do not influence work and quality of life

Fine

Symptoms relieved, activity limitations that influence work and quality of life

bad

No difference in or worsening of symptoms after versus before treatment

Patient selection

The following were indications for PEATCD and CR. (1) The patient had experienced failure of strict conservative treatment for at least 12 weeks. In our study, 3 patients accepted drug therapy and physical treatment, the left one was treated with epidural ejection; (2) single-level central or mediolateral soft herniation; (3) herniated disc fragment that migrated upward or downward but not free; (4) the symptom or discomfort was caused by the CDH. and (5) there is no evidence of instability in the cervical spine. The contraindications were as follows: (1) Patients with multiple-levels CDH or cervical spinal canal stenosis; (2) posterolateral herniation or foraminal stenosis; (3) previous surgery at the same segment; (4) calcification of the herniated disc or posterior osteophytes of the vertebral body; (5) obesity, (6) the herniation was induced by trauma.

Endoscopic instruments

The spinal endoscopy system (SPINENDOS GmbH., Munich, Germany) was comprised of a 4.3 mm working channel, an outer sheath with a 6.9 mm diameter, a 30°-angled scope with a continuous water irrigation system, a trephine with a 6.6 mm inner diameter and a 7.6 mm outer diameter, and a low-temperature radiofrequency ablation system (ArthroCare Co., Sunnyvale, CA, USA). The drill was made by NOUVAG AG, Goldach, Switzerland.

Operative technique

Under general anesthesia, the patient was placed in a supine position with the neck in slight extension. The caudal vertebra was chosen to be drilled for all patients. The entire process was monitored with C-arm fluoroscopy. We used a trephine to directly create the bony channel, which proceeded towards the posterosuperior edge of the targeted vertebra. We primarily confirmed the anterior surface of the drilled vertebra and then selected the channel position with a K-wire under C-arm fluoroscopy (Fig. 1). With the help of two-finger technique (The surgeon located the carotid artery as indicated by its pulsation with the index finger of the left hand and pushed it aside laterally. The tracheoesophagus was then pushed to the medial side with the middle finger), a safe window was created for the insertion of the K-wire and the following operations. The ultrasound examination intraoperative was beneficial if we couldn’t ensure that the vessels had been pushed aside. And the iohexol contrast agent was helpful for confirming the position of the esophagus under C-arm fluoroscopy. We made an approximately 8 mm incision, after which the serial dilators, working cannula and trephine were introduced. We turned the trephine gradually until its tip was located at the posterosuperior border of the vertebra (Fig. 2a and b). Then, the bone plug that was prepared for subsequent CR could be removed together with the trephine by moving it gently in all directions (Fig. 2c). We inserted the working cannula into the bony channel and then inserted the endoscopic system. Bleeding from soft tissues and the channel was resolved by radiofrequency ablation. We could observe some residual bone at the bottom of the channel due to the non-parallel plane between the posterior wall of the vertebra and the bottom of the channel (Fig. 2d). We used a diamond high-speed burr and rongeur to clear these remnants and make a consistent channel towards the herniated lesion. A blunt hook could be used to confirm the posterior wall of the vertebra when a satisfactory channel was established (Fig. 2e). Then, decompression was conducted. To ensure sufficient intraoperative decompression, a small window was made on the posterior longitudinal ligament to directly observe the pulse of the spinal cord (Fig. 2f). When the dural sac re-expansion became apparent, we removed the working cannula from the channel and ensured that no active bleeding was present in the channel. Then, bone grafting was conducted in the channel, in which prior shortening and pruning for the harvested bone had been performed. The insertion process was intently observed via an endoscopy, and the process was terminated when the surfaces of the vertebra and implant were parallel (Fig. 3a and b). We again examined the area for active bleeding before the working cannula and endoscopy were removed. A drainage tube was not necessary. Finally, the residual fluid in the cervical tissues was drained, and the incision was sutured.
Fig. 1
Fig. 1

a, b The position of the K-wire and the outline of the esophagus was confirmed under C-arm fluoroscopy

Fig. 2
Fig. 2

Trephination was terminated when the trephine tip was located at the posterosuperior border of C6 (a and b). The bone plug (c) could be removed by moving the trephine gently in all directions. Some residual bone (d) could be seen after inserting the endoscopic system due to the non-parallel plane of the trephine relative to the posterior edge of C6. A hook (e) was applied to determine the posterior border of C6, after which the hernia was removed. The dural sac re-expansion (f) became apparent when sufficient decompression was achieved

Fig. 3
Fig. 3

No active bleeding occurred after decompression (a), and bone grafting was conducted with the previously harvested bone plug (b)

Postoperative and follow-up care

Patients could manage their daily activities 1 day after the operation and could return to general office work 1 week postoperatively. All 4 patients underwent follow-up observation at 1, 3, 6, 12, and 22 months after surgery. At each follow-up stage, the results of the VAS, JOA score, modified Macnab criteria, and neurologic examinations were recorded. MRI was conducted 1 week after the operation to confirm decompression, and CT images were used to observe the bony channel at 1 week and 3 months after the operation.

Results

All the procedures were completed successfully by the same surgeon. Three interventions were performed at the C4–5 levels, and 1 intervention was performed at the C5–6 level. The average operation time was 83.75 min (70–105 min). The channel was established at the caudal vertebrae in all patients. Drainage tube was not necessary. The patient in Case 1 exhibited a swollen neck after the operation due to a relatively long operation time. However, no adverse effects were observed, and the tumid neck recovered completely within 2 h. Postoperatively, no manifestations of dysphagia, hematoma, esophageal perforation, or vascular and nerve injury were reported. The postoperative hospital stay was 1 day for the 4 patients. The clinical outcomes of VAS and JOA scores are shown in Table 3. According to the modified Macnab criteria, the clinical efficacy was excellent in 3 cases and good in 1 case after 22 months of follow-up care. Postoperative imaging studies showed that the herniated lesion was completely removed (Fig. 4), and the supplementary files showed the MRI images of the other 3 patients (see Additional file 1). According to the postoperative cervical CT images and radiographs, migration of the repaired bone or collapse of the drilled vertebra did not occur (Fig. 5). The channel disappeared nearly 3 months after the operation (Fig. 6). No instability, kyphosis, or loss of IDH in the cervical spine were observed.
Table 3

showed the clinical results of VAS and JOA scores during the postoperative periods

Cases

VAS

 

JOA

Pre

Post-1 m

Post-12 m

Final

 

Pre

Post-1 m

Post-12 m

Final

1

6

2

0

0

 

7

12

17

17

2

8

2

0.5

0.5

 

8

13

15

15.5

3

6

2.5

0

0

 

7

11

16

16

4

7

3

1

0

 

9

15

16

16

Average

6.75

2.38

0.38

0.13

 

7.75

12.75

16

16.13

All the patients got an immediate remission after operation, the pain was disappeared almost at the final follow-up stage, and the average improvement rates of JOA was 90.59%

Fig. 4
Fig. 4

A 43-year-old man was examined due to cervical spondylotic myelopathy. The MRI results showed a broad-based disc hernia at C5/6. The procedure was performed through the channel at C6, and repair was performed with autogenous bone. The postoperative MRI findings showed that the hernia mass was cleared. The preoperative MRI findings, namely, the T1 and T2 weighted sagittal views, are shown (a and b, respectively). Preoperative MRI, T1 weighted axial view (c). Postoperative MRI, T1 and T2 weighted sagittal views (d and e, respectively). Postoperative MRI, T1 weighted axial view (f)

Fig. 5
Fig. 5

CT images of the channel immediately postoperatively, including the axial plane view (a), coronal reconstruction view (b), sagittal reconstruction view (c), and three-dimensional view (d), showed the trajectory of the channel. No migration of the repaired bone occurred

Fig. 6
Fig. 6

CT images obtained 3 months after the operation, including the axial plane view (a), coronal reconstruction view (b), sagittal reconstruction view (c), and three-dimensional view (d), showed that the bone defect had almost completely disappeared. Neither disc space narrowing nor instability were observed

Discussion

The superior features of the endoscopic system include the lighting equipment, which supplies sufficient light to the operating area, the magnification system, and continuous irrigation with normal saline. Detailed vision can be acquired in the channel due to these advantages. Continuous irrigation is extremely important. First, the infection risk is further decreased by separating the surgical field from the air. Second, an endoscopic system can ensure relatively improved distinct vision through the hemostasis effect due to hydraulic pressure and exhaustion of blood along with lavage fluid.

Several researchers have previously reported conventional ATH and modified transcorporeal procedures [25, 26, 2835]. The best points of transcorporeal surgery include preservation of the cervical motion segment and decreasing iatrogenic damage to the pathologic disc. The transcorporeal method had an integrated development that progressed from a traditional open procedure to minimally invasive surgery and finally to the full-endoscopic method. Compared with either ACDF or the transdiscal approach, transcorporeal surgery can better address prolapse of CDH or lesions behind the vertebrae instead of corpectomy in some special situations. In the transcorporeal approach, the damage to the disc depends on the site of the herniated fragments. Injury to the cervical disc will not occur if the hernia deviates from the disc level.

In early procedures, limitations of the channel diameter and surgical vision were inevitable in both the traditional open and microendoscopic ATH. However, ATH under endoscopy can circumvent these limitations. The key point of this novel procedure is the accuracy of the channel trajectory. A diamond high-speed burr was used for channel establishment in most reported studies [31, 32, 35]. In contrast to the early procedures, a trephine was induced to establish the channel in our surgery. The process was dynamically monitored with C-arm fluoroscopy to ensure its depth of entry and the trajectory towards the herniated disc. The channel entrance should be centered relative to the objective drilled vertebra as much as possible to reduce damage to the longus colli muscle, which could reduce not only the subsequent intraoperative bleeding and the risk of postoperative hematoma, but also sympathetic trunk injury due to its anatomical position. The primary purpose of choosing a trephine to drill was to harvest sizable bone for later grafting to the channel. The anatomical integrity was retained, and complications related to bone harvesting from other regions or transplant reaction were avoided. Compared to the diamond high-speed burr, other advantages of using a trephine included better control of the orientation of the channel by the surgeon and a shorter operation time.

In 2010, Lowry combined ACDF with cervical transcorporeal microdecompression and vertebral body access CR for multiple-level CDH [36]. Lowery repaired the channel with a beta-tricalcium phosphate implant filled with locally harvested auto-graft and acquired good results. Although fractures of the drilled vertebrae were not observed, even without CR, in the reported studies [25, 26, 29, 32, 33, 37]. The bony defect was still present 3 months, even 1 year, after transcorporeal procedure in the reported literatures [31, 33]. Whether the risk of collapse will increase has not been reported for cases of patients with osteoporosis or an enlarged channel. In this study, a larger trephine (inner diameter: 6.6 mm, outer diameter: 7.6 mm) was applied to produce the bony channel (approximately 8 mm). Using a larger channel, we could ensure sufficient decompression instead of enlarging the bottom of the channel to obtain a better surgical field, which would make the channel irregular and subsequently increase the risk of repair implant migration. Furthermore, we could address hernias with a broader base (Fig. 4c). CR was conducted while considering the possible collapse of the drilled vertebrae due to the larger channel size. The repair implant was the bone plug harvested intraoperatively with a trephine, which could avoid rejection reaction and greatly decrease the cost. Appropriate pruning to match the harvested bone is necessary before grafting. Additionally, the parallel relationship of the anterior surface of the vertebra and the repair bone must be verified intraoperatively to prevent spinal cord injury due to oppression. Postoperative CT images showed no migration of the repair implementation, and the channel had disappeared almost 3 months after operation and there were no sclerotic changes in the channel. Moreover, no collapse of the drilled vertebrae, loss of IDH, changes of cervical physiological curve, or cervical kyphosis was observed.

Access-related complications in ACDF were avoided with endoscopy because no traction of cervical soft tissues was necessary [7, 8, 38]. Possible severe intraoperative complications included esophageal perforation and vascular injury. A two-finger technique was adopted to pull aside the esophagus and vessels. Additionally, the iohexol contrast agent, which is injected into the gastric tube, could sufficiently delineate the esophageal tract under C-arm fluoroscopy. Subsequently, we could determine whether the esophagus was impaled by observing the relative position of the K-wire and esophagus.

This is the first time anterior transcorporeal cervical discectomy with CR under percutaneous full-endoscopy has been reported. All symptoms of the 4 patients improved during the follow-up periods. Postoperative MRI also showed that the herniated lesion was completely removed. The inclusion criteria for PEATCD and CR was strict, patients with multiple CDH, obesity, or severe myelopathy was excluded. Patient with foraminal stenosis was also excluded because the “Key-hole” technique had been reported safely and effectively in that case [3941]. Previous study showed that the posterior osteophytes of vertebral body or calcification of the herniated disc fragment was difficult to remove completely [31]. Based on the reported literatures and our limited experiences, patients with central localized soft hernia and without spinal canal stenosis were the ideal candidate for PEATCD and CR [31]. This is a safe and economical novel surgery that offers an alternative for patients with CDH. Additional samples are necessary before widespread application is possible.

Conclusions

This is the first time that the anterior transcorporeal cervical discectomy with CR have been performed simultaneously under percutaneous full-endoscopy. This novel procedure retains as much anatomical integrity as possible and promotes the healing process of the bony channel by bone grafting. This is a feasible, safe, minimal invasion and novel procedure for patients with CDH.

Notes

Abbreviations

ACDF: 

Anterior cervical discectomy and fusion

ATH: 

Anterior transcorporeal herniotomy

CDH: 

Cervical disc herniation

CR: 

Channel repair

IDH: 

Intervertebral disc height

JOA: 

Japanese orthopedic association

PEATCD: 

Percutaneous full-endoscopic anterior transcorporeal cervical discectomy

VAS: 

Visual analogue score

Declarations

Acknowledgments

Thanks for my tutor for his careful modification to this manuscript and thanks for the support from my family.

Funding

The collection, analysis, and interpretation of the data in the study were financially supported by the Master’s Science Research Startup Funding of Zunyi Medical University (F-923). The design of the study was supported by the Doctoral Science Research Startup Funding of the Affiliated Hospital of Zunyi Medical University (2017–01). And the postoperative follow-up materials in the study were financially supported by the National Natural Science Foundation of China (31760266).

Authors’ contributions

QD and LQL composed and revised the manuscript and figures, respectively. WBL performed the surgery and WJK also participated as an assistant. GRC, XW, and JA collected the clinical materials and completed the table design. ASW is responsible for the postoperative care. And all the authors have read and approved the manuscript.

Ethics approval and consent to participate

The study is approved by The Ethical Committee of The Affiliated Hospital of Zunyi Medical College [2016 (19)], which belongs to the China Association for Ethical Studies. And the Informed Consent (written) was obtained from all patients included in this study.

Consent for publication

Not applicable.

Competing interests

Drs. Qian Du, Lan-Qiong Lei, Guang-Ru Cao, Wei-Jun Kong, Jun Ao, Xin Wang, An-Su Wang, and Wen-Bo Liao declare no competing interests in this study.

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

(1)
Department of Orthopaedic Surgery, Affiliated Hospital of Zunyi Medical University, Zunyi, 563000, Guizhou, China
(2)
Joint Orthopaedic Research Center of Zunyi Medical University & University of Rochester Medical Center (JCMR-ZMU & URMC), Zunyi Medical University, Zunyi, 563000, Guizhou, China
(3)
Institute of Health and Biomedical Innovation, Queensland University of Technology, Brisbane, Queensland, 4059, Australia
(4)
Translational Research Institute, School of Medicine, University of Queensland, Brisbane, Queensland, 4102, Australia

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