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Comparison of cage with plate versus tricortical iliac crest graft with plate fixation in anterior cervical discectomy and fusion: A retrospective study
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How to cite this article: Dobriyal AA, Srivastava A, Randhawa AS, Gupta P, Sharma BS. Comparison of cage with plate versus tricortical iliac crest graft with plate fixation in anterior cervical discectomy and fusion: A retrospective study. Adesh Univ J Med Sci Res. doi: 10.25259/AUJMSR_101_2025
Abstract
Objectives:
Anterior cervical discectomy and fusion (ACDF) is a widely accepted procedure for the management of degenerative cervical disc disease. Different fusion techniques, including cage with plate fixation and tricortical iliac crest graft (ICG) with plate fixation, are employed, but their comparative effectiveness remains debated. The present study aimed to compare clinical outcomes, fusion rates, and complications between these two techniques.
Material and Methods:
This retrospective study was conducted between 2015 and 2023 and included 194 patients with cervical disc disease who underwent ACDF (100 with cage and plate fixation, 94 with tricortical ICG and plate fixation). Patients were assessed for fusion, pain relief, functional outcomes (Odom’s criteria, Visual Analog Scale [VAS]), and complications.
Results:
The mean age was 50.2 ± 10.1 years in the cage group and 53.4 ± 6.5 years in the graft group, with a male predominance in both cohorts. Solid radiological fusion was achieved in 100% of patients in both groups at final follow-up. According to Odom’s criteria, excellent-to-good outcomes were observed in 83% of the cage group and 87% of the graft group (P = 0.001). The mean post-operative VAS was 45.32 ± 10.2 in the cage group and 41.5 ± 11.1 in the graft group (P = 0.034). Complications included dysphagia (6 in cage vs. 5 in graft), cage subsidence (2 cases), infection (4 in cage vs. 1 in graft), and donor-site pain in 20 graft patients.
Conclusion:
Both cages with plate fixation and tricortical ICG with plate fixation in ACDF provided high fusion rates and favorable functional outcomes, with no significant difference in overall efficacy. However, cage use reduced donor-site morbidity, whereas autograft provided robust biological fusion. The choice of technique should be individualized based on patient factors and surgeon preference.
Keywords
Anterior cervical discectomy
Cage
Fusion
Iliac crest graft
Plate fixation
INTRODUCTION
Cervical myelopathy is a disabling condition that commonly arises as a consequence of cervical spondylosis affecting vertebral structures. When cervical myelopathy develops secondary to degenerative spondylosis, it is known as cervical spondylotic myelopathy (CSM). Patients may present with impaired coordination, reduced manual dexterity, gait disturbance, urinary dysfunction, muscle weakness, sensory changes, and abnormal reflexes.[1]
The pathophysiology of CSM involves both static and dynamic spinal cord compression. Static compression results from osteophyte formation, disc degeneration, and ligamentum flavum hypertrophy. Dynamic compression arises from cervical motion – flexion increases disc bulging, and extension causes ligamentum thickening – leading to a fluctuant narrowing of the spinal canal. Cadaveric studies confirm that canal dimensions vary with motion, with flexion expanding the space compared to extension.[2,3] This cyclical compression contributes to ischemia and neuronal injury over time.
Age-related degeneration amplifies CSM pathogenesis; intervertebral disc dehydration, loss of height, and segmental instability diminish spinal canal capacity and impair cord perfusion.[4,5] If unaddressed, these changes lead to progressive neurological deterioration.
Anterior cervical discectomy and fusion (ACDF) is a standard surgical intervention for degenerative cervical disc disease and CSM. Initially described by Robinson and Smith, ACDF achieves decompression, restores disc height, and maintains spinal alignment while promoting stabilization and fusion.[6-9]
Fusion options after discectomy include tricortical iliac crest autografts, allografts, synthetic substitutes, and interbody cages, often supported with anterior plating.[10-12] Each method presents advantages and pitfalls: autografts have osteogenic properties but donor-site morbidity; standalone grafts risk subsidence and non-union; plating improves stability but can cause hardware-related complications such as plate loosening, screw failure, longer operative time, and soft tissue irritation.[10,11]
In this study, we evaluated two commonly employed strategies for ACDF:
Use of an autologous tricortical iliac crest bone graft combined with a locked anterior cervical plate, and
Use of a titanium interbody cage filled with cancellous bone cylinders obtained using a minimally invasive technique, also stabilized with a locked anterior cervical plate.[12]
Over the past two decades, comparative studies have shown equivalent fusion rates and outcomes between cages and autografts, with cages offering reduced operative time and donor-site pain.[13-17] Others support superior long-term biological integration using autografts, especially in multilevel fusions.[18-21] A systematic review by Verhagen et al. highlights variable outcomes across studies.[16]
Recent meta-analyses and systematic reviews maintain the controversy: while cages reduce donor-site morbidity, autografts still demonstrate strong fusion, particularly at longer follow-up.[17,21] Multicenter data suggest that the choice of technique may largely depend on surgeon preference, patient anatomy, and comorbidities, with both approaches achieving acceptable outcomes in properly selected cases.[22-26]
Technological advances have also introduced new implant designs. Stand-alone self-locking cages have demonstrated reductions in operative time, blood loss, dysphagia, and adjacent segment degeneration compared to cage-plus-plate constructs in single-level ACDF, while maintaining comparable fusion and subsidence rates.[10,11] Similarly, recent innovations such as bioactive glass-ceramic cages and 3D-printed porous titanium cages have shown promising fusion rates and biocompatibility when compared with conventional polyetheretherketone (PEEK) constructs.[18] These developments highlight an ongoing evolution in fusion technology, with efforts directed at improving implant integration and reducing morbidity.
Given this backdrop and persistent controversy, the present study was undertaken to compare two widely used ACDF techniques – cage with plate fixation versus tricortical iliac crest graft (ICG) with plate fixation – with respect to fusion success, functional outcomes, and post-operative complications, using long-term data from a single-center cohort.
MATERIAL AND METHODS
Study design and setting
This retrospective study was conducted in the Department of Neurosurgery, Mahatma Gandhi Hospital, Jaipur, between 2015 and 2023.
Patient selection
A total of 420 patients with cervical disc disease presented during the study, of whom 194 met the inclusion criteria. Patients were included if they had progressive spinal cord compression due to degenerative cervical disc prolapse, motor weakness of the upper or lower extremities, gait disturbance, clinical features of myelopathy or radiculopathy, and corresponding findings on X-ray, magnetic resonance imaging (MRI), or computed tomography scan. Exclusion criteria were cervical spine fracture or dislocation, infection, tumor, inflammatory or autoimmune disorders, and hereditary spastic paraplegia. Among the 194 eligible patients, 94 underwent ACDF with tricortical iliac crest bone graft and plate fixation, and 100 underwent ACDF with cage and plate fixation.
Consecutive patients who fulfilled the inclusion criteria during the study period were included to minimize selection bias. This was a retrospective cohort study; no randomization was performed, and patient allocation to cage versus ICG was determined by the surgeon’s decision and intraoperative factors. Masking/blinding was not applicable due to the retrospective surgical nature of the study. No formal sample size calculation was performed a priori; all eligible patients during the study were included.
Surgical technique
All procedures were performed by two experienced neurosurgeons using the standard Smith-Robinson anterior approach. Patients were positioned supine with a small support beneath the shoulders to achieve gentle cervical extension. The surgical level was confirmed intraoperatively using fluoroscopy. A transverse incision was made along the anterior cervical crease, followed by dissection through the platysma and fascial planes to expose the prevertebral fascia and longus colli muscles. After identification of the affected disc, discectomy was performed, and the endplates were partially curetted to reduce the risk of graft collapse or cage subsidence.
In the cage group, cage size was determined intraoperatively, and a titanium cage was filled with cancellous bone harvested from the iliac crest using a minimally invasive graft-harvesting sleeve. In the graft group, a tricortical iliac crest bone graft was obtained through a separate incision and inserted into the disc space. In both groups, fixation was augmented using a locked anterior cervical plate. Wounds were closed in layers over a drain.
Post-operative care and follow-up
All patients were immobilized postoperatively with a Philadelphia cervical collar. Assisted mobilization was initiated on the 1st post-operative day. The collar was continued for 3 months, after which patients began active and passive limb exercises. Patients were followed for a minimum of 9 months (Range: 9 months–3 years). Clinical evaluation included neurological assessment, pain relief, and functional recovery. Radiographs of the cervical spine (lateral view, flexion–extension views) were obtained to assess fusion and implant position.
Outcome measures
Functional outcomes were assessed using Odom’s criteria,[14,15] and pain intensity was measured with the Visual Analog Scale (VAS),[18,19] represented as a 100-mm horizontal line where 0 mm indicated no pain and 100 mm represented the worst pain imaginable. Neurological recovery was evaluated using the Medical Research Council grading for motor power, together with assessment of sensory, autonomic, and reflex functions. Radiological fusion was defined as the presence of bony trabeculae bridging the disc space. For cage constructs, successful fusion was additionally confirmed when the interspinous distance at the fusion level was <2 mm on flexion–extension radiographs.[15] Patients with persistent or worsening symptoms underwent MRI, whereas those with satisfactory clinical and radiological outcomes were not routinely subjected to post-operative MRI.
Statistical analysis
Statistical analysis was performed using IBM Statistical Package for the Social Sciences Statistics version 25.0 (IBM Corp, Armonk, NY). Continuous variables are presented as mean ± standard deviation (SD) and categorical variables as frequency (%). Between-group comparisons were performed using an independent samples t-test for continuous variables and a Chi-square test or Fisher’s exact test for categorical variables, as appropriate. P < 0.05 were considered statistically significant.
RESULTS
A total of 194 patients were included in the study: 100 underwent ACDF with cage and plate fixation, and 94 underwent ACDF with tricortical ICG and plate fixation.
Demographics
The mean age was 50.2 ± 10.1 years in the cage group and 53.4 ± 6.5 years in the graft group. In both groups, males were more common than females (65 vs. 35 in the cage; 64 vs. 30 in the graft). The mean follow-up duration was 16.4 ± 2.1 months in the cage group and 17.8 ± 1.5 months in the graft group. The most commonly involved level in both groups was C5–C6 (54 cases in cage, 50 in graft), followed by C6–C7. Complete demographic details are shown in [Table 1, Figures 1 and 2].
| Variable | Cage group | Tricortical graft with plate group |
|---|---|---|
| Number of patients | 100 | 94 |
| Mean age, (mean±SD) | 50.2±10.1 | 53.4±6.5 |
| Male | 65 | 64 |
| Female | 35 | 30 |
| Follow-up period (months), (mean±SD) | 16.4±2.1 | 17.8±1.5 |
| Involved level - C3-C4 | 5 | 8 |
| C4-C5 | 11 | 10 |
| C5-C6 | 54 | 50 |
| C6-C7 | 30 | 26 |
SD: Standard deviation


Fusion and functional outcomes
Solid radiological fusion was achieved in 100% of patients in both groups at final follow-up. According to Odom’s criteria, excellent-to-good outcomes were seen in 83 patients (83%) in the cage group and 82 patients (87%) in the graft group, while fair or poor results were observed in 7 and 12 patients, respectively (p = 0.001). Pain outcomes improved in both groups: mean post-operative VAS was 45.32 ± 10.2 in the cage group and 41.5 ± 11.1 in the graft group (p = 0.034). These findings are summarized in Table 2.
| Variable | Cage group (n=100) | Graft with plate (n=94) | p-value |
|---|---|---|---|
| Radiological fusion | |||
| Complete union | 100 | 94 | |
| Non-union | - | - | |
| Odom rating | |||
| Excellent | 45 | 42 | 0.001* |
| Good | 38 | 40 | |
| Fair | 5 | 10 | |
| Poor | 2 | 2 | |
| VAS (mean±SD) | 45.32±10.2 | 41.5±11.1 | 0.034 |
Values are mean±SD or n (%). VAS: Visual analog scale (0=No pain, 100=Worst pain). p value <0.05 = Significant. *highly significant
Radiological fusion is defined as bridging trabeculae and ≤2 mm interspinous motion. Between-group comparisons used an independent samples t-test for VAS and Chi-square test for categorical variables [Figures 3 and 4].


Complications
The overall complication rate was low in both groups. Dysphagia occurred in 6 cage patients and 5 graft patients, resolving within weeks. Cage subsidence was observed in 2 patients in the cage group, while no graft collapse was seen in the graft group. Superficial wound infection was observed in 4 cage patients and 1 graft patient, all managed successfully with antibiotics and dressings. Donor-site morbidity was unique to the graft group, with 20 patients reporting persistent iliac crest pain, 4 of whom required additional analgesics. Post-operative complications are shown in Table 3.
| Post-operative complications | Cage with plate | Graft with plate |
|---|---|---|
| Dysphagia | 6 | 5 |
| Cage subsidence | 2 | 0 |
| Infection | 4 | 1 |
| Surgical site pain | 2 | 1 |
| Graft site Pain | 0 | 20 |
DISCUSSION
ACDF is a well-established technique for the management of degenerative cervical spine disease associated with radiculopathy and myelopathy.[11] Over the years, multiple modifications of this procedure have been introduced, including the use of different graft materials and fixation devices. Despite extensive clinical use, no universal consensus has been reached regarding the superiority of any single technique.[15]
The fundamental objective of ACDF is to decompress the neural elements and achieve a stable fusion that maintains cervical alignment. Both tricortical ICGs with plate fixation and biomechanical interbody spacers, such as cages, effectively restore disc height, relieve compression, and increase foraminal dimensions through ligamentotaxis.[16] By restricting abnormal motion, fusion reduces radicular pain and may contribute to partial resorption of osteophytes.
In our study, most patients were in the 50–60-year age group, with a male predominance in both treatment groups. These demographic findings are consistent with prior literature. Spallone and Marchione reported a mean age of 49.1 ± 12.1 years in their cohort.[18] Sharma and Kishore, found a mean age of 51.07 ± 9.39 years in the autograft group and 47.3 ± 9.3 years in the PEEK cage group.[19] Similarly, studies by Sharma and Kishore, Siddiqui and Jackowski, Lee and Jang, Adam et al.[19,20,22,23] also reported a predominance of male patients.
In terms of functional outcome, excellent-to-good recovery was achieved in 83% of the cage group and 87% of the graft group (p = 0.001). These findings parallel those of Ayman and Galhom who reported 90% excellent-to-good outcomes in the cage group and 85% in the bone graft group.[24] Islam et al. also observed comparable functional improvement, with 93.3% of cage patients and 86.6% of autograft patients achieving excellent or good outcomes.[25] Pain relief was also significant in our series, with mean post-operative VAS scores of 45.32 ± 10.2 in the cage group and 41.5 ± 11.1 in the graft group (p = 0.034), consistent with Spallone and Marchione, who reported substantial improvement in both neck and arm pain after ACDF.[18]
Complication rates in our study were low and comparable between groups. Dysphagia was transient and observed in 6 patients in the cage group and 5 in the graft group, resolving spontaneously within weeks, similar to the findings of Ayman and Galhom[24] and Islam et al.[25] Cage subsidence was seen only in 2 cage patients, while donor-site morbidity, including persistent iliac crest pain, was unique to the autograft group, affecting 20 patients, with 4 requiring additional analgesic therapy. These findings reaffirm the trade-off between the biological fusion advantages of autografts and donor-site morbidity risks.
Recent literature continues to highlight this controversy. Alhashash et al. reported comparable clinical outcomes and fusion rates between cage constructs and grafts at 5-year follow-up, but noted less donor-site morbidity with cages.[27] Yang et al., in a meta-analysis, concluded that cage constructs significantly reduce perioperative complications, though long-term outcomes were similar to autografts.[17] Xu et al. observed that tricortical autografts may still provide superior biological fusion in multilevel cases, whereas cages offer predictable results in single-level procedures.[21] Contemporary reviews emphasize individualized decision-making, balancing the advantages of each technique against patient-specific factors.[26,28]
Our study adds to this evidence by demonstrating equivalent fusion and functional outcomes between cage and autograft with plate fixation, while highlighting the donor-site morbidity uniquely associated with iliac crest harvest.
Limitations
This study has certain limitations. It was retrospective and single-center in nature, with potential selection bias. Although the follow-up period ranged from 9 months to 3 years, a longer follow-up may better capture the durability of fusion and adjacent segment disease. We did not evaluate cost-effectiveness, which is an important factor in resource-limited settings.
Strengths
However, the strengths of this study include a relatively large sample size, standardized surgical techniques performed by experienced surgeons, and a comprehensive assessment of clinical, radiological, and functional outcomes.
CONCLUSION
The ACDF procedure is considered an optimal approach for the treatment of degenerative cervical disc disease, as it consistently yields favorable functional results and successful fusion. This can be achieved using either a cage with plate fixation or a tricortical ICG with plate fixation.
In our study, there was no notable difference in post-operative monitoring, fusion rates, or clinical and functional outcomes between the cage and tricortical ICG groups. The use of a tricortical ICG combined with a plate remains a highly effective treatment, providing strong fusion and sufficient stability with the addition of anterior plating. Conversely, the use of a cage serves as an equally efficient alternative, offering reduced surgical duration, reliable fusion outcomes, and fewer donor-site complications.
Further prospective multicenter studies with longer follow-up are warranted to validate these findings, assess cost-effectiveness, and evaluate newer cage designs and biomaterials that may further improve fusion rates and reduce complication profiles.
Ethical approval:
Institutional Review Board approval is not required as it is a retrospective study.
Declaration of patient consent:
The authors certify that they have obtained all appropriate patient consent forms. In the form, the patients have given their consent for their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.
Conflicts of interest:
There are no conflicts of interest.
Use of artificial intelligence (AI)-assisted technology for manuscript preparation:
The authors confirm that there was no use of artificial intelligence (AI)-assisted technology for assisting in the writing or editing of the manuscript and no images were manipulated using AI.
Financial support and sponsorship: Nil.
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