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Endoscope-assisted ACDF reduces complication rates and blood loss but increases operative timeEndoscope-assisted surgery shows fewer complications for cervical disease

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Key Takeaway
Note that EA-ACDF may reduce complication rates and blood loss but requires longer operative times.

This meta-analysis evaluated the efficacy and safety of endoscope-assisted anterior cervical discectomy and fusion (EA-ACDF) compared to conventional anterior cervical discectomy and fusion (CA-ACDF) in 755 patients with single-level degenerative cervical disease. The analysis synthesized data regarding perioperative metrics and clinical outcomes.

EA-ACDF was associated with a lower overall complication rate (RR 0.44; 95% CI 0.25 to 0.78) and reduced intraoperative blood loss (MD -17.31 mL; 95% CI -24.38 to -10.25). Additionally, patients undergoing EA-ACDF had lower postoperative drainage volumes (MD -10.97 mL; 95% CI -16.98 to -4.96) and shorter hospital stays (MD -0.67 days; 95% CI -1.16 to -0.17). However, EA-ACDF was associated with longer operative times (MD 17.31 min; 95% CI 11.38 to 23.23).

Clinical and radiographic outcomes, including Japanese Orthopaedic Association scores, Neck Disability Index, visual analogue scale scores, cervical lordosis, and fusion rates, showed no significant differences between the two techniques. The authors note that the certainty of evidence ranges from low to very low. While EA-ACDF may offer modest perioperative advantages, current evidence does not establish clinical superiority over conventional methods.

Living with degenerative cervical disease can be a struggle for your neck and your daily life. When surgery is an option, doctors often choose between traditional methods and newer techniques like endoscope-assisted surgery. This method uses a specialized scope to help the surgeon see more clearly during the procedure.

A review of data from 755 patients found that the endoscope-assisted approach led to lower blood loss and less drainage after surgery. It also resulted in shorter hospital stays and a lower overall complication rate compared to the traditional method. However, these benefits come with a trade-off: the surgery took about 17 minutes longer to complete.

While the surgical process showed some advantages in safety and recovery time, the actual clinical results were very similar between the two methods. Patients reported similar levels of pain and disability in both groups. It is important to note that the evidence for these findings is currently low to very low, meaning more research is needed to be certain of the results.

What this means for you:
Endoscope-assisted surgery may lower complication rates and blood loss, but it takes longer to perform.

Common questions

Is endoscope-assisted surgery safer than traditional surgery?

The data shows that endoscope-assisted surgery had a lower overall complication rate compared to the traditional method. However, the evidence for this finding is currently rated as low to very low certainty. You should talk to your doctor about which surgical approach is best for your specific condition.

How long does the surgery take with an endoscope?

The surgery using an endoscope took an average of 17.31 minutes longer than the traditional method. While it takes more time for the surgical team, it was associated with lower blood loss and shorter hospital stays for the patient.

Will I feel better after endoscope-assisted surgery?

Patients in the study reported similar levels of pain and disability regardless of which surgery they received. While the endoscope-assisted method had fewer complications, the clinical outcomes like the Neck Disability Index and pain scores were not significantly different between the two methods.

Study Details

Study typeMeta analysis
EvidenceLevel 1
PublishedNov 2026
View Original Abstract ↓
BackgroundEndoscope-assisted anterior cervical discectomy and fusion (EA-ACDF) has been introduced as a modified technique for the treatment of degenerative cervical disease, but its comparative efficacy and safety relative to conventional ACDF (CA-ACDF) remain uncertain. This systematic review and meta-analysis aimed to compare EA-ACDF with CA-ACDF for single-level degenerative cervical disease.MethodsPubMed, Embase, Web of Science, the Cochrane Library, CNKI, WanFang, VIP, and SinoMed were searched from inception through September 7, 2026. Comparative studies of EA-ACDF vs. CA-ACDF were included. Random-effects meta-analyses were performed. Methodological quality was assessed using the Newcastle–Ottawa Scale, and certainty of evidence was evaluated using GRADE.ResultsEleven retrospective comparative studies involving 755 patients were included. Compared with CA-ACDF, EA-ACDF was associated with longer operative time (MD = 17.31 min, 95% CI 11.38–23.23), but lower intraoperative blood loss (MD = −17.31 mL, 95% CI −24.38 to −10.25), postoperative drainage volume (MD = −10.97 mL, 95% CI −16.98 to −4.96), length of hospital stay (MD = −0.67 days, 95% CI −1.16 to −0.17), and overall complication rate (RR = 0.44, 95% CI 0.25–0.78). No significant between-group differences were observed in final Japanese Orthopaedic Association score, Neck Disability Index, visual analogue scale score, cervical lordosis, or fusion rate. The certainty of evidence ranged from low to very low.ConclusionEA-ACDF may offer modest perioperative advantages at the cost of longer operative time, while short- to mid-term clinical, radiographic, and fusion outcomes appear broadly similar. Current evidence does not establish clinical superiority.Systematic Review Registrationhttps://www.crd.york.ac.uk/PROSPERO/view/CRD420251123475, identifier CRD420251123475.
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