OBJECTIVE The management of cervical spondylotic myelopathy CSM presents a clinical conundrum, with cervical disc arthroplasty CDA and anterior cervical discectomy and fusion ACDF emerging as primary contenders. However, the comparative advantages and limitations of these interventions remain contentious. This meta-analysis aimed to scru-tinize the efficacy and safety profiles of CDA and ACDF inaddressing CSM METHODS Adhering rigorously to the PRISMA Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines, the authors conducted an exhaustive systematic search across reputable databases including PubMed, Embase, Web of Science, Cochrane Library, Scopus, and the Chinese National Knowledge Infrastructure. Randomized controlled trials evaluating the efficacy and safety of CDA versus ACDF for CSM were meticulously selected for comprehensive evaluation. RESULTSA total of 12 randomized controlled trials involving 2612 patients 1464 CDA, 1148 ACDF were included in this meta-analysis. The pooled results showed that compared with ACDF, CDA was associated with better overall success RR 1.21, 95 CI 1.06-1.37 p = 0.004 I2 = 71. In terms of Neck Disability Index and neck visual analog scale VAS, compared with ACDF, the CDA group showed superior performance at 6 weeks, 3 months, 6 months, 12 months, and 24 months after surgery. The performance on the arm VAS at 3 and 12 months after surgery was the same. The operative time for the CDA group was significantly longer than that of the ACDF group. There were no significant differ-ences in neurological success radiological success arm VAS scores at 6 weeks, 6 months, and 24 months postopera-tively range of motion SF-36 mental component summary and physical component summary scores surgical blood loss dysphagiadysphonia and rate of any adverse event. CONCLUSIONS In contrast to ACDF, CDA exhibited superior clinical efficacy and a more favorable safety profile in the management of CSM. Notably, discernible disparities were observed in the enhancement of neck pain as measured by the VAS within the initial postoperative year. It is imperative to note, however, that the body of evidence supporting these conclusions remains relatively scant, necessitating comprehensive validation through expanded multicenter randomized controlled trials encompassing substantial sample sizes. Systematic review registration no. CRD42024523510 www.crd.york.ac.ukprospero