Objective To compare the effectiveness of uniportal endoscopic transforaminal lumbar interbody fusion (Endo-TLIF), unilateral biportal endoscopic transforaminal lumbar interbody fusion (UBE-TLIF), and minimally invasive transforaminal lumbar interbody fusion (MIS-TLIF) in the treatment of single-level lumbar degenerative disease. Methods A retrospective analysis was conducted on 130 patients with single-level lumbar degenerative disease treated between January 2019 and December 2022. According to the surgical technique, patients were divided into the MIS-TLIF group (43 cases), the Endo-TLIF group (45 cases), and the UBE-TLIF group (42 cases). Baseline data, including age, gender, operated level, disease type, preoperative lower-extremity pain visual analogue scale (VAS) score, and Oswestry disability index (ODI), showed no significant difference among the three groups (P>0.05). Operation time, estimated intraoperative blood loss, postoperative hospital stays, and perioperative complications were recorded. Clinical symptoms were evaluated preoperatively and at 1 day, 1 month, 3 months, 1 year, and 2 years postoperatively using the lower-extremity pain VAS score and ODI. Interbody fusion was evaluated using the Suk method at 2 years postoperatively. Surgical outcomes and quality of life were assessed using the modified MacNab criteria and EuroQol-5 Dimensions (EQ-5D) at last follow-up. Results There was no significant difference in operation time among the three groups (P>0.05). The estimated intraoperative blood loss in MIS-TLIF group was the most, while that in Endo-TLIF group was the least, and there were significant differences among the three groups (P<0.05). The postoperative hospital stay was significantly shorter in the Endo-TLIF group and the UBE-TLIF group than in the MIS-TLIF group (P<0.05), while no significant difference was observed between the Endo-TLIF and UBE-TLIF groups (P>0.05). No serious complications, such as severe neurological injury or intervertebral space infection, occurred intraoperatively in any of the three groups. In the MIS-TLIF, Endo-TLIF, and UBE-TLIF groups, some patients experienced transient neurological dysfunction, minor dural tears, or delayed wound healing, respectively; however, there was no significant difference in the overall complication incidence among the three groups (9.30% vs 6.67% vs 7.14%, P>0.05). All patients in the three groups were followed up 24-36 months, with an average of 26.62 months. At all postoperative follow-up time points, both lower-extremity pain VAS scores and ODI in three groups significantly improved compared to the preoperative values (P<0.05). In intergroup comparisons, except that the VAS score at 1 day postoperatively in the Endo-TLIF group was significantly lower than that in the MIS-TLIF group (P<0.05), no significant difference was found in VAS scores or ODI among the three groups at the same follow-up time points (P>0.05). At 2 years postoperatively, the solid interbody fusion rate exceeded 92% in all three groups, and the excellent-to-good rate assessed by the modified MacNab criteria at last follow-up was greater than 90%. No significant difference was observed among the three groups in terms of interbody fusion status, surgical outcome grade, or EQ-5D score (P>0.05). Conclusion Endo-TLIF and UBE-TLIF achieve effectiveness and fusion rates comparable to those of MIS-TLIF for single-level lumbar degenerative disease, with advantages of less trauma, reduced blood loss, and faster recovery.
Citation:
LI Yiming, KONG Weiqing, LI Jie, MA Chao, REN Yongxin. Comparison of effectiveness between two endoscopic lumbar interbody fusion techniques and minimally invasive transforaminal lumbar interbody fusion for single-level lumbar degenerative disease. Chinese Journal of Reparative and Reconstructive Surgery, 2026, 40(3): 438-446. doi: 10.7507/1002-1892.202512031
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