Abstract
Purpose
Here, we introduce a novel strategy of awake unilateral biportal endoscopic (UBE) decompression, which applies conscious sedation combined with stepwise local anesthesia (LA) as an alternative to general anesthesia (GA). The study aims to evaluate the feasibility of awake UBE decompression for degenerative lumbar spinal stenosis (DLSS) in elderly patients.
Patients and Methods
This retrospective study included 31 consecutive patients who received awake UBE decompression for DLSS in our institution from January 2021 to March 2022. Clinical results were evaluated using patient-reported outcomes measures (PROM) including visual analog scale for leg pain (VAS-LP), Oswestry Disability Index (ODI), and modified MacNab criteria. The anesthesia effectiveness and intraoperative experience were evaluated by intraoperative VAS and satisfaction rating system.
Results
UBE decompression was successfully performed in all patients under LA combined with conscious sedation. 26 (83.9%) patients rated the intraoperative experience as satisfactory (excellent or good) and 5 (16.1%) as fair. The mean intraoperative VAS was 3.41±1.26. The VAS and ODI at each follow-up stage after surgery were significantly improved compared to preoperative scores (p < 0.01). At the last follow-up, 28 patients (90.3%) classified the surgical outcome as good or excellent, and 3 (9.7%) as fair. There were no serious complications or adverse reactions observed in the study.
Conclusion
Our preliminary results suggest that awake UBE decompression is a feasible and promising alternative for elderly patients with DLSS.
Abbreviations
UBE, unilateral biportal endoscopy; LA, local anesthesia; GA, general anesthesia; DLSS, degenerative lumbar spinal stenosis; PROM, patient-reported outcomes measures; VAS, visual analog scale; ODI, Oswestry disability index; ASS, awake spinal surgery; ULBD, unilateral laminotomy for bilateral decompression; PONV, postoperative nausea and vomiting; POD, postoperative delirium; ICH, intracranial hypertension; CT, computed tomography; MRI, magnetic resonance imaging.
Ethics Approval and Informed Consent
This study was approved by the ethics committee of Shengjing Hospital of China Medical University (2023PS854K), and the patient’s informed consent form was exempted, given the retrospective observational nature. This study was conducted in accordance with the Declaration of Helsinki.
Disclosure
The authors report no conflicts of interest in this work.