C1-ring osteosynthesis versus C1–2 fixation fusion in the treatment of unstable atlas fractures: a multicenter, prospective, randomized controlled study with 5-year follow-up

医学 骨合成 可视模拟标度 固定(群体遗传学) 颈部疼痛 外科 随机对照试验 地图集(解剖学) 人口 解剖 环境卫生 病理 替代医学
作者
Liang Yan,Jinpeng Du,Jun-Song Yang,Baorong He,Dingjun Hao,Bolong Zheng,Xiaobin Yang,Hui Hua,Tuan-Jiang Liu,Xiaodong Wang,Hua Guo,Jian Chen,Shaofei Wang,Shengzhong Ma,Sheng-li Dong
出处
期刊:Journal of neurosurgery [Journal of Neurosurgery Publishing Group]
卷期号:37 (2): 157-165 被引量:3
标识
DOI:10.3171/2021.12.spine211063
摘要

OBJECTIVE The aim of the present study was to compare the long-term effects of posterior C1-ring osteosynthesis and C1–2 fixation fusion in the treatment of unstable atlas fractures. METHODS A multicenter, prospective, randomized controlled trial was conducted to analyze 73 patients with atlas fractures who underwent posterior fixation. The intervention group was treated with C1-ring osteosynthesis, and the control group was treated with C1–2 fixation fusion. The patients were followed up for 6 months, 1 year, 2 years, and 5 years after the operation. RESULTS Fifty-two patients had complete data at the last follow-up. The visual analog scale (VAS) score for neck pain in the intervention group was lower than that in the control group (p < 0.001). The operation time, intraoperative blood loss, radiation dose, bedridden period, hospital stay, and cost in the intervention group were significantly lower than those in the control group (p < 0.001). At the last follow-up, the Neck Disability Index in the intervention group was higher than that of the control group, and the angle of flexion-extension and axial rotation in the intervention group were greater than those in the control group (p < 0.001). CONCLUSIONS In this study, the authors found that posterior C1-ring osteosynthesis is superior to C1–2 fixation fusion in terms of long-term relief of neck pain and preservation of the physiological function of the cervical vertebrae. This technique is a reliable choice for the treatment of unstable C1 fractures.

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