Influence of slippage reduction and correction of lumbosacral kyphosis by single-level posterior lumbar interbody fusion on spinal alignment in patients with dysplastic spondylolisthesis.

IF 1.6 Q3 CLINICAL NEUROLOGY Spine deformity Pub Date : 2024-11-01 Epub Date: 2024-06-27 DOI:10.1007/s43390-024-00917-9
Kazuki Takeda, Satoshi Suzuki, Masahiro Ozaki, Yohei Takahashi, Osahiko Tsuji, Narihito Nagoshi, Mitsuru Yagi, Morio Matsumoto, Masaya Nakamura, Kota Watanabe
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Abstract

Purpose: To investigate the influence of slippage reduction and correction of lumbosacral kyphosis by L5-S1 single-level posterior lumbar interbody fusion (PLIF) on spinal alignment and clinical outcomes including postoperative complications in patients with dysplastic spondylolisthesis (DS).

Methods: Twenty consecutive patients with symptomatic and severe DS who underwent L5-S1 single-level PLIF with a minimum of 2 years of follow-up after surgery were included. Clinical outcomes were evaluated using the Japanese Orthopaedic Association (JOA) and visual analog scale (VAS) scores for low back and leg pain obtained on preoperative and postoperative examinations. Postoperative instrumentation failure and L5 radiculopathy were also evaluated. The preoperative and postoperative spinopelvic parameters were measured.

Results: The JOA score significantly improved from 21.5 ± 4.8 (preoperative) to 27.0 ± 2.5 (postoperative), with a mean recovery rate of 75.0% ± 30.4%. The VAS score for low back pain significantly improved from 44.5 ± 30.1 (preoperative) to 11.5 ± 15.9 (postoperative), and that for leg pain significantly improved from 31.0 ± 33.2 (preoperative) to 5.0 ± 10.2 (postoperative). The slip percentage (% slip) significantly improved from 59.6% ± 13.5% (preoperative) to 25.2% ± 15.0% (postoperative). The lumbosacral angle (LSA) significantly improved from 12.3° ± 9.5° (preoperative) to 1.0° ± 4.9° (postoperative). L5-S1 PLIF led to significant improvement of lumbar lordosis (from 52.0° ± 15.9° to 59.7° ± 8.0°) and pelvic incidence - lumbar lordosis mismatch (from 23.9° ± 20.6° to 13.3° ± 10.0°). Correction of lumbosacral kyphosis had a significant positive correlation with postoperative pelvic tilt (PT) (r = 0.50, P = 0.02), while postoperative % slip did not have a significant correlation with postoperative PT.

Conclusions: L5-S1 PLIF for DS provided good clinical outcomes. Correction of lumbosacral kyphosis had a positive impact on regaining ideal spinopelvic balance and may be beneficial in the setting of treating DS.

Level of evidence iv:

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单层腰椎后路椎体间融合术减少滑动和矫正腰骶部后凸对发育不良脊柱滑脱患者脊柱排列的影响。
目的:研究通过L5-S1单水平后路腰椎椎体间融合术(PLIF)减少滑脱和矫正腰骶部后凸对脊柱排列和临床结果的影响,包括对发育不良性脊柱滑脱症(DS)患者术后并发症的影响:方法: 连续纳入20例接受L5-S1单层腰椎椎体间融合术(PLIF)且术后随访至少2年的无症状重度DS患者。采用日本骨科协会(JOA)和视觉模拟量表(VAS)对术前和术后检查中获得的腰痛和腿痛评分进行临床结果评估。此外,还对术后器械失败和 L5 根性病变进行了评估。对术前和术后脊柱骨盆参数进行了测量:结果:JOA评分从术前的21.5±4.8分明显提高到术后的27.0±2.5分,平均恢复率为75.0%±30.4%。腰痛的 VAS 评分从 44.5 ± 30.1(术前)明显改善到 11.5 ± 15.9(术后),腿痛的 VAS 评分从 31.0 ± 33.2(术前)明显改善到 5.0 ± 10.2(术后)。滑脱百分比(% slip)从术前的 59.6% ± 13.5% 显著改善到术后的 25.2% ± 15.0%。腰骶角(LSA)从术前的12.3° ± 9.5°明显改善到术后的1.0° ± 4.9°。L5-S1 PLIF 使腰椎前凸(从 52.0° ± 15.9° 到 59.7° ± 8.0°)和骨盆入射角-腰椎前凸不匹配(从 23.9° ± 20.6° 到 13.3° ± 10.0°)得到明显改善。腰骶椎后凸的矫正与术后骨盆倾斜(PT)呈显著正相关(r = 0.50,P = 0.02),而术后滑脱率与术后PT无显著相关性:结论:L5-S1 PLIF治疗DS具有良好的临床效果。腰骶椎后凸的矫正对恢复理想的脊柱骨盆平衡有积极影响,可能对治疗DS有益:
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来源期刊
CiteScore
3.20
自引率
18.80%
发文量
167
期刊介绍: Spine Deformity the official journal of the?Scoliosis Research Society is a peer-refereed publication to disseminate knowledge on basic science and clinical research into the?etiology?biomechanics?treatment?methods and outcomes of all types of?spinal deformities. The international members of the Editorial Board provide a worldwide perspective for the journal's area of interest.The?journal?will enhance the mission of the Society which is to foster the optimal care of all patients with?spine?deformities worldwide. Articles published in?Spine Deformity?are Medline indexed in PubMed.? The journal publishes original articles in the form of clinical and basic research. Spine Deformity will only publish studies that have institutional review board (IRB) or similar ethics committee approval for human and animal studies and have strictly observed these guidelines. The minimum follow-up period for follow-up clinical studies is 24 months.
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