Distal hyperlordotic distribution does not increase the risk of mechanical complications in adult spinal deformity patients undergoing long-construct fusion to the pelvis with optimal global sagittal alignment.

IF 1.7 Q3 CLINICAL NEUROLOGY
Spine deformity Pub Date : 2026-09-01 Epub Date: 2026-04-07 DOI:10.1007/s43390-026-01360-8
Lluís Vila, Sleiman Haddad, Eva Jacobs, Susana Núñez-Pereira, Javier Pizones, Anika Pupak, Gina Faragó, Alejandro Gómez-Rice, Ibrahim Obeid, Louis Boissière, Cécile Roscop, Yann Philippe Charles, Ahmet Alanay, Markus Loibl, Frank Kleinstück, Ferran Pellisé
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引用次数: 0

Abstract

Purpose: To assess whether distal hyperlordotic distribution (DHD), defined by the Lordosis Distribution Index (LDI) from the Global Alignment and Proportion (GAP) score, increases the risk of mechanical complications (MC) in adult spinal deformity (ASD) patients with optimal postoperative global sagittal alignment and total lordosis after long-construct fusion to the pelvis.

Methods: Retrospective analysis of a prospective, multicenter database. ASD patients undergoing fusion from L2 or higher to the pelvis with ≥ 2 years follow-up and optimal postoperative global alignment (RSA = 0) and total lordosis (RLL = 0), according to the GAP score, were included. Patients were classified into Ideal (LDI = 0) and DHD (LDI = 3) groups. Rates of MCs (stratified in PJK or PJF), reoperations, and functional outcomes were compared. A post-hoc non-inferiority analysis utilizing a 10% clinical margin was performed.

Results: A total of 125 patients met criteria (91 Ideal; 34 DHD). The DHD group, compared to the Ideal group, had a significantly lower preoperative pelvic incidence (50.9° vs. 57.2°, p = 0.014) and more frequently underwent three-column osteotomies (35.3% vs. 18.7%, p = 0.050). At 2-year follow-up, DHD was statistically non-inferior to the Ideal distribution regarding PJFs (absolute risk difference was -7.3%, 90% CI: -16.1% to 1.5%) and for PJKs (absolute risk difference was 1.5%, 90% CI: -6.0% to 9.0%). Reoperation rates (38.2% vs. 28.6%, p = 0.299) and patient-reported functional outcomes were comparable.

Conclusion: In ASD patients with pelvic fixation and optimal global alignment, DHD is statistically non-inferior to ideal distributions regarding the risk of MCs, including PJK and PJF, and reoperations. In addition to this, DHD represents a physiological scenario in patients with lower pelvic incidence. Future predictive models should focus on penalizing distal hypolordosis rather than universally penalizing DHD.

Level of evidence: III.

远端前凸过高的分布不会增加成人脊柱畸形患者采用最佳整体矢状位对骨盆进行长结构融合的机械并发症的风险。
目的:评估由全球对齐和比例(GAP)评分中的前凸分布指数(LDI)定义的远端前凸分布(DHD)是否会增加成人脊柱畸形(ASD)患者术后最佳整体矢状位对齐和骨盆长结构融合后全前凸的机械并发症(MC)的风险。方法:回顾性分析前瞻性多中心数据库。根据GAP评分,接受L2或更高部位骨盆融合且随访≥2年且术后最佳整体对齐(RSA = 0)和全前凸(RLL = 0)的ASD患者被纳入。将患者分为理想组(LDI = 0)和DHD组(LDI = 3)。比较MCs(按PJK或PJF分层)、再手术率和功能结局。采用10%临床裕度进行事后非劣效性分析。结果:共有125例患者符合标准(理想91例,DHD 34例)。与Ideal组相比,DHD组术前骨盆发生率显著降低(50.9°vs. 57.2°,p = 0.014),三柱截骨术发生率更高(35.3% vs. 18.7%, p = 0.050)。在2年的随访中,在PJFs(绝对风险差为-7.3%,90% CI: -16.1%至1.5%)和PJKs(绝对风险差为1.5%,90% CI: -6.0%至9.0%)方面,DHD在统计学上不逊于Ideal分布。再手术率(38.2% vs 28.6%, p = 0.299)和患者报告的功能结果具有可比性。结论:在盆腔固定和最佳整体对齐的ASD患者中,在MCs(包括PJK和PJF)和再手术的风险方面,DHD在统计学上不低于理想分布。除此之外,DHD在骨盆发病率较低的患者中代表了一种生理情景。未来的预测模型应侧重于惩罚远端畸形,而不是普遍惩罚多动症。证据水平:III。
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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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