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Validation of Sagittal Age-adjusted Score in Predicting Proximal Junctional Kyphosis/Failure and Clinical Outcomes Following Adult Spinal Deformity Surgery

医学 骨盆倾斜 矢状面 后凸 接收机工作特性 外科 冠状面 腰椎 脊柱畸形 回顾性队列研究 骶骨 畸形 前凸 脊柱融合术 核医学 口腔正畸科 脊柱侧凸 腰骶关节 腰椎 体质指数
作者
Sejun Park,Jin-Sung Park,Dong-Ho Kang,Kyunghun Jung,Minwook Kang,Choong-Won Jung,Hyun‐Jun Kim,Chong-Suh Lee
出处
期刊:Spine [Lippincott Williams & Wilkins]
卷期号:50 (14): 948-955 被引量:3
标识
DOI:10.1097/brs.0000000000005144
摘要

Study Design. A retrospective study. Objectives. To validate the sagittal age-adjusted score (SAAS) in predicting proximal junctional kyphosis/failure (PJK/F) and good clinical outcomes following adult spinal deformity (ASD) surgery. Summary of Background Data. SAAS is a relatively new assessment system that incorporates age-adjusted sagittal parameters of pelvic incidence (PI)-lumbar lordosis (LL), pelvic tilt (PT), and T1 pelvic angle (TPA) to predict the PJK/F. External validation is required to verify its clinical usefulness. Materials and Methods. We included patients with ASD undergoing ≥5-level fusion including the sacrum or pelvis. SAAS was calculated based on the scores of the three components: PI-LL, PT, and TPA. PJK/F rates and clinical outcomes were compared among the correction categories (undercorrection, matched correction, and overcorrection) for the SAAS as well as for each of the three components. PJK/F rates were compared according to the correction groups of the sagittal components and total SAAS using the χ 2 test. Receiver operating characteristic (ROC) analysis was performed to evaluate the predictive ability of overcorrection to develop PJK/F for the three sagittal parameters and SAAS. PROMs at final follow-up were compared among correction groups using ANOVA with Bonferroni post hoc corrections. Results. A total of 411 patients were included in the study (mean age: 69.3 y, mean body mass index: 25.9 kg/m 2 , total levels fused: 7.7 levels, and follow-up duration: 43.3 mo). Postoperative SAAS categories were as follow: undercorrection (13.4%), matched correction (30.2%), and overcorrection (56.4%). The PJK/F rates were significantly higher in the overcorrection group relative to PI-LL component ( P =0.001) as well as SAAS ( P =0.038) compared with undercorrection or matched correction groups. The clinical outcomes were best in patients who achieved matched correction relative to PI-LL component as well as SAAS compared with the other correction groups. However, the differentiating power of clinical outcomes across the correction categories was greater in the PI-LL component than in the SAAS. Conclusion. This study validated the efficacy of SAAS system to differentiate PJK/F development and good clinical outcomes. However, its differentiating power seems to be largely attributable to the function of the PI-LL component, as the PI-LL correction status better predicted PJK/F risk and clinical outcomes than SAAS.
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