TY - JOUR
T1 - Clinical Significance of Lordosis Orientation on Proximal Junctional Kyphosis Development in Long-Segment Fusion Surgery for Adult Spinal Deformity
AU - Park, Se Jun
AU - Kim, Hyun Jun
AU - Lee, Chong Suh
AU - Park, Jin Sung
AU - Jung, Choong Won
AU - Lee, Jong Shin
AU - Yang, Han Seok
N1 - Publisher Copyright:
© 2023 Elsevier Inc.
PY - 2024/3
Y1 - 2024/3
N2 - Objective: We sought to evaluate the clinical impact of lordosis orientation (LO) on proximal junctional kyphosis (PJK) development in adult spinal deformity surgery. Methods: This study included 152 patients who underwent low thoracic (T9–T12) to pelvis fusion and were followed up for ≥2 years. In the literature, 6 radiographic parameters representing LO were introduced, such as uppermost instrumented vertebra (UIV) slope, UIV inclination, UIV−femoral angle (UIVFA), thoracolumbar tilt, thoracolumbar slope, and lordosis tilt. Various clinical and radiographic factors including 6 LO parameters were investigated using logistic regression analysis to identify risk factors for PJK. Results: The mean age was 69.4 years, and 136 patients were females (89.5%). PJK developed in 65 patients (42.8%). Multivariate logistic regression analysis revealed that only small postoperative pelvic incidence (PI)–lumbar lordosis (LL) (odds ratio [OR] = 0.962, 95% confidence interval: 0.929–0.996, P = 0.030) and large UIVFA (OR = 1.089, 95% confidence interval: 1.028–1.154, P = 0.004) were significant for PJK development. UIVFA showed significantly positive correlation with pelvic tilt (CC = 0.509), thoracic kyphosis (CC = 0.384), and lordosis distribution index (CC = 0.223). UIVFA was also negatively correlated with sagittal vertical axis (CC = −0.371). However, UIVFA did not correlate with LL, PI-LL, or T1 pelvic angle. Conclusions: LO significantly increases the risk of PJK development in ASD surgery. Multivariate analysis revealed that smaller postoperative PI-LL and greater UIVFA were significant risk factors for PJK. Surgeons should avoid undercorrection and overcorrection to prevent PJK development.
AB - Objective: We sought to evaluate the clinical impact of lordosis orientation (LO) on proximal junctional kyphosis (PJK) development in adult spinal deformity surgery. Methods: This study included 152 patients who underwent low thoracic (T9–T12) to pelvis fusion and were followed up for ≥2 years. In the literature, 6 radiographic parameters representing LO were introduced, such as uppermost instrumented vertebra (UIV) slope, UIV inclination, UIV−femoral angle (UIVFA), thoracolumbar tilt, thoracolumbar slope, and lordosis tilt. Various clinical and radiographic factors including 6 LO parameters were investigated using logistic regression analysis to identify risk factors for PJK. Results: The mean age was 69.4 years, and 136 patients were females (89.5%). PJK developed in 65 patients (42.8%). Multivariate logistic regression analysis revealed that only small postoperative pelvic incidence (PI)–lumbar lordosis (LL) (odds ratio [OR] = 0.962, 95% confidence interval: 0.929–0.996, P = 0.030) and large UIVFA (OR = 1.089, 95% confidence interval: 1.028–1.154, P = 0.004) were significant for PJK development. UIVFA showed significantly positive correlation with pelvic tilt (CC = 0.509), thoracic kyphosis (CC = 0.384), and lordosis distribution index (CC = 0.223). UIVFA was also negatively correlated with sagittal vertical axis (CC = −0.371). However, UIVFA did not correlate with LL, PI-LL, or T1 pelvic angle. Conclusions: LO significantly increases the risk of PJK development in ASD surgery. Multivariate analysis revealed that smaller postoperative PI-LL and greater UIVFA were significant risk factors for PJK. Surgeons should avoid undercorrection and overcorrection to prevent PJK development.
KW - Adult spinal deformity
KW - Lordosis orientation
KW - Proximal junctional kyphosis
KW - Risk factor
KW - Uppermost instrumented vertebra−femoral angle
UR - https://www.scopus.com/pages/publications/85185490292
U2 - 10.1016/j.wneu.2023.12.082
DO - 10.1016/j.wneu.2023.12.082
M3 - Article
C2 - 38135150
AN - SCOPUS:85185490292
SN - 1878-8750
VL - 183
SP - e282-e292
JO - World Neurosurgery
JF - World Neurosurgery
ER -