Background
It is well reported that the patient’s age plays an important role associated with proximal junctional failure (PJF) development. Various characteristics of adult spinal deformity (ASD) patients were different between younger and older age groups. We hypothesized that the radiographic risk factors for PJF would different according to younger and older age groups. This study aimed to evaluate different radiographic risk factor of PJF according to the two age groups undergoing thoracolumbar fusion for ASD.
Methods
ASD patients aged ≥ 60 years who underwent thoracolumbar fusion from low thoracic level (T9~T12) to sacrum were included. The minimum follow-up duration was two years. PJF was defined as proximal junctional angle (PJA) ≥ 20°, fixation failure, fracture, myelopathy, or necessity of revision surgery. Using various radiographic risk factors including age-adjusted ideal pelvic incidence (PI)-lumbar lordosis (LL), univariate and multivariate analyses were performed separately according to the two age groups : <70 years and ≥70 years.
Results
A total of 186 patients were enrolled (mean age=68.5 years old, 90.3% female). Mean follow-up duration was 67.4 months. PJF developed in 98 patients (32.0%). There were fracture in 53 patients, PJA ≥ 20° in 26, fixation failure in 12, and myelopathy in 6. PJF developed more frequently in patients older than 70 years than in younger than 70 years. In patients aged less than 70 years, preoperative LL, PI-LL and change in LL were significant risk factors in univariate analysis. Multivariate analysis showed only change in LL was significant for PJF development (Odds ratio [OR]=1.025, p=0.021). On the other hand, in patients older than 70 years, postoperative LL, postoperative PILL, overcorrection relative to conventional PI-LL target (within ±10°) as well as age-adjusted ideal PI-LL target were significant. On multivariate analysis, only overcorrection of PI-LL relative to age-adjusted ideal target was a single significant factor to cause PJF (OR=5.250, p=0.024).
Conclusions
In patients younger than 70 years, greater change in LL was associated with PJF development regardless of PI-related value. However, in older patients, overcorrection of PI-LL relative to the age-adjusted PI-LL target was important to cause PJF.
