The study was a clinical retrospective study designed to investigate risk factors for long-term recurrent pain after PLIF in patients with lumbar degenerative disease and to improve patient outcomes
Study Type
OBSERVATIONAL
Enrollment
452
The study was retrospective and did not design an intervention
Medical record system and imaging system of the First Affiliated Hospital of Suzhou University
Suzhou, Jiangsu, China
SAS(Pain rating scale)
The visual analogue scale (VAS) was employed to determine the patient's perception of lower back pain or lower limb pain prior to surgery, as well as 12-18 months after surgery. (0-10 scale, with 0 being painless and 10 being the most painful)
Time frame: 12-18 months after surgery
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