Multivariate Analysis and Risk Factors Were Used to Predict the Short-term Postoperative Pain of Degenerative Lumbar Spine

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

936 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-09-20

Study Completion Date

2024-09-28

Brief Summary

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The objective of this retrospective clinical study wasto study the risk factors for short-term low back and leg pain after PLIF in patients with lumbar Degenerative disease, and to establish a risk prediction model for short-term low back and leg pain after PLIF based on relevant risk factors.

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Detailed Description

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Conditions

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Lumbar Disc Herniation Lumbar Degenerative Disease Sarcopenia

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

RETROSPECTIVE

Study Groups

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Rehabilitation Group

mild/non pain group with VAS\<3 at 3th months after PLIF.N=501

Magnetic Resonance Imaging with Contrast

Intervention Type OTHER

The study was retrospective and did not set interventions

Recurrent pain group

Recurrent pain group: recurrent pain group with VAS≥3 at 3th months after PLIF.N=435

Magnetic Resonance Imaging with Contrast

Intervention Type OTHER

The study was retrospective and did not set interventions

Interventions

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Magnetic Resonance Imaging with Contrast

The study was retrospective and did not set interventions

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

1. confirmed diagnosis of lumbar degenerative disease (spinal stenosis, disc herniation with lumbar instability, and lumbar spondylolisthesis), with no significant symptomatic relief after conservative treatment for more than 3 months, and in need of surgical intervention;
2. lumbar spinal fusion surgical treatment with PLIF;
3. grouping based on the presence or absence of a lumbar or limb pain with VAS ≥3 at the 3th month postoperative follow-up;
4. observational indicators including individual factors, surgical factors, spine-pelvis sagittal balance parameters, and paravertebral muscle parameters.

Exclusion Criteria

(1) those with a history of lumbar spine trauma, inflammation, tumor, or surgery; (2) those with congenital or acquired severe lumbar vertebral deformity; (3) those with severe neurological dysfunction; (4) those with incomplete baseline and follow-up data.

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes