This study was conducted in strict adherence to the principles of the Declaration of Helsinki15 and was approved by the Institutional Ethics Committee of North China Medical Health Group XingTai General Hospital (Approval No. ZCKT-2026-0018). All patients were informed of the study purpose, treatment protocols, and potential risks, and provided written informed consent. All study data were anonymized to ensure patient privacy.
Research subjects
This single-center retrospective observational study included patients with single-level LDH who underwent PELD in the orthopedics department of our hospital from January 2022 to September 2024. Among 123 initially screened patients, 101 were ultimately included after applying strict inclusion and exclusion criteria, all of whom completed at least one year of follow-up. Based on the modified MacNab criteria at one-year post-surgery, patients were classified into the favorable group (n = 76) and the unfavorable group (n = 25). The detailed process is shown in Figure 1.

Figure 1: Research flowchart. Flowchart of patient selection and grouping. Of 123 assessed patients, 101 with single-level LDH undergoing PELD were included and divided into Favorable (n = 76) and Unfavorable (n = 25) groups based on 1-year modified MacNab criteria. The analytical framework covered general clinical data, MRI parameters, and clinical outcomes (VAS, ODI, MacNab). Please click here to view a larger version of this figure.
Inclusion criteria
Age between 18 and 75 years; diagnosed with single-level LDH at L3/4, L4/5, or L5/S1 based on clinical symptoms, physical examination, and MRI/CT findings; presence of definite symptoms and signs of nerve root compression, with no response to at least 6 weeks of systematic conservative treatment (including bed rest, medication, physical therapy, etc.); underwent PELD surgery; postoperative follow-up duration of at least 1 year with complete clinical data.
Exclusion criteria
Multilevel LDH or a history of previous lumbar surgery; concomitant lumbar spondylolisthesis, lumbar spinal stenosis, spinal tumors, spinal infections, or spinal fractures; presence of cauda equina syndrome requiring emergency surgery; poor preoperative MRI image quality precluding accurate measurement; severe comorbid medical conditions (e.g., cardiac, pulmonary, hepatic, or renal insufficiency) rendering patients unfit for surgery; loss to follow-up or incomplete clinical data.
Surgical procedure
All surgeries were performed by the same experienced team of spine surgeons. The surgical approach (transforaminal, TF, or interlaminar, IL) was determined based on a comprehensive evaluation of the herniation morphology and anatomical constraints. Specifically, the TF approach was preferentially adopted for foraminal, extraforaminal, or central/paracentral herniations located below the pedicle level. Conversely, the IL approach was selected for highly migrated or sequestered fragments, particularly those migrating cephalad to the L5 pedicle or in patients with a high iliac crest, as previously described by Choi et al.16. This differentiated selection strategy ensured that the surgical trajectory aligned optimally with the target lesion.
Procedures were conducted under local anesthesia with or without intravenous sedation, with patients positioned prone. The target disc space was localized using C-arm fluoroscopy. A puncture needle was advanced into the spinal canal through Kambin's triangle or the interlaminar space, followed by guidewire insertion and sequential dilation to establish a working channel. A working endoscope (diameter 6.9 mm, 30° viewing angle) was introduced, and herniated nucleus pulposus tissue was removed under direct visualization to achieve nerve root decompression. Annuloplasty and hemostasis were performed using a radiofrequency probe. The working channel was then withdrawn, and the skin incision was sutured.
In cases presenting with preoperative DHI ≤25% or severe foraminal narrowing on MRI, additional foraminoplasty using a reamer or high-speed drill was performed at the discretion of the attending surgeon to enlarge Kambin's working zone and facilitate channel placement. However, given the retrospective design, the execution of this foraminoplasty was neither strictly standardized nor systematically documented in the operative notes, which precludes a quantitative analysis of its specific impact on clinical outcomes in this cohort.
Observation indicators
In this study, T0, T1, T2, and T3 were defined as preoperative, 1 week postoperative, 3 months postoperative, and 1 year postoperative, respectively.
General clinical data
Patient data, including age, sex, body mass index (BMI), disease duration, smoking history, history of diabetes mellitus, history of hypertension, surgical level, and surgical approach, were collected.
Measurement of MRI morphological parameters
All patients underwent preoperative lumbar MRI, including sagittal T1WI, T2WI, and axial T2WI sequences. Two experienced radiologists independently measured the parameters in a double-blind manner, with the average values used for analysis. Pfirrmann grade: Assessed on sagittal T2WI based on disc signal intensity, structure, height, and distinction between nucleus pulposus and annulus fibrosus, graded 1–511. Modic changes: Evaluated as signal changes in vertebral endplates and adjacent bone marrow, classified as none, type I (hypointense on T1WI, hyperintense on T2WI), type II (hyperintense on T1WI, iso- or slightly hyperintense on T2WI), or type III (hypointense on both T1WI and T2WI)12. Herniation type: Classified on axial T2WI as bulging, protrusion, extrusion, or sequestration17. Herniation location: Categorized as central, paracentral, foraminal, or far lateral4. Extent of migration: Measured on sagittal T2WI as the vertical distance from the upper or lower margin of the herniated fragment to the disc level, classified according to Lee et al.18 as no migration (grade 0), low-grade migration (<50% of disc height, grades 1–2), or high-grade migration (≥50% of disc height, grades 3–4). Spinal canal occupation ratio: Calculated on axial T2WI at the level of maximal herniation as (anteroposterior diameter of the herniation / anteroposterior diameter of the spinal canal) × 100%19,20. DHI: Measured on sagittal T2WI as [(anterior disc height + posterior disc height) / 2] / [(anterior-posterior diameter of upper vertebral body + anterior-posterior diameter of lower vertebral body) / 2] × 100%21. Foraminal area: Manually delineated and measured on axial T2WI at the maximal foraminal level using ImageJ software22,23. Maximum herniation area: Measured as the cross-sectional area of the herniated fragment on axial T2WI at the level of maximal herniation24.
Clinical outcome evaluation
Pain Assessment: Pain intensity was evaluated using the Visual Analog Scale (VAS) for low back pain (VAS-Back) and leg pain (VAS-Leg), with scores ranging from 0 (no pain) to 10 (worst imaginable pain)25,26. Functional Disability: Lumbar function was assessed using the Oswestry Disability Index (ODI)27,28. Modified MacNab Criteria: Evaluated at the 1-year follow-up, outcomes were classified as excellent (complete symptom resolution, return to normal activities), good (occasional pain, no interference with work or daily life), fair (improved symptoms but activity limitations), or poor (no improvement or worsened symptoms)29,30. “Excellent” and “good” outcomes were defined as a favorable prognosis, while “fair” and “poor” outcomes were defined as an unfavorable prognosis. The modified MacNab criteria were selected as the primary outcome measure because they provide a global, patient-centered assessment of surgical success that integrates pain relief, functional recovery, and return to daily activities—domains that are collectively more relevant to clinical decision-making than any single continuous scale. Additionally, the MacNab classification has been widely utilized and validated in PELD literature29,30, facilitating direct comparison with prior studies.
Sample size estimation
Sample size estimation was performed using G*Power software31. As a retrospective observational study, the sample size was determined based on the total number of patients meeting the inclusion and exclusion criteria during the study period, and its adequacy was verified through post-hoc power analysis. Based on previous relevant studies8, assuming an incidence of unfavorable prognosis following PELD of approximately 25% and using disc extrusion/sequestration as the primary exposure factor, a minimum of 89 participants was required with a two-sided α = 0.05 and a power (1-β) of 80%. A total of 101 patients were ultimately included in this study, meeting the statistical requirements.
Statistical analysis
Statistical analyses were performed using SPSS. Normality of continuous variables was assessed by the Shapiro-Wilk test. Normally distributed data were presented as mean ± SD and compared using independent-samples and paired t-tests. Non-normally distributed data were shown as median (Q1, Q3) and analyzed via the Mann-Whitney U test. Categorical variables were compared using the chi-square test. Pearson correlation and multivariate logistic regression were applied. All tests were two-sided, and P < 0.05 was deemed statistically significant.
For multivariate logistic regression analysis, the dependent variable was encoded as favorable prognosis = 1 and unfavorable prognosis = 0, resulting in 76 positive events. The number of covariates included in the final model must comply with the EPV principle32. Used variance inflation factor (VIF) to evaluate multicollinearity among MRI parameters; a VIF value <5 is considered acceptable.