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Original Article

Anat Cell Biol 2024; 57(4): 523-534

Published online December 31, 2024

https://doi.org/10.5115/acb.24.112

Copyright © Korean Association of ANATOMISTS.

Anatomical assessment of the Kambin’s triangle for percutaneous posterolateral transforaminal endoscopic surgery of lumbar intervertebral discs: a magnetic resonance imaging based study

Naeeme Nikpour1 , Zahra Fazelinejad1 , Mozhgan Sametzadeh1 , Mohammad Ardeshiri Lordjani2 , Ali Reza Eftekhari Moghadam3

1Department of Radiology, School of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, 2Department of Neurosurgery, School of Medicine, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, 3Department of Anatomical Science, Faculty of Medicine, Baqiyatallah University of Medical Sciences, Tehran, Iran

Correspondence to:Ali Reza Eftekhari Moghadam
Department of Anatomical Science, Faculty of Medicine, Baqiyatallah University of Medical Sciences, Tehran 61357-15794, Iran
E-mail: Eftekhari.anat@gmail.com

Received: April 29, 2024; Revised: August 6, 2024; Accepted: August 16, 2024

This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

The aim of the present study was to utilize magnetic resonance imaging (MRI) as a noninvasive tool for evaluation of the Kambin’s triangle safe zone. Lumbar MRIs of 67 healthy subjects were analyzed. On the coronal plane, the distance from the superior endplate to the nerve root exiting from the dura (distance a), the distance from the lateral aspect of the dura to the medial aspect of the nerve root (distance b), and the angle between the nerve root and plane of the corresponding disc (angle α) was measured. On the axial plane, the vertical distance from the upper facet surface to the exiting nerve root and root-disc distance was also measured. On the sagittal plane, foraminal height, diameter, nerve root-disc distance, and nerve root-pedicle distance were measured. On the coronal plane, right and left α angle was 50.78±4.43 (range, 48.52–51.84 degrees) and 51.07±4.08 (range, 49.25–51.91) degrees, respectively. Distance of right ‘a’ was 17.86±3.86 mm (range, 10.56–24.84 mm) and left ‘a’ was 18.03±3.73 mm (range, 10.98–24.82 mm), distance of right ‘b’ was 15.57±2.61 mm (range, 10.54–20.70 mm) and left ‘b’ was 15.46±2.68 mm (range, 10.93–19.23 mm). All these measurements increased as the spine level went down. Foraminal height and diameter decreased caudally. Nerve root-facet distance did not show change as the level went down. The study indicated that radiologic measurement is feasible to evaluate the anatomy of the Kambin’s triangle. At lower lumbar levels, the exiting nerve root is at risk of injury.

Keywords: Kambin’s triangle, Endoscopic discectomy, Magnetic resonance imaging, Lumbosacral regions, Spinal nerve

Roughly 70%–85% of individuals will experience low back pain (LBP) at least once in their lifetime. One of the primary causes is disc herniation (DH), which can result in radiculopathy due to both mechanical compression and chemical irritation [1]. Treatment for DH can be conservative or surgical. There are two main categories of surgical treatment for DH: open surgery and minimally invasive surgery [2-4]. Open discectomy approach requires dissection of anatomical structures, which increases the risk of iatrogenic morbidity [5, 6]. Percutaneous posterolateral transforaminal discectomy (PPTD) is a minimally invasive treatment for DH that was first introduced by Kambin and Gellman [7]. Current percutaneous posterolateral discectomies are based on a safe working zone in the posterolateral corner of the disc called Kambin’s triangle. Compared to traditional open surgery, percutaneous posterolateral discectomy has the following significant advantages: shortened operating time, reduced blood loss, and improved early recovery [8, 9]. However, perioperative complications limit further use of this procedure. Postoperative motor weakness due to root exiting injury is a complication of PPTD and is usually caused by the cannula placed in the Kambin’s zone near the nerve root [10-13]. According to topographical description, the Kambin triangle working zone is the region inside a right-angle triangle. The inferior border is formed by rim of the vertebral plate inferior to the target disc, the posterior border is formed by the lateral edge of the superior articular process of the next inferior vertebra, and the hypotenuse is provided by the medial border of the associated spinal nerve as it exits from the foramen (Fig. 1) [14-16]. The size of surgical equipment that can fit through Kambin’s triangle is restricted by its small dimensions.

Figure 1. Schematic diagram of the Kambin’s triangle (triangular safe zone) on the sagittal plane. The hypotenuse is bordered medially by the associated spinal nerve, posteriorly by the lateral edge of the superior articular process of the subsequent inferior vertebra, and inferiorly by the rim of the vertebral plate. KT, Kambin’s triangle.

The Kambin working zone’s dimensions and anatomic boundaries have been described by earlier studies using formalin-fixed cadavers [17-19]. However, the investigation of living individuals is rare. Furthermore, it is apparent that formalin may cause alterations in tissue and modify the Kambin triangle’s anatomical dimensions [20-22]. Therefore, radiologic evaluations are required to determine the Kambin’s zone on different anatomical planes. When compared to cadaveric studies, magnetic resonance images (MRIs) provide measurements that are more clinically accurate. It has been demonstrated that MRI has a special capacity to identify nerve architecture by suppressing fat and vascular signals [23-25].

The aim of the current study is to utilize MRI for evaluation of anatomic parameters of lumbosacral nerve root and adjacent structures in the Kambin working zone of the Iranian population, and further, to analyze the safety of PPTD procedure.

The Ethics Committee of the Ahvaz Jundishapur University of Medical Science assigned patient consent form for this research based on the ethical guidelines for medical and health study involving human subjects established by the Ministry of Health (IR.AJUMS.HGOLESTAN.REC.1401.080) (none of the patients’ identities were disclosed).

A total of 67 healthy volunteers, including 35 females and 32 males (mean age, 43.49 years old) were enrolled in this study. Patient inclusion criteria were: no symptoms or signs of lumbar radiculopathy, complete imaging data. Patients who met the following criteria were excluded: previous lumbar trauma, disc prolapse, lumbar deformity, history of lumbar spine surgery, lumbar spondylolisthesis, scoliosis, rheumatologic, or endocrine diseases. Further, radiography of anteroposterior and lateral views was performed to exclude the subjects of scoliosis, kyphosis, and other degenerative changes.

MRI protocol and measurements: MRI pulse sequences and all measurements of this study were carried out according to two investigations conducted by Guan et al. [24] and Hurday et al. [16]. Images were acquired using a 1.5 Tesla MRI scanner (Magnetom Avanto; Siemens Healthineers). Firstly, T2-weighted (T2W) sequence was performed on a sagittal plane from T12 to S2 with the following parameters: time of repetition (TR)=3,000 ms; time of echo (TE)=100 ms; section thickness, 2 mm; and field of view (FOV) 320×320 mm. On the transverse plane, T2W sequence was performed from L1 to S1 with the following parameters: repetition time TR=3,500 ms; TE=100 ms; section thickness, 3 mm; FOV with 200×200 mm. After that, MRI was done using a three-dimensional (3D) multiple echo recombined gradient echo (MEDIC) sequence on coronal plane (MR neurography). This sequence can suppress the vascular and fat signal to create nerve-selective images and demonstrate nerves in multiple anatomical sections. The imaging parameters were as follows: TR=30.0 ms; TE=12.0 ms; Flip angle=30°, section thickness, 1 mm; FOV: 320×320 mm; and matrix: 256×256 mm.

Figs. 24 show the measurement methods. For Kambin’s triangle assessment, the following measurements were taken on the coronal plane: 1) the distance of nerve root exiting from the dura to the superior endplate (distance a); 2) the distance from lateral aspect of the dura to the medial aspect of the nerve root along the superior endplate (distance b); and 3) the angle between the exiting nerve root and plane of the corresponding disc (angle α).

Figure 2. The magnetic resonance image shows the measurements related to the left side safety working zone at L4–L5 on the coronal plane. Distance a: the distance from the superior endplate to the nerve root exiting from the dura. Distance b: the distance from the lateral aspect of the dura to the medial aspect of the nerve root along the superior endplate. Angle α: the angle between the exiting nerve root and the plane of the corresponding disc.

Figure 3. Examples of the parameters that are calculated at the middle of the pedicle on the T1-weighted magnetic resonance imaging sagittal section. A, foramina height; B, middle foraminal diameter.

Figure 4. T2-weighted magnetic resonance image showing the parameters measured on the transverse plane at the superior margin of the disc. Gs, foraminal width; Hs, nerve root-disc distance; Ii, nerve root-facet distance.

The following measurements were made on the sagittal section (Fig. 3): 1) foraminal height: distance between inferior border of upper pedicle and superior border of lower pedicle (A), 2) foraminal diameter (B): the distance between the facet’s anterior surface and the disc’s posteromiddle corner (Fig. 3).

The following measurements were conducted on the transverse section (Fig. 4): The shortest distance between the anterior surface of a facet and the posterior surface of the vertebral body is known as the foraminal width (Gs). Nerve root-disc distance (Hs): the shortest path between the disc’s posterior surface and nerve root. The smallest distance between the nerve root and the facet’s anterior surface is known as the nerve root-facet distance (Ii). In all sections, disc levels from L1–L2 to L5–S1 were evaluated bilaterally and radiologic measurements were obtained independently by 2 experienced radiologists.

Statistical analysis

Descriptive statistics were used to report the primary results. The effects roles of age, sex and body mass index (BMI) on the outcome predictions were studied using multilevel mixed effects linear regression. Random intercept of the left and right sides nested within spine levels was added to the models. Model selection strategy involved the inclusion of all the three variables—age, sex, and BMI—in every models. P-value less than 0.1 (one-tailed significance level of 0.05) was regarded as the significance level. The sample size was considered as at least 20 individuals per each model covariate (at least 60 individuals). The statistical analyses were conducted in IBM SPSS Statistics 28 (IBM Co.).

There were a total of 67 patients, 35 females and 32 males (mean age, 43.49 years). The average values for the respective levels and planes are summarized in Tables 1-8. No significant differences were found when comparing the right and left measurements on sagittal, transverse, and coronal planes.

Table 1 . Measurement of Kambin’s triangle angle on the coronal plane

MeanMedianStandard deviationRangeMinimumMaximum
Rα148.5250.004.409233558
Rα250.9050.004.665184260
Rα352.2253.004.767214061
Rα450.4351.004.616233659
Rα551.8452.003.768194059
Lα149.2550.004.099184058
Lα250.8551.004.258214061
Lα352.7553.004.384244064
Lα450.6151.004.189204060
Lα551.9152.003.519164561


Table 2 . Comparison of mean value of distance ‘a’ from L1 to L5–S1 disc level

MeanMedianStandard deviationRangeMinimumMaximum
R a110.56710.0002.904915.06.021.0
R a214.47814.0003.607119.05.024.0
R a318.54518.5003.782717.010.027.0
R a420.91821.0003.808520.011.031.0
R a524.8423.0005.230024.014.038.0
L a110.98511.0002.667115.06.021.0
L a214.72414.0003.548718.06.024.0
L a318.63418.0003.602016.510.527.0
L a421.04821.0003.871420.011.031.0
L a524.82824.0005.012523.014.037.0


Table 3 . Comparison of mean value of distance ‘b’ from L1 to L5–S1 disc level

MeanMedianStandard deviationRangeMinimumMaximum
R b110.54510.0002.02409.57.016.5
R b212.07512.0002.165911.08.019.0
R b314.95515.0002.889014.09.023.0
R b419.59019.0002.989814.014.028.0
R b520.70120.0003.015213.015.028.0
L b110.93310.5002.179310.56.016.5
L b212.88113.0002.325914.08.022.0
L b315.20115.0002.545113.010.023.0
L b419.09018.5003.067316.014.030.0
L b519.23919.0003.335317.513.531.0


Table 4 . Comparison of mean value of foraminal height (h) (mm) on sagittal plane from L1 to L5–S1 disc level

MeanMedianStandard deviationRangeMinimumMaximum
R h118.84319.0001.72818.015.023.0
R h219.33619.0001.92749.015.024.0
R h318.59719.0002.529016.011.027.0
R h417.26317.0001.75138.013.021.0
R h515.57015.0002.093110.010.020.0
L h118.59019.0001.82359.013.022.0
L h219.33619.5001.998810.513.524.0
L h318.87319.0001.901610.014.024.0
L h416.94017.0002.118715.010.025.0
L h515.91016.0002.415112.010.022.0


Table 5 . Comparison of mean value of foraminal width on sagittal plane (w) (mm) from L1 to L5–S1 disc level

MeanMedianStandard deviationRangeMinimumMaximum
Rw17.8848.0001.00635.06.011.0
Rw28.4858.5001.02245.06.011.0
Rw38.4438.5001.14415.55.511.0
Rw48.3168.5001.12775.06.011.0
Rw57.9908.0001.07444.06.010.0
Lw18.1258.0000.99474.56.010.5
Lw28.7258.5001.06325.06.011.0
Lw38.2678.0001.02494.56.010.5
Lw48.5818.5001.09635.06.011.0
Lw58.1318.0000.97604.06.010.0


Table 6 . Transverse plane, foraminal width measurements (Gs) (mm) from L1 to L5–S1 disc level

MeanMedianStandard deviationRangeMinimumMaximum
R Gs15.3095.0001.18735.03.08.0
R Gs24.7765.0001.25875.03.08.0
R Gs34.3484.0001.15035.03.08.0
R Gs44.1934.0000.98834.13.07.1
R Gs54.2004.0000.97225.02.57.5
L Gs15.3405.0001.12324.53.07.5
L Gs24.7574.5001.33315.03.08.0
L Gs34.2914.0001.06654.03.07.0
L Gs44.0364.0000.98584.03.07.0
L Gs54.0454.0000.92403.53.06.5


Table 7 . Transverse plane, nerve root-disc distance (Hs) (mm) measurements from L1 to L5–S1 disc level

MeanMedianStandard deviationRangeMinimumMaximum
R Hs14.0574.0000.67833.12.45.5
R Hs23.7994.0000.69993.52.05.5
R Hs33.5343.5000.60012.72.35.0
R Hs43.7423.5000.74253.02.55.5
R Hs53.6423.5000.59012.52.55.0
L Hs14.0634.0000.77693.52.56.0
L Hs23.7934.0000.67833.02.55.5
L Hs33.6463.5000.70783.32.25.5
L Hs43.7403.5000.74513.02.55.5
L Hs53.6313.5000.61403.02.55.5


Table 8 . Transverse plane, nerve root-facet distance (Ii) (mm) measurements from L1 to L5–S1 disc level

MeanMedianStandard deviationRangeMinimumMaximum
RIi13.7373.5000.79733.52.56.0
RIi23.8913.8000.80113.52.56.0
RIi33.6393.5000.71883.02.55.5
RIi43.6103.5000.95004.52.57.0
RIi53.9783.8000.98504.03.07.0
LIi14.1374.0000.93684.52.57.0
LIi24.1124.0000.93024.02.56.5
LIi34.1044.0000.99154.52.06.5
LIi44.0134.0001.07414.52.57.0
LIi54.1584.0001.03125.02.57.5


On the coronal plane, the average of right and left angle α was 50.78±4.43 (range, 48.52–51.84 degrees) and 51.07±4.08 (range, 49.25–51.91) degrees, respectively. Distance of right ‘a’ was 17.86±3.86 mm (range, 10.56–24.84 mm) and left ‘a’ was 18.03±3.73 mm (range, 10.98–24.82 mm), distance of right ‘b’ was 15.57±2.61 mm (range, 10.54–20.70 mm) and left ‘b’ was 15.46±2.68 mm (range, 10.93–19.23 mm). For different levels, as the level went down, the values increased. The angles at L2–L3, L3–L4, and L5–S1 levels were larger than those at the upper levels. The mean values for the respective levels were shown in Tables 1-3.

On sagittal plane, foraminal height decreased caudally, biggest foraminal height was measured at L2–L3 (19.33±1.95 mm) and smallest at L5–S1 (15.74±2.1 mm) (Table 4). Foraminal diameters did not show changes at different levels, but could be arranged from longest to closest as follows: L2–L3>L3–L4>L4–L5>L5–S1>L1–L2 (Table 5).

On the transverse plane, Gs from L1 to L5–S1 showed a decrease as the disc level went down. The mean vertical distance from the facet surface to the posterior surface of vertebral body (distance Gs) was 4.56±1.10 for the right side, and 4.49±1.08 for left side (Table 6). Hs decreased caudally, and the mean value was 3.75±0.65 for the right side, and 3.77±0.69 for left side (Table 7). Ii did not show change as the spine level went down, and the mean value was 3.76±0.64 for right side, and 4.1±0.99 for left side (Table 8).

According to the conducted multilevel mixed effects models, the predictive roles of age, sex, and BMI for the radio anatomic factors were as the following (Table 9).

Table 9 . Multistage linear regression with mixed effect to predict radioanatomical indices

Covariates/outcomeCoefficientStandard errortSignificant95% confidence interval
LowerUpper
Model term/alpha
Intercept55.0013.413716.112<0.00148.29861.704
GENDER=0–0.4940.3417–1.4450.149–1.1650.177
Age (yr)–0.0180.0121–1.5050.133–0.0420.006
BMI (kg/m2)–0.1070.0375–2.8460.005a)–0.180–0.033
Var(Intercept)10.450-----
Var(Index_side(Index_number))1.4710.8221.7900.0730.4924.397
Model term/a
Intercept19.7624.57684.318<0.00110.77528.749
GENDER=0–1.8380.2705–6.795<0.001a)–2.369–1.307
Age (yr)0.0660.00966.832<0.001a)0.0470.084
BMI (kg/m2)–0.1310.0297–4.424<0.001a)–0.189–0.073
Var(Intercept)17.646-----
Var(Index_side(Index_number))26.366b)12.5302.1040.03510.38866.923
Model term/b
Intercept13.0543.32393.927<0.0016.52819.581
GENDER=0–0.9120.1915–4.764<0.001a)–1.288–0.536
Age (yr)0.0720.006810.603<0.001a)0.0590.085
BMI (kg/m2)–0.0070.0210–0.3250.745–0.0480.034
Var(Intercept)9.224-----
Var(Index_side(Index_number))14.917b)7.0732.1090.0355.88937.783
Model term/h
Intercept20.3771.823711.174<0.00116.79623.958
GENDER=0–0.3550.1569–2.2640.024a)–0.663–0.047
Age (yr)–0.0320.0056–5.731<0.001a)–0.043–0.021
BMI (kg/m2)–0.0310.0172–1.7960.073a)–0.0650.003
Var(Intercept)2.914-----
Var(Index_side(Index_number))1.8860.9202.0500.0400.7254.906
Model term/w
Intercept9.1220.828311.014<0.0017.49610.749
GENDER=0–0.0820.0847–0.9670.334–0.2480.084
Age (yr)–0.0140.0030–4.502<0.001a)–0.019–0.008
BMI (kg/m2)–0.0070.0093–0.7570.449–0.0250.011
Var(Intercept)0.616-----
Var(Index_side(Index_number))0.0560.0341.6510.0990.0170.183
Model term/Gs
Intercept5.8410.88836.575<0.0014.0967.585
GENDER=0–0.0990.0855–1.1620.246–0.2670.069
Age (yr)–0.0210.0030–7.043<0.001a)–0.027–0.015
BMI (kg/m2)–0.0120.0094–1.2620.207–0.0300.007
Var(Intercept)0.701-----
Var(Index_side(Index_number))0.2250.1141.9790.0480.0840.606
Model term/Hs
Intercept4.0680.54637.447<0.0012.9965.141
GENDER=00.0520.05550.9400.348–0.0570.161
Age (yr)<0.0010.0020–0.2530.800–0.0040.003
BMI (kg/m2)–0.0110.0061–1.8240.069a)–0.0230.001
Var(Intercept)0.268-----
Var(Index_side(Index_number))0.0240.0141.6270.1040.0070.078
Model term/Ii
Intercept4.1750.72765.739<0.0012.7475.604
GENDER=0–0.0330.0737–0.4530.651–0.1780.111
Age (yr)–0.0100.0026–3.662<0.001a)–0.015–0.004
BMI (kg/m2)0.0070.00810.8250.410–0.0090.023
Var(Intercept)0.477-----
Var(Index_side(Index_number))0.0330.0211.5580.1190.0090.114

GENDER=0, female; BMI, body mass index; Var(Intercept), residue variance; Var(Index_side(Index_number)), variance of side nested within lumbar spine number random effects; Gs, foraminal width; Hs, nerve root-disc distance; Ii, nerve root-facet distance; -, not abvailable. a)Significant association at P<0.01; b)Variance of random effect more than variance of residue.



α: each unit increase in BMI was associated with a 0.107-unit decrease in α (P=0.005). Age and sex did not show a considerable association (Table 9, Fig. 5).

Figure 5. (A) The severity of the correlation between the factors affecting alpha and (B) the model’s goodness of fit in prediction. GENDER=0, female; BMI, body mass index.

a: female caused a 1.838-unit decrease in a. Each year of increasing age caused a 0.066-unit increase in a. Each unit increase in BMI was associated with a 0.131-unit decrease in a (P>0.001) (Table 9, Fig. 6).

Figure 6. (A) The intensity of the correlation between the factors affecting a and (B) the model’s goodness of fit in prediction. GENDER=0, female; BMI, body mass index.

b: female sex caused a 0.912-unit decrease in b. Each year of increasing age caused a 0.072-unit increase in b (P>0.001). BMI did not show a significant relationship (Table 9, Fig. 7).

Figure 7. (A) The intensity of the correlation between the factors affecting b and (B) the model’s goodness of fit in prediction. GENDER=0, female; BMI, body mass index.

h: female gender caused a 0.355-unit decrease in h (P=0.024). Each year of increasing age caused a 0.034-unit decrease in h (P>0.001). Each unit increase in BMI was associated with a 0.031-unit decrease in h (Table 9, Fig. 8).

Figure 8. (A) The intensity of the correlation between the factors affecting h and (B) the model’s goodness of fit in prediction. GENDER=0, female; BMI, body mass index.

w: each year of increasing age caused a 0.014-unit decrease in w (P>0.001). Gender and BMI did not show a significant relationship with w (Table 9, Fig. 9).

Figure 9. (A) The intensity of the correlation between the factors affecting w and (B) the model’s goodness of fit in prediction. GENDER=0, female; BMI, body mass index.

Gs: each year of increasing age caused a 0.021-unit decrease in Gs (P>0.001). Gender and BMI did not show a significant relationship with Gs (Table 9, Fig. 10).

Figure 10. (A) The intensity of the correlation between the factors affecting Gs and (B) the model’s goodness of fit in prediction. GENDER=0, female; BMI, body mass index. Gs, foraminal width.

Hs: each unit increase in BMI caused a 0.011-unit decrease in Hs (P=0.069). Age and gender did not show a significant relationship with Hs (Table 9, Fig. 11).

Figure 11. (A) The intensity of the correlation between the factors affecting Hs and (B) the model’s goodness of fit in prediction. GENDER=0, female; BMI, body mass index. Hs, nerve root-disc distance.

The most common minimally invasive method for treating lumbar disc herniation is PPTD, particularly with regard to intraspinal decompression using the trans foraminal endoscopic spine system. The main goal of PPTD is to remove the herniated nucleus pulposus with the least damage and fewest complications to the musculoskeletal structure [15, 26].

The first definition of the safe working zone for the intervertebral foramen was given by Kambin in a 1991 study on the area of the human intervertebral foramen [27, 28]. The outer upper boundary of this area is the exiting nerve root, the medial boundary is the dural sac or traversing nerve root, the lower boundary is the upper end plate of the inferior vertebral body, and the posterior boundary is the superior articular process of the inferior vertebral body. To reduce the possibility of injury to the exiting nerve root, it is crucial to accurately identify the anatomic relationship between the outgoing nerve root and the superior articular process in Kambin’s triangle of the lumbar intervertebral foramen [27].

The majority of the literature focuses on research performed on cadavers, patients with degenerative spine, and symptomatic subjects [29]. Hoshide et al. [30] conducted an anatomic investigation on Kambin’s triangle and found that its border is a two-dimensional triangular region with an area of 60–108 mm2 which is located between the superior end plate of the inferior vertebral body, the superior articular process, and the exiting nerve root. Based on the cadaveric study, Mirkovic et al. [17] identified the “safe zone” as being 18.9 mm wide and 12.3 mm high, with the size increasing as the level went down. However, the current investigation showed a similar trend, with the largest distance observed located at the lowermost level (L5–S1). These findings are consistent with Guan et al.’s observation [24], which demonstrates the morphometric analysis of the working zone based on MR neurography. According to Guan’s research [24], the narrower Kambin’s angle at higher vertebral levels, the higher the risk of nerve root injury. The results of the current research showed that each unit increase in BMI was associated with a 0.107-unit decrease in α, which was not shown in previous studies. But no significant correlation was observed between gender and age. The investigation found that the mean distance (distance b) between the dura and the nerve root at the level of the superior endplate was 15.51±2.64 mm. This distance was comparable to the findings of Guan et al. [24] and was less than that of the cadaveric analysis. This difference might be the result of formalin fixation, tissue shrinkage and muscle traction. Furthermore, in cadaveric studies, anatomic structures greatly limit the access to L5–S1 level, thus restricting the sample size to a very small number [29].

In the present study, foraminal height decreased caudally and the biggest foraminal height was measured at L2–L3 and the smallest at L5–S1 level; This was consistent with the MRI studies done by Hurday et al. [16] and Al-Hadidi et al. [31] where they measured the mean foraminal height as 20.9±1.7 mm. In the study ahead, the mean foraminal diameters were 8.28±1.04 mm for both sides, and did not show changes at different levels. The research conducted by Min et al. [18] revealed that 15.6% of intervertebral foramens on the sagittal plane had diameters smaller than 7 mm. They concluded that the base dimension was the crucial factor when the disc space height was equal to or greater than that of the working device. According to Choi et al. [11] neural complication rates of PPTD operations decreased by 23% per each 1-mm increase in the distance based on a preoperative MRI scan.

In the current study, there was a decrease in both the Gs and Hs as the disc level went down. Due to limited visual control and the close proximity of the nerve root to the facet or disc, along with narrow Gs in the lower lumbar levels, there is a risk of injuring the exiting root. As a result, experts suggest inserting the working cannula as near as possible to the facet joint, rather than directly targeting the disc. This method should be easily accessible for the upper lumbar levels [11, 32, 33]. Therefore, it is recommended to undergo foraminoplasty in the lower lumbar region to improve the chances of a safer landing and minimize excessive manipulation of the spinal canal contents.

According to the multilevel mixed effects models, the predictive roles of age, sex, and BMI for the radio-anatomic factors showed that each unit increase in BMI was associated with a decrease in α (P=0.005). Age and sex did not show a considerable association. In the present study, ‘a, b,’ and h showed sexual dimorphism, and each year of increasing age caused increase in ‘a’ and ‘b’. Each unit increase in BMI was associated with a decrease in ‘a’ and h. These findings are compatible with previous research which found sexual dimorphism of the lumbar spine [34-36]. Compared with other studies, the unique value of this human MRI study is that we quantified sexual dimorphism in lumbar spines free of pathology and degeneration. Smith et al. [37] found no statistically significant differences between the inter vertebral foramen (IVF) dimensions of male and female in their study of cadavers. According to Vanharanta et al. [38] there is a statistically significant difference in the anterior-posterior dimensions of lumbar IVFs, with women’s IVFs being larger anterior-posterior dimensions than men’s. The findings of Cramer et al. [39] are consistent with the multistage linear regression analysis results of the current study. The different dimensions of Kambin’s triangle varies in the literature, possibly because of differences in the demographics of the study population, genetics, ethnicities, and formalin-fixed cadavers [19, 29, 40, 41]. It is difficult to analyze factors associated with the existence of a different shape of working zone separately because they may coexist in the same patient and at the same disc level. In the present study, multilevel mixed effects linear regression analysis for prediction of radio anatomic factors showed that age, gender and BMI are predictive factors for the working zone.

The present study, as the first research to evaluate the dimension of Kambin’s triangle and its related factors in Iran, reflects the inherent limitations of a cross-sectional study protocol. Firstly, a relatively small sample size may have decreased the statistical power. Therefore, a large sample, multicenter imaging study would be more helpful to analyze the Kambin’s triangle. Second, the aim was not to assess the relationship between the imaging findings and pain or disability. Third was the retrospective nature of the study, which no data exists regarding the sociodemographic condition of patients. Fourth, the inherent nature of conventional MRI which cannot detect cortical bone. Therefore, the results should be interpreted with care.

The present study showed that MR neurography is a practical, noninvasive diagnostic tool to evaluate the anatomical parameters of lumbosacral nerve root and adjacent structures in the working zone of Kambin’s triangle. On coronal plane, the average of α angle was 50.92±4.25 on both sides, and the distance of ‘a’ and ‘b’ decreased as the vertebral level went down. On sagittal plane, foraminal height decreased caudally, biggest foraminal height was measured at L2–L3 and smallest at L5–S1. On transverse plane, Gs from L1 to L5–S1 showed a decrease as the disc level went down. Additionally, this study suggests fewer maneuvers during PPTD, bearing in mind the proximity of the root to the instruments during foraminoplasty. To perform a safer procedure, 3D radiological measurement of the working zone is recommended before PPTD.

Conceptualization: AREM. Data acquisition: NN. Data analysis or interpretation: AREM, ZF. Drafting of the manuscript: AREM, NN. Critical revision of the manuscript: MS, MAL and ZF. Approval of the final version of the manuscript: all authors.

No potential conflict of interest relevant to this article was reported.

The research deputy of Ahvaz Jundishapur University of Medical Science, (grant number U-01128), funded this study.

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