2.1 Data Collection
This retrospective cohort study was approved by the Ethics Committee of Zhongshan Hospital. We collected the data of consecutive hospitalized patients of LDH treated with PTES in our hospital between January 2015 and December 2017. 101 patients who underwent PTES and met the following requirements were included in this study: (1) Patients complained of primarily radicular pain of unilateral leg; (2) Clear nerve root compression sign including positive Lasegue sign, sensory or movement disorder of the lower limbs and the reflex abnormalities of knee or ankle; (3) Imaging data confirmed the presence of single-level LDH and excluded other spinal diseases such as lumbar spondylolisthesis or lateral recess stenosis; (4) Conservative treatment failed.
In these patients, preoperative CT scan image confirmed that 46 of them had calcification at the herniated site. Patients with calcified herniation were included in CLDH group and the rest of them were included in ULDH (Uncalcified Lumbar Disc Herniation) group. The detailed grouping criteria is shown in Figure 1.
Table 1 summarizes the baseline date of two groups. The CLDH group was comprised of 46 patients and ULDH group included 55 patients. There was no statistical significance in age, gender, BMI, operation segment and follow-up time between two groups.
Table 1 The demographic data of CLDH and ULDH patients.
|
|
CLDH(n=46)
|
ULDH(n=55)
|
p-value
|
Age
|
|
49.57 ± 16.17
|
51.51 ± 16.07
|
0.547 a
|
Sex
|
M
|
26
|
31
|
0.987 b
|
F
|
20
|
24
|
|
BMI
|
|
24.38 ± 3.43
|
24.84 ± 3.15
|
0.482 a
|
Segments
|
L4-L5
|
26
|
36
|
0.358 b
|
L5-S1
|
20
|
19
|
Follow-up time (month)
|
|
24 (24-29)
|
24 (24-28)
|
0.285 c
|
a Exhibited in the format of “Mean ± standard deviation” and tested by Student’s t test.
b Pearson’s chi-squared test.
c Exhibited in the format of “Median (Min-Max)” and tested by Mann-Whitney U test.
2.2 Surgical techniques
All the surgeries were undertaken by the same senior surgeon. The patient was placed in a prone position on a radiolucent table with conscious sedation and C-arm was used for intraoperative fluoroscopic imaging.
The surface marking of anatomic disc space is a transverse line drawn along the metal rod which is placed transversely across the center of the target disc on the posteroanterior image. The entrance point locates at the corner of flat back turning to lateral side at the height of target disc, or cranially or slightly caudally. This entrance point, name “Gu’s point” was easy to determine without the fluoroscopy regardless of different age, gender and body size. The intersection of posterior midline and the transverse line was the aiming reference point. After local infiltration anesthesia with 1% lidocaine at the entrance point, an 18-gauge puncture needle was inserted anteromedially at an angle of about 45° (25°-75°, adjust based on the actual situation) to horizontal plane. Once the resistance disappeared, the needle tip should stay at posterior 1/3 of the intervertebral space or intracanal area close to posterior wall of the disc on lateral view and near the medial border of the pedicle on posteroanterior view, proving the success of the puncture. After dilating the puncture tract stepwise, a 6.3-mm diameter guiding rod was introduced over the guiding wire into the intervertebral foramen and an 8.8-mm diameter cannula with one-side opening was inserted over the guiding rod and docked at the superior facet. Then press down the cannula to decrease the inclination angle and a 7.5-mm diameter trephine was introduced through the cannula to remove the ventral bone of superior articular process to enlarge the foramen. When resistance disappeared, the distal end of the trephine should exceed the medial border of the pedicle on posteroanterior view and reach the posterior wall of disc on lateral view. This enlargement procedure was first introduced by us and was named “Press-Down Enlargement of Foramen”. In order to excise the calcification directly, the trephine was pressed down further to continue drilling until the distal end exceeded the midpoint between medial border of the pedicle and the spinous process on posteroanterior view and was across the posterior wall of disc on lateral view.
The 7.5-mm diameter working cannula was inserted over the guiding rod. The endoscope was introduced and the herniated tissue could be observed on screen generally. Remove the herniated tissue to free the compressed nerve root. The residual calcified tissue could be removed by small reamer, electric drill or ultrasonic osteotome. The freed nerve root always pulsated in pace with heart beat. After inquiring the patient to confirm the relieved symptoms, the endoscopic surgery could be completed.
Patients were immobilized within five hours after the surgery and left the hospital one day after operation. A flexible brace was used for two weeks. After leaving hospital, patients were encouraged to return to daily life and followed up regularly.
2.3 Pre- and Postoperative image
Before the surgery, patients received MRI to determine the herniated level and CT scan to confirm the presence of calcification. Posteroanterior and lateral X-rays were required to detect scoliosis or high iliac crest when the lower plate of L4 vertebral body was not higher than bilateral iliac crest. After operation, CT scan was undertaken to confirm the excision of calcification. Postoperative MRI images were acquired to evaluate decompression outcome and exclude hematoma and dural sac rupture or spinal fluid leakage.
2.4 Clinical follow-up
The pain intensity of the lower limbs was graded using Visual Analogue Scale (VAS) pain score before operation, immediately, one week, one month, two months, three months, six months, 12 months and 24 months after surgery. The therapeutic results were graded 24 months after discharge based on the MacNab criteria[9]. Clinical follow-up was carried out through outpatient or telephone follow-up.
During the follow-up, postoperative complications were recorded including infection, increased weakness of quadriceps, foot/toe extensor or triceps strength and residual or the recurrence of the herniation.
2.5 Statistical analysis
Data analysis was performed by SPSS, version 25.0 (IBM Corp., Armonk, New York, USA). Normal distribution of variable was tested by Shapiro-Wilk test. Normal distribution variable comparation between two groups was tested by Student’s t-test. Non-normal distribution variable and ordinal categorical variable was tested using Mann-Whitney U test. Unordered categorical variable was compared through Pearson’s Chi-squared test or Fisher’s exact test. All significance tests were two-tailed and p<0.05 was considered statistically significant.