Inclusion and exclusion criteria
Inclusion criteria: ① a diagnosis of lumbar degenerative disease, including lumbar disc herniation with intervertebral instability, lumbar spinal stenosis, lumbar spondylolisthesis ② with unilateral or bilateral lower limb symptoms (intermittent claudication or sciatica), after 3 months of conservative treatment, no obvious symptom relief was observed ③physical examination and imaging examination confirmed as a single level lumbar disease.
Exclusion criteria: ① lumbar spondylolisthesis≥2 degrees or accompanied by obvious spondylolysis② previous history of lumbar surgery ③ operative level infection, tumor or fracture ④combined with other severe cardiovascular and cerebrovascular diseases or other surgical contraindications
Baseline clinical data
A total of 87 consecutive patients between June 2016 and December 2019 with lumbar degenerative diseases who had undergone wiltse approach TLIF(29 cases), MIS-TLIF(28 cases) or PLIF(30 cases) in our department were included. There were 35 patients (44.9%) with unilateral lower limb pain, 29 patients (32.2%) with lower limb pain and numbness, and 20 patients (23.0%) with bilateral symptoms and 3 patients (3.4%) with simple low back pain. Twenty-eight patients (35.9%) presented unilateral or bilateral lower limb muscle strength decline to varying degrees. Cauda equina syndrome was present in 4 patients (4.6%).
All the patients underwent lumbar radiograph of anterior and lateral position, hyperextension and hyperflexion position, lumbar intervertebral disc CT, and lumbar MRI before surgery. Among them, 15 patients were with lumbar spondylolisthesis and 21 patients were with lumbar instability. All patients’ physical examination was consistent with imaging changes and all of them were confirmed as single-level degenerative diseases of the lumbar spine.
All patients in this study were informed and signed an informed consent, which was reviewed and approved by the ethics Committee of our hospital.
Cases of group
The patients were selected from the concurrent patients with similar age, weight and severity of the imaging and symptom, then were divided into 3 group according to the different treatment methods. Their baseline data showed no significant difference. Patients(n=29) who had received wiltse approach TLIF operation were in the wiltse group. Patients(n=28) who had received MIS-TILF (minimally invasive transforaminal lumbar interbody fusion) operation were in the MIS-TILF group. Patients(n=30) who had received traditional PLIF (posterior lumbar interbody fusion) operation were in the PLIF group. All surgery were conducted by the same surgeon (Wei Zhang).
Surgical procedures
Wiltse approach TLIF10
General anesthesia was used and patients were placed in prone position. (Step 1)Kirschner wire was used for positioning under c-arm X-ray fluoroscopy to determine the stage of responsibility. (Step 2) Bilateral access is provided thorough a midline skin incision with a length of about 8cm. The lumbar dorsal fascia was incised longitudinally at 2.5-3cm from the posterior midline. Blunt dissection by the fingers were used to separate the medial multifidus from the lateral longissimus muscle. (Step 3) Identify the junction of the facet joints and the transverse processes, and pedicle screw was installed. Then the new type retractor was fixed on the pedicle screw (figure 5 and figure6) (Step 4). After full decompression of contralateral spinal canal and nerve root canal, the diseased intervertebral disc was resected, the cartilage endplate was scraped and bone fragments as well as intervertebral fusion cage were implanted into the intervertebral space. (Step 5) Finally, rod system was installed. (Step 6) One drainage tube was placed beside the incision. (Step 7)
MIS-TILF (expandable tubular retractor assisted minimally invasive transforaminal interbody fusion)5
General anesthesia was used and patients were placed in prone position. (Step 1) The projection position of the adjacent pedicle of diseased segment were identified and marked by c-arm X-ray machine. With the assistance of fluoroscopy, percutaneous needle was used to locate the outer edge of each pedicle at the marking points respectively. (Step 2)Centering each puncture point,4 transverse incisions about 1.5cm in length were taken. The lumbar dorsal fascia was incised longitudinally. The space between the the medial multifidus and longissimus muscle was investigated and the articular facet joint were explored along this gap. After puncturing to the articular process with a puncture needle and inserting the guide wire along each puncture needle catheter, an expandable tubular retractor was inserted along the guide wire. The retractor was placed on the medial side of the articular process and on the upper margin of the intervertebral space in the responsible stage. (Step 3) After full decompression of spinal canal and nerve root canal, the diseased intervertebral disc was resected, the cartilage endplate was scraped and bone fragments and intervertebral fusion cage were implanted into the intervertebral space. If there were contralateral symptoms, the channel could be adjusted along the spinous process base to complete contralateral nerve root canal decompression, enlarge the contralateral nerve root canal and the central vertebral canal. After decompression and bone grafting, exit the working channel. (Step 4) Insert hollow pedicle screws into each pedicle along the guide wire. After the fluoroscopy position was satisfied, the pedicle screw rod system was installed. (Step 5) A drainage tube was placed through the incision on the decompression side. (Step 6)
Traditional PLIF
General anesthesia was used and patients were placed in prone position. (Step 1) Under the perspective of C-arm X-ray machine, kirschner wire is used to locate and determine the responsibility stage. (Step 2) The posterior midline incision with a length of about 10cm was taken. After the lumbar fascia was incised, the lateral paravertebral muscles along the spinous process are stripped to the bilateral facet joints. (Step 3) Then the pedicle screw rod system was installed. (Step 4) After full decompression of contralateral spinal canal and nerve root canal, the diseased intervertebral disc was resected, the cartilage endplate was scraped and bone fragments as well as intervertebral fusion cage were implanted into the intervertebral space. (Step 5) Finally, pedicle screw rod system was installed. (Step 6) One drainage tube was placed next to the incision. (Step 7)
Outcome measures
Perioperative indicators
Including intraoperative blood loss, postoperative drainage volume, operation time, fluoroscopy time, bed time.
Indicators of muscle injury
CK (Creatine kinase)
The serum CK level of patients were measured by enzyme coupling method before surgery, 1 day after surgery, 4 days after surgery, and 7 days after surgery, respectively, to evaluate the muscle injury intensity.
CK is the enzyme that catalyzes the reaction of creatine and adenosine triphosphate (ATP) to phosphocreatine and adenosine diphosphate (ADP). Serum creatine kinase (CK) concentrations have been used to investigate skeletal muscle injury caused by lumbar surgery. The normal CK level is considered to be 20 to 200 IU/L. In this study, serum CK was measured using spectrometry.
VAS (Visual analogue Score)
The lower back pain score and lower limb pain score were evaluated at 3 days and 3, 6 and 12 months after surgery, respectively.
The Visual Analogue Scale (VAS)has been in use for the measurement of pain. It is a self-reported scale consisting of a horizontal or vertical line, usually 10 centimetres long (100 mm) with anchor descriptors such as (in the pain context) “no pain” and “worst pain imaginable” referring to the pain status. An introductory question (with or without a time recall period) asks the patient to tick the line on the point that best refers to his/her pain. VAS is feasible for clinical research and practice.
ODI (Oswestry Disability Index)
In this study, patients were surveyed in 9 aspects except sexual life.
The ODI were evaluated before surgery and 3, 6 and 12 months after surgery, respectively.
Oswestry disability index (ODI) is a principal condition-specific outcome measures used in the management of spinal disorders, and to assess patient progress in routine clinical practice. The ODI score system includes 10 sections: pain intensity, personal care, lifting, walking, sitting, standing, sleeping, sex life, social life and traveling. For each section of six statements the total score is 5. Intervening statements are scored according to rank. If more than one box is marked in each section, take the highest score. If all10 sections are completed the score is calculated as follows: total scored out of total possible score×100.If one section is missed (or not applicable) the score is calculated: (total score/(5×number of questions answered))×100%.0%-20% is considered mild dysfunction, 21%-40% is moderate dysfunction, 41%-60% is severe dysfunction, and 61%-80% is considered as disability. For cases with score of 81%-100%, either long-term bedridden, or exaggerating the impact of pain on their life.
JOA score for low back pain
The JOA score for low back pain were evaluated before surgery and 3, 6 and 12 months after surgery, respectively
The Japanese Orthopaedic Association score for back pain (JOA score) was established for evaluating LBP and/or lumbar spinal diseases and has been used to estimate the severity of LBP or clinical outcomes. The JOA score consists of four subscales: Subjective symptoms, Clinical signs, Activities of daily living and Urinary bladder function, providing clinicians with significant information. JOA score is 29 in total.
Evaluation of intervertebral fusion
In this study, two methods were used to evaluate intervertebral fusion, including lumbar radiograph of hyperextension and hyperflexion position and lumbar CT in extension position at the last follow-up. The radiographs were interpreted as showing incomplete union if there was mobility of more than 3°, a remaining clear zone, or no definite bone connection11.Lumbar CT scan in hyperextension is considered to be incomplete fusion if there is a gas pattern, a remaining clear zone, or no definite bone connection.12-14
Evaluation of muscle atrophy and fatty infiltration
Lumbar MRI was used to evaluate the multifidus atrophy and fatty infiltration. The results, including the total cross-sectional area (CSA), lean CSA, ratio of lean-to-total CSA, were evaluated before surgery and at last follow-up after surgery according to the following methods. The CSA was measured at the operative level using the axial T2-weighted sequences with the RadiAnt DICOM Viewer software (Medixant. RadiAnt DICOM Viewer [Software]. Version 2020.2. Jul 19, 2020. URL: https://www.radiantviewer.com.).In order to identify the lean CSA, the region of interest (ROI) was drawn around the multifidus on both sides of the spinous process, excluding nearby fat, bone, and other tissues (Figure 1a). Ratio of multifidus atrophy = (preoperative CSA - postoperative CSA)/preoperative CSA. The ratio of lean-to-total CSA (Figure 1b) was utilized as an additional measurement of fatty infiltration as described in rotator cuff’s research (ratio of lean-to-total CSA = lean CSA /total CSA)15, 16.
Statistical method
SPSS 20.0.0 statistical software was used for data analysis. For measurement data, statistical analysis were performed utilizing one-way ANOVA if they obeyed normal distribution and satisfied homogeneity test of variance, otherwise, nonparametric test of rank conversion is used. Counting data were compared by using The Chi-square test. The test level was 0.05 on both sides, and p-value of ≤0.05 was considered statistically significant.