Method Article
This study evaluated endoscopic debridement for treating paravertebral abscesses in patients with spinal tuberculosis. Compared to conventional surgery, it significantly improved surgery time, blood loss, hospital stay, pain relief, and neurological outcomes, with fewer complications and no recurrences. These findings highlight its efficacy and safety. Further long-term studies are recommended.
Spinal tuberculosis (TB) remains a significant global health concern, necessitating the development of innovative treatment strategies. This clinical study aimed to evaluate the efficacy and safety of endoscopic debridement as a minimally invasive approach for treating paravertebral abscesses in patients with spinal tuberculosis. A total of 52 patients diagnosed with paravertebral tuberculosis abscesses were enrolled in this retrospective study. Patients were assigned to two groups: the endoscopic debridement group (n = 30) and the conventional open surgery group (n = 22), based on the type of surgery they received. Clinical outcomes were assessed at baseline, post-treatment, and follow-up visits at regular intervals, including surgery time, intraoperative blood loss, total hospital stay duration, pain relief, and neurological improvement. The results of this study demonstrate that endoscopic debridement is a highly effective treatment for paravertebral abscesses in patients with spinal TB. Patients in the endoscopic debridement group experienced significant improvements in surgery time, intraoperative blood loss, total hospital stay duration, pain relief, and neurological improvement compared to those in the conventional open surgery group. Additionally, the endoscopic approach resulted in fewer complications, such as wound infections and postoperative instability, with no cases of recurrence observed during the follow-up period. Therefore, this clinical study highlights the potential of endoscopic debridement as a safe and effective treatment modality for spinal tuberculosis. The technique not only effectively eliminates infected tissue but also ensures faster patient recovery and reduces postoperative complications. Additional research and long-term follow-up studies are necessary to confirm the long-term effectiveness and safety of endoscopic debridement as the standard treatment for spinal tuberculosis.
The risk of tuberculosis is increasing in the last decade due to the rise in drug-resistant tuberculosis bacterial strains and the prevalence of patients living with HIV. An estimated 10 million new cases of tuberculosis and 1.6 million deaths due to tuberculosis were reported globally in 2021 alone, an increase from 1.5 million in 20201. Tuberculosis of the bone and joints accounts for about 1%-2% of all patients with tuberculosis, and spinal tuberculosis accounts for 50% of all skeletal tuberculosis cases2. Spinal tuberculosis often causes pain and symptoms of systemic tuberculosis poisoning. In severe cases, it can lead to kyphotic deformity due to vertebral erosion, spinal cord injury, and paralysis. Active diagnosis and treatment can help relieve symptoms and create favorable conditions for neural recovery3,4.
The literature on treatments for thoracic and lumbar tuberculosis outlines several protocols, including a regimen of anti-TB drugs such as isoniazid, pyrazinamide, rifampicin, and ethambutol, various surgical approaches like anterior radical debridement with graft fusion or posterior debridement with fusion and fixation, as well as minimally invasive methods. Anti-TB chemotherapy is established as the principal treatment for spinal tuberculosis (ST). Surgery is recommended for cases demonstrating clear vertebral instability, non-response to chemotherapy, increasing spinal deformity, severe neurological deficits, or large paravertebral abscesses (PA) with or without compression of the epidural space. Reports indicate that 10% to 43% of spinal tuberculosis cases are complicated by severe kyphosis and neural functional damage, necessitating surgical treatment primarily to remove the lesion and relieve nerve compression5,6. The goal has always been to choose a safe, effective, and less invasive method for the treatment of spinal tuberculosis7,8. Minimally invasive spine surgeries (MIS) are frequently employed to treat degenerative spinal disorders. Among these, full endoscopic surgeries-an established subset of MIS-are effectively utilized for managing disc herniations and spinal stenosis. Nonetheless, their effectiveness in the debridement of vertebral tuberculosis lesions remains underexplored9,10.
Since January 2016, Urumqi Friendship Hospital has implemented minimally invasive anterior debridement to treat lumbar tuberculosis with paravertebral abscess. To provide a reference for future clinical practice, we compared the results of this unique method with traditional posterior fixation combined with anterior debridement techniques.
All procedures involved in the current study were approved by the ethical committee of Urumqi Friendship Hospital, and all patients agreed to the publication of their clinical material, provided their identity is not revealed. From January 2018 to January 2023, clinical and radiological materials, as well as blood work of patients treated with anterior debridement for lumbar tuberculosis with paravertebral abscess, were retrospectively analyzed. The diagnosis of spinal tuberculosis was confirmed by T-SPOT tests, spinal MRI and CT tests, and tissue acid-fast bacilli culture tests4,7,8. The commercial details of the equipment involved in this study are listed in the Table of Materials.
1. Preoperative preparation
2. Surgical procedure of endoscopic debridement
3. Postoperative care following endoscopic debridement
4. Traditional posterior debridement
5. Postoperative care following traditional posterior debridement
6. Outcome assessment
7. Statistical analysis
Fifty-two patients, including 28 males and 24 females, aged 18 to 73 years (50.2 ± 10.5) were included in the current study. Thirty patients were treated with minimally invasive anterior debridement and fusion (minimally invasive surgery group), while 22 patients underwent traditional open surgery (conventional surgery group). In the minimally invasive surgery group, there were 17 males and 13 females, aged 24-72 years (51.4 ± 9.1), including 18 single vertebral bodies and 12 double vertebral bodies. In the conventional surgery group, there were 13 males and 9 females, aged 18-65 years (48.6 ± 9.6), with 14 single vertebral bodies and 8 double vertebral bodies. There was no significant difference observed between the two groups in age, symptom duration, preoperative complications, and the number of involved vertebral segments (P > 0.05, Table 1). There was no significant difference observed between the two groups in age, symptom duration, preoperative complications, and the number of involved vertebral segments (P > 0.05).
Patients were followed up for 12-30 months (15.3 ± 3.2). With the gradual control of infection and pain, the erythrocyte sedimentation rate (ESR) of most cases decreased within one month after the operation. Although the ESR remained high in four patients with wound infections, it approached normal levels during the reexamination three months after surgery.
The total operative time was 74.3 ± 18.6 min in the minimally invasive group and 155.8 ± 29.4 min in the conventional surgery group. The difference between the two groups was statistically significant (P < 0.01). The volume of intraoperative hemorrhage was 81.0 mL ± 27.8 mL in the minimally invasive surgery group and 242.3 mL ± 45.3 mL in the conventional surgery group, with a statistically significant difference (P < 0.01). The Visual Analog Scale (VAS) score and Oswestry Disability Index (ODI) of the two groups improved significantly at three months and at the last follow-up compared to preoperative levels (P < 0.01, Table 2). Both the VAS score11 and ODI12 were better in the early postoperative period and at the last follow-up in the minimally invasive surgery group compared to the conventional surgery group (P < 0.05, Table 2). The operative time was longer in the conventional surgery group compared to the minimally invasive group; the volume of intraoperative hemorrhage was significantly lower in the minimally invasive group than in the conventional surgery group. The VAS score and ODI of the two groups improved significantly at three months and at the last follow-up compared to preoperative levels; both the VAS score and ODI were better in the early postoperative period and at the last follow-up in the minimally invasive surgery group compared to the conventional surgery group.
According to the ASIA classification13, there were six patients with spinal cord dysfunction before surgery. In the minimally invasive surgery group, there were two patients with grade D, while in the conventional surgery group, there were three patients with grade D and one patient with grade C. Except for one patient with grade D in the conventional surgery group, all other patients recovered to grade E.
The imaging data from the last follow-up showed that all patients achieved complete bone fusion. One patient in the conventional surgery group had a wound infection and was discharged after 2 weeks of dressing changes and antibacterial treatment. Postoperative lung infections were found in one patient in the conventional surgery group and in one patient in the minimally invasive surgery group. Additionally, there was one patient with gastrointestinal discomfort after surgery in the conventional surgery group. All complications were resolved with non-surgical intervention.
Figure 1: Endoscopic treatment of tuberculosis at L4-S1. (A) Sagittal MRI view of the spine showing tuberculosis at the L4-S1 level in a 65-year-old patient with paravertebral abscess. (B) Horizontal MRI view confirming the presence of tuberculosis at the same level. (C) Extracted diseased tissue following endoscopic surgery. Please click here to view a larger version of this figure.
Minimally invasive | Conventional | t/X2 value | P value | ||
Male/female | 17/13 | 13-09-2024 | 0.03 | 0.81 | |
Age | 51.4 ± 9.1 | 48.6 ± 9.6 | 1.1 | 0.3 | |
Symptom duration (months) | 5.5 ± 2.0 | 4.8 ± 1.3 | 1.58 | 0.12 | |
Complications | Cardiovascular | 8 | 6 | 0.07 | 0.8 |
Diabetes | 7 | 5 | 0.02 | 0.89 | |
Osteoporosis | 9 | 7 | 0.26 | 0.61 | |
Involved vertebrae | Single | 18 | 14 | 0.71 | 0.79 |
Double | 12 | 8 |
Table 1: Comparison of patient demographics and preoperative characteristics. There was no significant difference between the two groups in terms of age, symptom duration, preoperative complications, and the number of involved vertebral segments (P > 0.05).
Minimally invasive | Conventional | t value | P value | ||
Operation time, min | 74.3 ± 18.6 | 155.8 ± 29.4 | 6 | <0.01 | |
Intraoperative hemorrhage (mL) | 81.0 ± 27.8 | 242.3 ± 45.3 | 15.8 | <0.01 | |
Time for hospital stay (days) | 10.8 ± 2.8 | 15.2 ± 4.4 | 4.4 | <0.01 | |
VAS score | Before surgery | 5.6 ± 1.0 | 6.1 ± 1.0 | 2 | 0.08 |
3 months after surgery | 2.0 ± 0.9 | 3.5 ± 0.8 | 6.4 | <0.01 | |
At last follow up | 1.1 ± 0.7 | 2.4 ± 0.5 | 7.1 | <0.01 | |
ODI | Before surgery | 50.2 ± 8.4 | 53.1 ± 8.7 | 1.2 | 0.24 |
3 months after surgery | 22.9 ± 8.1 | 30.3 ± 6.5 | 3.5 | <0.01 | |
At last follow up | 3.3 ± 1.4 | 6.5 ± 2.1 | 6.4 | 0.01 | |
ESR | Before surgery | 38.1 ± 16.7 | 42.2 ± 15.9 | 0.91 | 0.37 |
At last follow up | 24.5 ± 9.3 | 21.2 ± 8.3 | 1.32 | 0.19 | |
CRP | Before surgery | 66.0 ± 25.7 | 67.2 ± 19.8 | 0.18 | 0.86 |
At last follow up | 26.8 ± 7.6 | 28.1 ± 9.3 | 0.53 | 0.6 |
Table 2: Surgical outcomes of minimally invasive vs. conventional surgery. Surgery duration was longer in the minimally invasive group compared to the conventional surgery group. The volume of intraoperative hemorrhage was significantly lower in the minimally invasive group than in the conventional surgery group. The VAS score and ODI for both groups improved significantly at 3 months and at the last follow-up compared to preoperative values. Both VAS score and ODI were better in the early postoperative period in the minimally invasive surgery group than in the conventional surgery group, as well as at the last follow-up.
The spine is one of the most common locations for tuberculosis, besides the lungs. If not treated in a timely manner, nerve function can be compromised, potentially leading to paralysis and other complications. The combination of anti-tuberculous drugs and surgical intervention is widely accepted as the approach to treat severe spinal tuberculosis. Surgical treatment is the most direct and effective method for these patients. The purpose of surgical treatment for spinal tuberculosis is to clear the abscess, restore stability to the spine, and relieve compression of the spinal cord and nerve roots15,16,17. Traditional open surgery involves significant trauma to the patient, substantial blood loss during the procedure, and an increased risk of postoperative infection, along with a prolonged hospital stay and lower overall treatment effectiveness. This surgical approach also has certain limitations and may not be suitable for patients with poor tolerance or compromised physical conditions18,19,20.
With the development of imaging technology and endoscopic techniques, minimally invasive spinal surgery has gradually replaced open surgeries. This technique features smaller incisions, higher safety, and lower levels of pain, making it suitable for various patients21,22. In cases of thoracic or lumbar tuberculosis with a paravertebral abscess but without severe neurological damage or significant kyphotic distortion, minimally invasive abscess debridement and drainage, along with chemotherapy, may provide a better treatment strategy. In the current study, we examined the efficacy of combining percutaneous catheter drainage with chemotherapy. The results indicated that the early Visual Analog Scale (VAS) score11 and Oswestry Disability Index (ODI)12 in the minimally invasive surgery group were better than those in the conventional surgery group. This improvement could be attributed to several factors: minimally invasive anterior abscess removal can avoid extensive tissue damage, protect the posterior column, and prevent injury to the spinal cord and nerve roots.
The results of this study are consistent with previous reports. In the study by Zhang et al.23, 106 patients with paraspinal abscesses due to spinal tuberculosis were treated using computed tomography-guided percutaneous catheter drainage and percutaneous catheter infusion chemotherapy. They found a significantly reduced erythrocyte sedimentation rate three months after surgery and solid bone fusion during an average follow-up of 7.21 years. In the study by Liu et al.24, 17 patients with upper cervical spine tuberculosis were treated using endoscopic anterior cervical debridement combined with posterior fixation and fusion. Significant postoperative neurological improvement was achieved in all patients, with most achieving excellent or good results as measured using the Kirkaldy-Willis criteria. However, few studies have compared the effectiveness and safety of minimally invasive endoscopic surgeries with traditional open-surgical approaches.
While providing direct evidence on the application of minimally invasive surgical treatment for paraspinal abscesses in patients with spinal tuberculosis, this study has several limitations. This is a retrospective study involving a relatively small number of patients, and the follow-up time is short compared to the studies by Zhang and Liu19,20. Multi-center studies with larger sample sizes are necessary for a more objective evaluation of this surgical technique.
In summary, it is essential to choose an appropriate operative measure to treat paravertebral abscesses in patients with spinal tuberculosis to achieve early and complete functional recovery without recurrence of infection. Anterior minimally invasive debridement and bone graft fusion in the treatment of lumbar tuberculosis with severe paraspinal abscesses have significant advantages over conventional methods in terms of early postoperative functional recovery and pain improvement. It is a safe and effective technique for the treatment of lumbar tuberculosis.
The authors declare no competing financial interests or other conflicts of interest.
None.
Name | Company | Catalog Number | Comments |
C-arm fluoroscope | GE Healthcare | https://www.gehealthcare.com/products/surgical-imaging/c-arms-for-orthopedics | |
Endoscope | JIOMAX (Germany) | https://www.joimax.com/en/products/ | used for the surgeical procedure |
SPSS | IBM, Chicago, IL | version 24.0 | software for statistocal analysis |
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