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Effectiveness and safety of percutaneous endoscopic debridement and drainage for spinal infections: a systematic review and meta-analysis

Abstract

Background

Spinal infections (SI) typically manifest with and pose a growing medical challenge. However, current evidence for treating SI is limited and inconclusive. Our aim was to assess the effectiveness and safety of percutaneous endoscopic disc decompression (PEDD) for SI.

Methods

On 20 October 2023, we searched the EMBASE, PubMed, Cochrane Library, China Biology Medicine Disc, China National Knowledge Infrastructure, and Wanfang databases for eligible studies. Cohort studies on SI treated with PEDD, reporting relevant effectiveness or safety outcomes. We assessed study quality using a modified Newcastle–Ottawa Scale and conducted a random-effects meta-analysis to calculate pooled results.

Results

Overall, 36 studies involving 925 patients were included. Erythrocyte sedimentation rate levels decreased significantly at 1-week postoperatively compared with preoperative levels (mean difference [MD] = − 13.48 [95% CI − 15.65 to − 11.31]) and continued to decrease over 3 months. Similarly, the c-reactive protein (CRP), visual analogue scale, and oswestry disability index scores significantly reduced postoperatively. The rates of excellent or good MacNab classification were 92.6% (95% CI 84.1–98.1%). Microbiological diagnostics revealed a 71.7% (95% CI 65.5–77.6%) positive rate in tissue cultures, surpassing blood cultures (odds ratio [OR] 2.72 [95% CI 1.01–7.30]). The rates of complication, reoperation, and mortality were 4.1% (95% CI 1.5–8.0%), 8.6% (95% CI 4.3–14.3%), and 1.7% (95% CI 0.4–4.1%), respectively. Subgroup analyses demonstrated a significantly lower reoperation rate in the group that discontinued antibiotics based on a normal CRP than in the fixed-duration group (2.7% [95% CI 0.3–7.7%] vs 20.1% [95% CI 14.5–26.3%], p = 0.0002). Conversely, ambulation 1 day postoperatively was associated with a higher reoperation rate than ambulation within 5–14 days (16.2% [95% CI 9.3–24.6%] vs 1.1% [95% CI 0.0–6.0%], p = 0.0060).

Conclusion

Our meta-analysis suggests that PEDD is a potentially effective and safe intervention for SI. Optimizing antibiotic discontinuation and postoperative care strategies may contribute to reducing reoperation rate. However, these findings require further validation from controlled studies.

Introduction

Spinal infection (SI) is an inflammatory condition, mainly caused by bacteria or other pathogens, with symptoms that may include persistent back pain, fever, malaise, localized swelling, and stiffness [1]. These infections are classified into primary infections, which are caused by blood or tissue transmission, and secondary infections, which are caused by surgical contamination [2]. The rising incidence of SI globally has been attributed to factors such as an aging population, increasing comorbidities, and higher rates of immunosuppression [3]. Untreated SI leads to debilitating complications including damage to spinal structures, neurological problems, sepsis, and death [4].

The management of SI primarily involves two strategies: conservative antibiotic therapy and surgical interventions. However, successful antibiotic treatment may extend over several weeks or even months to effectively combat the infection [5]. Surgical procedures for SI are known for their invasiveness and often require intricate postoperative care regimens [6,7,8]. Expanding upon the groundwork laid by percutaneous endoscopic lumbar discectomy (PELD), a pioneering technique known as percutaneous endoscopic debridement and drainage (PEDD) has emerged. PEDD employs percutaneous endoscopy to eliminate infectious materials, encompassing diseased tissues and purulent fluids. This less invasive approach shows promise, especially for patients contending with the complexities associated with SI [9, 10].

Mao et al. conducted meta-analyses in 2019 and 2024 to evaluate the effectiveness and safety of PEDD, incorporating 9 and 26 studies, respectively [6, 11]. However, both analyses were limited to three specific outcome measures: pain control satisfaction, microbiological positivity rate, and reoperation rate. Pain control satisfaction was defined as a Visual Analog Scale (VAS) score of ≤ 3 or an Oswestry Disability Index (ODI) score of ≤ 50 at the final follow-up. These outcomes, however, may be influenced by baseline preoperative pain levels and the duration of follow-up, which introduces potential biases. Consequently, there remains a need for more comprehensive and reliable outcome measures for a thorough evaluation. This study seeks to address these limitations by providing a more robust assessment of the efficacy and safety of PEDD in the treatment of SI.

Methods

Methods adhered to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) and the Assessing the Methodological Quality of Systematic Reviews (AMSTAR) guidelines [12, 13]. The study was registered in PROSPERO (CRD42023428502).

Search strategy

On 20 October 2023, we conducted a comprehensive search of the EMBASE, PubMed, Cochrane Library, China Biology Medicine disk, China National Knowledge Infrastructure, and Wanfang databases for eligible studies, without restrictions on the start date. Studies in all languages were included, and for non-English articles, translation was performed using professional translation services and/or institutional resources when necessary. The keyword combinations used for the search are detailed in Table 1. In addition, we manually checked the reference lists of all included studies and relevant review articles to identify any potentially missed studies.

Table 1 Search strategy

Study selection criteria

The inclusion criteria were: (1) cohort studies involving SI, including both primary and secondary infections, such as vertebral osteomyelitis, discitis, and epidural abscesses; (2) studies on the use of PEDD to treat SI, including unilateral or bilateral percutaneous endoscopic debridement; and (3) studies reporting of outcomes related to efficacy and/or safety. Primary infections were defined as those caused by blood or tissue transmission of pathogens, whereas secondary infections were defined as those resulting from surgical contamination during procedures. The diagnosis of SI primarily relies on microbiological evidence, including blood and tissue cultures or molecular diagnostics, as well as imaging studies such as X-ray, computed tomography (CT), and magnetic resonance imaging (MRI).

The exclusion criteria were: (1) studies with percutaneous endoscopic debridement without intraoperative irrigation or postoperative drainage; (2) studies with fewer than five participants; (3) studies involving vertebral fusion or fixation in conjunction with PEDD; (4) instances of duplicate publications; and (5) review articles, comments, case reports, letters, animal trials, or cadaveric studies.

Two investigators (GZZ and ZL) independently screened article titles and abstracts from the literature search. Full texts of potentially eligible studies were then assessed for final inclusion. Discrepancies, such as differing interpretations of the inclusion and exclusion criteria, were resolved through structured discussions. A third investigator (XSC) mediated by consulting the original study data and standardized scoring guidelines to ensure consensus.

Data extraction and quality assessment

In a preconceived and standardised data extraction form, information was collected regarding the name of the first author, year of publication, title, journal, study country, study design, study period, segment of surgery, proportion of tuberculosis (TB) cases, patient demographics, antibiotic usage strategy, type of intraoperative irrigation solution, postoperative continuation of irrigation, time to initiate postoperative ambulation, number of participants, outcomes of microbiological diagnostics, outcomes related to surgical effectiveness, and safety. Instances of reoperation or mortality attributed to antibiotic discontinuation were excluded from the analysis. Two investigators (GZZ and ZL) independently extracted the data from individual studies. Discrepancies were resolved through structured discussions. A third investigator (XSC) checked the extracted data, and disagreements were unanimously resolved.

We utilized a modified version of the Newcastle–Ottawa Scale (NOS) tailored to the characteristics of single-arm cohort studies. The revised scale includes six items, retaining key elements from the original, such as the representativeness of the study population and follow-up duration, while removing items specific to comparative studies (e.g., selection of the non-exposed cohort, ascertainment of exposure, and absence of outcomes at the start of the study). Additionally, new items were introduced to address the specific needs of single-arm studies, including clear inclusion and exclusion criteria, detailed descriptions of the surgical procedures and postoperative care, comprehensive documentation of patient demographic information, and explicit follow-up processes. Studies with NOS scores of 1–2, 3–4, and 5–6 were considered of low, moderate, and high quality, respectively. Two investigators (GZZ and ZL) independently assessed the methodological quality of the included studies using the modified NOS. Discrepancies, such as differences in scoring follow-up duration or the representativeness of the population, were resolved through structured discussions. A third investigator (XSC) acted as a mediator, referring to the original study data and standardized scoring guidelines to ensure a unanimous resolution.

Outcomes

Our primary outcomes comprised three domains: clinical parameters (erythrocyte sedimentation rate [ESR] and C-reactive protein [CRP]), patient-reported outcomes (Visual Analog Scale [VAS] for pain and Oswestry Disability Index [ODI] for functional impairment), and safety outcomes (complication rates, MacNab satisfaction scores, and reoperation rates). We pooled the mean values of ESR, CRP, VAS, and ODI at 1 day before surgery and at 1 day, 1 week, 1 month, 3 months, and 6 months after surgery. Only time points with data from more than three studies were included, using MD for comparison. We pooled the rates of culture-positive, MacNab (excellent or good), reoperation, mortality, and complications, with odds ratio (OR) employed for comparing the rates between the two groups. Furthermore, we conducted a subgroup analysis of reoperation rates based on several factors, including the type of infection, duration of antibiotic use, intraoperative irrigation, postoperative continuation of irrigation, and time to initiate ambulation. Using univariate meta-regression, we calculated the p values for each subgroup to determine whether the observed differences were significant.

Statistical analysis

Due to the high heterogeneity (I2 > 50%) and clinical diversity among the included studies, we opted to use a random-effects model to calculate the pooled results and their 95% confidence intervals (CI). Egger’s test was used to detect publication bias, and the trim-and-fill method was applied to adjust for it. Zero-event studies were included with continuity corrections to stabilize variance estimates, and sensitivity analyses were performed to assess the impact of outliers. For studies with missing data, only complete cases were analyzed. All p values were two-sided, with significance set at p < 0.05. Statistical analysis was performed using the “meta” package in R (version 3.4.3).

Results

Study selection and characteristics

Of the 8529 potentially eligible studies, 5425 were screened for titles and abstracts after removing duplicates, and 152 full-text articles were reviewed (Fig. 1). After a full-text review, 36 studies involving 925 individuals were included in the meta-analysis [10, 15,16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49].

Fig. 1
figure 1

Study selection

Among the 36 studies, 19 (52.8%), 11 (30.6%), and 3 (8.36%) originated from mainland China, Taiwan, and Japan, respectively, and the remaining three were from South Korea, India, and the United States. Twenty-eight studies (77.8%) were conducted in English, and eight (22.2%) were conducted in Chinese. Furthermore, among the interventions, 3 studies (8.3%) explored bilateral percutaneous endoscopic debridement, whereas 33 (91.7%) focused on unilateral percutaneous endoscopic debridement (Table 2).

Table 2 Detailed characteristics of individual study

Regarding intraoperative irrigation strategies, 21 (58.3%), eight (22.2%), and four studies (11.1%) employed physiological saline, antibiotic, and iodine solutions, respectively; whereas information on irrigation was not provided in three studies (8.36%). Concerning postoperative irrigation strategies, 5 studies (13.9%) used antibiotic solutions and 4 studies (11.1%) employed physiological saline; whereas postoperative irrigation was not conducted in 27 studies (75.0%). All nine studies reporting postoperative irrigation strategies were conducted in mainland China. Regarding postoperative ambulation strategies, 7 studies (19.4%) indicated that patients began ambulation one day after surgery, 7 studies (19.4%) recommended ambulation within 5–14 days, and 3 studies (8.36%) reported patients initiating ambulation between 21 and 60 days post surgery; whereas information on ambulation was not provided in 19 studies (52.8%).

Of the 36 studies, 22 (61.1%) were rated as high quality, whereas 14 (38.9%) were considered moderate quality. Fifteen studies (41.7%) lacked detailed information regarding the inclusion or exclusion criteria, and fifteen studies (41.7%) did not provide comprehensive follow-up information. Additionally, five studies (13.9%) had a follow-up duration of < 1 year and one study did not report the follow-up period (Supplementary Figs. S1, S2).

Primary outcomes

Assessment of the effectiveness of PEDD for SI

The 1-week postoperative ESR was significantly lower than the preoperative score (pooled MD = − 13.48 [95% CI − 15.65 to − 11.31, I2 = 33%]) (Supplementary Fig. S3), and ESR continued to decline within 3 months postoperation (See Table 3 and Fig. 2 for details). Similarly, the 1-week postoperative CRP was significantly lower than the preoperative score (pooled MD = − 26.77 [95% CI − 37.63 to − 15.91, I2 = 94%]) (Supplementary Fig. S4), and CRP continued to decline within 3 months postoperation.

Table 3 The outcomes of mean value
Fig. 2
figure 2

Postoperative trends of the mean values of ESR, CRP, VAS, and ODI

The 1-day postoperative VAS score was significantly lower than the preoperative score (pooled MD = − 3.70 [95% CI − 4.70 to − 2.70, I2 = 98%]) (Supplementary Fig. S5), and the VAS scores continued to decline within 3 months postoperation. Similarly, the 1-week postoperative ODI score was significantly lower than the preoperative score (pooled MD = − 30.18 [95% CI − 38.94 to − 21.43, I2 = 93%]) (Supplementary Fig. S6), and the ODI scores continued to decline within 3 months postoperation (See Table 3 and Fig. 2 for details).

Further, 8 cohorts of 164 individuals were eligible for calculating excellent or good rates in the MacNab classification. The pooled excellent or good rate in the MacNab classification was 92.6% (95% CI 84.1–98.1%; I2 = 70%) (Table 4 and Supplementary Fig. S7).

Table 4 The outcomes of rate

Although the Japanese Orthopaedic Association (JOA) score and other similar clinical outcome measures were collected, they were not reported in detail due to the limited number of studies that included these measures.

Assessment of PEDD safety for SI

Overall, 25 cohorts of 633 individuals were eligible for the complication rate analysis. The pooled complication rate was 4.1% (95% CI 1.5–8.0%; I2 = 74%) (Table 4 and Supplementary Fig. S8). A total of 36 complications were reported, of which 26 (72.2%) were mild and 7 (19.4%) were serious. The rate of mild complications was higher than that of serious complications (2.9% [95% CI 0.9–6.1%] vs 0.2% [95% CI 0.0–0.8%]). Additionally, 28 cohorts comprising 651 individuals were eligible for reoperation. The pooled reoperation rate was 8.6% (95% CI 4.3–14.3%; I2 = 80%) (Table 4 and Supplementary Fig. S9). Further, 26 cohorts of 625 individuals were eligible for reoperation stratified by the cause of uncontrolled infection or intractable pain due to kyphosis. The pooled reoperation rate caused by uncontrolled infection was 3.3% (95% CI 1.1–6.8%; I2 = 75%), and the pooled reoperation rate caused by kyphotic deformity was 3.4% (95% CI 1.0–7.3%; I2 = 79%).

Further, 15 cohorts comprising 359 individuals were eligible for evaluating the mortality rate. The pooled mortality rate was 1.7% (95% CI 0.4–4.1%; I2 = 41%) (Table 4 and Supplementary Fig. S10). Fifteen cohorts were eligible for assessing the mortality rate stratified by the cause of uncontrolled infection or morbidity. The pooled mortality rate caused by uncontrolled infection was 0.4% (95% CI 0.0–1.3%; I2 = 6%), and the pooled mortality rate caused by comorbidities was 0.6% (95% CI 0.0–2.0%; I2 = 35%).

Secondary outcomes

Outcomes of microbiological diagnostics

Next, 38 of 683 individuals were eligible for calculating the tissue culture positive rate. The pooled positive rate was 71.7% (95% CI 65.5–77.6%; I2 = 67%) (Table 4 and Supplementary Fig. S11). Further, 6 cohorts of 172 individuals were eligible for comparing the culture-positive rates between tissue and blood cultures. The pooled positive rates of tissue and blood cultures were 59.6% (95% CI 40.3–77.5%; I2 = 83%) and 35.5% (95% CI 25.5–46.3%; I2 = 46%), respectively. The pooled OR for the two positive rates in six studies was 2.72 (95% CI 1.01–7.30; I2 = 74%) (Supplementary Fig. S12).

Subgroup analysis of the reoperation rate

We performed a subgroup analysis on the reoperation rate, stratified by the duration of antibiotic usage, time to initiate ambulation, intraoperative irrigation, postoperative continuation of irrigation, type of infection, proportion of males, segment, and quality of study. Notably, significant differences emerged primarily within the subgroups of antibiotic usage duration and time to initiate ambulation (Table 5).

Table 5 Subgroup analysis of reoperation rate

Duration of antibiotic usage: The subgroup analysis revealed a significant difference in reoperation rates between the two antibiotic usage strategies. The group that discontinued antibiotics on the normal of inflammatory markers had a substantially lower reoperation rate than the group with a fixed duration strategy (2.7% [95% CI 0.3–7.7%, I2 = 77%] vs 20.1% [95% CI 14.5–26.3, I2 = 0%], p = 0.0002). This finding was consistent across the subgroup analyses of reoperation rates caused by uncontrolled infection and kyphotic deformity (Table 5).

Time to initiate postoperative ambulation: The timing of postoperative ambulation had a significant impact on reoperation rates. Patients who began walking 1 day postoperatively had a significantly higher reoperation rate than those who initiated ambulation 5–14 days post operation (16.2% [95% CI 9.3–24.6%, I2 = 53%] vs 1.1% [95% CI 0.0–6.0, I2 = 71%], p = 0.0060). Furthermore, for reoperation rates caused by kyphotic deformity, the group initiating ambulation 1 day post surgery had a significantly higher reoperation rate than the 5–14 day group (13.3% [95% CI 6.4–22.4%, I2 = 64%] vs 0.0% [95% CI 0.0–0.5, I2 = 0%], p < 0.0001). A similar trend was observed for reoperation rates because of uncontrolled infection; however, univariate meta-regression did not yield significant results (Table 5).

Comparing the effectiveness and safety of PEDD and open surgery

Four studies [20, 35, 39, 49] compared PEDD with open surgery for treating SI. Among them, three studies (comprising 107 patients) focused on VAS scores. No statistically significant differences were observed in preoperative VAS scores between PEDD and open surgery. However, postoperatively, PEDD showed a significantly lower VAS score at 1-week compared to open surgery (pooled MD = − 1.06 [95% CI − 1.24 to − 0.89, I2 = 0%]) (Supplementary Fig. S13).

Two studies (involving 86 patients) were eligible for comparing ODI scores. No statistically significant differences were found in preoperative ODI scores between PEDD and open surgery. However, in the postoperative period, PEDD demonstrated a significantly lower ODI score at 1-week compared to open surgery (pooled MD = − 7.02 [95% CI − 9.00 to − 5.04, I2 = 0%]) (Supplementary Fig. S14).

Three studies (involving 251 patients) were eligible for comparison among complication rates, and PEDD demonstrated a significantly lower complication rate than open surgery (pooled OR = 0.25 [95% CI 0.11–0.55, I2 = 0%]) (Supplementary Fig. S15). Additionally, three studies (involving 254 patients) were eligible for comparing hospitalisation duration, with PEDD revealing a shorter hospital stay than open surgery; however, this difference was not significant (pooled MD = − 19.79 [95% CI − 50.63 to 11.04, I2 = 100%]) (Supplementary Fig. S16).

Sensitivity analysis and publication bias

We performed a sensitivity analysis of the MD of the ESR at one week postoperatively and preoperatively and found no significant change in the pooled MD after excluding any of the studies (point estimates and 95% CIs for MD were less than 0), suggesting that the pooled MD was stable. For example, excluding study conducted by Cao et al. Resulted in an MD of − 13.61 (95% CI − 16.25 to − 10.96), while excluding study conducted by Hsu et al. led to an MD of − 13.17 (95% CI − 15.37 to − 10.97), showing minimal variation across the analyses. Similarly, sensitivity analyses for other primary outcomes also demonstrated stability (Supplementary Figs. S17, S18, S19, S20, S21, S22, S23, S24).

Egger’s test for publication bias was not significantly associated with primary outcomes, including complication (p = 0.4755), reoperation (p = 0.5607), mortality (p = 0.7730), and culture-positive rates (p = 0.5330). Similarly, publication bias was not significant for the pooled MD of ESR, CRP level and VAS and ODI scores (p > 0.05).

Discussion

We conducted a comprehensive systematic review and meta-analysis of 36 studies (925 patients) evaluating PEDD for SI treatment. Four key findings were as follows: First, there were significant postoperative reductions in ESR, CPR, VAS and ODI scores, persisting for 3 months. Second, the microbiological diagnostics rate of tissue culture after PEDD surpassed that of blood cultures. Third, the rates for excellent or good outcomes based on the MacNab classification, as well as complication, reoperation, and mortality rates, were 92.6%, 4.1%, 8.6%, and 1.7%, respectively. Finally, the group discontinuing antibiotics showed a significantly lower reoperation rate compared to CRP normalization, while the group ambulating 1-day postoperatively exhibited a higher reoperation rate compared to ambulation within 5–14 days.

In this study, we observed a significant reduction in inflammatory markers such as ESR and CRP one week postoperatively, with levels gradually approaching normal within the 1–3 month follow-up period. These findings suggest effective control of acute inflammation, which is clinically relevant as it reflects a reduced burden of infection and supports tissue healing. Pain, as measured by VAS scores, decreased significantly, with the average score falling below 4 by the 1-day mark. This rapid pain relief not only highlights the efficacy of PEDD in early symptom management but also facilitates patient mobility and accelerates rehabilitation, which are critical for recovery. Additionally, ODI scores showed significant improvement, dropping below 30 at 1 month. This indicates a marked reduction in disability and suggests that patients can resume normal daily activities, which is a key measure of functional recovery and quality of life [50]. Together, these findings underscore the clinical relevance of PEDD in achieving favorable short- and medium-term outcomes.

These improvements in inflammation, pain, and function resulted in a high rate of excellent or good outcomes (92.6%) based on the MacNab classification. Although no specific meta-analysis on the MacNab satisfaction rate for PEDD or other SI procedures exists, the pooled excellent or good rate for PELD in treating lumbar disc herniation is reported at 82.4% [50]. Patients with SI often experience a significant decline in quality of life due to chronic pain and infection, but symptom relief after surgery leads to notable improvements in satisfaction. In contrast, while PELD effectively alleviates nerve compression and related pain, its effectiveness may be limited by more complex lesions, such as free disc fragments or calcified foci, which could affect patient satisfaction.

We observed a complication rate of 4.1% for PEDD, with the majority (72.2%) being mild complications, such as limb numbness. When comparing this complication rate with that of similar procedures, it is noteworthy that biportal endoscopic surgery [50] and PELD [51] for treating lumbar disc herniation have reported complication rates of 7.9% and 3.1%, respectively. The complication rate associated with PEDD appears to be relatively acceptable. Overall, during the follow-up period, patients with SI treated with PEDD had a mortality rate of 1.7%, with only 0.4% attributed to uncontrolled infections. Kim et al. [52] investigated a cohort of 10 695 patients with pyogenic SI and reported a mortality rate of up to 1.2% at 12 weeks after onset, which increased to 3.3% when combined with infections at other sites. Additionally, Park et al. assessed 153 patients with hematogenous vertebral osteomyelitis who underwent open surgical treatment for infection, revealing that 10 patients (6.5%) died during hospitalisation, with 2 deaths (1.3%) directly linked to the infection [53]. Considering that the majority of patients undergoing PEDD treatment had previously failed antibiotic therapy or were elderly, and with the follow-up period exceeding 12 months in 15 studies reporting mortality rates, the observed 1.7% mortality rate in our study could be deemed acceptable.

Our study found a reoperation rate of 8.6% (95% CI 4.3–14.3%), which is similar to the results of Mao et al.'s 2024 [11] study (8% [95% CI 3–13%]). Furthermore, we conducted a comprehensive analysis of the underlying reasons for reoperations. Only 3.3% of reoperations were due to uncontrolled infections, while 3.4% were associated with spinal instability or intractable pain. These findings emphasize the importance of prioritizing infection control and considering factors related to spinal instability in order to reduce reoperation rates. Potential deformities and their consequences should also be taken into account postoperatively. For example, some studies have suggested that patients with severe local kyphosis (> 30°) or large bony defects (more than half of the vertebral body) may not be suitable candidates for PEDD treatment [20, 31]. Factors such as the location of infection can influence deformities in SI patients [54]. Future research should explore the relationship between the type or severity of deformities and the need for secondary surgery.

We conducted subgroup analyses of the reoperation rate and discovered that using a normal CRP as the criterion for discontinuing antibiotics and implementing antibiotic irrigation during and postoperatively may offer advantages for reducing the reoperation rate. However, early ambulation within 1-day postoperatively is associated with an increased reoperation rate. These findings highlight the potential to optimize clinical outcomes with PEDD by adjusting antibiotic administration and postoperative care strategies. Nonetheless, it is important to acknowledge certain limitations in our study, including the absence of comparative studies and the relatively limited sample sizes of the included studies. Therefore, further validation of these findings is warranted through well-designed randomised controlled trials.

In addition to its effectiveness in treating SI, PEDD offers the added benefit of obtaining tissue samples for bacterial culture. Mao et al. included 26 studies with 565 participants and reported a bacterial culture positivity rate of 73% [11]. Our analysis, which incorporated 30 studies with 683 participants, yielded a similar result of 71.7%. This relatively high positivity rate helps identify the most effective pathogen-specific antibiotics, avoiding unnecessary prolonged use of broad-spectrum antibiotics. This approach not only minimizes the risk of adverse effects but also supports antibiotic stewardship by reducing the development of antimicrobial resistance [34, 55, 56]. Moreover, our results revealed that tissue culture positivity rates were significantly higher than blood culture positivity rates, with an odds ratio of 2.72 (95% CI 1.01–7.30). These results highlight the diagnostic advantage of PEDD, as it allows for direct sampling of infected tissue, reducing the risk of false negatives associated with the lower sensitivity of blood cultures.

Our comparison of PEDD with open surgery revealed that PEDD offers notable advantages in pain relief (as indicated by VAS scores), functional recovery (ODI scores), and reduced complication rates. As a minimally invasive technique, PEDD also minimizes trauma, blood loss, and recovery time, making it a promising alternative for patients with mild infections or stable spinal conditions. However, it may not be suitable for individuals with complex or extensive infections that necessitate open surgery. Despite these benefits, the steep learning curve associated with PEDD (rooted in its foundation on PELD) highlights the importance of surgeon proficiency for successful outcomes [57]. Consequently, enhancing physician training and providing robust technical support are crucial for the wider adoption of PEDD and the optimization of clinical results.

This study has some limitations. First, most of the included studies were single-arm cohorts with small sample sizes. This could introduce bias and limit the generalisability of our findings. Second, only four studies directly compared PEDD with open surgery. Therefore, further comparative research is required to comprehensively understand the differences between the two approaches. Third, the predominance of studies originating from Asia (35 out of 36; 91.7%) may restrict the generalizability of these findings to populations in other regions. Fourth, substantial heterogeneity was observed among the included studies, likely stemming from differences in patient populations, surgical techniques, and antibiotic protocols. This heterogeneity poses challenges to drawing definitive conclusions from the available data. Finally, the variability in follow-up durations across studies may have impacted the consistency and interpretation of the reported outcomes.

Conclusions

PEDD is a potentially effective and safe intervention for SI. Optimizing antibiotic discontinuation and postoperative care strategies may contribute to reducing reoperation rate. However, these findings require further validation from controlled studies.

Availability of data and materials

The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.

Abbreviations

SI:

Spinal infection

PELD:

Percutaneous endoscopic lumbar discectomy

PEDD:

Percutaneous endoscopic debridement and drainage

ESR:

Erythrocyte sedimentation rate

CRP:

C-reactive protein

VAS:

Visual analogue scale

ODI:

Oswestry disability index

NOS:

Newcastle–Ottawa scale

OR:

Odds ratio

CI:

Confidence intervals

MD:

Mean difference

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Funding

Yunnan Fundamental Research Projects, 202301BE070001-036, Medical Joint Special Project of Kunming University of Science and Technology, KUST-AN2023004Z, KUST-AN2023018Y, Yunnan Xingdian Talent Support Project-Famous Doctor Project, XDYC-MY-2022-0071.

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GZZ, XRL, XSC and CS conceived and designed the study, collected the data, performed the formal analysis, curated the data, and wrote and prepared the original draft. GZZ and ZL collected the data and validated the study. All authors contributed to the methodology, interpreted the results, contributed to writing the manuscript, approved the final version, and had final responsibility for the decision to submit for publication.

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Correspondence to Xuesong Chen or Chao Song.

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Zhou, G., Liu, X., Liang, Z. et al. Effectiveness and safety of percutaneous endoscopic debridement and drainage for spinal infections: a systematic review and meta-analysis. J Orthop Surg Res 20, 135 (2025). https://doiorg.publicaciones.saludcastillayleon.es/10.1186/s13018-025-05540-6

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