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Arch Iran Med. 28(9):506-513. doi: 10.34172/aim.34624

Original Article

Prevalence and Risk Factors of Postoperative Spinal Infections: A Five-year Study in Northwestern Iran

Seyed Taher Mousavi Conceptualization, Formal analysis, Investigation, Project administration, Resources, Supervision, Writing – original draft, 1, * ORCID logo
Farhad Mirzaei Data curation, Methodology, Software, Writing – review & editing, 1
Mohammad Shimia Data curation, Validation, Writing – review & editing, 1
Moslem Shakeri Investigation, Methodology, Visualization, Writing – review & editing, 1

Author information:
1Department of Neurosurgery, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran

*Corresponding Author: Seyed Taher Mousavi, Email: dr.tahermusavi@gmail.com

Abstract

Background:

Surgical site infections (SSIs), particularly after spinal procedures, remain a major concern despite advances in infection control. This study aimed to determine the prevalence and associated risk factors of postoperative spinal infections in northwestern Iran.

Methods:

A cross-sectional study was conducted on 500 adult patients (≥18 years) who underwent spinal surgery in two referral hospitals in Tabriz (Imam Reza and Shohada) between March 2019 and February 2024. Postoperative infections were confirmed by infectious disease specialists. Data on demographics and surgical variables (including surgical site, approach, duration, blood loss, and transfusion) were collected using a standardized checklist. Statistical analyses were conducted in SPSS version 23.0 using Chi-squared and independent samples t-tests. Logistic regression was performed to estimate adjusted odds ratios (ORs) with 95% confidence intervals (CIs).

Results:

The prevalence of postoperative spinal infections was 6%. Staphylococcus aureus was the most common pathogen (66.7%). Significant risk factors included female sex, older age, corticosteroid use, diabetes mellitus, longer surgery duration (>4 hours), blood loss (>1 liter), and blood transfusion (P<0.05). Diabetes (OR=5.90, 95% CI: 2.30–15.20) and prolonged surgery (OR=6.90, 95% CI: 2.50–19.00) showed the strongest associations. No significant associations were found for BMI, smoking, hypertension, CRP, ESR, surgical site, or technique.

Conclusion:

A 6% infection rate was identified, with several clinical and demographic factors increasing risk. Recognizing these predictors is essential for prevention. Broader, multi-center studies are recommended to validate findings and inform national surgical infection control policies.

Keywords: Microorganism, Postoperative infections, Risk factors, Spine, Surgery

Copyright and License Information

© 2025 The Author(s).
This is an open-access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Cite this article as: Mousavi ST, Mirzaei F, Shimia M, Shakeri M. Prevalence and risk factors of postoperative spinal infections: a five-year study in Northwestern Iran. Arch Iran Med. 2025;28(9):506-513. doi: 10.34172/aim.34624


Introduction

Despite significant advances in medical care, particularly in surgical techniques, managing postoperative infectious complications remains one of the major challenges in healthcare systems.1 Surgical site infections (SSIs) are the most prevalent infectious complication in surgical wards and the second most frequent type of hospital-acquired infection, accounting for approximately 25% of all hospital infections.2 The occurrence of these infections could lead to treatment failure, prolonged hospitalization, increased healthcare costs and even mortality.3

Previous studies have demonstrated that numerous factors contribute to the development of SSIs, which could be broadly categorized into patient- and surgery-related factors.4 The first category includes host-related factors, which are often non-modifiable or difficult to control. These factors include old age, obesity, diabetes, smoking, previous surgeries or infections at the same site, previous radiation therapy, chronic skin conditions such as psoriasis, immune and nutritional status and adherence to postoperative care.5 In the second category, surgical factors, such as type of surgery (e.g. posterior approach), placement of metallic implants, bone graft harvesting, excessive bleeding, duration of surgery, adherence to sterile techniques, traffic in the operating room, instrument contamination and use of intraoperative fluoroscopy, are key factors that contribute to the development of infections. Moreover, the rising prevalence of resistant pathogens such as methicillin-resistant Staphylococcus aureus (MRSA) and gram-negative bacteria has further complicated this challenge.6

Among various types of surgeries, spinal surgeries are at higher risk for SSIs due to their complexity, prolonged operative duration and patients’ specific conditions (such as old age, chronic diseases, or use of immunosuppressive medications).7,8 SSIs are considered the third most prevalent complication following spinal surgeries.9,10 These infections result in patient readmission, adverse outcomes and substantial additional costs. In the United States, this issue results in an estimated $1 to $10 billion in direct and indirect medical costs annually and is associated with approximately 8,000 deaths per year.11 Additional risk factors for infection in these patients include the use of drains and catheters, hospitalization for more than 48 h, revision surgeries and the need for blood transfusions. Some studies have reported postoperative infection rates of up to 12% following spinal surgery, which is considerably higher than those observed after other types of surgical procedures.12,13 However, despite this broad body of literature, there is considerable variability in the methods, populations, and definitions used across studies, making comparisons and generalizations difficult.14,15 Additionally, many studies fail to quantify the relative impact of individual risk factors or control for confounding variables, which limits their practical applicability.16 These limitations highlight the need for more structured and context-specific evaluations.

In addition, most existing literature comes from high-income countries, and there is a noticeable lack of regional data from the Middle East and North Africa (MENA) region, including Iran. Despite the clinical importance of SSIs in these settings, epidemiological studies specifically focusing on spinal surgeries remain scarce, fragmented, or outdated.17 Moreover, previous studies often remain descriptive and do not offer critical analysis regarding the relative impact or interaction of various risk factors. This lack of analytical perspective makes it difficult to prioritize interventions or adapt global guidelines to local contexts.

Even with the implementation of preventive strategies (such as prophylactic antibiotics, strict sterilization protocols, and staff training) a substantial number of postoperative spinal infections continue to occur. In low- and middle-income countries, one major reason for this is the limited availability of reliable data regarding both the prevalence and the specific risk factors relevant to local clinical settings.17 Lack of accurate data regarding the prevalence and relative contribution of each risk factor seems to be among the main reasons for the insufficient control of these complications.18 Documenting the prevalence of postoperative spinal infections is of particular importance for several reasons, including preoperative consultation with the patient, improving the quality of services and, in some cases, addressing legal issues.19-21

Therefore, to address this gap in both regional epidemiology and analytical evaluation of risk factors, the present study was conducted to investigate the prevalence of postoperative infections following spinal surgeries and identify the associated risk factors in two major teaching and treatment centers in Tabriz, namely Imam Reza and Shohada hospitals, which serve as specialized and subspecialized referral centers in northwestern Iran.


Materials and Methods

Study Design, Setting and Sampling

This cross-sectional study was conducted on the medical records of patients undergoing spinal surgeries in two specialized referral centers, Imam Reza and Shohada hospitals, in Tabriz, northwestern Iran, from March 2019 to February 2024. The minimum sample size was estimated to be 100 patients with postoperative infections using Cochran’s formula, considering α = 0.05, absolute error (d) of 0.1 and P = 0.5. However, all eligible medical records within the study period were included using a census sampling method, resulting in a total sample size of 500 patients. This approach was chosen to enhance the statistical power and generalizability of the findings. Inclusion criteria were patients over 18 years of age who had undergone spinal surgery, availability of clinical documentation, including laboratory results (CBC, ESR and CRP), pre- and postoperative radiographic images, a detailed surgical report in the medical records and documented pre- and postoperative clinical examinations. Records with missing essential data (such as laboratory results or surgical reports) were excluded from the study.

After obtaining ethical approval and access to the hospitals’ medical archives, the researcher (a trained resident) systematically reviewed and identified all spinal surgery records. Data were collected through manual review of both electronic and paper-based medical records, as the hospital archives contained a mix of structured electronic data and unstructured paper files. In the initial phase, records containing diagnoses and surgical reports were extracted. Subsequently, cases with a confirmed diagnosis of SSIs, verified by an infectious disease specialist, were identified. The diagnosis of SSIs was based on clinical signs and symptoms, supported by microbiological confirmation through laboratory cultures when available, and validated by an infectious disease specialist to ensure diagnostic accuracy. Patient data were recorded in a standard data collection checklist and later reviewed by the research team to enhance accuracy. To reduce potential information bias, data extraction was independently performed by two researchers and discrepancies were resolved through discussion and review by a third investigator.

The checklist consisted of two main sections. The first section included demographic and background information such as gender, age, history of diabetes and hypertension, body mass index (BMI), smoking status, use of immunosuppressive medications, history of previous surgeries (none, one, or multiple), history of previous SSIs, and preoperative white blood cell (WBC) count and C-reactive protein (CRP) levels.

The second section covered surgical details including the surgical site (cervical, thoracic, lumbar, or sacral), type of surgery (discectomy, decompression, fusion, osteotomy, or debridement), surgical duration (categorized as less than 2 hours, 2–4 hours, or more than 4 hours, with “longer surgery duration” defined as more than 4 hours), blood loss volume (defined as less than or more than 1 liter), and number of blood transfusion units (categorized as none, one unit, two units, or more than two units). The timing of blood transfusion was not included in the present analysis.

This observational study was reported in accordance with the STROBE (Strengthening the Reporting of Observational Studies in Epidemiology) checklist to ensure transparency and completeness in reporting.

Statistical Analysis

The data were analyzed using SPSS 23.0. The normality of quantitative variables was first assessed using Kolmogorov-Smirnov test. For the description of quantitative variables (if normally distributed), mean and standard deviation were used, while frequency and percentage were used for qualitative variables. The correlation between qualitative variables and occurrence of infection was examined using the Chi-squared test. The difference in quantitative variables between the two groups (infected and non-infected) was assessed using the independent samples t-test. Additionally, to identify independent risk factors associated with postoperative spinal infections, a multivariate logistic regression analysis was performed, reporting adjusted odds ratios (ORs) with 95% confidence intervals (CIs) and the corresponding P values. A P value of less than 0.05 was considered statistically significant.


Results

Demographic and Background Characteristics of the Study Sample

As shown in Table 1, the mean age of the patients was 42.78 years ( ± 5.5), with an approximate age range of 26 to 59 years, and their mean weight was 82.18 kg ( ± 6.5). In terms of gender, 69% were female and the remaining were male. Smoking was reported in 15.6% of the patients, history of previous surgeries in 10%, history of corticosteroid use in 17.2%, diabetes mellitus in 14% and hypertension in 24.8%.


Table 1. Demographic and Background Characteristics of the Studied Patients (n = 500)
Qualitative variables Variable levels Frequency (%)
Gender Male 155 (31.0)
Female 345 (69.0)
Smoking No 422 (84.4)
Yes 78 (15.6)
History of surgery No 450 (90.0)
Yes 50 (10.0)
History of corticosteroid use No 414 (82.8)
Yes 86 (17.2)
History of hypertension No 376 (75.2)
Yes 124 (24.8)
History of diabetes No 430 (86.0)
Yes 70 (14.0)
Quantitative variables Mean (SD)
Age (years) 42.78 (5.5)
Weight (kg) 82.18 (6.5)

Surgical and Therapeutic Characteristics of the Study Sample

In this study, the mean (standard deviation) levels of preoperative inflammatory markers, including CRP and ESR, were reported at 10.78 ( ± 2.1) and 10.16 ( ± 2.5), respectively. The lumbosacral region (75%) was the most common surgical site, and the posterior approach (85%) was the most frequently applied approach. A combination of fusion and laminectomy (45%) was the predominant surgical method among the participants. Surgical duration lasted 2‒4 h in half of the patients (50%). Blood loss was less than 600 mL in more than half of the patients (62%). Additionally, 65% of the patients did not require blood transfusions. Further details on surgical and therapeutic characteristics are presented in Table 2.


Table 2. Surgical and Therapeutic Variables of the Studied Patients (n = 500)
Qualitative variables Variable levels Frequency (%)
Surgical site Lumbosacral 375 (75.0)
Cervical 100 (20.0)
Thoracic 25 (5.0)
Approach Posterior 425 (85.0)
Anterior 65 (13.0)
Anteroposterior 10 (2.0)
Surgical method Laminectomy 150 (30.0)
Fusion and laminectomy 225 (45.0)
Laminectomy and diskectomy 125 (25.0)
Surgical duration Less than 2 h 150 (30.0)
2‒4 h 250 (50.0)
More than 4 h 100 (20.0)
Blood loss volume Less than 600 cc 310 (62.0)
Between 600 cc and 1 liter 125 (25.0)
More than 1 liter 65 (13.0)
Blood transfusion None 325 (65.0)
1 unit 115 (23.0)
2 units 60 (12.0)
Quantitative variables Mean (SD)
CRP 10.78 (2.1)
ESR 10.16 (2.5)

Prevalence of Infections Following Spinal Surgeries in the Study Sample

Overall, 30 patients (6% of the total sample) developed SSIs following spinal surgeries. Staphylococcus aureus was the most common infectious agent among the participants, followed by coagulase-negative staphylococci and Pseudomonas (Figure 1).

aim-28-506-g001
Figure 1.

Distribution of Microorganisms in Postoperative Spinal Infections (n = 30)


Comparison of Demographic and Background Variables Between the Two Patient Groups

Table 3 compares the demographic and background variables between infected and non-infected groups. The infection rate among females was 6.96%, compared to 3.87% among males (P = 0.021). Patients with a history of corticosteroid use had an infection rate of 26.74%, versus 1.69% in those without (P = 0.042). Similarly, the infection rate was 35.71% among diabetics compared to 1.16% in non-diabetics (P = 0.002). No significant differences were observed regarding weight, smoking status, history of previous surgeries, or hypertension (P > 0.05).


Table 3. Comparison of demographic and background variables between the two groups of studied patients (n = 500)
Variables Variable levels Infection cases ( n ) Non-infection cases ( n ) Total cases ( n ) Infection within group (%) P value
Gender Male 6 149 155 3.87 0.021*
Female 24 321 345 6.96
Smoking No 12 410 422 2.84 0.230*
Yes 18 60 78 23.08
History of surgery No 13 437 450 2.89 0.390*
Yes 17 33 50 34.00
History of corticosteroid use No 7 407 414 1.69 0.042*
Yes 23 63 86 26.74
History of hypertension No 15 361 376 3.99 0.190*
Yes 15 109 124 12.10
History of diabetes No 5 425 430 1.16 0.002*
Yes 25 45 70 35.71
Quantitative variables Mean (SD) Mean (SD) Significance level
Age 55.18 (6.8) 34.29 (2.5) <0.001**
Weight 83.22 (8.2) 78.38 (4.5) 0.680**

* P value by chi-squared test, ** P value by independent samples t-test. significant P values are bold (values under 0.05).

Comparison of Surgical and Therapeutic Variables Between the Two Patient Groups

Table 4 presents the comparison of the surgical and therapeutic variables between patients with and without postoperative infections. As shown in the table, a surgical duration of more than 4 hours (with 20.0% infection rate in this group, P = 0.022), blood loss volume exceeding 1 liter (27.69% infection rate, P = 0.009), and receiving two units of blood transfusion (30.0% infection rate, P = 0.040) were significantly associated with the occurrence of SSIs. However, no significant correlation was found between postoperative infections and preoperative CRP and ESR levels, surgical site, surgical approach, or surgical method (P > 0.05).


Table 4. Comparison of Surgical and Therapeutic Variables Between the Two Groups of Studied Patients (n = 500)
Variables Variable levels Infection cases ( n ) Non-infection cases ( n ) Total cases ( n ) Infection within group (%) P value
Surgical site Lumbosacral 13 362 375 3.47 0.125*
Cervical 12 88 100 12.0
Thoracic 5 20 25 20.0
Approach Posterior 14 411 425 3.29 0.361*
Anterior 14 51 65 21.54
Anteroposterior 2 8 10 20.0
Surgical method Laminectomy 6 144 150 4.0 0.411*
Fusion and laminectomy 12 213 225 5.33
Laminectomy and diskectomy 12 113 125 9.6
Surgical duration Less than 2 h 5 145 150 3.33 0.022*
2‒4 h 5 250 255 1.96
More than 4 h 20 80 100 20.0
Blood loss volume Less than 600 cc 6 304 310 1.94 0.009*
Between 600 cc and 1 liter 6 119 125 4.8
More than 1 liter 18 47 65 27.69
Blood transfusion None 5 320 325 1.54 0.040*
1 unit 7 108 115 6.07
2 units 18 42 60 30.0
Quantitative variables Mean (SD) Mean (SD) Significance level
CRP 9.73 (4.1) 10.21 (2.0) **0.528
ESR 11.16 (3.5) 10.01 (2.1) **0.633

* P value by chi-squared test, ** P value by independent samples t-test. significant P values are bold (values under 0.05).

Table 5 presents the results of the multivariate logistic regression analysis evaluating independent risk factors associated with postoperative spinal infections. Adjusted ORs with their corresponding 95% CIs and P-values are reported for each category of the studied variables, with the reference groups clearly indicated. The analysis revealed that smoking significantly increases the risk of infection, with an adjusted OR of 3.80 (95% CI: 1.60 to 8.90, P = 0.003). A history of previous surgery and corticosteroid use were also significant risk factors, with adjusted ORs of 3.00 (95% CI: 1.20 to 7.50, P = 0.020) and 4.20 (95% CI: 1.70 to 10.30, P = 0.002), respectively. Diabetes mellitus demonstrated the strongest association with postoperative infection, with an adjusted OR of 5.90 (95% CI: 2.30 to 15.20, P < 0.001). Surgical site played an important role as well, with surgeries performed in the cervical and thoracic regions associated with higher infection risks compared to the lumbosacral region (adjusted ORs 3.70 and 6.80, respectively). Furthermore, surgical duration exceeding four hours and blood loss greater than one liter were strongly linked to increased infection risk, with adjusted ORs of 6.90 (P < 0.001) and 18.50 (P < 0.001), respectively. Blood transfusion was also a significant factor, with receiving one or two units increasing the infection risk (adjusted ORs of 3.90 and 25.50, respectively). Other variables such as male gender, history of hypertension, and surgical methods showed elevated ORs but did not reach statistical significance. These findings emphasize the importance of managing comorbidities like diabetes and corticosteroid use, along with optimizing surgical factors such as minimizing operative time and blood loss, to reduce the likelihood of postoperative spinal infections.


Table 5. Multivariate Logistic Regression Analysis of Risk Factors for Postoperative Spinal Infections
Variable Level Postoperative spinal infections
Adjusted OR (95% CI) P value
Gender Male 1.50 (0.70 – 3.20) 0.30
Female Ref Ref
Smoking Yes 3.80 (1.60 – 8.90) 0.003
No Ref Ref
History of surgery Yes 3.00 (1.20 – 7.50) 0.020
No Ref Ref
History of corticosteroid use Yes 4.20 (1.70 – 10.30) 0.002
No Ref Ref
History of hypertension Yes 2.10 (0.90 – 4.80) 0.080
No Ref Ref
History of diabetes Yes 5.90 (2.30 – 15.20)  < 0.001
No Ref Ref
Surgical site Cervical 3.70 (1.40 – 9.70) 0.008
Thoracic 6.80 (2.20 – 21.30) 0.001
Lumbosacral Ref Ref
Approach Anterior 7.40 (2.90 – 18.70)  < 0.001
Anteroposterior 6.80 (1.30 – 35.40) 0.022
Posterior Ref Ref
Surgical method Fusion and laminectomy 2.10 (0.80 – 5.70) 0.130
Laminectomy and diskectomy 2.40 (0.90 – 6.60) 0.086
Laminectomy Ref Ref
Surgical duration 2‒4 h 0.60 (0.18 – 2.00) 0.41
 > 4 h 6.90 (2.50 – 19.00)  < 0.001
 < 2 h Ref Ref
Blood loss volume 600 cc - 1 liter 2.30 (0.80 – 6.80) 0.11
 > 1 liter 18.50 (7.00 – 48.80)  < 0.001
 < 600 cc Ref Ref
Blood transfusion 1 unit 3.90 (1.20 – 12.30) 0.024
2 units 25.50 (8.60 – 75.60)  < 0.001
None Ref Ref

Discussion

The present study was conducted to investigate the prevalence of postoperative infections following spinal surgeries and the contributing factors. The results indicated postoperative infections occurred in 30 cases (6%). These findings were consistent with those of numerous similar national and international studies, suggesting that the prevalence of SSIs following spinal surgeries is similar across different countries and healthcare centers, despite some differences in infection rates and pathogen types. For example, Zarei et al reported a relatively low infection rate (6.8% in the case group and 4.5% in the control group) from Al-Zahra Hospital in Isfahan.22 In the study by Nota et al on 5,761 patients, the incidence of postoperative infections within 90 days was reported at 6%.23 These alignments suggest homogeneity in the factors contributing to infection rates. However, some studies have reported differing results, which may be attributed to factors such as type of surgeries, geographical location, sample size and patient inclusion criteria. For example, in the study by Al-Gamdi et al in Saudi Arabia, the infection rate was 4%.24 In the studies by Liu et al in the United States25 and Abolfotouh et al in Africa,17 the infection rates were 2.4% and 4.2%, respectively. These observed differences underscore the heterogeneity across healthcare systems, which may reflect variations in surgical infrastructure, ICU admission policies, antibiotic stewardship, and infection control protocols. Without accounting for these contextual differences, direct comparisons between settings may be limited in interpretability.

In the present study, among the common microbial factors, S. aureus, coagulase-negative staphylococci and Pseudomonas were identified as the most common pathogens associated with infections, respectively. In contrast, the study by Fakour et al in Razi hospital in Ahvaz reported Pseudomonas as the most common causative agent of infection, likely due to differences in settings and types of surgeries performed.26 Durkin et al found that the most common pathogens included S. aureus, coagulase-negative staphylococci and Escherichia coli.27 These differences may be attributed to variations in environmental conditions, study designs, populations studied and care practices at different centers, all of which could influence the final results. Such microbial variations could be also influenced by local antimicrobial policies, availability of infection surveillance systems, and differences in surgical asepsis standards, which were not consistently reported across studies.

Importantly, this study went beyond descriptive statistics by presenting adjusted ORs for several independent risk factors. Among patient-related variables, diabetes mellitus emerged as the strongest risk factor for postoperative spinal infections (adjusted OR = 5.90; 95% CI: 2.30–15.20; P < 0.001). Corticosteroid use was also significantly associated with infection (adjusted OR = 4.20; 95% CI: 1.70–10.30; P = 0.002), as was smoking (adjusted OR = 3.80; 95% CI: 1.60–8.90; P = 0.003), and prior surgery (adjusted OR = 3.00; 95% CI: 1.20–7.50; P = 0.020). In terms of surgical factors, longer surgical duration ( > 4 hours) showed a strong association with infection (adjusted OR = 6.90; P < 0.001), as did blood loss exceeding 1 liter (adjusted OR = 18.50; P < 0.001). Blood transfusion further increased the risk significantly, especially in patients receiving two units (adjusted OR = 25.50; P < 0.001). Surgical site was another determinant: surgeries in the thoracic (adjusted OR = 6.80) and cervical (adjusted OR = 3.70) regions had higher risks compared to the lumbosacral region. The strength of these associations highlights the importance of risk stratification, but also points to the need for further studies that control for setting-specific practices, such as surgical team experience, infection prevention protocols, and postoperative ICU care.

Consistent with our findings, Najafizadeh et al identified advanced age and a history of chemotherapy or radiotherapy as factors contributing to the occurrence of infection.28 However, in contrast to our results, no significant correlation was observed between infection and variables such as gender, smoking and diabetes. Furthermore, our findings were in line with other research that has confirmed the role of diabetes as a contributing factor to infections. Karamouzian et al identified diabetes as the most important risk factor for deep wound infections.29 Also, Soroush et al reported factors such as surgical duration, presence of drains, steroid use and low hemoglobin levels as independent predictors of infection.30 Mosleh et al reported a higher prevalence of infection among male patients and those under 35 years of age, particularly in emergency surgeries.31 Hojjat et al found a significant correlation between surgical wound infection and factors such as type of fracture, smoking, surgical duration, type of surgery and length of hospital stay.32 Additionally, Al-Gamdi et al showed that factors such as hypertension, prolonged hospital stay, prolonged surgical duration and use of multiple blood units play a significant role in increasing the risk of infection.24 Furthermore, Abolfotouh et al identified factors such as diabetes, smoking, reconstructive surgery and prolonged hospital stay as significant contributors to the occurrence of postoperative infections.17 Dong et al reported advanced age, prolonged surgical duration, blood loss exceeding 1,000 mL and history of diabetes as factors associated with an increased risk of SSIs.33 Similarly, Liu et al identified factors such as diabetes, low albumin and calcium levels, prolonged surgical duration, increased blood loss and decreased hemoglobin as major predictors of SSIs.25 These comparative findings, while valuable, should be interpreted cautiously due to likely heterogeneity in patient case-mix, surgical subspecialties, and hospital-level infection monitoring protocols that may not have been standardized across studies.

Finally, it should be noted that the observed differences in findings may be attributed to several factors, including geographical location, sample size, type of surgeries, patients’ demographic characteristics, and differences in inclusion and exclusion criteria across studies. These differences could account for the discrepancy between our results and those of other studies.

The results of this study, along with previous evidence, emphasize the importance of identifying high-risk patients before the surgery, closely monitoring patients during the procedure and ensuring the control of patient safety conditions. Using infection control protocols, reducing surgical duration and optimizing patient conditions before the surgery could help reduce the incidence of infections. Despite its significance, the present study has several limitations. First, its retrospective and cross-sectional design only allows for identification of associations, limiting causal inference and introducing potential biases inherent to retrospective data collection. Second, the study was conducted in a single region in northwestern Iran, which may affect the generalizability of the findings to other geographical areas or populations. Third, the microbial resistance profiles of isolated pathogens were not assessed, which could have provided important insights into treatment challenges. Finally, clinical outcomes related to postoperative infections, such as length of hospital stay or functional recovery, were not reported. Future research should aim to include multi-center data from diverse healthcare systems and explicitly examine how structural variations (such as ICU protocols, preoperative optimization strategies, and antibiotic stewardship) may affect infection rates. Prospective longitudinal design, broader geographic coverage, and inclusion of antimicrobial resistance and clinical outcomes are recommended.


Conclusion

In this study, the prevalence of postoperative spinal infections was reported at 6%. The most common microbial factors associated with infections were S. aureus, coagulase-negative staphylococci and Pseudomonas, in decreasing order of frequency. Data analysis revealed that certain variables, such as female gender, history of corticosteroid use, diabetes mellitus, surgical duration exceeding 2 hours, blood loss greater than 1 liter and receiving at least 2 units of blood transfusion, were significantly associated with an increased risk of postoperative infections. Additionally, the mean age of patients with infections was significantly higher than that of patients without infections. However, no significant correlation was found between the occurrence of infection and other variables, including weight, smoking, surgical history, hypertension, CRP, ESR, surgical site, type of approach or surgical method. Conducting further studies in other regions of the country could help identify factors influencing postoperative infections, develop preventive strategies and improve the quality of healthcare services in this field.


Competing Interests

The authors declare no conflict of interest regarding this study and its publication.

Data Availability Statement

The data that support the findings of this study are available from the corresponding author upon reasonable request.

Ethical Approval

This study was conducted with the approval of the Research Ethics Committee of Tabriz University of Medical Sciences (IR.TBZMED.FMD.REC.1403.009). In order to adhere to ethical principles, patients’ names and other personal information in their records were kept confidential, and only the variables relevant to the study were extracted. The results were published in aggregate form. Participants incurred no costs for participating in the study, and no additional therapeutic interventions beyond standard surgical procedures were applied to them.

Funding

This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors.


References

  1. Järbrink K, Ni G, Sönnergren H, Schmidtchen A, Pang C, Bajpai R. Prevalence and incidence of chronic wounds and related complications: a protocol for a systematic review. Syst Rev 2016; 5(1):152. doi: 10.1186/s13643-016-0329-y [Crossref] [ Google Scholar]
  2. Woo K, Song J, Adams V, Block LJ, Currie LM, Shang J. Exploring prevalence of wound infections and related patient characteristics in homecare using natural language processing. Int Wound J 2022; 19(1):211-21. doi: 10.1111/iwj.13623 [Crossref] [ Google Scholar]
  3. Reddy M, Gill SS, Wu W, Kalkar SR, Rochon PA. Does this patient have an infection of a chronic wound?. JAMA 2012; 307(6):605-11. doi: 10.1001/jama.2012.98 [Crossref] [ Google Scholar]
  4. Schimmel JJ, Horsting PP, de Kleuver M, Wonders G, van Limbeek J. Risk factors for deep surgical site infections after spinal fusion. Eur Spine J 2010; 19(10):1711-9. doi: 10.1007/s00586-010-1421-y [Crossref] [ Google Scholar]
  5. Martinengo L, Olsson M, Bajpai R, Soljak M, Upton Z, Schmidtchen A. Prevalence of chronic wounds in the general population: systematic review and meta-analysis of observational studies. Ann Epidemiol 2019; 29:8-15. doi: 10.1016/j.annepidem.2018.10.005 [Crossref] [ Google Scholar]
  6. Nampiaparampil DE. Prevalence of chronic pain after traumatic brain injury: a systematic review. JAMA 2008; 300(6):711-9. doi: 10.1001/jama.300.6.711 [Crossref] [ Google Scholar]
  7. Schuster JM, Rechtine G, Norvell DC, Dettori JR. The influence of perioperative risk factors and therapeutic interventions on infection rates after spine surgery: a systematic review. Spine (Phila Pa 1976) 2010; 35(9 Suppl):S125-37. doi: 10.1097/BRS.0b013e3181d8342c [Crossref] [ Google Scholar]
  8. Weinstein MA, McCabe JP, Cammisa FP Jr. Postoperative spinal wound infection: a review of 2,391 consecutive index procedures. J Spinal Disord 2000; 13(5):422-6. doi: 10.1097/00002517-200010000-00009 [Crossref] [ Google Scholar]
  9. Evaniew N, Khan M, Drew B, Peterson D, Bhandari M, Ghert M. Intrawound vancomycin to prevent infections after spine surgery: a systematic review and meta-analysis. Eur Spine J 2015; 24(3):533-42. doi: 10.1007/s00586-014-3357-0 [Crossref] [ Google Scholar]
  10. Strom RG, Pacione D, Kalhorn SP, Frempong-Boadu AK. Decreased risk of wound infection after posterior cervical fusion with routine local application of vancomycin powder. Spine (Phila Pa 1976) 2013; 38(12):991-4. doi: 10.1097/BRS.0b013e318285b219 [Crossref] [ Google Scholar]
  11. Wang X, Lin Y, Yao W, Zhang A, Gao L, Feng F. Surgical site infection in spinal surgery: a bibliometric analysis. J Orthop Surg Res 2023; 18(1):337. doi: 10.1186/s13018-023-03813-6 [Crossref] [ Google Scholar]
  12. Kang DG, Holekamp TF, Wagner SC, Lehman RA Jr. Intrasite vancomycin powder for the prevention of surgical site infection in spine surgery: a systematic literature review. Spine J 2015; 15(4):762-70. doi: 10.1016/j.spinee.2015.01.030 [Crossref] [ Google Scholar]
  13. Smith JS, Shaffrey CI, Sansur CA, Berven SH, Fu KM, Broadstone PA. Rates of infection after spine surgery based on 108,419 procedures: a report from the Scoliosis Research Society Morbidity and Mortality Committee. Spine (Phila Pa 1976) 2011; 36(7):556-63. doi: 10.1097/BRS.0b013e3181eadd41 [Crossref] [ Google Scholar]
  14. Korol E, Johnston K, Waser N, Sifakis F, Jafri HS, Lo M. A systematic review of risk factors associated with surgical site infections among surgical patients. PLoS One 2013; 8(12):e83743. doi: 10.1371/journal.pone.0083743 [Crossref] [ Google Scholar]
  15. Pop-Vicas A, Stern R, Osman F, Safdar N. Variability in infection surveillance methods and impact on surgical site infection rates. Am J Infect Control 2021; 49(2):188-93. doi: 10.1016/j.ajic.2020.06.211 [Crossref] [ Google Scholar]
  16. Matsumoto H, Simhon ME, Campbell ML, Vitale MG, Larson EL. Risk factors associated with surgical site infection in pediatric patients undergoing spinal deformity surgery: a systematic review and meta-analysis. JBJS Rev 2020; 8(3):e0163. doi: 10.2106/jbjs.Rvw.19.00163 [Crossref] [ Google Scholar]
  17. Abolfotouh SM, Khattab M, Zaman AU, Alnori O, Zakout A, Konbaz F. Epidemiology of postoperative spinal wound infection in the Middle East and North Africa (MENA) region. N Am Spine Soc J 2023; 14:100222. doi: 10.1016/j.xnsj.2023.100222 [Crossref] [ Google Scholar]
  18. Saeedinia S, Nouri M, Azarhomayoun A, Hanif H, Mortazavi A, Bahramian P. The incidence and risk factors for surgical site infection after clean spinal operations: a prospective cohort study and review of the literature. Surg Neurol Int 2015; 6:154. doi: 10.4103/2152-7806.166194 [Crossref] [ Google Scholar]
  19. Glotzbecker MP, Riedel MD, Vitale MG, Matsumoto H, Roye DP, Erickson M. What’s the evidence? Systematic literature review of risk factors and preventive strategies for surgical site infection following pediatric spine surgery. J Pediatr Orthop 2013; 33(5):479-87. doi: 10.1097/BPO.0b013e318285c507 [Crossref] [ Google Scholar]
  20. Patel N, Bagan B, Vadera S, Maltenfort MG, Deutsch H, Vaccaro AR. Obesity and spine surgery: relation to perioperative complications. J Neurosurg Spine 2007; 6(4):291-7. doi: 10.3171/spi.2007.6.4.1 [Crossref] [ Google Scholar]
  21. Piper KF, Tomlinson SB, Santangelo G, Van Galen J, DeAndrea-Lazarus I, Towner J. Risk factors for wound complications following spine surgery. Surg Neurol Int 2017; 8:269. doi: 10.4103/sni.sni_306_17 [Crossref] [ Google Scholar]
  22. Zarei MR, Tabesh H, Fazeli H, Aarabi A. The effect of incise drape on the incidence of surgical site infection following lumbar spine surgeries. J Isfahan Med Sch 2018; 36(498):1165-74. doi: 10.22122/jims.v36i498.10704 [Crossref] [ Google Scholar]
  23. Nota SP, Braun Y, Ring D, Schwab JH. Incidence of surgical site infection after spine surgery: what is the impact of the definition of infection?. Clin Orthop Relat Res 2015; 473(5):1612-9. doi: 10.1007/s11999-014-3933-y [Crossref] [ Google Scholar]
  24. Al-Gamdi SS, Alawi M, Bokhari R, Bajunaid K, Mukhtar A, Baeesa SS. Risk factors for surgical site infection following spinal surgery in Saudi Arabia: a retrospective case-control study. Medicine (Baltimore) 2021; 100(17):e25567. doi: 10.1097/md.0000000000025567 [Crossref] [ Google Scholar]
  25. Liu JM, Deng HL, Chen XY, Zhou Y, Yang D, Duan MS. Risk factors for surgical site infection after posterior lumbar spinal surgery. Spine (Phila Pa 1976) 2018; 43(10):732-7. doi: 10.1097/brs.0000000000002419 [Crossref] [ Google Scholar]
  26. Fakour M, Dasht Bozorg A, Latifi S, Mahdinasab S. Assessment of prevalence of infection following fracture fixation operation among patients admitted to orthopedics ward of Ahwaz Razi hospital during year 1383 to 1384. Jundishapur Sci Med J 2008;7(1):65-73. [Persian].
  27. Durkin MJ, Dicks KV, Baker AW, Moehring RW, Chen LF, Sexton DJ. Postoperative infection in spine surgery: does the month matter?. J Neurosurg Spine 2015; 23(1):128-34. doi: 10.3171/2014.10.Spine14559 [Crossref] [ Google Scholar]
  28. Najafizadeh M, Yasrebi SS, Dahim A, Zarei-Yazdeli M, Azadchehr MJ, Pahlavani H. Investigation of factors associated with surgical site infection after neurosurgery procedures in Kashan Shahid Beheshti hospital. Stud Med Sci 2024;35(2):84-92. [Persian].
  29. Karamouzian S, Keykhosravi E, Sarraf F, Noroozi M, Jangi Aghdam H. The incidence of deep wound infection after spinal instrumentation. Med J Mashhad Univ Med Sci 2012; 55(4):237-41. doi: 10.22038/mjms.2012.163.[Persian] [Crossref] [ Google Scholar]
  30. Soroush AR, Makarem J, Younesian M, Fazeli MS, Haji-Abdulbaqi M, Nouri M, et al. Surgical site infection and its contributing factors in general surgical patients. J Iran Med Council 2008;25:464-73. [Persian].
  31. Mosleh S, Baradaran Fard F, Jokar M, Akbari L, Aarabi A. Prevalence of surgical site infection after orthopedic surgery and some related factors at the selected hospitals of Isfahan University of Medical Sciences. Paramedical Sciences and Military Health 2019;13(4):43-53. [Persian].
  32. Hojjat M, Karimyar Jahromi M, Keshaei N, Salehifard A. Assessment of the prevalence of post-operation orthopedic wound infection in the orthopedic ward of Motahari hospital (2009-2010). Iran J Surg 2012;20(2):51-8. [Persian].
  33. Dong X, Zhou Y. Cross-sectional analysis of risk factors for surgical site infection secondary to spinal internal fixation via the posterior approach. J Int Med Res 2022; 50(5):3000605221099254. doi: 10.1177/03000605221099254 [Crossref] [ Google Scholar]

Submitted: 05 Jun 2025
Revised: 24 Jul 2025
Accepted: 10 Aug 2025
First published online: 01 Sep 2025
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