The risk factors of surgical site infection following posterior cervical spine surgery

DOI: https://doi.org/10.21203/rs.3.rs-331817/v1

Abstract

Background: Surgical site infection (SSI) is a common complication following posterior cervical spine surgery, imposing a high burden on patients and society. However, information about its characteristics and related risk factors is limited. We designed this study intended to address this issue.

Methods: From January 2011 through October 2020, a total of 405 patients diagnosed of cervical degenerative diseases (cervical spondylotic myelopathy, ossification of posterior longitudinal ligament and cervical disk herniation) who were treated with unilateral open-door lamnioplasty surgeries were enrolled in this study. We divided the patients into the SSI group and the non-SSI group and compared their patient-specific and procedure-specific factors. Univariate and multiple logistic regression analyses were performed to determine risk factors.

Results: There were significant differences between groups in subcutaneous fat thickness (FT) (P<0.001), ratio of subcutaneous FT to muscle thickness (MT) (P<0.001), preoperative  Japanese Orthopaedic Association(JOA)Scores (P< 0.003), preoperative serum albumin (P< 0.001), postoperative drainage (P<0.004), time of draining (P<0.001). Logistic regression analysis of these differences showed that ratio of subcutaneous FT/MT, preoperative JOA score, preoperative serum albumin and longer time of draining were significantly related to SSI (P<0.05).

Conclusion: Ratio of subcutaneous FT/MT, preoperative JOA score, preoperative serum albumin and longer time of draining are identified as the independent risk factors of SSI in posterior cervical spine surgeries. Identification of these risk factors could be useful in reducing SSI incidence and patients counseling.

Introduction

Surgical site infection (SSI) the most common complication after spinal surgery is an infection of the tissues, organs, or spaces exposed by surgeons during the performance of an invasive procedure1–3. SSI was classified as superficial, deep, or organ space. Compared with lumbar surgeries, cervical surgeries cases were associated with a significantly lower rate of infection4. Meanwhile, posterior cervical spine surgeries cases having a significantly higher rate of infection than anterior cervical surgeries cases with consequences ranging from superficial to deep infection5. The incidence of postoperative surgical site infections (SSIs) after posterior cervical spine surgeries is reported to range from 1.4–13%6,7. SSI leads to devastating outcomes including requires multiple readmissions, wound debridement or implant removal and increasing mortality, which results in readmission to the hospital, poor outcomes and additional hospitalization expenses causing patients’ physical, mental, and economic burdens8–10.

Although advances have been made in infection control practices, the incidence of SSI after posterior cervical surgery ranges from 1.3–14%, Several risk factors for SSI in posterior cervical spine surgeries are increasingly being investigated. Many estimated risk factors have been reported in previous studies, such as advanced age, higher body mass index (BMI > 30 kg/m2), smoking, diabetes, malnutrition (preoperative albumin level < 3.5 g/dL), history of infection in the surgical site, preoperative steroid therapy, blood loss, implant, and prolonged operative time (> 3 hours) 11–16. Meanwhile, bacterial culture indicated that the most common causative microorganisms of SSI in spinal surgery are Staphylococcus aureus and other members of Staphylococcus species17,18. However, the results in these previous studies were not always consistent and there were few studies about the risk factors of SSI following posterior cervical spine surgeries. In this study, we investigated the frequency of SSI and evaluated the risk factors for SSI in a Chinese population by comparing patient-related and procedure-related factors to identify cases of SSI and determine the factors that modify the risk of SSI to relief the burden on society.

Materials And Methods

Patient Population

This was a retrospective clinical study. From January 2011 to October 2020, 435 patients following posterior cervical spine surgeries at First Affiliated Hospital of Dalian Medical University and were included in this study and were observed for a minimum of 2 months postoperatively. 30 patients in this experiment were lost to follow-up among them. Information gathered included demographic details, cause of disorder, diagnosis, radiologic findings, and laboratory investigations. Preoperative, intraoperative, and postoperative findings were recorded. All patients aged 18 years or older who had cervical degenerative diseases (cervical spondylotic myelopathy, ossification of posterior longitudinal ligament and cervical disk herniation) treated by unilateral open-door lamnioplasty surgeries were included. The exclusion criteria were as follows: age < 18 years, traumatic fractures, and pathologic fractures (metastasis, tuberculosis) and 405 patients were enrolled. All surgical procedures were performed in operating rooms equipped with vertical laminar air flow. All surgical personnel wore body exhaust suits. We administered antibiotic prophylaxis just before surgery and 72 hours postoperatively for all patients. Each patient in the study underwent classic open-door lamnioplasty surgeries. A deep one-off negative pressure drain was inserted, and the fascia was closed meticulously, followed by closure of the wound. The drain was removed about 2 days postoperatively when the discharge was observed to be < 50 ml. The postoperative rehabilitation protocols were similar in all patients.

Identification of SSI

The diagnosis of SSI involves the interpretation of combined clinical, laboratory, and occasionally radiologic findings. SSI is considered as a diagnosis within 30 days of surgery in the absence of implants, and up to 1 year postoperatively in the presence of surgical implants. In this study, the definition of SSI was based on the Centers for Disease Control and Prevention definition. Superficial infection involves the skin and subcutaneous tissue only, occurring within 30 days after the operation, leading to pain, tenderness, redness, and heat over the site. Deep infection involves the fascia and muscle, occurring within 30 days after the operation (if no implant was left in place) or within 1 year (if the implant was left in place), often resulting in fever (> 38℃), pain, tenderness, and abscess formation. Organ infection includes septic discitis, vertebral osteomyelitis, and epidural abscess, leading to possible purulent drainage and abscess formation1. The microbiological culture results from all patients who experienced SSI were collected and recorded. In patients who underwent open debridement, microbiological cultures were taken to confirm the presence of SSI and to decide further treatment.

Data collection and outcome evaluations

The patients were divided into an SSI group and a non-SSI group in this study. We compared their patient-related factors such as: age, gender, BMI, muscle thickness(MT), subcutaneous fat thickness(FT), diabetes mellitus(DM), hypertension, ischemic heart disease, steroid use, rheumatoid arthritis, preoperative Japanese Orthopaedic Association(JOA)Scores, previous SSI, other infections such as pulmonary infection, urinary infection, and so on during the perioperative period, preoperative American Society of Anesthesiologists score, preoperative Visual Analogue Scale, preoperative temperature, preoperative white blood cell count, preoperative hematocrit, preoperative and postoperative hemoglobin, preoperative total lymphocyte count, preoperative serum albumin) and procedure-related factors (operative time, operated levels, estimated blood loss, postoperative drainage, time of draining, allogeneic blood transfusion, intraoperative rapid sterilizer use, local intrawound vancomycin antibiotic powder, dural tear, perioperative invasive vascular catheterization, postoperative prophylactic antibiotics).

Statistical Analysis

The mean and standard deviation were calculated for continuous variables; number and percentage were calculated for categorical variables. Firstly, a univariate logistic regression analysis was performed to evaluate the relationship between each categorical variable and SSI. The t-test or Mann-Whitney U test was used for continuous variables, depending on the data distribution (equal variance and normality or not). A P value < 0.05 was considered to be significant. Further, all the related variables were entered into the multivariate logistic regression model to determine the independent risk factors for SSI.

Results

The total incidence of SSI after posterior cervical spine surgery was 4.93% (20/405). The SSI group was composed of 11 men and 9 women, whose ages ranged from 55 to 73 years (median, 65 years). The non-SSI group was composed of 232 men and 153 women, whose ages ranged from 40 to 79 years (median, 61 years). Of the 20 patients with SSI cases, superficial in 15 and deep in 5 were treated with not only prolonging the use of antibiotics but also surgical debridement and VSD covered. All patients recovered well and with no implants removed.

Univariate analysis of patient demographics revealed several significant predictors of SSI including patient-related risk factors, procedure-related risk factors, and perioperative factors. Several medical comorbidities were associated with SSI rates including FT, Ratio of Subcutaneous FT to MT, preoperative JOA, preoperative serum albumin. Notable factors that were not predictive of SSI included diabetes mellitus, smoking, Gender, Age, BMI, MT and so are summarized in (Table 1). Univariate and multiple logistic regression analyses were used to evaluate the effect of each factor on the SSI (Table 2). Univariate logistic regression analysis showed that subcutaneous FT, Ratio of Subcutaneous FT to MT, preoperative JOA, preoperative serum albumin, postoperative drainage, time of draining were significant risk factors for SSI (P < 0.05). Multivariable logistic regression analysis identified four positive independent predictors of SSI including Ratio of Subcutaneous FT to MT, preoperative JOA, preoperative serum albumin, time of draining. Previous studies of risk factors for SSI in Posterior cervical spine surgery on Table 3.

Table 1

Risk Factors for SSI in Posterior Cervical Spine Surgery Using Univariate Analysis

Variable

SSI Group (n = 20)

Non-SSI Group (n = 385)

p value

Gender

9:11

153:232

0.640

Age

61.160

63.500

0.098

BMI

26.140

26.435

0.187

MT

36.880

36.950

0.714

FT

23.730

32.150

< 0.01

Radio of FT/MT

0.878

0.647

< 0.01

Smoking

6.000

121.000

0.893

Alcohol

3.000

67.000

1.000

DM

5.000

80.000

0.865

Hypertension

5.000

92.000

1.000

Ischemic heart disease

2.000

40.000

1.000

Rheumatoid arthritis

6.000

64.000

0.215

Chronic steroid usage

3.000

53.000

1.000

Previous SSI

2.000

36.000

1.000

ASA score

2.020

2.200

0.354

VAS score

7.249

7.300

0.924

Preoperative JOA score

7.618

5.850

< 0.01

Preoperative temperature

36.476

36.485

0.744

Preoperative white blood cells

7.487

7.493

0.699

Preoperative hematocrit

43.103

42.070

0.326

Preoperative total lymphocyte count, 109/L

1.918

1.965

0.589

Preoperative hemoglobin

136.647

136.150

0.967

Postoperative hemoglobin

107.239

103.150

0.377

Preoperative serum albumin (g/dL)

42.061

35.075

< 0.01

Operative time, minutes

140.234

142.000

0.441

Operated levels

3.722

3.800

0.447

Estimated blood loss, mL

430.208

435.000

0.129

Postoperative drainage, mL

269.325

406.500

0.005

Time of draining, hours

48.696

62.400

< 0.01

Perioperative invasive vascular catheterization

7.000

132.000

0.948

Intraoperative rapid sterilizer use

1.000

17.000

0.606

Local intrawound vancomycin antibiotic powder

8.000

153.000

0.982

Dural tear

4.000

35.000

0.221

Postoperative prophylactic antibiotics, days

4.213

4.250

< 0.01

Perioperative with other infections, n (%)

1.000

19.000

1.000

BMI, body mass index; MT, muscle thickness; FT, fat thickness; DM, diabetes mellitus; SSI, surgical site infection; ASA, American Society of Anesthesiologists; VAS, Visual Analogue Scale; JOA, Japanese Orthopaedic Association.

 

Table 2

Risk Factors for SSI in Posterior Cervical Spine Surgery Using Univariate and Multiple Logistic Regression Analysis

Variable

Univariate Logistic Regression Analysis

OR P

Multiple Logistic Regression Analysis

OR P C.I.

Preoperative serum albumin (g/dL)

0.795

< 0.01

0.83

< 0.01

0.745–0.925

FT

1.392

< 0.01

1.022

0.844

0.82–1.275

Radio of FT/MT

1.161

< 0.01

1.214

0.003

1.067–1.382

Preoperative JOA score

0.610

< 0.01

0.591

0.009

0.398–0.877

Postoperative drainage, mL

1.003

< 0.01

0.997

0.171

0.993–1.001

Time of draining, hours

1.044

< 0.01

8.347

0.011

1.020–1.170

FT, fat thickness; JOA, Japanese Orthopaedic Association.

 

Table 3

Previous Studies of Risk Factors for SSI in Posterior cervical Spine Surgery

Year

Study

Journal

Risk Factors

2012

Barnes [10]

Global Spine J

traumatic etiology, postoperative use of a collar

2013

Mehta [21]

J Bone Joint Surg Am

ratio of the FT to the lamina-to-skin distance

2016

Ojo [18]

Niger J Clin Pract

diabetes mellitus, obesity, and anemia

2016

Sebastian [33]

Spine J

BMI > 35, chronic steroid use,operative time > 197 minutes

2017

Cancienne [19]

Spine

preoperative cervical epidural steroid injections

2018

Herrick [24]

J Neurosurg Spine

no drain placement

2019

Cheng [22]

Spine J

BMI > 35, diabetes mellitus

2020

Fatima [23]

World Neurosurg

obesity

2020

Sridharan [11]

World Neurosurg

BMI ≥ 35.0

 

Discussion

SSI has been found to be the most common complication in spinal surgeries serious consequences like debridement negative impact on patient-reported clinical outcomes, potential need for instrumentation removal, and increasing patient mortality. Therefore, SSI causes huge healthcare and economic burden. Previous studies have shown that the SSI rate following posterior cervical spine surgery range from 1.4%-13% higher than anterior cervical spine5,6,19. In our study, patients who had surgery for osteomyelitis, discitis, epidural abscess, primary or metastatic tumors were excluded due to their inherent risk of SSI. the overall rate of clinically significant SSI after posterior cervical spine surgery was 4.93%. the incidence of SSI reported in our study was consistent with that reported previously in the literature.

In previous reports on SSI, many estimated risk factors were reported. However, there are many debates regarding the risk factors of SSI. In this study, we performed univariate and multivariate analyses to investigate the impact of related risk factors for development of SSI. In the univariate analysis, subcutaneous FT (P < 0.001), ratio of subcutaneous FT/MT (P < 0.001), preoperative JOA Scores (P < 0.01), preoperative serum albumin (P < 0.01), postoperative drainage (P < 0.01), time of draining (P < 0.001) were identified as significant risk factors. in the multivariate logistic regression model, we entered all variables, except for those identified in the univariate analysis as no significant (P > 0.05) effects. With subsequent multivariate analysis, we were able to identify 4 independent factors ratio of subcutaneous FT/MT (P < 0.01), preoperative JOA scores (P < 0.01), preoperative serum albumin (P < 0.001), time of draining (P < 0.001) influenced patients’ risks of SSI following posterior cervical spine surgeries.

High BMI was a recognized, independent risk factor in SSI following spine surgery11,20. Currently, more and more studies have found that the distribution of subcutaneous fat at the site of surgery not high BMI has been previously shown to affect the risk of SSI following lumbar spine fusion, with the subcutaneous FT being an independent risk factor for infection21–23. This association has also been previously shown to increase the risk of SSI after spine surgery procedures. Obese patients are at a greater risk of SSI because of the increased the subcutaneous FT at the surgical site. The increased FT may require a longer incision, wider dissection, and increased retraction. Operative time is also increased because of the increased difficulty of the surgery in these patients. As retraction is prolonged, the duration of decreased blood flow becomes longer, increasing tissue necrosis at the surgical site. Besides, redundant soft tissues and a poor wound healing environment making closure of the wound challenging, which were possible reasons for an increased risk of SSI resulting from tissue necrosis in obese patients. In the present study, the MT was not a risk factor for SSI, demonstrating that FT is at the highest risk for necrosis while MT not. Thick subcutaneous FT may allow for the development of a dead space after wound closure. This can play a role in the development of SSI following posterior cervical spine surgery. In this study, we demonstrated that the most useful predictor of incisional SSI is the ratio of FT/MT, which reflects the distribution of subcutaneous fat more accurately excluding individually influence.

At present, the relationship between SSI following posterior cervical spine surgeries and surgical site drains is still controversial. The surgical site drain was mainly started in cervical spine surgeries to prevent the formation of epidural hematoma or seroma which may cause neurological deficit and increasing the tension on the incisions resulting in wound-related complications namely SSI and wound dehiscence24. Wound drain apart from supposedly aiding in SSI prevention, could cause retrograde infection, increase post-operative blood loss which increases the need for blood transfusion. In our study, drainage time was an independent risk factor for postoperative SSI. In addition, Payhs et al.25 suggested that surgical site drains in the posterior cervical spine in combination with alcohol foam or vancomycin powder are associated with reduced odds of SSI among patients undergoing any posterior cervical spine surgery.

Current evidence demonstrates a strong and independent association between malnutrition and infectious and wound complications following posterior cervical spine surgeries15,16. Our results support the use of laboratory nutritional screening as a component of preoperative patient assessment and optimization to solve the difficulty of assessment of nutritional status of different people. In this study, decreased preoperative serum albumin (< 3.5 g/dL) significantly increased the risk of postoperative SSI. Additionally, low albumin level would suppress the patients’ immune function and impaired the wound healing, which increased the risk of SSI. Cooper et al.26 reported nutritional supplementation may provide a small reduction in infections in the spine trauma population. At present, the relationship between SSI following posterior cervical spine surgeries and preoperative malnutrition is still controversial, which needs to be confirmed by multicenter and large sample randomized controlled study.

At present, there are no study on the role of preoperative JOA score in SSI. In this study, we demonstrated an interesting result that preoperative JOA score was an independent risk factor of SSI following posterior cervical spine surgery. No clinical research pointed out this view before. A poor preoperative JOA score usually suggested to denervation, pressure sores and urinary retention. In one basic research, chronically denervated tissue is more susceptible to bacterial growth and difficulty in wound healing27,28. Poor nerve function may associate with difficulty getting out of bed resulting in pressure sores, and urinary retention may result in urinary tract infection. Those several reasons may attribute to SSI following posterior cervical spine surgery.

This study didn’t support for vancomycin predicting SSI possibly due to small infection rates while previous studies supported4,29−31. A possible theory for our results that are in contrast to those of other vancomycin studies is that local vancomycin may not have enough capacity to overcome the increased infection risk factors seen in patients undergoing fusion. Thus, the addition of other treatment modalities may be needed to prevent SSIs in the high-risk fusion population, such as improved nutrition or more stringent patient selection criteria. An additional consideration is that the current dosing of intrawound vancomycin may not be adequate, or the delivery of the medication does not last long enough in the local environment to completely control bacterial growth for these large, deep incisions.

In prior studies, DM was identified as a significant risk factor for SSI after spinal surgery32. However, in our study, DM was not significantly associated with SSI. Blood glucose were well controlled before operation, the smaller number of patients with DM, and the inclusion of several potential risk factors in the final multivariate logistic model may have been responsible for these results. Due to the same types of surgery, the intraoperative segments are mostly 3 or 4, so the operation time is relatively close. Similarly, gender, steroid use, current smoking, history of previous SSI, estimated blood loss, and surgical procedure were not identified as risk factors in our study, although they have been found to be significant risk factors for SSI in previous studies33.

First, this was a retrospective nonrandomized case-control study, and the number of patients with SSI in this study was relatively small.

Our study has several limitations. First, this was a retrospective nonrandomized case-control study, and the number of patients with SSI in this study was relatively small. The low rate of SSI could have prevented us from detecting correlations and statistical differences on some variables. Multicentric data pooling could help increase the included number of patients and overcome this limitation. Second, some variables that have potential to influence the development of SSI were not included because they were not considered before the start of the study, such as type of cervical pathology, anticoagulation used, neurological outcomes, cause of death and adverse reaction to transfusion. In addition, in some cases, such as those vancomycin-related reactions, and liver disease, the sample size was too small to allow investigation of their effects on SSI occurrence. Owing to these limitations, high-quality observational studies and basic experimental studies are still needed to investigate new risk factors for SSI further in the future.

Conclusions

A total of 20 SSIs (4.93%) occurred in 405 cases of posterior cervical spine surgeries. Incidence of SSI significantly prolonged hospitalization, increased hospitalization expenses. Ratio of subcutaneous FT to MT, preoperative JOA score, preoperative serum albumin and longer time of draining were found to be significantly associated with SSI after posterior cervical spine surgeries. Identification of these risk factors for SSI could be of great value in risk-benefit analysis of prophylaxis after posterior cervical spine surgeries, and adequate management of preoperative risk to reduce SSI incidence. In addition, the results could be used in counseling patients and their families during the consent process.

Abbreviations

SSI: Surgical site infection;BMI: Body mass index;JOA :Japanese Orthopaedic Association;DM: Diabetes mellitus;MT: Muscle thickness;FT: Fat thickness;ASA: American society of anesthesiologists;VAS: Visual analogue scale

Declarations

Acknowledgements

We would like to thank all the participants in the studies.

Authors’ contributions

CYA contributed to the study design, the writing of the paper, and drafting of the manuscript. LZH performed the surgeries and participated in the design of the study. YM, ZWT and XG collected and analyzed the data. LZH reviewed and edited the manuscript. All authors read and approved the final manuscript.

Funding

This study was supported by LiaoNing Revitalization Talents Program (XLYC1807131) and the Science and Technology Innovation Foundation of Dalian (2020JJ27SN070). The funders had no role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Availability of data and materials

All data used and analyzed during this study are available from the corresponding author upon reasonable request.

Ethics approval and consent to participate

This research was approved by the ethics committee of the First Affiliated Hospital of Dalian Medical University. And agreement to participate was given by the participants. Because of the retrospective nature of the study, informed consent was waived.

Consent for publication

Written informed consent for publication of their clinical details and/or clinical images was obtained from the patient/parent/guardian/relative of the patient.

Competing interests

The authors declare that they have no competing interests.

References

  1. Edwards JR, Peterson KD, Mu Y, et al. National Healthcare Safety Network (NHSN) report: data summary for 2006 through 2008, issued December 2009. American journal of infection control 2009;37:783-805.
  2. Shlobin NA, Cloney MB, Hopkins BS, et al. Surgical Site Infection, Readmission, and Reoperation After Posterior Long Segment Fusion. Spine 2020;Publish Ahead of Print.
  3. Mesregah MK, Chantarasirirat K, Formanek B, et al. Perioperative complications of inpatient and outpatient single-level posterior cervical foraminotomy: a comparative retrospective study. The spine journal : official journal of the North American Spine Society 2020;20:87-93.
  4. Martin JR, Adogwa O, Brown CR, et al. Experience with intrawound vancomycin powder for posterior cervical fusion surgery. Journal of neurosurgery. Spine 2015;22:26-33.
  5. Morishita S, Yoshii T, Okawa A, et al. Perioperative complications of anterior decompression with fusion versus laminoplasty for the treatment of cervical ossification of the posterior longitudinal ligament: propensity score matching analysis using a nation-wide inpatient database. The spine journal : official journal of the North American Spine Society 2019;19:610-6.
  6. Zhou J, Wang R, Huo X, et al. Incidence of Surgical Site Infection After Spine Surgery: A Systematic Review and Meta-analysis. Spine 2020;45:208-16.
  7. Harel R, Stylianou P, Knoller N. Cervical Spine Surgery: Approach-Related Complications. World neurosurgery 2016;94:1-5.
  8. Guo Q, Zhang M, Wang L, et al. Deep surgical site infection after anterior decompression and fusion with plate fixation for cervical spondylotic radiculopathy or myelopathy. Clinical neurology and neurosurgery 2016;141:13-8.
  9. Tsubouchi N, Fujibayashi S, Otsuki B, et al. Risk factors for implant removal after spinal surgical site infection. European spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society 2018;27:2481-90.
  10. Barnes M, Liew S. The incidence of infection after posterior cervical spine surgery: a 10 year review. Global spine journal 2012;2:3-6.
  11. Sridharan M, Malik AT, Kim J, et al. Does Increasing Body Mass Index Correlate with Adverse Outcomes Following Posterior Cervical Fusions? World neurosurgery 2020;133:e789-e95.
  12. Ogihara S, Murase S, Oguchi F, et al. Deep surgical site infection after posterior instrumented fusion for rheumatoid upper cervical subluxation treated with antibiotic-loaded bone cement: Three case reports. Medicine 2020;99:e20892.
  13. Nagoshi N, Kono H, Tsuji O, et al. Impact of Tobacco Smoking on Outcomes After Posterior Decompression Surgery in Patients With Cervical Spondylotic Myelopathy: A Retrospective Multicenter Study. Clinical spine surgery 2020;33:E493-e8.
  14. Zeng J, Sun X, Sun Z, et al. Negative Pressure Wound Therapy Versus Closed Suction Irrigation System in the Treatment of Deep Surgical Site Infection After Lumbar Surgery. World neurosurgery 2019;127:e389-e95.
  15. Guan J, Holland CM, Ravindra VM, et al. Perioperative malnutrition and its relationship to length of stay and complications in patients undergoing surgery for cervical myelopathy. Surgical neurology international 2017;8:307.
  16. Yao R, Zhou H, Choma TJ, et al. Surgical Site Infection in Spine Surgery: Who Is at Risk? Global spine journal 2018;8:5s-30s.
  17. Mok JM, Guillaume TJ, Talu U, et al. Clinical outcome of deep wound infection after instrumented posterior spinal fusion: a matched cohort analysis. Spine 2009;34:578-83.
  18. Ojo OA, Owolabi BS, Oseni AW, et al. Surgical site infection in posterior spine surgery. Nigerian journal of clinical practice 2016;19:821-6.
  19. Cancienne JM, Werner BC, Puvanesarajah V, et al. Does the Timing of Preoperative Epidural Steroid Injection Affect Infection Risk After ACDF or Posterior Cervical Fusion? Spine 2017;42:71-7.
  20. Gu W, Tu L, Liang Z, et al. Incidence and risk factors for infection in spine surgery: A prospective multicenter study of 1764 instrumented spinal procedures. American journal of infection control 2018;46:8-13.
  21. Mehta AI, Babu R, Sharma R, et al. Thickness of subcutaneous fat as a risk factor for infection in cervical spine fusion surgery. The Journal of bone and joint surgery. American volume 2013;95:323-8.
  22. Cheng CW, Cizik AM, Dagal AHC, et al. Body mass index and the risk of deep surgical site infection following posterior cervical instrumented fusion. The spine journal : official journal of the North American Spine Society 2019;19:602-9.
  23. Fatima N, Massaad E, Alvarez-Breckenridge C, et al. Does Obesity Correlate with Postoperative Complications After Elective Posterior Cervical Spine Fusion? World neurosurgery 2020;141:e231-e8.
  24. Herrick DB, Tanenbaum JE, Mankarious M, et al. The relationship between surgical site drains and reoperation for wound-related complications following posterior cervical spine surgery: a multicenter retrospective study. Journal of neurosurgery. Spine 2018;29:628-34.
  25. Pahys JM, Pahys JR, Cho SK, et al. Methods to decrease postoperative infections following posterior cervical spine surgery. The Journal of bone and joint surgery. American volume 2013;95:549-54.
  26. Cooper K, Glenn CA, Martin M, et al. Risk factors for surgical site infection after instrumented fixation in spine trauma. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2016;23:123-7.
  27. Hui PS, Pu LL, Kucukceleki A, et al. The effect of denervation on leukocyte function in soft tissue infection. Surgery 1999;126:933-8.
  28. Alison WE, Jr., Phillips LG, Linares HA, et al. The effect of denervation on soft-tissue infection pathophysiology. Plastic and reconstructive surgery 1992;90:1031-5.
  29. Caroom C, Tullar JM, Benton EG, Jr., et al. Intrawound vancomycin powder reduces surgical site infections in posterior cervical fusion. Spine 2013;38:1183-7.
  30. Strom RG, Pacione D, Kalhorn SP, et al. Decreased risk of wound infection after posterior cervical fusion with routine local application of vancomycin powder. Spine 2013;38:991-4.
  31. Haimoto S, Schär RT, Nishimura Y, et al. Reduction in surgical site infection with suprafascial intrawound application of vancomycin powder in instrumented posterior spinal fusion: a retrospective case-control study. Journal of neurosurgery. Spine 2018;29:193-8.
  32. El-Kadi M, Donovan E, Kerr L, et al. Risk factors for postoperative spinal infection: A retrospective analysis of 5065 cases. Surgical neurology international 2019;10:121.
  33. Sebastian A, Huddleston P, 3rd, Kakar S, et al. Risk factors for surgical site infection after posterior cervical spine surgery: an analysis of 5,441 patients from the ACS NSQIP 2005-2012. The spine journal : official journal of the North American Spine Society 2016;16:504-9.