Abstract
Study Design:
Literature review.
Objectives:
A review of the literature identifying preoperative risk factors for developing surgical site infections after spine surgery and discussion of the preventive strategies to minimize risks.
Methods:
A review of the literature and synthesis of the data to provide an updated review on the preoperative management of surgical site infection.
Results:
Preoperative prevention strategies of reducing surgical site infections in spine surgery remains a challenging problem. Careful mitigation of modifiable patient comorbidities, blood glucose control, smoking, obesity, and screening for pathologic microorganisms is paramount to reduce this risk. Individualized antibiotic regimens, skin preparation, and hand hygiene also play a critical role in surgical site infection prevention.
Conclusions:
This review of the literature discusses the preoperative preventive strategies and risk management techniques of surgical site infections in spine surgery. Significant decreases in surgical site infections after spine surgery have been noted over the past decade due to increased awareness and implementation of the prevention strategies described in this article. However, it is important to recognize that prevention of surgical site infection requires a system-wide approach that includes the hospital system, the surgeon, and the patient. Continued efforts should focus on system-wide implementation programs including careful patient selection, individualized antibiotic treatment algorithms, identification of pathologic organisms, and preoperative decolonization programs to further prevent surgical site infections and optimize patient outcomes.
Keywords: spine surgery, surgical site infection, preoperative antibiotics, prevention
Introduction
Surgical site infections (SSIs) represent a large proportion of hospital-acquired infections, 31% in a recent study in the acute care setting.1 Hospital-acquired infections have gained increased attention among the public, health care providers, and health care systems due to the benchmarking that occurs between facilities as well as changes in reimbursement models. SSIs are the most common infections treated by spinal surgeons and are associated with increased morbidity, mortality, cost, and inferior outcomes. Rates of SSI vary greatly based on the invasiveness of the procedure, underlying spinal pathology, and patient population.2 The rates of SSI are reported to be as low as 0.07% in patients undergoing anterior cervical discectomy and fusion, to 2.94% in posterior cervical surgery, 2.4% for spinal tumors, 8.8% in primary lumbar fusions, and 12.2% in revision lumbar fusions in a Medicare population.3-6
SSI after spine surgery poses a significant burden on patients and the health care system. It is estimated that in 2005 SSI extended hospital lengths of stay on average by 9.7 days and incurred an additional cost of $20 842 per admission.7 Blumberg et al found that the average cost of spine SSI treatment at a single tertiary referral center to be $16 242 per case.8 These figures do not include the indirect cost of SSI and therefore underestimate the overall financial burden. The impact of SSI is felt not only in cost but also in patient morbidity, mortality, and outcomes. Petilon et al performed a propensity case-control cohort study that found patients with deep infection after instrumented fusion had more back pain and were less likely to reach MCID (minimum clinically important difference) at 2 years compared with patients without infection.9 Additionally, Casper et al reported patients with spine SSI following elective surgery had increased mortality rates compared with controls at 1, 2, and 5 years with an overall mortality rate of 12%.10
As a result, there has been great focus across medicine and within the field of spine surgery to identify risk factors; optimize patients pre-, intra-, and postoperatively; as well as change surgical practice. In this article, we will highlight modifiable preoperative strategies to minimize the risk of SSI in spine surgery.
Patient Selection Optimization
Several underlying patient risk factors can be modified preoperatively to lessen the risk of SSI in spine surgery patients including optimizing hyperglycemic states, smoking cessation, obesity management, and screening for and eradicating methicillin-sensitive Staphylococcus aureus (MSSA)/methicillin-resistant Staphylococcus aureus (MRSA) in carriers.11,12 These modifiable risk factors need to be considered and optimized prior to elective spine surgery and their implications should be discussed carefully with the patient to achieve compliance.
Preoperative Blood Glucose Monitoring
The long-term sequelae and complications of diabetes leading to poor wound healing due to local ischemia secondary to microangiopathic changes have been well described.13 Due to the disruption of the vascular system in patients with diabetes, SSIs across all specialties are increased in this patient population. In a meta-analysis performed by Meng et al, the authors reported an odds ratio (OR) of 2.04 (95% confidence interval [CI] = 1.69-2.46) of increased infection rates among diabetic patients,11 who also have been shown to have worse patient-reported outcomes up to 2 years after spine surgery.14 In a study by Hikata et al, the authors evaluated 345 patients undergoing posterior thoracic and/or lumbar fusion surgery with instrumentation. The patients with preoperative diabetes had a 5-fold increase in infection rates. Subgroup analysis of these patients revealed that patients with hemoglobin A1C values <7 had a 0% infection rate, whereas patients with values >7 had an infection rate of 35.3%.15 Due to the reported increased rate of infection and worse outcomes in patients with diabetes, it is imperative that patients be screened for hemoglobin A1C values and tight control of blood glucose levels be achieved and documented prior to embarking on elective spine surgery.
Smoking Cessation
Aside from the known detriments of nicotine on bone healing, smoking is also implicated in increased SSIs. In the meta-analysis mentioned previously by Meng et al, smoking had an increased OR of infection of 1.17 (95% CI = 1.03-1.32) after spine surgery. In a systematic review performed by Thomsen et al, it was noted that surgical complications were nearly halved in patients who successfully stopped smoking prior to surgery, OR 0.56.16 Therefore, smoking cessation is a critical modifiable risk factor for SSI and imperative prior to elective spine surgery. The optimal preoperative intervention of smoking cessation techniques and duration of cessation remains unknown, but a recent Cochrane review suggests that a combination of cognitive therapy, behavioral therapy, and nicotine replacement therapy yields the best results and to be effective needs to be initiated 4 to 8 weeks prior to surgery as cessation less than 4 weeks does not appear to influence the risk of SSI.17
Obesity
With obesity rates reported in the United States at 34.9% of adults, SSI in this population remains a challenge as SSI rates are strongly correlated with obesity.18 In the meta-analysis performed by Meng et al, they reported an increased risk of infection in patients with a body mass index >30 kg/m2 with an OR of 2.13 (95% CI = 1.55-2.93), the strongest predictor of all 3 of the modifiable risk factors discussed thus far. In studies by Mehta et al, the distribution of adipose tissue, the skin-to-lamina distance, and the thickness of the subcutaneous tissue were significantly associated with increased SSI rates likely due to increased tissue disruption, creation of a larger dead space, and increased operative times.19,20 Additionally, obesity is associated with other comorbidities that may further increase risk for SSI including diabetes.21 Therefore, preoperative optimization of body weight is critical in order to minimize SSI. Interventions such as dietary counseling, referral to a bariatric surgeon for consideration of banding or gastric bypass procedures, as well as exercise counseling may be required prior to performing elective spine surgery. A caveat to substantial weight loss prior to surgery after bariatric surgery is malnutrition, especially as it pertains to bone health, with several studies noting a greater risk of osteoporosis, reduced bone mineral density, vitamin D deficiency, and an increased risk of spinal fracture.22-24
Bacterial Screening and Eradication
Gram positive bacteria continue to be the most common organism for spinal SSI. However, Abdul-Jabbar et al reviewed a single institution’s experience in a 5-year period of 239 spinal SSIs. Gram positive organisms accounted for the majority of infections but Gram negative microbes were identified in 30.5% of cases and were more common in those cases involving the sacrum. The most common pathogens isolated were Staphylococcus aureus (45.2%) and Staphylococcus epidermis (30.4%). Interestingly, Proprionibacterium acnes species was seen in 7.9% of patients in this series.25 Due to the preponderance of MSSA and MRSA SSIs and their colonization in healthy patients, screening programs have been designed in an attempt to preoperatively eradicate these organisms. Kim et al evaluated 7019 patients and identified 22.6% and 4.4% as MSSA and MRSA as carriers, respectively. In this study, they institutionalized a decolonization program entailing showering with 2% chlorhexidine once daily for 5 days and intranasal 2% mupirocin ointment twice daily for 5 days preoperatively and reported a significantly decreased rate of SSI from 0.45% to 0.19% for all elective orthopedic procedures.26 Several other studies, including a randomized, double-blinded, placebo-controlled trial, have supported these findings, albeit in the joint arthroplasty literature.27-29
Recently, concerns have been raised concerning the presence of P acnes colonization in instrumented spine surgery procedures. A study by Shifflett et al reported a series of 112 revision spine surgeries with no preoperative suspicion for infection in which intraoperative cultures were obtained. They identified 45 patients with positive cultures, staphylococcus species were present in 57.8%, and P acnes was present in 48.9%.30 Our identification of P acnes as a pathogen in spinal SSI is likely underreported given that it requires holding cultures for 14 days, and until recently was not identified as a pathogen. Further research is ongoing to help identify preventative strategies for limiting exposure to P acnes preoperatively.
Day of Surgery Optimization
Perioperative Antibiotics
Prevention of SSIs in spine surgery remains of paramount importance, and the use of prophylactic antibiotic therapy has been shown to reduce the risk of postoperative infection.31-34 The majority of the guidelines that have been established focus on the treatment of gram positive bacteria (staphylococcus), and the standard antibiotic of choice is cefazolin, a first-generation cephalosporin, which has a long half-life in bone and serum and efficacious in treating gram positive bacteria and some gram negative bacteria. This antimicrobial prevention strategy is effective in most elective spine surgeries, but as mentioned previously gram negative bacteria are becoming more prevalent and it is important to recognize patients that are at increased risk of harboring these gram negative species.35 In patients at risk of harboring gram negative species, not a normal component of the skin flora, such as incontinent patients or patients that have a history of urinary tract colonization and/or infection, should be carefully prescreened with urine cultures and have individualized additional antibiotic regimens administered. In the study by Núñez-Pereira et al, the authors studied an individualized antibiotic regimen based on preoperative risk factors for harboring gram negative bacteria and found a statistically decreased number of patients developing an SSI due to gram negative bacteria.35 The timing and the administration of prophylactic antibiotics within 30 minutes of surgery has been shown to significantly decrease the risk of SSI when compared with the timeframe of 30 to 60 minutes prior to incision, and for longer duration surgeries the antibiotic should be redosed every 4 hours.36 Other considerations are that for patients who have an allergy to beta-lactam antibiotics (penicillin), clindamycin should be substituted. The use of intravenous vancomycin should be used sparingly due to the risk of developing bacterial resistance but is the antibiotic of choice in patients who test positive for MRSA colonization preoperatively or who have a history of MRSA infections. Additionally, prophylactic antibiotics should only be administered for 24 hours postoperatively.
Recently, the use of intrawound vancomycin powder is rapidly being adopted for the prevention of SSIs in spine surgery.37,38 Topical vancomycin provides a high local concentration of antibiotic with minimal systemic absorption. Intrawound vancomycin powder is applied subfascially, suprafascially, or equally throughout. Approximately 24% of pediatric spine surgeons currently use intrawound vancomycin, and both adult- and pediatric consensus-based guidelines recommend that intrawound vancomycin be considered routinely in instrumented cases or cases with risk factors such as prolonged duration or significant patient comorbidities.39,40 Adverse events, though rare, include anaphylactic reaction, renal toxicity, and hearing loss.37,41 Although numerous reviews support the use of intrawound vancomycin powder in spine surgery, the majority of these studies are retrospective in nature.42-46 At least one randomized trial has reported conflicting evidence.47 These studies may be limited due to bias in study design, lack of precision, controls, and small sample sizes. Evaniew et al found that the pooled estimate from 8 observational studies indicated a statistically significant reduction in odds of infection with the use of intrawound vancomycin (OR = 0.19, 95% CI = −0.08 to 0.47, P = .0003).43 However, a randomized trial performed by Tubaki et al failed to demonstrate any benefit in 907 patients (OR = 0.96, 95% CI = −0.34 to 2.66, P = .93).47 A recent review performed by Ghobrial et al evaluating a total of 9721 patients found the SSI rate among the control and vancomycin-treated group to be 7.47% and 1.36%, respectively, with an overall adverse event rate of 0.3%.37 Despite the lack of support from Level 1 studies, intrawound vancomycin has been widely adopted and does appear to be safe and effective for reducing postoperative SSIs in spine surgery with a low rate of morbidity. Further high-quality studies defining the dosage and delineating the exact population of efficacy are warranted.
Skin Antisepsis
The goal of intraoperative skin preparation of the surgical field is to sterilize the skin just prior to skin incision. The most commonly used commercial preparations are iodine and chlorhexidine combined with isopropyl alcohol compounds. Mechanisms of action are variable depending on the antiseptic compound being utilized, and there is no definitive clinical evidence that one skin preparation solution effectively lowers SSI rates compared with others. Three prospective randomized controlled trials in orthopedic surgery have compared the effectiveness of antiseptic preparations in eradicating skin flora.48-50 Savage et al50 found no difference between ChloraPrep (2% chlorhexidine and 70% isopropyl alcohol; Enturia, El Paso, Texas) and DuraPrep (0.7% available iodine and 74% isopropyl alcohol; 3M Healthcare, St Paul, Minnesota) in the rate of positive culture results after skin preparation. On the contrary, Ostrander et al48 and Saltzman et al49 found that ChloraPrep was superior to the other agents, with lower rates of positive cultures. When translated to rates of SSI, however, the ideal skin preparation solution remains unclear. Swenson et al51 found that the lowest infection rates were seen with the use of DuraPrep, compared with Betadine and ChloraPrep, and Darouiche et al52 found the lowest infection rates were in the ChloraPrep group compared with the Betadine group. A recent meta-analysis evaluating 10 randomized controlled trials concluded that alcohol-based agents are likely superior to aqueous solutions53; thus, use of either DuraPrep or ChloraPrep would provide adequate intraoperative skin preparation.
Hand Hygiene and Surgical Gloves
Hand hygiene plays a crucial role in preventing SSIs. Current commercially available solutions are generally either chlorhexidine-based or povidone iodine–based solutions. A recent Cochrane review found no evidence that one type of hand antisepsis is better than another in reducing SSIs.54 Although chlorhexidine-based scrubs were shown to reduce skin colony counts more effectively, this did not translate into incidence of postoperative infection rates.54,55 In a randomized trial with 4387 consecutive patients, Parienti et al found that hand rubbing with an aqueous alcohol solution was as effective as traditional hand scrubbing with antiseptic soap in SSI prevention.56 Importantly, the hand-rubbing protocol was better tolerated and faster, with improved compliance rates.
With regard to surgical gloves, double gloving significantly reduces glove perforations and also allows earlier detection of perforation when the inside gloves are of a different color, which theoretically reduces rates of SSI.57 Furthermore, Rehman et al showed that removal of outer gloves, as opposed to wearing the same pair of double gloves, prior to handling instrumentation in posterior spinal fusions resulted in a significant reduction of infection rates from 3.35% to 0.48%.58 Additionally, Bible et al found that bacterial contamination of the operative microscope was found to be significant after spine surgery, particularly around the optic eyepieces. The authors recommend changing gloves after making adjustments to the optic eyepieces and avoid handling any portion of the drape above the eyepieces.59
Conclusion
This review of the literature discusses the preoperative preventive strategies and risk management techniques of SSIs in spine surgery. Even though we have seen significant decreases in SSIs after spine surgery over the past decade due to increased awareness and implementation of the prevention strategies described in this article, it is important to recognize that prevention of SSI requires a system-wide approach that includes the hospital system, the surgeon, and the patient. Continued efforts should focus on system-wide implementation of careful patient selection, individualized antibiotic treatment algorithms, identification of pathologic organisms, and preoperative decolonization programs to further prevent SSIs and optimize patient outcomes.
Footnotes
Declaration of Conflicting Interests: The author(s) declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.
Funding: The author(s) disclosed receipt of the following financial support for the research, authorship, and/or publication of this article: This Supplement was supported by funding from AOSpine North America.
References
- 1. Magill SS, Hellinger W, Cohen J, et al. Prevalence of healthcare-associated infections in acute care hospitals in Jacksonville, Florida. Infect Control Hosp Epidemiol. 2012;33:283–291. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2. 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;473:1612–1619. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3. Ghobrial GM, Harrop JS, Sasso RC, et al. Anterior cervical infection: presentation and incidence of an uncommon postoperative complication. Global Spine J. 2017;7(1 suppl):12S–16S. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4. Sebastian A, Huddleston P, 3rd, Kakar S, Habermann E, Wagie A, Nassr A. Risk factors for surgical site infection after posterior cervical spine surgery: an analysis of 5441 patients from the ACS NSQIP 2005-2012. Spine J. 2016;16:504–509. [DOI] [PubMed] [Google Scholar]
- 5. Karhade AV, Vasudeva VS, Dasenbrock HH, et al. Thirty-day readmission and reoperation after surgery for spinal tumors: a National Surgical Quality Improvement Program analysis. Neurosurg Focus. 2016;41:E5. [DOI] [PubMed] [Google Scholar]
- 6. Manoso MW, Cizik AM, Bransford RJ, Bellabarba C, Chapman J, Lee MJ. Medicaid status is associated with higher surgical site infection rates after spine surgery. Spine (Phila Pa 1976). 2014;39:1707–1713. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 7. de Lissovoy G, Fraeman K, Hutchins V, Murphy D, Song D, Vaughn BB. Surgical site infection: incidence and impact on hospital utilization and treatment costs. Am J Infect Control. 2009;37:387–397. [DOI] [PubMed] [Google Scholar]
- 8. Blumberg TJ, Woelber E, Bellabarba C, Bransford R, Spina N. Predictors of increased cost and length of stay in the treatment of postoperative spine surgical site infection [published online July 21, 2017]. Spine J. doi:10.1016/j.spinee.2017.07.173. [DOI] [PubMed] [Google Scholar]
- 9. Petilon JM, Glassman SD, Dimar JR, Carreon LY. Clinical outcomes after lumbar fusion complicated by deep wound infection: a case-control study. Spine (Phila Pa 1976). 2012;37:1370–1374. [DOI] [PubMed] [Google Scholar]
- 10. Casper DS, Zmistowski B, Hollern DA, et al. The effect of postoperative spinal infections on patient mortality [published online June 9, 2017]. Spine (Phila Pa 1976). doi:10.1097/BRS.0000000000002277. [DOI] [PubMed] [Google Scholar]
- 11. Meng F, Cao J, Meng X. Risk factors for surgical site infections following spinal surgery. J Clin Neurosci. 2015;22:1862–1866. [DOI] [PubMed] [Google Scholar]
- 12. Xing D, Ma JX, Ma XL, et al. A methodological, systematic review of evidence-based independent risk factors for surgical site infections after spinal surgery. Eur Spine J. 2013;22:605–615. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13. Goodson WH, 3rd, Hung TK. Studies of wound healing in experimental diabetes mellitus. J Surg Res. 1977;22:221–227. [DOI] [PubMed] [Google Scholar]
- 14. Armaghani SJ, Archer KR, Rolfe R, Demaio DN, Devin CJ. Diabetes is related to worse patient-reported outcomes at two years following spine surgery. J Bone Joint Surg Am. 2016;98:15–22. [DOI] [PubMed] [Google Scholar]
- 15. Hikata T, Iwanami A, Hosogane N, et al. High preoperative hemoglobin A1c is a risk factor for surgical site infection after posterior thoracic and lumbar spinal instrumentation surgery. J Orthop Sci. 2014;19:223–228. [DOI] [PubMed] [Google Scholar]
- 16. Thomsen T, Tønnesen H, Møller AM. Effect of preoperative smoking cessation interventions on postoperative complications and smoking cessation. Br J Surg. 2009;96:451–461. [DOI] [PubMed] [Google Scholar]
- 17. Thomsen T, Villebro N, Møller AM. Interventions for preoperative smoking cessation. Cochrane Database Syst Rev. 2014;(3):CD002294. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18. Ogden CL, Carroll MD, Kit BK, Flegal KM. Prevalence of childhood and adult obesity in the United States, 2011-2012. JAMA. 2014;311:806–814. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19. Mehta AI, Babu R, Karikari IO, et al. 2012 Young Investigator Award winner: the distribution of body mass as a significant risk factor for lumbar spinal fusion postoperative infections. Spine (Phila Pa 1976). 2012;37:1652–1656. [DOI] [PubMed] [Google Scholar]
- 20. Mehta AI, Babu R, Sharma R, et al. Thickness of subcutaneous fat as a risk factor for infection in cervical spine fusion surgery. J Bone Joint Surg Am. 2013;95:323–328. [DOI] [PubMed] [Google Scholar]
- 21. Ganz ML, Wintfeld N, Li Q, Alas V, Langer J, Hammer M. The association of body mass index with the risk of type 2 diabetes: a case-control study nested in an electronic health records system in the United States. Diabetol Metab Syndr. 2014;6:50. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22. Costa TL, Paganotto M, Radominski RB, Kulak CM, Borba VC. Calcium metabolism, vitamin D and bone mineral density after bariatric surgery. Osteoporos Int. 2015;26:757–764. [DOI] [PubMed] [Google Scholar]
- 23. Nakamura KM, Haglind EG, Clowes JA, et al. Fracture risk following bariatric surgery: a population-based study. Osteoporos Int. 2014;25:151–158. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24. Ravindra VM, Godzik J, Guan J, et al. Prevalence of vitamin D deficiency in patients undergoing elective spine surgery: a cross-sectional analysis. World Neurosurg. 2015;83:1114–1119. [DOI] [PubMed] [Google Scholar]
- 25. Abdul-Jabbar A, Berven SH, Hu SS, et al. Surgical site infections in spine surgery: identification of microbiologic and surgical characteristics in 239 cases. Spine (Phila Pa 1976). 2013;38:E1425–E1431. [DOI] [PubMed] [Google Scholar]
- 26. Kim DH, Spencer M, Davidson SM, et al. Institutional prescreening for detection and eradication of methicillin-resistant Staphylococcus aureus in patients undergoing elective orthopaedic surgery. J Bone Joint Surg Am. 2010;92:1820–1826. [DOI] [PubMed] [Google Scholar]
- 27. Bode LG, Kluytmans JA, Wertheim HF, et al. Preventing surgical-site infections in nasal carriers of Staphylococcus aureus . N Engl J Med. 2010;362:9–17. [DOI] [PubMed] [Google Scholar]
- 28. Rao N, Cannella BA, Crossett LS, Yates AJ, Jr, McGough RL, 3rd, Hamilton CW. Preoperative screening/decolonization for Staphylococcus aureus to prevent orthopedic surgical site infection: prospective cohort study with 2-year follow-up. J Arthroplasty. 2011;26:1501–1507. [DOI] [PubMed] [Google Scholar]
- 29. Sporer SM, Rogers T, Abella L. Methicillin-resistant and methicillin-sensitive Staphylococcus aureus screening and decolonization to reduce surgical site infection in elective total joint arthroplasty. J Arthroplasty. 2016;31(9 suppl):144–147. [DOI] [PubMed] [Google Scholar]
- 30. Shifflett GD, Bjerke-Kroll BT, Nwachukwu BU, et al. Microbiologic profile of infections in presumed aseptic revision spine surgery. Eur Spine J. 2016;25:3902–3907. [DOI] [PubMed] [Google Scholar]
- 31. Fogelberg EV, Zitzmann EK, Stinchfield FE. Prophylactic penicillin in orthopaedic surgery. J Bone Joint Surg Am. 1970;52:95–98. [PubMed] [Google Scholar]
- 32. Pavel A, Smith RL, Ballard A, Larsen IJ. Prophylactic antibiotics in clean orthopaedic surgery. J Bone Joint Surg Am. 1974;56:777–782. [PubMed] [Google Scholar]
- 33. Leaper D Burman-Roy S Palanca A et al. ; Guideline Development Group . Prevention and treatment of surgical site infection: summary of NICE guidance. BMJ. 2008;337:a1924. [DOI] [PubMed] [Google Scholar]
- 34. Watters WC, 3rd, Baisden J, Bono CM, et al. Antibiotic prophylaxis in spine surgery: an evidence-based clinical guideline for the use of prophylactic antibiotics in spine surgery. Spine J. 2009;9:142–146. [DOI] [PubMed] [Google Scholar]
- 35. Núñez-Pereira S, Pellisé F, Rodríguez-Pardo D, et al. Individualized antibiotic prophylaxis reduces surgical site infections by gram-negative bacteria in instrumented spinal surgery. Eur Spine J. 2011;20(suppl 3):397–402. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36. Steinberg JP, Braun BI, Hellinger WC, et al. ; Trial to Reduce Antimicrobial Prophylaxis Errors (TRAPE) Study Group. Timing of antimicrobial prophylaxis and the risk of surgical site infections: results from the trial to reduce antimicrobial prophylaxis errors. Ann Surg. 2009;250:10–16. [DOI] [PubMed] [Google Scholar]
- 37. Ghobrial GM, Cadotte DW, Williams K, Jr, Fehlings MG, Harrop JS. Complications from the use of intrawound vancomycin in lumbar spinal surgery: a systematic review. Neurosurg Focus. 2015;39:E11. [DOI] [PubMed] [Google Scholar]
- 38. Savage JW, Anderson PA. An update on modifiable factors to reduce the risk of surgical site infections. Spine J. 2013;13:1017–1029. [DOI] [PubMed] [Google Scholar]
- 39. Glotzbecker MP, Vitale MG, Shea KG, Flynn JM; POSNA committee on the Quality, Safety, Value Initiative (QSVI). Surgeon practices regarding infection prevention for pediatric spinal surgery. J Pediatr Orthop. 2013;33:694–699. [DOI] [PubMed] [Google Scholar]
- 40. Vitale MG, Riedel MD, Glotzbecker MP, et al. Building consensus: development of a Best Practice Guideline (BPG) for surgical site infection (SSI) prevention in high-risk pediatric spine surgery. J Pediatr Orthop. 2013;33:471–478. [DOI] [PubMed] [Google Scholar]
- 41. Gans I, Dormans JP, Spiegel DA, et al. Adjunctive vancomycin powder in pediatric spine surgery is safe. Spine (Phila Pa 1976). 2013;38:1703–1707. [DOI] [PubMed] [Google Scholar]
- 42. Bakhsheshian J, Dahdaleh NS, Lam SK, Savage JW, Smith ZA. The use of vancomycin powder in modern spine surgery: systematic review and meta-analysis of the clinical evidence. World Neurosurg. 2015;83:816–823. [DOI] [PubMed] [Google Scholar]
- 43. 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;24:533–542. [DOI] [PubMed] [Google Scholar]
- 44. 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;15:762–770. [DOI] [PubMed] [Google Scholar]
- 45. Khan NR, Thompson CJ, DeCuypere M, et al. A meta-analysis of spinal surgical site infection and vancomycin powder. J Neurosurg Spine. 2014;21:974–983. [DOI] [PubMed] [Google Scholar]
- 46. Molinari RW, Khera OA, Molinari WJ., 3rd Prophylactic intraoperative powdered vancomycin and postoperative deep spinal wound infection: 1512 consecutive surgical cases over a 6-year period. Eur Spine J. 2012;21(suppl 4):S476–S482. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 47. Tubaki VR, Rajasekaran S, Shetty AP. Effects of using intravenous antibiotic only versus local intrawound vancomycin antibiotic powder application in addition to intravenous antibiotics on postoperative infection in spine surgery in 907 patients. Spine (Phila Pa 1976). 2013;38:2149–2155. [DOI] [PubMed] [Google Scholar]
- 48. Ostrander RV, Botte MJ, Brage ME. Efficacy of surgical preparation solutions in foot and ankle surgery. J Bone Joint Surg Am. 2005;87:980–985. [DOI] [PubMed] [Google Scholar]
- 49. Saltzman MD, Nuber GW, Gryzlo SM, Marecek GS, Koh JL. Efficacy of surgical preparation solutions in shoulder surgery. J Bone Joint Surg Am. 2009;91:1949–1953. [DOI] [PubMed] [Google Scholar]
- 50. Savage JW, Weatherford BM, Sugrue PA, et al. Efficacy of surgical preparation solutions in lumbar spine surgery. J Bone Joint Surg Am. 2012;94:490–494. [DOI] [PubMed] [Google Scholar]
- 51. Swenson BR, Hedrick TL, Metzger R, Bonatti H, Pruett TL, Sawyer RG. Effects of preoperative skin preparation on postoperative wound infection rates: a prospective study of 3 skin preparation protocols. Infect Control Hosp Epidemiol. 2009;30:964–971. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 52. Darouiche RO, Wall MJ, Jr, Itani KM, et al. Chlorhexidine-alcohol versus povidone-iodine for surgical-site antisepsis. N Engl J Med. 2010;362:18–26. [DOI] [PubMed] [Google Scholar]
- 53. Sidhwa F, Itani KM. Skin preparation before surgery: options and evidence. Surg Infect (Larchmt). 2015;16:14–23. [DOI] [PubMed] [Google Scholar]
- 54. Tanner J, Dumville JC, Norman G, Fortnam M. Surgical hand antisepsis to reduce surgical site infection. Cochrane Database Syst Rev. 2016;(1):CD004288. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 55. Fletcher N, Sofianos D, Berkes MB, Obremskey WT. Prevention of perioperative infection. J Bone Joint Surg Am. 2007;89:1605–1618. [DOI] [PubMed] [Google Scholar]
- 56. Parienti JJ, Thibon P, Heller R, et al. ; Antisepsie Chirurgicale des mains Study Group. Hand-rubbing with an aqueous alcoholic solution vs traditional surgical hand-scrubbing and 30-day surgical site infection rates: a randomized equivalence study. JAMA. 2002;288:722–727. [DOI] [PubMed] [Google Scholar]
- 57. Tanner J, Parkinson H. Double gloving to reduce surgical cross-infection. Cochrane Database Syst Rev. 2006;(3):CD003087. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 58. Rehman A, Rehman AU, Rehman TU, Freeman C. Removing outer gloves as a method to reduce spinal surgery infection. J Spinal Disord Tech. 2015;28:E343–E346. [DOI] [PubMed] [Google Scholar]
- 59. Bible JE, O’Neill KR, Crosby CG, Schoenecker JG, McGirt MJ, Devin CJ. Microscope sterility during spine surgery. Spine (Phila Pa 1976). 2012;37:623–627. [DOI] [PubMed] [Google Scholar]