The practice parameters for perioperative infection control vary among clinicians. The results of almost 200 practicing neuromodulation physicians presented here provide information on basic infection control practices for both SCS trials and implants. Compared to the survey by Provenzano et al, there has not been a substantial increase in the use of antibiotics among clinicians (> 80% vs > 82%) for SCS trials (
27). Nonetheless, there continues to be a significant portion of physicians who do not adhere to the NACC guidelines. Our data suggest 47% and 56% of physicians utilize antibiotics for trials and implants, respectively, as a single dose or up to 24 hours, which is in compliance with NACC guidelines. Approximately 39% of providers extend antibiotic use up to more than 5 days for implants. As compared to Provenzano et al, the number of clinicians that continue antibiotics in the postoperative period has decreased to 35% from 50.5% for SCS trials and to 39% from 57% for implants (
27). This decrease may reflect the NACC guidelines’ recommendation to consider discontinuing antibiotics within 24 hours for implantation (
22). Indeed, infections associated with SCS are the most common complication after implantation (
23). This can lead to not only explantation and infection in the epidural space, but also increased morbidity, and increased healthcare costs (
23,
28). However, studies indicate prolonged antibiotic use in the post-operative period does not improve outcomes and may contribute to multidrug-resistant bacteria, including MRSA, which can lead to increased morbidity and mortality (
22,
29,
30). On the other hand, 17% (34/181) of clinicians do not use antibiotics prior to performing an SCS trial and 4% (8/195) prior to an SCS implant despite evidence that the preoperative use of antibiotics, independent of surgery type, results in a 50% decrease in the incidence of wound infections (
23,
25).
NACC guidelines help establish standard practices in order to improve patient safety. For the purposes of antibiotic use, they recommend pre-procedure antibiotic use and discontinuation of antibiotics within 24 hours (
22). NACC guidelines endorse tailoring antibiotics to community, hospital, and resistance patterns of organisms (
22). They further recommend that for most SCS procedures, a single dose of a cephalosporin, such as cefazolin, is appropriate (
22). Cefazolin is favorable in terms of having a high safety profile, low cost, and activity against common organisms, such as MSSA, that cause SSIs (
28,
31). In patients with a beta-lactam allergy, clindamycin or vancomycin can be considered (
22). However, vancomycin should be reserved for patients with MRSA colonization, as seen on nasal swab (
22,
28,
32,
33). This is important to help limit multidrug resistant infections, including vancomycin-resistant strains (
34). In addition, vancomycin is less effective than cefazolin in preventing MSSA related SSIs (
28,
35). The antibiotic should be administered intravenously approximately 30 - 60 minutes prior to incision, with the exception of vancomycin which should be administered 120 minutes prior to incision (
22,
28).
Our results also indicate that a large percentage of clinicians (82% and 69%) are not testing for MSSA or MRSA prior to a SCS trial or implant, despite level IA evidence from the NACC guidelines to decolonize MRSA prior to the procedure (
22). This underutilized diagnostic test can help identify patients who are carriers of MSSA and MRSA and is recommended by the NACC guidelines (
22). Because being either a MSSA or MRSA carrier is the most important risk factor of SSIs, these patients are at a significantly higher risk of developing an infection (
22,
36-
39). Both MSSA and MRSA are commonly located in the anterior nares, perianal, and groin regions (
22). Pre-procedure nasal swab testing for both MSSA and MRSA, allows for the detection of these bacteria to not only signify when to decolonize the patient, but to administer appropriate antibiotics, such as vancomycin. Decolonization entails application of mupirocin nasal ointment and chlorhexidine wash prior the procedure (
22). About to 1/3 of the population are carriers of S. aureus, illustrating that nasal swabs are cost effective manner to identify a large portion of patients who are at higher risk of infection (
22,
40). Despite this, nasal screening may not detect up to 20% of patients with colonization (
41). On the other hand, it is not clear if universal decolonization may be beneficial (
41). Decolonization with mupirocin may also lead to mupirocin resistance S. aureus, which can potentially cause failure of decolonization (
41). More information is needed to determine optimization of decolonization.
There continue to be obstacles in which ongoing education and NACC guidelines are not implemented by physicians. The duration of antibiotic use in SCS and nasal swab testing vary widely among practicing physicians. Provenzano et al published in 2013, and nearly 7 years later, our results remain comparable (
27). The barriers to adoption of best antibiotic prophylaxis measures may include lack of accessibility of information and consensus guidelines, ongoing education regarding guidelines, and physicians' adherence to their routine practices.
4.1. Limitations
There are several limitations in our study. The survey link was emailed to over 6000 members with active general membership through the American Society of Regional Anesthesia and Spine Intervention Society. Membership through these societies included physicians with a variety of practices and, of which a small portion perform neuromodulation procedures, such as spinal cord stimulation. We were unable to send the survey to societies for neuromodulation due to logistical reasons. We estimated that 10-20% of the recipients were eligible to respond to the questionnaire. In addition, there are overlapping members between the two societies, making it difficult to account for the true number of interventional pain physicians who perform SCS within these groups. This may have influenced the response rate to be lower as the overlap was unknown. The questionnaire also did not investigate further details, including the class of antibiotics administered, timing of antibiotic administration, weight-based antibiotic dosing, and the reasoning behind physicians’ common antibiotic administration practices. The study also did not assess the use of direct wound application of antibiotics (e. g. vancomycin powder). Ideally, a larger study would provide more information regarding antibiotic use and nasal swab use as typical practices for pain physicians.
4.2. Conclusions
The use of perioperative infection control practices continues to vary among neuromodulation clinicians. Surgical site infections are the most common complication for spinal cord stimulation and are associated with increased morbidity and mortality. The NACC provides guidelines to provide a consensus to improve patient safety and standardize practices. In regard to antibiotic administration, the NACC advocates that a single pre-operative dose of antibiotics is largely sufficient. Antibiotic should be tailored to nasal swab testing, weight-based dosing, and discontinuation of antibiotics within 24 hours. More education is needed to continue to refine guidelines and recommendations, and more importantly, to disperse the information to practicing pain physicians. Our data suggest the majority of physicians do not utilize nasal swabs to determine MSSA and MRSA presence. Although most physicians administer antibiotics peri-procedurally for both trial and permanent phases, they administer them for typically longer durations than recommended by the NACC. There also continues to remain a significant portion of physicians who do not administer antibiotics. This review gives initial data regarding the use of antibiotics from a large group of interventional pain physicians, allowing providers to review how the majority of pain physicians practice with regards to antibiotic usage. Further analysis and questionnaires should be performed to determine how physicians select antibiotics.