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During Perioperative Nurses Week this November 10-16, we encourage you to recognize the invaluable contributions of your perioperative nurses and nurse leaders....
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By: Hellen Johnson
Published: 5/7/2019
You're probably aware that most surgical site infections are caused by patients' microbial skin flora flaking into surgical wounds. You also know skin prepping eliminates resident and transient microbes on the body's first line of defense against infection and prevents the growth of microorganisms around the incision site. But are you certain your staff applies pre-op skin prep solutions correctly and allows enough time for them to dry? Don't count on it. National statistics show that surgical teams follow proper application instructions and allow for adequate dry times in fewer than half of all cases.
You need to ensure your staff isn't part of that troubling trend, and internal audits are a proven way to identify where gaps in best practices are occurring. There are many competency tools available to help guide observations of your team in prepping action, including AORN's Competency Verification Tool for Skin Antisepsis (osmag.net/VkY7jQ) or the Agency for Healthcare Research and Quality's (AHRQ) Surgical Skin Preparation Audit Tool (osmag.net/jHM3mS). Some tips for effective auditing include:
Don't hesitate to engage industry professionals to assist with evaluating and improving compliance with best practices. These industry reps are well versed in their products' directions for use and can provide an element of objectivity in the assessment process. In many cases, they will also provide interventions to improve compliance in those areas demonstrating need.
Most experts agree that education is key to improving compliance with best prepping practices. Importantly, discuss the evidence behind dry times and application techniques. For example, studies involving 2% chlorhexidine gluconate (CHG)/70% isopropyl alcohol prep solutions have shown that a back-and-forth application technique, starting with the least contaminated area and moving to the most contaminated area, is the most effective means of working the solution into the outer layer of the skin. This allows for killing of the bacteria that reside there, while minimizing redistribution of bacteria. After observing your staff's prepping techniques, capitalize on all available opportunities to provide them with feedback and education that will improve their techniques:
Efforts to improve compliance with best practices might also include limiting the number of skin prep products your facility uses. At the Infectious Disease Society of America's 2018 ID Week conference, researchers from the University of Texas Southwestern Medical Center presented the results of their experience auditing skin prep compliance. After finding that staff applied the appropriate prep in only 3% of cases and followed dry times only 41% of the time, they knew they not only had to educate staff. They also had to limit the skin prep agents available at the institution.
They found that the facility had 9 different product options and that, for povidone-iodine solutions, the scrub and paint directions for use differed between 2 and 3 different manufacturers. As a result, the researchers chose to reduce the number of prep solutions available for use in an effort to limit the variability of appropriate application techniques and dry times. Their efforts worked: Prep time compliance for 2% CHG/70% isopropyl alcohol and aqueous CHG solutions went from 6% to 50% and from 0% to 40%, respectively. Dry time compliance for aqueous CHG and povidone-iodine solutions jumped from 48% to 84% and from 14% to 78%, respectively.
Your surgical team might not know as much about SSI prevention as you might think, so have them brush up on these basics of pre-op skin asepsis.
1. No prep is best. The effort to identify the ultimate prep solution is a much-debated issue with a conflicting body of evidence. Most infection prevention organizations do not recommend one antiseptic for all procedures. In their most recent SSI guidelines, the CDC recommends skin preparation with an alcohol-based agent "unless contraindicated." The World Health Organization recommends using alcohol-based antiseptic solutions containing chlorhexidine gluconate (CHG), noting that there is moderate quality evidence supporting the use of alcohol-based agents over aqueous agents. AORN recommends that a multidisciplinary team of perioperative RNs, physicians and infection preventionists should select a product "based on a review of current research literature and FDA approval status, in accordance with the health care organization's product evaluation and selection process."
2. Application techniques vary. A prep manufacturer's instructions for use are based on research the company has done on the best method of application for its specific antiseptic. For example, most povidone-iodine solution manufacturers recommend a circular application technique in which the product is applied from the least to the most contaminated areas. Most CHG product manufacturers, on the other hand, recommend a firm back-and-forth method of application, though also from least to most contaminated area.
3. Hair removal is optional. The link between hair removal at the surgical site and SSI risk is limited. Many of the studies performed on the topic did not use standardized definitions of SSIs, were underpowered and are roughly 20 years old. Where there is consensus is that hair should not be removed with razors as the evidence clearly demonstrates small microabrasions created in the skin increases the risk for SSIs. Current recommendations from AORN and the CDC state that hair removal should not be performed unless the presence of hair at the surgical site will interfere with the procedure. If hair must be removed, AORN recommends the use of clippers or a depilatory, while the CDC preferentially recommends clippers. AORN emphasizes the importance of removing hair outside the OR and with vacuum-assisted clippers or wet clipping to avoid dispersal of loose hair particles.
4. Size matters. Both AORN and the Association for Surgical Technologists recommend prepping an area that is wider than the planned incision. This additional prepped space allows for unforeseen developments such as the need to extend the incision or create an additional incision, the use of drains, or conversion of an endoscopic procedure to an open procedure. Additionally, following the manufacturer recommendations for the maximal treatment area per antiseptic applicator is key to avoiding inadequate skin disinfection.
You've identified prepping problem areas and implemented a process improvement plan, so what's next? Post-intervention audits measure the success of your efforts to improve prepping practices and identify new and persistent challenges. It's also imperative that your staff receive repeated education on prepping guidelines, technique demonstration and scientific rationale for best practices.
Ultimately, if you want to maintain the gains you achieve with an intervention, continue to measure compliance. Adopting a shifting schedule of random audits throughout the year or conducting a regular audit review of your electronic medical records to verify that preps were allowed to dry adequately before draping can help those compliance percentages to keep moving in the right direction and continue the climb above 50%. OSM
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