infection control and hospital epidemiology june 2007, vol. 28, no. 6 concise communication Evaluation of the Microbiology of Soft-Tissue Abscesses in the Era of Community-Associated Strains of Methicillin-Resistant Staphylococcus aureus: An Argument for Empirical Contact Precautions Thomas R. Talbot, MD, MPH; Joseph J. Nania, MD; Patty W. Wright, MD; Ian Jones, MD; Dominik Aronsky, MD, PhD To ascertain the microbiology of skin abscesses, emergency department records were reviewed to identify patients with debrided skin abscesses. Methicillin-resistant Staphylococcus aureus was isolated from 255 (67.6%) of 377 culture samples from episodes in the adult cohort and from 145 (79.7%) of 182 culture samples from episodes in the pediatric cohort. Thus, empirical use of contact precautions for patients with skin abscesses should be strongly considered. Infect Control Hosp Epidemiol 2007; 28:730-732 Recently, the number of infections due to antibiotic-resistant strains of Staphylococcus aureus has increased dramatically.1 In particular, the emergence of community-associated strains of methicillin-resistant S. aureus (MRSA) has become a growing concern.2,3 To prevent transmission of MRSA, the Centers for Disease Control and Prevention (CDC) recommends that any patient with MRSA infection or colonization be placed under contact precautions in medical settings.4 Such precautions have reduced the transmission of MRSA but can also be costly to implement.5 According to CDC guidelines, the care of a patient with a soft-tissue abscess involves only the use of standard precautions for anticipated exposure to blood or body fluids during dressing changes; use of other precautions for routine patient contact is not recommended, except for those who are caring for a patient with an uncovered or inadequately covered draining lesion or with an abscess due to a multidrug-resistant organism, such as MRSA, instances which require contact precautions.4 With the emergence of community-associated strains of MRSA, it is unclear whether these isolation recommendations should be altered. We hypothesized that MRSA is now the predominant cause of skin abscesses in adults and children. As such, empirical use of contact precautions may be warranted for all types of patient care activities performed for such persons to prevent secondary MRSA transmission. methods We conducted a retrospective, descriptive epidemiologic study to ascertain the microbiology of skin and soft-tissue abscesses in patients who presented to an emergency department at a tertiary care academic medical center. The study population included all adult patients (ie, patients aged 18 years or older) and pediatric patients (ie, those aged less than 18 years) who met the following 3 criteria. (1) The patient visited the emergency department during the period from November 1, 2004, through October 31, 2005. (2) The patient presented with 1 of 4 complaints coded in the International Classification of Diseases, Ninth Edition (ICD-9): “infection of skin” (686.9), “mass/superficial swelling” (782.2), “insect bite” (919.4), or “sting: snake, lizard, spider” (989.5), as recorded in the computerized emergency department record. (3) The patient underwent an incision and drainage procedure, as determined by institutional accounting data. Persons with a surgical site infection, laceration infection, or abscess at a site other than the skin (eg, odontogenic or perirectal abscess) were excluded from the study cohort. Investigators (T.R.T., J.J.N., and P.W.W.) conducted chart reviews to confirm the presence and location of the abscess (by provider diagnosis or description of expressed purulent matter upon incision and drainage). Microbiologic data collected included the time of culture sample collection, time of final pathogen identification, and culture results. The study was approved by the Vanderbilt University institutional review board. Comparisons were made between abscess episodes in which specimens were obtained for culture (hereafter, cultured episodes) and episodes in which specimens were not obtained (hereafter, noncultured episodes) using the Fisher exact test. Data are reported per episode of infection. Analyses were conducted using Stata software, version 7.0 (Stata). results Of 764 abscesses that were debrided, 63 were excluded due to the presence of an alternate diagnosis. Among the 701 episodes included, 486 (69%) occurred in adult patients and 215 (31%) occurred in pediatric patients (Table). During the study period, 43 (8.9%) of the adult patients and 8 (3.7%) of the pediatric patients presented on multiple occasions with skin abscesses that were debrided. In both the adult and pediatric cohorts, the most common anatomic sites for abscesses were the extremities and the pelvis. Specimens for culture were obtained for a majority of episodes (78% of adult episodes and 85% of pediatric episodes). Cultured episodes were significantly more likely to occur in male patients (49% of cultured episodes vs 38% of noncultured episodes; P p .02), more often involved abscesses located on the pelvis (28% vs 18%; P ! .001), and less often involved abscesses located on the upper extremities (25% vs 32%; P p .03). When cultured and noncultured abscess episodes were compared, there were no significant differences in patient age or the frequency of other abscess sites. soft-tissue abscesses, mrsa, and contact precautions 731 table. Characteristics of Episodes of Debrided Soft-Tissue Abscess in Adult and Pediatric Emergency Department Patients Variable Patient age, mean (range), years Male sex, % of patients Location of abscessb Head Chest Back Upper extremity Abdomen Pelvis Lower extremity Not noted Culture results Abscess culture performed S. aureus isolated (% of cultured episodes) MRSA isolated (% of cultured episodes) Time to pathogen identification,c mean (95% CI), days Adult patient episodes (n p 486) Pediatric patient episodes (n p 215) 32.4 (18-77) 44.4 7.8 (0.2-18)a 51.6 49 12 21 137 35 122 145 0 (10.1) (2.5) (4.3) (28.2) (7.2) (25.1) (29.8) 18 7 4 43 19 62 60 2 (8.4) (3.3) (1.9) (20.0) (8.8) (28.8) (27.9) (0.9) 377 (77.6) 182 (84.7) 298 (79.1) 169 (92.9) 255 (67.6) 145 (79.7) 2.4 (2.3-2.4) 2.2 (2.1-2.3) note. Data are no. (%) of episodes, unless otherwise indicated. Cultured episode, episode of cutaneous abscess from which a culture sample was obtained; CI, confidence interval; MRSA, methicillin-resistant S. aureus. a Due to rounding, the value for the upper age range of the pediatric cohort (17.96) and the lower age range of the adult cohort (18.04) both equal 18. b Counts sum to more than the total number of episodes because there were multiple concurrent abscesses at different anatomic locations during some episodes. c Time from specimen collection to final pathogen identification and susceptibility testing. Among the adult cohort, MRSA was isolated in 255 (52.5%) of 486 abscess episodes and in 255 (67.6%) of 377 cultured episodes (Figure). Of the 25 soft-tissue abscess episodes in the adult cohort that required hospitalization, culture yielded MRSA in 14 (56%). Among the pediatric cohort, MRSA was isolated in 145 (67.4%) of 215 abscess episodes and in 145 (79.7%) of 182 cultured episodes. Of the 27 abscess episodes in the pediatric cohort that required hospitalization, culture yielded MRSA in 21 (78%). Episodes requiring hospitalization occurred significantly more often in males and more often involved abscesses on the abdomen or upper extremities (data not shown). The mean time from culture sample collection to final identification of a causative pathogen was 2.4 days (95% CI, 2.3-2.4) for episodes in the adult cohort and 2.2 days (95% CI, 2.1-2.3) for episodes in the pediatric cohort. diatric nasal carriage of MRSA has increased 10-fold in Nashville in 4 years,6 and reports of severe MRSA infections in previously healthy persons are increasing.2 Augmenting these findings, the present study confirms that MRSA causes a sub- discussion In a remarkably short period of time, the incidence of infection and colonization with MRSA has markedly increased.1 MRSA now accounts for three-fourths of all pediatric community-onset S. aureus skin infections in some centers,3 pe- figure. Culture findings for episodes of cutaneous abscess in emergency department patients, by pathogen (abscess episodes in adults, n p 377; abscess episodes in pediatric patients, n p 182). MRSA, methicillin-resistant Staphylococcus aureus; MSSA, methicillin-sensitive S. aureus. 732 infection control and hospital epidemiology june 2007, vol. 28, no. 6 stantial majority of debrided soft-tissue abscesses in both adult and pediatric emergency department patients, which mirrors other recently reported data on adults with softtissue infections presenting to university-affiliated emergency departments.7 In light of these findings, methods to prevent MRSA transmission in healthcare settings, such as the use of isolation precautions, must be increasingly emphasized. Use of contact precautions (in which care providers wear gowns and gloves if direct contact with the patient or the patient’s environment is anticipated, and private rooms or cohorting of patients is used) is a cornerstone of efforts to reduce MRSA transmission4 and is recommended for all patients with either MRSA infection or colonization. In contrast, in the absence of infection or colonization with an antibiotic-resistant pathogen, current guidelines recommend use of contact precautions for patients with a skin or soft-tissue abscess only if the lesion is not covered by a dressing or the dressing does not contain drainage adequately.4 The finding that MRSA causes the majority of these infections, however, argues for the use of empirical contact precautions for all patients with a skin or softtissue abscess because of concerns about colonization with multidrug-resistant bacteria and the risk of secondary transmission of MRSA by healthcare workers. Although most patients with a skin or soft-tissue abscess in our study did not require hospitalization, transmission of MRSA from infected (and presumptively colonized) individuals to other patients via healthcare workers may have occurred, even during the limited time spent in the emergency department before discharge. Empirical use of contact precautions for patients presenting with a soft-tissue abscess who require hospitalization may have an even greater impact, as use of empirical precautions would have averted more than 2 days of unprotected exposure, compared with precautions implemented after identification of MRSA. In 2003, the Society for Healthcare Epidemiology of America (SHEA) recommended a comprehensive strategy to prevent MRSA transmission in healthcare settings, including screening and empirical isolation of persons at high risk for MRSA carriage.8 The findings of the current study may also impact isolation practices in healthcare institutions that have fully implemented the SHEA recommendations. Specifically, the classification of high-risk patients is determined institutionally, on the basis of patient populations and pathogen prevalence,5 and may include prior healthcare exposures, antimicrobial use, and severity of comorbid illnesses. However, as community-associated MRSA soft-tissue infections often occur in previously healthy persons without prior healthcare exposure, such individuals may not be deemed high-risk by healthcare providers. In summary, MRSA was responsible for over two-thirds of all adult episodes of debrided skin and soft-tissue infections and for three-fourths of all pediatric episodes. These findings argue that implementation of empirical contact precautions for all patients with soft-tissue abscesses should be considered. acknowledgments We acknowledge Jennifer Pritchett for the linkage to the institutional financial data and C. Buddy Creech MD, MPH, and William Schaffner, MD, for their critical review of the manuscript. Financial support. T.R.T. has received research funding from Nabi Pharmaceuticals and support from GlaxoSmithKline. Potential conflicts of interest. All authors report no conflicts of interest relevant to this article. From the Division of Infectious Diseases in the Department of Medicine (T.R.T., P.W.W.), the Division of Infectious Diseases in the Department of Pediatrics (J.J.N.), and the Departments of Preventive Medicine (T.R.T.), Emergency Medicine (I.J., D.A.), and Biomedical Informatics (D.A.), Vanderbilt University School of Medicine, Nashville, Tennessee. Address reprint requests to Thomas R. Talbot, MD MPH, A-2200 Medical Center North, 1161 21st Avenue South, Vanderbilt University Medical Center, Nashville, TN 37232 (tom.talbot@vanderbilt.edu). Presented in part: 16th Annual Scientific Meeting of the Society of Healthcare Epidemiology of America; Chicago, IL; March 19, 2006 (Abstract 50). Received June 20, 2006; accepted September 5, 2006; electronically published April 19, 2007. 䉷 2007 by The Society for Healthcare Epidemiology of America. All rights reserved. 0899-823X/2007/2806-0017$15.00. DOI: 10.1086/516799 references 1. National Nosocomial Infections Surveillance (NNIS) System Report, data summary from January 1992 through June 2004, issued October 2004. Am J Infect Control 2004; 32:470-485. 2. Fridkin SK, Hageman JC, Morrison M, et al. Methicillin-resistant Staphylococcus aureus disease in three communities. N Engl J Med 2005; 352: 1436-1444. 3. Kaplan SL, Hulten KG, Gonzalez BE, et al. Three-year surveillance of community-acquired Staphylococcus aureus infections in children. Clin Infect Dis 2005; 40:1785-1791. 4. Garner JS. Guideline for isolation precautions in hospitals. The Hospital Infection Control Practices Advisory Committee. Infect Control Hosp Epidemiol 1996; 17:53-80. 5. Jackson M, Jarvis WR, Scheckler WE. HICPAC/SHEA—conflicting guidelines: what is the standard of care? Am J Infect Control 2004; 32:504-511. 6. Creech CB 2nd, Kernodle DS, Alsentzer A, Wilson C, Edwards KM. Increasing rates of nasal carriage of methicillin-resistant Staphylococcus aureus in healthy children. Pediatr Infect Dis J 2005; 24:617-621. 7. Moran GJ, Krishnadasan A, Gorwitz RJ, et al. Methicillin-resistant S. aureus infections among patients in the emergency department. N Engl J Med 2006; 355:666-674. 8. Muto CA, Jernigan JA, Ostrowsky BE, et al. SHEA guideline for preventing nosocomial transmission of multidrug-resistant strains of Staphylococcus aureus and enterococcus. Infect Control Hosp Epidemiol 2003; 24:362-386.