Skin and soft-tissue infections in suburban primary care: epidemiology of methicillin-resistant Staphylococcus aureus and observations on abscess management
© Weiss et al; licensee BioMed Central Ltd. 2011
Received: 18 May 2010
Accepted: 7 February 2011
Published: 7 February 2011
Reports from urban medical centers suggest that methicillin-resistant Staphylococcus aureus (MRSA) has become the most common cause of skin and soft-tissue infections (SSTIs). Risk factors for MRSA have been identified but have not been clinically useful.
From May 2006-April 2007, we performed an observational study of 529 SSTIs among ambulatory patients in the urgent care departments of a large suburban primary-care practice. SSTIs were included if they produced pus or fluid. The proportion of MRSA was determined overall (defined as prevalence) and by SSTI diagnosis. Potential risk factors for MRSA were examined with multivariate analysis, and descriptive statistics were generated for follow-up and abscess management. The prevalence of MRSA was 22% and did not rise during the study. MRSA was isolated from 36% of abscesses, 15% of cellulitis, and 14% of other SSTIs. Independent risk factors for MRSA included a prior history of MRSA (adjusted odds ratio [aOR], 41.05; 95% confidence interval [CI], 11.4-147.3), a close contact with prior MRSA (aOR, 12.83; 95% CI, 4.2-39.2), erythema ≥10 cm (aOR, 2.59; 95% CI, 1.5-4.4), and abscess diagnosis (aOR, 3.19; 95% CI, 2.1-5.0). Prior MRSA had a positive predictive value of 88% for current MRSA. When both abscess diagnosis and erythema ≥10 cm were present, the proportion of MRSA was 59%. The vast majority of SSTIs (96 percent) resolved or improved within one week. Most abscesses, even small ones, were treated with antibiotics. Resource utilization was highest in those abscesses with erythema ≥10 cm.
The prevalence of MRSA is relatively low among SSTIs in suburban primary care. However, MRSA is common in the subgroup of abscesses with large erythema. While the effectiveness of adjunctive antibiotic therapy for large abscesses is unknown, drugs chosen for these infections should be active against MRSA. Most non-abscess SSTIs do not require treatment with a MRSA-active drug, and antibiotics are probably overused for small abscesses. A history of prior MRSA should be recorded in a patient's health record.
The prevalence of methicillin-resistant Staphylococcus aureus (MRSA) in skin and soft-tissue infections (SSTIs) has reached epidemic proportions in the United States (US) according to studies published since 2004 [1–7]. The emergence of MRSA has been particularly rapid in some areas [3, 4, 7]. MRSA is resistant to beta-lactam antibiotics such as cephalexin and dicloxacillin which are traditionally used to treat SSTIs . With the rising prevalence of MRSA, many SSTIs may be inadequately treated if clinicians continue to rely on beta-lactam agents. Conversely, SSTIs not caused by MRSA may be treated unnecessarily with MRSA-active drugs.
Most MRSA isolates from SSTIs in the United States are descended from a clone of MRSA known as USA-300 [5, 6]. These isolates contain the SCCmec IV gene complex which conveys methicillin resistance [2, 9], and are termed community-associated MRSA (CA-MRSA) for lack of traditional risk factors linked to healthcare-associated infection [8, 9]. While CA-MRSA isolates are usually susceptible to tetracycline and trimethoprim-sulfamethoxazole (TMP/SMX), and have been universally susceptible to vancomycin, substantial resistance to both clindamycin and fluoroquinolones has been reported [2, 4, 6, 7]. Multiple risk factors for CA-MRSA have been identified in both outbreak [10–12] and endemic [2, 5, 6, 13–16] settings, but they appear to have limited clinical usefulness [6, 14]. Follow-up data suggest timely resolution in most SSTIs caused by MRSA [6, 17–20]. However, there have been reports of delayed treatment response [21–24], high hospitalization rates [4, 25], and severe infections [26, 27].
Early studies of endemic CA-MRSA were performed primarily in outpatient clinics, emergency departments, and hospitals associated with urban medical centers that serve indigent populations [1–7]. In addition, the types and sizes of SSTIs examined in some of these studies were not clearly defined [1, 3–5, 7]. To address these limitations, we investigated the epidemiology of MRSA in SSTIs among ambulatory patients from suburban areas in the San Francisco Bay Area (Bay Area). We classified SSTIs by diagnosis group and maximum erythema size, and also described initial treatment decisions and resource utilization in the management of abscesses.
This was an observational study of purulent or fluid-producing SSTIs that were sampled for bacterial culture among ambulatory patients from May 1, 2006 through April 30, 2007. Incision and drainage (I&D) of abscesses and culturing of pus and fluid from SSTIs were usual care prior to the study. Clinical decisions regarding procedures, cultures, antibiotics, and charting in the electronic health record (EHR) remained at the discretion of providers.
The study took place in the adult and pediatric urgent care departments (urgent care) of the Palo Alto Medical Foundation, Palo Alto Division (PAMF-PA), which have over 50,000 patient visits annually. PAMF-PA provides primary and specialty care to an ambulatory patient population of approximately 300,000 persons in the Bay Area, The primary care providers (PCPs) in the family medicine, internal medicine, and pediatrics departments at PAMF-PA frequently refer patients to urgent care for I&D of abscesses and for intravenous infusions of antibiotics. The study was funded by PAMF-PA.
Patients of any age were considered for inclusion in the study if a new SSTI was diagnosed by an urgent care provider and a bacterial culture was obtained from the infection site. An SSTI was considered new if there was no previous history of SSTI, or if greater than one month had elapsed since resolution of erythema and pus or fluid in a previous SSTI. Patients were excluded if they had a nonbacterial skin disorder (e.g. herpes simplex infection or trauma without infection) or a noncutaneous bacterial infection (e.g. vaginitis or peri-rectal abscess). Patients were not excluded if they had a history of risk factors for healthcare-associated MRSA.
The proportions of MRSA, methicillin-sensitive Staphylococcus aureus (MSSA), and Streptococcal species were determined overall and by three diagnosis groups: abscesses (discrete collections of pus including furuncles and carbuncles), cellulitis (spreading erythema with bullous or open purulent, moist, or fluid-producing areas), and other SSTIs (felon, folliculitis, impetigo, paronychia, septic bursitis, inflamed sebaceous cyst, and miscellaneous). The overall proportion of a bacterial isolate was termed its prevalence. Demographics and potential risk factors for MRSA versus non-MRSA culture results were examined. Erythema, an easily ascertained measure of infection size, was defined as the maximum dimension of erythema in any direction measured in cm. If erythema was not recorded in the EHR, an estimate was imputed using standard anthropometric tables  where possible. Erythema ≥10 cm was considered "large" erythema. Injection drug use was not examined because a previous case series of MRSA SSTIs at our institution revealed no patient with this history (unpublished data). Follow-up status was assessed as better or resolved, worse or no change, or lost to follow-up at last patient contact within seven days of the initial visit. Initial treatment selections for abscesses included antibiotic therapy (started or continued at the initial visit), I&D, both antibiotic and I&D, or neither antibiotic nor I&D. An antibiotic selection was considered "active" if the isolate was confirmed susceptible to the drug by laboratory testing. Repeat I&D and ≥3 follow-up visits were considered variables potentially affected by initial antibiotic selections. Resources utilized for abscess management (in addition to an oral antibiotic and/or initial I&D) were outpatient intravenous therapy (IV), hospitalization, repeat I&D, and ≥3 follow-up visits. Resource utilization was described by erythema size.
Reports listing all wound and body fluid culture results were reviewed thrice weekly to identify possible SSTIs for the study. Inclusion of SSTIs and assignment of diagnosis group was based on initial provider assessment and consensus between two authors (CW and PK). The visit during which the initial bacterial culture was performed was the initial visit. Specimens for aerobic culture were obtained with a Culturette EZ II™ transport swab (Becton Dickinson, Franklin Lakes, New Jersey) and were processed and cultured at the Mills-Peninsula Hospital Laboratory (San Mateo, CA) utilizing standard techniques . The Dade Behring Microscan system was used to determine antibiotic susceptibilities. The D-zone test was done on isolates that were erythromycin-resistant and clindamycin-susceptible to confirm clindamycin susceptibility.
A standardized SSTI template was available for provider use in the EHR. Data were extracted from the SSTI template or other EHR notes. As a proxy for individual income and education data, the socioeconomic status (SES) of the zip codes in which patients resided was examined using the US Postal Service  and US Census 2000 . Follow-up status was determined by EHR review and telephone calls made on days 3 and 7 after the initial visit. Up to two calls per patient were made on both days. Initial treatment selections and resource utilization for abscesses were recorded. The total number of I&D procedures performed in urgent care during the study period was provided by the information technology department at PAMF-PA.
All SSTIs, including those with no growth, were included in the analysis. Descriptive statistics were generated after data entry in Epi Info software, version 3.3.2, February 9, 2005 (CDC, Atlanta, Georgia). Analysis of potential risk factors for MRSA was performed for MRSA versus non-MRSA and for MRSA versus MSSA. Continuous variables were analyzed with the t-test and dichotomous variables with the chi-square test. Multivariate analysis was performed using logistic regression with variables either considered clinically important or with a significant association to specific outcome variables at the 0.05 significance level, using SAS, version 8.2 (Cary, North Carolina). Odds ratios (OR) and 95 percent confidence intervals (CI) were calculated. Separate models were created for demographical/historical variables and clinical variables.
The Institutional Review Board of the PAMF-PA approved the study. Verbal consent was obtained for follow-up telephone calls.
Demographical characteristics (N = 513)
17 days-93 years
Primary care at PAMF-PA
High income zip codes*(1)
High education zip codes*(2)
Proportion of bacterial isolates in skin and soft-tissue infections overall and by diagnosis group
MRSA, No. (%)
MSSA, No. (%)
Strep, No. (%)
All SSTI (N = 529)
Abscess (N = 185)
Cellulitis (N = 183)
Other SSTIs (N = 161)
The proportion of MRSA was highest in abscesses and lower in cellulitis and other SSTIs. If cases of folliculitis (10 of 20 [50 percent] positive for MRSA) were excluded from the other SSTIs group, the proportion of MRSA was only 8 percent. The monthly prevalence of MRSA and the monthly frequency of all SSTIs showed no overall increase during the study period.
Cumulative susceptibilities for MRSA isolates were 100 percent to TMP/SMX and vancomycin, 94 percent to tetracycline, 88 percent to clindamycin, and 45 percent to levofloxacin. Among the 14 MRSA isolates resistant to clindamycin, five were identified as having inducible resistance by the D-zone test.
Demographical and historical variables: overall, and MRSA vs. non-MRSA
All isolates, No. (%)
MRSA, No. (%)
Non-MRSA, No. (%)
Unadjusted OR (95% CI)
Adjusted OR (95% CI)*
(N = 529)
(N = 115)
(N = 414)
Age < 65 years
2.25 (1.0-4.9), P = 0.002
4.18 (2.4-7.4), P < 0.001
41.05 (11.4-147.3), P < 0.001
12.83 (4.2-39.2), P < 0.001
2.21 (1.3-3.8), P = 0.05
Clinical variables: overall, and MRSA vs. non-MRSA
All isolates, No. (%) of observations
MRSA, No. (%)
Non-MRSA, No. (%)
Unadjusted OR (95% CI)
Adjusted OR (95% CI)*
Erythema ≥10 cm
3.2 (2.0 - 5.2)
2.59 (1.5-4.4), P < 0.001
(N = 529)
(N = 115)
(N = 414)
Head and neck
(N = 529)
(N = 115)
(N = 414)
3.19 (2.1-5.0), P < 0.001
Proportion of MRSA by erythema size (N = 500)
MRSA, No./0-4 cm, No.(%)
MRSA, No./5-9 cm, No.(%)
MRSA, No./≥10 cm, No.(%)
All SSTIs (N = 500)
Abscess (N = 178)
Cellulitis (N = 165)
Other SSTIs (N = 157)
Follow-up was available for 399 (75 percent) of 529 SSTIs, 383 (96 percent) of which improved or resolved within seven days of initial visit, with no difference between MRSA and non-MRSA SSTIs (p = 0.60). Patients lost to follow-up were less likely to have erythema ≥10 cm (p = 0.004).
Initial antibiotic selections for abscesses (N = 172)
Abscesses, No. (%)
Beta-lactam plus MRSA-active
Resource* utilization for abscesses by erythema size (N = 143)†
0-4 cm erythema (N = 63)
5-9 cm erythema (N = 41)
≥10 cm erythema (N = 39)
≥3 Follow-Up visits
In this study of purulent or fluid-producing SSTIs, the prevalence of MRSA was 22 percent. This is substantially below the 42 to 64 percent range previously reported in the US [1–7]. While MRSA overall was less common in our patients, its proportion varied by risk factors. For example, when both abscess diagnosis and large erythema were present, MRSA was isolated in almost 60 percent of cases. Other risk factors for MRSA included a history of prior MRSA in the patient or a close contact, and age <65 years. A history of prior MRSA in the patient had a positive predictive value for current MRSA of 88 percent. Most abscesses were treated empirically with antibiotics, although selection of a drug to which the isolate was susceptible did not affect the outcomes we measured. Seventeen percent of abscesses did not undergo I&D at the initial visit, and 13 percent required a repeat I&D. Resource utilization for abscesses was highest for those with large erythema.
There are several possible explanations for the relatively low prevalence of MRSA in our patients. First, MRSA may have simply emerged more slowly in our region. Indeed, the prevalence of MRSA has been shown to vary geographically [6, 25]. However, a surge of MRSA in SSTIs in the Bay Area [1, 2] preceding our study makes this unlikely. Second, demographical differences may have contributed to a disparity in MRSA prevalence. Our patients resided in suburban zip codes with relatively high SES, and most had established primary care. In contrast, patients in earlier studies were identified in hospital-based clinics and emergency departments of urban medical centers that serve the poor [1–7]. Urban areas with the lowest income levels have been shown to have the highest incidence rates of MRSA , possibly related to clustering of MRSA cases in public housing and incarceration . Third, the distribution of SSTIs into abscesses, cellulitis, and other SSTIs was almost equal in our study. By comparison, abscesses predominated in several previous studies [1, 2, 6]. The lower proportion of abscesses in our study could have decreased the prevalence of MRSA as we found MRSA to be more common in abscesses. Finally, SSTIs in our study were not limited to those caused by S. aureus [4, 5]. Limiting our analysis to S. aureus alone would have resulted in a MRSA prevalence of 42 percent.
Our findings have implications for the treatment of SSTIs in primary care. For example, clinicians should consider diagnosis type when making antibiotic selections. We found that most culturable, non-abscess SSTIs are caused by bacteria other than MRSA. In fact, in the other SSTIs diagnosis group the proportion of MRSA was only 8 percent if cases of folliculitis, a potential precursor to abscess formation, were excluded. MRSA also appears to be uncommon in non-culturable cellulitis which is usually caused by Streptococcal species [33, 34] and responds to beta-lactam antibiotics . In contrast, we found MRSA to be common in abscesses with large erythema. Thus, antibiotics chosen for these infections should be MRSA-active based on local susceptibility testing. However, the imperative for antibiotic treatment of abscesses remains unclear [35–37]. Two randomized, controlled trials (RCTs) of TMP/SMX versus placebo for the treatment of skin abscesses after I&D showed no benefit of drug therapy in reducing treatment failure [38, 39]. From this standpoint, the high level of antibiotic coverage for abscesses observed in our study (93 percent) seems excessive. However, in both RCTs there were fewer new lesions in the TMP/SMX group after follow-up, leaving open the possibility of a drug benefit. Also, most abscesses in these studies had erythema or induration of <10 cm. Thus, the validity of their results for larger abscesses is unclear. One observational study of 531 community-acquired SSTIs (mostly abscesses) caused by MRSA that excluded "minor or superficial skin infections" found that lack of an active antibiotic was a risk factor for treatment failure . While we did not find an effect of active antibiotic therapy on the frequency of repeat I&D or follow-up visits for abscesses, the generalizability of our results is limited by the small sample size and observational design of our study.
In addition, some I&D procedures may be delayed or inadequate. While we are not aware of validated criteria by which to make these judgments, it is reasonable for clinicians to consider aspiration or ultrasound imaging if the presence of pus is unclear, or surgical consultation if there is doubt about the examiner's ability to perform an I&D.
Finally, greater resources are expended on abscesses with large erythema. Why some abscesses are large at presentation is unknown. Possible modifiable factors include delay in seeking medical care, attempts at self-treatment (e.g. squeezing or even incising the abscess), delayed or inadequate I&D, and inappropriate antibiotic selection or route of antibiotic delivery.
Our study also has implications for the prevention of SSTIs caused by MRSA. The strong association of prior MRSA in the patient or a close contact with current MRSA suggests that persistent MRSA colonization in the individual , and transmission of MRSA in households  contribute to incident MRSA SSTIs. The smaller proportion of SSTIs caused by MRSA among patients ≥65 years may reflect lower potential exposure through skin-to-skin contact or contaminated fomites as the elderly more typically live alone . De-colonization and limiting fomite exposure among household contacts are two possible strategies for limiting the spread of MRSA in the community.
There are several limitations to our study. First, only SSTIs that produced pus or fluid were included in the study. Excluding non-culturable cellulitis, which is largely Streptococcal in origin [33, 34], may have biased our estimation of the prevalence of MRSA upward. Second, the decision to culture an SSTI was left to the discretion of the provider. We do not know how many culturable SSTIs were not cultured. However, the observation that 68 percent of SSTIs undergoing I&D in urgent care during the study period were included in the study suggests case identification was good. Third, 25 percent of our patients were lost to follow-up and our follow-up extended to only one week. We may have missed some treatment failures or late complications. Finally, the small sample size and lack of experimental design of our study limited our ability to detect a treatment effect of active antibiotic therapy on outcomes for abscesses.
Future studies are needed to confirm the high proportion of MRSA in large abscesses, to examine the effect of adjunctive antibiotics in the treatment of abscesses (especially large abscesses), to define quality measures for I&D, and to determine why some SSTIs are large at presentation.
The prevalence of MRSA is relatively low in a broad range of SSTIs diagnosed in suburban primary care. In contrast, MRSA is the most common isolate in abscesses with large erythema. Empirical antibiotic treatment, if selected for these infections, should be active against MRSA. Many non-abscess SSTIs do not require empirical coverage for MRSA and over-treatment of small abscesses with antibiotics appears to be common.
Documentation of prior MRSA in health records may alert clinicians to the high probability of MRSA in subsequent culturable SSTIs.
We would like to thank Andrea Enright for her participation in the initial design and development of the study. We would also like to thank Nancy Hinojosa, Talayeh Nikpay, and Cliff Olson for technical assistance with the electronic health record, and Sukyung
Chung, Sara Cody, Laura Eaton, Harold Luft, Latha Palaniappan, and Henry Chambers for critically reviewing the manuscript.
Palo Alto Medical Foundation.
- Young DM, Harris HW, Charlebois ED, Chambers H, Campbell A, Perdreau-Remington F, Lee C, Mankani M, Mackersie R, Schecter W: An epidemic of methicillin-resistant Staphylococcus aureus soft tissue infections among medically underserved patients. Arch Surg. 2004, 139: 947-953. 10.1001/archsurg.139.9.947.PubMedView ArticleGoogle Scholar
- Frazee BW, Lynn J, Charlebois ED, Lambert L, Lowery D, Perdreau-Remington F: High prevalence of methicillin-resistant Staphylococcus aureus in emergency department skin and soft tissue infections. Ann Emerg Med. 2005, 45: 311-320. 10.1016/j.annemergmed.2004.10.011.PubMedView ArticleGoogle Scholar
- Moran GJ, Amii RN, Abrahamian FM, Talan DA: Methicillin-resistant Staphylococcus aureus in community-acquired skin infections. Emerg Infect Dis. 2005, 11: 928-930.PubMedPubMed CentralView ArticleGoogle Scholar
- Clancy MJ, Graepler A, Breese PE, Price CS, Burman WJ: Widespread emergence of methicillin resistance in community-acquired Staphylococcus aureus infections in Denver. South Med J. 2005, 98: 1069-1075. 10.1097/01.smj.0000184800.83171.f7.PubMedView ArticleGoogle Scholar
- King MD, Humphrey BJ, Wang YF, Kourbatova EV, Ray SM, Blumberg HM: Emergence of community-acquired methicillin-resistant Staphylococcus aureus USA 300 clone as the predominant cause of skin and soft-tissue infections. Ann Intern Med. 2006, 144: 309-317.PubMedView ArticleGoogle Scholar
- Moran GJ, Krishnadasan A, Gorwitz RJ, Fosheim GE, McDougal LK, Carey RB, Talan DA: Methicillin-resistant S. aureus infections among patients in the emergency department. N Engl J Med. 2006, 355: 666-674. 10.1056/NEJMoa055356.PubMedView ArticleGoogle Scholar
- Johnson JK, Khoie T, Shurland S, Kreisel K, Stine OC, Roghmann M: Skin and soft tissue infections caused by methicillin-resistant Staphylococcus aureus USA 300 clone. Emerg Infect Dis. 2007, 13: 1195-1200.PubMedPubMed CentralView ArticleGoogle Scholar
- Community-Associated MRSA Information for Clinicians. [http://www.cdc.gov/ncidod/dhqp/ar_mrsa_ca_clinicians.html]
- Naimi TS, LeDell KH, Como-Sabetti K, Borchardt SM, Boxrud DJ, Etienne J, Johnson SK, Vandenesch F, Fridkin S, O'Boyle C, Danila RN, Lynfield L: Comparison of community- and health care-associated methicillin-resistant Staphylococcus aureus infection. JAMA. 2003, 290: 2976-2984. 10.1001/jama.290.22.2976.PubMedView ArticleGoogle Scholar
- Campbell KM, Vaughn AF, Russell KL, Smith B, Jimenez DL, Barrozo CP, Minarcik JR, Crum NF, Ryan MA: Risk factors for community-associated methicillin-resistant Staphylococcus aureus infections in an outbreak of disease among military trainees in San Diego, California, in 2002. J Clin Microbiol. 2004, 42: 4050-4053. 10.1128/JCM.42.9.4050-4053.2004.PubMedPubMed CentralView ArticleGoogle Scholar
- Begier EM, Frenette K, Barrett NL, Mshar P, Petit S, Boxrud DJ, Watkins-Colwell K, Wheeler S, Cebelinski EA, Glennen A, Nguyen D, Hadler JL: A high morbidity outbreak of methicillin-resistant Staphylococcus aureus among players on a college football team, facilitated by cosmetic body shaving and turf burns. Clin Infect Dis. 2004, 39: 1446-1453. 10.1086/425313.PubMedView ArticleGoogle Scholar
- Turabelidze G, Lin M, Wolkoff B, Dodson D, Gladbach S, Zhu B: Personal hygiene and methicillin-resistant Staphylococcus aureus infection. Emerg Infect Dis. 2006, 12: 422-427.PubMedPubMed CentralView ArticleGoogle Scholar
- Community-associated methicillin-resistant Staphylococcus aureus infections in Pacific Islanders--Hawaii, 2001-2003. MMWR. 2004, 53: 767-770.
- Miller LG, Perdreau-Remington F, Bayer AS, Diep B, Tan N, Bharadwa K, Tsui J, Perlroth J, Shay A, Tagudar G, Ibebuogu U, Spellberg B: Clinical and epidemiologic characteristics cannot distinguish community-associated methicillin-resistant Staphylococcus aureus infection from methicllin-susceptible S. aureus infection: a prospective investigation. Clin Infect Dis. 2007, 44: 471-482. 10.1086/511033.PubMedView ArticleGoogle Scholar
- Hota B, Ellenbogen C, Hayden MK, Aroutcheva A, Rice TW, Weinstein RA: Community-associated methicillin-resistant Staphylococcus aureus skin and soft tissue infections at a public hospital--do public housing and incarceration amplify transmission?. Arch Intern Med. 2007, 167: 1026-1033. 10.1001/archinte.167.10.1026.PubMedView ArticleGoogle Scholar
- Cohen AL, Shuler C, McAllister S, Fosheim GE, Brown MG, Abercrombie D, Anderson K, McDougal LK, Drenzek C, Arnold K, Jernigan J, Gorwitz R: Methamphetamine use and methicillin-resistant Staphylococcus aureus skin infections. Emerg Infect Dis. 2007, 13: 1707-1713.PubMedPubMed CentralView ArticleGoogle Scholar
- Lee MC, Rios AM, Fonseca Aten M, Mejias A, Cavuoti D, McCracken GH, Hardy RD: Management and outcome of children with skin and soft tissue abscesses caused by community-acquired methicillin-resistant Staphylococcus aureus. Pediatr Infect Dis. 2004, 23: 123-127. 10.1097/01.inf.0000109288.06912.21.View ArticleGoogle Scholar
- Barnes EV, Dooley DP, Hepburn MJ, Baum SE: Outcomes of community-acquired, methicillin-resistant Staphylococcus aureus soft tissue infections treated with antibiotics other than vancomycin. Mil Med. 2006, 171: 504-507.PubMedView ArticleGoogle Scholar
- Ruhe JJ, Smith N, Bradsher RW, Menon A: Community-onset methicillin-resistant Staphylococcus aureus skin and soft-tissue infections: impact of antimicrobial therapy on outcome. Clin Infect Dis. 2007, 44: 777-784. 10.1086/511872.PubMedView ArticleGoogle Scholar
- Rajendran PM, Young D, Maurer T, Chambers H, Perdreau-Remington F, Ro P, Harris H: Randomized, double-blind, placebo-controlled trial of cephalexin for treatment of uncomplicated skin abscesses in a population at risk for community-acquired methicillin-resistant Staphyloccocus aureus infection. Antimicrob Agents Chemother. 2007, 51: 4044-4048. 10.1128/AAC.00377-07.PubMedPubMed CentralView ArticleGoogle Scholar
- Iyer S, Jones DH: Community-acquired methicillin-resistant Staphylococcus aureus skin infection: a retrospective analysis of clinical presentation and treatment of a local outbreak. J Am Acad Dermatol. 2004, 50: 854-858. 10.1016/j.jaad.2003.12.043.PubMedView ArticleGoogle Scholar
- Szumowski JD, Cohen DE, Kanaya F, Mayer KH: Treatment and outcomes of infections by methicillin-resistant Staphylococcus aureus at an ambulatory clinic. Antimicrob Agents Chemother. 2007, 51: 423-428. 10.1128/AAC.01244-06.PubMedPubMed CentralView ArticleGoogle Scholar
- Miller LG, Quan C, Shay A, Mostafaie K, Tan N, Matayoshi K, Cronin J, Tan J, Tagudar G, Bayer AS: A prospective investigation of outcomes after hospital discharge for endemic, community-acquired methillin-resistant and -susceptible Staphylococcus aureus skin infection. Clin Infect Dis. 2007, 44: 483-492. 10.1086/511041.PubMedView ArticleGoogle Scholar
- Davis SL, Perri MB, Donabedian SM, Manierski C, Singh A, Vager D, Haque NZ, Speirs K, Muder RR, Robinson-Dunn B, Hayden MK, Zervos MJ: Epidemiology and outcomes of community-associated methicillin-resistant Staphylococcus aureus infection. J Clin Microbiol. 2007, 45: 1705-1711. 10.1128/JCM.02311-06.PubMedPubMed CentralView ArticleGoogle Scholar
- Fridkin SK, Hageman JC, Morrison M, Thomson Sanza L, Como-Sabetti K, Jernigan JA, Harriman K, Harrison LH, Lynfield R, Farley MM: Methicillin-resistant Staphylococcus aureus in three communities. N Engl J Med. 2005, 352: 1436-1444. 10.1056/NEJMoa043252.PubMedView ArticleGoogle Scholar
- Miller LG, Perdreau-Remington F, Rieg G, Sheherbano M, Perlroth J, Bayer AS, Tang AW, Phung TO, Spellberg B: Necrotizing fasciitis caused by community-associated methicillin-resistant Staphylococcus aureus in Los Angeles. N Engl J Med. 2005, 352: 1445-1453. 10.1056/NEJMoa042683.PubMedView ArticleGoogle Scholar
- Pannaraj PS, Hulten KG, Gonzalez BE, Mason EO, Kaplan SL: Infective pyomyositis in children in the era of community-acquired, methicillin-resistant Staphylococcus aureus infection. Clin Infect Dis. 2006, 43: 953-960. 10.1086/507637.PubMedView ArticleGoogle Scholar
- Anthropometric reference data for children and adults: U.S. population, 1999-2002. [http://www.cdc.gov/nchs/data/ad/ad361.pdf]
- Performance standards for antimicrobial susceptibility testing: 17th informational supplement. M100-S17. 2007, Wayne, Pa.: Clinical and Laboratory Standards Institute
- USPS Zip Code Lookup. [http://zip4.usps.com/zip4/citytown_zip.jsp]
- American FactFinder. [http://factfinder.census.gov/home/saff/main.html?_lang=en]
- Liu C, Graber CJ, Karr M, Diep BA, Basuino L, Schwartz BS, Enright MC, O'Hanlon SJ, Thomas JC, Perdreau-Remington F, Gordon S, Gunthorpe H, Jacobs R, Jensen P, Leoung G, Rumack JS, Chambers HF: A population-based study of the incidence and molecular epidemiology of methicillin-resistant Staphylococcus aureus disease in San Francisco, 2004-2005. Clin Infect Dis. 2008, 46: 1637-1646. 10.1086/587893.PubMedView ArticleGoogle Scholar
- Bernard P, Bedane C, Mounier M, Denis F, Catanzano G, Bonnetblanc JM: Streptococcal cause of erysipelas and cellulitis in adults. Arch Dermatol. 1989, 125: 779-782. 10.1001/archderm.125.6.779.PubMedView ArticleGoogle Scholar
- Jeng A, Beheshti M, Li J, Nathan R: The role of beta-hemolytic Streptococci in causing diffuse, nonculturable cellulitis. Medicine. 2010, 89: 217-226. 10.1097/MD.0b013e3181e8d635.PubMedView ArticleGoogle Scholar
- Gorwitz RJ: The role of ancillary antimicrobial therapy for treatment of uncomplicated skin infections in the era of community-associated methicillin-resistant Staphylococcus aureus. Clin Infect Dis. 2007, 44: 785-787. 10.1086/511884.PubMedView ArticleGoogle Scholar
- Chambers HF, Moellering RC, Kamitsuka P: Management of skin and soft-tissue infection. N Engl J Med. 2008, 359: 1063-1067. 10.1056/NEJMclde0708359.PubMedView ArticleGoogle Scholar
- Talan DA: The lack of antibiotic efficacy for simple abscesses: have matters come to a head?. Ann Emerg Med. 2010, 55: 412-414. 10.1016/j.annemergmed.2010.02.024.PubMedView ArticleGoogle Scholar
- Duong M, Markwell S, Peter J, Barenkamp S: Randomized, controlled trial of antibiotics in the management of community-acquired skin abscesses in the pediatric patient. Ann Emerg Med. 2010, 55: 401-407. 10.1016/j.annemergmed.2009.03.014.PubMedView ArticleGoogle Scholar
- Schmitz GR, Bruner D, Pitotti R, Olderog C, Livengood T, Williams J, Huebner K, Lightfoot J, Ritz B, Bates C, Schmitz M, Mete M, Deye G: Randomized controlled trial of trimethoprim-sulfamethoxazole for uncomplicated skin abscesses in patients at risk for community-associated methicillin-resistant Staphylococcus aureus infection. Ann Emerg Med. 2010, 56: 283-287. 10.1016/j.annemergmed.2010.03.002.PubMedView ArticleGoogle Scholar
- Robicsek A, Beaumont J, Peterson L: Duration of colonization with methicillin-resistant Staphylococcus aureus. Clin Infect Dis. 2009, 48: 910-913. 10.1086/597296.PubMedView ArticleGoogle Scholar
- Mollema F, Richardus J, Behrendt M, Vaessen N, Lodder W, Hendriks W, Verbrugh H, Vos M: Transmission of methicillin-resistant Staphylococcus aureus to household contacts. J Clin Microbiol. 2010, 48: 202-207. 10.1128/JCM.01499-09.PubMedPubMed CentralView ArticleGoogle Scholar
- America's Families and Living Arrangements: 2003. [http://www.census.gov/prod/2004pubs/p20-553.pdf]
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