News & Updates

Dr. Paul Kamitsuka published in the New England Journal of Medicine

September 04, 2008

Incision and Drainage plus Anti-MRSA Therapy

First, although decisions regarding the choice of empirical antibiotics should be made on the basis of local resistance data when possible, the likelihood that our patient has a community-associated MRSA infection is considerable. He is an athlete with exposure to skin flora through physical contact in geographic locales across the United States. In a study of acute skin and soft-tissue infections in patients presenting to emergency departments in 11 U.S. cities, 59% of the infections were due to community-associated MRSA (range, 15 to 74).6 Nonetheless, it is advisable to obtain a sample for culture at the time of incision and drainage, not only to focus current treatment but also to have susceptibility data in case the infection recurs and eradication of community-associated MRSA is needed.

Second, although it has long been accepted that most MRSA soft-tissue abscesses may be treated with incision and drainage alone,13 recent data suggest that antibiotics may play a more important role in treating abscesses due to community- associated MRSA. Unlike traditional MRSA strains,20 community-associated MRSA strains often produce Panton-Valentine leukocidin, a pore-forming cytotoxin associated with increased tissue destruction. In a retrospective cohort study of 492 adults with 531 independent episodes of skin and soft-tissue infections with community associated MRSA, most of whom underwent incision and drainage, therapy was successful in 95% of those receiving an active antibiotic as compared with 87% of those who did not.10 Use of an inactive antimicrobial agent was an independent predictor of treatment failure on logistic regression analysis (adjusted odds ratio, 2.80; 95% confidence interval, 1.26 to 6.22; P = 0.01). Szumowski et al.21 found, in a retrospective review of 399 sequential cases of culture-confirmed S. aureus skin and soft-tissue infections, including 227 cases of MRSA infection, use of an antibiotic to which the isolate was sensitive was associated with an increased likelihood of clinical resolution (odds ratio, 5.91, as compared with no such use), after adjustment for incision and drainage and human immunodeficiency virus status. Finally, in a prospective observational study of a pediatric population, Lee et al.8 found that an infected site more than 5 cm in diameter treated by means of incision and drainage was less likely to respond in the absence of effective antibiotic therapy than with such therapy. Our patient's abscess is 5 cm in diameter.

A third consideration is whether providing effective antibiotics will decrease the risk of persistent carriage and thereby prevent recurrent infection as well as spread of community-associated MRSA to others. The answer to this question awaits further study, although in the absence of hard data clinicians often find themselves attempting to break the cycle of recurrent infection with the combined use of systemic antibiotics and topical antiseptics. Recurrent skin and soft-tissue infection is a vexing characteristic of community-associated MRSA, with estimates of recurrence ranging from 10%22 to 23.8%.21 Although some of these recurrences may be due to infection with a different community-associated MRSA strain, others result from persistent cutaneous carriage of the original strain after resolution of the initial infection. The spread of community-associated MRSA to household contacts is also problematic. Zafar et al.23 found that 20% of household contacts of patients with community- associated MRSA skin and soft-tissue infections carried MRSA, with half the MRSA strains related to the patient's infective isolate. A previous study reported household MRSA-carriage rates of 14.5%.24 Anecdotal evidence suggests that more than 60% of households of children hospitalized with community-associated MRSA infections include one or more family members who had a putative MRSA infection in the previous 6 months.22 The likelihood of clinical infection after colonization by community-associated MRSA appears to be considerable. Ellis et al.,25 in a prospective observational study of soldiers, found that soft tissue infections developed over a period of 8 to 10 weeks in 9 of 24 (38%) of those with community-associated MRSA in their nares, as compared with only 8 of 229 (3%) of those with nasal carriage of MSSA (P<0.001).

For our athlete, eager to resolve his infection before next week's game, the provision of an antibiotic effective against community-associated MRSA, perhaps with the use of 2% chlorhexidine for bathing, appears to be prudent.

No potential conflict of interest relevant to this article was reported.

From Wilmington Health and the Department of Medicine, University of North Carolina School of Medicine, Wilmington.

1. Burn JI, Curwen MP, Huntsman RG, Shooter RA. A trial of penicillin V: response of penicillin-resistant staphylococcal infections to penicillin. BMJ 1957;2:193-6.
2. Anderson J. Dispensability of post-operative penicillin in septic-hand surgery. BMJ 1958;2:1569-71.
3. Rutherford WH, Hart D, Calderwood JW, Merrett JD. Antibiotics in surgical treatment of septic lesions. Lancet 1970;1:1077-80.
4. Macfie J, Harvey J. The treatment of acute superficial abscesses:a prospective clinical trial. Br J Surg 1977;64:264-6.
5. Llera JL, Levy RC. Treatment of cutaneous abscess: a doubleblind clinical study. Ann Emerg Med 1985;14:15-9.
6. Moran GJ, Krishnadasan A, Gorwitz RJ, et al. Methicillinresistant S. aureus infections among patients in the emergency department. N Engl J Med 2006;355:666-74.
7. Fridkin SK, Hageman JC, Morrison M, et al. Methicillin-resistant Staphylococcus aureus disease in three communities. N Engl J Med 2005;352:1436-44. [Erratum, N Engl J Med 2005;352:2362.]
8. Lee MC, Rios AM, Aten MF, et al. Management and outcome of children with skin and soft tissue abscesses caused by community- acquired methicillin-resistant Staphylococcus aureus. Pediatr Infect Dis J 2004;23:123-7.
9. Giordano PA, Elston D, Akinlade BK, et al. Cefdinir vs. cephalexin for mild to moderate uncomplicated skin and skin structure infections in adolescents and adults. Curr Med Res Opin 2006;22:2419-28.
10. 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;44:777-84.
11. Rajendran PM, Young D, Maurer T, et al. Randomized, doubleblind, placebo-controlled trial of cephalexin for treatment of uncomplicated skin abscesses in a population at risk for community-acquired methicillin-resistant Staphylococcus aureus infection. Antimicrob Agents Chemother 2007;51:4044-8.
12. Swartz MN. Cellulitis. N Engl J Med 2004;350:904-12.
13. Stevens DL, Bisno AL, Chambers HF, et al. Practice guidelines for the diagnosis and management of skin and soft-tissue infections. Clin Infect Dis 2005;41:1373-406. [Errata, Clin Infect Dis 2005;41:1830, 2006;42:1219.]
14. Eron LJ, Lipsky BA. Use of cultures in cellulitis: when, how, and why? Eur J Clin Microbiol Infect Dis 2006;25:615-7.
15. Peralta G, Padron E, Roiz MP, et al. Risk factors for bacteremia in patients with limb cellulitis. Eur J Clin Microbiol Infect Dis 2006;25:619-26.16. F, Brooks GF. Characterization of antimicrobial resistance in Streptococcus pyogenes from the San Francisco Bay area of northern California. J Clin Microbiol 1999;37:1727-31.
17. Moellering RC Jr. Current treatment options for community acquired methicillin-resistant Staphylococcus aureus infection. Clin Infect Dis 2008;46:1032-7.
18. Kaplan SL, Hulten KG, Gonzalez BE, et al. Three-year surveillance of community-acquired Staphylococcus aureus infections in children. Clin Infect Dis 2005;40:1785-91.
19. King MD, Humphrey BJ, Wang YF, Kourbatova EV, Ray SM, Blumberg HM. Emergence of community-acquired methicillinresistant Staphylococcus aureus USA 300 clone as the predominant cause of skin and soft-tissue infections. Ann Intern Med 2006;144:309-17.
20. Moellering RC. The growing menace of community-acquired methicillin-resistant Staphylococcus aureus. Ann Intern Med 2006;144:368-70.
21. 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;51:423-8.
22. Daum RS. Skin and soft-tissue infections caused by methicillin-resistant Staphylococcus aureus. N Engl J Med 2007;357:380- 90. [Erratum, N Engl J Med 2007;357:1357.]
23. Zafar U, Johnson LB, Hanna M, et al. Prevalence of nasal colonization among patients with community-associated methicillin- resistant Staphylococcus aureus infection and their household contacts. Infect Control Hosp Epidemiol 2007;28:966-9.
24. Calfee DP, Durbin LJ, Germanson TP, Toney DM, Smith EB, Farr BM. Spread of methicillin-resistant Staphylococcus aureus (MRSA) among household contacts of individuals with nosocomially acquired MRSA. Infect Control Hosp Epidemiol 2003;24:422-6.
25. Ellis MW, Hospenthal DR, Dooley DP, Gray PJ, Murray CK. Natural history of community-acquired methicillin-resistant Staphylococcus aureus colonization and infection in soldiers. Clin Infect Dis 2004;39:971-9.
Copyright 2008 Massachusetts Medical Society.