Cellulitis: getting it right

Commentary

James Ducharme, MD CM, FRCP

Department of Emergency Medicine, Dalhousie University; Department of Emergency Medicine, Atlantic Health Sciences Corporation, Saint John, NB

CJEM 2005;7(4):235-236

See also: EM Advances

We have once again learned that what was thought to be simple is not. Evidence is required to better guide the clinician -- at times I wonder if I know anything at all.

Cellulitis seems at first glance to be a straightforward infection that should respond to readily available antibiotics, guaranteeing excellent outcomes. Certainly most emergency physicians treat it as such, giving it little extra thought in their busy clinical workload. Yet, in this issue, Murray and colleagues have prospectively identified an overall failure rate of 18.7% when treating cellulitis in the outpatient setting.1 There is no way to know if this is a high or low rate of failure, for we appear to lack historical data describing treatment failure rates for inpatients. It is entirely possible that the identified failure rate may be the best we can achieve within practical practice patterns; then again it might not. As the authors state, the emergency medicine literature has been to date woefully inadequate in studying this change in clinical practice. We can only hope that this lacune will soon be corrected.

There is no magic in admitting a patient: irrespective of venue, if (infected) tissue levels of antibiotics surpass the established minimal inhibitory concentration for greater than 60% of the time, treatment success should be assured. If emergency physicians treated patients with the same antibiotic regimen as presently performed on the ward, they should expect to have the same results. Unfortunately, an observational study such as the one by Murray and colleagues could not establish that patients receiving therapy achieved the criterion of adequate tissue levels. Brown and associates reported a much lower failure rate when combining both oral and intravenous (IV) therapy, probably attaining higher tissue levels in their study; there again levels were not measured.2 It would be interesting to see if the IV treatment failures in Murray and colleagues' study clustered more in the cefazolin/probenicid arm than the ceftriaxone arm, for we are reasonably certain about 24-hour tissue levels for the latter but not the former when providing a once-a-day regimen.

This study did not identify pathogens or their resistance patterns. This is not a criticism, for it is a difficult process at best for cellulitis, and rarely done in the emergency department with immunocompetent patients. It raises the question, however, whether some of the treatment failures were due to bacterial resistances, or whether bacteria other than those covered were responsible. When considering any standardized algorithm, these questions will have to be addressed. This has become crucial with the rapid emergence of community-based MRSA (methicillin-resistant Staphylococcus aureus) skin infections.3

We require even more inclusive studies than this one if we are to define severity. Murray and colleagues state that there was poor inter-rater reliability in judging severity. They have made this observation after having excluded from their cohort almost all patients we would normally consider at risk: diabetics, immunocompromised patients, or those they considered a priori to have a severe infection. It might be difficult to further break down grades of severity when the above groups are excluded. Given the unreliability of "severity assessment," future studies should not exclude those traditional high-risk patients, or at least should limit exclusion criteria to enroll the most externally valid patient sample.

We have once again learned that what was thought to be simple is not. Evidence is required to better guide the clinician -- at times I wonder if I know anything at all.

References

  1. Murray H, Stiell I, Wells G. Treatment failure in emergency department patients with cellulitis. Can J Emerg Med 2005;7(4): 228-34.
  2. Brown G, Chamberlain R, Goulding J, Clarke A. Ceftriaxone versus cefazolin with probenecid for severe skin and soft tissue infections. J Emerg Med 1996;14(5):547-51.
  3. Methicillin-resistant Staphylococcus aureus infections among competitive sports participants -- Colorado, Indiana, Pennsylvania, and Los Angeles County, 2000-2003. MMWR Morbid Mortal Wkly Rep 2003;52:793-5.