JANUARY 30, 2007
VOLUME 4 NO. 2

EDITORIAL

Guest editorial

Not just another superbug


Over the past few years an increasing number of reports from the US have suggested that a new community-associated strain of Staphylococcus aureus with resistance to methicillin (CA-MRSA) has replaced conventional methicillin susceptible S aureus as a significant pathogen in healthy community dwelling individuals. A recent report demonstrated that MRSA was the most common identifiable cause of skin and soft tissue infections amongst patients presenting to emergency departments in 11 American cities. Similar reports have also emerged in Canada.

What is this new pathogen and what does it mean for us? This pathogen is unique in that it is not merely a hospital associated MRSA which is now found in the community. This pathogen has a completely different antimicrobial susceptibility profile. In addition, the CA-MRSA variant has been seen to affect persons who may live in crowded environments with suboptimal hygiene. It's also been noted to harbour the Panton-Valentine leukocidin (PVL) toxin which is lethal for neutrophils and speculated to be the key factor responsible for the cutaneous abscesses and necrotizing pneumonias. This virulence factor is not traditionally observed in the healthcare associated MRSA strains.

In reviewing epidemiological trends over the past few years, it looks like CA-MRSA is with us to stay. It's impossible to effectively predict which patient will become infected, though one can speculate based on high risk groups. It's harder to know which antimicrobial therapy should be initiated, when and how. To address some of these questions "Guidelines for the Prevention and Management of Community Associated Methicillin Resistant Staphylococcus aureus (CA-MRSA): A Perspective for Canadian Healthcare Practitioners" has been drafted (see "Are you ready for the superbug?"). This report provides a practical approach to the diagnosis and management of infections caused by CA-MRSA. Thankfully, this pathogen is susceptible to agents such as trimethoprim sulfamethoxazole (TMP/SMX), doxycycline, clindamycin and the quinolones.

Clearly the diagnosis and therapy for CA-MRSA related infections currently falls in that gray area that is between the art and science of medicine since clinical acumen is required to establish the diagnosis and initiate an empiric treatment as CA-MRSA in Canada has not replaced conventional strains of S aureus. Until that time, however, we will continue to contemplate how best to diagnose this pathogen. The new Canadian recommendations are certainly of great benefit in helping guide diagnosis, treatment and in some cases, potentially decolonization. — Dr John M Embil, MD, FRCPC, Associate Professor, University of Manitoba and Medical Director, Infection Prevention and Control Program, Health Sciences Centre and Winnipeg Regional Health Authority.

 

 

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