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Table 1.  

Isolate and Patient Characteristics for 300 Veterans who had Staphylococcus aureus bacteremia
at 4 Veterans Affairs Medical Centers, USA, 2004–2008*

Table 2.  

Infection Characteristics for 300 Veterans who had Staphylococcus aureus Bacteremia
at 4 Veterans Affairs Medical Centers, USA, 2004–2008

Table 3.  

Patient and Infection Characteristics for 300 Veterans with Staphylococcus aureus Bacteremia
and Association with Illicit Drug Use at 4 Veterans Affairs Medical Centers, USA, 2004–2008*

Table 4.  

Patient and Infection Characteristics for 300 Veterans with Staphylococcus aureus Bacteremia
and Association with USA300 MRSA at 4 Veterans Affairs Medical Centers, USA, 2004–2008*

Table 5.  

Independent Risk Factors for USA300 MRSA Bacteremia
Among 300 Veterans at 4 Veterans Affairs Medical Centers, USA, 2004–2008*

CME

Illicit Drug Use and the Risk of USA300 Methicillin-Resistant Staphylococcus aureus Infections With Bacteremia

  • Authors: Kristen M. Kreisel, PhD; J. Kristie Johnson, PhD; O. Colin Stine, PhD; Michelle D. Shardell, PhD; Alan J. Lesse, MD; Fred M. Gordin, MD; Michael W. Climo, MD; Mary-Claire Roghmann, MD, MS
  • CME Released: 8/16/2010
  • THIS ACTIVITY HAS EXPIRED FOR CREDIT
  • Valid for credit through: 8/16/2011, 11:59 PM EST
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Target Audience and Goal Statement

This activity is intended for primary care clinicians, infectious disease specialists, and other specialists who care for patients at risk for community-acquired MRSA infection.

The goal of this activity is to review the epidemiology of community-acquired MRSA and its changing pattern of acquisition.

Upon completion of this activity, participants will be able to:

  1. Examine the association of illicit drug use with USA300 MRSA infection, including risk factors for acquisition and transmission
  2. Describe characteristics of illicit drug users who acquire MRSA and the changing pattern of risk from 2004 to 2008 in the United States with implications for management and prevention


Disclosures

As an organization accredited by the ACCME, Medscape, LLC, requires everyone who is in a position to control the content of an education activity to disclose all relevant financial relationships with any commercial interest. The ACCME defines "relevant financial relationships" as financial relationships in any amount, occurring within the past 12 months, including financial relationships of a spouse or life partner, that could create a conflict of interest.

Medscape, LLC, encourages Authors to identify investigational products or off-label uses of products regulated by the US Food and Drug Administration, at first mention and where appropriate in the content.


Author(s)

  • J. Kristie Johnson, PhD

    University of Maryland, Baltimore

    Disclosures

    Disclosure: J. Kristie Johnson, PhD, has disclosed the following relationships:
    Received grants for clinical research from: Becton, Dickinson and Company

  • O. Colin Stine, PhD

    University of Maryland, Baltimore

    Disclosures

    Disclosure: O. Colin Stine, PhD, has disclosed no relevant financial relationships.

  • Michelle D. Shardell, PhD

    University of Maryland, Baltimore

    Disclosures

    Disclosure: Michelle D. Shardell, PhD, has disclosed no relevant financial relationships.

  • Eli N. Perencevich, MD, MS

    University of Maryland, Baltimore, Maryland; VA Maryland Health Care System, Baltimore, Maryland

    Disclosures

    Disclosure: Eli N. Perencevich, MD, MS, has disclosed the following relationships:
    Received grants for clinical support from: Pfizer Inc.

  • Alan J. Lesse, MD

    VA Western New York Healthcare System, Buffalo, New York; University at Buffalo, Buffalo, New York

    Disclosures

    Disclosure: Alan J. Lesse, MD, has disclosed no relevant financial relationships.

  • Fred M. Gordin, MD

    Washington DC VA Medical Center, Washington, DC; George Washington University, Washington, DC

    Disclosures

    Disclosure: Fred M. Gordin, MD, has disclosed no relevant financial relationships.

  • Michael W. Climo, MD

    Hunter Holmes McGuire VA Medical Center, Richmond, Virginia; Medical College of Virginia at Virginia Commonwealth University, Richmond, Virginia

    Disclosures

    Disclosure: Michael W. Climo, MD, has disclosed the following relationships:
    Served as an advisor or consultant for: Biosynexus Incorporated
    Received grants for clinical research from: Biosynexus Incorporated

  • Mary-Claire Roghmann, MD, MS

    University of Maryland, Baltimore, Maryland; VA Maryland Health Care System, Baltimore, Maryland

    Disclosures

    Disclosure: Mary-Claire Roghmann, MD, MS, has disclosed no relevant financial relationships.

Editor(s)

  • Carol Snarey

    Copyeditor, Emerging Infectious Diseases

    Disclosures

    Disclosure: Carol Snarey has disclosed no relevant financial relationships.

CME Author(s)

  • Désirée Lie, MD, MSEd

    Clinical Professor of Family Medicine, Director of Research and Faculty Development, University of California, Irvine at Orange, California

    Disclosures

    Disclosure: Désirée Lie, MD, MSEd, has disclosed the following relevant financial relationship:
    Served as a nonproduct speaker for: "Topics in Health" for Merck Speaker Services

CME Reviewer(s)

  • Sarah Fleischman

    CME Program Manager, Medscape, LLC

    Disclosures

    Disclosure: Sarah Fleischman has disclosed no relevant financial relationships.

  • Laurie E. Scudder, DNP, NP

    CME Accreditation Coordinator, Medscape, LLC

    Disclosures

    Disclosure: Laurie E. Scudder, DNP, NP, has disclosed no relevant financial relationships.


Accreditation Statements

    For Physicians

  • This activity has been planned and implemented in accordance with the Essential Areas and policies of the Accreditation Council for Continuing Medical Education through the joint sponsorship of Medscape, LLC and Emerging Infectious Diseases. Medscape, LLC is accredited by the ACCME to provide continuing medical education for physicians.

    Medscape, LLC designates this educational activity for a maximum of 0.50 AMA PRA Category 1 Credit(s)™ . Physicians should only claim credit commensurate with the extent of their participation in the activity.

    Medscape, LLC staff have disclosed that they have no relevant financial relationships.

    Contact This Provider

For questions regarding the content of this activity, contact the accredited provider for this CME/CE activity noted above. For technical assistance, contact [email protected]


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CME

Illicit Drug Use and the Risk of USA300 Methicillin-Resistant Staphylococcus aureus Infections With Bacteremia: Results

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Results

We identified 300 patients with S. aureus bacteremia at the 4 participating sites during the study period. Strains having all 3 genetic factors (PVL, ACME, and spa type motif MBQBLO) were classified as USA300 MRSA, and a random sample of these isolates showed 100% sensitivity and specificity by PFGE. Isolates with none of these genetic factors were classified as non-USA300 MRSA, and a random sample of these isolates also showed 100% sensitivity and specificity by PFGE. Isolates with 1 or 2 of the genetic factors were also designated as non-USA300 MRSA; 18% of these isolates were found to be USA300 MRSA by PFGE, resulting in 100% sensitivity and 82% specificity of the laboratory algorithm for identifying USA300 MRSA. Sixty-seven (22%) of the infections were caused by USA300 MRSA, 117 (39%) by non-USA300 MRSA, and 116 (39%) by MSSA.

Patient and infection characteristics of the study population are presented in Table 1 and Table 2 . Of all patients with S. aureus bacteremia, 22 (7%) were illicit drug users, 13 (59%) with injection drugs. The patients had a mean age of 68 years and were almost all male (98%). Infections were classified as nosocomial in 172 (57%) patients, 83 (48%) of which were central-line associated. Sixteen (5%) patients were infected with HIV and 80 (27%) had a previous episode of colonization or infection with MRSA.

Compared with patients who did not use illicit drugs, illicit drug users were younger (mean age 51 vs. 69; p<0.0001; Table 3 ) and more likely to be African American (17% vs. 3%; p<0.0001). Illicit drug users were more likely to have HIV (38% vs. 6%; p<0.0001) or endocarditis (16% vs. 6%; p = 0.04) and less likely to have acquired their infection nosocomially (3% vs. 13%; p = 0.003) than patients who did not use illicit drugs. Illicit drug users were significantly more likely to have a bacteremic infection caused by USA300 MRSA than by all other S. aureus strains, compared with patients who did not use illicit drugs (RR 3.04, 95% confidence interval [CI] 1.99-4.64; p<0.0001; Table 4 ). Age (mean age 63 vs. 69 years; p = 0.0004) and a nosocomial acquisition of infection (RR 0.44, 95% CI 0.29-0.69; p = 0.0002) were both negatively associated with USA300 MRSA bacteremia.

Using binomial regression, illicit drug users were significantly more likely to have USA300 MRSA bacteremia compared with patients not using illicit drugs, controlling for year of presentation (adjusted RR [aRR] 3.00, 95% CI 1.88-4.36; p<0.0001; Table 5 ). This result was due to an increase in the proportion of S. aureus bacteremic infections caused by the USA300 MRSA strain in patients who did not use illicit drugs over the study period, while the proportion in patients using illicit drugs remained relatively stable after 2004. Stratified by year of presentation (categorized as early [January 1, 2004-March 31, 2006] vs. late [April 1, 2006-June 30, 2008] years of presentation), the association of illicit drug use with USA300 MRSA bacteremia decreased over the study period (RR in early years of presentation 4.63, 95% CI 2.36-9.07; p<0.0001; RR for late years of presentation 2.45, 96% CI 1.38-4.35; p = 0.02). The association of illicit drug use and USA300 MRSA bacteremia weakened over the study period, although the trend was not statistically significant (p = 0.23 for trend over time; Figure).

Figure.

Enlarge

Association Between Illicit Drug Use and USA300 Methicillinresistant Staphylococcus aureus Bacteremia among 300 Veterans at 4 Veterans Affairs Medical Centers, USA, 2004–2008 (generalized linear model p value for trend over time = 0.23). †No illicit drug users had a bacteremic infection caused by USA300 MRSA in 2006.