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CME / ABIM MOC / CE

Vital Signs: Epidemiology and Recent Trends in Methicillin-Resistant and in Methicillin-Susceptible Staphylococcus aureus Bloodstream Infections — United States

  • Authors: Athena P. Kourtis, MD, PhD, MPH; Kelly Hatfield, MSPH; James Baggs, PhD; Yi Mu, PhD; Isaac See, MD; Erin Epson, MPH; Joelle Nadle, MPH; Marion A. Kainer, MD; Ghinwa Dumyati, MD; Susan Petit, MD; Susan M. Ray, MD; David Ham, MD; Catherine Capers, MA; Heather Ewing, MPH; Nicole Coffin, MA; L. Clifford McDonald, MD; John Jernigan, MD; Denise Cardo, MD
  • CME / ABIM MOC / CE Released: 5/23/2019
  • THIS ACTIVITY HAS EXPIRED FOR CREDIT
  • Valid for credit through: 5/23/2020, 11:59 PM EST
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Target Audience and Goal Statement

This activity is intended for infectious disease physicians, critical care physicians, internists, nurses, pharmacists, public health officials, and other physicians who treat and manage patients with methicillin-resistant Staphylococcus aureus (MRSA) and methicillin-susceptible S aureus (MSSA) infections.

The goal of this activity is to describe updated estimates of MRSA and MSSA bloodstream infections and associated in-hospital mortality, according to recent data from the Emerging Infections Program (EIP) population surveillance and 2 large electronic health record (EHR) data sets from more than 400 US acute care hospitals.

Upon completion of this activity, participants will:

  • Describe updated estimates of MRSA and MSSA bloodstream infections and associated in-hospital mortality, according to recent EIP data and 2 large EHR data sets from more than 400 US acute care hospitals
  • Determine possible reasons for changing trends in MRSA and MSSA bloodstream infections and associated in-hospital mortality, according to recent EIP data and 2 large EHR data sets from more than 400 US acute care hospitals
  • Explain clinical and public health implications of changing trends in MRSA and MSSA bloodstream infections and associated in-hospital mortality, according to recent EIP data and 2 large EHR data sets from more than 400 U.S. acute care hospitals


Disclosures

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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.


Authors

  • Athena P. Kourtis, MD, PhD, MPH

    Division of Healthcare Quality Promotion
    National Center for Emerging and Zoonotic Infectious Diseases
    CDC
    Atlanta, Georgia

    Disclosures

    Disclosure: Athena P. Kourtis, MD, PhD, MPH, has disclosed no relevant financial relationships.

  • Kelly Hatfield, MSPH

    Division of Healthcare Quality Promotion
    National Center for Emerging and Zoonotic Infectious Diseases
    CDC
    Atlanta, Georgia

    Disclosures

    Disclosure: Kelly Hatfield, MSPH, has disclosed no relevant financial relationships.

  • James Baggs, PhD

    Division of Healthcare Quality Promotion
    National Center for Emerging and Zoonotic Infectious Diseases
    CDC
    Atlanta, Georgia

    Disclosures

    Disclosure: James Baggs, PhD, has disclosed no relevant financial relationships.

  • Yi Mu, PhD

    Division of Healthcare Quality Promotion
    National Center for Emerging and Zoonotic Infectious Diseases
    CDC
    Atlanta, Georgia

    Disclosures

    Disclosure: Yi Mu, PhD, has disclosed no relevant financial relationships.

  • Isaac See, MD

    Division of Healthcare Quality Promotion
    National Center for Emerging and Zoonotic Infectious Diseases
    CDC
    Atlanta, Georgia

    Disclosures

    Disclosure: Isaac See, MD, has disclosed no relevant financial relationships.

  • Erin Epson, MPH

    California Department of Public Health
    Sacramento, California

    Disclosures

    Disclosure: Erin Epson, MPH, has disclosed no relevant financial relationships.

  • Joelle Nadle, MPH

    California Emerging Infections Program
    Oakland, California

    Disclosures

    Disclosure: Joelle Nadle, MPH, has disclosed no relevant financial relationships.

  • Marion A. Kainer, MD

    Tennessee Emerging Infections Program
    Nashville, Tennessee

    Disclosures

    Disclosure: Marion A. Kainer, MD, has disclosed no relevant financial relationships.

  • Ghinwa Dumyati, MD

    New York-Rochester Emerging Infections Program
    University of Rochester Medical Center
    Rochester, New York

    Disclosures

    Disclosure: Ghinwa Dumyati, MD, has disclosed no relevant financial relationships.

  • Susan Petit, MD

    Connecticut Emerging Infections Program
    New Haven, Connecticut

    Disclosures

    Disclosure: Susan Petit, MD, has disclosed no relevant financial relationships.

  • Susan M. Ray, MD

    Georgia Emerging Infections Program
    Atlanta Georgia

    Disclosures

    Disclosure: Susan M. Ray, MD, has disclosed no relevant financial relationships.

  • David Ham, MD

    Division of Healthcare Quality Promotion
    National Center for Emerging and Zoonotic Infectious Diseases
    CDC
    Atlanta, Georgia

    Disclosures

    Disclosure: David Ham, MD, has disclosed no relevant financial relationships.

  • Catherine Capers, MA

    Division of Healthcare Quality Promotion
    National Center for Emerging and Zoonotic Infectious Diseases
    CDC
    Atlanta, Georgia

    Disclosures

    Disclosure: Catherine Capers, MA, has disclosed no relevant financial relationships.

  • Heather Ewing, MPH

    Division of Healthcare Quality Promotion
    National Center for Emerging and Zoonotic Infectious Diseases
    CDC
    Atlanta, Georgia

    Disclosures

    Disclosure: Heather Ewing, MPH, has disclosed no relevant financial relationships.

  • Nicole Coffin, MA

    Division of Healthcare Quality Promotion
    National Center for Emerging and Zoonotic Infectious Diseases
    CDC
    Atlanta, Georgia

    Disclosures

    Disclosure: Nicole Coffin, MA, has disclosed no relevant financial relationships.

  • L. Clifford McDonald, MD

    Division of Healthcare Quality Promotion
    National Center for Emerging and Zoonotic Infectious Diseases
    CDC
    Atlanta, Georgia

    Disclosures

    Disclosure: L. Clifford McDonald, MD, has disclosed no relevant financial relationships.

  • John Jernigan, MD

    Division of Healthcare Quality Promotion
    National Center for Emerging and Zoonotic Infectious Diseases
    CDC
    Atlanta, Georgia

    Disclosures

    Disclosure: John Jernigan, MD, has disclosed no relevant financial relationships.

  • Denise Cardo, MD

    Division of Healthcare Quality Promotion
    National Center for Emerging and Zoonotic Infectious Diseases
    CDC
    Atlanta, Georgia

    Disclosures

    Disclosure: Denise Cardo, MD, has disclosed no relevant financial relationships.

CME Author

  • Laurie Barclay, MD

    Freelance writer and reviewer, Medscape, LLC

    Disclosures

    Disclosure: Laurie Barclay, MD, has disclosed no relevant financial relationships.

CME Reviewer

  • Esther Nyarko, PharmD

    Associate CME Clinical Director, Medscape, LLC

    Disclosures

    Disclosure: Esther Nyarko, PharmD, has disclosed no relevant financial relationships.

Nurse Planner

  • Amy Bernard, MS, BSN, RN-BC, CHCP

    Lead Nurse Planner, Medscape, LLC

    Disclosures

    Disclosure: Amy Bernard, MS, BSN, RN-BC, CHCP, has disclosed no relevant financial relationships.


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    For Physicians

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

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

    Successful completion of this CME activity, which includes participation in the evaluation component, enables the participant to earn up to 0.50 MOC points in the American Board of Internal Medicine's (ABIM) Maintenance of Certification (MOC) program. Participants will earn MOC points equivalent to the amount of CME credits claimed for the activity. It is the CME activity provider's responsibility to submit participant completion information to ACCME for the purpose of granting ABIM MOC credit.

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  • Awarded 0.50 contact hour(s) of continuing nursing education for RNs and APNs; none of these credits is in the area of pharmacology.

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  • Medscape, LLC designates this continuing education activity for 0.50 contact hour(s) (0.050 CEUs) (Universal Activity Number JA0007105-0000-19-120-H01-P).

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CME / ABIM MOC / CE

Vital Signs: Epidemiology and Recent Trends in Methicillin-Resistant and in Methicillin-Susceptible Staphylococcus aureus Bloodstream Infections — United States

Authors: Athena P. Kourtis, MD, PhD, MPH; Kelly Hatfield, MSPH; James Baggs, PhD; Yi Mu, PhD; Isaac See, MD; Erin Epson, MPH; Joelle Nadle, MPH; Marion A. Kainer, MD; Ghinwa Dumyati, MD; Susan Petit, MD; Susan M. Ray, MD; David Ham, MD; Catherine Capers, MA; Heather Ewing, MPH; Nicole Coffin, MA; L. Clifford McDonald, MD; John Jernigan, MD; Denise Cardo, MDFaculty and Disclosures
THIS ACTIVITY HAS EXPIRED FOR CREDIT

CME / ABIM MOC / CE Released: 5/23/2019

Valid for credit through: 5/23/2020, 11:59 PM EST

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Abstract and Introduction

Abstract

Introduction: Staphylococcus aureus is one of the most common pathogens in health care facilities and in the community, and can cause invasive infections, sepsis, and death. Despite progress in preventing methicillin-resistant S. aureus (MRSA) infections in health care settings, assessment of the problem in both health care and community settings is needed. Further, the epidemiology of methicillin-susceptible S. aureus (MSSA) infections is not well described at the national level.

Methods: Data from the Emerging Infections Program (EIP) MRSA population surveillance (2005–2016) and from the Premier and Cerner Electronic Health Record databases (2012–2017) were analyzed to describe trends in incidence of hospital-onset and community-onset MRSA and MSSA bloodstream infections and to estimate the overall incidence of S. aureus bloodstream infections in the United States and associated in-hospital mortality.

Results: In 2017, an estimated 119,247 S. aureus bloodstream infections with 19,832 associated deaths occurred. During 2005–2012 rates of hospital-onset MRSA bloodstream infection decreased by 17.1% annually, but the decline slowed during 2013–2016. Community-onset MRSA declined less markedly (6.9% annually during 2005–2016), mostly related to declines in health care–associated infections. Hospital-onset MSSA has not significantly changed (p = 0.11), and community-onset MSSA infections have slightly increased (3.9% per year, p<0.0001) from 2012 to 2017.

Conclusions and Implications for Public Health Practice: Despite reductions in incidence of MRSA bloodstream infections since 2005, S. aureus infections account for significant morbidity and mortality in the United States. To reduce the incidence of these infections further, health care facilities should take steps to fully implement CDC recommendations for prevention of device- and procedure-associated infections and for interruption of transmission. New and novel prevention strategies are also needed.

Introduction

Staphylococcus aureus is a major cause of community- and health care–associated infections,[1] ranging from superficial skin and soft tissue infections (SSTI) to invasive infections, sepsis, and death. Methicillin-resistant S. aureus (MRSA) has long been recognized as a pathogen associated with health care settings; however, in the 1990s, community-associated MRSA infections, causing mostly SSTI, emerged in the United States.[2] Substantial progress has been achieved in preventing MRSA bloodstream infections in U.S. health care facilities[3–5] after widespread introduction of enhanced infection control efforts in acute-care hospitals.

Although the rates of hospital-onset MRSA bloodstream infections have substantially decreased, evidence from the National Healthcare Safety Network (NHSN) and from the Emerging Infections Program (EIP) surveillance system suggests that the decline might have slowed in more recent years;[4,6] the United States is not on track to meet the 2020 goal of the Healthcare-Associated Infection National Action Plan of a 50% reduction in hospital-onset MRSA bloodstream infections from the 2015 baseline.[7] Moreover, to protect patients, expanded efforts are needed to prevent methicillin-susceptible S. aureus (MSSA), which causes approximately half of all health care–associated S. aureus infections.[8] There is little information on the current epidemiology of MSSA infections in the United States, and available data might not be nationally representative.[9–11]

A critical assessment of recent trends and incidence of both MRSA and MSSA invasive disease in the United States is crucial to informing public health policy and formulating a framework of approaches to further prevent S. aureus infections. In this report, recent data from the EIP population surveillance and two large electronic health record (EHR) data sets from over 400 U.S. acute care hospitals were used to update estimates of MRSA and MSSA bloodstream infections, and to estimate associated in-hospital mortality.