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Featured researches published by Jeffrey C. Hageman.


Clinical Infectious Diseases | 2008

Vancomycin-Resistant Staphylococcus aureus in the United States, 2002–2006

Dawn M. Sievert; James T. Rudrik; Jean B. Patel; L. Clifford McDonald; Melinda J. Wilkins; Jeffrey C. Hageman

BACKGROUND This report compares the clinical characteristics, epidemiologic investigations, infection-control evaluations, and microbiologic findings of all 7 of the cases of vancomycin-resistant Staphylococcus aureus (VRSA) infection in the United States during the period 2002-2006. METHODS Epidemiologic, clinical, and infection-control information was collected. VRSA isolates underwent confirmatory identification, antimicrobial susceptibility testing, pulsed-field gel electrophoresis, and typing of the resistance genes. To assess VRSA transmission, case patients and their contacts were screened for VRSA carriage. RESULTS Seven cases were identified from 2002 through 2006; 5 were reported from Michigan, 1 was reported from Pennsylvania, and 1 was reported from New York. All VRSA isolates were vanA positive and had a median vancomycin minimum inhibitory concentration of 512 microg/mL. All case patients had a history of prior methicillin-resistant S. aureus and enterococcal infection or colonization; all had several underlying conditions, including chronic skin ulcers; and most had received vancomycin therapy prior to their VRSA infection. Person-to-person transmission of VRSA was not identified beyond any of the case patients. Infection-control precautions were evaluated and were consistent with established guidelines. CONCLUSIONS Seven patients with vanA-positive VRSA have been identified in the United States. Prompt detection by microbiology laboratories and adherence to recommended infection control measures for multidrug-resistant organisms appear to have prevented transmission to other patients.


Emerging Infectious Diseases | 2006

Severe community-acquired pneumonia due to Staphylococcus aureus, 2003-04 influenza season

Jeffrey C. Hageman; Timothy M. Uyeki; John S. Francis; Daniel B. Jernigan; J. Gary Wheeler; Carolyn B. Bridges; Stephen J. Barenkamp; Dawn M. Sievert; Arjun Srinivasan; Meg C. Doherty; Linda K. McDougal; George Killgore; Uri Lopatin; Rebecca Coffman; J. Kathryn MacDonald; Sigrid K. McAllister; Gregory E. Fosheim; Jean B. Patel; L. Clifford McDonald

S. aureus community-acquired pneumonia has been reported from 9 states.


Pediatrics | 2008

Influenza-Associated Pediatric Mortality in the United States: Increase of Staphylococcus aureus Coinfection

Lyn Finelli; Anthony E. Fiore; Rosaline Dhara; Lynnette Brammer; David K. Shay; Laurie Kamimoto; Alicia M. Fry; Jeffrey C. Hageman; Rachel J. Gorwitz; Joseph S. Bresee; Timothy M. Uyeki

OBJECTIVE. Pediatric influenza-associated death became a nationally notifiable condition in the United States during 2004. We describe influenza-associated pediatric mortality from 2004 to 2007, including an increase of Staphylococcus aureus coinfections. METHODS. Influenza-associated pediatric death is defined as a death of a child who is younger than 18 years and has laboratory-confirmed influenza. State and local health departments report to the Centers for Disease Control and Prevention demographic, clinical, and laboratory data on influenza-associated pediatric deaths. RESULTS. During the 2004–2007 influenza seasons, 166 influenza-associated pediatric deaths were reported (n = 47, 46, and 73, respectively). Median age of the children was 5 years. Children often progressed rapidly to death; 45% died within 72 hours of onset, including 43% who died at home or in an emergency department. Of 90 children who were recommended for influenza vaccination, only 5 (6%) were fully vaccinated. Reports of bacterial coinfection increased substantially from 2004–2005 to 2006–2007 (6%, 15%, and 34%, respectively). S aureus was isolated from a sterile site or endotracheal tube culture in 1 case in 2004–2005, 3 cases in 2005–2006, and 22 cases in 2006–2007; 64% were methicillin-resistant S aureus. Children with S aureus coinfection were significantly older and more likely to have pneumonia and acute respiratory distress syndrome than those who were not coinfected. CONCLUSIONS. Influenza-associated pediatric mortality is rare, but the proportion of S aureus coinfection identified increased fivefold over the past 3 seasons. Research is needed to identify risk factors for influenza coinfection with invasive bacteria and to determine the impact of influenza vaccination and antiviral agents in preventing pediatric mortality.


Annals of Emergency Medicine | 2009

Staphylococcus aureus Community-Acquired Pneumonia During the 2006 to 2007 Influenza Season

Joan Brunkard; Zachary Moore; Philip J. Budge; Kathryn E. Arnold; Gregory E. Fosheim; Lyn Finelli; Susan E. Beekmann; Philip M. Polgreen; Rachel J. Gorwitz; Jeffrey C. Hageman

STUDY OBJECTIVE Staphylococcus aureus is a cause of community-acquired pneumonia that can follow influenza infection. In response to a number of cases reported to public health authorities in early 2007, additional case reports were solicited nationwide to better define S. aureus community-acquired pneumonia during the 2006 to 2007 influenza season. METHODS Cases were defined as primary community-acquired pneumonia caused by S. aureus occurring between November 1, 2006, and April 30, 2007. Case finding was conducted through an Emerging Infections Network survey and through contacts with state and local health departments. RESULTS Overall, 51 cases were reported from 19 states; 37 (79%) of 47 with known susceptibilities involved infection with methicillin-resistant S. aureus (MRSA). The median age of case patients was 16 years, and 44% had no known pertinent medical history. Twenty-two (47%) of 47 case patients with information about other illnesses were diagnosed with a concurrent or antecedent viral infection during their illness, and 11 of 33 (33%) who were tested had laboratory-confirmed influenza. Of the 37 patients with MRSA infection, 16 (43%) were empirically treated with antimicrobial agents recommended for MRSA community-acquired pneumonia. Twenty-four (51%) of 47 patients for whom final disposition was known died a median of 4 days after symptom onset. CONCLUSION S. aureus continues to cause community-acquired pneumonia, with most reported cases caused by MRSA and many occurring with or after influenza. In this series, patients were often otherwise healthy young people and mortality rates were high. Further prospective investigation is warranted to clarify infection incidence, risk factors, and preventive measures.


Journal of the American Geriatrics Society | 2004

Comparison of Routine Glove Use and Contact-Isolation Precautions to Prevent Transmission of Multidrug-Resistant Bacteria in a Long-Term Care Facility

William E. Trick; Robert A. Weinstein; Patricia L. DeMarais; Wanda Tomaska; Catherine Nathan; Sigrid K. McAllister; Jeffrey C. Hageman; Thomas W. Rice; Glennis Westbrook; William R. Jarvis

Objectives: To compare routine glove use by healthcare workers for all residents, without use of contact‐isolation precautions, with contact‐isolation precautions for the care of residents who had vancomycin‐resistant enterococci or methicillin‐resistant Staphylococcus aureus isolated from a clinical culture


Emerging Infectious Diseases | 2009

Vancomycin-resistant Staphylococcus aureus, Michigan, USA, 2007

Jennie Finks; Eden Wells; Teri Lee Dyke; Nasir Husain; Linda Plizga; Renuka Heddurshetti; Melinda J. Wilkins; James T. Rudrik; Jeffrey C. Hageman; Jean B. Patel; Corinne E. Miller

Vancomycin-resistant Staphylococcus aureus (VRSA) infections, which are always methicillin-resistant, are a rare but serious public health concern. We examined 2 cases in Michigan in 2007. Both patients had underlying illnesses. Isolates were vanA-positive. VRSA was neither transmitted to or from another known VRSA patient nor transmitted from patients to identified contacts.


Clinical Infectious Diseases | 2005

A National Survey of Severe Influenza-Associated Complications among Children and Adults, 2003–2004

Laura Jean Podewils; Laura A. Liedtke; L. Clifford McDonald; Jeffrey C. Hageman; Larry J. Strausbaugh; Thea Kølsen Fischer; Daniel B. Jernigan; Timothy M. Uyeki; Matthew J. Kuehnert

This report summarizes findings of a national survey conducted among infectious diseases consultants to assess complications associated with influenza during the 2003-2004 influenza season. The survey identified severe complications, including secondary infection with Staphylococcus aureus and deaths among children and adults, as well as perceived shortages in rapid diagnostic tests and influenza vaccine.


Diagnostic Microbiology and Infectious Disease | 2008

Occurrence of a USA300 vancomycin-intermediate Staphylococcus aureus

Jeffrey C. Hageman; Jean B. Patel; Patrick Franklin; Karen Miscavish; Linda K. McDougal; David Lonsway; Fazle N. Khan

A vancomycin-intermediate Staphylococcus aureus (VISA) isolated from the blood of a 46-year-old patient with endocarditis was determined to be pulsed-field type USA300, daptomycin nonsusceptible, and positive for the Panton-Valentine leukocidin genes. Development of the VISA phenotype does not appear limited to traditional health care strains of S. aureus.


Clinical Infectious Diseases | 2006

Management of Persistent Bacteremia Caused by Methicillin-Resistant Staphylococcus aureus: A Survey of Infectious Diseases Consultants

Jeffrey C. Hageman; Laura A. Liedtke; Rebecca Sunenshine; Larry J. Strausbaugh; L. Clifford McDonald; Fred C. Tenover

We conducted a survey in 2005 of infectious diseases consultants and asked about persistent bacteremia due to methicillin-resistant Staphylococcus aureus. Many consultants perceived an increase in the frequency of illness, and, when presented with vancomycin minimum inhibitory concentrations approaching the limit of the susceptible range, most consultants indicated that they would switch to newer antimicrobial agents for treatment.


Emerging Infectious Diseases | 2013

Methicillin-Resistant Staphylococcus aureus Colonization of the Groin and Risk for Clinical Infection among HIV-infected Adults

Philip J. Peters; John T. Brooks; Sigrid K. McAllister; Brandi Limbago; H. Ken Lowery; Gregory E. Fosheim; Jodie L. Guest; Rachel J. Gorwitz; Monique Bethea; Jeffrey C. Hageman; Rondeen Mindley; Linda K. McDougal; David Rimland

Data on the interaction between methicillin-resistant Staphylococcus aureus (MRSA) colonization and clinical infection are limited. During 2007–2008, we enrolled HIV-infected adults in Atlanta, Georgia, USA, in a prospective cohort study. Nares and groin swab specimens were cultured for S. aureus at enrollment and after 6 and 12 months. MRSA colonization was detected in 13%–15% of HIV-infected participants (n = 600, 98% male) at baseline, 6 months, and 12 months. MRSA colonization was detected in the nares only (41%), groin only (21%), and at both sites (38%). Over a median of 2.1 years of follow-up, 29 MRSA clinical infections occurred in 25 participants. In multivariate analysis, MRSA clinical infection was significantly associated with MRSA colonization of the groin (adjusted risk ratio 4.8) and a history of MRSA infection (adjusted risk ratio 3.1). MRSA prevention strategies that can effectively prevent or eliminate groin colonization are likely necessary to reduce clinical infections in this population.

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Rachel J. Gorwitz

Centers for Disease Control and Prevention

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Scott K. Fridkin

Centers for Disease Control and Prevention

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Sigrid K. McAllister

Centers for Disease Control and Prevention

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Fred C. Tenover

Centers for Disease Control and Prevention

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Gregory E. Fosheim

Centers for Disease Control and Prevention

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Jean B. Patel

Centers for Disease Control and Prevention

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Linda K. McDougal

Centers for Disease Control and Prevention

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Timothy M. Uyeki

Centers for Disease Control and Prevention

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Arjun Srinivasan

Centers for Disease Control and Prevention

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Daniel B. Jernigan

National Center for Immunization and Respiratory Diseases

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