2012 Summer Meeting
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Clinical Impact of MRSA Bacteremia with Reduced Vancomycin Susceptibility
Track:
Education Sessions (CE)
Program Code: 114-L01
Date: Wednesday, June 13, 2012
Time: 8:00 AM to 10:30 AM EST
Location:
327, Level 300
PRESENTER(S):
Dr. Tonya Crawford, PharmD, BCPS, Assistant Professor of Clinical Sciences, Roosevelt University
Thomas Lodise,
PharmD, Associate Professor,
Albany College of Pharmacy and Health Sciences
Dr. Thomas Lodise is an Associate Professor at Albany College of Pharmacy and Health Sciences, Albany, New York. Dr. Lodise, a 1999 summa cum laude doctor of pharmacy graduate of Temple University School of Pharmacy, joined the faculty at Albany College of Pharmacy in August 2002. Prior to Albany College of Pharmacy, he completed the APhA-ASHPaccredited Pharmacy Practice Residency at Thomas Jefferson University Hospital, Philadelphia, Pennsylvania in 2000 and the Infectious Diseases Pharmacotherapy and Outcomes Fellowship at Wayne State University, Detroit, Michigan in 2002.
Integrating his dual interests in research and patient care, his current research focuses on the epidemiology and outcomes of bacterial infections, and his work explores antibiotic exposure-response relationships among patients. He has published over 60 peer-reviewed articles in reputable scientific journals, including Clinical Infectious Diseases, Antimicrobial Agents and Chemotherapy, Chest, and Journal of Antimicrobial Chemotherapy.
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Keith Rodvold,
PharmD, FCCP, Professor,
University of Illinois at Chicago
Keith A. Rodvold, PharmD, was appointed as an Assistant Professor in the Department of Pharmacy Practice at the University of Illinois at Chicago in 1984, was promoted to the rank of Associate Professor with tenure in 1989, and to the rank of Professor in 1994. In addition, he is also a Professor of Medicine in Pharmacy in the College of Medicine at the University of Illinois at Chicago. Dr. Rodvold received his bachelors of science and doctor of pharmacy degrees from the University of Minnesota. He completed his research fellowship in clinical pharmacokinetics and pharmacology at St. Paul-Ramsey Medical Center and the University of Minnesota.
Dr. Rodvold is currently conducting research in the area of clinical pharmacokinetics and pharmacodynamics of antiinfective. Dr. Rodvold has authored more than 150 original research and review publications and 35 book chapters, and he is coeditor of the textbook Drug Interactions in Infectious Diseases. The American College of Clinical Pharmacy presented Dr. Rodvold with the 2003 Russell R. Miller Award in recognition of his sustained and outstanding contributions to the literature of clinical pharmacy. He is an active member of numerous professional societies and has been elected Fellow of the Infectious Diseases Society of America, the American College of Clinical Pharmacology, and the American College of Clinical Pharmacy.
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PROGRAM CHAIR:
Dr. Tonya Crawford, PharmD, BCPS, Assistant Professor of Clinical Sciences, Roosevelt University
Description
In this session, experts will 1) review the susceptibility methods utilized to detect vancomycin MICs, 2) define predicative factors of MRSA blood isolates with high vancomycin MICs, 3) compare and contrast outcomes of patient diagnosed with MRSA bacteremia with high vancomycin MICs to those with low, and 4) evaluate other therapeutic options to treat MRSA bacteremia. At the conclusion, attendees will have a better understanding of how to appropriately manage patients diagnosed with MRSA bacteremia with high vancomycin MICs.
LEARNER OUTCOMES:
- Analyze the difference in clinical outcomes of patients with MRSA bacteremia with high vancomycin MICs to those with low vancomycin MICs.
- Define predicative factors of the development of MRSA bacteremia with high (defined as 1.5 g/mL) vancomycin MICs.
- Discuss challenges and realities when implementing these concepts in your institution.
- Distinguish susceptibility methods utilized to detect vancomycin MICs.
- Evaluate other treatment options with MRSA activity to treat MRSA bacteremia with high vancomycin MICs.