Vancomycin-resistant staphylococcus aureus in the United States, 2002-2006

被引:333
作者
Sievert, Dawn M. [1 ,2 ]
Rudrik, James T. [2 ]
Patel, Jean B. [1 ]
McDonald, L. Clifford [1 ]
Wilkins, Melinda J. [2 ]
Hageman, Jeffrey C. [1 ]
机构
[1] Ctr Dis Control & Prevent, Div Healthcare Qual Promot, Atlanta, GA 30333 USA
[2] Michigan Dept Community Hlth, Lansing, MI USA
关键词
D O I
10.1086/527392
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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 mg/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.
引用
收藏
页码:668 / 674
页数:7
相关论文
共 40 条
[31]   Alterations of cell wall structure and metabolism accompany reduced susceptibility to vancomycin in an isogenic series of clinical isolates of Staphylococcus aureus [J].
Sieradzki, K ;
Tomasz, A .
JOURNAL OF BACTERIOLOGY, 2003, 185 (24) :7103-7110
[32]   Vancomycin-resistant Staphylococcus aureus isolate from a patient in Pennsylvania [J].
Tenover, FC ;
Weigel, LM ;
Appelbaum, PC ;
McDougal, LK ;
Chaitram, J ;
McAllister, S ;
Clark, N ;
Killgore, G ;
O'Hara, CM ;
Jevitt, L ;
Patel, JB ;
Bozdogan, B .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2004, 48 (01) :275-280
[33]   SPECIFIC DETECTION OF METHICILLIN-RESISTANT STAPHYLOCOCCUS SPECIES BY MULTIPLEX PCR [J].
VANNUFFEL, P ;
GIGI, J ;
EZZEDINE, H ;
VANDERCAM, B ;
DELMEE, M ;
WAUTERS, G ;
GALA, JL .
JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (11) :2864-2867
[34]   TREATMENT OF INFECTIONS DUE TO METHICILLIN-RESISTANT STAPHYLOCOCCUS-AUREUS [J].
WATANAKUNAKORN, C .
ANNALS OF INTERNAL MEDICINE, 1982, 97 (03) :376-378
[35]   High-level vancomycin-resistant staphylococcus aureus isolates associated with a polymicrobial biofilm [J].
Weigel, Linda M. ;
Donlan, Rodney M. ;
Shin, Dong Hyeon ;
Jensen, Bette ;
Clark, Nancye C. ;
McDougal, Linda K. ;
Zhu, Wenming ;
Musser, Kimberlee A. ;
Thompson, Jill ;
Kohlerschinidt, Donna ;
Dumas, Nellie ;
Limberger, Ronald J. ;
Patel, Jean B. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2007, 51 (01) :231-238
[36]   Genetic analysis of a high-level vancomycin-resistant isolate of Staphylococcus aureus [J].
Weigel, LM ;
Clewell, DB ;
Gill, SR ;
Clark, NC ;
McDougal, LK ;
Flannagan, SE ;
Kolonay, JF ;
Shetty, J ;
Killgore, GE ;
Tenover, FC .
SCIENCE, 2003, 302 (5650) :1569-1571
[37]   THE EMERGENCE OF METHICILLIN-RESISTANT STAPHYLOCOCCUS-AUREUS [J].
WENZEL, RP .
ANNALS OF INTERNAL MEDICINE, 1982, 97 (03) :440-442
[38]   Vancomycin-resistant Staphylococcus aureus in the absence of vancomycin exposure [J].
Whitener, CJ ;
Park, SY ;
Browne, FA ;
Parent, LJ ;
Julian, K ;
Bozdogan, B ;
Appelbaum, PC ;
Chaitram, J ;
Weigel, LM ;
Jernigan, J ;
McDougal, LK ;
Tenover, FC ;
Fridkin, SK .
CLINICAL INFECTIOUS DISEASES, 2004, 38 (08) :1049-1055
[39]  
ZHU WL, 2006, ANTIMICROB AGENTS CH
[40]  
2005, INVESTIGATION CONTRO