Real-Time PCR Testing for mecA Reduces Vancomycin Usage and Length of Hospitalization for Patients Infected with Methicillin-Sensitive Staphylococci

被引:43
作者
Nguyen, David T. [1 ]
Yeh, Ellen [1 ]
Perry, Sharon [2 ]
Luo, Robert F. [1 ]
Pinsky, Benjamin A. [1 ]
Lee, Betty P. [5 ]
Sisodiya, Deepak [4 ]
Baron, Ellen Jo [1 ,3 ]
Banaei, Niaz [1 ,2 ,3 ]
机构
[1] Stanford Univ, Sch Med, Dept Pathol, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Med, Div Infect Dis & Geog Med, Stanford, CA 94305 USA
[3] Stanford Hosp & Clin, Clin Microbiol Lab, Palo Alto, CA 94304 USA
[4] Stanford Hosp & Clin, Dept Pharm, Palo Alto, CA 94304 USA
[5] Lucile Packard Childrens Hosp, Dept Pharm, Palo Alto, CA 94304 USA
关键词
COAGULASE-NEGATIVE STAPHYLOCOCCI; AUREUS BACTEREMIA; CLINICAL MICROBIOLOGY; ANTIBIOTIC-RESISTANCE; IMPACT; THERAPY; CEPHALOSPORINS; INTERVENTIONS; PATHOGENESIS; LUGDUNENSIS;
D O I
10.1128/JCM.02150-09
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Nucleic acid amplification tests (NAATs) have revolutionized infectious disease diagnosis, allowing for the rapid and sensitive identification of pathogens in clinical specimens. Real-time PCR testing for the mecA gene (mecA PCR), which confers methicillin resistance in staphylococci, has the added potential to reduce antibiotic usage, improve clinical outcomes, lower health care costs, and avoid emergence of drug resistance. A retrospective study was performed to identify patients infected with methicillin-sensitive staphylococcal isolates who were receiving vancomycin treatment when susceptibility results became available. Vancomycin treatment and length of hospitalization were compared in these patients for a 6-month period before and after implementation of mecA PCR. Among 65 and 94 patients identified before and after mecA PCR, respectively, vancomycin usage (measured in days on therapy) declined from a median of 3 days (range, 1 to 44 days) in the pre-PCR period to 1 day (range, 0 to 18 days) in the post-PCR period (P < 0.0001). In total, 38.5% (25/65) of patients were switched to beta-lactam therapy in the pre-PCR period, compared to 61.7% (58/94) in the post-PCR period (P = 0.004). Patient hospitalization days also declined from a median of 8 days (range, 1 to 47 days) in the pre-PCR period to 5 days (range, 0 to 42 days) in the post-PCR period (P = 0.03). Real-time PCR testing for mecA is an effective tool for reducing vancomycin usage and length of stay of hospitalized patients infected with methicillin-sensitive staphylococci. In the face of ever-rising health care expenditures in the United States, these findings have important implications for improving outcomes and decreasing costs.
引用
收藏
页码:785 / 790
页数:6
相关论文
共 34 条
[11]   Real-time PCR in clinical microbiology: Applications for a routine laboratory testing [J].
Espy, MJ ;
Uhl, JR ;
Sloan, LM ;
Buckwalter, SP ;
Jones, MF ;
Vetter, EA ;
Yao, JDC ;
Wengenack, NL ;
Rosenblatt, JE ;
Cockerill, FR ;
Smith, TF .
CLINICAL MICROBIOLOGY REVIEWS, 2006, 19 (01) :165-+
[12]   Impact of rapid in situ hybridization testing on coagulase-negative staphylococci positive blood cultures [J].
Forrest, Graerne N. ;
Mehta, Sanjay ;
Weekes, Elizabeth ;
Lincalis, Durry P. ;
Johnson, Jennifer K. ;
Venezia, Richard A. .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2006, 58 (01) :154-158
[13]   From clinical microbiology to infection pathogenesis:: How daring to be different works for Staphylococcus lugdunensis [J].
Frank, Kristi L. ;
del Pozo, Jose Luis ;
Patel, Robin .
CLINICAL MICROBIOLOGY REVIEWS, 2008, 21 (01) :111-+
[14]   The effect of vancomycin and third-generation cephalosporins on prevalence of vancomycin-resistant enterococci in 126 US adult intensive care units [J].
Fridkin, SK ;
Edwards, JR ;
Courval, JM ;
Hill, H ;
Tenover, FC ;
Lawton, R ;
Gaynes, RP ;
McGowan, JE .
ANNALS OF INTERNAL MEDICINE, 2001, 135 (03) :175-183
[15]   Bacteremic pneumonia due to Staphylococcus aureus:: A comparison of disease caused by methicillin-resistant and methicillin-susceptible organisms [J].
González, C ;
Rubio, M ;
Romero-Vivas, J ;
González, M ;
Picazo, JJ .
CLINICAL INFECTIOUS DISEASES, 1999, 29 (05) :1171-1177
[16]   Clinical relevance of increasing glycopeptide MICs against Staphylococcus aureus [J].
Gould, Ian M. .
INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2008, 31 :1-9
[17]   Outcome of vancomycin treatment in patients with methicillin-susceptible Staphylococcus aureus bacteremia [J].
Kim, Sung-Han ;
Kim, Kye-Hyung ;
Kim, Hong-Bin ;
Kim, Nam-Joong ;
Kim, Eui-Chong ;
Oh, Myoung-Don ;
Choe, Kang-Won .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2008, 52 (01) :192-197
[18]   Limitations of vancomycin in the management of resistant staphylococcal infections [J].
Kollef, Marin H. .
CLINICAL INFECTIOUS DISEASES, 2007, 45 :S191-S195
[19]   Structural basis for the β-lactam resistance of PBP2a from methicillin-resistant Staphylococcus aureus [J].
Lim, D ;
Strynadka, NCJ .
NATURE STRUCTURAL BIOLOGY, 2002, 9 (11) :870-876
[20]   Improving the appropriateness of vancomycin use by sequential interventions [J].
Lipsky, BA ;
Baker, CA ;
McDonald, LL ;
Suzuki, NT .
AMERICAN JOURNAL OF INFECTION CONTROL, 1999, 27 (02) :84-90