PNA FISH: Present and future impact on patient management

被引:34
作者
Forrest, Groeme N. [1 ]
机构
[1] Univ Maryland, Div Infect Dis, Baltimore, MD 21201 USA
关键词
cost-effectiveness; fluorescence in situ hybridization; peptide nucleic acid; real-time assay;
D O I
10.1586/14737159.7.3.231
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Inappropriate and inaccurate antimicrobial therapy can lead to adverse patient outcomes and also the development of antimicrobial resistance. Peptide nucleic acid (PNA) fluorescence in situ hybridization (FISH) gives rapid reporting with highly sensitive and specific results to clinicians within 3 h after blood cultures turn positive, thereby offering targeted therapeutics where necessary. It is simple to establish compared with real-time PCR and has resulted in significant cost savings for hospitals. PNA FISH is a promising future technology for the microbiology laboratory that will impact on patient management and clinical guidelines. This article will review the clinical data supporting these new technologies.
引用
收藏
页码:231 / 236
页数:6
相关论文
共 44 条
[1]   Cost savings with implementation of PNA FISH testing for identification of Candida albicans in blood cultures [J].
Alexander, BD ;
Ashley, ED ;
Reller, LB ;
Reed, SD .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2006, 54 (04) :277-282
[2]  
[Anonymous], 16 EUR C CLIN MICR I
[3]   Comparison of three PCR primer sets for identification of vanB gene carriage in feces and correlation with carriage of vancomycin-resistant enterococci:: Interference by vanB-containing anaerobic bacilli [J].
Ballard, SA ;
Grabsch, EA ;
Johnson, PDR ;
Grayson, ML .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2005, 49 (01) :77-81
[4]   Evaluation of three rapid methods for the direct identification of Staphylococcus aureus from positive blood cultures [J].
Chapin, K ;
Musgnug, M .
JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (09) :4324-4327
[5]  
Cockerill FR, 2003, ARCH PATHOL LAB MED, V127, P1112
[6]   The impact of antimicrobial resistance on health and economic outcomes [J].
Cosgrove, SE ;
Carmeli, Y .
CLINICAL INFECTIOUS DISEASES, 2003, 36 (11) :1433-1437
[7]   Evaluation of the IDI-MRSA assay for detection of methicillin-resistant Staphylococcus aureus from nasal and rectal specimens pooled in a selective broth [J].
Desjardins, M ;
Guibord, C ;
Lalonde, B ;
Toye, B ;
Ramotar, K .
JOURNAL OF CLINICAL MICROBIOLOGY, 2006, 44 (04) :1219-1223
[8]   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-+
[9]   Peptide nucleic acid fluorescence in situ hybridization-based identification of Candida albicans and its impact on mortality and antifungal therapy costs [J].
Forrest, G. N. ;
Mankes, K. ;
Jabra-Rizk, M. A. ;
Weekes, E. ;
Johnson, J. K. ;
Lincalis, D. P. ;
Venezia, R. A. .
JOURNAL OF CLINICAL MICROBIOLOGY, 2006, 44 (09) :3381-3383
[10]   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