The Clinical Impact of Rapid, Direct MALDI-ToF Identification of Bacteria from Positive Blood Cultures

被引:45
作者
French, Kathryn [1 ,2 ]
Evans, Jason [1 ,3 ]
Tanner, Hannah [1 ]
Gossain, Savita [1 ]
Hussain, Abid [1 ]
机构
[1] Heart England NHS Fdn Trust, Publ Hlth Lab Birmingham, Publ Hlth England, Birmingham, W Midlands, England
[2] Royal Wolverhampton NHS Trust, New Cross Hosp, Dept Microbiol, Wolverhampton, W Midlands, England
[3] Univ Hosp Llandough, Publ Hlth Wales, Wales Ctr Mycobacteria, Penarth, S Glam, Wales
关键词
DESORPTION-IONIZATION-TIME; FLIGHT MASS-SPECTROMETRY;
D O I
10.1371/journal.pone.0169332
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background Faster identification of bacterial isolates from blood cultures can enable earlier clinical intervention for patients with sepsis. We evaluated the clinical impact of direct identification of micro-organisms from positive blood cultures using MALDI-ToF. Method Positive blood cultures with organisms seen on Gram stain were included over a four week period. For each patient case, comparison was made between the clinical advice given on day one with only a Gram stain result, and the follow up advice given on day two with the benefit of organism identification. Culture results were then compared with direct MALDI-ToF identification. Results For 73 of 115 cases (63.5%), direct organism identification was obtained by MALDI-ToF. Of those 73, 70 (95.5%) had a result concordant with that of the plate culture. In 28 of the 115 cases (24.3%) direct MALDI-ToF identification on day one would have had a clear clinical benefit. In 11 cases it would have helped to identify the potential source of bacteraemia. In 11 cases it would have indicated a different antibiotic regimen on day one, with five patients receiving appropriate antibiotics 24 hours earlier. For 14 cases the blood culture isolate could have been designated as unlikely to be clinically significant. Conclusion We have demonstrated that organism identification on day one of blood culture positivity can have a direct clinical impact. Faster identification using MALDI-ToF assists the clinician in assessing the significance of a blood culture isolate on day one. It can allow earlier appropriate choice of antimicrobial agent, even in the absence of susceptibility testing, and help narrow down the potential source of infection providing a focus for further investigation in a more timely way than conventional techniques alone.
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共 15 条
[1]   Comparison of the MALDI Biotyper System Using Sepsityper Specimen Processing to Routine Microbiological Methods for Identification of Bacteria from Positive Blood Culture Bottles [J].
Buchan, Blake W. ;
Riebe, Katherine M. ;
Ledeboer, Nathan A. .
JOURNAL OF CLINICAL MICROBIOLOGY, 2012, 50 (02) :346-352
[2]   Using Matrix-Assisted Laser Desorption Ionization-Time of Flight Mass Spectrometry To Detect Carbapenem Resistance within 1 to 2.5 Hours [J].
Burckhardt, Irene ;
Zimmermann, Stefan .
JOURNAL OF CLINICAL MICROBIOLOGY, 2011, 49 (09) :3321-3324
[3]   Impact of Matrix-Assisted Laser Desorption Ionization Time-of-Flight Mass Spectrometry on the Clinical Management of Patients With Gram-negative Bacteremia: A Prospective Observational Study [J].
Clerc, Olivier ;
Prod'hom, Guy ;
Vogne, Christelle ;
Bizzini, Alain ;
Calandra, Thierry ;
Greub, Gilbert .
CLINICAL INFECTIOUS DISEASES, 2013, 56 (08) :1101-1107
[4]   Microorganisms direct identification from blood culture by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry [J].
Ferreira, L. ;
Sanchez-Juanes, F. ;
Porras-Guerra, I. ;
Garcia-Garcia, M. I. ;
Garcia-Sanchez, J. E. ;
Gonzalez-Buitrago, J. M. ;
Munoz-Bellido, J. L. .
CLINICAL MICROBIOLOGY AND INFECTION, 2011, 17 (04) :546-551
[5]   Detection of NDM-1, VIM-1, KPC, OXA-48, and OXA-162 Carbapenemases by Matrix-Assisted Laser Desorption Ionization-Time of Flight Mass Spectrometry [J].
Hrabak, Jaroslav ;
Studentova, Vendula ;
Walkova, Radka ;
Zemlickova, Helena ;
Jakubu, Vladislav ;
Chudackova, Eva ;
Gniadkowski, Marek ;
Pfeifer, Yvonne ;
Perry, John D. ;
Wilkinson, Kathryn ;
Bergerova, Tamara .
JOURNAL OF CLINICAL MICROBIOLOGY, 2012, 50 (07) :2441-2443
[6]   Rapid identification of pathogens directly from blood culture bottles by Bruker matrix-assisted laser desorption laser ionization-time of flight mass spectrometry versus routine methods [J].
Jamal, Wafaa ;
Saleem, Rola ;
Rotimi, Vincent O. .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2013, 76 (04) :404-408
[7]   Identification of Bacteria in Blood Culture Broths Using Matrix-Assisted Laser Desorption-Ionization Sepsityper™ and Time of Flight Mass Spectrometry [J].
Kok, Jen ;
Thomas, Lee C. ;
Olma, Thomas ;
Chen, Sharon C. A. ;
Iredell, Jonathan R. .
PLOS ONE, 2011, 6 (08)
[8]   Duration of hypotension before initiation of effective antimicrobial therapy is the critical determinant of survival in human septic shock [J].
Kumar, Arland ;
Roberts, Daniel ;
Wood, Kenneth E. ;
Light, Bruce ;
Parrillo, Joseph E. ;
Sharma, Satendra ;
Suppes, Robert ;
Feinstein, Daniel ;
Zanotti, Sergio ;
Taiberg, Leo ;
Gurka, David ;
Kumar, Aseem ;
Cheang, Mary .
CRITICAL CARE MEDICINE, 2006, 34 (06) :1589-1596
[9]   Identification of Blood Culture Isolates Directly from Positive Blood Cultures by Use of Matrix-Assisted Laser Desorption Ionization-Time of Flight Mass Spectrometry and a Commercial Extraction System: Analysis of Performance, Cost, and Turnaround Time [J].
Lagace-Wiens, Philippe R. S. ;
Adam, Heather J. ;
Karlowsky, James A. ;
Nichol, Kimberly A. ;
Pang, Paulette F. ;
Guenther, Jodi ;
Webb, Amanda A. ;
Miller, Crystal ;
Alfa, Michelle J. .
JOURNAL OF CLINICAL MICROBIOLOGY, 2012, 50 (10) :3324-3328
[10]   Impact of rapid microbial identification directly from positive blood cultures using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry on patient management [J].
Martiny, D. ;
Debaugnies, F. ;
Gateff, D. ;
Gerard, M. ;
Aoun, M. ;
Martin, C. ;
Konopnicki, D. ;
Loizidou, A. ;
Georgala, A. ;
Hainaut, M. ;
Chantrenne, M. ;
Dediste, A. ;
Vandenberg, O. ;
Van Praet, S. .
CLINICAL MICROBIOLOGY AND INFECTION, 2013, 19 (12) :E568-E581