A randomised controlled trial of matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDITOF-MS) versus conventional microbiological methods for identifying pathogens: Impact on optimal antimicrobial therapy of invasive bacterial and fungal infections in Vietnam

•MALDITOF MS provided more rapid identification of invasive bacterial and fungal pathogens than conventional microbiology.•MALDITOF MS did not increase the proportion of patients on optimal therapy at 24 or 48 hours after positive culture.•MALDITOF MS did not increase the proportion of patients rece...

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Published inThe Journal of infection Vol. 78; no. 6; pp. 454 - 460
Main Authors Nadjm, Behzad, Dat, Vu Quoc, Campbell, James I., Dung, Vu Tien Viet, Torre, Alessandro, Tu, Nguyen Thi Cam, Van, Ninh Thi Thanh, Trinh, Dao Tuyet, Lan, Nguyen Phu Huong, Trung, Nguyen Vu, Hang, Nguyen Thi Thuy, Hoi, Le Thi, Baker, Stephen, Wolbers, Marcel, Chau, Nguyen Van Vinh, Van Kinh, Nguyen, Thwaites, Guy E., van Doorn, H. Rogier, Wertheim, Heiman F.L.
Format Journal Article
LanguageEnglish
Published England Elsevier Ltd 01.06.2019
W.B. Saunders
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Abstract •MALDITOF MS provided more rapid identification of invasive bacterial and fungal pathogens than conventional microbiology.•MALDITOF MS did not increase the proportion of patients on optimal therapy at 24 or 48 hours after positive culture.•MALDITOF MS did not increase the proportion of patients receiving adequate therapy at 24 hours after positive culture.•The most common reason for therapy being sub-optimal was use of overly broad spectrum or unnecessary multiple antibiotics. We assessed the impact of MALDITOF-MS on the timeliness of optimal antimicrobial therapy through a parallel-arm randomised controlled trial in two hospitals in Vietnam. We recruited patients with a pathogen (bacterial or fungal) cultured from a normally sterile sample. Samples were randomly assigned (1:1) to identification by MALDITOF-MS or conventional diagnostics. The primary outcome was the proportion on optimal antimicrobial therapy within 24 h of positive culture, determined by a blinded independent review committee. Trial registered at ClinicalTrials.gov (NCT02306330). Among 1005 randomised patients, pathogens were isolated from 628 (326 intervention, 302 control), with 377 excluded as likely contaminants or discharged/died before positive culture. Most isolates were cultured from blood (421/628, 67.0%). The proportion receiving optimal antimicrobial therapy within 24 h (the primary outcome) or 48 h of growth was not significantly different between MALDITOF-MS and control arms (135/326, 41.4% vs 120/302, 39.7%; Adjusted Odds ration (AOR) 1.17, p = 0.40 and 151/326, 46.3% vs 141/302, 46.7%; AOR 1.05 p = 0.79, respectively). MALDITOF-MS, in the absence of an antimicrobial stewardship programme, did not improve the proportion on optimal antimicrobial therapy at 24 or 48 h after first growth in a lower-middle income setting with high rates of antibiotic resistance.
AbstractList • MALDITOF MS provided more rapid identification of invasive bacterial and fungal pathogens than conventional microbiology. • MALDITOF MS did not increase the proportion of patients on optimal therapy at 24 or 48 hours after positive culture. • MALDITOF MS did not increase the proportion of patients receiving adequate therapy at 24 hours after positive culture. • The most common reason for therapy being sub-optimal was use of overly broad spectrum or unnecessary multiple antibiotics.
OBJECTIVESWe assessed the impact of MALDITOF-MS on the timeliness of optimal antimicrobial therapy through a parallel-arm randomised controlled trial in two hospitals in Vietnam. METHODSWe recruited patients with a pathogen (bacterial or fungal) cultured from a normally sterile sample. Samples were randomly assigned (1:1) to identification by MALDITOF-MS or conventional diagnostics. The primary outcome was the proportion on optimal antimicrobial therapy within 24 h of positive culture, determined by a blinded independent review committee. Trial registered at ClinicalTrials.gov (NCT02306330). RESULTSAmong 1005 randomised patients, pathogens were isolated from 628 (326 intervention, 302 control), with 377 excluded as likely contaminants or discharged/died before positive culture. Most isolates were cultured from blood (421/628, 67.0%). The proportion receiving optimal antimicrobial therapy within 24 h (the primary outcome) or 48 h of growth was not significantly different between MALDITOF-MS and control arms (135/326, 41.4% vs 120/302, 39.7%; Adjusted Odds ration (AOR) 1.17, p = 0.40 and 151/326, 46.3% vs 141/302, 46.7%; AOR 1.05 p = 0.79, respectively). CONCLUSIONSMALDITOF-MS, in the absence of an antimicrobial stewardship programme, did not improve the proportion on optimal antimicrobial therapy at 24 or 48 h after first growth in a lower-middle income setting with high rates of antibiotic resistance.
We assessed the impact of MALDITOF-MS on the timeliness of optimal antimicrobial therapy through a parallel-arm randomised controlled trial in two hospitals in Vietnam. We recruited patients with a pathogen (bacterial or fungal) cultured from a normally sterile sample. Samples were randomly assigned (1:1) to identification by MALDITOF-MS or conventional diagnostics. The primary outcome was the proportion on optimal antimicrobial therapy within 24 h of positive culture, determined by a blinded independent review committee. Trial registered at ClinicalTrials.gov (NCT02306330). Among 1005 randomised patients, pathogens were isolated from 628 (326 intervention, 302 control), with 377 excluded as likely contaminants or discharged/died before positive culture. Most isolates were cultured from blood (421/628, 67.0%). The proportion receiving optimal antimicrobial therapy within 24 h (the primary outcome) or 48 h of growth was not significantly different between MALDITOF-MS and control arms (135/326, 41.4% vs 120/302, 39.7%; Adjusted Odds ration (AOR) 1.17, p = 0.40 and 151/326, 46.3% vs 141/302, 46.7%; AOR 1.05 p = 0.79, respectively). MALDITOF-MS, in the absence of an antimicrobial stewardship programme, did not improve the proportion on optimal antimicrobial therapy at 24 or 48 h after first growth in a lower-middle income setting with high rates of antibiotic resistance.
•MALDITOF MS provided more rapid identification of invasive bacterial and fungal pathogens than conventional microbiology.•MALDITOF MS did not increase the proportion of patients on optimal therapy at 24 or 48 hours after positive culture.•MALDITOF MS did not increase the proportion of patients receiving adequate therapy at 24 hours after positive culture.•The most common reason for therapy being sub-optimal was use of overly broad spectrum or unnecessary multiple antibiotics. We assessed the impact of MALDITOF-MS on the timeliness of optimal antimicrobial therapy through a parallel-arm randomised controlled trial in two hospitals in Vietnam. We recruited patients with a pathogen (bacterial or fungal) cultured from a normally sterile sample. Samples were randomly assigned (1:1) to identification by MALDITOF-MS or conventional diagnostics. The primary outcome was the proportion on optimal antimicrobial therapy within 24 h of positive culture, determined by a blinded independent review committee. Trial registered at ClinicalTrials.gov (NCT02306330). Among 1005 randomised patients, pathogens were isolated from 628 (326 intervention, 302 control), with 377 excluded as likely contaminants or discharged/died before positive culture. Most isolates were cultured from blood (421/628, 67.0%). The proportion receiving optimal antimicrobial therapy within 24 h (the primary outcome) or 48 h of growth was not significantly different between MALDITOF-MS and control arms (135/326, 41.4% vs 120/302, 39.7%; Adjusted Odds ration (AOR) 1.17, p = 0.40 and 151/326, 46.3% vs 141/302, 46.7%; AOR 1.05 p = 0.79, respectively). MALDITOF-MS, in the absence of an antimicrobial stewardship programme, did not improve the proportion on optimal antimicrobial therapy at 24 or 48 h after first growth in a lower-middle income setting with high rates of antibiotic resistance.
Author Wertheim, Heiman F.L.
Hang, Nguyen Thi Thuy
Hoi, Le Thi
Trinh, Dao Tuyet
Wolbers, Marcel
Lan, Nguyen Phu Huong
Campbell, James I.
Tu, Nguyen Thi Cam
Torre, Alessandro
Van, Ninh Thi Thanh
Chau, Nguyen Van Vinh
Trung, Nguyen Vu
van Doorn, H. Rogier
Van Kinh, Nguyen
Thwaites, Guy E.
Nadjm, Behzad
Dat, Vu Quoc
Baker, Stephen
Dung, Vu Tien Viet
AuthorAffiliation c Department of Infectious Diseases, Hanoi Medical University, Hanoi, Viet Nam
d National Hospital for Tropical Diseases, Hanoi, Viet Nam
e Hospital for Tropical Diseases, Ho Chi Minh City, Viet Nam
f Department of Medical Microbiology, RadboudUMC, Nijmegen, The Netherlands
b Centre for Tropical Medicine & Global Health, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, United Kingdom
a Oxford University Clinical Research Unit, Hanoi & Ho Chi Minh City, Viet Nam
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Keywords Bacteraemia
Vietnam
Matrix-assisted laser desorption-ionization mass spectrometry
Microbiological techniques
Antibacterial agents
Language English
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Snippet •MALDITOF MS provided more rapid identification of invasive bacterial and fungal pathogens than conventional microbiology.•MALDITOF MS did not increase the...
We assessed the impact of MALDITOF-MS on the timeliness of optimal antimicrobial therapy through a parallel-arm randomised controlled trial in two hospitals in...
OBJECTIVESWe assessed the impact of MALDITOF-MS on the timeliness of optimal antimicrobial therapy through a parallel-arm randomised controlled trial in two...
• MALDITOF MS provided more rapid identification of invasive bacterial and fungal pathogens than conventional microbiology. • MALDITOF MS did not increase the...
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elsevier
SourceType Open Access Repository
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Index Database
Publisher
StartPage 454
SubjectTerms Adult
Anti-Bacterial Agents - therapeutic use
Antibacterial agents
Antifungal Agents - therapeutic use
Bacteraemia
Bacteremia - diagnosis
Bacteremia - drug therapy
Bacteremia - microbiology
Bacteria - drug effects
Bacteria - isolation & purification
Female
Fungi - drug effects
Fungi - isolation & purification
Humans
Male
Matrix-assisted laser desorption-ionization mass spectrometry
Microbiological Techniques
Middle Aged
Mycoses - diagnosis
Mycoses - drug therapy
Mycoses - microbiology
Prospective Studies
Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
Time Factors
Treatment Outcome
Vietnam
Title A randomised controlled trial of matrix-assisted laser desorption ionization-time of flight mass spectrometry (MALDITOF-MS) versus conventional microbiological methods for identifying pathogens: Impact on optimal antimicrobial therapy of invasive bacterial and fungal infections in Vietnam
URI https://dx.doi.org/10.1016/j.jinf.2019.03.010
https://www.ncbi.nlm.nih.gov/pubmed/30914268
https://search.proquest.com/docview/2198557619
https://pubmed.ncbi.nlm.nih.gov/PMC6529875
Volume 78
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