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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.
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.
Afiliação
  • Nadjm B; Oxford University Clinical Research Unit, Hanoi & Ho Chi Minh City, Viet Nam; Centre for Tropical Medicine & Global Health, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, United Kingdom. Electronic address: bnadjm@oucru.org.
  • Dat VQ; Oxford University Clinical Research Unit, Hanoi & Ho Chi Minh City, Viet Nam; Department of Infectious Diseases, Hanoi Medical University, Hanoi, Viet Nam.
  • Campbell JI; Oxford University Clinical Research Unit, Hanoi & Ho Chi Minh City, Viet Nam; Centre for Tropical Medicine & Global Health, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, United Kingdom.
  • Dung VTV; Oxford University Clinical Research Unit, Hanoi & Ho Chi Minh City, Viet Nam.
  • Torre A; Oxford University Clinical Research Unit, Hanoi & Ho Chi Minh City, Viet Nam.
  • Tu NTC; Oxford University Clinical Research Unit, Hanoi & Ho Chi Minh City, Viet Nam.
  • Van NTT; Oxford University Clinical Research Unit, Hanoi & Ho Chi Minh City, Viet Nam.
  • Trinh DT; National Hospital for Tropical Diseases, Hanoi, Viet Nam.
  • Lan NPH; Hospital for Tropical Diseases, Ho Chi Minh City, Viet Nam.
  • Trung NV; National Hospital for Tropical Diseases, Hanoi, Viet Nam.
  • Hang NTT; National Hospital for Tropical Diseases, Hanoi, Viet Nam.
  • Hoi LT; National Hospital for Tropical Diseases, Hanoi, Viet Nam.
  • Baker S; Oxford University Clinical Research Unit, Hanoi & Ho Chi Minh City, Viet Nam; Centre for Tropical Medicine & Global Health, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, United Kingdom.
  • Wolbers M; Oxford University Clinical Research Unit, Hanoi & Ho Chi Minh City, Viet Nam.
  • Chau NVV; Hospital for Tropical Diseases, Ho Chi Minh City, Viet Nam.
  • Van Kinh N; National Hospital for Tropical Diseases, Hanoi, Viet Nam.
  • Thwaites GE; Oxford University Clinical Research Unit, Hanoi & Ho Chi Minh City, Viet Nam; Centre for Tropical Medicine & Global Health, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, United Kingdom.
  • van Doorn HR; Oxford University Clinical Research Unit, Hanoi & Ho Chi Minh City, Viet Nam; Centre for Tropical Medicine & Global Health, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, United Kingdom.
  • Wertheim HFL; Centre for Tropical Medicine & Global Health, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, United Kingdom; Department of Medical Microbiology, RadboudUMC, Nijmegen, The Netherlands.
J Infect ; 78(6): 454-460, 2019 06.
Article em En | MEDLINE | ID: mdl-30914268
OBJECTIVES: 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. METHODS: 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). RESULTS: 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). CONCLUSIONS: 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.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Bactérias / Técnicas Microbiológicas / Bacteriemia / Espectrometria de Massas por Ionização e Dessorção a Laser Assistida por Matriz / Fungos / Micoses Tipo de estudo: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies Limite: Adult / Female / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Revista: J Infect Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Bactérias / Técnicas Microbiológicas / Bacteriemia / Espectrometria de Massas por Ionização e Dessorção a Laser Assistida por Matriz / Fungos / Micoses Tipo de estudo: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies Limite: Adult / Female / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Revista: J Infect Ano de publicação: 2019 Tipo de documento: Article