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640. Randomized Clinical Trial Evaluating Clinical Impact of RAPid IDentification and Antimicrobial Susceptibility Testing for Gram-Negative Bacteremia (RAPIDS-GN)

BACKGROUND: Rapid blood culture diagnostics increase cost and have unclear benefit for patients with Gram-negative bacilli (GNB) bloodstream infections (BSIs). We conducted a multicenter, prospective randomized controlled trial (RAPIDS-GN), comparing outcomes of patients with GNB BSI who had blood c...

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Autores principales: Banerjee, Ritu, Komarow, Lauren, Virk, Abinash, Rajapakse, Nipunie S, Schuetz, Audrey, Dylla, Brenda, Earley, Michelle, Lok, Judith, Kohner, Peggy, Ihde, Sherry, Cole, Nicolynn, Hines, Lisa, Reed, Katelyn, Garner, Omai, Chandrasekaran, Sukantha, de St. Maurice, Annabelle M, Kanatani, Meganne, Curello, Jennifer, Arias, Rubi, Swearingen, William, Doernberg, Sarah B, Patel, Robin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6811091/
http://dx.doi.org/10.1093/ofid/ofz360.708
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author Banerjee, Ritu
Banerjee, Ritu
Komarow, Lauren
Virk, Abinash
Rajapakse, Nipunie S
Schuetz, Audrey
Dylla, Brenda
Earley, Michelle
Lok, Judith
Kohner, Peggy
Ihde, Sherry
Cole, Nicolynn
Hines, Lisa
Reed, Katelyn
Garner, Omai
Chandrasekaran, Sukantha
de St. Maurice, Annabelle M
Kanatani, Meganne
Curello, Jennifer
Arias, Rubi
Swearingen, William
Doernberg, Sarah B
Patel, Robin
Patel, Robin
author_facet Banerjee, Ritu
Banerjee, Ritu
Komarow, Lauren
Virk, Abinash
Rajapakse, Nipunie S
Schuetz, Audrey
Dylla, Brenda
Earley, Michelle
Lok, Judith
Kohner, Peggy
Ihde, Sherry
Cole, Nicolynn
Hines, Lisa
Reed, Katelyn
Garner, Omai
Chandrasekaran, Sukantha
de St. Maurice, Annabelle M
Kanatani, Meganne
Curello, Jennifer
Arias, Rubi
Swearingen, William
Doernberg, Sarah B
Patel, Robin
Patel, Robin
author_sort Banerjee, Ritu
collection PubMed
description BACKGROUND: Rapid blood culture diagnostics increase cost and have unclear benefit for patients with Gram-negative bacilli (GNB) bloodstream infections (BSIs). We conducted a multicenter, prospective randomized controlled trial (RAPIDS-GN), comparing outcomes of patients with GNB BSI who had blood culture testing with standard of care (SOC) culture and antibiotic susceptibility testing (AST) vs. rapid organism identification (ID) and phenotypic AST using the Accelerate Pheno System (AXDX). METHODS: Subjects with blood culture Gram stain showing GNB were randomized to receive SOC testing with antimicrobial stewardship review (AS) or AXDX plus SOC testing with AS, at two academic medical centers between October 2017 and October 2018. SOC testing included rapid MALDI-TOF mass spectrometry ID and agar dilution or broth microdilution AST. In a modified intention to treat analysis, subjects were excluded if: Gram stain was erroneous, culture was positive during off-hours, blood culture in the prior week had GNB, they were deceased/on comfort care, or admitted to a nonparticipating hospital. The primary outcome was time to first antibiotic modification within 72 hours after randomization. Subjects without antibiotic modifications were assigned a time of 72 hours. No censoring was observed. T-tests and Wilcoxon rank-sum tests were used for statistical analyses. RESULTS: Of 500 randomized subjects, 448 were included (226 SOC, 222 AXDX). Groups did not differ in baseline characteristics (Table 1). Median (IQR) hours to first antibiotic modification was faster in the AXDX vs. SOC group [8.6 (2.6, 27.6) vs. 14.9 (3.3, 41.1)], P = 0.02 (Figure 1). Median (IQR) hours to first Gram-negative antibiotic modification (including escalation and de-escalation) was faster in the AXDX than SOC group [17.4 (4.9, 72) vs. 42.1 (10.1, 72)], P < 0.001 (Figure 2). Groups did not differ in clinical outcomes (Table 2). Mean (S.D.) time to results was faster for AXDX than SOC for organism ID [2.7 (1.2) h vs. 15.6 (20.3) h, P < 0.001] and AST [13 (55.7) h vs. 54.6 (45.5) h, P < 0.001]. CONCLUSION: In the largest trial to evaluate the clinical impact of a blood culture diagnostic for GNB BSI, we found that rapid organism ID and phenotypic AST led to faster changes in antibiotic therapy for Gram-negative bacteremia. [Image: see text] [Image: see text] [Image: see text] [Image: see text] DISCLOSURES: Ritu Banerjee, MD, PhD, Accelerate Diagnostics: Grant/Research Support; BioFire: Research Grant; Biomerieux: Research Grant; Roche: Research Grant Robin Patel, MD, ASM and IDSA: Other Financial or Material Support, Travel reimbursement, editor’s stipends; CD Diagnostics, Merck, Hutchison Biofilm Medical Solutions, Accelerate Diagnostics, ContraFect, TenNor Therapeutics Limited, Shionogi: Grant/Research Support; Curetis, Specific Technologies, NextGen Diagnostics, PathoQuest, Qvella: Consultant; NBME, Up-to-Date, the Infectious Diseases Board Review Course: Honorarium recipient, Other Financial or Material Support; Patent on Bordetella pertussis/parapertussis PCR issued, a patent on a device/method for sonication with royalties paid by Samsung to Mayo Clinic, and a patent on an anti-biofilm substance issued: Other Financial or Material Support, Patents.
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spelling pubmed-68110912019-10-28 640. Randomized Clinical Trial Evaluating Clinical Impact of RAPid IDentification and Antimicrobial Susceptibility Testing for Gram-Negative Bacteremia (RAPIDS-GN) Banerjee, Ritu Banerjee, Ritu Komarow, Lauren Virk, Abinash Rajapakse, Nipunie S Schuetz, Audrey Dylla, Brenda Earley, Michelle Lok, Judith Kohner, Peggy Ihde, Sherry Cole, Nicolynn Hines, Lisa Reed, Katelyn Garner, Omai Chandrasekaran, Sukantha de St. Maurice, Annabelle M Kanatani, Meganne Curello, Jennifer Arias, Rubi Swearingen, William Doernberg, Sarah B Patel, Robin Patel, Robin Open Forum Infect Dis Abstracts BACKGROUND: Rapid blood culture diagnostics increase cost and have unclear benefit for patients with Gram-negative bacilli (GNB) bloodstream infections (BSIs). We conducted a multicenter, prospective randomized controlled trial (RAPIDS-GN), comparing outcomes of patients with GNB BSI who had blood culture testing with standard of care (SOC) culture and antibiotic susceptibility testing (AST) vs. rapid organism identification (ID) and phenotypic AST using the Accelerate Pheno System (AXDX). METHODS: Subjects with blood culture Gram stain showing GNB were randomized to receive SOC testing with antimicrobial stewardship review (AS) or AXDX plus SOC testing with AS, at two academic medical centers between October 2017 and October 2018. SOC testing included rapid MALDI-TOF mass spectrometry ID and agar dilution or broth microdilution AST. In a modified intention to treat analysis, subjects were excluded if: Gram stain was erroneous, culture was positive during off-hours, blood culture in the prior week had GNB, they were deceased/on comfort care, or admitted to a nonparticipating hospital. The primary outcome was time to first antibiotic modification within 72 hours after randomization. Subjects without antibiotic modifications were assigned a time of 72 hours. No censoring was observed. T-tests and Wilcoxon rank-sum tests were used for statistical analyses. RESULTS: Of 500 randomized subjects, 448 were included (226 SOC, 222 AXDX). Groups did not differ in baseline characteristics (Table 1). Median (IQR) hours to first antibiotic modification was faster in the AXDX vs. SOC group [8.6 (2.6, 27.6) vs. 14.9 (3.3, 41.1)], P = 0.02 (Figure 1). Median (IQR) hours to first Gram-negative antibiotic modification (including escalation and de-escalation) was faster in the AXDX than SOC group [17.4 (4.9, 72) vs. 42.1 (10.1, 72)], P < 0.001 (Figure 2). Groups did not differ in clinical outcomes (Table 2). Mean (S.D.) time to results was faster for AXDX than SOC for organism ID [2.7 (1.2) h vs. 15.6 (20.3) h, P < 0.001] and AST [13 (55.7) h vs. 54.6 (45.5) h, P < 0.001]. CONCLUSION: In the largest trial to evaluate the clinical impact of a blood culture diagnostic for GNB BSI, we found that rapid organism ID and phenotypic AST led to faster changes in antibiotic therapy for Gram-negative bacteremia. [Image: see text] [Image: see text] [Image: see text] [Image: see text] DISCLOSURES: Ritu Banerjee, MD, PhD, Accelerate Diagnostics: Grant/Research Support; BioFire: Research Grant; Biomerieux: Research Grant; Roche: Research Grant Robin Patel, MD, ASM and IDSA: Other Financial or Material Support, Travel reimbursement, editor’s stipends; CD Diagnostics, Merck, Hutchison Biofilm Medical Solutions, Accelerate Diagnostics, ContraFect, TenNor Therapeutics Limited, Shionogi: Grant/Research Support; Curetis, Specific Technologies, NextGen Diagnostics, PathoQuest, Qvella: Consultant; NBME, Up-to-Date, the Infectious Diseases Board Review Course: Honorarium recipient, Other Financial or Material Support; Patent on Bordetella pertussis/parapertussis PCR issued, a patent on a device/method for sonication with royalties paid by Samsung to Mayo Clinic, and a patent on an anti-biofilm substance issued: Other Financial or Material Support, Patents. Oxford University Press 2019-10-23 /pmc/articles/PMC6811091/ http://dx.doi.org/10.1093/ofid/ofz360.708 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Abstracts
Banerjee, Ritu
Banerjee, Ritu
Komarow, Lauren
Virk, Abinash
Rajapakse, Nipunie S
Schuetz, Audrey
Dylla, Brenda
Earley, Michelle
Lok, Judith
Kohner, Peggy
Ihde, Sherry
Cole, Nicolynn
Hines, Lisa
Reed, Katelyn
Garner, Omai
Chandrasekaran, Sukantha
de St. Maurice, Annabelle M
Kanatani, Meganne
Curello, Jennifer
Arias, Rubi
Swearingen, William
Doernberg, Sarah B
Patel, Robin
Patel, Robin
640. Randomized Clinical Trial Evaluating Clinical Impact of RAPid IDentification and Antimicrobial Susceptibility Testing for Gram-Negative Bacteremia (RAPIDS-GN)
title 640. Randomized Clinical Trial Evaluating Clinical Impact of RAPid IDentification and Antimicrobial Susceptibility Testing for Gram-Negative Bacteremia (RAPIDS-GN)
title_full 640. Randomized Clinical Trial Evaluating Clinical Impact of RAPid IDentification and Antimicrobial Susceptibility Testing for Gram-Negative Bacteremia (RAPIDS-GN)
title_fullStr 640. Randomized Clinical Trial Evaluating Clinical Impact of RAPid IDentification and Antimicrobial Susceptibility Testing for Gram-Negative Bacteremia (RAPIDS-GN)
title_full_unstemmed 640. Randomized Clinical Trial Evaluating Clinical Impact of RAPid IDentification and Antimicrobial Susceptibility Testing for Gram-Negative Bacteremia (RAPIDS-GN)
title_short 640. Randomized Clinical Trial Evaluating Clinical Impact of RAPid IDentification and Antimicrobial Susceptibility Testing for Gram-Negative Bacteremia (RAPIDS-GN)
title_sort 640. randomized clinical trial evaluating clinical impact of rapid identification and antimicrobial susceptibility testing for gram-negative bacteremia (rapids-gn)
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6811091/
http://dx.doi.org/10.1093/ofid/ofz360.708
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