Evidence map›Paper›PMID 26197846›Full record

Trial reportClinical infectious diseases : an official publication of the Infectious Diseases Society of America2015

Randomized Trial of Rapid Multiplex Polymerase Chain Reaction-Based Blood Culture Identification and Susceptibility Testing.

Ritu Banerjee, Christine B Teng, Scott A Cunningham, Sherry M Ihde, James M Steckelberg, James P Moriarty, Nilay D Shah, Jayawant N Mandrekar, Robin Patel

2 registry-linked trialsOpen access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 288 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
288citing papers in PubMed, 6 pooled it
30.0field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT01898208 nacompletednot on this map

Rapid Identification and Susceptibility Testing of Pathogens Growing in Blood Culture Bottles - A Quality Improvement Theragnostic Stewardship Project

TypeinterventionalSponsorMayo ClinicRan2013 to 2014Enrolled743ConditionsBacteremia, Fungemia, Bloodstream InfectionArmsFilmArray testing, Antimicrobial Stewardship, Bacterial culture, Susceptibility testing
NCT03876990 nacompletednot on this mapstarted 2019, after this paper: background citation

Clinical and Medico-economic Evaluation of a Rapid Test (ePlex-BCID®, GenMark) for the Diagnosis of Bacteremia or Fungemia From Positive Blood Culture Bottles, Combining Fast Identification of Bacteria and Fungi and Evaluation of Bacterial Resistance to First Line Antibiotics.

TypeinterventionalSponsorUniversity Hospital, GrenobleRan2019 to 2021Enrolled312ConditionsBacteremia Sepsis, FungemiaArmsMultiplex PCR, Current strategy alone
3 · Its place in the literature

Who cites it

288 citing papers in PubMed, 6 syntheses or guidelines pooled it, 538 citations in OpenAlex.

  1. Pooled it
  2. Guideline
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  10. Clinical impact and cost-consequence analysis of ePlex® blood culture identification panels for the rapid diagnosis of bloodstream infections: a single-center randomized controlled trial.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2024
    Trial
  11. Randomized Trial Evaluating Clinical Impact of RAPid IDentification and Susceptibility Testing for Gram-negative Bacteremia: RAPIDS-GN.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2021
    Trial
  12. Article
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  14. Methicillin-resistant Staphylococcus aureus.Nature reviews. Disease primers · 2026
    Review
  15. Review
  16. Observational
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228 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 2 countries.

Ritu BanerjeeDivision of Pediatric Infectious Diseases, Mayo Clinic, Rochester, Minnesota.
Christine B TengDepartment of Pharmacy, National University of Singapore and Tan Tock Seng Hospital, Singapore.
Scott A CunninghamDivision of Laboratory Medicine and Pathology.
Sherry M IhdeDivision of Laboratory Medicine and Pathology.
James M SteckelbergDivision of Infectious Diseases.
James P MoriartyDivision of Health Care Policy and Research.
Nilay D ShahDivision of Health Care Policy and Research.
Jayawant N MandrekarDepartment of Health Sciences Research, Mayo Clinic, Rochester, Minnesota.
Robin PatelDivision of Laboratory Medicine and Pathology Division of Infectious Diseases.
Office of Infectious Diseases · USMayo Clinic in Florida · USNational University of Singapore · SGWinnMed · US

Funding

Antibacterial Resistance Leadership Group (ARLG)UM1AI104681 · NIAID · DUKE UNIVERSITY · PI Vance G. Fowler, Henry F HENRY CHAMBERS · 2013 to 2026
$180.8M
Mayo Clinic Center for Translational Science ActivitiesKL2TR000136 · NCATS · MAYO CLINIC ROCHESTER · PI KHOSLA, SUNDEEP · 2012 to 2015
$6.6M
NCATS NIH HHS KL2 TR000136NIAID NIH HHS UM1 AI104681NIAID NIH HHS UM1AI104681
6 · The paper itself

Abstract

backgroundThe value of rapid, panel-based molecular diagnostics for positive blood culture bottles (BCBs) has not been rigorously assessed. We performed a prospective randomized controlled trial evaluating outcomes associated with rapid multiplex PCR (rmPCR) detection of bacteria, fungi, and resistance genes directly from positive BCBs.

methodsA total of 617 patients with positive BCBs underwent stratified randomization into 3 arms: standard BCB processing (control, n = 207), rmPCR reported with templated comments (rmPCR, n = 198), or rmPCR reported with templated comments and real-time audit and feedback of antimicrobial orders by an antimicrobial stewardship team (rmPCR/AS, n = 212). The primary outcome was antimicrobial therapy duration. Secondary outcomes were time to antimicrobial de-escalation or escalation, length of stay (LOS), mortality, and cost.

resultsTime from BCB Gram stain to microorganism identification was shorter in the intervention group (1.3 hours) vs control (22.3 hours) (P < .001). Compared to the control group, both intervention groups had decreased broad-spectrum piperacillin-tazobactam (control 56 hours, rmPCR 44 hours, rmPCR/AS 45 hours; P = .01) and increased narrow-spectrum β-lactam (control 42 hours, rmPCR 71 hours, rmPCR/AS 85 hours; P = .04) use, and less treatment of contaminants (control 25%, rmPCR 11%, rmPCR/AS 8%; P = .015). Time from Gram stain to appropriate antimicrobial de-escalation or escalation was shortest in the rmPCR/AS group (de-escalation: rmPCR/AS 21 hours, control 34 hours, rmPCR 38 hours, P < .001; escalation: rmPCR/AS 5 hours, control 24 hours, rmPCR 6 hours, P = .04). Groups did not differ in mortality, LOS, or cost.

conclusionsrmPCR reported with templated comments reduced treatment of contaminants and use of broad-spectrum antimicrobials. Addition of antimicrobial stewardship enhanced antimicrobial de-escalation. CLINICAL TRIALS REGISTRATION: NCT01898208.

Indexed as

Drug Resistance, BacterialAdultAgedAged, 80 and overAnti-Bacterial AgentsBacteremiaBacteriaFemaleHumansMaleMicrobial Sensitivity TestsMiddle AgedMolecular TypingMultiplex Polymerase Chain ReactionProspective StudiesAnti-Bacterial Agentsantimicrobial stewardshipblood culturediagnosticPCR

Identifiers

PMID26197846
PMCPMC4560903
OpenAlexW2159643438

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.