Evidence map›Paper›PMID 37843121›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2023

The Antibacterial Resistance Leadership Group: Scientific Advancements and Future Directions.

Henry F Chambers, Heather R Cross, Maria Souli, Scott R Evans, Robin Patel, Vance G Fowler, Antibacterial Resistance Leadership Group

Open access · greenAbstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.7field-weighted citation impact, top 15% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 1 country.

Henry F ChambersDivision of Infectious Diseases, Department of Medicine, University of California -San Francisco, San Francisco, California, USA.
Heather R CrossDuke Clinical Research Institute, Duke University School of Medicine, Durham, North Carolina, USA.
Maria SouliDuke Clinical Research Institute, Duke University School of Medicine, Durham, North Carolina, USA.
Scott R EvansDepartment of Biostatistics, George Washington University, Washington, DC, USA.
Robin PatelDivision of Infectious Diseases, Mayo Clinic, Rochester, Minnesota, USA.
Vance G FowlerDuke Clinical Research Institute, Duke University School of Medicine, Durham, North Carolina, USA.ORCID 0000-0002-8048-0897
Antibacterial Resistance Leadership Group
Duke University · USGeorge Washington University · USMayo Clinic in Florida · USUniversity of California, San Francisco · US

Funding

Antibacterial Resistance Leadership Group (ARLG)UM1AI104681 · NIAID · DUKE UNIVERSITY · PI Vance G. Fowler, Henry F HENRY CHAMBERS · 2013 to 2026
$180.8M
NIAID NIH HHS UM1 AI104681
6 · The paper itself

Abstract

In this overview, we describe important contributions from the Antibacterial Resistance Leadership Group (ARLG) to patient care, clinical trials design, and mentorship while outlining future priorities. The ARLG research agenda is focused on 3 key areas: gram-positive infections, gram-negative infections, and diagnostics. The ARLG has developed an innovative approach to clinical trials design, the desirability of outcome ranking (DOOR), which uses an ordinal measure of global outcome to assess both benefits and harms. DOOR was initially applied to observational studies to determine optimal dosing of vancomycin for methicillin-resistant Staphylcococcus aureus bacteremia and the efficacy of ceftazidime-avibactam versus colistin for the treatment of carbapenem-resistant Enterobacterales infection. DOOR is being successfully applied to the analysis of interventional trials and, in collaboration with the US Food and Drug Administration (FDA), for use in registrational trials. In the area of diagnostics, the ARLG developed Master Protocol for Evaluating Multiple Infection Diagnostics (MASTERMIND), an innovative design that allows simultaneous testing of multiple diagnostic platforms in a single study. This approach will be used to compare molecular assays for the identification of fluoroquinolone-resistant Neisseria gonorrhoeae (MASTER GC) and to compare rapid diagnostic tests for bloodstream infections. The ARLG has initiated a first-in-kind randomized, double-blind, placebo-controlled trial in participants with cystic fibrosis who are chronically colonized with Pseudomonas aeruginosa to assess the pharmacokinetics and antimicrobial activity of bacteriophage therapy. Finally, an engaged and highly trained workforce is critical for continued and future success against antimicrobial drug resistance. Thus, the ARLG has developed a robust mentoring program targeted to each stage of research training to attract and retain investigators in the field of antimicrobial resistance research.

Indexed as

Anti-Bacterial AgentsLeadershipCarbapenemsCeftazidimeColistinDrug Resistance, BacterialHumansMicrobial Sensitivity TestsAnti-Bacterial AgentsCarbapenemsCeftazidimeColistinantibacterial agentsantibacterial resistancebacterial infectionsclinical trialsdiagnostics

Identifiers

PMID37843121
PMCPMC10578046
OpenAlexW4387661666

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 Socratic graph.