Evidence map›Paper›PMID 27986734›Full record

ArticleBMJ open2016

How to measure the impacts of antibiotic resistance and antibiotic development on empiric therapy: new composite indices.

Josie S Hughes, Amy Hurford, Rita L Finley, David M Patrick, Jianhong Wu, Andrew M Morris

Open access · goldAbstract read
In one paragraph

Article in BMJ open, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.5field-weighted citation impact, top 8% 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

14 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. A Nonprofit Drug Development Model Is Part of the Antimicrobial Resistance (AMR) Solution.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2022
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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

6 authors at 5 institutions in 1 country.

Josie S HughesCentre for Disease Modelling, York University, Toronto, Ontario, Canada.
Amy HurfordDepartment of Biology and Department of Mathematics and Statistics, Memorial University of Newfoundland, St. John's, Newfoundland, Canada.
Rita L FinleyCentre for Food-borne, Environmental and Zoonotic Infectious Diseases, Public Health Agency of Canada, Guelph, Ontario, Canada.
David M PatrickCentre for Disease Control, Vancouver, British Columbia, Canada.
Jianhong WuCentre for Disease Modelling, York University, Toronto, Ontario, Canada.
Andrew M MorrisDepartment of Medicine, Mount Sinai Hospital and University Health Network, Toronto, Ontario, Canada.
York University · CABC Centre for Disease Control · CAMemorial University of Newfoundland · CAPublic Health Agency of Canada · CAUniversity of Toronto · CA

Funding

CIHR
6 · The paper itself

Abstract

objectivesWe aimed to construct widely useable summary measures of the net impact of antibiotic resistance on empiric therapy. Summary measures are needed to communicate the importance of resistance, plan and evaluate interventions, and direct policy and investment. DESIGN, SETTING AND

participantsAs an example, we retrospectively summarised the 2011 cumulative antibiogram from a Toronto academic intensive care unit. OUTCOME MEASURES: We developed two complementary indices to summarise the clinical impact of antibiotic resistance and drug availability on empiric therapy. The Empiric Coverage Index (ECI) measures susceptibility of common bacterial infections to available empiric antibiotics as a percentage. The Empiric Options Index (EOI) varies from 0 to 'the number of treatment options available', and measures the empiric value of the current stock of antibiotics as a depletable resource. The indices account for drug availability and the relative clinical importance of pathogens. We demonstrate meaning and use by examining the potential impact of new drugs and threatening bacterial strains.

conclusionsIn our intensive care unit coverage of device-associated infections measured by the ECI remains high (98%), but 37-44% of treatment potential measured by the EOI has been lost. Without reserved drugs, the ECI is 86-88%. New cephalosporin/β-lactamase inhibitor combinations could increase the EOI, but no single drug can compensate for losses. Increasing methicillin-resistant Staphylococcus aureus (MRSA) prevalence would have little overall impact (ECI=98%, EOI=4.8-5.2) because many Gram-positives are already resistant to β-lactams. Aminoglycoside resistance, however, could have substantial clinical impact because they are among the few drugs that provide coverage of Gram-negative infections (ECI=97%, EOI=3.8-4.5). Our proposed indices summarise the local impact of antibiotic resistance on empiric coverage (ECI) and available empiric treatment options (EOI) using readily available data. Policymakers and drug developers can use the indices to help evaluate and prioritise initiatives in the effort against antimicrobial resistance.

Indexed as

Drug Resistance, BacterialAnti-Bacterial AgentsCatheter-Related InfectionsHumansIntensive Care UnitsMicrobial Sensitivity TestsPneumonia, Ventilator-AssociatedRetrospective StudiesAnti-Bacterial Agentsantimicrobial resistanceburden of resistancecomposite indexcumulative antibiogramdevice-associated infection

Identifiers

PMID27986734
PMCPMC5168677
OpenAlexW2566694113

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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 OpenQuestion graph.