Evidence map›Paper›PMID 30052813›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2018

Difficult-to-Treat Resistance in Gram-negative Bacteremia at 173 US Hospitals: Retrospective Cohort Analysis of Prevalence, Predictors, and Outcome of Resistance to All First-line Agents.

Sameer S Kadri, Jennifer Adjemian, Yi Ling Lai, Alicen B Spaulding, Emily Ricotta, D Rebecca Prevots, Tara N Palmore, Chanu Rhee, Michael Klompas, John P Dekker and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 377 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
377citing papers in PubMed, 3 pooled it
10.7field-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.

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

377 citing papers in PubMed, 3 syntheses or guidelines pooled it, 547 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Trial
  6. Trial
  7. Is less always more? Ceftazidime/avibactam alone or in combination to treat infections caused by Pseudomonas aeruginosa: a retrospective observational multi-centre cohort study.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2026
    Observational
  8. A review of bloodstream infections-pathogens, pathogenesis, diagnostic strategies, treatment methods-challenges and future aspects.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2026
    Review
  9. Review
  10. Global epidemiology of carbapenem-resistantJAC-antimicrobial resistance · 2026
    Review
  11. Review
  12. Article
  13. Article
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  17. In vitro activity of aztreonam-avibactam against carbapenem-resistant Pseudomonas aeruginosa from Southern Brazil.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2026
    Article
  18. Article
  19. Long-Term Environmental Surveillance ofPathogens (Basel, Switzerland) · 2026
    Article
  20. Article

317 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 6 institutions in 1 country.

Sameer S KadriCritical Care Medicine Department, National Institutes of Health Clinical Center, Bethesda, Maryland.
Jennifer AdjemianEpidemiology Unit, Laboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda.
Yi Ling LaiEpidemiology Unit, Laboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda.
Alicen B SpauldingEpidemiology Unit, Laboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda.
Emily RicottaEpidemiology Unit, Laboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda.
D Rebecca PrevotsEpidemiology Unit, Laboratory of Clinical Immunology and Microbiology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda.
Tara N PalmoreNational Institutes of Health Clinical Center, Bethesda, Maryland.
Chanu RheeDepartment of Medicine, Brigham and Women's Hospital.
Michael KlompasDepartment of Medicine, Brigham and Women's Hospital.
John P DekkerDepartment of Laboratory Medicine, National Institutes of Health Clinical Center, Bethesda.
John H PowersClinical Research Directorate/Clinical Monitoring Research Program, Leidos Biomedical Research, Inc., NCI Campus at Frederick, Maryland.
Anthony F SuffrediniCritical Care Medicine Department, National Institutes of Health Clinical Center, Bethesda, Maryland.
David C HooperDivision of Infectious Diseases, Massachusetts General Hospital and Harvard Medical School, Boston.
Scott FridkinDivision of Healthcare Quality and Promotion, Centers for Disease Control and Prevention, Atlanta, Georgia.
Robert L DannerCritical Care Medicine Department, National Institutes of Health Clinical Center, Bethesda, Maryland.
National Institutes of Health Antimicrobial Resistance Outcomes Research Initiative (NIH–ARORI)
National Institutes of Health · USNational Institutes of Health Clinical Center · USBrigham and Women's Hospital · USHarvard University · USCenters for Disease Control and Prevention · USLeidos (United States) · US

Funding

Application of Genomic Approaches to Bacterial Pathogenesis and Mechanisms of Antimicrobial ResistanceZIAAI001249 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI DEKKER, JOHN · 2019 to 2025
$13.7M
Epidemiology of Mycobacterial InfectionsZIAAI001035 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI PREVOTS, D. REBECCA · 2009 to 2025
$11.6M
Epidemiology of Antibiotic ResistanceZIAAI001215 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI PREVOTS, DEBORAH · 2016 to 2019
$629k
Objective Evaluation of Variation in Sepsis Incidence, Mortality, and CareK08HS025008 · AHRQ · HARVARD PILGRIM HEALTH CARE, INC. · PI RHEE, CHANU · 2017 to 2019
$450k
Preclinical and Clinical Investigations of Severe Infection and Critical Illness ZIACL008060 · CLC · CLINICAL CENTER · PI DANNER, ROBERT L · 2009 to 2025
$0k
Next Generation Sequencing Methods in Molecular MicrobiologyZIACL080020 · CLC · CLINICAL CENTER · PI DEKKER, JOHN · 2015 to 2018
$0k
Big Data- Epidemiology of Antimicrobial ResistanceZIACL090046 · CLC · CLINICAL CENTER · PI KADRI, SAMEER · 2017 to 2025
$0k
AHRQ HHS K08 HS025008NCI NIH HHS HHSN261200800001E
6 · The paper itself

Abstract

Background: Resistance to all first-line antibiotics necessitates the use of less effective or more toxic "reserve" agents. Gram-negative bloodstream infections (GNBSIs) harboring such difficult-to-treat resistance (DTR) may have higher mortality than phenotypes that allow for ≥1 active first-line antibiotic. Methods: The Premier Database was analyzed for inpatients with select GNBSIs. DTR was defined as intermediate/resistant in vitro to all ß-lactam categories, including carbapenems and fluoroquinolones. Prevalence and aminoglycoside resistance of DTR episodes were compared with carbapenem-resistant, extended-spectrum cephalosporin-resistant, and fluoroquinolone-resistant episodes using CDC definitions. Predictors of DTR were identified. The adjusted relative risk (aRR) of mortality was examined for DTR, CDC-defined phenotypes susceptible to ≥1 first-line agent, and graded loss of active categories. Results: Between 2009-2013, 471 (1%) of 45011 GNBSI episodes at 92 (53.2%) of 173 hospitals exhibited DTR, ranging from 0.04% for Escherichia coli to 18.4% for Acinetobacter baumannii. Among patients with DTR, 79% received parenteral aminoglycosides, tigecycline, or colistin/polymyxin-B; resistance to all aminoglycosides occurred in 33%. Predictors of DTR included urban healthcare and higher baseline illness. Crude mortality for GNBSIs with DTR was 43%; aRR was higher for DTR than for carbapenem-resistant (1.2; 95% confidence interval, 1.0-1.4; P = .02), extended-spectrum cephalosporin-resistant (1.2; 1.1-1.4; P = .001), or fluoroquinolone-resistant (1.2; 1.0-1.4; P = .008) infections. The mortality aRR increased 20% per graded loss of active first-line categories, from 3-5 to 1-2 to 0. Conclusion: Nonsusceptibility to first-line antibiotics is associated with decreased survival in GNBSIs. DTR is a simple bedside prognostic measure of treatment-limiting coresistance.

Indexed as

Drug Resistance, Multiple, BacterialAdolescentAdultAgedAnti-Bacterial AgentsBacteremiaCarbapenemsDatabases, FactualFemaleFluoroquinolonesGram-Negative BacteriaGram-Negative Bacterial InfectionsHospitalsHumansMaleMicrobial Sensitivity TestsAnti-Bacterial AgentsCarbapenemsFluoroquinolones

Identifiers

PMID30052813
PMCPMC6260171
OpenAlexW2883234304

What OpenQuestion 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 OpenQuestion graph.