Evidence map›Paper›PMID 30264119›Full record

Trial reportJAMA2018

Effect of Algorithm-Based Therapy vs Usual Care on Clinical Success and Serious Adverse Events in Patients with Staphylococcal Bacteremia: A Randomized Clinical Trial.

Thomas L Holland, Issam Raad, Helen W Boucher, Deverick J Anderson, Sara E Cosgrove, P Suzanne Aycock, John W Baddley, Anne-Marie Chaftari, Shein-Chung Chow, Vivian H Chu and 21 more

2 registry-linked trialsOpen access · bronzeAbstract readComparative StudyEquivalence TrialMulticenter Study
In one paragraph

Trial report in JAMA, 2018. 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 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
5.3field-weighted citation impact, top 3% 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.

NCT01191840 phase2completednot on this map

A Multi-Center, Randomized, Open-Label, Comparative Study to Assess the Safety and Efficacy of a Treatment Algorithm to Reduce the Use of Vancomycin in Adult Patients With Blood Stream Infections Due to Staphylococci

TypeinterventionalSponsorDuke UniversityRan2011 to 2017Enrolled509ConditionsBacteremiaArmsVancomycin
NCT06211829 completednot on this mapstarted 2022, after this paper: background citation

An Evaluation of a Antimicrobial Stewardship Recommendation Bundle for Staphylococcus Aureus Bloodstream Infections

TypeobservationalSponsorMethodist Health SystemRan2022 to 2025Enrolled77ConditionsBacterial Infections
3 · Its place in the literature

Who cites it

36 citing papers in PubMed, 72 citations in OpenAlex.

  1. Cefazolin for Methicillin-SusceptibleThe New England journal of medicine · 2026
    Trial
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Current management ofFujita medical journal · 2024
    Article
  13. Low-Risk Staphylococcus aureus Bacteremia Patients Do Not Require Routine Diagnostic Imaging: A Multicenter, Retrospective, Cohort Study.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2024
    Article
  14. Article
  15. Article
  16. Article
  17. Clinically Adjudicated Reference Standards for Evaluation of Infectious Diseases Diagnostics.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2023
    Article
  18. Review
  19. Article
  20. Intravenous versus Oral Step-Down for the Treatment ofPharmacy (Basel, Switzerland) · 2022
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

31 authors at 20 institutions in 3 countries.

Thomas L HollandDuke University Medical Center, Durham, North Carolina.
Issam RaadThe University of Texas MD Anderson Cancer Center, Houston.
Helen W BoucherTufts Medical Center, Boston, Massachusetts.
Deverick J AndersonDuke University Medical Center, Durham, North Carolina.
Sara E CosgroveJohns Hopkins University School of Medicine, Baltimore, Maryland.
P Suzanne AycockDuke Clinical Research Institute, Durham, North Carolina.
John W BaddleyUniversity of Alabama at Birmingham.
Anne-Marie ChaftariThe University of Texas MD Anderson Cancer Center, Houston.
Shein-Chung ChowDuke Clinical Research Institute, Durham, North Carolina.
Vivian H ChuDuke University Medical Center, Durham, North Carolina.
Manuela CarugatiDuke University Medical Center, Durham, North Carolina.
Paul CookBrody School of Medicine, East Carolina University, Greenville, North Carolina.
G Ralph CoreyDuke University Medical Center, Durham, North Carolina.
Anna Lisa CrowleyDuke University Medical Center, Durham, North Carolina.
Jennifer DalyUniversity of Massachusetts Medical School, Worcester.
Jiezhun GuDuke Clinical Research Institute, Durham, North Carolina.
Ray HachemThe University of Texas MD Anderson Cancer Center, Houston.
James HortonCarolinas Medical Center, Charlotte, North Carolina.
Timothy C JenkinsDenver Health, Denver, Colorada.
Donald LevineWayne State University, Detroit, Michigan.
Jose M MiroHospital Clinic-IDIBAPS, University of Barcelona, Barcelona, Spain.
Juan M PericasHospital Clinic-IDIBAPS, University of Barcelona, Barcelona, Spain.
Paul RiskaAlbert Einstein College of Medicine, Bronx, New York.
Zachary RubinDavid Geffen School of Medicine, University of California at Los Angeles.
Mark E RuppUniversity of Nebraska Medical Center, Omaha.
John SchrankGreenville Health System, Greenville, South Carolina.
Matthew SimsBeaumont Health System, Royal Oak, Michigan.
Dannah WrayMedical University of South Carolina, Charleston.
Marcus ZervosHenry Ford Health System, Detroit, Michigan.
Vance G FowlerDuke University Medical Center, Durham, North Carolina.
Staphylococcal Bacteremia Investigators
Clinical Research Institute · USDuke Medical Center · USThe University of Texas MD Anderson Cancer Center · USAlbert Einstein College of Medicine · USBeaumont Health · USCarolinas Medical Center · USConsorci Institut D'Investigacions Biomediques August Pi I Sunyer · ESEast Carolina University · USHenry Ford Health System · USHospital Clínic de Barcelona · ESJohns Hopkins Medicine · USMedical University of South Carolina · USPrisma Health · USTufts Medical Center · USUniversity of Alabama at Birmingham · USUniversity of California, Los Angeles · USUniversity of Colorado Denver · USUniversity of Massachusetts Chan Medical School · USUniversity of Nebraska Medical Center · USWayne State University · US

Funding

Mentoring Patient Oriented Research in Antibiotic-Resistant BacteriaK24AI093969 · NIAID · DUKE UNIVERSITY · PI FOWLER, VANCE G. · 2011 to 2020
$1.6M
NIAID NIH HHS K24 AI093969
6 · The paper itself

Abstract

Importance: The appropriate duration of antibiotics for staphylococcal bacteremia is unknown. Objective: To test whether an algorithm that defines treatment duration for staphylococcal bacteremia vs standard of care provides noninferior efficacy without increasing severe adverse events. Design, Setting, and Participants: A randomized trial involving adults with staphylococcal bacteremia was conducted at 16 academic medical centers in the United States (n = 15) and Spain (n = 1) from April 2011 to March 2017. Patients were followed up for 42 days beyond end of therapy for those with Staphylococcus aureus and 28 days for those with coagulase-negative staphylococcal bacteremia. Eligible patients were 18 years or older and had 1 or more blood cultures positive for S aureus or coagulase-negative staphylococci. Patients were excluded if they had known or suspected complicated infection at the time of randomization. Interventions: Patients were randomized to algorithm-based therapy (n = 255) or usual practice (n = 254). Diagnostic evaluation, antibiotic selection, and duration of therapy were predefined for the algorithm group, whereas clinicians caring for patients in the usual practice group had unrestricted choice of antibiotics, duration, and other aspects of clinical care. Main Outcomes and Measures: Coprimary outcomes were (1) clinical success, as determined by a blinded adjudication committee and tested for noninferiority within a 15% margin; and (2) serious adverse event rates in the intention-to-treat population, tested for superiority. The prespecified secondary outcome measure, tested for superiority, was antibiotic days among per-protocol patients with simple or uncomplicated bacteremia. Results: Among the 509 patients randomized (mean age, 56.6 [SD, 16.8] years; 226 [44.4%] women), 480 (94.3%) completed the trial. Clinical success was documented in 209 of 255 patients assigned to algorithm-based therapy and 207 of 254 randomized to usual practice (82.0% vs 81.5%; difference, 0.5% [1-sided 97.5% CI, -6.2% to ∞]). Serious adverse events were reported in 32.5% of algorithm-based therapy patients and 28.3% of usual practice patients (difference, 4.2% [95% CI, -3.8% to 12.2%]). Among per-protocol patients with simple or uncomplicated bacteremia, mean duration of therapy was 4.4 days for algorithm-based therapy vs 6.2 days for usual practice (difference, -1.8 days [95% CI, -3.1 to -0.6]). Conclusions and Relevance: Among patients with staphylococcal bacteremia, the use of an algorithm to guide testing and treatment compared with usual care resulted in a noninferior rate of clinical success. Rates of serious adverse events were not significantly different, but interpretation is limited by wide confidence intervals. Further research is needed to assess the utility of the algorithm. Trial Registration: ClinicalTrials.gov Identifier: NCT01191840.

Indexed as

AlgorithmsStaphylococcus aureusAdultAgedAged, 80 and overAnti-Bacterial AgentsBacteremiaCoagulaseConfidence IntervalsDrug Administration ScheduleFemaleHumansIntention to Treat AnalysisMaleMiddle AgedSingle-Blind MethodAnti-Bacterial AgentsCoagulase

Identifiers

PMID30264119
PMCPMC6233609
OpenAlexW2894198721

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.