Evidence map›Paper›PMID 42210178›Full record

ArticleBMC infectious diseases2026

The impact of follow-up blood cultures on mortality and management in patients with gram-negative bloodstream infections: a validation cohort study.

Joshua T Thaden, Felicia Ruffin, Lawrence P Park, Parisa Farahani, Divyam Goel, Joshua B Parsons, Vance G Fowler, Stacey A Maskarinec

Abstract readValidation Study
In one paragraph

Article in BMC infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
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

8 authors.

Joshua T ThadenDivision of Infectious Diseases, Department of Medicine, Duke University, DUMC Box 102359, Durham, NC, 27710, USA. Joshua.Thaden@duke.edu.
Felicia RuffinDivision of Infectious Diseases, Department of Medicine, Duke University, DUMC Box 102359, Durham, NC, 27710, USA.
Lawrence P ParkDivision of Infectious Diseases, Department of Medicine, Duke University, DUMC Box 102359, Durham, NC, 27710, USA.
Parisa FarahaniDivision of Infectious Diseases, Department of Medicine, Duke University, DUMC Box 102359, Durham, NC, 27710, USA.
Divyam GoelDuke University School of Medicine, DUMC Box 102359, Durham, NC, 27710, USA.
Joshua B ParsonsDivision of Infectious Diseases, Department of Medicine, Duke University, DUMC Box 102359, Durham, NC, 27710, USA.
Vance G FowlerDivision of Infectious Diseases, Department of Medicine, Duke University, DUMC Box 102359, Durham, NC, 27710, USA.
Stacey A MaskarinecDivision of Infectious Diseases, Department of Medicine, Duke University, DUMC Box 102359, Durham, NC, 27710, USA.

Funding

HLA Fine Mapping to Elucidate S. aureus SusceptibilityR01AI165671 · NIAID · DUKE UNIVERSITY · PI FOWLER, VANCE G., SCOTT, WILLIAM K · 2021 to 2025
$3.8M
Staphylococcus aureus Cardiac Device Infections - From the Vascular ViewpointK23HL159275 · NHLBI · DUKE UNIVERSITY · PI Stacey A Maskarinec · 2022 to 2026
$897k
Characterization of a Novel E. coli Type III Secretion System Associated with Increased Patient MortalityK08AI171183 · NIAID · DUKE UNIVERSITY · PI Joshua T Thaden · 2022 to 2026
$895k
NHLBI NIH HHS K23 HL159275NIAID NIH HHS K08 AI171183NIAID NIH HHS R01 AI165671NIH HHS 1R01-AI165671NIH HHS K08-AI171183NIH HHS K23-HL159275
6 · The paper itself

Abstract

backgroundThe practice of obtaining follow-up blood cultures (FUBCs) in patients with gram-negative bloodstream infections (GN-BSI) remains controversial. The current study had two goals: (1) to internally validate our earlier findings of decreased mortality in patients with FUBCs and increased mortality in those with persistent GN-BSI, and (2) to identify mechanisms by which FUBCs might impact clinical care and outcome.

methodsAdults with GN-BSI at Duke University were enrolled from 2015 to 2021. Cox proportional hazards models with propensity score-weighting were used to examine associations of FUBCs and positive FUBCs with attributable and all-cause in-hospital mortality. Immortal time bias was addressed by treating FUBCs as a time-dependent variable and through sensitivity analyses. To understand the potential impact of FUBCs on clinical care, matched cohorts were generated (n = 41 in each group): (1) no FUBCs, (2) FUBCs negative for growth, and (3) FUBCs positive for growth (i.e., persistent GN-BSI). Infection-related consultations, imaging studies, and procedures were determined for each matched cohort.

resultsOf the 1291 patients in this study, FUBCs were obtained in 78% (1012 patients) and positive in 20% (199 patients). After adjusting for immortal time bias, obtaining FUBCs remained associated with decreased attributable mortality (Hazard ratio [HR] 0.39; 95% confidence interval [CI] 0.32-0.49; p < 0.0001). Persistent GN-BSI was associated with increased attributable mortality (HR 1.77; 95% CI, 1.24-2.52; p = 0.002). Obtaining FUBCs was associated with subsequent infectious diseases (ID) consultation (No FUBCs: 2/41 [5%]; FUBCs: 21/82 [26%]; p < 0.0001). This finding was primarily due to patients with persistent GN-BSI (FUBCs negative: 6/41 [15%]; FUBCs positive: 15/41 [37%]; p = 0.04). Patients with persistent GN-BSI had a higher rate of source control procedures (FUBCs positive: 12/41 [29%]; All others: 11/82 [13%]); p = 0.05).

conclusionsObtaining FUBCs was associated with decreased mortality. This mortality effect could stem from increased ID consults after FUBCs and increased source control procedures following positive FUBCs.

Indexed as

BacteremiaBlood CultureGram-Negative Bacterial InfectionsAdultAgedCohort StudiesFemaleFollow-Up StudiesGram-Negative BacteriaHospital MortalityHumansMaleMiddle AgedProportional Hazards ModelsBacteremiaBloodstream infectionFollow-up blood cultureGram negative

Identifiers

PMID42210178
PMCPMC13425979

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.