Evidence map›Paper›PMID 39657016›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2025

Association Between the Sequence of β-Lactam and Vancomycin Administration and Mortality in Patients With Suspected Sepsis.

Yutaka Kondo, Michael Klompas, Caroline S McKenna, Theodore R Pak, Claire N Shappell, Laura DelloStritto, Chanu Rhee

Abstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing papers in PubMed
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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

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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

2 citing papers in PubMed.

  1. Review
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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Yutaka KondoDepartment of Population Medicine, Harvard Pilgrim Health Care Institute, Boston, Massachusetts, USA.ORCID 0000-0003-1072-7089
Michael KlompasDepartment of Population Medicine, Harvard Pilgrim Health Care Institute, Boston, Massachusetts, USA.ORCID 0000-0001-8641-4498
Caroline S McKennaDepartment of Population Medicine, Harvard Pilgrim Health Care Institute, Boston, Massachusetts, USA.
Theodore R PakDepartment of Population Medicine, Harvard Pilgrim Health Care Institute, Boston, Massachusetts, USA.ORCID 0000-0002-1676-2523
Claire N ShappellDepartment of Population Medicine, Harvard Pilgrim Health Care Institute, Boston, Massachusetts, USA.ORCID 0000-0002-8316-1496
Laura DelloStrittoDepartment of Population Medicine, Harvard Pilgrim Health Care Institute, Boston, Massachusetts, USA.
Chanu RheeDepartment of Population Medicine, Harvard Pilgrim Health Care Institute, Boston, Massachusetts, USA.ORCID 0000-0002-9537-4245

Funding

INFECTIOUS DISEASE AND BASIC MICROBIOLOGICAL MECHANISMST32AI007061 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI Marcia B Goldberg · 1985 to 2026
$12.1M
AHRQ HHS K08 HS029518AHRQ HHS K08 HS030118AHRQ HHS R01 HS027170AHRQ HHS R01HS027170CDC HHS U54CK000611Ministry of Education 22KK0264National Institute of Allergy and Infectious Diseases T32AI007061NCEZID CDC HHS U54 CK000611NIAID NIH HHS T32 AI007061
6 · The paper itself

Abstract

backgroundTimely antibiotic initiation is critical to sepsis management, but there are limited data on the impact of giving β-lactams first versus vancomycin first among patients prescribed both agents.

methodsWe retrospectively analyzed all adults admitted to 5 US hospitals from 2015-2022 with suspected sepsis (blood culture collected, antibiotics administered, and organ dysfunction) treated with vancomycin and a broad-spectrum β-lactam within 24 hours of arrival. We estimated associations between β-lactam- versus vancomycin-first strategies and in-hospital mortality using inverse probability weighting (IPW) to adjust for potential confounders.

resultsAmong 25 391 patients with suspected sepsis, 21 449 (84.4%) received β-lactams first and 3942 (15.6%) received vancomycin first. Compared with the β-lactam-first group, patients administered vancomycin first tended to be less severely ill, had more skin/musculoskeletal infections (20.0% vs 7.8%), and received β-lactams a median of 3.5 hours later relative to emergency department arrival. On IPW analysis, the β-lactam-first strategy was associated with lower mortality (adjusted odds ratio [aOR]: .89; 95% CI: .80-.99). Point estimates were directionally similar but nonsignificant in a sensitivity analysis using propensity score matching rather than IPW (aOR: .94; 95% CI: .82-1.07) and in subgroups of patients with positive blood cultures, methicillin-resistant Staphylococcus aureus cultures, and those administered antipseudomonal β-lactams.

conclusionsAmong patients with suspected sepsis prescribed vancomycin and β-lactam therapy, β-lactam administration before vancomycin was associated with a modest reduction in in-hospital mortality. These findings support prioritizing β-lactam therapy in most patients with sepsis but merit confirmation in randomized trials given the risk of residual confounding in observational analyses.

Indexed as

Anti-Bacterial Agentsbeta-LactamsSepsisVancomycinAdultAgedAged, 80 and overFemaleHospital MortalityHumansMaleMiddle AgedRetrospective StudiesUnited StatesAnti-Bacterial Agentsbeta-LactamsVancomycinantibacterial agentsantibioticsantibiotic sequencesepsisβ-lactam

Identifiers

PMID39657016
PMCPMC12043061

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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.