Evidence map›Paper›PMID 40236356›Full record

ArticleCureus2025

Impact of Shipping Transit Time on Central Laboratory Processing of Total Colony Forming Units (CFU) and Staphylococcus aureus Detection.

Randy W Loftus, Franklin Dexter, Jeremiah R Brown

Abstract read
In one paragraph

Article in Cureus, 2025. 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

3 authors.

Randy W LoftusAnesthesiology and Perioperative Medicine, Mayo Clinic Rochester, Rochester, USA.
Franklin DexterAnesthesia, University of Iowa, Iowa City, USA.
Jeremiah R BrownEpidemiology, Dartmouth Geisel School of Medicine, Lebanon, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCentral laboratory processing of anesthesia work area reservoir samples is used to improve infection control measures. Reservoir samples returning ≥ 100 colony forming units (CFU) and

methodsWe conducted a retrospective analysis involving seven geographically dispersed hospitals over a 4.2-year (October 1, 2018 to December 31, 2022) study period. We chose geographically dispersed sites considering variation in ambient shipping conditions and time. Stopcocks sampled at the end of surgery were shipped to a central laboratory, plated to sheep's blood agar, incubated for 24hr at 36°C, CFU/mL quantified, and distinct isolates assessed by colony morphology, Gram stain, simple rapid tests (e.g., coagulase, oxidase, lactose fermentation, catalase), and selective growth medium.

resultsA total of 969 stopcock samples were analyzed. The percentage of stopcocks with CFU ≥ 100 was stable following sample collection from days 3 to 32 (odds ratio (OR) 1.0086/day, 95% confidence interval (CI) 0.9868-1.0309/day) and from sample kit preparation from days 3 to 143 (OR 1.0044/day, 95% CI 0.9991-1.0099/day).

conclusionsWhen utilizing a central laboratory for processing anesthesia workspace reservoir stopcock set samples, there is stability of ≥ 100 CFU for up to 32 days from collection and up to 143 days from kit preparation.

Indexed as

central clinical laboratorycolony forming units (cfu)detections aureusshipment stabilitytransit time

Identifiers

PMID40236356
PMCPMC11998623

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Registered trials

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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.