Evidence map›Paper›PMID 42262094›Full record

ArticleJournal of clinical microbiology2026

A myco-management problem: improving utilization of fungal and mycobacterial smear and culture.

Sarah M Schrader, Vamsi Thiriveedhi, John A Branda, Sarah E Turbett, Erik H Klontz

Abstract read
In one paragraph

Article in Journal of clinical microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Sarah M SchraderDepartment of Pathology, Massachusetts General Hospital, , Boston, Massachusetts, USA.ORCID 0000-0003-4141-531X
Vamsi ThiriveedhiDepartment of Pathology, Massachusetts General Hospital, , Boston, Massachusetts, USA.
John A BrandaDepartment of Pathology, Massachusetts General Hospital, , Boston, Massachusetts, USA.
Sarah E Turbett *Department of Pathology, Massachusetts General Hospital, , Boston, Massachusetts, USA.ORCID 0000-0002-3603-8110
Erik H Klontz *Department of Pathology, Massachusetts General Hospital, , Boston, Massachusetts, USA.ORCID 0000-0002-1923-972X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fungal and mycobacterial smear and culture are often inappropriately ordered, straining clinical laboratory resources and risking patient harm from false-positive results. To identify opportunities for optimization, we assessed utilization and yield of fungal and mycobacterial smear and culture over five years at a large academic medical center in an area of low tuberculosis prevalence. Positive rates were generally lower for non-respiratory specimens compared to respiratory specimens, prompting us to focus on collection method (swab vs non-swab) and location (operating room [OR] vs non-OR) for non-respiratory specimens. For non-respiratory fungal smear and culture, swabs demonstrated poor recovery of mold in culture, and positive smear results from swabs rarely affected clinical management (6/3,611 cases [0.17%]). Positive rates were significantly lower among OR specimens. For mycobacterial smear and culture, positive rates were exceedingly low for non-respiratory specimens (smear: 70/23,661 [0.3%]; culture: 278/23,918 [1.2%]). Swabs were inferior for mycobacterial culture, and positive smear results from swabs rarely impacted clinical management (3/7,398 cases [0.04%]). Among patients with at least one non-respiratory mycobacterial smear or culture over a two-year period, the smear or culture was diagnostic in only 32/4,572 (0.70%), 31 (96.9%) of whom had risk factors for mycobacterial infection. The smear result changed clinical management in only 5/4,497 cases (0.11%). Our results reveal considerable overutilization of fungal and mycobacterial smear and culture for non-respiratory specimens and confirm the low yield of non-respiratory swabs for mold and mycobacterial detection. These data inform strategies to optimize fungal and mycobacterial diagnostic testing in clinical laboratories. IMPORTANCE: Fungal and mycobacterial infections are associated with specific risk factors. However, diagnostic studies for fungal and mycobacterial infections, including fungal and mycobacterial smear and culture, are often inappropriately ordered in clinical scenarios where the probability of infection is low. Due to the manual nature of these tests, high volumes of unnecessary testing strain limited clinical laboratory resources. In addition, patients can be harmed by false-positive results. In this study, we analyzed the results of fungal and mycobacterial smear and culture performed over five years at a large academic medical center in a location with low tuberculosis prevalence to identify strategies to reduce unnecessary testing. Implementation of these strategies could allow clinical laboratories to optimize fungal and mycobacterial diagnostic testing and more efficiently use limited clinical laboratory resources without compromising patient care.

Indexed as

FungiMicrobiological TechniquesMycobacteriumMycobacterium InfectionsMycosesAcademic Medical CentersBacilloscopyBacteriological TechniquesHumansSpecimen Handlingfungal diagnosticsmycobacterial diagnosticstest utilization

Identifiers

PMID42262094
PMCPMC13343888

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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.