Evidence map›Paper›PMID 35298491›Full record

Observational studyPloS one2022

Outcomes of implementation of the FilmArray meningoencephalitis panel in a tertiary hospital between 2017 and 2020.

TeeKeat Teoh, James Powell, Jillian O'Keeffe, Eoghan Donlon, Lisa Dillon, Marie Lenihan, Amanda Mostyn, Lorraine Power, Peter Boers, Patrick J Stapleton and 2 more

Abstract readObservational Study
In one paragraph

Observational study in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
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  3. 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

12 authors.

TeeKeat TeohDepartment of Clinical Microbiology, University Limerick Hospital Group, Limerick, Ireland.ORCID 0000-0003-2362-4994
James PowellDepartment of Clinical Microbiology, University Limerick Hospital Group, Limerick, Ireland.
Jillian O'KeeffeDepartment of Clinical Microbiology, University Limerick Hospital Group, Limerick, Ireland.
Eoghan DonlonDepartment of Neurology, University Limerick Hospital Group, Limerick, Ireland.
Lisa DillonDepartment of Clinical Microbiology, University Limerick Hospital Group, Limerick, Ireland.
Marie LenihanDepartment of Clinical Microbiology, University Limerick Hospital Group, Limerick, Ireland.
Amanda MostynDepartment of Clinical Microbiology, University Limerick Hospital Group, Limerick, Ireland.
Lorraine PowerDepartment of Clinical Microbiology, University Limerick Hospital Group, Limerick, Ireland.
Peter BoersDepartment of Neurology, University Limerick Hospital Group, Limerick, Ireland.
Patrick J StapletonDepartment of Clinical Microbiology, University Limerick Hospital Group, Limerick, Ireland.
Nuala H O'ConnellDepartment of Clinical Microbiology, University Limerick Hospital Group, Limerick, Ireland.
Colum P DunneCentre for Interventions in Infection, Inflammation & Immunity (4i), Limerick, Ireland.ORCID 0000-0002-5010-3185

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAcute meningoencephalitis is encountered commonly in the acute hospital setting and is associated with significant morbidity and mortality, in addition to significant healthcare costs. Multiplex PCR panels now allow syndromic testing for central nervous system infection. The BioFire® FilmArray® Meningoencephalitis (ME) allows testing of 14 target pathogens using only 0.2mls of cerebrospinal fluid (CSF). We conducted a retrospective observational study to assess the performance of the assay and secondarily to observe the clinical utility of negative results by comparing clinical outcomes of aseptic meningitis to bacterial and viral meningoencephalitis.

methodsData for CSF samples tested using the FilmArray ME panel from October 2017 to October 2020 were analysed. Detection of bacterial and viral targets was analysed. Admission to critical care area, 90-day readmission rates, average length of stay and 30-day and 90-day mortality were analysed for three groups with following diagnoses: bacterial meningitis, viral meningoencephalitis, or aseptic meningitis.

resultsFrom October 2017 to October 2020, 1926 CSF samples were received in the Clinical Microbiology laboratory. Of those, 543 CSF samples from 512 individual patients were tested using the FilmArray ME panel. Twenty-one bacterial targets and 56 viral targets were detected during the study period. For viral targets, the cumulative specificity was 98.9% (95% confidence interval: 93.1-99.9) when compared to the reference laboratory methods. The outcomes for 30- and 90-day mortality of the aseptic meningitis group were non-inferior relative to the viral meningoencephalitis and bacterial meningitis group. Patients with bacterial meningitis had a longer average length of stay. Aseptic meningitis was associated with a higher 90-day readmission rate than the other 2 groups, but without statistical significance.

conclusionIn our hands, implementation of the FilmArray ME panel was relatively straightforward. We experienced a transition in our workflow processes that enabled streamlining of CSF diagnostics and the safe removal of Gram staining in those samples being tested by this molecular assay. Coupled to this improvement, there was a positive clinical impact on patient care due to rapid turnaround time to results.

Indexed as

EncephalitisMeningitisMeningitis, AsepticMeningitis, ViralMeningoencephalitisBacteriaHumansMultiplex Polymerase Chain ReactionTertiary Care Centers

Identifiers

PMID35298491
PMCPMC8929653

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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.