Evidence map›Paper›PMID 35840825›Full record

ArticleIrish journal of medical science2023

Establishing a committee for antemortem reviews of suspect Creutzfeldt-Jakob disease cases in Ireland.

Conor Fearon, Rachel Howley, Seamus Looby, Amber Byrne, Josephine Heffernan, Ciara Heeney, Alan Beausang, Jane Cryan, Michael Farrell, Sean O'Dowd and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Irish journal of medical science, 2023. 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, top 93% of its field
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, 0 citations in OpenAlex.

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

11 authors at 2 institutions in 1 country.

Conor Fearon *Department of Neuropathology, Beaumont Hospital, Dublin 9, Ireland.
Rachel Howley *Department of Neuropathology, Beaumont Hospital, Dublin 9, Ireland.
Seamus LoobyDepartment of Neuroradiology, Beaumont Hospital, Dublin 9, Ireland.
Amber ByrneDepartment of Neuropathology, Beaumont Hospital, Dublin 9, Ireland.
Josephine HeffernanDepartment of Neuropathology, Beaumont Hospital, Dublin 9, Ireland.
Ciara HeeneyDepartment of Neuropathology, Beaumont Hospital, Dublin 9, Ireland.
Alan BeausangDepartment of Neuropathology, Beaumont Hospital, Dublin 9, Ireland.
Jane CryanDepartment of Neuropathology, Beaumont Hospital, Dublin 9, Ireland.
Michael FarrellDepartment of Neuropathology, Beaumont Hospital, Dublin 9, Ireland.
Sean O'DowdDepartment of Neurology, Tallaght University Hospital, Dublin 24, Ireland. sean.odowd@tuh.ie.
Francesca BrettDepartment of Neuropathology, Beaumont Hospital, Dublin 9, Ireland. francescabrett@beaumont.ie.ORCID http://orcid.org/0000-0002-7453-4027
Beaumont Hospital · IETrinity College Dublin · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCreutzfeldt-Jakob disease (CJD) is a rapidly progressive, neurodegenerative disease. In Ireland, clinical diagnostics and laboratory testing remain the responsibility of the managing clinician and the Neuropathology Department at the Beaumont Hospital, respectively. Centralized review of individual cases is not undertaken.

aimsTo determine how diagnostic processes for CJD could be improved in Ireland and to outline the structure and referral process for a new CJD review panel at the Beaumont Hospital.

methodsWe surveyed Irish neurologists' experiences on the management of CJD in Ireland. We measured turnaround times (TAT) for CSF samples referred for diagnostic CJD testing. Finally, we retrospectively reviewed imaging of autopsy-proven CJD cases to compare with initial reports.

resultsNinety-three percent of neurologists supported a national central review of suspect CJD cases. A second clinical opinion was considered to be of likely benefit by 79%. Additionally, 93% reported that a centralized review of neuroradiology would be useful. All respondents felt that expediting turnaround of CSF analysis would be of benefit. The average TAT for CSF testing was 35.4 days. In retrospective review of imaging, all patients demonstrated MRI findings consistent with CJD. However, in only one of these cases were the initial pre-autopsy radiological findings reported as being consistent with CJD.

conclusionsThese findings support the need for improvements to the Irish National CJD Surveillance Unit to maximize antemortem diagnostic accuracy. On foot of this, a clinical CJD Multidisciplinary Team (CJD MDT) has been established to provide a second opinion on (i) the patient's clinical history, (ii) neuroradiology and (iii) and neurophysiology reports (where available).

Indexed as

Creutzfeldt-Jakob SyndromeNeurodegenerative DiseasesBiopsyHumansIrelandRetrospective StudiesCreutzfeldt-Jakob diseasePrion disease

Identifiers

PMID35840825
PMCPMC9286704
OpenAlexW4285591610

What OpenQuestion holds

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LicenceCC BY
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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.