Evidence map›Paper›PMID 38993737›Full record

ArticleJournal of hematology2024

Recurrent Infection in a Young Female Patient Recently Diagnosed With Primary Evans Syndrome Without Neutropenia.

Jennie An, Preye Amaruntowa, Waleed Ahmed, Ali Khan, Muhammad Shahzad

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PubMed Full text at PMC Publisher
In one paragraph

Article in Journal of hematology, 2024. 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.

Jennie AnSt. James School of Medicine, Anguilla, Park Ridge, IL 60068, USA.ORCID https://orcid.org/0009-0004-6348-9381
Preye AmaruntowaSt. James School of Medicine, Anguilla, Park Ridge, IL 60068, USA.
Waleed AhmedSt. James School of Medicine, Anguilla, Park Ridge, IL 60068, USA.
Ali KhanSt. James School of Medicine, Anguilla, Park Ridge, IL 60068, USA.
Muhammad ShahzadSt. James School of Medicine, Anguilla, Park Ridge, IL 60068, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Evans syndrome (ES) is a rare autoimmune condition of unknown etiology that occurs in a small subset of patients diagnosed, either sequentially or concomitantly, with immune thrombocytopenia (ITP) or warm autoimmune hemolytic anemia (AIHA). Neutropenia is present occasionally. Diagnosis is based on exclusion with a median age of 52 years of age. Here we have a case of a young patient with ES presenting with recurrent infection. ES should be included in differential diagnoses for patients presenting with AIHA, ITP, cytopenias or recurrent infection as the prognosis is more favorable when diagnosis is made early and symptoms are still mild.

Indexed as

Autoimmune cytopeniaAutoimmune hemolytic anemiaCoombs testImmune thrombocytopeniaImmunoglobulinsNeutropeniaThrombocytopenia

Identifiers

PMID38993737
PMCPMC11236364

What OpenQuestion holds

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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.