Evidence map›Paper›PMID 41233813›Full record

ReviewOrphanet journal of rare diseases2025

Common features of rare disease patients in the emergency department: a systematised literature review.

Sandra Pflock, Hannah Carolina Mücke, Rajan Somasundaram, Eva Diehl-Wiesenecker

Abstract readReview
In one paragraph

Review in Orphanet journal of rare diseases, 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

4 authors.

Sandra PflockDepartment of Emergency Medicine, Campus Benjamin Franklin, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Hindenburgdamm 30, 12203, Berlin, Germany. sandra.pflock@charite.de.ORCID 0009-0004-2949-2210
Hannah Carolina MückeDepartment of Emergency Medicine, Campus Benjamin Franklin, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Hindenburgdamm 30, 12203, Berlin, Germany.
Rajan SomasundaramDepartment of Emergency Medicine, Campus Benjamin Franklin, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Hindenburgdamm 30, 12203, Berlin, Germany.
Eva Diehl-WieseneckerDepartment of Emergency Medicine, Campus Benjamin Franklin, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Hindenburgdamm 30, 12203, Berlin, Germany.ORCID 0000-0002-4058-9337

Funding

Projekt DEAL
6 · The paper itself

Abstract

backgroundPatients with rare diseases (RD) may present to the emergency department (ED) with an acute manifestation of an undiagnosed RD. If not identified, some of these patients may suffer from increased morbidity, mortality and worse outcomes compared to patients with more common diseases. Unfortunately, patients with RD often present with common symptoms, e.g. abdominal pain, making it even more difficult for ED physicians to identify those patients. Thus, strategies are needed to determine when certain RD should be suspected in the ED. We aimed to identify common features of RD through a systematised literature review of a predefined set of RD.

methodsEmbase and MEDLINE were searched for eligible studies published in all years up to November 2023. Studies reporting clinical characteristics of patients who presented to the ED with one out of a predefined set of eight RD were included: acute hepatic porphyria, Fabry disease, familial Mediterranean fever, hereditary angioedema, hereditary hemorrhagic telangiectasia, myasthenia gravis, paroxysmal nocturnal hemoglobinuria and thrombotic thrombocytopenic purpura. Clinical characteristics, symptoms and family history were extracted to explore potential common features. Database searches, title, abstract and full-text screening and data extraction were conducted by a single reviewer.

resultsOf the 4 732 articles identified, 18 were included in the review. For two RD no articles and for three RD only one article could be included. All but two prospective studies were retrospective chart reviews or case series reporting on small patient cohorts (n = 3 - 75 patients). The common features of patients were: age under 65 years, recurrent symptoms affecting multiple organ systems, normal or nonspecific findings in routine laboratory tests and imaging, presence of trigger factors and a positive family history of similar symptoms or RD.

conclusionThis review highlights the limited knowledge about RD in the ED setting. Some common features of RD patients were identified that could aid future research in developing risk stratification algorithms to facilitate early detection and treatment of RD in the ED. To our knowledge, this is the first literature review to explore the common features of patients with RD in the ED.

Indexed as

Emergency Service, HospitalRare DiseasesEmergency Room VisitsHumansAcute hepatic porphyriaCommon featuresEmergency departmentEmergency physicianInborn errors of metabolismRare diseases

Identifiers

PMID41233813
PMCPMC12616910

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.