Evidence map›Paper›PMID 41567200›Full record

Observational studyFrontiers in immunology2025

From hypereosinophilia to hypereosinophilic syndrome: real-world application of a two-tailed approach for HES diagnosis.

Stefania Nicola, Richard Borrelli, Irene Ridolfi, Luca Lo Sardo, Simone Negrini, Monica Fornero, Nicolò Rashidy, Federica Corradi, Iuliana Badiu, Eleonora Cerutti and 4 more

Abstract readObservational Study
In one paragraph

Observational study in Frontiers in immunology, 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

14 authors.

Stefania Nicola *Struttura Complessa a Direzione Universitaria (SCDU) Immunologia e Allergologia, Azienda Ospedaliera (AO) Ordine Mauriziano di Torino - C.so Re Umberto, Torino, Italy.
Richard Borrelli *Struttura Complessa a Direzione Universitaria (SCDU) Immunologia e Allergologia, Azienda Ospedaliera (AO) Ordine Mauriziano di Torino - C.so Re Umberto, Torino, Italy.
Irene RidolfiStruttura Complessa a Direzione Universitaria (SCDU) Immunologia e Allergologia, Azienda Ospedaliera (AO) Ordine Mauriziano di Torino - C.so Re Umberto, Torino, Italy.
Luca Lo SardoStruttura Complessa a Direzione Universitaria (SCDU) Immunologia e Allergologia, Azienda Ospedaliera (AO) Ordine Mauriziano di Torino - C.so Re Umberto, Torino, Italy.
Simone NegriniStruttura Complessa a Direzione Universitaria (SCDU) Immunologia e Allergologia, Azienda Ospedaliera (AO) Ordine Mauriziano di Torino - C.so Re Umberto, Torino, Italy.
Monica ForneroDipartimento di Scienze Mediche - Università degli Studi di Torino - C.so Dogliotti, Torino, Italy.
Nicolò RashidyStruttura Complessa a Direzione Universitaria (SCDU) Immunologia e Allergologia, Azienda Ospedaliera (AO) Ordine Mauriziano di Torino - C.so Re Umberto, Torino, Italy.
Federica CorradiStruttura Complessa a Direzione Universitaria (SCDU) Immunologia e Allergologia, Azienda Ospedaliera (AO) Ordine Mauriziano di Torino - C.so Re Umberto, Torino, Italy.
Iuliana BadiuStruttura Complessa a Direzione Universitaria (SCDU) Immunologia e Allergologia, Azienda Ospedaliera (AO) Ordine Mauriziano di Torino - C.so Re Umberto, Torino, Italy.
Eleonora CeruttiStruttura Complessa (SC) Farmacia Ospedaliera - Azienda Ospedaliera (AO) Ordine Mauriziano di Torino - C.so Re Umberto, Torino, Italy.
Giulia CostanzoMedical Science and Public Health, University of Cagliari - Via Università, Cagliari, Italy.
Stefano Del GiaccoMedical Science and Public Health, University of Cagliari - Via Università, Cagliari, Italy.
Giovanni Rolla *Dipartimento di Scienze Mediche - Università degli Studi di Torino - C.so Dogliotti, Torino, Italy.
Luisa Brussino *Struttura Complessa a Direzione Universitaria (SCDU) Immunologia e Allergologia, Azienda Ospedaliera (AO) Ordine Mauriziano di Torino - C.so Re Umberto, Torino, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Hypereosinophilic Syndrome (HES) is a rare disorder with a heterogeneous clinical presentation. If not recognized, it can lead to diagnostic delay and worse prognosis. Our study aimed to describe the real-world scenario of patients presenting with hypereosinophilia (HE), diagnosed with HES in an Italian Immunology Excellence University Centre. In addition, we also assessed the feasibility of a two-tailed approach for HES diagnosis, which consists of proceeding from the beginning with the differential diagnosis and systematic evaluation of organ damage. Methods: A retrospective observational single-center study was conducted. All patients underwent blood and instrumental tests to simultaneously identify HES etiology and any organ damage, through a process we called the "two-tailed approach". Results: Two hundred forty-seven patients with HE referred to our center underwent the two-tailed approach. Due to either the presence of a straightforward underlying disease associated with HE, or the lack of sustained hypereosinophilia, 168 patients (68.0%) were excluded from the study. Seventy-nine patients (31 females, 39.2%) with a mean age of 54.9 years were finally diagnosed with HES. 19 (24.1%) patients were diagnosed with reactive HES, 15 (19.0%) with overlap HES, 1 (1.3%) with myeloid-HES, 10 (12.7%) with lymphocytic HES, and 8 (10.1%) with idiopathic HES. Sixty-three patients showed involvement of at least two organs: the lung (32/63, 50.7%), the skin (24/63, 38.1%), the bowel (23/63, 36.5%), and the peripheral nervous system (25.4%). Eight patients (8/63, 12.7%) showed heart involvement. The diagnosis was achieved in 4 ± 1.8 months, and no deaths were observed. Conclusion: HE is a common reason for consultations with allergists and clinical immunologists, and the two-tailed approach, which tests simultaneously for diagnosis and organ damage, should be implemented from the initial evaluation of patients with HE. The lower rate of idiopathic HES diagnosis and the higher frequency of heart involvement we found confirm the usefulness of the tool in reducing the risk of mistakes in classifying HES subtypes and the diagnostic delay, thus allowing prompt and tailored treatment and better outcomes.

Indexed as

Hypereosinophilic SyndromeAdultAgedDiagnosis, DifferentialFemaleHumansMaleMiddle AgedRetrospective StudiesEGIDEGPAheart involvementhypereosinophiliahypereosinophilic syndrome (HES)mepolizumabsingle-center reporttwo-tailed approach

Identifiers

PMID41567200
PMCPMC12815814

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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.