Evidence map›Paper›PMID 40301132›Full record

ArticleEuropean journal of pediatrics2025

Glanzmann thrombasthenia: a multi-center study of demographics, clinical spectrum, and treatment efficacy.

Laila M Sherief, Magdy El Ekiaby, Mahmoud El-Hawy, Eslam Elhawary, Amira A Nazim, Samar M Elbahy

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in European journal of pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

6 authors.

Laila M SheriefPediatric Department, Faculty of Medicine, Zagazig University, Zagazig, Egypt.ORCID http://orcid.org/0000-0003-2088-4213
Magdy El EkiabyShabrawishi Hospital Blood Transfusion and Hemophilia Treatment Center, Giza, Egypt.ORCID http://orcid.org/0000-0002-3881-1605
Mahmoud El-HawyPediatric Department, Faculty of Medicine, Menoufia University, Menoufia, Egypt.ORCID http://orcid.org/0000-0002-3420-922X
Eslam ElhawaryPediatric Department, Faculty of Medicine, Tanta University, Tanta, Egypt.ORCID http://orcid.org/0000-0002-4460-1567
Amira A NazimPediatric Department, Mansoura Health Insurance Hospital, Mansoura, Egypt.
Samar M ElbahyPediatric Department, Faculty of Medicine, Benha University, Benha, Egypt. samar.elbahy@fmed.bu.edu.eg.ORCID http://orcid.org/0000-0001-8465-3794

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glanzmann thrombasthenia (GT) is a rare inherited bleeding disorder caused by quantitative or qualitative defects of platelet integrin GPIIb/IIIa (CD41 and CD61). This study intended to describe the demographics, clinical features, and treatment response of GT patients in several hematology centers in Egypt. A cross-sectional multi-center study involved 87 children (<18 years old) diagnosed with GT. Clinical data were recorded as bleeding manifestations, response to treatment modalities, and laboratory results. The study included eighty-seven children (61 females and 26 males) with a median age of 8 years. Sixty-one children (55.2%) were born to parents who were consanguineous. The median age at presentation was 3 years (birth-14 years). The most frequent initial presenting symptom was epistaxis (39.1%), followed by cutaneous bleeding (29.9%), gastrointestinal bleeding (23%), heavy menstrual bleeding (19.5%), bleeding per gum (10.3%), and post-circumcision bleeding (5.7%), while one patient initially presented with intracranial hemorrhage (1.1%). These also constituted common bleeding sites. Eighty children (92%) received treatment. Platelet transfusions were given to 65 patients, with a response rate of 73.8%, and recombinant factor VII concentrates were given to 71 patients, with a response rate of 90.1%. Type I GT represented most of our patients (79.3%), followed by type III (11.5%) and type II (9.2%). No significant correlation was found between CD41/CD61 expression and other parameters as the patient's age, bleeding frequency, and treatment response. There was no evident difference between the three forms of GT regarding clinical characteristics such as bleeding severity or response to treatment. What is known: • Glanzmann thrombasthenia is the most common inherited platelet function abnormality. • Treatment is based on general supportive measures, platelet transfusion and recombinant factor VIIa. What is new: • Glanzmann thrombasthenia is an underestimated disorder, with a significant delay in diagnosis. • Although it has three types, there is no significant variation in bleeding phenotype between them.

Indexed as

Platelet TransfusionThrombastheniaAdolescentChildChild, PreschoolCross-Sectional StudiesEgyptFactor VIIaFemaleHemorrhageHumansInfantInfant, NewbornMaleRecombinant ProteinsTreatment OutcomeFactor VIIarecombinant FVIIaRecombinant ProteinsBleedingGlanzmann thrombastheniaPlateletsRecombinant factor VII

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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.