# European Management of Glanzmann's Thrombasthenia: A Survey of Current Clinical Practice

**Authors:** Mathieu Fiore, Andrea Artoni, Robert Klamroth, Mary Mathias, Roger Schutgens, Roseline d'Oiron

PMC · DOI: 10.1111/hae.70114 · Haemophilia · 2025-09-11

## TL;DR

This paper surveys European practices for managing Glanzmann's thrombasthenia, a rare blood disorder, to identify areas for improving patient care and standardizing treatment.

## Contribution

The study provides the first comprehensive survey of clinical practices for Glanzmann's thrombasthenia across Europe, highlighting inconsistencies and areas needing standardization.

## Key findings

- Physicians showed consensus on peri-operative treatment and use of recombinant factor VIIa.
- Only 53% of respondents in most countries screen for anti-αIIbβ3 antibodies.
- Access to HLA-matched platelet concentrates is limited for 55% of respondents.

## Abstract

Glanzmann's thrombasthenia is a rare inherited platelet disorder characterized by a lack of platelet aggregation. Patients tend to be diagnosed in early childhood with treatment strategies involving a multifaceted approach to prevent and manage bleeding episodes. Unfortunately, there is currently no European consensus regarding the management of GT.

This initiative aimed to gain an understanding of current clinical management of GT across Europe, with the aim of aligning best practice and improving patient outcomes.

The authors, on behalf of the EAHAD Glanzmann Working Group, administered an online survey of 57 questions to European haematologists currently involved in the management of patients with GT. The survey covered topics related to diagnosis, treatment access and selection, immunization, peri‐operative management and use of second‐line therapies.

Responses reflected physician consensus around some topics, including peri‐operative treatment, use of recombinant factor VIIa, and concerns around antibody development. However, more varied responses were received on topics such as antibody screening (anti‐αIIbβ3 antibodies screening conducted by ≤53% of respondents in all countries of interest except France), access to HLA‐matched platelet concentrates (none or limited for 55% of respondents) and duration of platelet transfusions for major surgery (13%–31% for 1, 2, 3 and 4 or more days of transfusions).

Establishing comprehensive guidelines to manage GT will enhance patient outcomes by ensuring patients receive high‐quality and effective care as well as standardize care across different healthcare settings.

## Linked entities

- **Diseases:** Glanzmann's thrombasthenia (MONDO:0031332)

## Full-text entities

- **Diseases:** bleeding (MESH:D006470), GT (MESH:D013915), inherited platelet disorder (MESH:D001791)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12612366/full.md

## References

29 references — full list in the complete paper: https://tomesphere.com/paper/PMC12612366/full.md

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Source: https://tomesphere.com/paper/PMC12612366