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Research into the development of shortness of breath after blood transfusion

Pathophysiology of respiratory transfusion complications: an international multicenter case control study - Pathophysiology of respiratory transfusion complications (Photon)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON58168
Enrollment
300
Registered
2025-05-06
Start date
2026-01-01
Completion date
Unknown
Last updated
2025-12-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Respiratory transfusion complications Shortness of breath due to blood transfusion

Interventions

All patients developing a respiratory transfusion complication collected by participating blood banks. Cases will be matched to patients not developing a respiratory transfusion reaction on age, admit

Sponsors

Amsterdam UMC
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All adult patients developing a transfusion complication as reported to hemovigilance agencies world-wide.  Patients matched on transfusion type, age, sex, and admittance diagnosis, not developing a respiratory transfusion complication.January 2015 – present. 

Exclusion criteria

Exclusion criteria: Local objection of patients to sharing data of materials for research purposes.

Design outcomes

Primary

MeasureTime frame
The incidence of different types of respiratory transfusion complications related to specific blood product types and clinical parameters (e.g., mortality, risk factors). As well as the occurrence of anti–human leukocyte antigen class I/II antibodies, anti–human neutrophil antigen antibodies or non-HLA antibodies in patient and recipient samples. In addition, the influence and biological effects of plasma, micro-particles, lipids and other storage products with regard to respiratory transfusion complications will be determined.

Secondary

MeasureTime frame
This study is a descriptive study for research purposes and only includes objective data collected as part of routine care including waste material. Only standard proceedings will be performed. This study does not result in any risk, interventions or burdens to patients and/or family. 

Countries

Australia, Belgium, Canada, Denmark, France, Germany, Netherlands, Turkey, United Kingdom, United States

Contacts

Public ContactA.L> Peters

Amsterdam UMC

a.l.peters@amsterdamumc.nl020-5669111

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)