Atypical Hemolytic Uremic Syndrome, Microangiopathic Hemolytic Anemia, Microparticles, Thrombotic Thrombocytopenic Purpura
Conditions
Brief summary
The investigators propose to characterize MPs in aHUS and TTP both at the onset and throughout treatment. The investigators believe that the number, size, and cell origin of MPs will differ between these two diseases. The hypothesis is that endothelial derived MPs will be higher in number and comprise a larger portion of the MP population in aHUS and that platelet MPs will comprise a larger number and greater proportion of MPs in TTP. The investigators believe that MP identity and number can be used to reliably differentiate between aHUS and TTP at disease onset.
Interventions
None listed
Sponsors
Study design
Eligibility
Inclusion criteria
* Patients with MAHA, TTP, and/or aHUS
Exclusion criteria
* Prisoners
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Microparticle/Nanoparticle number (an absolute number) | an average of 3 months |
| Microparticle/Nanoparticle size (in nanometers or micrometers) | an average of 3 months |
| Microparticle/Nanoparticle identity (identity of cell type from which they are derived) | an average of 3 months |
Secondary
| Measure | Time frame |
|---|---|
| Morbidities | 3 months |
| Mortality | 3 months |
Countries
United States