Diagnostic and risk criteria for HSCT-associated thrombotic microangiopathy: a study in children and young adults

Author:

Jodele Sonata1,Davies Stella M.1,Lane Adam1,Khoury Jane2,Dandoy Christopher1,Goebel Jens3,Myers Kasiani1,Grimley Michael1,Bleesing Jack1,El-Bietar Javier1,Wallace Gregory1,Chima Ranjit S.4,Paff Zachary4,Laskin Benjamin L.5

Affiliation:

1. Division of Bone Marrow Transplantation and Immune Deficiency,

2. Division of Biostatistics and Epidemiology,

3. Division of Nephrology and Hypertension, and

4. Division of Critical Care Medicine, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH; and

5. Division of Nephrology, The Children’s Hospital of Philadelphia, Philadelphia, PA

Abstract

Key Points Proteinuria and elevated markers of complement activation at TMA diagnosis are associated with poor outcome. Clinical interventions should be considered in HSCT patients with these high-risk features at the time TMA is diagnosed.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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