Delayed Plasma Clot Lysis in Adult Patients with Primary Immune Thrombocytopenia (ITP)

Theresa Schramm,Jennifer Machacek,Michael Fillitz,Barbara Dixer,Peter Quehenberger,Dino Mehic,Cihan Ay,Ingrid Pabinger,Johanna Gebhat

Blood（2021）

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摘要

Introduction: Primary immune thrombocytopenia (ITP) is an orphan disease characterized by very low platelet counts. Patients have heterogeneous bleeding phenotypes, which are not only determined by platelet counts, also a paradoxically increased thrombotic risk has been observed.

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