Thrombotic microangiopathy (TMA) encompasses several overlapping clinical syndromes with different etiologies, based on a common pathologic lesion; TMA symptoms include but are not limited to consumptive thrombocytopenia with purpuric capillary bleeding, microangiopathic hemolytic anemia (MAHA), and microvascular thrombosis.
Hematopoietic stem cell transplant associated (TA)-TMA has an exceedingly high mortality rate with limited therapeutic options. In a new study published in TRANSFUSION, Fujiwara and colleagues retrospectively evaluated 254 hematopoietic stem cell transplant patients for development of TA-TMA and subsequently treatment and clinical course. Among the 16 patients with TA-TMA, 9 were initially treated with recombinant thrombomodulin and 7 were treated with standard first-line treatment. While 7 of 9 patients (77.8%) treated with recombinant thrombomodulin recovered from TA-TMA without complications, 0 of the 7 patients (0%) with standard treatment recovered. Further research is needed, but recombinant thrombomodulin may provide assistance in treatment of TA-TMA.
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