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FDA Approves First Treatment for Congenital Thrombotic Thrombocytopenic Purpura

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The genetically engineered protein product is safe, effective for the rare inherited blood clotting disorder

Tolerable Treatments Lacking for Higher-Risk Myelodysplastic Syndromes

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61 percent of 200 patients with higher-risk MDS were subsequently hospitalized within six months of diagnosis

Efgartigimod Efficacious, Safe for Primary Immune Thrombocytopenia

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More patients receiving efgartigimod reached primary end point of sustained platelet count response

Risk for Intracerebral Hemorrhage May Be Transmissible Via Blood Transfusion

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Risk was increased for those receiving transfusion from donors who later developed multiple spontaneous intracerebral hemorrhages

Red Cross Appeals for Donors During National Blood Shortage

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Back-to-back climate-related disasters have hampered blood collection efforts, and a summer shortfall has made the shortage worse

Concizumab May Be Effective Prophylaxis for Hemophilia A or B With Inhibitors

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Overall median annualized bleeding rate was 0 with concizumab

Prognostic Factors ID’d for Stage IIIb AL Amyloidosis

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Symptom onset to diagnosis longer than six months, bone marrow plasmacytosis ≥10 percent associated with shorter overall survival

Misdiagnosis Common for Suspected Myelodysplastic Neoplasms

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About one-third of cases were reclassified following central review; receipt of inappropriate meds reported in 7 percent of misdiagnosed cases

International Prognostic Scoring System-Molecular Changes Clinical Management

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For nearly half of patients with myelodysplastic syndromes, results could change clinical care

Tranexamic Acid Does Not Up Functional Outcome After Major Trauma

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No improvement seen in favorable functional outcome at six months, but reduced risk of death at 28 days after injury