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  2. Jul 17, 2023 · Explain the treatment and management options available for aplastic anemia. Summarize interprofessional team strategies for enhancing care coordination and communication to advance treatment of aplastic anemia and improve outcomes.

  3. To diagnose AA, there must be at least two of the following, haemoglobin concentration (Hb) <100 g/L, platelet count <50 × 109/L and neutrophil count <1.5 × 109/L. Reticulocyte count is useful in delineating the severity of AA. The majority (70%–80%) of cases are idiopathic.

  4. Oct 1, 2021 · This topic reviews the treatment and prognosis of AA in adults. For adults, the evaluation of pancytopenia; pathogenesis, clinical manifestations, and diagnosis of AA; and hematopoietic cell transplantation for AA are discussed separately. (See "Approach to the adult with pancytopenia" and "Aplastic anemia: Pathogenesis, clinical manifestations ...

  5. Jun 6, 2021 · Establishing a diagnosis of aplastic anemia (AA) can be challenging, but it is absolutely critical to appropriate management, especially differentiating between acquired and inherited forms of the disease.

    • Amy E. DeZern, Jane E. Churpek
    • 10.1182/bloodadvances.2021004345
    • 2021
    • Blood Adv. 2021 Jun 22; 5(12): 2660-2671.
  6. Mar 16, 2017 · Treatment strategy in patients with acquired aplastic anemia. Patients are stratified according to whether or not they have an HLA-identical sibling. In young patients (<40 years) with a matched donor, allogeneic BMT is first-line therapy.

    • Andrea Bacigalupo
    • 2017
  7. The standard first-line treatment for newly diagnosed acquired severe/very severe AA patients is horse anti-thymocyte globulin and ciclosporin-based immunosuppressive therapy (IST) with eltrombopag or allogeneic haemopoietic stem cell transplant (HSCT) from a matched sibling donor.

  8. Nov 11, 2017 · Approach to diagnosis and treatment of acquired aplastic anemia. Initial screening evaluation of a patient with aplastic anemia is required to document pancytopenia with a hypocellular marrow, followed by testing to exclude alternative diagnoses.

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