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Therapy of aplastic anemia with sequential antithymocyte globulin and cyclosporin

✍ Scribed by Gary C. Doolittle; David C. Bodensteiner; Barry S. Skikne; Mammo Amare


Publisher
John Wiley and Sons
Year
1991
Tongue
English
Weight
221 KB
Volume
36
Category
Article
ISSN
0361-8609

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✦ Synopsis


Five consecutive patients with severe aplastic anemia were treated with antithymocyte globulin followed by cyclosporin A. All received antithymocyte globulin initially, and because of lack of response within a 4 week period, cyclosporin was administered subsequently. Hematologic improvement occurred within four months of initiation of cyclosporin. Four patients no longer require blood product support, while one remains transfusion-dependent. In two patients, thrombocytopenia developed when the cyclosporin was tapered but re-institution of the drug resulted in a prompt improvement of counts. These observations indicate that the sequential use of antithymocyte globulin and cyclosporin may be an effective therapeutic approach in the treatment of severe aplastic anemia.


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The development of alloantibodies to platelets is a major problem in the supportive management of thrombocytopenia in patients with severe aplastic anemia. We report here a case of aplastic anemia refractory to platelet transfusion. An immunosuppressant, cyclosporin A, which was used for the therapy