Macitentan Administration for Pulmonary Hypertension Due to β-thalassemia with Multiple Organ Failure
Kento Takagi,
Hajime Kasai,
Hiroyuki Tani
et al.
Abstract:A 51-year-old Thai woman diagnosed with β-thalassemia underwent regular blood transfusion and ironchelating therapy. However, after voluntarily discontinuing treatment, the patient developed progressive dyspnea and was diagnosed with pulmonary hypertension following right heart catheterization. Despite resuming blood transfusions, her condition did not improve. Because the patient had a history of multiple organ failure, curative treatment for β-thalassemia was not feasible, and macitentan was administered. De… Show more
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