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Ticlopidine-associated aplastic anemia. A case report and review of literature
1Department of Internal Medicine, Veterans General Hospital-Kaoshiung, Taiwan, R.O.C.
Abstract:
Serious hematologic complications associated with ticlopidine have been reported, including aplastic anemia. We report here an additional case of fatal aplastic anemia due to ticlopidine. A 66-year-old male patient developed fever and pancytopenia 2 months after ticlopidine was started. Despite the administration of granulocyte colony-stimulating factor (G-CSF) and broad-spectrum antibiotics, as well as aggressive red cell and platelet transfusions, the patient died 16 days after admission due to septic shock. Eighteen other cases of ticlopidine-induced aplastic anemia published in the English literature are also reviewed and presented here. Eight of the total 19 patients (including the one reported here) have died, mostly due to infection. Of the seven who received supportive treatment only, four had spontaneous recovery. Nine cases were treated with G-CSF or granulocyte-macrophage colony-stimulating factor (GM-CSF), and response was observed in only four of them. Several other cases were treated with high-dose corticosteroids or androgens; however, it was not possible to evaluate the efficacy of these treatments because of the limited number of cases. In the absence of satisfactory treatment for ticlopidine-induced aplastic anemia at present, it may be reasonable to try antilymphocyte globulin or cyclosporine. Also, great efforts should be made in the prevention and management of infection accompanying this disease.
Insights
Ticlopidine can cause fatal aplastic anemia, a serious blood disorder. Early recognition and infection management are crucial for patients experiencing this rare but severe adverse drug reaction.
Area of Science:
- Hematology
- Pharmacology
- Toxicology
Background:
- Ticlopidine is an antiplatelet medication with known serious hematologic side effects.
- Aplastic anemia is a rare but life-threatening condition where the bone marrow fails to produce sufficient blood cells.
Observation:
- A case of fatal aplastic anemia in a 66-year-old male following ticlopidine use is presented.
- Review of 18 additional cases reveals a high mortality rate, primarily due to infection.
Findings:
- Supportive care alone resulted in spontaneous recovery in 4 of 7 patients.
- Growth factors like G-CSF or GM-CSF showed limited efficacy, with response in only 4 of 9 treated cases.
- The efficacy of corticosteroids or androgens remains unevaluated due to small sample sizes.
Implications:
- Current treatments for ticlopidine-induced aplastic anemia are unsatisfactory.
- Antilymphocyte globulin or cyclosporine may be potential therapeutic options.
- Vigilant prevention and management of infections are critical for patient survival.