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Pregnancy in beta-thalassemia trait carriers: an uneventful journey
Constantinos Tsatalas1, Panagiota Chalkia, Despoina Pantelidou
1Department of Haematology, Democritus University of Thrace Medical School, Alexandroupolis, Greece. ktsatala@med.duth.gr
Abstract:
Normochromic normocytic anemia during pregnancy reflects the significant increase in plasma volume, which disproportionately exceeds the increase in the red cell volume. In beta-thalassemia (beta-thal) trait carriers who become pregnant the plasma volume expansion may cause more pronounced anemia because the anemia of pregnancy is added to the pre-existed hypochromic microcytic anemia. In beta-thal women, pregnancy outcome and obstetric complications do not differ from the general population. Anemia in beta-thal carriers is generally not severe enough to warrant anxiety. No specific therapy is indicated and pregnant women generally require only supportive care with an anticipated favorable pregnancy outcome.
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