Clinical and Parasitological Characteristics of Puerperal Malaria
1Medical Research Unit, Albert Schweitzer Hospital, Lambaréné, Gabon; 2Institute for Tropical Medicine, Department of Parasitology, University of Tübingen, Tübingen, Germany; 3Department of Internal Medicine I, Division of Infectious Diseases, Medical University of Vienna, Vienna, Austria
Background.
Women with semi‐immunity to malaria who live in regions where the disease is endemic are at increased risk for more frequent and severe episodes of malaria during pregnancy. Recent findings indicate that this increased risk might persist beyond delivery, but the underlying mechanisms for this change in risk are poorly understood.
Methods.One hundred fifty women were included in a cohort study in Lambaréné, Gabon, and were actively followed up weekly for 10 weeks after delivery, as were nonpregnant control women who had been matched to them by location and age. Parasites in samples of placenta and blood were genotyped by use of polymerase chain reaction amplification of the merozoite surface antigen 2 gene and the subtelomeric variable open reading frame gene of Plasmodium falciparum.
Results.Eleven puerperal women had cases of clinical malaria, compared with 1 control woman (rate ratio, 9.8; 
). Eighteen puerperal women had P. falciparum parasitemia, compared with 6 control women (rate ratio, 2.7; 
). Five of 16 puerperal women (31%) with parasitemia on follow‐up had identical parasites in their placentas and blood, and 11 of these cases (69%) were the result of reinfection. Puerperal women remained at equal risk for the development of parasitemia throughout the first 10 weeks after delivery. Use of bed nets, use of chloroquine prophylaxis during pregnancy, presence of malaria episodes during pregnancy, gravidity, and age were not associated with the acquisition of parasitemia during follow‐up.
Conclusions.Compared with nonpregnant women, puerperal women have a considerably increased risk for the development of malaria and/or parasitemia. This increased risk is caused both by the recurrence of P. falciparum parasitemia and by the increased susceptibility to new infections, although the latter plays a more significant role.
Received 29 July 2004; accepted 17 September 2004; electronically published 4 February 2005.
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