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. 2013;8(2):e56183.
doi: 10.1371/journal.pone.0056183. Epub 2013 Feb 25.

Intermittent preventive treatment in pregnant women is associated with increased risk of severe malaria in their offspring

Whitney E Harrington  1 , Robert Morrison, Michal Fried, Patrick E Duffy
Affiliations

Intermittent preventive treatment in pregnant women is associated with increased risk of severe malaria in their offspring

Whitney E Harrington et al. PLoS One. 2013.

Abstract

Background: In areas of widespread sulfadoxine-pyrimethamine resistance, intermittent treatment in pregnancy (IPTp) fails to prevent placental malaria (PM) and may exacerbate drug resistant infections. Because PM predicts increased susceptibility to parasitemia during infancy, we hypothesized that IPTp would also increase susceptibility to malaria infection and disease in the offspring.

Methods: In a birth cohort from NE Tanzania, we evaluated the association between maternal IPTp use and risk of parasitemia and severe malaria in the offspring. Using Cox Proportional Hazards Models as well as Generalized Estimating Equations, we evaluated the effects of IPTp on the entire cohort and on subgroups stratified by PM status at delivery.

Results and conclusions: Offspring of PM+ women who received IPTp had a dose-dependent decrease in time to first parasitemia (AHR = 2.13, p = 0.04 [95%CI: 1.04, 4.38]). Among all offspring, IPTp was associated with earlier first severe malaria episode (AHR = 2.32, p = 0.02 [95%CI: 1.12, 4.78]) as well as increased overall odds of severe malaria (AOR = 2.31, p = 0.03 [95%CI: 1.09, 4.88]). Cost-benefit analyses of IPTp regimens should consider the long term effects on offspring in addition to pregnancy outcomes.

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Conflict of interest statement

Competing Interests: The authors have declared that no competing interests exist.

Figures

Figure 1
Figure 1. IPTp is associated with earlier first parasitemia among offspring of PM+ women.
Kaplan-Meier curves of time to first parasitemia by maternal IPTp status (A) or dose (B). 1 dose: AHR = 3.71, p = 0.04 [95% CI: 1.07, 12.78]; 2(+) doses: AHR = 10.89, p = 0.003 [95%CI: 2.25, 52.78].
Figure 2
Figure 2. IPTp is associated with earlier first severe malaria episode.
Kaplan-Meier curves of time to first severe malaria episode by maternal IPTp status (A) or dose (B). 1 dose: AHR = 1.17, p = 0.8 [95% CI: 0.45, 3.07]; 2(+) doses: AHR = 2.76, p = 0.03 [95% CI: 1.11, 6.85].
Figure 3
Figure 3. IPTp is associated with increased overall odds of severe malaria.
Severe malaria as a fraction of positive bloodsmears by age of the child and maternal IPTp status (A) or dose (B), bandwidth one week. 1 dose: AOR = 1.43, p = 0.4 [95%CI: 0.62, 3.30]; 2(+) doses: AOR = 2.81, p = 0.008 [95%CI: 1.31, 6.01].
See this image and copyright information in PMC

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