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International Journal of Epidemiology 2001;30:1303-1308
© International Epidemiological Association 2001


Perinatal epidemiology

Effect of prenatal treatment on mother to child transmission of Toxoplasma gondii: retrospective cohort study of 554 mother-child pairs in Lyon, France

RE Gilberta, L Grasa, M Wallonb, F Peyronb, AE Adesa and DT Dunna,c

a Centre for Paediatric Epidemiology and Biostatistics, Institute of Child Health, London, UK.
b Laboratoire de Parasitologie et de Pathologie Exotique, Hôpital de la Croix Rousse, Lyon, France.
c Medical Research Council Clinical Trials Unit, London, UK.

Dr Ruth Gilbert, Centre for Paediatric Epidemiology and Biostatistics, Institute of Child Health, 30 Guilford Street, London WC1N 1EH, UK.

Abstract

Background The aim of prenatal serological screening for toxoplasmosis is to identify and treat maternal infection as soon as possible in order to prevent transmission of the parasite to the fetus. However, despite widespread provision of prenatal toxoplasma screening across Europe, the effectiveness of prenatal treatment is uncertain. The study aimed to determine the effect of the timing and type of prenatal treatment on mother to child transmission of Toxoplasma gondii.

Method A cohort of 554 infected pregnant women were identified in Lyon, France between 1987 and 1995 and their children were followed to determine congenital infection status. We determined the effect of prenatal treatment on transmission by examining the effect of the delay between maternal seroconversion and start of treatment. We also compared the effect of the type of treatment and no treatment on the risk of mother to child transmission. Analyses were adjusted for gestation at maternal seroconversion.

Results Compared to treatment within 4 weeks from seroconversion, the adjusted odds ratios (OR) for mother to child transmission after a treatment delay of 4–7 weeks was 1.29 (95% CI : 0.61, 2.73) and after more than 8 weeks, 1.44 (95% CI : 0.60, 3.31). The adjusted OR associated with spiramycin alone compared with pyrimethamine-sulfadiazine treatment was 0.91 (95% CI : 0.45, 1.84) and the OR for no treatment compared with pyrimethamine-sulfadiazine treatment was 1.06 (95% CI : 0.37, 3.03).

Conclusions The authors hypothesize that the absence of an effect of prenatal treatment is due to transmission before the start of treatment.

Keywords Congenital toxoplasmosis, treatment, vertical transmission

Accepted 24 May 2001


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This article has been cited by other articles:


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Int J EpidemiolHome page
L Gras, R. Gilbert, A. Ades, and D. Dunn
Effect of prenatal treatment on the risk of intracranial and ocular lesions in children with congenital toxoplasmosis
Int. J. Epidemiol., December 1, 2001; 30(6): 1309 - 1313.
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Home page
Int J EpidemiolHome page
A. Eskild and P. Magnus
Commentary: Little evidence of effective prenatal treatment against congenital toxoplasmosis--the implications for testing in pregnancy
Int. J. Epidemiol., December 1, 2001; 30(6): 1314 - 1315.
[Full Text] [PDF]


Home page
Int J EpidemiolHome page
P Thulliez
Commentary: Efficacy of prenatal treatment for toxoplasmosis: a possibility that cannot be ruled out
Int. J. Epidemiol., December 1, 2001; 30(6): 1315 - 1316.
[Full Text] [PDF]



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