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Prenatal therapy with pyrimethamine + sulfadiazine vs spiramycin to reduce placental transmission of toxoplasmosis: a multicenter, randomized trial.
- Source :
-
American journal of obstetrics and gynecology [Am J Obstet Gynecol] 2018 Oct; Vol. 219 (4), pp. 386.e1-386.e9. Date of Electronic Publication: 2018 Jun 02. - Publication Year :
- 2018
-
Abstract
- Background: The efficacy of prophylaxis to prevent prenatal toxoplasmosis transmission is controversial, without any previous randomized clinical trial. In France, spiramycin is usually prescribed for maternal seroconversions. A more potent pyrimethamine + sulfadiazine regimen is used to treat congenital toxoplasmosis and is offered in some countries as prophylaxis.<br />Objective: We sought to compare the efficacy and tolerance of pyrimethamine + sulfadiazine vs spiramycin to reduce placental transmission.<br />Study Design: This was a randomized, open-label trial in 36 French centers, comparing pyrimethamine (50 mg qd) + sulfadiazine (1 g tid) with folinic acid vs spiramycin (1 g tid) following toxoplasmosis seroconversion.<br />Results: In all, 143 women were randomized from November 2010 through January 2014. An amniocentesis was later performed in 131 cases, with a positive Toxoplasma gondii polymerase chain reaction in 7/67 (10.4%) in the pyrimethamine + sulfadiazine group vs 13/64 (20.3%) in the spiramycin group. Cerebral ultrasound anomalies appeared in 0/73 fetuses in the pyrimethamine + sulfadiazine group, vs 6/70 in the spiramycin group (P = .01). Two of these pregnancies were terminated. Transmission rates, excluding 18 children with undefined status, were 12/65 in the pyrimethamine + sulfadiazine group (18.5%), vs 18/60 in the spiramycin group (30%, P = .147), equivalent to an odds ratio of 0.53 (95% confidence interval, 0.23-1.22) and which after adjustment tended to be stronger (P = .03 for interaction) when treatment started within 3 weeks of seroconversion (95% confidence interval, 0.00-1.63). Two women had severe rashes, both with pyrimethamine + sulfadiazine.<br />Conclusion: There was a trend toward lower transmission with pyrimethamine + sulfadiazine, but it did not reach statistical significance, possibly for lack of statistical power because enrollment was discontinued. There were also no fetal cerebral toxoplasmosis lesions in the pyrimethamine + sulfadiazine group. These promising results encourage further research on chemoprophylaxis to prevent congenital toxoplasmosis.<br /> (Copyright © 2018. Published by Elsevier Inc.)
- Subjects :
- Adult
Antiprotozoal Agents administration & dosage
Drug Therapy, Combination
Female
France
Humans
Infectious Disease Transmission, Vertical prevention & control
Pregnancy
Prenatal Care
Pyrimethamine administration & dosage
Pyrimethamine therapeutic use
Sulfadiazine administration & dosage
Sulfadiazine therapeutic use
Toxoplasmosis transmission
Toxoplasmosis, Congenital prevention & control
Treatment Outcome
Antiprotozoal Agents therapeutic use
Pregnancy Complications, Infectious drug therapy
Toxoplasmosis drug therapy
Subjects
Details
- Language :
- English
- ISSN :
- 1097-6868
- Volume :
- 219
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- American journal of obstetrics and gynecology
- Publication Type :
- Academic Journal
- Accession number :
- 29870736
- Full Text :
- https://doi.org/10.1016/j.ajog.2018.05.031