Patients who decline to undergo amniocentesis may opt to take pyrimethamine-sulfadiazine plus folinic acid from diagnosis of maternal toxoplasmosis infection ≥14 weeks until delivery since fetal infection cannot be excluded and treatment may improve outcome. If the patient does not want prolonged treatment, we suggest treatment for at least 8 weeks and until results from a fetal ultrasound after 22 weeks are available and negative for anomalies, with the understanding that the risk is not eliminated because a normal ultrasound does not exclude the possibility of congenital toxoplasmosis.
PCR: polymerase chain reaction; T. gondii: Toxoplasma gondii. * Routine screening is not performed in all countries. Where screening is performed, frequency of screening during pregnancy varies among protocols. A discussion of serologic diagnosis can be found in the UpToDate content on diagnostic testing for toxoplasmosis infection. ¶ Patients who begin spiramycin before 14 weeks can continue this drug until PCR results from the amniocentesis at 18 weeks are available to guide further treatment decisions; alternatively, they may switch to pyrimethamine-sulfadiazine at 14 weeks and continue pyrimethamine-sulfadiazine until PCR results from the amniocentesis at 18 weeks are available. Refer to UpToDate content on toxoplasmosis in pregnancy for a detailed discussion. Δ When possible, amniocentesis at ≥18 weeks is timed to be at least 2 weeks after documentation of seroconversion (or 4 weeks after the estimated date of maternal primary infection) to improve diagnostic performance. ◊ Counsel the patient on the likelihood of congenital defects. Most cases are not severe enough to warrant pregnancy termination; however, patients consider multiple personal factors in making this decision. § The appearance of fetal lesions suggestive of infection on ultrasound following a negative PCR is rare. Nevertheless, because of the rare residual risk of congenital toxoplasmosis after a primary infection despite a negative amniocentesis, ultrasound follow-up is suggested every 4 to 6 weeks.
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