First-Line Treatment for Toxoplasmosis
The first-line treatment for toxoplasmosis is pyrimethamine combined with sulfadiazine, plus leucovorin (folinic acid) supplementation. 1, 2
Treatment Regimens Based on Patient Population
For Congenital Toxoplasmosis
- Pyrimethamine: Loading dose of 2 mg/kg/day for 2 days, then 1 mg/kg/day for 2-6 months, followed by 1 mg/kg three times weekly 1
- Sulfadiazine: 50 mg/kg twice daily 1
- Leucovorin (folinic acid): To minimize pyrimethamine-associated hematologic toxicity 1
- Duration: 12 months of treatment 1
For Acquired Toxoplasmosis in HIV-Infected Individuals
- Pyrimethamine: 2 mg/kg/day for 3 days, followed by 1 mg/kg/day 1
- Sulfadiazine: 25-50 mg/kg four times daily 1
- Leucovorin: 10-25 mg/day 1
- Duration: Acute therapy for 6 weeks, assuming clinical and radiological improvement 1
For Pregnant Women with Toxoplasmosis
Treatment approach varies based on gestational age and fetal infection status:
Before 16 weeks of pregnancy:
After 16 weeks or confirmed fetal infection:
- Switch to pyrimethamine/sulfadiazine plus folinic acid 1
Monitoring During Treatment
- Complete blood count: Weekly while on daily pyrimethamine and at least monthly while on less frequent dosing 1
- Monitor for adverse effects:
Alternative Regimens for Sulfa-Allergic Patients
- Clindamycin (5.0-7.5 mg/kg orally 4 times daily; maximum 600 mg/dose) with pyrimethamine and leucovorin 1
- Azithromycin (900-1,200 mg/day) with pyrimethamine and leucovorin has been used in adults but is less studied in children 1
Important Considerations and Precautions
- Leucovorin must always be administered with pyrimethamine to prevent bone marrow toxicity 1, 2
- Continue leucovorin for 1 week after pyrimethamine discontinuation due to the long half-life of pyrimethamine 1
- Pyrimethamine is contraindicated in the first trimester of pregnancy due to teratogenic effects 2
- Pyrimethamine should be used with caution in patients with seizure disorders, impaired renal or hepatic function 2
- Keep pyrimethamine out of reach of children as they are extremely susceptible to adverse effects from overdose 2
Treatment Efficacy
The German approach of using spiramycin until 16 weeks of pregnancy followed by at least 4 weeks of combination therapy with pyrimethamine, sulfadiazine, and folinic acid has shown very low rates of mother-to-child transmission (4.8%) compared to other European cohort studies (30%) 1, 3.
This treatment protocol prioritizes early intervention to reduce both transmission rates and severity of disease in infected infants, which directly impacts morbidity, mortality, and quality of life outcomes.