The prevention of congenital toxoplasmosis using a combination of Spiramycin and Cotrimoxazole: The long-time experience of a tertiary referral centre

Trop Med Int Health. 2024 Aug;29(8):697-705. doi: 10.1111/tmi.14021. Epub 2024 Jun 6.

Abstract

Background: Toxoplasmosis is a parasitic infection caused by Toxoplasma gondii and is responsible for gestational and congenital infections worldwide. The current standard therapy is based on the administration of Spiramycin to prevent trans-placental transmission. Other therapies are being studied to reduce the rates of foetal transmission and symptomatic congenital infection.

Objectives: We report our long-standing experience in maternal toxoplasmosis infection treatment using a combination of Spiramycin-Cotrimoxazole, assessing its effectiveness in preventing vertical transmission compared to the expected incidence of congenital infection.

Methods: We retrospectively collected cases of pregnant women referred to our centre for suspected toxoplasmosis infection according to Lebech criteria, treated with Spiramycin-Cotrimoxazole.

Results: Of 1364 women referred to our centre, postnatal follow-up of primary toxoplasmosis was available in 562 cases (73.9%). The overall vertical transmission rate was 3.4% in women treated immediately with Spiramycin-Cotrimoxazole after the diagnosis of infection. In comparison, it was 7.7% in women undergoing the same therapy but late or with poor compliance. The foetal transmission rate was 71.4% in untreated cases. All the infected newborns of mother treated adequately with Spiramycin-Cotrimoxazole were asymptomatic afterbirth, while 6/21 infected infants of the inadequate Spiramycin-Cotrimoxazole therapy group had postnatal sequelae (28.5%). The incidence of transmission after appropriate Spiramycin-Cotrimoxazole therapy was significantly lower than the expected rate reported in literature.

Conclusions: A combination of Spiramycin and Cotrimoxazole is safe and effective in preventing foetal congenital toxoplasmosis and reducing sequelae in case of in-utero infection. The timing and adherence to the therapy are crucial to lowering the risk of congenital infection and neonatal morbidity.

Keywords: Cotrimoxazole; Spiramycin; pregnancy; toxoplasma; toxoplasmosis.

MeSH terms

  • Adult
  • Anti-Bacterial Agents / therapeutic use
  • Antiprotozoal Agents / therapeutic use
  • Drug Therapy, Combination
  • Female
  • Humans
  • Infant, Newborn
  • Infectious Disease Transmission, Vertical* / prevention & control
  • Pregnancy
  • Pregnancy Complications, Parasitic* / drug therapy
  • Pregnancy Complications, Parasitic* / epidemiology
  • Pregnancy Complications, Parasitic* / prevention & control
  • Retrospective Studies
  • Spiramycin* / therapeutic use
  • Tertiary Care Centers*
  • Toxoplasmosis / drug therapy
  • Toxoplasmosis / epidemiology
  • Toxoplasmosis / prevention & control
  • Toxoplasmosis / transmission
  • Toxoplasmosis, Congenital* / drug therapy
  • Toxoplasmosis, Congenital* / epidemiology
  • Toxoplasmosis, Congenital* / prevention & control
  • Trimethoprim, Sulfamethoxazole Drug Combination* / therapeutic use

Substances

  • Spiramycin
  • Trimethoprim, Sulfamethoxazole Drug Combination
  • Anti-Bacterial Agents
  • Antiprotozoal Agents