TORCH Testing in Pregnant Women: Evidence-Based Recommendations
Primary Recommendation
Routine universal TORCH screening is not recommended for all pregnant women in the United States; instead, testing should be targeted based on specific clinical indications, risk factors, or concerning ultrasound findings. 1, 2
Standard Screening Approach by TORCH Component
Syphilis (The "O" in TORCH)
- All pregnant women must be screened with serologic testing at the first prenatal visit 1
- High-risk women require repeat testing in the third trimester (28 weeks) and again at delivery 1
- Universal delivery screening is mandated in many states; no infant should be discharged without maternal syphilis status documented at least once during pregnancy 1
- Any woman delivering a stillborn infant after 20 weeks must be tested 1
Hepatitis B (Part of "Other")
- All pregnant women must be screened for HBsAg at the first prenatal visit 1
- Repeat testing late in pregnancy for HBsAg-negative women at high risk (injection drug users, women with concurrent STDs) 1
HIV (Part of "Other")
- HIV testing should be offered to all pregnant women at the first prenatal visit 1
Toxoplasmosis
- Routine universal screening is NOT recommended for low-risk pregnant women 1, 2
- Targeted screening should be offered when:
- Ultrasound findings suggest TORCH infection (intracranial calcification, microcephaly, hydrocephalus, ascites, hepatosplenomegaly, severe IUGR) 2
- Maternal symptoms suggest acute infection 1
- Patient has known risk factors for T. gondii exposure 2
- Maternal clinical signs: thrombocytopenia (7.1% infection rate) or elevated liver enzymes (3.0% infection rate) 3
Rubella
- No routine prenatal screening is specified in current U.S. guidelines, though immunity status is typically assessed as part of standard prenatal care 1
Cytomegalovirus (CMV)
- Routine universal screening is NOT recommended 1
- Consider testing when:
Herpes Simplex Virus (HSV)
- Routine prenatal serologic screening is NOT recommended 1, 4
- Routine serial cultures are NOT indicated for women with history of recurrent genital herpes in the absence of third-trimester lesions 1
- Cultures at delivery may guide neonatal management for women with recurrent herpes history 1
Critical Testing Principles
When TORCH Testing is Indicated
Maternal-related indications (higher yield): 3
- Fever with thrombocytopenia (7.1% infection rate)
- Elevated liver enzymes (3.0% infection rate)
- Gastroenteritis with systemic symptoms
- Clinical suspicion of acute infection
Fetal-related indications (lower yield but important): 2, 3
- Intracranial calcification
- Microcephaly
- Hydrocephalus
- Ascites
- Hepatosplenomegaly
- Severe intrauterine growth restriction
- Polyhydramnios or oligohydramnios
Laboratory Confirmation Requirements
All positive results from commercial laboratories must be confirmed at reference laboratories before intervention, particularly for toxoplasmosis where approximately 60% of positive IgM results are false positives 1, 5
For suspected acute toxoplasmosis: 1, 2
- Send samples directly to toxoplasmosis reference laboratory to avoid delays
- Repeat testing within 2-3 weeks
- Consider starting spiramycin immediately without waiting for confirmatory results
- IgG avidity testing helps determine timing of infection
Special Populations
HIV-Infected Pregnant Women
- Test for T. gondii IgG antibodies at initial HIV diagnosis; if positive, obtain IgM to rule out acute infection 4
- Screen for CMV if CD4+ count <100/mm³ due to reactivation risk 4
- Syphilis screening at first visit with repeat testing in third trimester if at continued risk 4
- HSV serologic testing has no routine value 4
Immunocompromised Women
- Screening for toxoplasmosis is recommended due to reactivation risk and potential for toxoplasmosis encephalitis 2
Common Pitfalls to Avoid
- Screening only symptomatic or high-risk women for toxoplasmosis will miss up to 50% of infected pregnant women at risk of transmission 1
- Misinterpreting positive IgG alone as active infection rather than past exposure 5
- Failing to confirm positive results from non-reference laboratories, especially for toxoplasmosis IgM 1, 5
- Testing for toxoplasmosis via amniocentesis before 18 weeks gestation or less than 4 weeks after suspected maternal infection leads to false-negative results 2
- Ordering routine serial HSV cultures in asymptomatic women with recurrent herpes history 1
Clinical Context
The evidence demonstrates that maternal-indicated TORCH testing (based on clinical symptoms) has significantly higher yield than fetal-indicated testing (based on ultrasound findings alone), detecting 10.8% of neonates with confirmed TORCH infection versus lower rates with fetal indications 3. However, both approaches remain important as they identify different at-risk populations.