When should TORCH (Toxoplasmosis, Other, Rubella, Cytomegalovirus, Herpes) infections be tested for in pregnant women?

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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:
    • Ultrasound findings suggest congenital infection 2
    • Maternal symptoms suggest primary infection 1
    • HIV-infected women with CD4+ counts <100/mm³ (high risk for CMV disease reactivation) 4
    • Maternal clinical signs: thrombocytopenia or elevated liver enzymes 3

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.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Toxoplasmosis in pregnancy: prevention, screening, and treatment.

Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC, 2013

Research

TORCH testing in HIV-infected women.

Clinical obstetrics and gynecology, 1999

Guideline

Interpretation and Management of TORCH Infections

Praxis Medical Insights: Practical Summaries of Clinical Guidelines, 2025

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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