Polymerase chain reaction (PCR) test for fetal toxoplasmosis


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Polymerase chain reaction (PCR) test for fetal toxoplasmosis


Polymerase chain reaction (PCR) is a method of duplicating DNA strands from a tiny sample of blood, hair, or tissue. PCR is used to identify infectious diseases, genetic conditions, and genetic links between people.

When a pregnant woman has toxoplasmosis, a PCR test on amniotic fluid is used to learn whether her fetus is also infected. PCR is preferred over a fetal blood test for antibodies because:1

  • Collecting amniotic fluid through amniocentesis is considered safer than fetal blood sampling.
  • PCR is better than antibody testing to detect toxoplasmosis.
  • PCR can be done earlier in a pregnancy than a blood test for antibodies. Because first- and second-trimester fetal infection carry the highest risk of birth defects and mental retardation, earlier test results are important to parents who are considering ending such a pregnancy.

In rare cases, PCR produces false-positive or false-negative test results. Follow-up testing and fetal ultrasound monitoring for hydrocephalus can help confirm PCR test results.

PCR is seldom used to diagnose toxoplasmosis in adults. Antibody testing of a blood sample is easier and more widely available.

References


Citations

  1. Jones J, et al. (2003). Congenital toxoplasmosis. American Family Physician, 76(10): 2131–2138.

Credits


Author Maria G. Essig, MS, ELS
Editor Susan Van Houten, RN, BSN, MBA
Associate Editor Pat Truman, MATC
Primary Medical Reviewer Adam Husney, MD - Family Medicine
Primary Medical Reviewer Joy Melnikow, MD, MPH - Family Medicine
Specialist Medical Reviewer Gregory A L Davies, MD, FRCSC, FACOG - Maternal-Fetal Medicine
Last Updated June 27, 2007

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Last updated: June 27, 2007
Author: Maria G. Essig, MS, ELS
Reviewed By: Joy Melnikow, MD, MPH - Family Medicine, Gregory A L Davies, MD, FRCSC, FACOG - Maternal-Fetal Medicine
Editors: Susan Van Houten, RN, BSN, MBA, Pat Truman, MATC

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