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STD Testing During Pregnancy

What tests for sexually transmitted diseases and other conditions should pregnant women have?

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• Part 1: STDs During Pregnancy
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Part 2: How Common Are STDs During Pregnancy?
 

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"I just found out that I have herpes ... I am still in shock as I thought I was careful and this proves nobody can be careful enough I guess. ... I wonder if I caught it before him or did I get it from him but he has no symptoms. Also I am pregnant and dealing with stress, pregnancy, herpes, can really be a problem..."
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What You Need to Know About Genital Herpes
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Chlamydia - The Silent Epidemic
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Gonorrhea - Symptoms, Treatments, Prevention
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Hepatitis Resources
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Pregnancy Resource Center

by Tracee Cornforth

No woman is safe from contracting a sexually transmitted disease. Age, race, ethnicity, religion, social status and education level do not play a role in determing which women may be affected by sexually transmitted diseases. The Centers for Disease Control STD Treatment Guidelines (2002) recommends the following screening tests for all pregnant women:

  • All pregnant women should be offered voluntary HIV testing at the first prenatal visit. Reasons for refusal of testing should be explored, and testing should be reoffered to pregnant women who initially declined testing. Retesting in the third trimester (preferably before 36 weeks' gestation) is recommended for women at high risk for acquiring HIV infection (i.e., women who use illicit drugs, have STDs during pregnancy, have multiple sex partners during pregnancy, or have HIV-infected partners). In addition, women who have not received prenatal counseling should be encouraged to be tested for HIV infection at delivery.

  • A serologic test for syphilis should be performed on all pregnant women at the first prenatal visit. In populations in which use of prenatal care is not optimal, rapid plasma reagin (RPR)-card test screening (and treatment, if that test is reactive) should be performed at the time a pregnancy is confirmed. Patients who are at high risk for syphilis, are living in areas of excess syphilis morbidity, are previously untested, or have positive serology in the first trimester should be screened again early in the third trimester (28 weeks' gestation) and at delivery. Some states require all women to be screened at delivery. Infants should not be discharged from the hospital unless the syphilis serologic status of the mother has been determined at least one time during pregnancy and preferably again at delivery. Any woman who delivers a stillborn infant should be tested for syphilis.

  • A serologic test for hepatitis B surface antigen (HBsAg) should be performed on all pregnant women at the first prenatal visit. HBsAg testing should be repeated late in pregnancy for women who are HBsAg negative but who are at high risk for HBV infection (e.g., injection-drug users and women who have concomitant STDs).

  • A test for Chlamydia trachomatis should be performed at the first prenatal visit. Women under the age of 25 and those at increased risk for chlamydia (i.e., women who have a new or more than one sex partner) also should be tested during the third trimester to prevent maternal postnatal complications and chlamydial infection in the infant. Screening during the first trimester might enable prevention of adverse effects of chlamydia during pregnancy. However, evidence for preventing adverse effects during pregnancy is lacking. If screening is performed only during the first trimester, a longer period exists for acquiring infection before delivery.

  • A test for Neisseria gonorrhoeae should be performed at the first prenatal visit for women at risk or for women living in an area in which the prevalence of N. gonorrhoeae is high. A repeat test should be performed during the third trimester for those at continued risk.

  • A test for hepatitis C antibodies (anti-HCV) should be performed at the first prenatal visit for pregnant women at high risk for exposure. Women at high risk include those with a history of injection-drug use, repeated exposure to blood products, prior blood transfusion, or organ transplants.

  • Evaluation for bacterial vaginosis (BV) may be conducted at the first prenatal visit for asymptomatic patients who are at high risk for preterm labor (e.g., those who have a history of a previous preterm delivery). Current evidence does not support routine testing for BV.

  • A Papanicolaou (Pap) smear should be obtained at the first prenatal visit if none has been documented during the preceding year.

Other STD-related concerns are as follows:

  • HBsAg-positive women should be reported to the local and/or state health department to ensure that they are entered into a case-management system and that appropriate prophylaxis is provided for their infants. In addition, household and sex contacts of HBsAg-positive women should be vaccinated.

  • No treatment is available for anti-HCV-positive pregnant women. However, all women found to be anti-HCV-positive should receive appropriate counseling. No vaccine is available to prevent HCV transmission.

  • In the absence of lesions during the third trimester, routine serial cultures for HSV are not indicated for women who have a history of recurrent genital herpes. Prophylactic cesarean section is not indicated for women who do not have active genital lesions at the time of delivery.

  • The presence of genital warts is not an indication for cesarean section.

  • Not enough evidence exists to recommend routine screening for Trichomonas vaginalis in asymptomatic pregnant women.

Not all health care providers routinely perform these tests and pregnant women should ask for them if they are not recommended by their clinicians. Diagnostic tests for sexually transmitted diseases are constantly becoming more accurate; even if you have been tested for STDs in the past, you need to be retested whenever pregnancy occurs.

Information contained in this article is adapted from material available at the Centers for Disease Control and Prevention, National Center for HIV, STD and TB Prevention, Division of Sexually Transmitted Diseases Prevention

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