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CDC Updates Guidance for the Care of Pregnant Women with Possible Zika Virus Exposure

JUL 31, 2017 | CONTAGION® EDITORIAL STAFF
The Centers for Disease Control and Prevention (CDC) has responded to the declining prevalence of Zika virus in the Americas, as well as emerging evidence "indicating prolonged detection of Zika immunglobulin M (IgM) antibodies,” by updating its interim guidance for US healthcare providers who are treating pregnant women with possible Zika virus exposure.

The authors of the guidance note that as prevalence of the disease continues to decline, the likelihood of false-positive test results is conversely increasing. This may be because recent evidence suggests that Zika virus IgM antibodies can persist in the body for > 12 weeks after infection. As such, the authors note that IgM test results cannot always reliably distinguish between an infection that occurred during the current pregnancy and one that occurred before the current pregnancy, particularly for women who had potential exposure to the virus previous to their current pregnancy.” Healthcare providers should mention the limitations to current testing methods when counseling pregnant women on the risks and benefits involved in testing for the virus during their pregnancy.

Ultimately, the new guidance stresses the use of a “shared decision-making model” for testing and screening pregnant women. In this model, patients work closely with healthcare providers to make important decisions regarding testing and care. These decisions are informed by “patient preferences and values, clinical judgment, and a balanced assessment of risks and expected outcomes.”

According to the guidance, some of the key updated recommendations include:

  • Having healthcare providers ask all pregnant women in the United States and US territories about potential exposure to Zika virus both before and during current pregnancies; this should happen at each prenatal care visit.

  • Pregnant women who report potential Zika virus exposure or present with associated symptoms should be tested to diagnose the cause of their symptoms. The updated recommendation calls for a concurrent Zika virus nucleic acid test (NAT) and serologic testing "as soon as possible through 12 weeks after symptom onset."

  • Healthcare providers should offer Zika virus NAT testing a total of 3 times during pregnancy to symptomatic pregnant women who have ongoing potential exposure to the virus. The authors note that IgM testing is no longer a routine recommendation because IgM is capable of persisting for months after infection. As such, the test cannot reliably answer the question of whether the infection occurred during pregnancy or not. Furthermore, the authors write that pregnant women who are given a diagnosis of laboratory-confirmed Zika virus any time during their pregnancies, are not recommended to receive any additional testing. However, they do say that pregnant women without laboratory-confirmed diagnosis should be offered NAT testing as soon as they start prenatal care. If healthcare providers do not detect Zika virus RNA, “2 additional [NAT] tests should be offered [to these women] during the course of pregnancy coinciding with prenatal visits.”


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