Prevention and treatment of Zika virus in Canada
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Published by: The Public Health Agency of Canada
Issue: Volume 42-5: Virus Zika
Date published: May 5, 2016
Volume 42-5, May 5, 2016: Virus Zika
Canadian recommendations on the prevention and treatment of Zika virus: Update
Zika Working Group1 on behalf of the Committee to Advise on Tropical Medicine and Travel (CATMAT)*
1 Members of the Zika Working Group are listed in the Acknowledgments section
Zika Working Group on behalf of the Committee to Advise on Tropical Medicine and Travel (CATMAT). Canadian Recommendations on the Prevention and Treatment of Zika virus: Update. Can Comm Dis Rep 2016;42:101-11. https://doi.org/10.14745/ccdr.v42i05a01
Updated guidance has been published. Refer to the updated Zika Virus Prevention and Treatment Recommendations.
Table of contents
- Risk to travellers
- Areas of risk
- Prevention - Decision to travel to areas of risk
- Prevention of sexual transmission
- Laboratory Diagnosis
- Screening and Management
- Evaluation of non-pregnant travellers returning from endemic countries
- Evaluation in the context of pregnancy
- Evaluation of the infant born to a woman diagnosed with ZIKV infection or with suspected congenital ZIKV infection
- Recommendations for ZIKV
- Additional resources and useful links
Background: Zika virus (ZIKV) has recently emerged as a disease of significant public health concern. Currently, a large outbreak is occurring predominantly located in the Americas. ZIKV infection is a cause of microcephaly and other congenital abnormalities and can cause post-infectious neurologic complications such as Guillain-Barré syndrome.
Objective: To review current knowledge of ZIKV infection and to provide guidance to health care professionals who provide advice to Canadians who may be impacted by ZIKV infection.
Methods: This Statement was developed by a working group of the Committee to Advise on Tropical Medicine and Travel (CATMAT). Recommendations are based on a literature review and clinical judgment.
Results: All travellers should use personal protective measures against mosquito bites including insect repellents and protection of living areas against mosquito entry. Pregnant women should avoid travel to areas designated by the Public Health Agency of Canada as being of concern because of ongoing ZIKV transmission. Women planning a pregnancy should consult with their health care provider and consider postponing travel to these areas. All other travellers may wish to consider deferring travel to designated areas based on risk tolerance, values, and preferences.
Sexual transmission of ZIKV from male partners has been documented and couples should practice abstinence or use condoms for the duration of a pregnancy, while in a risk area, or until viral shedding has likely ceased. In the absence of clear data, we make the assumption that viral shedding is unlikely to persist beyond 6 months for men and two months for non-pregnant women.
Health care providers should take a travel history from their pregnant patients including relevant information related to the travel history of their partner(s). Screening and management recommendations are provided for all travellers including potentially contagious male partners, pregnant women (symptomatic and asymptomatic), and the fetus or infant of potentially infected women. There is no specific antiviral therapy for the treatment of ZIKV infection.
Conclusion: Robust quantitative assessments for the full spectrum of ZIKV-associated risks are not possible. This reflects, among other things, uncertainties related to the likelihood of infection among travellers to ZIKV-affected areas, vertical transmission from mother to fetus, sexual transmission (from symptomatic or asymptomatic partners), and serious ZIKV-associated sequelae among travellers. Given this uncertainty, as well as the potentially severe effects of ZIKV infection on the fetus, recommendations are conservative. CATMAT will update its recommendations as new information becomes available.
Zika virus (ZIKV) infection is caused by a flavivirus transmitted through the bite of an infected Aedes mosquito, mainly Aedes aegypti. Aedes albopictus has also been associated with transmission of ZIKV Footnote 3. Although infections in humans were documented in the 1950s, ZIKV has only recently emerged as a disease of significant public health concern. Currently, there is a large outbreak underway in the Americas with transmission also occurring in some other countries. Outbreaks have also recently occurred on islands in the South Pacific and in Cabo Verde. Before this, known areas of endemic transmission were limited to Asia and Africa, and transmission rates in these areas are generally low. It is likely that the virus will continue to spread because the mosquito vectors are found in many tropical and subtropical regions and in some warmer temperate regions Footnote 4,Footnote 5.
A major concern with the current outbreak is the spatial and temporal clustering of ZIKV activity with an increase in the incidence of children born with microcephaly, defined as a head circumference measurement below the third percentile and disproportionate to the weight and length percentile measurements Footnote 6,Footnote 7. A recent epidemiologic study also demonstrated a strong association of ZIKV and microcephaly in the population of French Polynesia, where an outbreak took place from 2013-2015 Footnote 8. The role of ZIKV in microcephaly is further supported by detection of ZIKV viral genome in amniotic fluid, placenta and tissues of affected fetuses and neonates Footnote 1,Footnote 9, and the pattern of microcephaly associated with ZIKV appears to be within the context of a broader syndrome that may be distinct from that caused by other fetal insults Footnote 9. Based on the available evidence, a causal relationship between prenatal ZIKV infection and infant microcephaly or other severe brain anomalies has been acknowledged in the scientific community Footnote 10.
Although disease is usually mild in adults, ZIKV infection can cause neurologic sequelae such as Guillain-Barré syndrome (GBS) Footnote 7,Footnote 11. A recent case control study done in French Polynesia estimates a 0.24 in 1000 risk for developing GBS in persons infected with ZIKV. This is comparable to the risk of 0.25 to 0.65/1000 observed following Campylobacter jejuni infection. There are also reports of acute disseminated encephalomyelitis (ADEM) following ZIKV infection Footnote 12.
Finally, there are multiple reports of sexual transmission of ZIKV from infected males to their partner(s), including male-to-male Footnote 2,Footnote 13,Footnote 14,Footnote 15,Footnote 16, suggesting that this event is not a rare occurrence.
The purposes of this statement are to review our current knowledge of ZIKV infection and to provide guidelines for health care providers on prevention and management of ZIKV disease.
This statement was developed by a working group of the Committee to Advise on Tropical Medicine and Travel (CATMAT). Members of the working group were from CATMAT, the Public Health Agency of Canada (the Agency) and the Society of Obstetricians and Gynaecologists of Canada. Each member was a volunteer, and none declared a relevant conflict of interest. This guideline complements existing CATMAT statements including the Statement on Personal Protective Measures to Prevent Arthropod bites Footnote 17 and the Statement on Pregnancy and Travel Footnote 18. A literature search for evidence related to ZIKV was conducted. Guidelines and reports from international and national public health organizations including, but not limited to, the Centers for Disease Control in the United States, the Pan American Health Organization and the World Health Organization, were also retrieved and reviewed.
ZIKV was first isolated from monkeys in Uganda in 1947. Soon after (1952), human infections were detected in Uganda and Tanzania Footnote 19,Footnote 20. However, human infections were rarely reported until 2007, when the first major outbreak of ZIKV disease occurred on the island of Yap (Micronesia) in the southwestern Pacific Ocean Footnote 21. Between 2013 and 2015, additional outbreaks occurred on islands and archipelagos from the Pacific region including a large outbreak in French Polynesia Footnote 22,Footnote 23 and another in Cabo Verde Footnote 24. In 2014, local transmission in the Americas was reported for the first time on Easter Island Footnote 25. ZIKV has since spread to a wide region of the Americas including, at the time of updating, more than 43 countries and territories. It is anticipated that ZIKV will continue to spread through the Americas, in particular in tropical and subtropical regions Footnote 27,Footnote 28.
The mosquitoes associated with ZIKV can be active during the day and night, with biting activity often peaking in the morning and later in the afternoon. In vertebrate hosts, the incubation period is usually three to 12 days, with blood viremia (the period when ZIKV is present in the blood) usually lasting for three to five days Footnote 29,Footnote 30. Viremia has typically been detected only during symptoms, although a case of prolonged viremia during pregnancy has been reported Footnote 31. It is uncertain whether viremia is detectable prior to symptoms, or during asymptomatic infection. If bitten by a competent mosquito while viremic, the human (or other) host can infect the mosquito thereby completing the transmission cycle Footnote 28. Vertical transmission between mother and developing fetus also presumably occurs during this viremic period Footnote 32,Footnote 33. Other described routes of transmission include blood product transfusion Footnote 34 and sexual transmission from men after symptomatic infection Footnote 13,Footnote 14,Footnote 15,Footnote 16. Viral RNA has been detected in the semen of males previously known to have symptomatic disease at very high levels; how long this persists, and whether it can occur in males who were infected but asymptomatic is not known. Viral RNA has also been detected in saliva Footnote 23 or urine Footnote 35,Footnote 36 more than a week after clearance of blood viremia. Neutralizing antibodies for ZIKV are detectable after infection, and by extrapolation from other flaviviruses, post-infection immunity is presumed to be long lasting.
Sexual transmission of ZIKV from infected women to their sexual partners and from persons who are asymptomatically infected has not been reported; however, there is insufficient evidence to exclude these as routes of transmission.
ZIKV RNA has been detected in breast milk; however, there have not been any documented reports of transmission to infants through breastfeeding Footnote 19. At this time, the World Health Organization (WHO) considers that “the benefits of breastfeeding for the infant and mother outweigh any potential risk of Zika virus transmission through breast milk” Footnote 37. CATMAT shares this opinion.
Approximately 20-25% of persons infected with ZIKV will manifest symptoms, including fever, myalgia, pruritis, eye pain, and maculopapular rash Footnote 21,Footnote 38. Early clinical manifestations are generally similar to other arboviral infections including dengue and chikungunya Footnote 38,Footnote 39. Thus, the differential diagnosis of a febrile returned traveller from the Americas will likely include these arboviral entities, as well as malaria Footnote 40 and other viral infections Footnote 41,Footnote 42.
Post-infection neurologic complications, such as Guillain-Barré synfrome (GBS), have been reported from many of the countries affected by the current ZIKV outbreak Footnote 11,Footnote 30,Footnote 43,Footnote 44. They include French Polynesia where a case-control study estimated that the odds of positive ZIKV serology was substantially greater in GBS cases compared to matched controls (OR 59.7; 95% CI 10.4 to ∞) Footnote 45. In this same study, and based on a ZIKV population seroprevalence of 0.66, the risk of GBS following ZIKV infection was estimated at approximately 1/4,000. Other neurological manifestations have also been reported in association with ZIKV infection, e.g., acute myelitis, meningoencephalitis, and acute disseminated encephalomyelitis Footnote 12,Footnote 46,Footnote 47, suggesting that the neurological spectrum of sequelae associated with ZIKV may be broader than previously thought.
Clinically relevant thrombocytopenia and subcutaneous hematomas have been reported in a small number of cases Footnote 48,Footnote 49. Deaths from other causes have also been reported Footnote 50,Footnote 51.
Brazil, French Polynesia and several other affected countries (e.g., Colombia) Footnote 7 have reported infant microcephaly associated with ZIKV infection. Ocular abnormalities and other congenital malformations such as arthrogryposis and hydrops fetalis have also been described Footnote 52,Footnote 53,Footnote 54. Although the full impact of ZIKV infection during pregnancy remains to be described, there is now consensus that infection can cause fetal congenital anomalies Footnote 8,Footnote 10. Although the likelihood of serious fetal harm following infection is unknown there is evidence to suggest that it is not a rare occurrence. For example, a recent case series from Brazil suggests that infection is associated with serious outcomes including fetal death, placental insufficiency, fetal growth restriction, and central nervous system (CNS) injury (12/42 ZIKV-infected females on whom Doppler ultrasonography was performed) Footnote 55. A retrospective study of patients in French Polynesia suggested that the impact of ZIKV was primarily through infections occurring during the first trimester (when it was estimated to result in an approximately 1% risk of microcephaly) Footnote 8.
Reviews of the epidemiology of ZIKV, as well as the causal association of ZIKV and microcephaly have been recently published Footnote 10.
The Agency has published an assessment of the risk of ZIKV to Canadians Footnote 56. It concludes:
- For most infected travellers, ZIKV will have little or no health impact (Low impact, with medium confidence). However, severe outcomes (e.g., GBS) might occur in some affected individuals (High impact, medium confidence).
- There could be Very High impact (with medium confidence) to the unborn children of women who become infected with ZIKV while pregnant.
- Sexual transmission, from symptomatic male travellers to a sexual partner(s) who has(ve) not travelled, has been reported. Because the likelihood of infection with ZIKV is considered low, so too is the likelihood of transmission via this route (Low likelihood, medium confidence). However, if a man becomes infected with ZIKV, the likelihood of transmission to his sexual partner(s) is assessed as Medium (low confidence).
This assessment also considered factors that might affect the likelihood or impact of ZIKV infection. While evidence is very limited in this regard, several plausible relationships were identified:
- Conditions at higher elevations (≥ 2,000 m) are generally not supportive of viral replication in, or survival of, Aedes aegypti populations. Correspondingly, the relative likelihood of infection with ZIKV might be substantially lower for travellers (depending on how much time they spend at higher compared to lower elevations) to such areas.
- All else held equal, the likelihood of infection is higher in countries/areas that are reporting high levels of ZIKV activity compared to those that are not.
- The likelihood of infection is likely lower for shorter travel durations and/or when staying in protected environments (e.g., well screened and air-conditioned accommodations, transiting through an airport in a risk area). This might also apply to situations where the traveller is staying in an isolated location, i.e. where there are relatively few residents who might support sustained transmission.
CATMAT stresses that, at this time, robust quantitative assessments for the full spectrum of ZIKV-associated risks are not possible. This reflects, among other things, uncertainties related to: the likelihood that travellers will be infected with ZIKV, the likelihood that travellers infected with ZIKV will manifest serious sequelae like GBS, and the probability that maternal infection during pregnancy will lead to fetal infection. Given this uncertainty, as well as the potentially severe effects of ZIKV infection on the fetus, our recommendations are conservative. However, we also realize that there might be circumstances where a patient is unable to or unsure about whether to adhere to our guidance. In this situation, we believe it is appropriate to consider factors such as those identified above to help inform the decision-making process (also see below, decision to travel to risk areas).
There is widespread transmission over much of South and Central America, the Caribbean, but not temperate areas of Argentina and Chile. An up to date list of countries to which our recommendations apply is maintained by the Agency.
There are areas of Africa and Asia where ZIKV transmission has previously occurred, or is considered endemic with very low potential for transmission to travellers. These are not currently designated as risk areas by the Agency, nor are countries/territories where ZIKV has been reported, but only in travellers and/or as a result of sexual transmission.
Health care providers should discuss with travellers what is known and what is not known about ZIKV to help their patients make an informed choice about travel based on this guideline and the ZIKV information on the Government of Canada’s ZIKV webpage. Factors to consider include:
- The possibility of serious sequelae such as post-infection neurologic complications (e.g., GBS, ADEM).
- The potential for ZIKV infection during pregnancy to have a severe impact of the fetus.
- The potential for sexual transmission from men to their sexual partners, which is particularly relevant to couples who are actively trying to conceive.
- The potential for co-morbidities to predispose to more serious outcomes (there is little specific evidence in this regard, though it is reasonable to expect such impacts).
- Patients’ values and preferences (including risk perception and risk tolerance).
- The potential impacts of following the recommendation on a couple’s reproductive plans.
- The large uncertainties that continue to hamper the development of robust risk assessments for Canadians.
- Itinerary- specific factors (see section on risk to Canadian travellers) that might affect the likelihood of being exposed to ZIKV.
CATMAT recommends that pregnant women avoid travel to areas of risk. Women planning a pregnancy should consult with their health care provider and consider postponing travel to areas of risk as defined above. Pregnant women and those planning a pregnancy who choose to travel to areas of risk or for whom travel cannot be avoided are strongly advised to use Personal Protective Measures (PPM) against insect bites (see below for more detail). As for travellers generally (see previous section), health care providers should help their patients make an informed decision regarding travel or other aspects of ZIKV prevention. The risk of severe adverse outcomes of pregnancy deserves particular emphasis.
There is no vaccine or immunoprophylaxis that protects against ZIKV infection. CATMAT recommends that all travellers to areas of risk should be advised to strictly adhere to recommendations for the use of personal protective measures against mosquito bites (see below). Because the mosquitoes that transmit ZIKV can bite at any time (including during daylight hours), PPM should be used through all hours of the day and night. In addition to ZIKV, PPM provide protection against other vector-associated diseases such as malaria, dengue, and chikungunya. Recommendations for PPM can be found in CATMAT’s Statement on Personal Protective Measures to Prevent Arthropod Bites Footnote 17. These are summarized below:
Personal protective measures to prevent arthropod bites
1) Cover up:
- Wear light-coloured, long-sleeved, loose fitting, tucked-in shirts, long pants, shoes or boots (not sandals), and a hat.
2) Use insect repellent on exposed skin:
- It is recommended that adults use repellents that contain DEET (20-30%) or icaridin (20%).
- It is recommended that children six months to twelve years of age use repellents that contain icaridin (20%). As a second choice, this age group can use repellents with age-appropriate DEET concentrations as per label. Since publication of the PPM guidelines, p-Menthane-3,8-diol 20% has become available in Canada and is an option.
- If bites cannot be avoided using a physical barrier, consider use of up to 10% DEET or 10% icaridin for infants under six months of age.
3) Protect living areas from mosquito entry:
- Stay in a well-screened or completely enclosed air-conditioned room.
- Reduce your risk in work and accommodation areas by closing eaves, eliminating holes in roofs and walls and closing any other gaps.
4) If mosquito entry into living quarters cannot be otherwise prevented (e.g. by screening):
- Use a bed net (e.g. for sleeping or resting inside), preferably treated with insecticide.
- Netting can also be used to protect children in playpens, cribs, or strollers.
- Bed nets will also provide protection against diseases like malaria.
5) Apply a permethrin insecticide to clothing and other travel gear for greater protection:
- Although permethrin clothing treatments are not widely available in Canada, travel health clinics can advise you how to purchase permethrin and pre-treated gear before or during your trip.
- Permethrin-treated clothing is effective through several washes.
- Always follow label instructions when using permethrin.
- Do not use permethrin directly on skin.
Insect repellents, insecticide treated bed nets and permethrin treated clothing/clothing treatments have been reviewed for safety in Canada and/or the United States. They are considered safe, including for children, pregnant and breastfeeding women if used in accordance with label directions.
ZIKV RNA has been detected in semen two months after acute illness Footnote 16,Footnote 57. It is not known how long viral shedding in semen can last, how often this might happen when infection is asymptomatic, or how easily virus can be transmitted by sexual contact. The number of reports of sexual transmission has been increasing, suggesting this may not be a rare occurrence. When properly used, condoms should minimize the risk of sexual transmission.
If travel to a risk area is unavoidable, pregnant woman and male partners should practise abstinence or use condoms until more is known about the prolonged viral shedding of ZIKV in semen. If the male partner of pregnant female has been in a risk area the couple should practice abstinence or use condoms for the full duration of the pregnancy (including after return).
Based on current information on the incubation period and duration of viremia, and the unclear duration of viral persistence in tissues, women planning a pregnancy should wait at least two months after their return from an area of risk before trying to conceive. For couples where the male partner has travelled in an area of risk, it is reasonable to delay trying to conceive for six months.
Men who have returned from a risk area and who wish to reduce the possibility of sexual transmission to their partner (outside of the context of pregnancy) can do so through appropriate use of condoms. Although transmission has so far only been reported after symptomatic infection, and it is plausible that the risk after asymptomatic infection is lower, there are no data to support making different recommendations for symptomatic or asymptomatic men. Use of condoms likely provides the greatest protection in the first weeks following illness, but given the potential for long-term persistence in semen, condom use should be considered for six months after return from a risk area.
Laboratory testing for ZIKV infection is fully described below. In theory, based on information from other similar viral infections, the absence of ZIKV-specific antibodies two weeks or more after the last possible exposure implies that the individual has never been infected, and is not contagious to sexual partners or to the fetus. Such seronegative individuals could consider discontinuing measures to intensively follow the pregnancy for ZIKV-related complications, as well as measures to prevent sexual transmission. The absence of ZIKV RNA in a semen sample might indicate absence of contagiousness, but there are no data to support this practice at this time, and there remains the theoretical risk of poor test sensitivity for some ZIKV strains. However, at this time, serology and RNA testing in Canada is only available for symptomatic individuals and pregnant women. Testing of asymptomatic individuals (men or non-pregnant women) is not routinely offered.
Molecular testing using reverse-transcriptase PCR (RT-PCR) is conducted by some provincial laboratories in Canada. The National Microbiology Laboratory provides provincial support, along with confirmatory testing. Sensitivity and specificity are unknown, but presumed to be high, at least in the initial few days of illness, since ZIKV appears to circulate in the blood for the first three to five days after onset of symptoms Footnote 27. ZIKV RNA may be present in urine for a few days after it is no longer detectable in blood Footnote 27,Footnote 58. Information about the National Microbiology Laboratory guidelines and testing recommendations are available on the Government of Canada's website.
At the National Microbiology Laboratory, serologic testing is currently performed using a Centers for Disease Control in the United States based in-house IgM enzyme linked immunosorbent assay (ELISA) followed by a confirmatory ZIKV plaque reduction neutralization test (PRNT) Footnote 36. Antibodies appear approximately five to six days after onset of symptoms Footnote 30. For the acutely unwell patient with less than 10 days of symptoms, both RT-PCR and serology should be requested to maximize sensitivity. For the convalescent patient with symptom onset over 10 days ago, only serology should be requested. Appropriate diagnostic specimens for RT-PCR testing include plasma/serum, urine, cerebrospinal fluid (CSF), amniotic fluid and placental tissue. Serology is usually only performed on serum; however, viral antibodies may be detected in CSF in some cases of neurological disease.
As ZIKV is a member of the flaviviridae, serologic tests, including the IgM ELISA, may be cross-reactive with other flaviviruses such as dengue, West Nile, and Yellow Fever (including among vaccine recipients) Footnote 4. Confirmation of ZIKV therefore rests on amplification of viral RNA by RT-PCR, or by confirmatory PRNT serologic testing. Confirmatory testing generally requires neutralizing IgG production, which may appear later than IgM. The specificity of the IgM ELISA is limited particularly during secondary flavivirus infections. Patients whose serum samples are IgM positive and have ZIKV-specific antibodies confirmed through PRNT are confirmed cases of viral infection. However, it is also recommended for equivocal cases that acute and convalescent sera be collected 2-3 weeks apart to document a seroconversion or a diagnostic increase (four-fold or greater) in virus specific neutralizing antibodies. This is because individuals previously infected with or vaccinated against flaviviruses may exhibit cross reactivity in PRNT tests making them difficult to interpret.
PCR for ZIKV can be performed on amniotic fluid (when amniocentesis is technically feasible) to confirm infection of the fetus. At this time, the risk of adverse outcomes of pregnancy if the fetus is infected with ZIKV is unknown, so the risk of the procedure must be weighed against the clinical utility of this test result. A negative PCR result likely means that the fetus is not currently infected, but would not eliminate the possibility of previous infection. It is not known when ZIKV RNA would be expected to appear in amniotic fluid after infection, or how long it is likely to be detectable. There is some evidence that viral RNA may persist in amniotic fluid for months Footnote 59.
For postnatal diagnosis of congenital infection, PCR for ZIKV can be performed on placental tissue, umbilical cord blood or infant blood, and CSF for confirmation of congenital infection. It is possible, however, that infants or fetuses infected weeks prior to specimen sampling will no longer have detectable viral RNA.
Testing for ZIKV infection (PCR) should be considered in the diagnosis of any ill traveller with compatible epidemiologic and clinical history, when symptom onset is within three days after arrival in, to 14 days after departing from an area of risk. Testing for other similar viral infections and for malaria should also be done as appropriate.
Serologic testing may be considered for male returned travellers whose clinically compatible illness has resolved, and are at least two weeks post exposure, in order to assess for potential contagiousness to sexual partners. The same would theoretically apply to males who have travelled and remain asymptomatic but testing is not currently being offered to this group in Canada. Testing an asymptomatic individual simply out of curiosity concerning their serostatus would not be a prudent use of limited resources. Given that neurologic disorders like GBS have occurred following ZIKV infection, returning travellers should be counselled to report any neurologic symptoms to their doctor. In the event of the diagnosis of GBS or other unusual neurologic syndrome, a travel history for the patient and any male sexual partners should be elicited. If ZIKV infection is thought to be potentially associated with the illness, a specialist should be consulted.
Health care providers should take a travel history from their pregnant patients including relevant information related to the travel history of their partner(s). Any patient who indicates that they or their partner have recently travelled to an area of risk should be further evaluated.
Screening of asymptomatic pregnant women should be discussed on a case-by-case basis between the woman and her health care provider. Screening would consist of serology at least two weeks after the last potential exposure, as well as fetal ultrasounds, at a frequency to be determined in consultation with the woman’s obstetrician, at least until serology is shown to be negative. The usefulness of serology will depend partly on the turn-around time for results, which can be discussed with the local laboratory. The decision to test should include consideration of how the results of the screening tests would be used to inform subsequent decisions. Diagnosis and identification of poor fetal outcomes will allow for appropriate counselling.
Pregnant women and their partners may be justifiably concerned about the risk of ZIKV infection to their fetus and may want to receive counselling to decide the best course of action, including the question of termination. The risk of vertical infection (with clinical sequelae) in the setting of symptomatic or asymptomatic maternal infection in a given trimester of pregnancy is unknown, but appears highest in the first trimester Footnote 8. However severe sequelae have been reported after infection at all stages of pregnancy Footnote 55. This uncertainty makes pregnancy counselling a difficult prospect. Regardless, discussion and informed decision making regarding options for management of ZIKV infection in pregnancy (much like any other congenital infection or congenital anomaly) requires thorough consultation with a Maternal Fetal Medicine Specialist or another specialist familiar with reproductive infectious diseases. As understanding of the risks of ZIKV infection in pregnancy becomes clearer, so too will the related counselling messages, which in turn will allow each patient to make her own individual decision about her pregnancy.
Testing (including PCR) should be offered to pregnant women with acute signs and symptoms compatible with ZIKV. As described above, for the acutely unwell patient with less than 10 days of symptoms, both RT-PCR and serology should be requested to maximize sensitivity. For the convalescent patient with symptom onset over 10 days ago, only serology should be requested. Repeated ultrasound monitoring is indicated, unless the woman is found to be negative on laboratory testing. A woman whose fetus is suspected of having a congenital anomaly should also be offered testing if she or her partner has travelled to any location where ZIKV transmission may be occurring, even at a low level.
The risk of microcephaly or other adverse pregnancy outcomes for a woman known to be infected with ZIKV cannot be estimated from currently available data. Although measurements of head circumference and biparietal diameter may occur as early as 15 weeks, there is no defined gestational age by which microcephaly can be ruled out. Serial monitoring by ultrasound with close attention to measurement trends over time is recommended. It is possible that changes in intracranial anatomy may not be elucidated until well into the third trimester, or later.
Serial ultrasounds (every 3-4 weeks) are recommended in pregnant women with confirmed or suspected (if testing results are pending) ZIKV infection in pregnancy, and for asymptomatic pregnant travellers returning from areas of risk while awaiting diagnosis, to help define risk and counsel the mother. Should CNS calcifications or fetal microcephaly be noted at ultrasonography of the asymptomatic pregnant returned traveller, then specific ZIKV testing of the fetus (e.g., amniocentesis) should be considered to help define the likely cause of the anomaly.
Evaluation of the infant born to a woman diagnosed with ZIKV infection or with suspected congenital ZIKV infection
Infants born to women with confirmed or suspected ZIKV infection in pregnancy, or those with microcephaly, intracranial calcifications or other symptoms of congenital ZIKV infection in whom the mother had potential exposure to the virus, should be tested. This testing should include serology, PCR of serum (umbilical cord or infant sample), and PCR of placenta; if CSF is sampled, this can also be sent for PCR and serology. Infants with suspected or confirmed congenital ZIKV infection should also undergo further work-up including: routine lab tests (CBC and liver enzymes), head ultrasound, ophthalmologic examination, and hearing evaluation. Infants with confirmed congenital ZIKV infection should have neurodevelopmental monitoring throughout infancy to assess the potential for long term sequelae.
Infants born to women with symptoms of active ZIKV infection around the time of delivery are at risk for perinatal transmission of the disease. In the limited number of reported cases to date, perinatally infected infants have exhibited either no or mild symptoms and laboratory findings (rash, thrombocytopenia) Footnote 32. Regardless, such infants should be monitored closely given the unclear spectrum of potential illness in this emerging infection. Testing with serology and serum PCR during acute illness is recommended. In such cases, care should be taken to ensure a thorough work up for other important and treatable causes of congenital infections, such as cytomegalovirus and toxoplasma.
Currently there is no specific antiviral therapy for the treatment of ZIKV infection. Treatment is supportive with antipyretics (acetaminophen in pregnancy), hydration and rest. Aspirin and other non-steroidal anti-inflammatory drugs (NSAIDs) should be avoided until dengue can be ruled out to reduce the risk of hemorrhage Footnote 60. Symptomatic disease typically lasts for up to seven days. Urgent medical care is recommended for any symptoms associated with GBS, and treating health care providers should be made aware of recent travel to area with ZIKV circulation and/or symptoms of ZIKV infection.
If ZIKV infection is confirmed in the setting of pregnancy, referral to a Maternal Fetal Medicine Specialist or specialist familiar with Reproductive Infectious Diseases should be made. If microcephaly, intracranial calcifications or other abnormalities are identified, appropriate counselling by a Neonatologist and Pediatric Infectious Diseases Specialist on potential neurodevelopmental outcome should be offered to parents.
- Government of Canada – For health professionals: Zika Virus
- Government of Canada: Countries with reported locally acquired Zika virus infection
- Government of Canada – Travel health notice: Zika virus infection: Global Update
- Pan American Health Organization – Zika Virus Infection
This statement was developed by the Zika Working Group: Libman M (chair), Boggild A, Bui Y, Brophy J, Drebot M, Geduld J, McCarthy A, Safronetz D, Schofield S, Tataryn J, Vanschalkwyk J, Yudin M.
CATMAT acknowledges and appreciates the contribution of Alex Demarsh and Tanya Christidis to the statement.
CATMAT members: McCarthy A (Chair), Acharya A, Boggild A, Brophy J, Bui Y, Crockett M, Greenaway C, Libman M, Teitelbaum P and Vaughan S.
Liaison members: Audcent T (Canadian Paediatric Society), Gershman M (United States Centers for Disease Control and Prevention) and Pernica J (Association of Medical Microbiology and Infectious Disease Canada).
Ex officio members: Marion D (Canadian Forces Health Services Centre, Department of National Defence), McDonald P (Division of Anti-Infective Drugs, Health Canada) and Schofield S (Pest Management Entomology, Department of National Defence).
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