Guidance for Investigation and Management of Zika Virus Infection

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Guidance for Investigation and Management of Zika Virus Infection Update: February 11, 2016 Public Health Agency of Canada has issued recommendations from the Committee to Advise on Tropical Medicine and Travel (CATMAT) on the prevention and treatment of Zika virus. http://www.healthycanadians.gc.ca/publications/diseases-conditionsmaladies-affections/committee-statement-treatment-prevention-zika-declarationcomite-traitement-prevention/index-eng.php Women should wait at least two months after returning from an area with Zika virus transmission before trying to conceive. Men who have travelled to an area with Zika virus transmission should use condoms with a partner who is or could become pregnant for two months after their return. Consider using condoms for the duration of the pregnancy after travel to an area with Zika virus transmission. Consider testing asymptomatic pregnant women with a history of travel to an area with Zika virus transmission. Serial obstetrical ultrasounds are recommended every three to four weeks for all pregnant travelers returning from an area with Zika virus transmission. Defer blood donation for 21 days after returning from a country with Zika virus transmission. Key Points: The main risk factor for Zika virus infection is travel to an affected area Obtain travel history from all pregnant women Testing is only indicated for persons with symptoms and relevant travel history Test for dengue and chikungunya as well

There is no prophylaxis or treatment so postponement of travel or avoidance of mosquito bites is advised Investigations are ongoing regarding the association between Zika virus disease and fetal microcephaly and Guillain-Barré syndrome Recommendations for the prevention of sexual transmission are expected soon Defer blood donation for 21 days after returning from a country with Zika transmission Background Zika virus, first described in Rhesus monkeys in the Zika forest, Uganda in 1947, has led to outbreaks in Africa, Asia and the Oceanic Pacific region. In late 2015, Zika virus was reported for the first time in a number of countries in Central and South America with a concomitant 20-fold increase in microcephaly rates in affected parts of Brazil. This association is currently under investigation. The list of countries reporting transmission is evolving and now includes many Caribbean nations. The World Health Organization website has an up to date list of affected nations: http://www.who.int/csr/don/archive/disease/zika-virus-infection/en/ On February 1, 2016 the Director General of the World Health Organization declared that: The recent cluster of microcephaly cases and other neurological disorders reported in Brazil, following a similar cluster in French Polynesia in 2014, constitutes a Public Health Emergency of International Concern. Zika virus and Pregnancy The current outbreak of Zika virus disease in Brazil has occurred simultaneously with a marked increase in the number of infants born with microcephaly and intracranial calcification, compared to previous years. In some of these cases, Zika virus RNA has been isolated from infants with microcephaly and from fetal losses from women infected with the virus. There is limited data on the outcomes of Zika virus infection during pregnancy. At this time there is nothing to suggest that pregnant women are more susceptible or suffer more severe symptoms. Investigations are underway to determine the association between infant microcephaly and maternal Zika virus infection February 11, 2016 Page 2

Transmission Zika virus is a mosquito-borne single-strand RNA flavivirus transmitted by Aedes mosquitoes. This species also transmits dengue and chikungunya viruses. It is a day-biting mosquito with highest activity in the hours just after sunrise and just before sunset. This vector is established in subtropical, tropical, and temperate regions but not in Canada, therefore local transmission here is highly unlikely. Evidence of Zika virus transmission through sexual intercourse is emerging. There is also some evidence for vertical transmission and transmission via blood transfusion (as the virus is known to circulate in the blood for about one week). Currently, no published guidelines or recommendations have been published by the Public Health Agency of Canada or the Centers for Disease Control in Atlanta regarding sexual transmission. Clinical Features An estimated 80% of Zika virus infections are asymptomatic The incubation period ranges from 3 to 12 days Symptoms are usually mild and fatalities are rare Symptoms usually last about 2 to 7 days Symptoms include: o fever (often less than 38.5ºC) o nonpurulent conjunctivitis o maculopapular rash (face and body) o arthralgias Diagnosis Preliminary diagnosis is based on clinical features and a history of travel to an area with Zika virus transmission. Diagnostic tests for Zika virus infection are available through the NL Public Health Laboratory via the National Microbiology Laboratory in Winnipeg. There are two types of testing currently available: 1. Zika virus RT-PCR The test of choice for direct detection of viral RNA Recommended in suspected cases within 7 days of onset of symptoms Submit serum and urine, and, if indicated, cerebrospinal fluid (CSF) Viral RNA in urine may persist up to 10 days or more after symptoms are noted. This may be considered an alternative or additional sample for RT-PCR testing. February 11, 2016 Page 3

o o o Serum is submitted in the yellow/gold serum separator tube (SST) Urine can be submitted in any sterile container CSF (1.0 ml) is in a sterile container (usually the specific CSF tube). Turnaround time for RT PCR is about 2 days. 2. Serology Detection of Zika virus IgG and IgM antibodies at least 4 days after symptom onset Serum samples collected after 7 days can be tested for Zika virus antibody Confirmation of Zika virus-specific antibody in serum samples can be challenging, particularly in the case of previous infection with a related Flavivirus, such as dengue. This is due to the cross-reactivity of diagnostic Flavivirus antibody assays. Turnaround time for serology is about 2-4 weeks. Who should be tested? Any patient with: o a history of travel to an area with Zika virus transmission -ANDo two or more symptoms consistent with Zika virus infection during or within 2 weeks of travel Pregnant women with: o a history of travel to an area with Zika virus transmission -ANDo two or more symptoms consistent with Zika virus infection during or within 2 weeks of travel -ORo ultrasound findings of fetal microcephaly or intracranial calcification Mothers of newborns with microcephaly who have a history of travel to an area with Zika virus transmission Infants: o with microcephaly or intracranial calcifications born to women who traveled to or resided in an area with Zika virus transmission while pregnant ORo born to mothers with positive or inconclusive test results for Zika virus infection February 11, 2016 Page 4

Prevention There is no vaccine and no specific antiviral treatment for Zika virus, therefore prevention is paramount. Travelers are advised to use appropriate measures to protect against mosquito bites. This includes use of repellants, protective clothing, and bed nets. Pregnant women are advised to postpone travel to affected areas. If this is not possible, measures to avoid mosquito bites should be strictly observed. Further information on prevention of mosquito bites can be found at: http://travel.gc.ca/travelling/health-safety/insect-bite On January 28, 2016 Canadian Blood Services has changed its donor criteria to mitigate the risk of Zika virus entering the national blood supply. They are asking all potential donors who have recently travelled to places other than Canada, the continental United States and Europe to donate prior to departure or one month following their return to Canada. For more information: https://www.blood.ca/en/media/changes-to-donor-criteria-planned-due-to-zikavirus Treatment There is no specific treatment for Zika virus infection. Symptomatic treatment with analgesics and fluids will suffice in most cases. Avoidance of acetylsalicylic acid and other nonsteroidal anti-inflammatory drugs is recommended until dengue infection has been excluded. Notifiable Disease Zika virus is a notifiable disease in NL. Areas with Zika Virus Transmission The World Health Organization website has an up to date list of affected nations: http://www.who.int/csr/don/archive/disease/zika-virus-infection/en/ February 11, 2016 Page 5

References Heymann DL. Control of Communicable Diseases Manual. 20th edition. Washington D.C. USA: American Public Health Association, 2015. Musso D, Roche C, Robin E, Nhan T, Teissier A, Cao-Lormeau VM. Potential sexual transmission of Zika virus. Emerg Infect Dis. 2015 Feb;21(2):359-361. Pan American Health Organization. Zika virus infection: step by step guide on Risk Communications and Community Engagement. 2016. Retrieved Febrauary 1, 2016 from http://www.paho.org/hq/index.php?option=com_docman&task=doc_view&itemid=270&gid=33 051&lang=en Petersen EE, Staples JE, Meaney-Delman, D, et al. Interim Guidelines for Pregnant Women During a Zika Virus Outbreak United States, 2016. MMWR Morb Mortal Wkly Rep 2016;65:30 33. DOI: http://dx.doi.org/10.15585/mmwr.mm6502e1 Public Health Agency of Canada. What Health Professionals Need to Know about Zika Virus. January 29, 2016. http://healthycanadians.gc.ca/diseases-conditions-maladies-affections/diseasemaladie/zika-virus/professionals-professionnels-eng.php?id=health_prof World Health Organization. Zika virus factsheet. January 2016. Retrieved February 1, 2016 from http://www.who.int/mediacentre/factsheets/zika/en/ World Health Organization. Zika virus disease: Questions and answers. January 20, 2016. Retrieved February 1, 2016 from http://who.int/features/qa/zika/en/ World Health Organization. WHO Director-General summarizes the outcome of the Emergency Committee regarding clusters of microcephaly and Guillain-Barré syndrome. Retrieved February 2, 2016 from: http://www.who.int/mediacentre/news/statements/2016/emergency-committeezika-microcephaly/en/ February 11, 2016 Page 6