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PRACTICE POINT Zika virus: What does a physician caring for children in Canada need to know? Joan L Robinson; Canadian Paediatric Society Infectious Diseases and Immunization Committee Paediatr Child Health (2017) 22 (1): 48-51. Posted: Mar 30 2017 Abstract Zika virus (ZIKV) was recently recognized to be ter atogenic. The diagnosis of congenital ZIKV syn drome should be considered in children with unex plained microcephaly, intracranial calcifications, ventriculomegaly or major structural central ner vous system abnormalities. Management is evolv ing but suggestions are provided for children with findings compatible with congenital infection and for those born to women with potential exposure during pregnancy. Key words: Congenital infection, Microcephaly, Teratogen, Zika virus EPIDEMIOLOGY Zika virus (ZIKV) is an RNA virus and member of the flavivirus family, which includes West Nile, dengue, Japanese encephalitis, St. Louis encephalitis and yel low fever viruses. ZIKV was first detected in monkeys in 1947 in the Zika Forest, Uganda. A small number of human cases with nonspecific features were docu mented in Africa and Asia over the subsequent 60 years [1]. Then, in 2007, ZIKV infected an estimated 73% of the population of Yap Island in the South Pacif ic [2]. Outbreaks were subsequently recognized in 2013 to 2014 in French Polynesia, the Cook Islands, New Caledonia, and Easter Island [2]. ZIKV was detected in Brazil in 2015 [2] but may have been present there since 2013 [3]. During 2016, locally acquired cases have been documented in most countries in South America and the Caribbean, Mexico, and the USA (in Florida and Texas only, as of March 1, 2017) (see www.cdc.gov/zika/geo/index.html). ZIKV is spread by the bite of Aedes aegypti mosqui toes and less commonly Aedes albopictus, neither of which is known to be established in Canada (see https://elifesciences.org/content/4/e08347 for maps of worldwide Aedes distribution). Because patients are commonly asymptomatic yet viremic, it is not surpris ing that transmission via blood products occurs. ZIKV has been detected in semen for ≥181 days [4] and in female genital secretions for up to 3 weeks [5]; male-tofemale, female-to-male and male-to-male sexual trans mission have been documented (www.cdc.gov/zika/hcproviders/clinical-guidance/sexualtransmission.html). CLINICAL FEATURES The estimated incubation period is 3 to 12 days. Most infections (75% to 80%) are asymptomatic. Common features of symptomatic infections are maculopapular rash (typically pruritic, starting proximally and spread ing to the limbs, with associated edema), low-grade fever, arthralgias (especially of small joints in the hands and feet), myalgias, headache and nonpurulent conjunctivitis. Recovery is usually complete within 3 to 14 days. Features overlap with disease caused by dengue and chikungunya viruses, which are transmit ted by the same mosquitoes. A small number of cases have had unusual features, including myelitis or encephalitis (with detection of ZIKV in cerebrospinal fluid [CSF]) [6], hearing loss, genitourinary symptoms, hematospermia, hypotension [2], thrombotic thrombocytopenia [7] and death [6][8]. Guillain-Barré syndrome (GBS) has been associated with ZIKV infection, with an estimated incidence of 0.24/1000 total cases in French Polynesia [9] and 1.73/1000 symptomatic cases in the USA and US terri tories as of November 16, 2016 [10]. Onset is median only 7 days following initial ZIKV symptoms, with paresthesias and facial palsy possibly being more INFECTIOUS DISEASES AND IMMUNIZATION COMMITTEE, CANADIAN PAEDIATRIC SOCIETY | 1 common than usual [11]. It is not clear whether any cas es have occurred in children. CONGENITAL ZIKV SYNDROME (CZS) ZIKV is neurotropic in mice when injected into the peri toneum [12], but was not suspected to be teratogenic in humans until an unusual cluster of microcephaly was noted in Brazil in 2015. It appears that CZS cases commonly have severe microcephaly, cerebral atro phy, abnormal cortical development, callosal hypopla sia and diffuse subcortical calcifications [13][14]. Micro cephaly with normal brain imaging was described in 0 of 11 [13] and 16 of 27 cases [14]; interpretation of these discordant results is not clear. Head circumference can be normal with ventriculomegaly [13]. Infants with se vere microcephaly from CZS have redundant scalp consistent with fetal brain disruption sequence. Abnor mal fetal tone can result in clubfoot or fetal akinesia deformation sequence (arthrogryposis); the latter was described in 3 of 11 proven [13] and 7 of 104 possible cases [15]. Microphthalmia, cataracts, and retinal ab normalities have been described in a small number of CZS cases [13][16]. Sensorineural hearing loss was doc umented in 5 of 70 cases (7%) [17]. Intrauterine growth retardation is common. A recent review article summarized the features of CZS that distinguish it from other congenital infections as follows: “[1] severe microcephaly with partially col lapsed skull; [2] thin cerebral cortices with subcortical calcifications; [3] macular scarring and focal pigmentary retinal mottling; [4] congenital contractures; and [5] marked early hypertonia and symptoms of extrapyra midal involvement [18].” There are no consistent reports of congenital abnormalities outside of the central ner vous system (CNS). Congenital ZIKV infection without CNS involvement undoubtedly occurs but has not been described to date [19]; presumably such cases would be labelled “congenital ZIKV infection,” rather than CZS. Strong evidence that ZIKV causes CZS emerged from a case-controlled study where ZIKV was detected in the amniotic fluid and/or brain/CSF of fetuses and in fants in 13 of 32 cases and 0 of 62 controls [14]. It is surprising that 60 years elapsed between the first de tection of ZIKV in humans and the recognition that it is teratogenic. One possible explanation for the sudden explosion of cases of CZS is that recent outbreaks are Asian-lineage ZIKV, while the original cases were African-lineage ZIKV. The Asian lineage generates higher level viremia and therefore may more readily in fect a population and cross the placenta [20]. Another theory is that “antibodymediated enhancement” caused by ZIKV interacting with pre-existing dengue virus antibodies, which are common in Brazilians, led to teratogenicity [21]. The incidence and risk of CZS with ZIKV infection dur ing pregnancy are unknown. Most, but not all mothers of infants with CZS recalled a rash during pregnancy [13][19]. Microcephaly occurred in an estimated 0.76% to 1.27% of infants born to women with first trimester ZIKV in French Polynesia [22]. A study from Brazil esti mated 1% to 13% risk, depending on the ZIKV infec tion rate and the degree of overreporting of micro cephaly [23]. More alarming data reported abnormal inutero ultrasounds in 13 of 45 cases of ZIKV during pregnancy in Brazil (29%) [24]. CZS has been de scribed mainly with first trimester infection but also with second and third trimester infection [13][19]. There are two reports of subependymal cysts and lenticulostriate vasculopathy (findings suggestive of injury to the de veloping brain) on postnatal ultrasound following ma ternal infection at 36 weeks gestation; one of the in fants affected had ZIKV detected in urine [25]. Perinatal transmission appears to be benign. It was documented in two infants; one had a rash and the other was asymptomatic [26]. DIAGNOSIS Diagnosis is by: 1. Serology (IgM or IgG or neutralizing antibody) or 2. Detection of ZIKV RNA by polymerase reaction (PCR) testing. IgM becomes positive about 7 days following symptom onset, with IgG appearing about 3 days later [27]. IgG presumably persists indefinitely. It is estimated that IgM persists 3 months [27]. Both IgM and IgG can crossreact with other flaviviruses and therefore must be confirmed to be ZIKV antibodies by a plaque reduc tion neutralization test (PRNT). If PRNT titres for both dengue and ZIKV are identified, the result will be as sessed as “indeterminate.” Current testing in Canada consists only of IgM with PRNT done when IgM is pos itive or when IgM is negative but the requisition clari fies that exposure is remote. PCR testing on blood is usually only positive during the first 4 days of symptoms [27]. However, viremia persist ed for ≥71 days in one pregnant woman [28] and ≥67 days in CZS [29], possibly because fetuses have pro longed viremia from immature immune systems; ZIKV crosses the placenta, yielding persistent maternal 2 | ZIKA VIRUS: WHAT DOES A PHYSICIAN CARING FOR CHILDREN IN CANADA NEED TO KNOW? viremia. PCR on urine is usually positive on days 2 through 9 following symptom onset [27]. See Figures 1 and 2 for guidance on testing in different scenarios or with positive laboratory results. Figure 1. Investigating infants or children with features suggestive of congenital Zika syndrome. 1Negative maternal ZIKV serology more than 4 weeks after exposure rules out ZIKV infection and congenital ZIKV infection. However, since one may wait weeks for re sults, sending specimens for PCR and testing the child simultaneously is advised. Assuming that the child has not travelled to a ZIKV-endemic country, they should only have positive ZIKV serology if the mother tests positive. Discuss with an ID physician or microbiologist if results are positive only from the child. CMV cytomegalovirus; CNS central nervous system; CSF cerebrospinal fluid; ID infectious diseases; IgM Immune globulin; LCMV lymphocytic choriomeningitis virus; MRI magnetic resonance imaging; PCR polymerase chain reaction; PRNT plaque reduction neutralization test; U/S ultrasound; ZIKV Zika virus INFECTIOUS DISEASES AND IMMUNIZATION COMMITTEE, CANADIAN PAEDIATRIC SOCIETY | 3 Figure 2. Management of infants born to women with potential exposure to ZIKV during pregnancy. 4 | ZIKA VIRUS: WHAT DOES A PHYSICIAN CARING FOR CHILDREN IN CANADA NEED TO KNOW? 1Travel to a ZIKV-endemic country during pregnancy or sexual contact during pregnancy with a male who travelled to a ZIKV-endemic country in the preceding 6 months. CMV cytomegalovirus; ID infectious diseases; IgM immune globulin; MRI magnetic resonance imaging; PCR polymerase chain reaction; ZIKV Zika virus. Delayed onset of hearing loss is well described in in fants with congenital rubella or cytomegalovirus who are asymptomatic at birth; there may also be late se quelae with congenital ZIKV infection. Therefore, all women with potential ZIKV exposure during pregnancy should be identified. When the exposure is noted only after delivery, ZIKV serology should be requested on the mother or infant. The algorithm in Figure 2 is fol lowed when results are positive or indeterminate. Testing is generally not advised for asymptomatic or symptomatic children with exposure to ZIKV after birth, unless they require hospitalization. However, when considering testing a febrile traveller for arboviruses, add ZIKV if appropriate. Travel history should be as certained from all children with GBS. PREVENTION There is no treatment for ZIKV infections. Several vac cines are in development and may be licensed as early as 2018. Travellers to areas with ZIKV should use per sonal protective measures (i.e., bed nets, appropriate clothing and mosquito repellents) to prevent mosquito bites day and night, both inside and outside (See www.cps.ca/documents/position/preventing-mosquitoand-tick-bites and www.phac-aspc.gc.ca/publicat/ccdrrmtc/12vol38/acs-dcc-3/index-eng.php). Those who are or may become pregnant and their sexual partners should avoid travel to affected areas, where practical (https://travel.gc.ca/travelling/advisories). Although ZIKV RNA has been detected in breast milk, the virus is not thought to be infectious. However, some experts advise caution with breastfeeding during acute ZIKV infection. There was a case of transmis sion from a dying elderly man with very high grade viremia to his son [10], but nonsexual person-to-person transmission appears to be rare. However, routine in fection control precautions always apply. Pending more data on transmission, pregnant women should employ meticulous hand hygiene when they have di rect contact with infants with congenital ZIKV infection. For more detail (particularly about adults), see www.phac-aspc.gc.ca/publicat/ccdr-rmtc/16vol42/drrm42-5/ar-01-eng.php? id=zika_virus_16_phac_catmat. Acknowledgements This practice point was reviewed by the Fetus and Newborn and Community Paediatrics Committees of the Canadian Paediatric Society, as well as by the CPS Developmental Paediatrics Section executive. It has also been reviewed by investigators for the Cana dian Paediatric Surveillance Program (CPSP) Severe Microcephaly Study. References 1. Posen HJ, Keystone JS, Gubbay JB, Morris SK. Epi demiology of Zika virus, 1947–2007. BMJ Global Health 2016;1(2):e00087. http://gh.bmj.com/content/1/2/ e000087 (Accessed December 1, 2016). 2. Plourde AR , Block EM. A literature review of Zika virus. Emerg Infect Dis 2016;22(7):1185–92. 3. Faria NR , Azevedo RS, Kraemer MU, et al. Zika virus in the Americas: Early epidemiological and genetic find ings. Science 2016;352(6283):345–9. 4. Barzon L, Pacenti M, Franchin E, et al. Infection dynam ics in a traveller with persistent shedding of Zika virus RNA in semen for six months after returning from Haiti to Italy, January 2016. Euro Surveill 2016;21(32). 5. Prisant N, Breurec S, Moriniere C, Bujan L, Joguet G. Zika virus genital tract shedding in infected women of childbearing age. Clin Infect Dis 2017;64(1):107–9. 6. Soares CN, Brasil P, Carrera RM, et al. Fatal encephali tis associated with Zika virus infection in an adult. J Clin Virol 2016;83:63–5. 7. Chraïbi S, Najioullah F, Bourdin C, et al. Two cases of thrombocytopenic purpura at onset of Zika virus infec tion. J Clin Virol 2016;83:61–2. 8. Swaminathan S, Schlaberg R , Lewis J, Hanson KE, Couturier MR . Fatal Zika virus infection with secondary nonsexual transmission. N Engl J Med 2016;375(19): 1907–9. 9. Cao-Lormeau VM, Blake A, Mons S, et al. Guillain-Barre syndrome outbreak associated with Zika virus infection in French Polynesia: A case-control study. Lancet 2016;387(10027):1531–9. 10. Centers for Disease Control and Prevention. Zika virus/ Case counts in the U.S. (as of November 23, 2016): http://www.cdc.gov/zika/geo/united-states.html (Ac cessed December 1, 2016). 11. Parra B, Lizarazo J, Jiménez-Arango JA, et al. GuillainBarré syndrome associated with Zika virus infection in Colombia. N Engl J Med 2016; 37(16)5:1513–23. 12. Dick GW. Zika virus. II. Pathogenicity and physical prop erties. Trans R Soc Trop Med Hyg 1952;46(5):521–34. INFECTIOUS DISEASES AND IMMUNIZATION COMMITTEE, CANADIAN PAEDIATRIC SOCIETY | 5 13. Melo AS, Aguiar RS, Amorim MM, et al. Congenital Zika virus infection: Beyond neonatal microcephaly. JAMA Neurol 2016;73(12):1407–16. 14. de Araújo TV, Rodrigues LC, de Alencar Ximenes RA, et al. Association between Zika virus infection and micro cephaly in Brazil, January to May, 2016: Preliminary re port of a case-control study. Lancet Infect Dis 2016;16(12):1356–63. 15. van der Linden V, Filho EL, Lins OG, et al. Congenital Zika syndrome with arthrogryposis: Retrospective case series study. BMJ 2016;354:i3899. doi: 10.1136/ bmj.i3899. 16. Ventura CV, Maia M, Bravo-Filho V, Góis AL, Belfort R , Jr. Zika virus in Brazil and macular atrophy in a child with microcephaly. Lancet 2016;387(10015):228. 17. Leal MC, Muniz LF, Ferreira TS, et al. Hearing loss in in fants with microcephaly and evidence of congenital Zika virus infection – Brazil, November 2015-May 2016. MMWR Morb Mortal Wkly Rep 2016;65(34):917–9. 18. Moore CA, Staples JE, Dobyns WB, et al. Characteriz ing the pattern of anomalies in congenital Zika syn drome for pediatric clinicians. JAMA Pediatr 2016 Nov 3. doi: 10.1001/jamapediatrics.2016.3982. [Epub ahead of print]. 19. França GV, Schuler-Faccini L, Oliveira WK, et al. Con genital Zika virus syndrome in Brazil: A case series of the first 1501 livebirths with complete investigation. Lancet 2016;388(10047):891–7. 20. Russell PK. The Zika pandemic – A perfect storm? PLoS Negl Trop Dis 2016;10(3):e0004589. doi:10.1371/ journal.pntd.0004589. 21. Durbin AP. Dengue antibody and Zika: Friend or foe? Trends Immunol 2016;37(10):635–36. 22. Cauchemez S, Besnard M, Bompard P, et al. Associa tion between Zika virus and microcephaly in French Polynesia, 2013–15: A retrospective study. Lancet 2016;387(10033):2125–32. 23. Johannsson MA, Mier-y-Teran-Romero L, Reefhuis J, Gilboa SM, Hills SL. Zika and the risk of microcephaly. N Engl J Med 2016;375(1):1–4. 24. Brasil P, Pereira JP, Jr., Raja Gabaglia C, et al. Zika virus infection in pregnant women in Rio de Janeiro – 25. 26. 27. 28. 29. Preliminary report. N Engl J Med 2016;375(24):2321– 34. Soares de Souza A, Moraes Dias C, Braga FD, et al. Fetal infection by Zika virus in the third trimester: Report of 2 cases. Clin Infect Dis 2016;63(12):1622–25. Besnard M, Lastere S, Teissier A, et al. Evidence of perinatal transmission of Zika virus, French Polynesia, December 2013 and February 2014. Euro Surveill 2014;19(13)pii: 20751. Atif M, Azeem M, Sarwar MR , Bashir A. Zika virus dis ease: A current review of the literature. Infection 2016;44(6):695–705. Driggers RW, Ho CY, Korhonen EM, et al. Zika virus in fection with prolonged maternal viremia and fetal brain abnormalities. N Engl J Med 2016;374(22):2142–51. Oliveira DB, Almeida FJ, Durigon EL, et al. Prolonged shedding of Zika virus associated with congenital infec tion. N Engl J Med 2016;375(12):1202–4. CPS INFECTIOUS DISEASES AND IMMUNIZATION COMMITTEE Members: Natalie A Bridger MD; Shalini Desai MD; Ruth Grimes MD (Board Representative); Timothy Mailman MD; Joan L Robinson MD (Chair); Marina Salvadori MD (past member); Otto G Vanderkooi MD Liaisons:Upton D Allen MBBS, Canadian Pediatric AIDS Research Group; Tobey Audcent MD, Committee to Advise on Tropical Medicine and Travel (CATMAT), Public Health Agency of Canada; Carrie Byington MD, Committee on Infectious Diseases, American Academy of Pediatrics; Nicole Le Saux MD, Immunization Monitoring Program, ACTive (IMPACT); Fahamia Koudra MD, College of Family Physicians of Canada; Rhonda Kropp BScN MPH, Public Health Agency of Canada; Jane McDonald MD, Association of Medical Microbiology and Infectious Disease Canada; Dorothy L Moore MD, National Advisory Committee on Immunization (NACI) Consultant: Noni E MacDonald MD Principal author: Joan L Robinson MD Also available at www.cps.ca/en © Canadian Paediatric Society 2017 The Canadian Paediatric Society gives permission to print single copies of this document from our website. to reprint or reproduce copies, please see our policy.IN CANADA NEED TO KNOW? 6For |permission ZIKA VIRUS: WHAT DOES Amultiple PHYSICIAN CARING FORcopyright CHILDREN Disclaimer: The recommendations in this position statement do not indicate an exclusive course of treatment or procedure to be followed. Variations, taking in to account individual circumstances, may be appropriate. Internet addresses are current at time of publication.