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Table  

Zika-related outcomes Any laboratory evidence of confirmed or possible Zika virus infection during pregnancy (n = 1,450) No. (%) Pregnancies with nucleic acid test-confirmed Zika virus infection (n = 943)§ No. (%)
Zika-associated birth defect 87 (6) 62 (7)
Neurodevelopmental abnormality possibly associated with congenital Zika virus infection** 136 (9) 99 (10)
Zika-associated birth defect and neurodevelopmental abnormality possibly associated with congenital Zika virus infection 20 (1) 17 (2)
Total with Zika-associated birth defect, neurodevelopmental abnormality possibly associated with congenital Zika virus infection, or both 203 (14) 144 (15)
Microcephaly
Microcephaly at birth†† 64 (4) 44 (5)
Postnatal-onset microcephaly only§§ 20 (1) 12 (1)
Total with microcephaly 84 (6) 56 (6)

Outcomes among children aged ≥1 year from pregnancies with any laboratory evidence of confirmed or possible Zika virus infection (n = 1,450) and with nucleic acid test-confirmed Zika virus infection (n = 943) and with reported follow-up care* — U.S. Zika Pregnancy and Infant Registry (USZPIR), U.S. territories and freely associated states, February 1, 2017-June 1, 2018

* Any clinical care at age >14 days reported to the USZPIR.
Includes maternal, placental, or infant laboratory evidence of confirmed or possible Zika virus infection during pregnancy based on presence of Zika virus RNA by a positive nucleic acid test (e.g., reverse transcription-polymerase chain reaction [RT-PCR]), serologic evidence of a Zika virus infection, or serologic evidence of an unspecified flavivirus infection.
§ Includes maternal, placental, or infant laboratory evidence of confirmed Zika virus infection during pregnancy based on presence of Zika virus RNA by a positive nucleic acid test (e.g., RT-PCR).
Includes Zika-associated birth defect detected from birth to age 2 years with or without neurodevelopmental abnormality possibly associated with congenital Zika virus infection. Zika-associated birth defects include selected congenital brain anomalies (intracranial calcifications; cerebral atrophy; abnormal cortical formation; corpus callosum abnormalities; cerebellar abnormalities; porencephaly; hydranencephaly; ventriculomegaly/hydrocephaly); selected congenital eye anomalies (microphthalmia or anophthalmia; coloboma; cataract; intraocular calcifications; chorioretinal anomalies involving the macula, excluding retinopathy of prematurity; and optic nerve atrophy, pallor, and other optic nerve abnormalities); and/or microcephaly at birth (birth head circumference <3rd percentile for infant sex and gestational age based on INTERGROWTH-21st online percentile calculator (http://intergrowth21.ndog.ox.ac.uk/)).
** Includes neurodevelopmental abnormality possibly associated with congenital Zika virus infection detected from birth to age 2 years, with or without Zika-associated birth defect. Neurodevelopmental abnormalities possibly associated with congenital Zika virus infection include hearing abnormalities; congenital contractures; seizures; body tone abnormalities; movement abnormalities; swallowing abnormalities; possible developmental delay; possible visual impairment; and/or postnatal-onset microcephaly (two most recent head circumference measurements reported from follow-up care <3rd percentile for child's sex and age based on World Health Organization child growth standards; downward trajectory of head circumference percentiles with most recent <3rd percentile. Age at measurement was adjusted for gestational age in infants born at <40 weeks' gestational age, through age 24 months chronological age).
†† Microcephaly at birth is a subset of Zika-associated birth defects and was defined as birth head circumference <3rd percentile for infant sex and gestational age based on INTERGROWTH-21st online percentile calculator (http://intergrowth21.ndog.ox.ac.uk/)).
§§ Postnatal-onset microcephaly is a subset of neurodevelopmental abnormalities possibly associated with congenital Zika virus infection and was defined as two most recent head circumference measurements reported from follow-up care <3rd percentile for child's sex and age based on World Health Organization child growth standards; downward trajectory of head circumference percentiles with most recent <3rd percentile. Age at measurement was adjusted for gestational age in infants born at <40 weeks' gestational age, through age 24 months chronological age).

Box  

Zika-associated birth defects: Selected structural anomalies of the brain or eyes present at birth (congenital) and detected from birth to age 2 years. Microcephaly at birth, with or without low birthweight, was included as a structural anomaly.
  • Selected congenital brain anomalies: intracranial calcifications; cerebral atrophy; abnormal cortical formation (e.g., polymicrogyria, lissencephaly, pachygyria, schizencephaly, gray matter heterotopia); corpus callosum abnormalities; cerebellar abnormalities; porencephaly; hydranencephaly; ventriculomegaly/hydrocephaly.
  • Selected congenital eye anomalies: microphthalmia or anophthalmia; coloboma; cataract; intraocular calcifications; chorioretinal anomalies involving the macula (e.g., chorioretinal atrophy and scarring, macular pallor, and gross pigmentary mottling), excluding retinopathy of prematurity; optic nerve atrophy, pallor, and other optic nerve abnormalities.
  • Microcephaly at birth: birth head circumference <3rd percentile for infant sex and gestational age based on INTERGROWTH-21st online percentile calculator (http://intergrowth21.ndog.ox.ac.uk/).
Neurodevelopmental abnormalities possibly associated with congenital Zika virus infection: Consequences of neurologic dysfunction detected from birth (congenital) to age 2 years. Postnatal-onset microcephaly was included as a neurodevelopmental abnormality.
  • Hearing abnormalities: Hearing loss or deafness documented by testing, most frequently auditory brainstem response (ABR). Includes sensorineural hearing loss, mixed hearing loss, and hearing loss not otherwise specified. Failed newborn hearing screen is not sufficient for diagnosis.
  • Congenital contractures: Multiple contractures (arthrogryposis) and isolated clubfoot documented at birth. Brain anomalies must be documented for isolated clubfoot, but not for arthrogryposis.
  • Seizures: Documented by electroencephalogram or physician report. Includes epilepsy or seizures not otherwise specified; excludes febrile seizures.
  • Body tone abnormalities: Hypertonia or hypotonia documented at any age in conjunction with 1) a failed screen or assessment for gross motor function; 2) suspicion or diagnosis of cerebral palsy from age 1 year to age 2 years; or 3) assessment by a physician or other medical professional, such as a physical therapist.
  • Movement abnormalities: Dyskinesia or dystonia at any age; suspicion or diagnosis of cerebral palsy from age 1 year to age 2 years.
  • Swallowing abnormalities: Documented by instrumented or noninstrumented evaluation, presence of a gastrostomy tube, or physician report.
  • Possible developmental delay: Abnormal result from most recent developmental screening (i.e., failed screen for gross motor domain or failed screen for ≥2 developmental domains at the same time point or age); developmental evaluation; or assessment review by developmental pediatrician. Results from developmental evaluation are considered the gold standard if available.
  • Possible visual impairment: Includes strabismus (esotropia or exotropia), nystagmus, failure to fix and follow at age <1 year; diagnosis of visual impairment at age ≥1 year.
  • Postnatal-onset microcephaly: Two most recent head circumference measurements reported from follow-up care <3rd percentile for child's sex and age based on World Health Organization child growth standards; downward trajectory of head circumference percentiles with most recent measurement <3rd percentile. Age at measurement was adjusted for gestational age in infants born at <40 weeks' gestational age through age 24 months chronological age.

Surveillance case classification — children, neonate to 2 years of age, born to mothers with any evidence of Zika virus infection during pregnancy

CME / CE

Vital Signs: Zika-Associated Birth Defects and Neurodevelopmental Abnormalities Possibly Associated With Congenital Zika Virus Infection — US Territories and Freely Associated States, 2018

  • Authors: Marion E. Rice, MPH; Romeo R. Galang, MD; Nicole M. Roth, MPH; Sascha R. Ellington, MSPH; Cynthia A. Moore, MD, PhD; Miguel Valencia-Prado, MD; Esther M. Ellis, PhD; Aifili John Tufa, MPH; Livinson A. Taulung, DCHMS; Julia M. Alfred; Janice Pérez-Padilla, MPH; Camille A. Delgado-López, MPH; Sherif R. Zaki, MD; Sarah Reagan-Steiner, MD; Julu Bhatnagar, PhD; John F. Nahabedian III, MS; Megan R. Reynolds, MPH; Marshalyn Yeargin-Allsopp, MD; Laura J. Viens, MD; Samantha M. Olson, MPH; Abbey M. Jones, MPH; Madelyn A. Baez-Santiago, PhD; Philip Oppong-Twene, MBChB; Kelley VanMaldeghem, MPH; Elizabeth L. Simon, MPH; Jazmyn T. Moore, MPH; Kara D. Polen, MPH; Braeanna Hillman, MPH; Ruta Ropeti; Leishla Nieves-Ferrer, MS; Mariam Marcano-Huertas; Carolee A. Masao, DCHMS; Edlen J. Anzures; Ransen L. Hansen, Jr; Stephany I. Pérez-Gonzalez, MPH; Carla P. Espinet-Crespo, MPH; Mildred Luciano-Román; Carrie K. Shapiro-Mendoza, PhD; Suzanne M. Gilboa, PhD; Margaret A. Honein, PhD
  • CME / CE Released: 10/2/2018
  • THIS ACTIVITY HAS EXPIRED FOR CREDIT
  • Valid for credit through: 10/2/2019, 11:59 PM EST
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Target Audience and Goal Statement

This activity is intended for obstetricians/ gynecologists, infectious disease clinicians, neurologists, nurses, pediatricians, psychiatrists, public health officials, and other clinicians caring for children born to mothers exposed to Zika virus during pregnancy.

Clinicians will become aware of the frequency and type of birth defects and neurodevelopmental abnormalities seen among children born to mothers with laboratory evidence of possible Zika virus infection.

Upon completion of this activity, participants will be able to:

  1. Describe the frequency of Zika-associated birth defects and/or neurodevelopmental abnormalities possibly associated with congenital Zika virus infection in infants born to mothers with laboratory evidence of possible Zika virus infection reported to the US Zika Pregnancy and Infant Registry (USZPIR)
  2. Explain clinical and public health implications of these findings from USZPIR regarding Zika-associated birth defects and/or neurodevelopmental abnormalities in infants born to mothers with laboratory evidence of possible Zika virus infection
  3. Determine potential limitations of these findings from USZPIR regarding Zika-associated birth defects and/or neurodevelopmental abnormalities in infants born to mothers with laboratory evidence of possible Zika virus infection


Disclosures

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Medscape, LLC, encourages Authors to identify investigational products or off-label uses of products regulated by the US Food and Drug Administration, at first mention and where appropriate in the content.


Authors

  • Marion E. Rice, MPH

    Division of Congenital and Developmental Disorders, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention (CDC), Atlanta, Georgia; Oak Ridge Institute for Science and Education, Oak Ridge, Tennessee

    Disclosures

    Disclosure: Marion E. Rice, MPH, has disclosed no relevant financial relationships.

  • Romeo R. Galang, MD

    Division of Congenital and Developmental Disorders, National Center on Birth Defects and Developmental Disabilities, CDC, Atlanta, Georgia

    Disclosures

    Disclosure: Romeo R. Galang, MD, has disclosed no relevant financial relationships.

  • Nicole M. Roth, MPH

    Division of Congenital and Developmental Disorders, National Center on Birth Defects and Developmental Disabilities, CDC, Atlanta, Georgia

    Disclosures

    Disclosure: Nicole M. Roth, MPH, has disclosed no relevant financial relationships.

  • Sascha R. Ellington, MSPH

    Division of Reproductive Health, National Center for Chronic Disease Prevention and Health Promotion, CDC, Atlanta, Georgia

    Disclosures

    Disclosure: Sascha R. Ellington, MSPH, has disclosed no relevant financial relationships.

  • Cynthia A. Moore, MD, PhD

    Division of Congenital and Developmental Disorders, National Center on Birth Defects and Developmental Disabilities, CDC, Atlanta, Georgia

    Disclosures

    Disclosure: Cynthia A. Moore, MD, PhD, has disclosed no relevant financial relationships.

  • Miguel Valencia-Prado, MD

    Puerto Rico Department of Health, San Juan, Puerto Rico

    Disclosures

    Disclosure: Miguel Valencia-Prado, MD, has disclosed no relevant financial relationships.

  • Esther M. Ellis, PhD

    US Virgin Islands Department of Health, St Croix, US Virgin Islands

    Disclosures

    Disclosure: Esther M. Ellis, PhD, has disclosed no relevant financial relationships.

  • Aifili John Tufa, MPH

    American Samoa Department of Health, Pago Pago, American Samoa

    Disclosures

    Disclosure: Aifili John Tufa, MPH, has disclosed no relevant financial relationships.

  • Livinson A. Taulung, DCHMS

    Kosrae Department of Health Services, Port Vila, Vanuatu, Federated States of Micronesia

    Disclosures

    Disclosure: Livinson A. Taulung, DCHMS, has disclosed no relevant financial relationships.

  • Julia M. Alfred

    Republic of Marshall Islands Ministry of Health and Human Services, Delap, Majuro, Marshall Islands

    Disclosures

    Disclosure: Julia M. Alfred has disclosed no relevant financial relationships.

  • Janice Pérez-Padilla, MPH

    Division of Vector-Borne Diseases, National Center for Emerging and Zoonotic Infectious Diseases, CDC, Atlanta, Georgia

    Disclosures

    Disclosure: Janice Pérez-Padilla, MPH, has disclosed no relevant financial relationships.

  • Camille A. Delgado-López, MPH

    Puerto Rico Department of Health, San Juan, Puerto Rico

    Disclosures

    Disclosure: Camille A. Delgado-López, MPH, has disclosed no relevant financial relationships.

  • Sherif R. Zaki, MD

    Division of High-Consequence Pathogens and Pathology, National Center for Emerging and Zoonotic Infectious Diseases, CDC, Atlanta, Georgia

    Disclosures

    Disclosure: Sherif R. Zaki, MD, has disclosed no relevant financial relationships.

  • Sarah Reagan-Steiner, MD

    Division of High-Consequence Pathogens and Pathology, National Center for Emerging and Zoonotic Infectious Diseases, CDC, Atlanta, Georgia

    Disclosures

    Disclosure: Sarah Reagan-Steiner, MD, has disclosed no relevant financial relationships.

  • Julu Bhatnagar, PhD

    Division of High-Consequence Pathogens and Pathology, National Center for Emerging and Zoonotic Infectious Diseases, CDC, Atlanta, Georgia

    Disclosures

    Disclosure: Julu Bhatnagar, PhD, has disclosed no relevant financial relationships.

  • John F. Nahabedian III, MS

    Division of Congenital and Developmental Disorders, National Center on Birth Defects and Developmental Disabilities, CDC, Atlanta, Georgia

    Disclosures

    Disclosure: John F. Nahabedian III, MS, has disclosed no relevant financial relationships.

  • Megan R. Reynolds, MPH

    Division of Congenital and Developmental Disorders, National Center on Birth Defects and Developmental Disabilities, CDC, Atlanta, Georgia

    Disclosures

    Disclosure: Megan R. Reynolds, MPH, has disclosed no relevant financial relationships.

  • Marshalyn Yeargin-Allsopp, MD

    Division of Congenital and Developmental Disorders, National Center on Birth Defects and Developmental Disabilities, CDC, Atlanta, Georgia

    Disclosures

    Disclosure: Marshalyn Yeargin-Allsopp, MD, has disclosed no relevant financial relationships.

  • Laura J. Viens, MD

    Division of Congenital and Developmental Disorders, National Center on Birth Defects and Developmental Disabilities, CDC, Atlanta, Georgia

    Disclosures

    Disclosure: Laura J. Viens, MD, has disclosed no relevant financial relationships.

  • Samantha M. Olson, MPH

    Division of Congenital and Developmental Disorders, National Center on Birth Defects and Developmental Disabilities, CDC, Atlanta, Georgia

    Disclosures

    Disclosure: Samantha M. Olson, MPH, has disclosed no relevant financial relationships.

  • Abbey M. Jones, MPH

    Division of Congenital and Developmental Disorders, National Center on Birth Defects and Developmental Disabilities, CDC, Atlanta, Georgia

    Disclosures

    Disclosure: Abbey M. Jones, MPH, has disclosed no relevant financial relationships.

  • Madelyn A. Baez-Santiago, PhD

    Division of Congenital and Developmental Disorders, National Center on Birth Defects and Developmental Disabilities, CDC, Atlanta, Georgia

    Disclosures

    Disclosure: Madelyn A. Baez-Santiago, PhD, has disclosed no relevant financial relationships.

  • Philip Oppong-Twene, MBChB

    Division of Congenital and Developmental Disorders, National Center on Birth Defects and Developmental Disabilities, CDC, Atlanta, Georgia

    Disclosures

    Disclosure: Philip Oppong-Twene, MBChB, has disclosed no relevant financial relationships.

  • Kelley VanMaldeghem, MPH

    Division of Congenital and Developmental Disorders, National Center on Birth Defects and Developmental Disabilities, CDC, Atlanta, Georgia

    Disclosures

    Disclosure: Kelley VanMaldeghem, MPH, has disclosed no relevant financial relationships.

  • Elizabeth L. Simon, MPH

    Division of Congenital and Developmental Disorders, National Center on Birth Defects and Developmental Disabilities, CDC Atlanta, Georgia

    Disclosures

    Disclosure: Elizabeth L. Simon, MPH, has disclosed no relevant financial relationships.

  • Jazmyn T. Moore, MPH

    Division of Congenital and Developmental Disorders, National Center on Birth Defects and Developmental Disabilities, CDC, Atlanta, Georgia

    Disclosures

    Disclosure: Jazmyn T. Moore, MPH, has disclosed no relevant financial relationships.

  • Kara D. Polen, MPH

    Division of Congenital and Developmental Disorders, National Center on Birth Defects and Developmental Disabilities, CDC, Atlanta, Georgia

    Disclosures

    Disclosure: Kara D. Polen, MPH, has disclosed no relevant financial relationships.

  • Braeanna Hillman, MPH

    U.S. Virgin Islands Department of Health

    Disclosures

    Disclosure: Braeanna Hillman, MPH, has disclosed no relevant financial relationships.

  • Ruta Ropeti

    American Samoa Department of Health, Pago Pago, American Samoa

    Disclosures

    Disclosure: Ruta Ropeti has disclosed no relevant financial relationships.

  • Leishla Nieves-Ferrer, MS

    Puerto Rico Department of Health, San Juan, Puerto Rico

    Disclosures

    Disclosure: Leishla Nieves-Ferrer, MS, has disclosed no relevant financial relationships.

  • Mariam Marcano-Huertas

    Puerto Rico Department of Health, San Juan, Puerto Rico

    Disclosures

    Disclosure: Mariam Marcano-Huertas has disclosed no relevant financial relationships.

  • Carolee A. Masao, DCHMS

    Kosrae Department of Health Services, Port Vila, Vanuatu, Federated States of Micronesia

    Disclosures

    Disclosure: Carolee A. Masao, DCHMS, has disclosed no relevant financial relationships.

  • Edlen J. Anzures

    Republic of Marshall Islands Ministry of Health and Human Services, Delap, Majuro, Marshall Islands

    Disclosures

    Disclosure: Edlen J. Anzures has disclosed no relevant financial relationships.

  • Ransen L. Hansen, Jr.

    Republic of Marshall Islands Ministry of Health and Human Services, Delap, Majuro, Marshall Islands

    Disclosures

    Disclosure: Ransen L. Hansen, Jr, has disclosed no relevant financial relationships.

  • Stephany I. Pérez-Gonzalez, MPH

    Puerto Rico Department of Health, San Juan, Puerto Rico

    Disclosures

    Disclosure: Stephany I. Pérez-Gonzalez, MPH, has disclosed no relevant financial relationships.

  • Carla P. Espinet-Crespo, MPH

    Puerto Rico Department of Health, San Juan, Puerto Rico

    Disclosures

    Disclosure: Carla P. Espinet-Crespo, MPH, has disclosed no relevant financial relationships.

  • Mildred Luciano-Román

    Puerto Rico Department of Health, San Juan, Puerto Rico

    Disclosures

    Disclosure: Mildred Luciano-Román has disclosed no relevant financial relationships.

  • Carrie K. Shapiro-Mendoza, PhD

    Division of Reproductive Health, National Center for Chronic Disease Prevention and Health Promotion, CDC, Atlanta, Georgia

    Disclosures

    Disclosure: Carrie K. Shapiro-Mendoza, PhD, has disclosed no relevant financial relationships.

  • Suzanne M. Gilboa, PhD

    Division of Congenital and Developmental Disorders, National Center on Birth Defects and Developmental Disabilities, CDC, Atlanta, Georgia

    Disclosures

    Disclosure: Suzanne M. Gilboa, PhD, has disclosed no relevant financial relationships.

  • Margaret A. Honein, PhD

    Division of Congenital and Developmental Disorders, National Center on Birth Defects and Developmental Disabilities, CDC, Atlanta, Georgia

    Disclosures

    Disclosure: Margaret A. Honein, PhD, has disclosed no relevant financial relationships.

CME Author(s)

  • Laurie Barclay, MD

    Freelance writer and reviewer, Medscape, LLC

    Disclosures

    Disclosure: Laurie Barclay, MD, has disclosed the following relevant financial relationships:
    Owns stock, stock options, or bonds from: Pfizer

CME Reviewer(s)

  • Amy Bernard, MS, BSN, RN-BC, CHCP

    Lead Nurse Planner, Medscape, LLC

    Disclosures

    Disclosure: Amy Bernard, MS, BSN, RN-BC, CHCP, has disclosed no relevant financial relationships.


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CME / CE

Vital Signs: Zika-Associated Birth Defects and Neurodevelopmental Abnormalities Possibly Associated With Congenital Zika Virus Infection — US Territories and Freely Associated States, 2018

Authors: Marion E. Rice, MPH; Romeo R. Galang, MD; Nicole M. Roth, MPH; Sascha R. Ellington, MSPH; Cynthia A. Moore, MD, PhD; Miguel Valencia-Prado, MD; Esther M. Ellis, PhD; Aifili John Tufa, MPH; Livinson A. Taulung, DCHMS; Julia M. Alfred; Janice Pérez-Padilla, MPH; Camille A. Delgado-López, MPH; Sherif R. Zaki, MD; Sarah Reagan-Steiner, MD; Julu Bhatnagar, PhD; John F. Nahabedian III, MS; Megan R. Reynolds, MPH; Marshalyn Yeargin-Allsopp, MD; Laura J. Viens, MD; Samantha M. Olson, MPH; Abbey M. Jones, MPH; Madelyn A. Baez-Santiago, PhD; Philip Oppong-Twene, MBChB; Kelley VanMaldeghem, MPH; Elizabeth L. Simon, MPH; Jazmyn T. Moore, MPH; Kara D. Polen, MPH; Braeanna Hillman, MPH; Ruta Ropeti; Leishla Nieves-Ferrer, MS; Mariam Marcano-Huertas; Carolee A. Masao, DCHMS; Edlen J. Anzures; Ransen L. Hansen, Jr; Stephany I. Pérez-Gonzalez, MPH; Carla P. Espinet-Crespo, MPH; Mildred Luciano-Román; Carrie K. Shapiro-Mendoza, PhD; Suzanne M. Gilboa, PhD; Margaret A. Honein, PhDFaculty and Disclosures
THIS ACTIVITY HAS EXPIRED FOR CREDIT

CME / CE Released: 10/2/2018

Valid for credit through: 10/2/2019, 11:59 PM EST

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Abstract and Introduction

Abstract

Introduction: Zika virus infection during pregnancy causes serious birth defects and might be associated with neurodevelopmental abnormalities in children. Early identification of and intervention for neurodevelopmental problems can improve cognitive, social, and behavioral functioning.

Methods: Pregnancies with laboratory evidence of confirmed or possible Zika virus infection and infants resulting from these pregnancies are included in the U.S. Zika Pregnancy and Infant Registry (USZPIR) and followed through active surveillance methods. This report includes data on children aged ≥1 year born in U.S. territories and freely associated states. Receipt of reported follow-up care was assessed, and data were reviewed to identify Zika-associated birth defects and neurodevelopmental abnormalities possibly associated with congenital Zika virus infection.

Results: Among 1,450 children of mothers with laboratory evidence of confirmed or possible Zika virus infection during pregnancy and with reported follow-up care, 76% had developmental screening or evaluation, 60% had postnatal neuroimaging, 48% had automated auditory brainstem response-based hearing screen or evaluation, and 36% had an ophthalmologic evaluation. Among evaluated children, 6% had at least one Zika-associated birth defect identified, 9% had at least one neurodevelopmental abnormality possibly associated with congenital Zika virus infection identified, and 1% had both.

Conclusion: One in seven evaluated children had a Zika-associated birth defect, a neurodevelopmental abnormality possibly associated with congenital Zika virus infection, or both reported to the USZPIR. Given that most children did not have evidence of all recommended evaluations, additional anomalies might not have been identified. Careful monitoring and evaluation of children born to mothers with evidence of Zika virus infection during pregnancy is essential for ensuring early detection of possible disabilities and early referral to intervention services.

Introduction

Zika virus infection during pregnancy can cause serious birth defects, including structural abnormalities of the brain and eye.[1-7] As infants with congenital Zika virus infection get older, problems such as epilepsy, vision loss, and developmental delays have been increasingly recognized.[8] Early identification of and intervention for adverse neurodevelopmental outcomes have been determined to improve cognitive, social, and behavioral functioning and to be cost effective to society in general.[9-12]

The most critical time to intervene and promote optimal brain development is during the first 3 years of life.[9] To facilitate early identification and intervention, CDC released clinical guidance for the evaluation and management of infants with possible congenital Zika virus infection in January 2016.[13] The guidance was based largely on existing guidelines for pediatric health promotion and care;[14] expert opinion was incorporated from clinicians and researchers with knowledge of congenital infections and of clinical care of infants with birth defects as described in early reports.[15-18] Recommendations for the care and management of infants with possible congenital Zika virus exposure and infants with one or more clinical findings consistent with congenital Zika virus syndrome have remained largely unchanged through subsequent updates.[19] Standard evaluation* at birth and during each well-child visit is recommended for all infants and young children with possible prenatal Zika virus exposure.[13,19] Laboratory testing for Zika virus is recommended for infants born to mothers with laboratory evidence of confirmed or possible Zika virus infection during pregnancy and for infants with one or more clinical findings consistent with congenital Zika syndrome born to mothers with possible Zika virus exposure, regardless of maternal testing results. In addition to a standard evaluation, infants born to mothers with laboratory evidence of confirmed or possible Zika virus infection during pregnancy should have a cranial ultrasound or other brain imaging and a comprehensive ophthalmologic evaluation performed by age 1 month to detect subclinical brain and eye findings.[19]

To better understand the effects of Zika virus infection during pregnancy on mothers and children from a national surveillance perspective, CDC collaborated with state, territorial, and local health departments on the U.S. Zika Pregnancy and Infant Registry (USZPIR) to monitor pregnancy and infant/child outcomes among pregnancies with laboratory evidence of confirmed or possible Zika virus infection (www.cdc.gov/pregnancy/zika/research/registry.html). The USZPIR currently monitors outcomes of approximately 7,300 pregnancies, over 4,800 of which are reported from the U.S. territories and freely associated states§ (https://www.cdc.gov/pregnancy/zika/data/pregwomen-uscases.html). This report is the first to provide data on Zika-associated birth defects and neurodevelopmental abnormalities possibly associated with congenital Zika virus infection identified during infancy and early childhood among children aged ≥1 year who were born in the U.S. territories and freely associated states.§