4.7 Article

Early Clinical Infancy Outcomes for Microcephaly and/or Small for Gestational Age Zika-Exposed Infants

期刊

CLINICAL INFECTIOUS DISEASES
卷 70, 期 12, 页码 2663-2672

出版社

OXFORD UNIV PRESS INC
DOI: 10.1093/cid/ciz704

关键词

Zika; congenital Zika syndrome; microcephaly; proportional microcephaly; small for gestational age (SGA)

资金

  1. Departamento de Ciencia e Tecnologia do Ministerio da Saude do Brasil
  2. Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior [CAPES/88887.116627/2016-01]
  3. National Institute of Allergy and Infectious Diseases [AI28697, AI1259534-01]
  4. National Eye Institute of the National Institutes of Health (NIH)/National Center for Advancing Translational Science of the University of California-Los Angeles Clinical and Translational Science Institute [AI129847-01, UL1TR001881]
  5. Thrasher Research Fund [20164370]
  6. UK Department for International Development

向作者/读者索取更多资源

Background. Zika-exposed infants with microcephaly (proportional or disproportional) and those who are small for gestational age without microcephaly should be closely followed, particularly their growth trajectories. They are at high risk of adverse outcomes in the first year of life.Antenatal Zika virus (ZIKV) exposure may lead to adverse infant outcomes including microcephaly and being small for gestational age (SGA). ZIKV-exposed infants with a diagnosis of microcephaly (proportional [PM] or disproportional [DM]) or SGA at birth were evaluated with anthropometric measurements and health outcomes. Methods. Infants had laboratory-confirmed ZIKV exposure in Brazil. PM, DM, or SGA classification was based on head circumference and weight. First-year growth parameters and clinical outcomes were recorded with analyses performed. Results. Among the 156 ZIKV-exposed infants, 14 (9.0%) were SGA, 13 (8.3%) PM, 13 (8.3%) DM, and 116 (74.4%) were neither SGA nor had microcephaly (NSNM). High rates of any neurologic, ophthalmologic, and hearing abnormalities were observed for PM (100%), DM (100%), and SGA (42.9%) vs NSNM infants (18.3%; P <.001); odds ratio [OR], 3.4 (95% confidence interval [CI], 1.1-10.7) for SGA vs NSNM. Neuroimaging abnormalities were seen in 100% of PM and DM and in 42.9% of SGA vs NSNM infants 16%; (P <.001); OR 3.9 (95% CI, 1.2-12.8) for SGA vs NSNM. Growth rates by z score, particularly for microcephaly infants, were poor after birth but showed improvement beyond 4 months of life. Conclusions. ZIKV-exposed infants with microcephaly (PM and DM) had similarly high rates of adverse outcomes but showed improvement in growth measurements beyond 4 months of life. While SGA infants had fewer adverse outcomes compared with microcephaly infants, notable adverse outcomes were observed in some; their odds of having adverse outcomes were 3 to 4 times greater compared to NSNM infants.

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