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      Social and economic impacts of congenital Zika syndrome in Brazil: Study protocol and rationale for a mixed-methods study

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          Abstract

          Global concern broke out in late 2015 as thousands of children in Brazil were born with microcephaly, which was quickly linked to congenital infection with Zika virus (ZIKV). ZIKV is now known to cause a wider spectrum of severe adverse outcomes—congenital Zika syndrome (CZS)—and also milder impairments. This study aimed to explore the social and economic impacts of CZS in Brazil. Data was collected through mixed methods across two settings: Recife City and Jaboatão dos Guararapes in Pernambuco State (the epicentre of the epidemic), and the city of Rio de Janeiro (where reports of ZIKV infection and CZS were less frequent). Data was collected May 2017-January 2018. Ethical standards were adhered to throughout the research. In-depth qualitative interviews were conducted with: mothers and other carers of children with CZS (approximately 30 per setting), pregnant women (10-12 per setting), men and women of child-bearing age (16-20 per setting), and health professionals (10-12 per setting). Thematic analysis was undertaken independently by researchers from at least two research settings, and these were shared for feedback.

          A case-control study was undertaken to quantitatively explore social and economic differences between caregivers of a child with CZS (cases) and caregivers with an unaffected child (controls). We aimed to recruit 100 cases and 100 controls per setting, from existing studies. The primary caregiver, usually the mother, was interviewed using a structured questionnaire to collect information on: depression, anxiety, stress, social support, family quality of life, health care and social service use, and costs incurred by families. Multivariable logistic regression analyses were used to compare outcomes for cases and controls. Costs incurred as a result of CZS were estimated from the perspective of the health system, families and society. Modelling was undertaken to estimate the total economic burden of CZS from those three perspectives.

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          Zika Virus Infection in Pregnant Women in Rio de Janeiro - Preliminary Report.

          Background Zika virus (ZIKV) has been linked to neonatal microcephaly. To characterize the spectrum of ZIKV disease in pregnancy, we followed patients in Rio de Janeiro to describe clinical manifestations in mothers and repercussions of acute ZIKV infection in fetuses. Methods We enrolled pregnant women in whom a rash had developed within the previous 5 days and tested blood and urine specimens for ZIKV by reverse-transcriptase-polymerase-chain-reaction assays. We followed the women prospectively and collected clinical and ultrasonographic data. Results A total of 88 women were enrolled from September 2015 through February 2016; of these 88 women, 72 (82%) tested positive for ZIKV in blood, urine, or both. The timing of acute ZIKV infection ranged from 5 to 38 weeks of gestation. Predominant clinical features included pruritic descending macular or maculopapular rash, arthralgias, conjunctival injection, and headache; 28% had fever (short-term and low-grade). Women who were positive for ZIKV were more likely than those who were negative for the virus to have maculopapular rash (44% vs. 12%, P=0.02), conjunctival involvement (58% vs. 13%, P=0.002), and lymphadenopathy (40% vs. 7%, P=0.02). Fetal ultrasonography was performed in 42 ZIKV-positive women (58%) and in all ZIKV-negative women. Fetal abnormalities were detected by Doppler ultrasonography in 12 of the 42 ZIKV-positive women (29%) and in none of the 16 ZIKV-negative women. Adverse findings included fetal deaths at 36 and 38 weeks of gestation (2 fetuses), in utero growth restriction with or without microcephaly (5 fetuses), ventricular calcifications or other central nervous system (CNS) lesions (7 fetuses), and abnormal amniotic fluid volume or cerebral or umbilical artery flow (7 fetuses). To date, 8 of the 42 women in whom fetal ultrasonography was performed have delivered their babies, and the ultrasonographic findings have been confirmed. Conclusions Despite mild clinical symptoms, ZIKV infection during pregnancy appears to be associated with grave outcomes, including fetal death, placental insufficiency, fetal growth restriction, and CNS injury.
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            Zika Virus and Birth Defects--Reviewing the Evidence for Causality.

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              Characterizing the Pattern of Anomalies in Congenital Zika Syndrome for Pediatric Clinicians

              Zika virus infection can be prenatally passed from a pregnant woman to her fetus. There is sufficient evidence to conclude that intrauterine Zika virus infection is a cause of microcephaly and serious brain anomalies, but the full spectrum of anomalies has not been delineated. To inform pediatric clinicians who may be called on to evaluate and treat affected infants and children, we review the most recent evidence to better characterize congenital Zika syndrome.
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                Author and article information

                Contributors
                Role: ConceptualizationRole: Funding AcquisitionRole: InvestigationRole: MethodologyRole: Project AdministrationRole: SupervisionRole: Writing – Original Draft PreparationRole: Writing – Review & Editing
                Role: ConceptualizationRole: Data CurationRole: Formal AnalysisRole: Funding AcquisitionRole: InvestigationRole: MethodologyRole: Project AdministrationRole: SupervisionRole: Writing – Review & Editing
                Role: ConceptualizationRole: Data CurationRole: Funding AcquisitionRole: InvestigationRole: MethodologyRole: Project AdministrationRole: SupervisionRole: Writing – Review & Editing
                Role: Data CurationRole: Formal AnalysisRole: InvestigationRole: MethodologyRole: SupervisionRole: Writing – Review & Editing
                Role: ConceptualizationRole: Data CurationRole: Formal AnalysisRole: Funding AcquisitionRole: InvestigationRole: MethodologyRole: Project AdministrationRole: SupervisionRole: Writing – Review & Editing
                Role: Data CurationRole: Formal AnalysisRole: InvestigationRole: MethodologyRole: SoftwareRole: Writing – Review & Editing
                Role: Formal AnalysisRole: InvestigationRole: MethodologyRole: SupervisionRole: Writing – Review & Editing
                Role: ConceptualizationRole: Funding AcquisitionRole: MethodologyRole: SupervisionRole: Writing – Review & Editing
                Role: Data CurationRole: Formal AnalysisRole: InvestigationRole: MethodologyRole: Project AdministrationRole: SupervisionRole: Writing – Review & Editing
                Role: Formal AnalysisRole: InvestigationRole: MethodologyRole: Project AdministrationRole: Writing – Review & Editing
                Role: Formal AnalysisRole: InvestigationRole: MethodologyRole: Project AdministrationRole: SupervisionRole: Writing – Review & Editing
                Role: Formal AnalysisRole: InvestigationRole: MethodologyRole: Project AdministrationRole: SupervisionRole: Writing – Review & Editing
                Role: ConceptualizationRole: Formal AnalysisRole: InvestigationRole: MethodologyRole: Project AdministrationRole: SupervisionRole: Writing – Review & Editing
                Role: Formal AnalysisRole: InvestigationRole: MethodologyRole: Project AdministrationRole: SupervisionRole: Writing – Review & Editing
                Role: Data CurationRole: Formal AnalysisRole: InvestigationRole: MethodologyRole: Project AdministrationRole: SupervisionRole: Writing – Review & Editing
                Role: Formal AnalysisRole: InvestigationRole: MethodologyRole: Project AdministrationRole: Writing – Review & Editing
                Role: Data CurationRole: Formal AnalysisRole: InvestigationRole: MethodologyRole: Project AdministrationRole: SupervisionRole: Writing – Review & Editing
                Journal
                Wellcome Open Res
                Wellcome Open Res
                Wellcome Open Res
                Wellcome Open Research
                F1000 Research Limited (London, UK )
                2398-502X
                11 September 2019
                2018
                : 3
                : 127
                Affiliations
                [1 ]International Centre for Evidence in Disability, Clinical Research Department, London School of Hygiene & Tropical Medicine, London, UK
                [2 ]Aggeu Magalhães Institute, FIOCRUZ/PE, Recife, Brazil
                [3 ]Faculty of Medicine, University of Pernambuco, Recife, Brazil
                [4 ]Fernando Figueira Maternal and Children's Institute, Rio de Janeiro, Brazil
                [5 ]Department of Social Medicine, Federal University of Pernambuco, Recife, Brazil
                [6 ]Postgraduate Programme in Public Health, Federal University of Pernambuco, Recife, Brazil
                [7 ]Faculty of Public Health and Policy, London School of Hygiene & Tropical Medicine, London, UK
                [8 ]Department of Economics, City University London, London, UK
                [9 ]Department of Infectious Disease Epidemiology, London School of Hygiene & Tropical Medicine, London, UK
                [10 ]Public Health Department, Federal University of Pernambuco, Recife, Brazil
                [1 ]RTI International, Research Triangle Park, NC, USA
                [1 ]RTI International, Research Triangle Park, NC, USA
                Clinical Research Unit, Department of Infectious and Tropical Disease, London School of Hygiene and Tropical Medicine, UK
                [1 ]Law School, University of Brasília, Brasília, Brazil
                Clinical Research Unit, Department of Infectious and Tropical Disease, London School of Hygiene and Tropical Medicine, UK
                Author notes

                No competing interests were disclosed.

                Competing interests: No competing interests were disclosed.

                Competing interests: No competing interests were disclosed.

                Competing interests: No competing interests were disclosed.

                Competing interests: No competing interests were disclosed.

                Competing interests: No competing interests were disclosed.

                Author information
                https://orcid.org/0000-0002-8952-0023
                https://orcid.org/0000-0002-3600-7250
                https://orcid.org/0000-0002-2034-0294
                https://orcid.org/0000-0001-7694-4233
                https://orcid.org/0000-0002-5572-0609
                https://orcid.org/0000-0002-7199-3797
                https://orcid.org/0000-0002-3363-4232
                https://orcid.org/0000-0002-7511-9925
                https://orcid.org/0000-0003-0035-8419
                https://orcid.org/0000-0001-8532-5346
                Article
                10.12688/wellcomeopenres.14838.2
                6807146
                31667356
                9b859c1f-fe58-4d8b-94bc-d5ad93807863
                Copyright: © 2019 Kuper H et al.

                This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 15 August 2019
                Funding
                Funded by: Horizon 2020
                Award ID: 734584
                Funded by: Wellcome Trust
                Award ID: 206016
                This study was supported by The Wellcome Trust and the Department for International Development (grant: 206016/Z/17/Z). This study was also supported by a supplementary grant from the European Union’s Horizon 2020 research and innovation programme, under Zika-PLAN grant agreement no. 734584.
                The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Study Protocol
                Articles

                zika,congenital zika syndrome,economic,social,depression,anxiety,brazil

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