[Access of children with congenital Zika virus syndrome to public policies].

IF 1.8 4区 医学 Q3 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Cadernos de saude publica Pub Date : 2025-02-07 eCollection Date: 2025-01-01 DOI:10.1590/0102-311XPT014624
Ana Cristina Pannain L Kaufman, Andre Reynaldo Santos Périssé, Cristina Barroso Hofer
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Abstract

Congenital Zika syndrome (CZS) is responsible for several malformations, including microcephaly. This study aimed to describe children's access to social public policies: lifetime benefit (E60) created in the face of the Zika virus public health emergency (Espin-ZIKV) or Continuous Cash Benefit/Type 87 (BPC/E87). Thus, this study compares the children's access before and after Espin-ZIKV. This was a cross-sectional study, with data extraction and description from the Brazilian Information System on Live Births (SINASC), the Registry of Public Health Events-Microcephaly (Resp-Microcephaly), and the Unified System for Benefits Information (SUIBE), from 2013 to 2021. We describe the E60 that were still active at the time of SUIBE data extraction in May, 2023. We compared the granting of BPC/E87 for microcephaly in 2013 and 2021 (before and after Espin-ZIKV). Of the 20,000,859 live births from 2015-2021, 20,464 suspected cases of CZS were reported in Resp-Microcephaly; 20% of affected patients received some social benefit: 705 received E60 and 3,822 received BPC/E87. The national average of BPC/E87 granted in 2013 for microcephaly was eight for every 100,000 live births (before Espin-ZIKV), while in 2021 it was five BPC/E87 for every 100,000 live births (after Espin-ZIKV) (p < 0.01). We observed 689 children with active E60 (from 3 to 8 years of age), in May, 2023. The study showed low social protection for children with suspected CZS. However, of those who benefited from the E60, 98% had active benefits in 2023, demonstrating the important survival of the benefited children. A reduction in the mean number of BPC/E87 grants for microcephaly without specified cause was observed after Espin-ZIKV.

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[先天性寨卡病毒综合征儿童获得公共政策的途径]。
先天性寨卡综合征(CZS)可导致包括小头畸形在内的几种畸形。本研究旨在描述儿童获得社会公共政策的途径:面对寨卡病毒突发公共卫生事件(Espin-ZIKV)创建的终身福利(E60)或连续现金福利/ 87型(BPC/E87)。因此,本研究比较了Espin-ZIKV之前和之后儿童的访问。这是一项横断面研究,数据提取和描述来自2013年至2021年巴西活产信息系统(SINASC)、公共卫生事件-小头症登记处(rep - microcephaly)和福利信息统一系统(SUIBE)。我们描述了在2023年5月进行subbe数据提取时仍处于活动状态的E60。我们比较了2013年和2021年(在Espin-ZIKV之前和之后)对小头症的BPC/E87批准情况。在2015-2021年的20,000,859例活产婴儿中,repr -小头畸形报告了20,464例疑似cz病例;20%的受影响患者接受了一些社会福利:705人接受了E60, 3822人接受了BPC/E87。2013年,全国小头畸形平均每10万活产婴儿中获得8例BPC/E87(在埃斯平-寨卡病毒之前),而2021年每10万活产婴儿中获得5例BPC/E87(在埃斯平-寨卡病毒之后)(p < 0.01)。我们于2023年5月观察了689例活动性E60患儿(3 - 8岁)。该研究显示,疑似cz儿童的社会保护水平较低。然而,在那些受益于E60的人中,98%的人在2023年有积极的福利,这表明受益儿童的重要生存。在感染了Espin-ZIKV后,观察到无特定原因的小头症BPC/E87的平均拨款数量减少。
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来源期刊
Cadernos de saude publica
Cadernos de saude publica 医学-公共卫生、环境卫生与职业卫生
CiteScore
5.30
自引率
7.10%
发文量
356
审稿时长
3-6 weeks
期刊介绍: Cadernos de Saúde Pública/Reports in Public Health (CSP) is a monthly journal published by the Sergio Arouca National School of Public Health, Oswaldo Cruz Foundation (ENSP/FIOCRUZ). The journal is devoted to the publication of scientific articles focusing on the production of knowledge in Public Health. CSP also aims to foster critical reflection and debate on current themes related to public policies and factors that impact populations'' living conditions and health care. All articles submitted to CSP are judiciously evaluated by the Editorial Board, composed of the Editors-in-Chief and Associate Editors, respecting the diversity of approaches, objects, and methods of the different disciplines characterizing the field of Public Health. Originality, relevance, and methodological rigor are the principal characteristics considered in the editorial evaluation. The article evaluation system practiced by CSP consists of two stages.
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