Healthcare gaps and inequities following hospitalisation for COVID-19 in Brazil's universal healthcare system: a patient-engaged survey of Long COVID healthcare needs, use and barriers.

IF 4.1 2区 医学 Q1 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH
Margareth Crisóstomo Portela, Claudia Caminha Escosteguy, Sheyla Maria Lemos Lima, Michelle Bernardino, Bárbara do Nascimento Caldas, Letícia Soares, Maurício Teixeira Leite de Vasconcellos, Mônica Martins, Carla Lourenço Tavares de Andrade, Natalie Perez Baginski, Gabriela Góes, Brenda Sabaine, Marta Cavalcanti, Danielle Furtado, Elisabeth Stelson, Flora Cornish, Emma-Louise Aveling
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引用次数: 0

Abstract

Background: Long COVID (LC) is an infection-associated chronic condition (IACC) that tends to be neglected by healthcare systems. Studies of post-COVID healthcare utilisation find elevated levels of use but have mainly been conducted in high-income settings. In the context of Brazil's universal health system (SUS), our patient-engaged study aimed to map healthcare needs, use, and access barriers related to LC up to 24 months following COVID-19 hospitalisation, in the interest of informing health system planning for an equitable LC response.

Methods: A cohort survey included a probabilistic sample of hospitalised COVID-19-confirmed individuals aged ≥ 18, who had been discharged from public hospitals in Rio de Janeiro between December 2020 and November 2022. Socio-demographic and clinical data were collected, including self-reported LC symptoms, self-reported LC, healthcare needs, use, and access barriers.

Results: In a sample of 556 participants, corresponding to an estimated population of 11,328 individuals, 50.0% (95%CI 44.3-55.6%) reported healthcare needs in the six months prior, due to new-onset or worsened conditions after COVID-19. Almost 45.0% did not complete high school, while 26.5% lived below the poverty line (~ US$6.85 per day), indicating a high proportion of socially vulnerable individuals. High prevalence of LC symptoms, self-reported LC, and new diagnoses were observed. Healthcare needs were associated with acute disease severity, number of LC symptoms, and new post-COVID diagnoses, including cardiovascular and kidney diseases, and endocrine and musculoskeletal disorders. Significant gaps existed between need and access to services, and part of the access to services involved substantial out-of-pocket expenditure. These gaps were particularly pronounced for specialised medical services, scans/imaging, post-COVID rehabilitation services, and mental healthcare. Despite a universal health system, those with higher monthly incomes (above R$1,500 or ~ US$250) were more likely to have accessed specialised medical care.

Conclusions: The SUS is not meeting the high need for LC healthcare, raising concerns about deepening health inequities. In Brazil, as elsewhere, LC joins other IACCs in becoming an invisibilised epidemic, with LC patients, especially those unable to pay for care, neglected amid general healthcare backlogs. A comprehensive pandemic response must include dedicated efforts to surveil and treat the long-term impacts of infection.

巴西全民医疗体系中因COVID-19住院后的医疗差距和不公平现象:针对长期COVID-19医疗需求、使用和障碍的患者参与调查
背景:长冠状病毒病(LC)是一种容易被卫生保健系统忽视的感染相关慢性疾病(IACC)。对covid - 19后医疗保健利用率的研究发现,使用水平有所上升,但主要是在高收入环境中进行的。在巴西全民卫生系统(SUS)的背景下,我们的患者参与研究旨在绘制COVID-19住院后24个月内与LC相关的医疗保健需求、使用和获取障碍,以便为卫生系统规划提供信息,以实现公平的LC应对。方法:采用队列调查方法,抽取2020年12月至2022年11月期间从巴西里约热内卢公立医院出院的年龄≥18岁的住院covid -19确诊患者作为概率样本。收集社会人口学和临床数据,包括自我报告的LC症状、自我报告的LC、医疗保健需求、使用和获取障碍。结果:在556名参与者的样本中,对应于11,328人的估计人口,50.0% (95%CI 44.3-55.6%)报告了由于新发或COVID-19后病情恶化而在6个月内的医疗保健需求。近45.0%的人没有完成高中学业,26.5%的人生活在贫困线以下(每天约6.85美元),表明社会弱势群体的比例很高。观察到LC症状、自我报告LC和新诊断的高发率。医疗保健需求与急性疾病严重程度、LC症状数量和新冠肺炎后诊断相关,包括心血管和肾脏疾病、内分泌和肌肉骨骼疾病。在需要和获得服务之间存在着巨大的差距,获得服务的一部分需要大量的自付费用。这些差距在专业医疗服务、扫描/成像、covid后康复服务和精神卫生保健方面尤为明显。尽管有全民医疗保健系统,但月收入较高(超过1,500雷亚尔或约250美元)的人更有可能获得专业医疗服务。结论:SUS不能满足LC医疗保健的高需求,引起了对深化卫生不公平的担忧。在巴西,与其他地方一样,LC与其他iacc一起成为一种无形的流行病,LC患者,特别是那些无力支付医疗费用的患者,在一般医疗积压中被忽视。全面的大流行病应对措施必须包括专门努力监测和治疗感染的长期影响。
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来源期刊
CiteScore
7.80
自引率
4.20%
发文量
162
审稿时长
28 weeks
期刊介绍: International Journal for Equity in Health is an Open Access, peer-reviewed, online journal presenting evidence relevant to the search for, and attainment of, equity in health across and within countries. International Journal for Equity in Health aims to improve the understanding of issues that influence the health of populations. This includes the discussion of political, policy-related, economic, social and health services-related influences, particularly with regard to systematic differences in distributions of one or more aspects of health in population groups defined demographically, geographically, or socially.
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