Suppr超能文献

[复杂护理、高成本与收入损失:患有罕见健康状况的儿童和青少年家庭的常见问题]

[Complex care, high cost, and loss of income: frequent issues for families of children and adolescents with rare health conditions].

作者信息

Pinto Márcia, Madureira Adelino, Barros Letícia Baptista de Paula, Nascimento Marcos, Costa Ana Carolina Carioca da, Oliveira Nicole Velloso de, Albernaz Lidianne, Campos Daniel de Souza, Horovitz Dafne Dain Gandelman, Martins Antilia Januária, Moreira Martha Cristina Nunes

机构信息

Instituto Nacional de Saúde da Mulher, da Criança e do Adolescente Fernandes Figueira, Fundação Oswaldo Cruz, Rio de Janeiro, Brasil.

出版信息

Cad Saude Publica. 2019 Sep 9;35(9):e00180218. doi: 10.1590/0102-311X00180218.

Abstract

Estimates point to more than seven thousand rare diseases already identified, representing 6 to 10% of all diseases. In Brazil, a rare disease is defined as one that affects up to 65 persons per 100,000. The quantification of costs for the families of patients with such conditions and their impact on income provides information capable of supporting public policies for these youngsters. The study aimed to estimate the cost and loss of earnings, viewed from the perspective of families of children and adolescents with cystic fibrosis, mucopolysaccharidosis, and osteogenesis imperfecta. The study included 99 families of patients treated at a national referral hospital for rare diseases in Rio de Janeiro, based on the principal caregiver's report. The descriptive data analysis showed that the median direct nonmedical cost for families was BRL 2,156.56 (USD 570) for cystic fibrosis, BRL 1,060.00 (USD 280) for mucopolysaccharidosis, and BRL 1,908.00 (USD 505) for osteogenesis imperfecta. Loss of earnings exceeded 100% for all three diseases. A total of 54% of families fail to receive any social benefits. The estimate of coping costs indicated that 69% of the families had incurred loans and that 22.5% had sold household assets to cope with the treatment costs. Catastrophic expenditures were observed in families dealing with the three diseases. The results unveil costs that are rarely estimated, and not only in the field of rare diseases. The findings point to a major burden on the families' income. It is important to incorporate such studies in the discussion of financing, the incorporation of new technologies, and the supply of health services.

摘要

据估计,目前已确认的罕见病超过7000种,占所有疾病的6%至10%。在巴西,罕见病被定义为每10万人中受影响人数至多为65人的疾病。对这类疾病患者家庭的费用及其对收入的影响进行量化,可为针对这些青少年的公共政策提供支持信息。该研究旨在从患有囊性纤维化、黏多糖贮积症和成骨不全症的儿童及青少年家庭的角度,估算费用和收入损失。基于主要照顾者的报告,该研究纳入了在里约热内卢一家全国罕见病转诊医院接受治疗的99个患者家庭。描述性数据分析表明,囊性纤维化患者家庭的直接非医疗费用中位数为2156.56巴西雷亚尔(570美元),黏多糖贮积症患者家庭为1060.00巴西雷亚尔(280美元),成骨不全症患者家庭为1908.00巴西雷亚尔(505美元)。所有这三种疾病的收入损失均超过100%。共有54%的家庭未获得任何社会福利。应对费用的估算表明,69%的家庭举了债,22.5%的家庭变卖了家庭资产以支付治疗费用。在应对这三种疾病的家庭中观察到了灾难性支出。研究结果揭示了很少被估算的费用,而且不仅在罕见病领域。研究结果表明家庭收入负担沉重。将此类研究纳入融资、新技术引入及卫生服务供应的讨论中很重要。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验