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Economic burden of sickle cell disease in Brazil

BACKGROUND: Sickle cell disease (SCD) may cause several impacts to patients and the whole society. About 4% of the population has the sickle cell trait in Brazil, and 60,000 to 100,000 have SCD. However, despite recognizing the significant burden of disease, little is known about SCD costs. OBJECTIV...

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Autores principales: Silva-Pinto, Ana Cristina, Costa, Fernando F., Gualandro, Sandra Fatima Menosi, Fonseca, Patricia Belintani Blum, Grindler, Carmela Maggiuzzu, Souza Filho, Homero C. R., Bueno, Carolina Tosin, Cançado, Rodolfo D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9202914/
https://www.ncbi.nlm.nih.gov/pubmed/35709301
http://dx.doi.org/10.1371/journal.pone.0269703
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author Silva-Pinto, Ana Cristina
Costa, Fernando F.
Gualandro, Sandra Fatima Menosi
Fonseca, Patricia Belintani Blum
Grindler, Carmela Maggiuzzu
Souza Filho, Homero C. R.
Bueno, Carolina Tosin
Cançado, Rodolfo D.
author_facet Silva-Pinto, Ana Cristina
Costa, Fernando F.
Gualandro, Sandra Fatima Menosi
Fonseca, Patricia Belintani Blum
Grindler, Carmela Maggiuzzu
Souza Filho, Homero C. R.
Bueno, Carolina Tosin
Cançado, Rodolfo D.
author_sort Silva-Pinto, Ana Cristina
collection PubMed
description BACKGROUND: Sickle cell disease (SCD) may cause several impacts to patients and the whole society. About 4% of the population has the sickle cell trait in Brazil, and 60,000 to 100,000 have SCD. However, despite recognizing the significant burden of disease, little is known about SCD costs. OBJECTIVE: To estimate SCD societal costs based on disease burden modelling, under Brazilian societal perspective. METHODS: A disease burden model was built considering the societal perspective and a one-year time horizon, including direct medical and indirect costs (morbidity and mortality). The sum of life lost and disability years was considered to estimate disability-adjusted life years (DALYs). Data from a public database (DATASUS) and the prevalence obtained from literature or medical experts were used to define complications prevalence and duration. Costs were defined using data from the Brazilian public healthcare system table of procedures and medications (SIGTAP) and the human capital method. RESULTS: Annual SCD cost was 413,639,180 USD. Indirect cost accounted for the majority of burden (70.1% of the total; 290,158,365 USD vs 123,480,816 USD). Standard of care and chronic complications were the main source of direct costs among adults, while acute conditions were the main source among children. Vaso-occlusive crisis represented the complication with the highest total cost per year in both populations, 11,400,410 USD among adults and 11,510,960 USD among children. CONCLUSIONS: SCD management may impose an important economic burden on Brazilian society that may reach more than 400 million USD per year.
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spelling pubmed-92029142022-06-17 Economic burden of sickle cell disease in Brazil Silva-Pinto, Ana Cristina Costa, Fernando F. Gualandro, Sandra Fatima Menosi Fonseca, Patricia Belintani Blum Grindler, Carmela Maggiuzzu Souza Filho, Homero C. R. Bueno, Carolina Tosin Cançado, Rodolfo D. PLoS One Research Article BACKGROUND: Sickle cell disease (SCD) may cause several impacts to patients and the whole society. About 4% of the population has the sickle cell trait in Brazil, and 60,000 to 100,000 have SCD. However, despite recognizing the significant burden of disease, little is known about SCD costs. OBJECTIVE: To estimate SCD societal costs based on disease burden modelling, under Brazilian societal perspective. METHODS: A disease burden model was built considering the societal perspective and a one-year time horizon, including direct medical and indirect costs (morbidity and mortality). The sum of life lost and disability years was considered to estimate disability-adjusted life years (DALYs). Data from a public database (DATASUS) and the prevalence obtained from literature or medical experts were used to define complications prevalence and duration. Costs were defined using data from the Brazilian public healthcare system table of procedures and medications (SIGTAP) and the human capital method. RESULTS: Annual SCD cost was 413,639,180 USD. Indirect cost accounted for the majority of burden (70.1% of the total; 290,158,365 USD vs 123,480,816 USD). Standard of care and chronic complications were the main source of direct costs among adults, while acute conditions were the main source among children. Vaso-occlusive crisis represented the complication with the highest total cost per year in both populations, 11,400,410 USD among adults and 11,510,960 USD among children. CONCLUSIONS: SCD management may impose an important economic burden on Brazilian society that may reach more than 400 million USD per year. Public Library of Science 2022-06-16 /pmc/articles/PMC9202914/ /pubmed/35709301 http://dx.doi.org/10.1371/journal.pone.0269703 Text en © 2022 Silva-Pinto et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Silva-Pinto, Ana Cristina
Costa, Fernando F.
Gualandro, Sandra Fatima Menosi
Fonseca, Patricia Belintani Blum
Grindler, Carmela Maggiuzzu
Souza Filho, Homero C. R.
Bueno, Carolina Tosin
Cançado, Rodolfo D.
Economic burden of sickle cell disease in Brazil
title Economic burden of sickle cell disease in Brazil
title_full Economic burden of sickle cell disease in Brazil
title_fullStr Economic burden of sickle cell disease in Brazil
title_full_unstemmed Economic burden of sickle cell disease in Brazil
title_short Economic burden of sickle cell disease in Brazil
title_sort economic burden of sickle cell disease in brazil
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9202914/
https://www.ncbi.nlm.nih.gov/pubmed/35709301
http://dx.doi.org/10.1371/journal.pone.0269703
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