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Cost analysis of acute care resource utilization among individuals with sickle cell disease in a middle-income country
BACKGROUND: The costs associated with the treatment of sickle cell disease (SCD) are understudied in low and middle-income countries (LMIC). We evaluated the cost of treating SCD-related acute complications and the potential cost-savings of hydroxyurea in a specialized hematology center in Brazil. M...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8742916/ https://www.ncbi.nlm.nih.gov/pubmed/34998394 http://dx.doi.org/10.1186/s12913-021-07461-6 |
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author | Lobo, Clarisse Moura, Patricia Fidlarczyk, Delaine Duran, Jane Barbosa, Roberto Oliveira, Thais do Nascimento, Emilia Matos Bhakta, Nickhill Hankins, Jane S. |
author_facet | Lobo, Clarisse Moura, Patricia Fidlarczyk, Delaine Duran, Jane Barbosa, Roberto Oliveira, Thais do Nascimento, Emilia Matos Bhakta, Nickhill Hankins, Jane S. |
author_sort | Lobo, Clarisse |
collection | PubMed |
description | BACKGROUND: The costs associated with the treatment of sickle cell disease (SCD) are understudied in low and middle-income countries (LMIC). We evaluated the cost of treating SCD-related acute complications and the potential cost-savings of hydroxyurea in a specialized hematology center in Brazil. METHODS: The costs (US dollars) of emergency department (ED) and hospitalizations from SCD-related complications between 01.01.2018 and 06.30.2018 were ascertained using absorption and micro-costing approaches. The reasons for acute hospital visits were grouped as: 1) vaso-occlusive (VOC) pain, 2) infection, 3) anemia exacerbation, and 4) chronic organ damage complications. Hydroxyurea adherence was estimated by medication possession ratio (MPR) during the study period. RESULTS: In total, 1144 patients, median age 17 years (range 0–70), 903 (78.9%) with HbSS/HbSβ(0)-thalassemia, 441 (38.5%) prescribed hydroxyurea, visited the ED, of whom 381 (33%) were admitted. VOC accounted for 64% of all ED visits and 60% of all admissions. Anemia exacerbation was the most expensive reason for ED visit ($321.87/visit), while chronic organ damage carried the highest admission cost ($2176.40/visit). Compared with other genotypes, individuals with HbSS/HbSβ(0)-thalassemia were admitted more often (79% versus 21%, p < 0.0001), and their admission costs were higher ($1677.18 versus $1224.47/visit, p = 0.0001). Antibiotics and analgesics accounted for 43% and 42% of the total ED costs, respectively, while housing accounted for 46% of the total admission costs. Costs of ED visits not resulting in admissions were lower among HbSS/HbSβ(0)-thalassemia individuals with hydroxyurea MPR ≥65% compared with visits by patients with MPR <65% ($98.16/visit versus $182.46/visit, p = 0.0007). No difference in admission costs were observed relative to hydroxyurea use. DISCUSSION: In a LMIC hematology-specialized center, VOCs accounted for most acute visits from patients with SCD, but costs were highest due to anemia exacerbation. Analgesics, antibiotics, and housing drove most expenses. Hydroxyurea may reduce ED costs among individuals with HbSS/HbSβ(0)-thalassemia but is dependent on adherence level. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12913-021-07461-6. |
format | Online Article Text |
id | pubmed-8742916 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-87429162022-01-10 Cost analysis of acute care resource utilization among individuals with sickle cell disease in a middle-income country Lobo, Clarisse Moura, Patricia Fidlarczyk, Delaine Duran, Jane Barbosa, Roberto Oliveira, Thais do Nascimento, Emilia Matos Bhakta, Nickhill Hankins, Jane S. BMC Health Serv Res Research BACKGROUND: The costs associated with the treatment of sickle cell disease (SCD) are understudied in low and middle-income countries (LMIC). We evaluated the cost of treating SCD-related acute complications and the potential cost-savings of hydroxyurea in a specialized hematology center in Brazil. METHODS: The costs (US dollars) of emergency department (ED) and hospitalizations from SCD-related complications between 01.01.2018 and 06.30.2018 were ascertained using absorption and micro-costing approaches. The reasons for acute hospital visits were grouped as: 1) vaso-occlusive (VOC) pain, 2) infection, 3) anemia exacerbation, and 4) chronic organ damage complications. Hydroxyurea adherence was estimated by medication possession ratio (MPR) during the study period. RESULTS: In total, 1144 patients, median age 17 years (range 0–70), 903 (78.9%) with HbSS/HbSβ(0)-thalassemia, 441 (38.5%) prescribed hydroxyurea, visited the ED, of whom 381 (33%) were admitted. VOC accounted for 64% of all ED visits and 60% of all admissions. Anemia exacerbation was the most expensive reason for ED visit ($321.87/visit), while chronic organ damage carried the highest admission cost ($2176.40/visit). Compared with other genotypes, individuals with HbSS/HbSβ(0)-thalassemia were admitted more often (79% versus 21%, p < 0.0001), and their admission costs were higher ($1677.18 versus $1224.47/visit, p = 0.0001). Antibiotics and analgesics accounted for 43% and 42% of the total ED costs, respectively, while housing accounted for 46% of the total admission costs. Costs of ED visits not resulting in admissions were lower among HbSS/HbSβ(0)-thalassemia individuals with hydroxyurea MPR ≥65% compared with visits by patients with MPR <65% ($98.16/visit versus $182.46/visit, p = 0.0007). No difference in admission costs were observed relative to hydroxyurea use. DISCUSSION: In a LMIC hematology-specialized center, VOCs accounted for most acute visits from patients with SCD, but costs were highest due to anemia exacerbation. Analgesics, antibiotics, and housing drove most expenses. Hydroxyurea may reduce ED costs among individuals with HbSS/HbSβ(0)-thalassemia but is dependent on adherence level. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12913-021-07461-6. BioMed Central 2022-01-08 /pmc/articles/PMC8742916/ /pubmed/34998394 http://dx.doi.org/10.1186/s12913-021-07461-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Lobo, Clarisse Moura, Patricia Fidlarczyk, Delaine Duran, Jane Barbosa, Roberto Oliveira, Thais do Nascimento, Emilia Matos Bhakta, Nickhill Hankins, Jane S. Cost analysis of acute care resource utilization among individuals with sickle cell disease in a middle-income country |
title | Cost analysis of acute care resource utilization among individuals with sickle cell disease in a middle-income country |
title_full | Cost analysis of acute care resource utilization among individuals with sickle cell disease in a middle-income country |
title_fullStr | Cost analysis of acute care resource utilization among individuals with sickle cell disease in a middle-income country |
title_full_unstemmed | Cost analysis of acute care resource utilization among individuals with sickle cell disease in a middle-income country |
title_short | Cost analysis of acute care resource utilization among individuals with sickle cell disease in a middle-income country |
title_sort | cost analysis of acute care resource utilization among individuals with sickle cell disease in a middle-income country |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8742916/ https://www.ncbi.nlm.nih.gov/pubmed/34998394 http://dx.doi.org/10.1186/s12913-021-07461-6 |
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