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Availability of Genetic Tests in Public Health Services in Brazil: Data from the Brazilian Rare Diseases Network

INTRODUCTION: The Brazilian Policy for Comprehensive Care for People with Rare Diseases (BPCCPRD) was published in 2014, accrediting several reference centers and incorporating many genetic tests for the diagnosis of rare diseases (RDs). The Brazilian Network of Rare Diseases (RARAS) comprises more...

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Autores principales: de Oliveira, Bibiana Mello, Neiva, Mariane Barros, Carvalho, Isabelle, Schwartz, Ida Vanessa Doederlein, Alves, Domingos, Félix, Temis Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10614440/
https://www.ncbi.nlm.nih.gov/pubmed/37356424
http://dx.doi.org/10.1159/000531547
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author de Oliveira, Bibiana Mello
Neiva, Mariane Barros
Carvalho, Isabelle
Schwartz, Ida Vanessa Doederlein
Alves, Domingos
Félix, Temis Maria
author_facet de Oliveira, Bibiana Mello
Neiva, Mariane Barros
Carvalho, Isabelle
Schwartz, Ida Vanessa Doederlein
Alves, Domingos
Félix, Temis Maria
author_sort de Oliveira, Bibiana Mello
collection PubMed
description INTRODUCTION: The Brazilian Policy for Comprehensive Care for People with Rare Diseases (BPCCPRD) was published in 2014, accrediting several reference centers and incorporating many genetic tests for the diagnosis of rare diseases (RDs). The Brazilian Network of Rare Diseases (RARAS) comprises more than 40 institutions that offer diagnosis and treatment for RDs in Brazil. This network includes Reference Services for Rare Diseases (RDRS), Reference Services for Newborn Screening (NSRS), and University Hospitals distributed in all Brazilian regions. OBJECTIVE: The aim of the study was to map the availability and distribution of the BPCCPRD diagnostic procedures in the Brazilian Unified Health System through RARAS. METHOD: Data were collected through a questionnaire on the Research Electronic Data Capture platform, with 22 questions regarding the availability of procedures. Thirty-seven coordinators from RARAS participating centers received the questionnaire link for participation by email from August/2020 to March/2021. All participating institutions ethically approved this project. RESULTS: Of the 37 institutions, 23 (62.16%) offered cytogenetic tests, 20 (54.05%) offered molecular procedures, and 22 (59.46%) offered inborn errors of metabolism diagnostic tests. The Southern blot analysis, enzyme assays on cultured tissue and urinary organic acid tests had the highest outsourcing rate. On the other hand, the procedures most frequently performed on-site were bone marrow karyotype and long-term cultured karyotype. It was observed that 10 of the 37 centers (27%) did not provide access to investigated procedures (on-site or outsourced). The North and Midwest regions stood out in terms of the unavailability of such techniques in at least 40% of the evaluated institutions. DISCUSSION AND CONCLUSION: This study reveals large discrepancies in the supply of diagnostic procedures in the Brazilian territory. Moreover, there is a broad collaboration between services through the outsourcing of multiple diagnostic techniques to address this issue. Finally, this work corroborates the importance of mapping services for the diagnosis and treatment of individuals with RDs to propose actions for the better supply and distribution of these procedures.
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spelling pubmed-106144402023-10-31 Availability of Genetic Tests in Public Health Services in Brazil: Data from the Brazilian Rare Diseases Network de Oliveira, Bibiana Mello Neiva, Mariane Barros Carvalho, Isabelle Schwartz, Ida Vanessa Doederlein Alves, Domingos Félix, Temis Maria Public Health Genomics Research Article INTRODUCTION: The Brazilian Policy for Comprehensive Care for People with Rare Diseases (BPCCPRD) was published in 2014, accrediting several reference centers and incorporating many genetic tests for the diagnosis of rare diseases (RDs). The Brazilian Network of Rare Diseases (RARAS) comprises more than 40 institutions that offer diagnosis and treatment for RDs in Brazil. This network includes Reference Services for Rare Diseases (RDRS), Reference Services for Newborn Screening (NSRS), and University Hospitals distributed in all Brazilian regions. OBJECTIVE: The aim of the study was to map the availability and distribution of the BPCCPRD diagnostic procedures in the Brazilian Unified Health System through RARAS. METHOD: Data were collected through a questionnaire on the Research Electronic Data Capture platform, with 22 questions regarding the availability of procedures. Thirty-seven coordinators from RARAS participating centers received the questionnaire link for participation by email from August/2020 to March/2021. All participating institutions ethically approved this project. RESULTS: Of the 37 institutions, 23 (62.16%) offered cytogenetic tests, 20 (54.05%) offered molecular procedures, and 22 (59.46%) offered inborn errors of metabolism diagnostic tests. The Southern blot analysis, enzyme assays on cultured tissue and urinary organic acid tests had the highest outsourcing rate. On the other hand, the procedures most frequently performed on-site were bone marrow karyotype and long-term cultured karyotype. It was observed that 10 of the 37 centers (27%) did not provide access to investigated procedures (on-site or outsourced). The North and Midwest regions stood out in terms of the unavailability of such techniques in at least 40% of the evaluated institutions. DISCUSSION AND CONCLUSION: This study reveals large discrepancies in the supply of diagnostic procedures in the Brazilian territory. Moreover, there is a broad collaboration between services through the outsourcing of multiple diagnostic techniques to address this issue. Finally, this work corroborates the importance of mapping services for the diagnosis and treatment of individuals with RDs to propose actions for the better supply and distribution of these procedures. S. Karger AG 2023-06-23 /pmc/articles/PMC10614440/ /pubmed/37356424 http://dx.doi.org/10.1159/000531547 Text en © 2023 The Author(s).Published by S. Karger AG, Basel https://creativecommons.org/licenses/by-nc/4.0/This article is licensed under the Creative Commons Attribution-NonCommercial 4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission.
spellingShingle Research Article
de Oliveira, Bibiana Mello
Neiva, Mariane Barros
Carvalho, Isabelle
Schwartz, Ida Vanessa Doederlein
Alves, Domingos
Félix, Temis Maria
Availability of Genetic Tests in Public Health Services in Brazil: Data from the Brazilian Rare Diseases Network
title Availability of Genetic Tests in Public Health Services in Brazil: Data from the Brazilian Rare Diseases Network
title_full Availability of Genetic Tests in Public Health Services in Brazil: Data from the Brazilian Rare Diseases Network
title_fullStr Availability of Genetic Tests in Public Health Services in Brazil: Data from the Brazilian Rare Diseases Network
title_full_unstemmed Availability of Genetic Tests in Public Health Services in Brazil: Data from the Brazilian Rare Diseases Network
title_short Availability of Genetic Tests in Public Health Services in Brazil: Data from the Brazilian Rare Diseases Network
title_sort availability of genetic tests in public health services in brazil: data from the brazilian rare diseases network
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10614440/
https://www.ncbi.nlm.nih.gov/pubmed/37356424
http://dx.doi.org/10.1159/000531547
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