Literature DB >> 22533694

The challenges of incorporating genetic testing in the unified national health system in Brazil.

Débora Gusmão Melo1, Jorge Sequeiros.   

Abstract

Genetic diseases and congenital anomalies are the second most common cause of infant mortality in Brazil. In 2009, the Ministry of Health established the National Policy for Integral Attention in Clinical Genetics in the Brazilian Unified National Health System (UNHS). This policy is not yet regulated, and there is a fear that, in the name of the comprehensiveness of health care, genetic testing might be carried out without due care and criteria, increasing costs to the UNHS. Currently, only a small population has access to genetic testing, through teaching hospitals or private health care. The biggest challenge in Brazil, in this area, is to be able to set the right standards and assessment processes about clinical utility, testing priorities, dispersal of resources, and distribution of skilled professionals. Expanding access to users of the Brazilian UNHS will mean mining the technical, social, and ethical aspects about medical genetics services.

Entities:  

Mesh:

Year:  2012        PMID: 22533694     DOI: 10.1089/gtmb.2011.0286

Source DB:  PubMed          Journal:  Genet Test Mol Biomarkers        ISSN: 1945-0257


  9 in total

1.  Genomic analysis in the clinic: benefits and challenges for health care professionals and patients in Brazil.

Authors:  Patrícia Ashton-Prolla; José Roberto Goldim; Filippo Pinto E Vairo; Ursula da Silveira Matte; Jorge Sequeiros
Journal:  J Community Genet       Date:  2015-06-04

2.  Genetics in primary health care and the National Policy on Comprehensive Care for People with Rare Diseases in Brazil: opportunities and challenges for professional education.

Authors:  Débora Gusmão Melo; Pamela Karen de Paula; Stephania de Araujo Rodrigues; Lucimar Retto da Silva de Avó; Carla Maria Ramos Germano; Marcelo Marcos Piva Demarzo
Journal:  J Community Genet       Date:  2015-04-18

3.  Ethical, social, and cultural issues related to clinical genetic testing and counseling in low- and middle-income countries: a systematic review.

Authors:  Adrina Zhong; Benedict Darren; Bethina Loiseau; Li Qun Betty He; Trillium Chang; Jessica Hill; Helen Dimaras
Journal:  Genet Med       Date:  2018-08-03       Impact factor: 8.822

4.  [Neonatal screening for hemoglobinopathies in São Carlos, São Paulo, Brazil: analysis of a series of cases].

Authors:  Camila de Azevedo Silva; Letícia Botigeli Baldim; Geiza César Nhoncanse; Isabeth da Fonseca Estevão; Débora Gusmão Melo
Journal:  Rev Paul Pediatr       Date:  2015-01-23

5.  Genetic counseling and presymptomatic testing programs for Machado-Joseph Disease: lessons from Brazil and Portugal.

Authors:  Lavínia Schuler-Faccini; Claudio Maria Osorio; Flavia Romariz; Milena Paneque; Jorge Sequeiros; Laura Bannach Jardim
Journal:  Genet Mol Biol       Date:  2014-03       Impact factor: 1.771

6.  Ethical, social, and cultural issues related to clinical genetic testing and counseling in low- and middle-income countries: protocol for a systematic review.

Authors:  Adrina Zhong; Benedict Darren; Helen Dimaras
Journal:  Syst Rev       Date:  2017-07-11

Review 7.  What Health System Challenges Should Responsible Innovation in Health Address? Insights From an International Scoping Review.

Authors:  Pascale Lehoux; Federico Roncarolo; Hudson Pacifico Silva; Antoine Boivin; Jean-Louis Denis; Réjean Hébert
Journal:  Int J Health Policy Manag       Date:  2019-02-01

8.  Costs of genetic testing: Supporting Brazilian Public Policies for the incorporating of molecular diagnostic technologies.

Authors:  Rosane Paixão Schlatter; Ursula Matte; Carisi Anne Polanczyk; Patrícia Koehler-Santos; Patricia Ashton-Prolla
Journal:  Genet Mol Biol       Date:  2015-08-21       Impact factor: 1.771

9.  Rare single gene disorders: estimating baseline prevalence and outcomes worldwide.

Authors:  Hannah Blencowe; Sowmiya Moorthie; Mary Petrou; Hanan Hamamy; Sue Povey; Alan Bittles; Stephen Gibbons; Matthew Darlison; Bernadette Modell
Journal:  J Community Genet       Date:  2018-08-14
  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.